Testosterone level, androgen receptor polymorphism, and depressive symptoms in middle-aged men

Background: Testosterone (T) level declines progressively with age. Psychiatric symptoms of T deficiency (e.g., dysphoria, fatigue, irritability, low libido) are also symptoms of depression, and appear to be variably expressed. Methods: We assessed independent measures of hypothalamic-pituitary-gona...

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Veröffentlicht in:Biological psychiatry (1969) 2001-09, Vol.50 (5), p.371-376
Hauptverfasser: Seidman, Stuart N, Araujo, Andre B, Roose, Steven P, McKinlay, John B
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Sprache:eng
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Zusammenfassung:Background: Testosterone (T) level declines progressively with age. Psychiatric symptoms of T deficiency (e.g., dysphoria, fatigue, irritability, low libido) are also symptoms of depression, and appear to be variably expressed. Methods: We assessed independent measures of hypothalamic-pituitary-gonadal axis functioning, i.e., total T level and androgen receptor (AR) CAG repeat length (CAG RL), a genetic trait marker associated with AR function; and depression (diagnosed by above-threshold score on the Center for Epidemiologic Studies-Depression Scale [CES-D]) in 1000 men (mean age = 62.6 years; SD = 8.3) who participated in the Massachusetts Male Aging Study. Results: There were 110 (11%) men with “depression” (CES-D score ≥ 16) in the analysis sample. Neither total T level nor CAG RL was associated with depression in bivariate analyses. Among men with shorter CAG RLs, the percentage of men with depression was 21.6% in the lowest subgroup of total T (defined by quintiles) and 4.2% in the highest subgroup of total T. This was confirmed in simple logistic regression models with depression as the dependent variable and continuous total T as the predictor, run separately within the three CAG RL subgroups: depression was significantly and inversely associated with total T in men with shorter CAG RLs but not in men with moderate and longer CAG RLs. Conclusions: CAG isotype, a genetic trait marker of androgen receptor function, may mediate the expression of the central nervous system effects of T deficiency in men.
ISSN:0006-3223
1873-2402
DOI:10.1016/S0006-3223(01)01148-9