Baillargeon Jean-Patrice, Carpentier André
Department of Medicine, Division of Endocrinology, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Fertil Steril. 2007 Oct;88(4):886-93. doi: 10.1016/j.fertnstert.2006.12.055. Epub 2007 Jun 7.
To determine the effect of reducing insulin secretion on hyperandrogenemia in lean normoinsulinemic women with polycystic ovary syndrome (PCOS) and normal metabolic insulin sensitivity.
Transversal assessment at baseline and prospective follow-up of lean PCOS group after 8 days of diazoxide, which reduces insulin secretion, and 1 month of leuprolide, which suppresses LH.
Clinical research center of an academic hospital.
PATIENT(S): Nine lean women (body mass index <or=25 kg/m(2)) with PCOS and normal insulin levels, as well as 17 lean healthy women.
INTERVENTION(S): Lean PCOS women were reassessed after 8 days of diazoxide and after 1 month of leuprolide, which suppresses LH.
MAIN OUTCOME MEASURE(S): Androgen levels and insulin-stimulated glucose disposal (metabolic insulin sensitivity), determined by euglycemic-hyperinsulinemic clamp (M-value).
RESULT(S): Mean M-value of lean PCOS women (48.5 micromol/kg.min) was similar to lean control subjects (52.9 micromol/kg.min). They also had comparable anthropometric measures, lipids, fibrinogen, and plasminogen activator inhibitor 1. The LH did not change significantly after diazoxide, but was almost suppressed after leuprolide in the PCOS group. Androstenedione decreased significantly after diazoxide and even more after leuprolide. However, free T significantly decreased only after diazoxide in lean PCOS women. Diazoxide also increased SHBG significantly in this group.
CONCLUSION(S): In women with typical PCOS and normal insulin levels and metabolic insulin sensitivity, reducing insulin secretion significantly decreased androgen and increased SHBG levels. These results suggest that insulin contributes to hyperandrogenemia even in PCOS women with normal metabolic insulin sensitivity, which might be due to increased sensitivity of their androgenic insulin pathway.
确定在患有多囊卵巢综合征(PCOS)且代谢胰岛素敏感性正常的瘦型正常胰岛素血症女性中,降低胰岛素分泌对高雄激素血症的影响。
对瘦型PCOS组在使用降低胰岛素分泌的二氮嗪8天以及使用抑制促黄体生成素(LH)的亮丙瑞林1个月后进行基线横向评估和前瞻性随访。
一家学术医院的临床研究中心。
9名患有PCOS且胰岛素水平正常的瘦型女性(体重指数≤25kg/m²)以及17名瘦型健康女性。
瘦型PCOS女性在使用二氮嗪8天后以及使用抑制LH的亮丙瑞林1个月后重新进行评估。
通过正常血糖高胰岛素钳夹技术(M值)测定雄激素水平和胰岛素刺激的葡萄糖处置(代谢胰岛素敏感性)。
瘦型PCOS女性的平均M值(48.5微摩尔/千克·分钟)与瘦型对照受试者(52.9微摩尔/千克·分钟)相似。她们在人体测量指标、血脂、纤维蛋白原和纤溶酶原激活物抑制剂1方面也具有可比性。PCOS组使用二氮嗪后LH无显著变化,但使用亮丙瑞林后几乎被抑制。二氮嗪后雄烯二酮显著下降,亮丙瑞林后下降更明显。然而,瘦型PCOS女性仅在使用二氮嗪后游离睾酮显著下降。二氮嗪在该组中还显著增加了性激素结合球蛋白(SHBG)。
在具有典型PCOS且胰岛素水平和代谢胰岛素敏感性正常的女性中,降低胰岛素分泌可显著降低雄激素水平并增加SHBG水平。这些结果表明,即使在代谢胰岛素敏感性正常的PCOS女性中,胰岛素也会导致高雄激素血症,这可能是由于其雄激素胰岛素途径的敏感性增加所致。