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患有多囊卵巢疾病的克罗米芬反应者和无反应者的血清胰岛素

Serum insulin in clomiphene responders and nonresponders with polycystic ovarian disease.

作者信息

Espinosa de los Monteros A, Ayala J, Sanabria L C, Parra A

机构信息

Endocrine Department, Instituto Nacional de Perinatología, Mexico City, Mexico, D.F.

出版信息

Rev Invest Clin. 1995 Sep-Oct;47(5):347-53.

PMID:8584804
Abstract

OBJECTIVE

To investigate insulin levels in women with polycystic ovarian disease (PCOD) who are responders or nonresponders to clomiphene citrate (CC).

DESIGN

Open and prospective study.

SETTING

Outpatient infertility clinic of a third level medical institution.

PATIENTS

Ten healthy women (group 1) and 35 PCOD women classified as responders (group 2 n = 10) or nonresponders (group 3 n = 25) on the basis of serum progesterone > or = 19 nmol/L in response to CC repeatedly administered in doses up to 250 mg/day for five days; they were further subdivided if body mass index (BMI) was below (N) or above (H) mean + 3 SD of group 1.

INTERVENTIONS

Blood samples were obtained in a 100-g, 2-hours oral glucose tolerance test (OGTT).

MAIN OUTCOME MEASURES

Serum glucose, insulin, free testosterone (free-T), dehydroepiandrosterone sulphate (DHEA-S), and androstenedione (A) were determined in the samples OGTT and the areas under the curve (AUC) were calculated.

RESULTS

Group 3 had higher BMI, basal LH, and insulin and AUC insulin than groups 1 and 2; free-T was higher in groups 2 and 3 than in group 1, and basal PRL was higher in group 2 compared to groups 1 and 3. When BMI < or = 25.4 kg/m2 (mean + 1 SD of group 1) 77% of the PCOD cases responded (10 out of 13) whereas none with BMI > 25.4 responded to CC (n = 22) irrespectively of basal insulin concentration or AUC insulin.

CONCLUSION

Moderate to excessive overweight seems more frequently and closely associated to a negative CC response in women with PCOD than hyperinsulinemia.

摘要

目的

研究多囊卵巢疾病(PCOD)患者中,对枸橼酸氯米芬(CC)有反应者和无反应者的胰岛素水平。

设计

开放性前瞻性研究。

地点

某三级医疗机构的门诊不孕诊所。

患者

10名健康女性(第1组)和35名PCOD女性,根据血清孕酮≥19 nmol/L,将其分为对CC有反应者(第2组,n = 10)或无反应者(第3组,n = 25),CC每日剂量高达250 mg,连续服用5天;若体重指数(BMI)低于(N)或高于(H)第1组均值 + 3标准差,则进一步细分。

干预措施

在100 g、2小时口服葡萄糖耐量试验(OGTT)中采集血样。

主要观察指标

测定OGTT样本中的血清葡萄糖、胰岛素、游离睾酮(free-T)、硫酸脱氢表雄酮(DHEA-S)和雄烯二酮(A),并计算曲线下面积(AUC)。

结果

第3组的BMI、基础促黄体生成素(LH)、胰岛素和胰岛素AUC高于第1组和第2组;第2组和第3组的free-T高于第1组,第2组的基础催乳素(PRL)高于第1组和第3组。当BMI≤25.4 kg/m²(第1组均值 + 1标准差)时,77%的PCOD病例有反应(13例中的10例),而BMI>25.4的病例无论基础胰岛素浓度或胰岛素AUC如何,对CC均无反应(n = 22)。

结论

对于PCOD女性,中度至过度超重似乎比高胰岛素血症更频繁、更密切地与CC阴性反应相关。

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