Tuesday, 15 July 2014

claim the side effects of drinking alcohol


Long-term effects of alcohol


The long-term effects of alcohol (ethanol) consumption range from cardioprotective health benefits for low to moderate alcohol consumption in industrialized societies with higher rates of cardiovascular disease[2][3] to severe detrimental effects in cases of chronic alcohol abuse.[4] High levels of alcohol consumption are associated with an increased risk of alcoholismmalnutritionchronic pancreatitisalcoholic liver disease, and cancer. In addition, damage to the central nervous system and peripheral nervous systemcan occur from chronic alcohol abuse.[5][6] The long-term use of alcohol is capable of damaging nearly every organ and system in the body.[7] The developing adolescent brain is particularly vulnerable to the toxic effects of alcohol.[8] In addition, the developing fetal brain is also vulnerable, and fetal alcohol syndrome (FAS) may result if pregnant mothers consume alcohol.
The inverse relation in Western cultures between alcohol consumption and cardiovascular disease has been known for over 100 years.[9] Many physicians do not promote alcohol consumption, however, given the many health concerns associated with it. Some suggest that alcohol should be regarded as a recreational drug, and prefer exercise and good nutrition to combat cardiovascular disease.[10][11] Others have argued that the benefits of moderate alcohol consumption may be outweighed by other increased risks, including those of injuriesviolencefetal damage, liver disease, and certain forms of cancer.

Withdrawal effects and dependence are also almost identical.[13] Alcohol at moderate levels has some positive and negative effects on health. The negative effects include increased risk of liver diseasesoropharyngeal canceresophageal cancer andpancreatitis. Conversely moderate intake of alcohol may have some beneficial effects on gastritis and cholelithiasis.[14] Of the total number of deaths and diseases caused by alcohol, most happen to the majority of the population who are moderate drinkers, rather than the heavy drinker minority.[15] Chronic alcohol misuse and abuse has serious effects on physical and mental health. Chronic excess alcohol intake, or alcohol dependence, can lead to a wide range of neuropsychiatric orneurological impairment, cardiovascular disease, liver disease, and malignant neoplasms. The psychiatric disorders which are associated with alcoholism include major depressiondysthymiamaniahypomaniapanic disorderphobiasgeneralized anxiety disorderpersonality disordersschizophreniasuicideneurologic deficits (e.g. impairments of working memory,emotionsexecutive functionsvisuospatial abilities and gait and balance) and brain damage. Alcohol dependence is associated with hypertensioncoronary heart disease, and ischemic strokecancer of the respiratory system, and alsocancers of the digestive systemliverbreast and ovaries. Heavy drinking is associated with liver disease, such as cirrhosis.[16]Excessive alcohol consumption can have a negative impact on aging.

Recent studies have focused on understanding the mechanisms by which moderate alcohol consumption confers cardiovascular benefit.[18] One study has suggested a beneficial effect of alcohol on patients with hypertension.

Alcohol-related death


Over-consumption of alcohol causes many deaths worldwide. The overall mortality from alcohol use was found to be similar to that of the effect of physical inactivity.[20] A review in 2009 found that "the net effect of alcohol consumption on health is detrimental, with an estimated 3.8% of all global deaths and 4.6% of global disability-adjusted life-years attributable to alcohol."[21]
Extensive research of Western cultures has consistently shown increased survival associated with light to moderate alcohol consumption.[22] A 23-year prospective study of 12,000 male British physicians aged 48–78, found that overall mortality was significantly lower in current drinkers compared to non-drinkers even after correction for ex-drinkers. This benefit was strongest for ischemic heart disease, but was also noted for other vascular disease and respiratory disease. Death rate amongst current drinkers was higher for 'alcohol augmentable' disease such as liver disease and oral cancers, but these deaths were much less common than cardiovascular and respiratory deaths. The lowest mortality rate was found for consumption of 8 to 14 'units' per week. In the UK a unit is defined as 10ml or 8g of pure alcohol.[23] Higher consumption increased overall mortality rate, but not above that of non-drinkers.[24] Other studies have found age-dependent mortality risks of low-to-moderate alcohol use: an increased risk for individuals aged 16-34 (due to increased risk of cancers, accidents, liver disease, and other factors), but a decreased risk for individuals ages 55+ (due to lower incidence of ischemic heart disease).

This is consistent with other research that found a J-curve dependency between alcohol consumption and total mortality among middle aged and older men. While the mortality rates of ex-drinkers and heavy drinkers are significantly elevated, the all-cause mortality rates may be 15-18% lower among moderate drinkers. Although the definition of a drinkvaries between studies and countries, this meta-analysis found that low levels of alcohol intake, defined as 1-2 drinks per day for women and 2-4 drinks per day for men, was associated with lower mortality than abstainers.[26] This claim was challenged by another study[27][28] that found that in certain low quality studies occasional drinkers or ex-drinkers were included as abstainers, resulting in the increased mortality in that group. However, the J-curve for total and CHD mortality was reconfirmed by studies that took the mentioned confounders into account. There seems to be little discussion of what proportion of individuals classified as abstainers are those already at greater risk of mortality due to chronic conditions and do not or cannot consume alcohol for reasons of health or harmful interactions with medication.

The observed decrease in mortality of light-to-moderate drinkers compared to never drinkers might be partially explained by superior health and social status of the drinking group;[33] however, the protective effect of alcohol in light to moderate drinkers remains significant even after adjusting for these confounders.[30][32] Additionally, confounders such as underreporting of alcohol intake might lead to the underestimation of how much mortality is reduced in light-to-moderate drinkers.[29][34]
A 2010 study confirmed the beneficial effect of moderate alcohol consumption on mortality.[32] Subjects were grouped into abstainers, light, moderate, and heavy drinkers. The order of mortality rates from lowest to highest were moderate, light, heavy, and abstainers. The increased risk for abstainers was twice the mortality rate as for moderate drinkers. This study specifically sought to control for confounding factors including the problem of ex-drinkers considered as non-drinkers.[32] According to another study, drinkers with heavy drinking occasions (six or more drinks at a time) have a 57% higher all-cause mortality than drinkers without heavy drinking occasions.[35]
Mortality is lowest among young abstainers and highest among young heavy drinkers.[36]
In contrast to studies of Western cultures, research in other cultures has yielded some opposite findings. The landmark INTERHEART Study has revealed that alcohol consumption in South Asians was not protective against CAD in sharp contrast to other populations who benefit from it.[37] In fact Asian Indians who consume alcohol had a 60% higher risk of heart attack which was greater with local spirits (80%) than branded spirits (50%).[38] The harm was observed in alcohol users classified as occasional as well as regular light, moderate, and heavy consumers.[38]
Another large study of 4465 subjects in India also confirmed the possible harm of alcohol consumption on coronary risk in men. Compared to lifetime abstainers, alcohol users had higher blood sugar (2 mg/dl), blood pressure (2 mm Hg) levels, and the HDL-C levels (2 mg/dl) and significantly higher tobacco use (63% vs. 21%).[38]

Death rates in various countries


Many countries collect statistics on alcohol-related deaths. While some categories relate to short-term effects, such as accidents, many relate to long-term effects of alcohol.

