多囊卵巢综合征不同表型的临床特征和生化参数评估。

Mymensingh medical journal : MMJ Pub Date : 2025-10-01
F Sharmin, T T Mirza, T Latif, S Shamsi, K Nigar, T Sharmin, S Akter, N S Komola, P Das, S Ferdoushi, F A Islam, H Akhter
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引用次数: 0

摘要

多囊卵巢综合征(PCOS)是一种多基因、多因素的疾病,被认为是育龄妇女最常见的内分泌问题。胰岛素抵抗、高雄激素和肥胖显著影响多囊卵巢综合征的病理生理过程。本研究旨在评估不同表型多囊卵巢综合征的临床和生化参数。横断面描述性观察性研究于2018年1月至2019年6月在孟加拉国Mymensingh医学院医院进行,目的是选择107例PCOS患者。数据采用SPSS 22.0软件进行分析。本研究的定量变量采用均值和标准差进行汇总,定性变量采用百分比进行汇总。不同表型的生化参数比较采用t检验。A型最多(59.8%),其次是B型(14.9%)、D型(14.0%)和C型(11.2%)。生化高雄激素血症以表型A最高(57.8%),其次为表型B(36.4%)和表型C(6.1%)。A、B、C、D型患者的平均年龄分别为22.92±6.36、20.81±3.69、24.82±5.96、21.94±4.12岁。各表型亚群均以中高阶层城市家庭居多。体重指数(BMI)、腰围和腰臀比在所有表型中均增加,但在表型A和b中增加较多。血压无显著变化。表型A表现为少经(50.47%)、闭经(7.48%)和月经过多(1.87%)。多数B型(13.08%)和D型(12.15%)表现为少经。所有C型患者(11.2%)月经周期正常。多毛症以A型和b型多见。A型多表现为严重痤疮(19.6%)、黑棘皮病(38.3%)、体重增加(34.6%)和生育能力低下(18.7%)。表现型A和表现型B血清总胆固醇和甘油三酯较高,而血清HDL较低。表型划分有助于更好地了解多囊卵巢综合征的病理生理,疾病的严重程度,也有助于预测不良反应。此外,识别各种表型具有诊断意义,也有助于提供适当的治疗和患者预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of Clinical Profile and Biochemical Parameters in Diverse Phenotypes of Polycystic Ovarian Syndrome.

Polycystic ovary syndrome (PCOS) is a polygenic and multifactorial condition, considered as the most common endocrine problem of women in reproductive age. Insulin resistance, hyper-androgenism and obesity significantly influence the pathophysiological process of PCOS. This study was designed to estimate clinical and biochemical parameters in different phenotypes of PCOS. The cross sectional descriptive type of observational study was carried out at Mymensingh Medical College Hospital, Bangladesh from January 2018 to June 2019 among purposively selected 107 patients with PCOS. Data were analyzed by computer software, SPSS, version 22.0. Quantitative variables of this study were summarized using mean and standard deviation and qualitative variables were summarized by percentage. Biochemical parameters in different phenotypes were compared with t-test. Phenotype A was found in highest number (59.8%) followed by phenotype B (14.9%), phenotype D (14.0%) and phenotype C (11.2%). Biochemical hyper-androgenism was observed highest in phenotype A (57.8%) followed by phenotype B (36.4%) and phenotype C (6.1%). Biochemical or clinical hyper-androgenism was not observed among patients of phenotype D. Mean age of phenotype A, B, C and D were 22.92±6.36, 20.81±3.69, 24.82±5.96 and 21.94±4.12 years respectively. All the phenotypic subgroups were found higher in the high and middle class urban family. Body mass index (BMI), waist circumference and waist hip ratio were increased in all phenotypes but more in phenotype A and B. Blood pressure had no significant change. Phenotype A presented with oligo-menorrhea (50.47%), amenorrhea (7.48%) and menorrhagia (1.87%). Majority of phenotype B (13.08%) and D (12.15%) presented with oligo-menorrhea. All the phenotype C (11.2%) had normal menstrual cycle. Hirsutism was more in phenotype A and B. Phenotype A presented with more severe acne (19.6%), acanthosis nigricans (38.3%), weight gain (34.6%) and subfertility (18.7%) than others. Phenotype A and B had high serum total cholesterol and triglyceride but low serum HDL. Phenotypic division helps in better understanding the pathophysiology of PCOS, severity of the disease and also helps in predicting the adverse effects. Moreover, identifying various phenotypes have diagnostic implications and also assist in providing appropriate treatment and prognosticating the patients.

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