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Muscle Dissatisfaction and Muscle-Enhancing Substance Use: A Population-Based Twin Study in Young Adult Men

Published online by Cambridge University Press:  21 February 2012

Anu Raevuori*
Affiliation:
Department of Public Health, University of Helsinki, Finland. [email protected]
Anna Keski-Rahkonen
Affiliation:
Department of Public Health, University of Helsinki, Finland; Obesity Research Unit, Department of Psychiatry, Helsinki University Central Hospital, Finland; Department of Epidemiology, Columbia University, United States of America.
Richard J. Rose
Affiliation:
Department of Psychology, Indiana University, Bloomington, Indiana, United States of America.
Aila Rissanen
Affiliation:
Obesity Research Unit, Department of Psychiatry, Helsinki University Central Hospital, Finland.
Jaakko Kaprio
Affiliation:
Department of Public Health, University of Helsinki, Finland; Department of Mental Health, National Public Health Institute, Helsinki, Finland.
*
*Address for correspondence: Dr. Anu Raevuori, Department of Public Health, PO Box 41, 00014 University of Helsinki, Finland.

Abstract

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In the population-based FinnTwin16 study, proportions of genetic and environmental factors contributing to muscle dissatisfaction and muscle-enhancing substance use were assessed in 319 pairs of twin brothers: 141 monozygotic (MZ) and 178 dizygotic (DZ) pairs. In addition there were 86 twin individuals from pairs in which only one co-twin responded. Of all respondents, 30% experienced high muscle dissatisfaction. The corresponding proportion of muscle-enhancing substance use was 10%. The subjects were similar in age (23.8 years, 95% confidence interval [CI] 23.76–23.84), body mass index (23.7, 95% CI 23.5–23.9), and waist circumference (84.5 cm, 95% CI 83.7–85.2), independent of their muscle dissatisfaction or muscle-enhancing substance use status and independent of their zygosity. The MZ polychoric correlation for muscle dissatisfaction was .39 (95% CI .17–.58) and .27 for DZ pairs (95% CI .07–.46). The MZ tetrachoric correlation for muscle-enhancing substance use was .65 (95% CI .28–.87) and .56 for DZ pairs (95% CI .26–.78). The AE model, where additive genetic factors (A) accounted for 42% (95% CI .23–.59) and unique environmental factors (E) 58% (95% CI .41–.77) of the liability, provided the best fit for muscle dissatisfaction. The CE model, where common environmental factors (C) accounted for 60% (95% CI .37–.77) and unique environmental factors (E) 40% (95% CI .23–.63) of the liability, provided the best fit for muscle-enhancing substance use. Both genetic and unique (nonfamilial) environmental factors are involved in muscle dissatisfaction in the population. Nongenetic factors (both familial and non-familial) appear to best explain the use of muscle-enhancing substances.

Type
Articles
Copyright
Copyright © Cambridge University Press 2006