Russia


One study claims that "excessive alcohol consumption in Russia, particularly by men, has in recent years caused more than half of all the deaths at ages 15-54 years."[39]However, there are some difficulties with this study. For instance the same study also found a protective effect of heavy drinking on breast cancer mortality. This contradicts the well established scientific view that alcohol increases breast cancer risk.[40] On this account in further correspondence it was advised that "careful interpretation of mortality statistics in relation to alcohol use is needed, taking into account other relevant risk factors, incidence, and survival."[41]
The authors replied that "whether or not the apparent shortfall in breast cancer mortality among heavy drinkers is real, it accounts for only about 0·1% of adult deaths in Russia. Careful interpretation of it is therefore of little relevance to the findings for alcohol and overall mortality".

United Kingdom[edit]

A governmental report from Britain has found that "There were 8,724 alcohol-related deaths in 2007, lower than 2006, but more than double the 4,144 recorded in 1991. The alcohol-related death rate was 13.3 per 100,000 population in 2007, compared with 6.9 per 100,000 population in 1991."[42] In Scotland, the NHS estimate that in 2003 one in every 20 deaths could be attributed to alcohol.[43] A 2009 report noted that the death rate from alcohol-related disease was 9,000, a number three times that of 25 years previously.[44]

United States[edit]

The Centers for Disease Control and Prevention report, "From 2001–2005, there were approximately 79,000 deaths annually attributable to excessive alcohol use. In fact, excessive alcohol use is the 3rd leading lifestyle-related cause of death for people in the United States each year."[45] A 1993 study estimated US deaths through alcohol at 100,000.[46]

Longevity[edit]

In a 2010 long-term study of an older population, the beneficial effects of moderate drinking were confirmed. Both abstainers and heavy drinkers showed an increased mortality of about 50% over moderate drinkers after adjustment for confounding factors.[47]
Some animal studies have found increased longevity with exposure to various alcohols. The roundworm Caenorhabditis elegans has been used as a model for aging and age-related diseases.[48] The lifespan of these worms has been shown to double when fed 0.005% ethanol, but does not markedly increase at higher concentrations. Supplementing starved cultures with n-propanol and n-butanol also extended lifespan.[49]

Cardiovascular system


A meta-analysis of 34 studies found a reduced risk of mortality from coronary heart disease in men who drank 2 - 4 drinks per day and women who drank 1 - 2 drinks per day.[26]Alcohol has been found to have anticoagulant properties.[50][51] Thrombosis is lower among moderate drinkers than abstainers.[52] A meta-analysis of randomized trials found that alcohol consumption in moderation decreases serum levels of fibrinogen, a protein that promotes clot formation, while it increases levels of tissue type plasminogen activator, an enzyme that helps dissolve clots.[53] These changes were estimated to reduce coronary heart disease risk by about 24%. Another meta-analysis in 2011 found favorable changes in HDL cholesterol, adiponectin, and fibrinogen associated with moderate alcohol consumption.[54]
Also, serum levels of C-reactive protein (CRP), a marker of inflammation and predictor of CHD (coronary heart disease) risk, are lower in moderate drinkers than in those who abstain from alcohol, suggesting that alcohol consumption in moderation might have anti-inflammatory effects.[55][56][57]
Despite epidemiological evidence, many have cautioned against recommendations for the use of alcohol for health benefits. A physician from the World Health Organisationlabeled such alcohol promotion as "ridiculous and dangerous".[58][59] One reviewer has noted, "Despite the wealth of observational data, it is not absolutely clear that alcohol reduces cardiovascular risk, because no randomized controlled trials have been performed. Alcohol should never be recommended to patients to reduce cardiovascular risk as a substitute for the well-proven alternatives of appropriate diet, exercise, and drugs."[60] It has been argued[who?] that the health benefits from alcohol are at best debatable and may have been exaggerated by the alcohol industry. Some investigators hold that alcohol should be regarded as a recreational drug with potentially serious adverse effects on health and should not be promoted for cardio-protection.[10]
Nevertheless, a large prospective non-randomized study has shown that moderate alcohol intake in individuals already at low risk based on body mass index, physical activity, smoking, and diet, yields further improvement in cardiovascular risk.[61] Furthermore, a multicenter randomized diet study published in 2013 found that a Mediterranean-diet, which included an encouragement to daily wine consumption in habitual drinkers, led to a dramatic reduction in cardiovascular events.[62]

Peripheral arterial disease[edit]

A prospective study published in 1997 found "moderate alcohol consumption appears to decrease the risk of PAD in apparently healthy men."[63] In a large population-based study, moderate alcohol consumption was inversely associated with peripheral arterial disease in women but not in men. But when confounding by smoking was considered, the benefit extended to men. The study concluded "an inverse association between alcohol consumption and peripheral arterial disease was found in nonsmoking men and women."[64][65]

Intermittent claudication[edit]

A study found that moderate consumption of alcohol had a protective effect against intermittent claudication. The lowest risk was seen in men who drank 1 to 2 drinks per day and in women who drank half to 1 drink per day.[66]

Heart attack and stroke[edit]

Drinking in moderation has been found to help those who have suffered a heart attack survive it.[67][68][69] However, excessive alcohol consumption leads to an increased risk ofheart failure.[70] A review of the literature found that half a drink of alcohol offered the best level of protection. However, they noted that at present there have been no randomised trials to confirm the evidence which suggests a protective role of low doses of alcohol against heart attacks.[71] However, moderate alcohol consumption is associated with hypertension.[12] There is an increased risk of hypertriglyceridemiacardiomyopathyhypertension, and stroke if 3 or more standard drinks of alcohol are taken per day.[72]

Cardiomyopathy[edit]

Large amount of alcohol over the long term can lead to alcoholic cardiomyopathy. Alcoholic cardiomyopathy presents in a manner clinically identical to idiopathic dilated cardiomyopathy, involving hypertrophy of the musculature of the heart that can lead to congestive heart failure.[73]

Hematologic diseases[edit]

Alcoholics may have anemia from several causes;[74] they may also develop thrombocytopenia from direct toxic effect on megakaryocytes, or from hypersplenism.

Nervous system[edit]

Results of the ISCD 2010 study ranking the levels of damage caused by drugs, in the opinion of drug-harm experts. When harm to self and others is summed, alcohol was the most harmful of all drugs considered, scoring 72%.
Chronic heavy alcohol consumption impairs brain development, causes alcohol dementiabrain shrinkagephysical dependence, increases neuropsychiatric and cognitive disorders and causes distortion of the brain chemistry. At present, due to poor study design and methodology, the literature is inconclusive on whether moderate alcohol consumption increases the risk of dementia or decreases it.[75]Evidence for a protective effect of low to moderate alcohol consumption on age related cognitive decline and dementia has been suggested by some research, however, other research has not found a protective effect of low to moderate alcohol consumption.[76] Some evidence suggests that low to moderate alcohol consumption may speed up brain volume loss.[77] Chronic consumption of alcohol may result in increased plasma levels of the toxic amino acid homocysteine;[78][79] which may explain alcohol withdrawal seizures,[80] alcohol-induced brain atrophy[81] and alcohol-related cognitive disturbances.[82] Alcohol's impact on the nervous system can also include disruptions of memory and learning (see Effects of alcohol on memory), such as resulting in a blackout phenomenon.

