Walch Katharina, Grimm Christoph, Zeillinger Robert, Huber Johannes C, Nagele Friedrich, Hefler Lukas A
Department of Obstetrics and Gynecology, University of Vienna Medical School, Vienna, Austria.
Fertil Steril. 2004 Jun;81(6):1638-41. doi: 10.1016/j.fertnstert.2004.01.021.
To investigate the association of a common polymorphism of the interleukin-6 gene (IL6) promoter with the occurence and the clinical characteristics of polycystic ovary syndrome (PCOS).
Prospective, case-control study.
Academic research institution.
PATIENT(S): Sixty-two patients with PCOS and 94 healthy controls.
INTERVENTION(S): Peripheral venous puncture, ultrasonography, oral glucose tolerance test (OGTT), questionnaire.
MAIN OUTCOME MEASURE(S): Genotype analysis with respect to the common -174 G/C polymorphism of the IL6 gene promoter, analysis of testosterone (T), androstendione, and sex hormone binding globulin serum levels, and evaluation of the OGTT.
RESULT(S): Allele frequencies among women with PCOS and controls were 62.9% and 64.4%, respectively, for the wild-type G allele, and 37.1% and 35.6%, respectively, for the mutant C allele. We ascertained a significant association between presence of at least one mutant C allele and the clinical characteristics of affected women: these women were more likely to present with a body mass index >27 kg/m(2), elevated total T serum levels, and a pathological OGTT result.
CONCLUSION(S): A common polymorphism of the IL6 promoter, although not associated with the presence of PCOS, is associated with the clinical characteristics of women affected by this condition.
探讨白细胞介素-6基因(IL6)启动子的一种常见多态性与多囊卵巢综合征(PCOS)的发生及临床特征之间的关联。
前瞻性病例对照研究。
学术研究机构。
62例PCOS患者和94例健康对照者。
外周静脉穿刺、超声检查、口服葡萄糖耐量试验(OGTT)、问卷调查。
对IL6基因启动子常见的-174 G/C多态性进行基因分型分析,分析睾酮(T)、雄烯二酮和性激素结合球蛋白的血清水平,并评估OGTT。
PCOS患者和对照者中,野生型G等位基因的频率分别为62.9%和64.4%,突变型C等位基因的频率分别为37.1%和35.6%。我们确定至少存在一个突变型C等位基因与受影响女性的临床特征之间存在显著关联:这些女性更有可能出现体重指数>27 kg/m²、总T血清水平升高以及OGTT结果异常。
IL6启动子的一种常见多态性虽然与PCOS的存在无关,但与受该疾病影响女性的临床特征有关。