Partial androgen deficiency in aging type 2 diabetic men and its relationship to glycemic control

被引:77
作者
Corrales, JJ
Burgo, RM
García-Berrocal, B
Almeida, M
Alberca, I
González-Buitrago, JM
Orfao, A
Miralles, JM
机构
[1] Univ Salamanca, Serv Endocrinol, Dept Med, Salamanca, Spain
[2] Univ Salamanca, Serv Bioquim, Dept Bioquim, Salamanca, Spain
[3] Univ Salamanca, Serv Citometria Flujo, Dept Med, Salamanca, Spain
[4] Univ Salamanca, Hematol Serv, Dept Med, Salamanca, Spain
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2004年 / 53卷 / 05期
关键词
D O I
10.1016/j.metabol.2003.12.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aging in the male is associated with both a higher incidence of type 2 diabetes and hypogonadism. However, little information is available about the complex of symptoms and hormonal changes related to partial androgen deficiency in aging (called andropause) in type 2 diabetic men. Here, for the first time, we used a combination of clinical and hormonal criteria to define andropause and to analyze the relationships between the androgen environment and glucose metabolism in 55 type 2 diabetic men (63.6 +/- 7.9 years, mean +/- SD). Low plasma levels of total testosterone ( less than or equal to 53.4 ng/mL) and free testosterone ( less than or equal to 11 pg/mL) were found in 20% and 54.5%, respectively, of the diabetic men. The fraction of diabetic men with subnormal levels of total testosterone increased with aging: 14.2% (50 to 59 years), 17.4% (60 to 69 years) and 36% ( > 70 years). The corresponding figures for subnormal values of free testosterone were 38%, 69.6%, and 54.5%, respectively. In the whole group of type 2 diabetic men, no significant linear correlations between total or free testosterone with fasting plasma glucose, insulin, C-peptide, or fructosamine values could be established. Total testosterone was positively correlated with glycosylated haemoglobin (HbA(1c)) levels (r = .322, P = .01). Although fasting plasma glucose was marginally higher in aging type 2 diabetic patients with andropause than in those without andropause (162 +/- 6.9 v 139 +/- 8.9, mean +/- SEM, P = .05), there were no differences between both subgroups for plasma fasting insulin, C-peptide, fructosamine, or HbA(1c) levels. Replacement therapy (150 mg intramuscular [IM] of enanthate of testosterone every 14 days for 6 months) was applied in 10 type 2 diabetic men with clinical features of andropause associated with subnormal concentrations of serum testosterone. The treatment induced significant increases in total plasma testosterone (baseline: 3.9 +/- 0.3; at 6 months: 7.1 +/- 0.9 ng/mL, mean SEM, P = .003) and free testosterone (baseline: 9.3 +/- 0.6; at 6 months 17.6 +/- 2.4 pg/mL, P = .003), but had a neutral effect on overall glycemic control. These data show a high prevalence of andropause in aging type 2 diabetic men and suggest that the endogenous androgen environment, as well as correction of the partial androgen deficiency, do not have a meaningful effect on glycemic control. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:666 / 672
页数:7
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