Strokes[edit]

Epidemiological studies of middle-aged populations generally find the relationship between alcohol intake and the risk of stroke to be either U- or J-shaped.[83][84][85][86] There may be very different effects of alcohol based on the type of stroke studied. The predominate form of stroke in Western cultures is ischemic, whereas non-western cultures have more hemorrhagic stroke. In contrast to the beneficial effect of alcohol on ischemic stroke, consumption of more than 2 drinks per day increases the risk of hemorrhagic stroke. The National Stroke Association estimates this higher amount of alcohol increases stroke risk by 50%.[87] "For stroke, the observed relationship between alcohol consumption and risk in a given population depends on the proportion of strokes that are hemorrhagic. Light-to-moderate alcohol intake is associated with a lower risk of ischemic stroke which is likely to be, in part, causal. Hemorrhagic stroke, on the other hand, displays a loglinear relationship with alcohol intake."[88]

Brain[edit]

Alcohol abuse is associated with widespread and significant brain lesions. Alcohol related brain damage is not only due to the direct toxic effects of alcohol; alcohol withdrawal, nutritional deficiency, electrolyte disturbances, and liver damage are also believed to contribute to alcohol-related brain damage.[89] The long-term effects of alcohol on brain chemistry is an important cause of chronic fatigue.[90]

Cognition and dementia[edit]

Excessive alcohol intake is associated with impaired prospective memory. This impaired cognitive ability leads to increased failure to carry out an intended task at a later date, for example, forgetting to lock the door or to post a letter on time. The higher the volume of alcohol consumed and the longer consumed, the more severe the impairments.[91] One of the organs most sensitive to the toxic effects of chronic alcohol consumption is the brain. In France approximately 20% of admissions to mental health facilities are related to alcohol-related cognitive impairment, most notably alcohol-related dementia. Chronic excessive alcohol intake is also associated with serious cognitive decline and a range of neuropsychiatric complications. The elderly are the most sensitive to the toxic effects of alcohol on the brain.[92] There is some inconclusive evidence that small amounts of alcohol taken in earlier adult life is protective in later life against cognitive decline and dementia.[93] However, a study concluded, "Our findings suggest that, despite previous suggestions, moderate alcohol consumption does not protect older people from cognitive decline."[94]
Acetaldehyde is produced from ethanol metabolism by the liver. The acetaldehyde is further metabolized by the enzyme acetaldehyde dehydrogenase. A deficiency of this enzyme is not uncommon in individuals from Northeastern Asia as pointed out in a study from Japan.[95] This study has suggested these individuals may be more susceptible to late-onsetAlzheimer's disease, however this higher risk is associated with the enzyme deficiency not with alcohol consumption. Individuals with this defect generally do not drink alcohol.
Wernicke-Korsakoff syndrome is a manifestation of thiamine deficiency, usually as a secondary effect of alcohol abuse.[96] The syndrome is a combined manifestation of two eponymous disorders, Korsakoff's Psychosis and Wernicke's encephalopathy, named after Drs. Sergei Korsakoff and Carl Wernicke. Wernicke's encephalopathy is the acute presentation of the syndrome and is characterised by a confusional state while Korsakoff's psychosis main symptoms are amnesia and executive dysfunction.[97]

Essential tremor


Essential tremors can be temporarily relieved in up to two-thirds of patients by drinking small amounts of alcohol.[98]
Ethanol is known to activate aminobutyric acid type A (GABAA) and inhibit N-methyl-D-aspartate (NMDA) glutamate receptors, which are both implicated in essential tremor pathology [99] and could underlie the ameliorative effects.[100][101] Additionally, the effects of ethanol have been studied in different animal essential tremor models.
For more details on this topic, see Essential tremor

Sleep[edit]

Main article: Alcohol use and sleep
Chronic use of alcohol used to induce sleep can lead to insomnia. Frequent moving between sleep stages occurs, with awakenings due to headaches and diaphoresis. Stopping chronic alcohol abuse can also lead to profound disturbances of sleep with vivid dreams. Chronic alcohol abuse is associated with NREM stage 3 and 4 sleep as well as suppression of REM sleep and REM sleep fragmentation. During withdrawal REM sleep is typically exaggerated as part of a rebound effect.[102]

Mental health effects[edit]

High rates of major depressive disorder occur in heavy drinkers and those who abuse alcohol. Whether it is more true that major depressive disorder causes self-medicating alcohol abuse, or the increased incidence of the disorder in alcohol abusers is caused by the drinking, is not known though some evidence suggests drinking causes the disorder.[103] Alcohol misuse is associated with a number of mental health disorders and alcoholics have a very high suicide rate.[104] A study of people hospitalised for suicide attempts found that those who were alcoholics were 75 times more likely to go on to successfully commit suicide than non-alcoholic suicide attempters.[105] In the general alcoholic population the increased risk of suicide compared to the general public is 5-20 times greater. About 15 percent of alcoholics commit suicide. Abuse of other drugs is also associated with an increased risk of suicide. About 33 percent of suicides in the under 35s are due to alcohol or other substance misuse.[106]
Social skills are significantly impaired in people suffering from alcoholism due to the neurotoxic effects of alcohol on the brain, especially the prefrontal cortex area of the brain. The social skills that are impaired by alcohol abuse include impairments in perceiving facial emotions, prosody perception problems and theory of mind deficits; the ability to understand humour is also impaired in alcohol abusers.[107]
Studies have shown that alcohol dependence relates directly to cravings and irritability.[108] Another study has shown that alcohol use is a significant predisposing factor towardsantisocial behavior in children.[109] Depression, anxiety and panic disorder are disorders commonly reported by alcohol dependent people. Alcoholism is associated with dampened activation in brain networks responsible for emotional processing (e.g. the amygdala and hippocampus).[110] Evidence that the mental health disorders are often induced by alcohol misuse via distortion of brain neurochemistry is indicated by the improvement or disappearance of symptoms that occurs after prolonged abstinence, although problems may worsen in early withdrawal and recovery periods.[111][112][113] Psychosis is secondary to several alcohol-related conditions including acute intoxication and withdrawal after significant exposure.[114] Chronic alcohol misuse can cause psychotic type symptoms to develop, more so than with other drugs of abuse. Alcohol abuse has been shown to cause an 800% increased risk of psychotic disorders in men and a 300% increased risk of psychotic disorders in women which are not related to pre-existing psychiatric disorders. This is significantly higher than the increased risk of psychotic disorders seen from cannabis use making alcohol abuse a very significant cause of psychotic disorders.[115] Approximately 3 percent of people who are alcohol dependent experience psychosis during acute intoxication or withdrawal. Alcohol-related psychosis may manifest itself through a kindling mechanism. The mechanism of alcohol-related psychosis is due to distortions to neuronal membranes, gene expression, as well as thiamin deficiency. It is possible in some cases that alcohol abuse via a kindling mechanism can cause the development of a chronic substance-induced psychotic disorder, i.e. schizophrenia. The effects of an alcohol-related psychosis include an increased risk of depression and suicide as well as psychosocial impairments.[114] However, moderate wine drinking has been shown to lower the risk for depression.[116]
While alcohol initially helps social phobia or panic symptoms, with longer term alcohol misuse can often worsen social phobia symptoms and can cause panic disorder to develop or worsen, during alcohol intoxication and especially during the alcohol withdrawal syndrome. This effect is not unique to alcohol but can also occur with long term use of drugs which have a similar mechanism of action to alcohol such as the benzodiazepines which are sometimes prescribed as tranquillizers to people with alcohol problems.[117]Approximately half of patients attending mental health services for conditions including anxiety disorders such as panic disorder or social phobia suffer from alcohol orbenzodiazepine dependence. It was noted that every individual has an individual sensitivity level to alcohol or sedative hypnotic drugs and what one person can tolerate without ill health another will suffer very ill health and that even moderate drinking can cause rebound anxiety syndromes and sleep disorders. A person who is suffering the toxic effects of alcohol will not benefit from other therapies or medications as they do not address the root cause of the symptoms.[118]

Digestive system and weight gain


The impact of alcohol on weight-gain is contentious: some studies find no effect, others find decreased[120] or increased effect on weight gain.
Alcohol use increases the risk of chronic gastritis (stomach inflammation);[4][121] it is one cause of cirrhosishepatitis, and pancreatitis in both its chronic and acute forms.

