Insulin sensitivity and hyperprolactinemia

被引:59
作者
Tuzcu, A [1 ]
Bahceci, M
Dursun, M
Turgut, C
Bahceci, S
机构
[1] Dicle Univ, Tip Fak, TR-21280 Diyarbakir, Turkey
[2] Univ Dicle, Sch Med, Dept Histol & Embryol, Diyarbakir, Turkey
[3] Univ Dicle, Sch Med, Dept Endocrinol & Metab, Diyarbakir, Turkey
[4] Univ Dicle, Sch Med, Dept Gastroenterol, Diyarbakir, Turkey
[5] Univ Dicle, Sch Med, Dept Biochem, Diyarbakir, Turkey
关键词
hyperprolactinemia; insulin resistance; HOMA; androgenic hormones and obesity;
D O I
10.1007/BF03345182
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It has been shown that prolactin (PRL) induces glucose intolerance, hyperinsulinemia and insulin resistance in several animal species. In women with microprolactinomas, the sensitivity to insulin is lower in hyperprolactinemia than in normoprolactinemia. Thirty non-obese women with hyperprolactinemia and 30 healthy non-obese women were included into the study. Age, body weight (bw), height, body mass index (BMI), waist circumference, hip circumference and waist to hip ratio of both patients with hyperprolactinemia and control subjects were not different. Mean serum prolactin level was higher in hyperprolactinemic patients than in control group (84.5 +/- 51.1 ng/ml and 13.8 +/- 5.3 ng/ml respectively, p<0.002). Mean HOMA-(%B) index of hyperprolactinemic patients was higher than in control subjects (121 +/- 49 and 84 +/- 38, respectively, p<0.02). Mean HOMA-(%S) index was lower in hyperprolactinemic patients (56 39 and 105 55, respectively, p<0.006). Serum total testosterone, free testosterone, androstenedione, estradiol, cortisol, sex hormone binding globulin and DHEA-S levels in both hyperprolactinemic women and healthy subjects, statistically did not show any difference between the two groups. The present data indicate that hyperprolactinemia is associated with an insulin-resistant state. This resistant state may not be a result of obesity, androgenic hormones, and SHBG or pregnancy. It may be the result of serum free fatty acids (FFA) levels, decrement in the number of insulin receptors (by a down-regulation of insulin receptors) or post-binding defect in insulin action or more. (C) 2003, Eclitrice Kurtis.
引用
收藏
页码:341 / 346
页数:6
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