Hepatic adverse effects of performance-enhancing drugs in Iranian male bodybuilders

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Article Type:
Research/Original Article (دارای رتبه معتبر)
Abstract:
Background and aim

Studies have shown that performance-enhancing drugs (PEDs) especially anabolic steroids cause liver damage. There is no study on the PEDs effects on the liver of bodybuilding athletes in Bushehr city (Iran).  Aim of this study was to evaluate the hepatic effects of PEDs, particularly anabolic steroids in male bodybuilders in Bushehr.

Methods

Demographic information, exercise program, use of PEDs, alcohol and dietary supplements were recorded in male bodybuilders using a questionnaire. Participants were divided into three groups: 1) current users (CU), 2) non-current users (NCU), and 3) non-users (NU). The serum levels of alanine transaminase (ALT), aspartate transaminase (AST) and bilirubin were measured in the athletes by using the commercially available kits. The data were analyzed by using one-way analysis of variance.

Results

Two-hundred and three bodybuilders with the age range of 18-50 years, body mass index of 18.6-40 kg/m2, and average of 6 years exercise were included in the study. In the present study, 8.9% of athletes were current users, 39.9% were non-current users, and 51.2% were non-users. Athletes have been used anabolic steroids, stimulants, growth hormone, and insulin. The average period of PEDs use in athletes was 60 days/year by simultaneous oral and injection routes. The serum levels of ALT (p = 0.003), AST (p = 0.000) and bilirubin (p = 0.023) were significantly different between the three groups. The serum levels of ALT (p = 0.000) and AST in current users were higher than non-user athletes, while only the AST level in non-current users was higher than non-users (p = 0.044).

Conclusion

The use of anabolic steroids with other PEDs may raise the serum level of hepatic enzymes in male bodybuilders. This effect may be the sign of PEDs-induced hepatic injury in these athletes.

Language:
Persian
Published:
Physiology and Pharmacology, Volume:2 Issue: 2, 2018
Pages:
118 to 127
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