Metabolic syndrome[edit]

A study concluded, "Mild to moderate alcohol consumption is associated with a lower prevalence of the metabolic syndrome, with a favorable influence on lipids, waist circumference, and fasting insulin. This association was strongest among whites and among beer and wine drinkers."[122] This is also true for Asians. A J-curve association between alcohol intake and metabolic syndrome was found: "The results of the present study suggest that the metabolic syndrome is negatively associated with light alcohol consumption (1–15 g alcohol/d) in Korean adults". However, "odds ratios for the metabolic syndrome and its components tended to increase with increasing alcohol consumption."[123]

Gallbladder effects[edit]

Research has found that drinking reduces the risk of developing gallstones. Compared with alcohol abstainers, the relative risk of gallstone disease, controlling for age, sex, education, smoking, and body mass index, is 0.83 for occasional and regular moderate drinkers (< 25 ml of ethanol per day), 0.67 for intermediate drinkers (25-50 ml per day), and 0.58 for heavy drinkers. This inverse association was consistent across strata of age, sex, and body mass index."[124] Frequency of drinking also appears to be a factor. "An increase in frequency of alcohol consumption also was related to decreased risk. Combining the reports of quantity and frequency of alcohol intake, a consumption pattern that reflected frequent intake (5-7 days/week) of any given amount of alcohol was associated with a decreased risk, as compared with nondrinkers. In contrast, infrequent alcohol intake (1-2 days/week) showed no significant association with risk.

A large self-reported study published in 1998 found no correlation between gallbladder disease and multiple factors including smoking, alcohol consumption, hypertension, and coffee consumption.[126] A retrospective study from 1997 found vitamin C (ascorbic acid) supplement use in drinkers was associated with a lower prevalence of gallbladder disease, but this association was not seen in non-drinkers.[127]

Liver disease[edit]

Alcoholic liver disease is a major public health problem. For example in the United States up to two million people have alcohol-related liver disorders.[128] Chronic alcohol abuse can cause fatty livercirrhosis and alcoholic hepatitis. Treatment options are limited and consist of most importantly discontinuing alcohol consumption. In cases of severe liver disease, the only treatment option may be a liver transplant from alcohol abstinent donors. Research is being conducted into the effectiveness of anti-TNFs. Certain complementary medications, e.g., milk thistle and silymarin, appear to offer some benefit.[128][129] Alcohol is a leading cause of liver cancer in the Western world, accounting for 32-45% of hepatic cancers. Up to half a million people in the United States develop alcohol-related liver cancer.[130][131] Moderate alcohol consumption also increases the risk of liver disease.[12]

Pancreatitis[edit]

Alcohol abuse is a leading cause of both acute pancreatitis and chronic pancreatitis.[132][133] Alcoholic pancreatitis can result in severe abdominal pain and may progress topancreatic cancer.[134] Chronic pancreatitis often results in intestinal malabsorption, and can result in diabetes.[135]

Other systems


Respiratory system[edit]

Chronic alcohol ingestion can impair multiple critical cellular functions in the lung.[citation needed] These cellular impairments can lead to increased susceptibility to serious complications from lung disease. Recent research cites alcoholic lung disease as comparable to liver disease in alcohol-related mortality.[citation needed] Alcoholics have a higher risk of developing acute respiratory distress syndrome (ARDS) and experience higher rates of mortality from ARDS when compared to non-alcoholics.[citation needed] Despite these effects, a large prospective study has shown a protective effect of moderate alcohol consumption on respiratory mortality.[24]

Kidney stones

Research indicates that drinking alcohol is associated with a lower risk of developing kidney stones. One study concludes, "Since beer seemed to be protective against kidney stones, the physiologic effects of other substances besides ethanol, especially those of hops, should also be examined."[136] "...consumption of coffee, alcohol, and vitamin C supplements were negatively associated with stones."[137] "After mutually adjusting for the intake of other beverages, the risk of stone formation decreased by the following amount for each 240-ml (8-oz) serving consumed daily: caffeinated coffee, 10%; decaffeinated coffee, 10%; tea, 14%; beer, 21%; and wine, 39%."[138] "...stone formation decreased by the following amount for each 240-mL (8-oz) serving consumed daily: 10% for caffeinated coffee, 9% for decaffeinated coffee, 8% for tea, and 59% for wine." (CIdata excised from last two quotes.).

Sexual dysfunction

Long term excessive intake of alcohol can lead to damage to the central nervous system and the peripheral nervous system resulting in loss of sexual desire and impotence in men.[140] This can result due to a reduction of testosterone from ethanol-induced testicular atrophy, resulting in increased feminisation of males and is a clinical feature of alcohol abusing males who have cirrhosis of the liver.[141]

Hormonal Imbalance

Excessive alcohol intake can result in hyperoestrogenisation.[142] It has been speculated that alcohol beverages may contain estrogen like compounds. In men, high levels of estrogen can lead to testicular failure and the development of feminine traits including development of male breasts, called gynecomastia.] In women, increased levels of estrogen due to excessive alcohol intake have been related to an increased risk of breast cancer.

Diabetes mellitus

A meta-analysis found with data from 477,200 individuals determined the dose-response relationships by sex and end point using lifetime abstainers as the reference group. The search revealed 20 cohort studies that met our inclusion criteria. A U-shaped relationship was found for both sexes. Compared with lifetime abstainers, the relative risk (RR) for type 2 diabetes among men was most protective when consuming 22 g/day alcohol (RR 0.87 [95% CI 0.76–1.00]) and became deleterious at just over 60 g/day alcohol (1.01 [0.71–1.44]). Among women, consumption of 24 g/day alcohol was most protective (0.60 [0.52–0.69]) and became deleterious at about 50 g/day alcohol (1.02 [0.83–1.26]).
Because former drinkers may be inspired to abstain due to health concerns, they may actually be at increased risk of developing diabetes, known as the sick-quitter effect. Moreover, the balance of risk of alcohol consumption on other diseases and health outcomes, even at moderate levels of consumption, may outweigh the positive benefits with regard to diabetes.
Additionally, the way in which alcohol is consumed (i.e., with meals or bingeing on weekends) affects various health outcomes. Thus, it may be the case that the risk of diabetes associated with heavy alcohol consumption is due to consumption mainly on the weekend as opposed to the same amount spread over a week.[146] In the United Kingdom "advice on weekly consumption is avoided".
Also, a twenty year twin study from Finland has shown that moderate alcohol consumption may reduce the risk of type 2 diabetes in men and women. However, binge drinking and high alcohol consumption was found to increase the risk of type 2 diabetes in women. [147] A study in mice has suggested a beneficial effect of alcohol in promoting insulin sensitivity.[148]

Rheumatoid arthritis

Regular consumption of alcohol is associated with an increased risk of gouty arthritis[149][150] and a decreased risk of rheumatoid arthritis. Two recent studies report that the more alcohol consumed, the lower the risk of developing rheumatoid arthritis. Among those who drank regularly, the one-quarter who drank the most were up to 50% less likely to develop the disease compared to the half who drank the least.[156]
The researchers noted that moderate alcohol consumption also reduces the risk of other inflammatory processes such as cardiovascualar disease. Some of the biological mechanisms by which ethanol reduces the risk of destructive arthritis and prevents the loss of bone mineral density (BMD), which is part of the disease process.[157]
A study concluded, "Alcohol either protects from RA or, subjects with RA curtail their drinking after the manifestation of RA".[158] Another study found, "Postmenopausal women who averaged more than 14 alcoholic drinks per week had a reduced risk of rheumatoid arthritis..."[159]

Osteoporosis

Moderate alcohol consumption is associated with higher bone mineral density in postmenopausal women. "...Alcohol consumption significantly decreased the likelihood [ofosteoporosis]."[160] "Moderate alcohol intake was associated with higher BMD in postmenopausal elderly women."[161] "Social drinking is associated with higher bone mineral density in men and women [over 45]."[162] However, alcohol abuse is associated with bone loss.

Skin[edit]

Chronic excessive alcohol abuse is associated with a wide range of skin disorders including urticariaporphyria cutanea tardaflushing, cutaneous stigmata of cirrhosispsoriasis,pruritusseborrheic dermatitis and rosacea.[165]
A 2010 study concluded, "Nonlight beer intake is associated with an increased risk of developing psoriasis among women. Other alcoholic beverages did not increase the risk of psoriasis in this study."[166]

Immune system

Bacterial infection

There is a protective effect of alcohol consumption against active infection with H. pylori[167] In contrast, alcohol intake (comparing those who drink > 30g of alcohol per day to non-drinkers) is not associated with higher risk of duodenal ulcer. Excessive alcohol consumption seen in alcoholics is a known risk factor for pneumonia.

Common cold


A study on the common cold found that "Greater numbers of alcoholic drinks (up to three or four per day) were associated with decreased risk for developing colds because drinking was associated with decreased illness following infection. However, the benefits of drinking occurred only among nonsmokers. [...] Although alcohol consumption did not influence risk of clinical illness for smokers, moderate alcohol consumption was associated with decreased risk for nonsmokers."[169]
Another study concluded, "Findings suggest that wine intake, especially red wine, may have a protective effect against common cold. Beer, spirits, and total alcohol intakes do not seem to affect the incidence of common cold.


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Steroids Side Effects


Most of the time, when steroids are mentioned, they’re brought up as the reason a particular athlete can run so fast, hit so many home runs, or make so many tackles. They are also claimed to have extraordinarily harsh side effects and for causing severely unforgiving and permanent damage. Everybody´s seen movies like "The Program" where steroids ruin a young athlete´s life, or perhaps "The Aaron Henry Story" on HBO, where a young athlete suffers lifelong problems from his steroid abuse. Most recently, I saw the movie "Spiderman" where the villain, the Green Goblin, admits to having his superhuman strength and psychotic personality from using "performance enhancers"!
I´m here to assure you that those types of horror stories are few and far between, and after consulting with literally hundreds of athletes and bodybuilders, I've almost never heard of anything even remotely resembling the popular "horror stories" we see in the media almost daily. I´ve certainly never seen anyone become Green Goblin-like from using them, either.

By reading this article, coaches, athletes, parents and teachers will learn the truth about anabolic steroid side effects, and will be able to make their own informed decisions regarding them. But I suspect that after reading what I have to say, as well as what the scientific literature says, the question of how bad steroids are will be a different question entirely; the only question remaining will be "why didn´t anyone tell me this before?"
When I initially started research for this piece, I consulted not only real-life athletes who had vast experience with anabolic steroid use, but also scientific and medical journals. The picture that unfolded before me was very different from the one typically painted by the mass media, and certainly much different than the one I found on www.steroidabuse.org, www.dea.org, and www.drugabuse.gov. Honestly, my research on the governmental sites revealed very little useful information. There were numerous unfounded claims, and plenty of talk about money being put into “studies”. In reality, the government "studies" on anabolic steroids were not medical studies at all. They were surveys given to various age groups, on steroid use, in order to generate statistics. There was nothing of medical value or scientific merit on those sites, despite the endless parade of doctors that seemed to be against their use. Here´s an example of one of the more absurd claims made on one of those sites:

Anabolic Steroid Side Effects:

1. Inhibition of Natural Hormones


The inhibition of natural hormones is likely the most common and probable side effect experienced from the use of anabolic steroids. In almost all cases, taking hormones will send a message to your endocrine system to reduce or stop producing it. This is because your body wants to remain in a very balanced state -- called ‘homeostasis’. To maintain homeostasis, the body seeks to avoid having too much or too little of any particular hormone. In the case of anabolic steroids, the brain signals the testicles to slow down, or even stop producing (depending on the type and amount of steroids taken) testosterone when there is too much circulating. Unfortunately, this happens when any kind of hormone is added into the body, so even if an athlete is not using testosterone, but is using other anabolic steroids, the body will still send this signal 99% of the time. Of course different steroids cause varying degrees of inhibition ranging from total shut down of endogenous (natural) testosterone production, to very mild reductions, where some natural hormones are still being produced and circulating. In almost all cases, this inhibition is over once the steroids aren´t active in the body anymore. In the following charts, we can see a mirror image of the level of activity during steroid (Nandrolone) administration, compared with the level of natural testosterone being produced. In other words, as the level of steroid rises (chart 2), the level of testosterone falls (chart 1), and vice versa.
level of testosterone falls - chart
Now, as that first chart shows, testosterone levels fell when Nandrolone (an anabolic steroid was administered, but interestingly, the following chart shows an almost identical mirror image, where the Nandrolone levels in the blood rise. What this indicates is that the amount of this particular steroid in the blood is directly and proportionately inhibiting natural testosterone production. Here´s the chart:
level of testosterone rises - chart
Most athletes who use anabolic steroids accept all of this as a necessary price to pay in order to experience the benefits from using steroids. In an effort to combat this, athletes have experimented throughout the years with various compounds to avoid or at least limit this problem. Human Chorionic Gonadotropin, anti-estrogens, and Selective Estrogen Receptor Antagonists (SERMs) are all used during a cycle, or after (or both) with this goal in mind. The following table shows the various hormonal levels of former steroid users who haven´t used them for a year (*called "ex-abusers" by the nice people who funded the test) versus current users (*abusers):
What we see in this chart is not surprising to anyone who is actually familiar with steroids, and not with media-hype. In people studied who haven t used steroids for a year, ALL of their measured hormones (testosterone, estrogen) were within the NORMAL RANGE! Clearly, the effects that steroids have on your hormones are reversible and the horror stories we’ve all read in the media about people who never regained normal hormonal function after one cycle are greatly exaggerated. I think anyone who is familiar with "After School Specials" about steroids will be very surprised at learning this fact. As for "The Aaron Henry Story" on HBO, I can t imagine how he has suffered side effects well into his 40’s when the steroid users in this study were totally fine after one year, and in some cases used more than he did!
(*Journal of Steroid Biochemistry and Molecular Biology. 84 (2003) 369-375)

2. Steroid Effects and Liver Damage

d-anabol,Dianabol,SteroidsLiver damage is probably the most sensationalized of all the possible steroid side effects. The media often focuses on this particular problem as if it occurs with every steroid, and in every person who takes them. Nothing could be further than the truth. Most anabolic steroids which are ingested orally pass through the liver, which functions as the body´s filtration system. When something goes through the liver, it is broken down by various enzymes, then passed along into the bloodstream. Most research on orally administered anabolic steroids focus on the fact that liver enzymes are elevated following ingestion. But does this necessarily mean that the liver is being damaged, does it? Of course not. Commonly, studies that focus on steroid toxicity often use absurd doses, or incorrectly focus on liver activity instead of damage. The liver functions as the filter for the human body, it´s going to be activated whenever something (not just a steroid) passes through it. Does that show that steroids damage the liver? Let´s see what the scientists say.

There was an eight-week study done in 1999, which looked at the effects of an 8-week cycle of oral steroids. The steroids examined were Halotestin (Fluoxymesterone), Dianabol (methylandrostanolone), or Winstrol (Stanozolol) on rats at the dose of 2mg/kg-body weight, administered five times a week for 8 weeks. That s almost 200mgs/day of any of those steroids, for a 200lb user. That is, generally speaking, much more than the average person would use on a cycle. In fact, I have never, in my years of researching steroids and speaking with athletes, heard of anybody using even close to 200mgs/day of Halotestin, Winstrol, or Dianabol, ever!
At the end of that study, in vivo, each rat still had liver enzyme levels that were within normal range!
(*Med Sci Sports Exerc. 1999 Feb;31(2):243-50, Rat liver lysosomal and mitochondrial activities are modified by anabolic-androgenic steroids. Molano F, Saborido A, Delgado J, Moran M, Megias A.)
In another study, 16 bodybuilders using steroids were compared to 12 bodybuilders who were not. Then the bodybuilders who had used steroids stopped taking them for three months, at which points, the researchers found that liver enzymes had returned to the same levels as the non users. After only 3 months!
(*Int J Sports Med 1996 Aug;17(6):429-33, Body composition, cardiovascular risk factors and liver function in long-term androgenic-anabolic steroids using bodybuilders three months after drug withdrawal. Hartgens F, Kuipers H, Wijnen JA, Keizer HA.)

We can see from the chart below that ex-steroid users have totally normal liver enzymes one year after they stop using. In fact, for some liver enzymes, even the current users have normal scores!
(*Journal of Steroid Biochemistry and Molecular Biology. 84 (2003) 369-375)

3. Steroid Effects on Cholesterol (Blood Lipid Profile)

Steroids can lower HDL cholesterol, and raise LDL cholesterol. HDL (high density lipoprotein, commonly referred to as "good cholesterol") helps to protect the arteries by bringing unused cholesterol to the liver where it is broken down. LDL on the other hand has the opposite effect. Some steroids can therefore cause high cholesterol levels with low HDL and high LDL. Some steroids are, of course, very mild on blood lipids, while others are notably harsh. In both cases, however, it is likely that a return to within normal parameters would occur shortly after steroid discontinuation.

 

4. Gynocomastia (Development of breast tissue in males)

The development of gynecomastia or feminization of the breast tissue in males is possible with anabolic steroids. This is due to an excess of estrogen being present in the body, through a process known as "aromatization" whereby androgens like testosterone are converted to estrogen. This excess estrogen then finds its way to the receptors in breast tissue and binds to them. This results in the possibility of female-like breast tissue, which must sometimes be removed by surgery. Most athletes experience itchiness of the nipples, followed by pain. Since this develops over several days, usually, the athlete has more than enough time to discontinue the use of the compounds he´s taking, or to attempt to counteract the breast tissue development while remaining on the cycle. The two most common ways to counteract gynecomastia are the use an anti-estrogen like Nolvadex or Clomiphene Citrate (best taken post-cycle) or Letrozole, a very strong Aromatase Inhibitor (AI)/anti-estrogenic compound is employed during cycle to effectively starve the growth of nourishing estrogen.
The initiation and progression of breast development involves a variety of pituitary (and ovarian, in women) hormones, as well as various local mediators. As you can see in the following chart, testosterone has the ability to aromatize (convert to estrogen), and eventually become part of the cascade of hormones that contribute to the development of breast tissue:
(GYNECOMASTIA: ETIOLOGY, DIAGNOSIS, AND TREATMENT Chapter 14 - Ronald S. Swerdloff, MD, Jason Ng, MD, and Gladys E. Palomeno, MD, March 1, 2004)

5. Acne and Anabolic Steroids

Anabolic steroids can cause the development of acne. However, the extent to which it is experienced can be due to a number of varying factors, with the particular steroids and exact dosages used being primary. The skin´s sebaceous glands have a particularly high affinity to Dihydrotestosterone, which is an androgen the body naturally produces from testosterone via the enzyme 5-alpha Reductase. Increased sebaceous gland activity promotes oily skin which can combine with bacteria and dead skin (normal wear and tear) eventually causing pores to become clogged more quickly than the body can cleanse them. This of course, is preventable by using only particular steroids, cleansing the skin regularly, and perhaps using a topical anti-androgen.
(1. Am J Clin Dermatol. 2002;3(8):571-8. 2. Clin Dermatol. 2004 Sep-Oct;22(5):419-28. 3. Pol Merkuriusz Lek. 2004 May;16(95):490-2.)

6. Roid Rage

Increased aggressiveness is often claimed to occur with anabolic steroid use. Although it´s highly rare (less than 5%), significant psychiatric symptoms have been found in some steroid users, including aggression and increased violence, mania, and even psychosis. However, it must be noted that in the studies performed there was no control group, making their results spurious at best. It can be logically assumed that naturally aggressive people (those with certain aggressive traits) are simply more inclined to use steroids, which further skews any research results. Can steroids enhance such aggressiveness? Possibly. Can steroids be to blame for anti-social, psychotic, "roid-rage" type of behaviors? Probably not. The evidence just isn´t there to support that such theories.
In fact, a landmark study was performed which examined different doses of testosterone administration on men aged 20-50, who had a variety of experience with steroids from having used them previously to not at all prior to the study. A variety of psychological tests were performed at the outset of the study as well as at the end. It was found was that no participant in the study had become violent as a result of the testosterone injections they had been receiving, although some said they felt more aggressive. This clearly indicates that there is a high level of control over possible violent or aggressive behavior that can result from steroid use. The researchers also noted that in terms of the psychological tests performed, some subjects showed little or no response to testosterone, with regards to psychological measures, while others experienced significant changes. Thus, general temperament clearly plays a large role in how one responds psychologically to steroid administration. In addition, when this study was compared with others, similar results were found:
Out of 109 cases studied, only 5 people exhibited Psychological (Manic or Hypomanic) effects. (*Archives of General Psychiatry, Volume 57, February 2000.)

7. Steroids and Baldness


Steroids can possibly cause men to start balding if they have a genetic predisposition towards Male Pattern Baldness. The gene for baldness is thought to reside in the X (male) chromosome exclusively, so a good general indication of whether someone is genetically predisposed towards being bald is to look at the men on their mothers side. Chances are that if the majority of them are bald, then the person will be carrying that gene too. The reason steroids can cause premature balding is that the scalp reacts to Dihydrotestosterone (DHT) quite strongly, and many steroids can either convert to DHT or are derived from it. Some anti-baldness medications can prevent this, such as Finasteride and Dutesteride. This is, of course, merely a cosmetic effect, and poses no real health issues. It could be catastrophic to a potential career with any one of a number of 80´s rock bands, but other than that, I can´t really see any real problems associated with hair loss; especially since it can be avoided when proper steps are taken and certain steroids are avoided.

8. Cardiovascular Problems from Anabolic Steroids


Anabolic steroids have been linked with cardiovascular issues. Part of this may be due to their effects on Blood Lipids (see above). But some of it is due to the fact that many steroid users have been found to have enlarged ventricles. This is actually very common in bodybuilders as well as powerlifters and other types of athletes, and is more indicative of the effect of weight training on the heart, rather than solely steroid use.

9. Virilization (Development of male characteristics in women)


This term refers masculinization, or development of male sexual characteristics that females could potentially suffer from steroid use. This side effect on women is often reversible after steroids are discontinued. Some typical signs of virilization are the development of a deeper voice, hirsuitism (growth of excess body hair), enlargement of external genitalia (clitoral enlargement), and possible male pattern baldness, or acne on the face or body. This is all dependent, of course, on the compounds used as well as the dosages employed. Personally, I have witnessed the most permanent of these effects to be the deepening of the voice due to the hypertrophy (growth) of the vocal chords. This is typically the most unwelcome side effect, as it makes it very obvious when a woman is using steroids. Of course, if this begins, the best course of action is to cease taking all steroids immediately. There are several ways to reverse this effect, the most common being to undergo a medical procedure known as vocal chord scraping. And yes, it´s exactly what it sounds like.

10. Stunted Growth (height)

clenbuterol,steroids,clenThe use of some steroids can possibly stunt the growth potential of still maturing children, teens and young adults. This is only possible with certain steroids, and not with others. In fact, certain steroids have been used in clinical settings to improve growth rates in children. It is probable that the premature closure of the epiphysial cartilage, which is most likely caused by aromatizable steroids, will lead to a possible growth inhibiting effect, and could ultimately result in a shorter adult height. This is most likely an irreversible side effect, as the growth plates would have fused and can not "re-open". Anavar (Oxandrolone) has been used to improve the height of growth stunted children, and it is probable that most other DHT-derived steroids could also be used for this purpose as could certain anti-estrogens.
In 99.9% of humans, the process of bone elongation ends at around the mid to late teen years. At this point, the growth plates are obliterated and disappear, after which no more elongation (typified by an increase in limb length, i.e. height) can take place. Elongation of the bone occurs here and at a second epiphysis at the end. The proliferation of the cartilage happens very quickly, actually fast enough to keep ahead of the bone generation that´s "chasing" it, called ossification, which is just the replacement of cartilage by bone. As long as the cartilage growth "stays ahead" of the bone, you grow taller, as bone replaces cartilage. When the bone finally catches the cartilage (because the cartilage slows its growth rate, not the bone), it ossifies, and "seals" the growth plate.
Here´s a growth plate picture, enhanced by radioactive dye (GP= Growth Plate), so you can sort of see the bone "catching" up with the cartilage.
(Human Anatomy and Physiology, 6th Edition, John W. Hole jr., Wm. C. Brown Publishers.)

10. Prostate Enlargement

Once again, this is only a possible side effect, but steroids can potentially cause enlargement of the prostate. The media-perpetuated claim of possible prostate cancer seems to be wholly unfounded, according to most research. In many cases, this enlargement is quickly remedied upon cessation ofanabolic steroid use. The first period of prostate prostate growth, occurs during puberty and occurs as a result of the testicular secretion of androgens. Then, much later on in life, there is often a second stage of growth. Although this was originally deemed to be a result of Dihydrotestosterone’s actions in the body, it is more likely due to estrogen combined with a small amount of either DHT or Testosterone. Thus, it’s not hard to imagine that taking steroids can potentially cause this type of prostate enlargement and cause trouble for a steroid taking athlete. Typically, a product such as Finasteride or Dutesteride is taken to avoid this problem, with a high degree of success.

11. High Blood Pressure

This problem is possibly the most easily remedied of all steroid side effects. It’s very common for steroid using athletes attempting to gain maximum bulk to abstain from all aerobic activity. This causes the body to work much harder to circulate blood. The typical water and sodium retention induced by certain steroids can also contribute to this side effect. If blood pressure is measured regularly to ensure that the value is not higher than 140/90, there should be no problems.

12. Kidney Problems

Certain anabolic steroid usage may place greater strain on the kidneys. Since kidneys are involved in the filtration and excretion processes, when a foreign substance is administered, they necessarily work harder. Some steroid users have noticed very dark urine while on a cycle, and this is indicative of the kidneys working overtime to accomplish their goal. One of the major offenders of this seems to be Trenbolone, which turns the user’s urine a very dark color. This problem is alleviated when enough water is consumed daily. Also, even though I know you’re probably getting sick of hearing this from me, the possibility of side effects is dependant on the dosage and type of administered compounds. Some steroids (Nandrolones) are even used to help treat people with kidney problems! So clearly, they aren’t as bad as they’re made out to be with regards to possible negative kidney-related side effects.

13. Immune System Changes

There is a large amount of data indicating that anabolic steroids may have some effect(s) on modulating the immune system. As with most potential side effects, this is largely dose and compound dependent. There is strong evidence that different analogues impact the immune system in differing ways. Testosterone and certain analogues have been shown to be possibly immunosuppressive, while Nandrolone and still other compounds have demonstrated immunostimulating properties. Both, however, have been found to be beneficial when given to AIDS patients, who clearly have an already compromised immune system. This is because the increase in lean body mass that those steroids can provide is consistent with an enhanced ability to fight off infections, enhanced survival rates, and a better quality of life.
(1.Int J Immunopharmacol. 1995 Nov;17(11):857-63. 2. J Steroid Biochem Mol Biol. 1990 Sep;37(1):71-6 3. AIDS. 1996 Jun;10(7):745-52. 4. Journal of Neuroimmunology 83 1998, 162-67.)

14. Growth of Excessive Body Hair

As expressed above in ‘Virilization’ steroids typically cause an increase in body hair growth. In a manner very similar to adolescence, the period when hair sprouts in places it formerly wasn’t due to the exposure of unusually high amounts of sex hormones, steroids serve as a synthetic initiator. Quite simply put, the rapid influx of sex hormones stimulates body hair development. This side effect is occurs in both males and females, and the hair growth can appear anywhere on the body with the exception of the head (where the opposite effect is sometimes seen due to the large number of DHT receptors). In women, this hair growth most often increases in traditionally manly locations on the body such as the face and back, but also increases on the legs, armpits, pubic region, arms, torso, hands/knuckles and feet. Although steroid discontinuation, reverses the irregular growth, it does not reverse or thin any hair grown during steroid administration. For men, such hair growth is barely noticeable except among the decisively less hairy members of the population, and even then it doesn’t really present a problem.
Effects of androgenic-anabolic steroids in athletes. Hartgens F, Kuipers H., Sports Med. 2004;34(8):513-54.

14. Water Retention and Bloating

Bloating, a.k.a. excess water retention is a very likely side effect of specific anabolic steroids. Generally speaking short-ester testosterone (Testosterone Propionate) and DHT-derived steroids (with the exception of Dianabol) do not cause significant bloating. Some 19-Nors, Dianabol, and medium to long-ester testosterones have a greater aromatization rate and excess estrogen typically (but not always) equates to greater muscle blurring water retention. For this reason such steroids are often included within bulking cycles and avoided during cutting cycles. Also contributing to the bloating are moderate to high levels of sodium, sugar, and synthetic sweetners like those found in diet drinks.
It's true that estrogen is required for optimal muscle development, which often makes bloating is an acceptable side effect during off-season training. Thus, there are periods of training during which athletes and bodybuilders are less concerned with, and affected by bloating. However, when seconds count, success is measured in inches, and muscular presentation readiness is of great importance, bloating is often off-set in numerous ways. Firstly, the above high propensity for bloating steroids and food sources are avoided. Secondly, with regard to steroid use AIs and SERMs (anti-estrogenics explained earlier) are employed to reduce estrogenic activity, and thereby promote lean, bloat-free physiques. The third weapon against bloat used by the athlete comes in the form of diuretics which flush extra fluids from the body. Some are mild (mostly mineral & herbal), others (mostly prescription) can be harsh, but both should be used respectfully to prevent debilitating cramping which can hinder both performance and presentation.
Psychological characteristics of adolescent steroid users. Burnett KF, Kleiman ME., Adolescence. 1994 Spring;29(113):81-9., Counseling Psychology Program, School of Education, University of Miami, Coral Gables, Florida 33124.

16. Sterility in Males and Females

Anavar,var,SteroidsTemporary sterility is a common side effect of steroids in both males and females. In fact, anabolic steroids are so proficient at this that they have actually been studied and approved by the World Health Organization as a male contraceptive possibility. Steroids do this by disrupting the various hormones in women which potentiate the ability to have regular menstrual cycles. In men, steroids lower Follicle Stimulating Hormone (FSH) to the point where normal production of sperm is not possible. This isn´t to say that nobody on a cycle has every conceived; quite the opposite, actually. There' ve been legions of "happy accidents" reported to me by athletes who were on cycles and thought they couldn´t possibly conceive.
Sterility caused by steroids is temporary, of course, and reverses post-cycle. This reversal is typically sped up by the post-cycle therapy which often involves the use of SERMs such as Nolvadex or Clomid , and/or Human Chorionic Gonadotropin.
(1. Fertil Steril. 2004 Jan;81(1):226. 2. Urology. 2000 Oct 1;56(4):669.3. J Clin Endocrinol Metab. 1985 Oct;61(4):746-52 4. Fertil Steril. 1994 May;61(5):911-4. 5. Andrologia. 1985 Sep-Oct;17(5):497-501 6. Urol Clin North Am. 1986 Aug;13(3):455-63.)

Steroid Effects Myth:

Believing Everything You Hear

Ok, so this last side effect isn´t really a steroid effect at all. But it’s true, nonetheless. It´s my hope that you read this entire article and were surprised and possibly even a little outraged. Maybe you were outraged with how casually I seem to treat a very serious topic, but more likely than not, you were outraged at the fact that most of what you´ve come to believe about steroids and their reportedly horrible side effects has been greatly exaggerated. The simple fact of the matter is that anabolic steroids, like any medication, can cause a host of unwanted side effects. I´m certainly not suggesting otherwise. What I am suggesting is that a more logical and rational view be taken of them. The literature suggests that these drugs are safe when used in a clinical setting; my numerous interviews and experience with athletes suggests that this also holds true outside the clinical setting.
Please don´t misinterpret my position as being pro-steroid, anti-media, or anti-government. To do so would be to miss the point of this work entirely. I have the utmost respect for the media for providing the services that they do. I also have the utmost respect for the government and those who serve this country.
Anabolic steroid side effects are a very real and possible concern for those who decide to use them. My position, therefore, is one that I hope is consistent with both the media’s as well as the government’s position. I simply wish to tell the truth, and allow my reader to make the best and most informed decisions possible. In that regard, I think this article has served its purpose.


Corticosteroids: Side Effects and Solutions


If you have inflammation, there is no quicker or more efficient way to control it than with corticosteroids. But while these powerful anti-inflammatory drugs can be lifesavers, they can also cause some pretty nasty side effects. To reduce the risk ofcorticosteroids’ side effects, doctors recommend taking the lowest dose needed for the shortest period of time that gets inflammation under control.
If you need to take corticosteroids for more than a week or two, never stop taking them abruptly – your doctor will give you instructions for tapering your dose while watching for signs that inflammation isn’t sufficiently controlled, says Donald R. Miller, professor and chair of the department of pharmacy practice at North Dakota State University, Fargo.
Miller also recommends the following to minimize the risk (or appearance) of some of corticosteroids’ most troublesome side effects:
Weight gain: Steroids affect your metabolism and the way your body stores fat. While taking corticosteroids you may feel famished, prompting you to eat excessively and gain weight. You may notice fat accumulation around your abdomen, even if you’ve never had it there before. You may also retain fluids and feel bloated.
Solution: Watch your calories and exercise regularly to try to prevent excessive weight gain. Particularly watch your salt intake, which can increase fluid build-up. And take heart: If you do gain weight, it won’t likely linger forever. Most people start to lose it relatively easily once they discontinue steroids.
Susceptibility to infection: While corticosteroids help suppress the body’s destructive immune response to itself, they can also suppress the response to infection, allowing even minor infections to become serious.
Solution: Be sure to get an annual flu shot and ask your doctor about the pneumonia vaccine. Do not get any live vaccines – including the measles, mumps, rubella and chickenpox vaccines – which may actually cause you to become sick with the illness you are trying to prevent, says Miller. Practice prevention by washing your hands frequently and avoiding crowds and contact with people you know are sick. If you notice any signs of infection – a dry cough, fever or painful urination, for example – call your doctor immediately.
Thin skin: Corticosteroids inhibit the production of collagen, a chief component of skin, resulting in thinning and weakening of the skin evidenced by stretch marks, easy bruising and the appearance of capillaries beneath the skin.
Solution: While there is little, if anything, you can do to stop skin thinning, there are a number of products – including collagen hydrolysate or vitamin E creams – may reduce the appearance of stretch marks. Cosmetic products can be useful for camouflaging tiny blood vessels or bruising on the face.
Cataracts and glaucoma: Using corticosteroids can worsen or increase your risk of two eye problems: cataracts, the clouding of the eye’s lens, and glaucoma, the build up of pressure in the eye.
Solution: To reduce your risk of cataracts, avoid other causes such as direct sunlight and cigarette smoking. While cataracts cannot be reversed, regular eye exams will alert your doctor to a possible problem, which may necessitate changing your medication or lowering the dose. Regular eye exams are also important to check for glaucoma, which can be treated and often reversed if detected early.
Bone loss: One of the most common and potentially debilitating side effects of corticosteroids is thinning of the bones, which can lead to painful and debilitating fractures.
Solutions: While taking corticosteroids it’s more important than ever to get enough calcium (1500 mg daily) and vitamin D (800 mg daily). It’s also important to get regular weight-bearing exercise, such as walking or dancing. If you are going to be on corticosteroids more than three months, Miller recommends speaking to your doctor about a bone density scan and the possibility of taking an osteoporosis medication called a bisphosphonate.