Andrology, Women's Endocrinology and Gender Incongruence Unit, Department of Experimental Clinical and Biomedical Sciences "Mario Serio," University of Florence, Florence, Italy.
Gynecology Unit, Department of Biomedical, Experimental and Clinical Sciences "Mario Serio," University of Florence, Florence, Italy.
Front Endocrinol (Lausanne). 2021 Mar 29;12:641446. doi: 10.3389/fendo.2021.641446. eCollection 2021.
PCOS is one of the most common endocrine disorders and NAFLD is one of its most dangerous metabolic consequences. The diagnosis of NAFLD is not a practical task and the condition is at risk of being overlooked. The use of simpler but still reliable surrogate markers is necessary to identify women with a high likelihood of NAFLD. The aim of this study was to evaluate the clinical correlates of NAFLD Liver Fat Score (NAFLD-LFS) in women with oligomenorrhea and/or hirsutism. Furthermore, the study aimed to evaluate whether, among the hormonal parameters evaluated in such women, possible hallmarks of NAFLD may be identified. To this purpose, 66 women who attended our Outpatient Clinic for oligomenorrhea and/or hyperandrogenism were included in the study. In order to validate the results obtained in the first cohort, a second independent sample of 233 women evaluated for female sexual dysfunction (FSD) was analyzed. In cohort 1, NAFLD-LFS positively correlated with metabolic and inflammatory parameters. Among the hormone parameters, NAFLD-LFS showed no significant relationships with androgens but a significant negative correlation with SHBG (p<0.0001) that therefore appeared as a candidate hallmark for pathologic NAFLD-LFS. The ROC analysis showed a significant accuracy (81.1%, C.I.69.1-93.0, p <0.0001) for SHBG in identifying women with a pathological NAFLD-LFS. In particular, a SHBG 33.4 nmol/l was recognized as the best threshold, with a sensitivity of 73.3% and a specificity of 70.7%. In order to validate this SHBG as a marker of metabolic impairment possible related with the presence of NAFLD, we tested this threshold in cohort 2. FSD women with SHBG <33.4 nmol/l had worse metabolic parameters than women with SHBG ≥33.4 nmol/l and a significantly higher NAFLD-LFS even after adjusting for confounders (B=4.18 [2.05; 6.31], p=0.001). In conclusion, this study provides a new evidence in the diagnostic process of NAFLD, showing that the measurement of SHBG, which is routinely assessed in the workup of women referred for possible PCOS, could identify women at higher metabolic risk, thus detecting those who may deserve further targeted diagnostic assessment.
多囊卵巢综合征(PCOS)是最常见的内分泌疾病之一,非酒精性脂肪性肝病(NAFLD)是其最危险的代谢后果之一。NAFLD 的诊断不是一项实际任务,而且该病症有被忽视的风险。因此,有必要使用更简单但仍然可靠的替代标志物来识别患有 NAFLD 可能性高的女性。本研究旨在评估月经稀少和/或多毛症妇女的非酒精性脂肪性肝病肝脏脂肪评分(NAFLD-LFS)的临床相关性。此外,本研究旨在评估在这些女性中评估的激素参数中,是否可以确定非酒精性脂肪性肝病的可能特征。为此,纳入了 66 名因月经稀少和/或高雄激素血症而就诊于我院门诊的女性。为了验证第一组队列中获得的结果,还分析了第二组 233 名因女性性功能障碍(FSD)就诊的女性的独立样本。在队列 1 中,NAFLD-LFS 与代谢和炎症参数呈正相关。在激素参数中,NAFLD-LFS 与雄激素无显著相关性,但与 SHBG 呈显著负相关(p<0.0001),因此 SHBG 似乎是病理性 NAFLD-LFS 的候选特征。ROC 分析显示 SHBG 对识别病理性 NAFLD-LFS 具有显著的准确性(81.1%,置信区间为 69.1-93.0,p<0.0001)。特别是,33.4 nmol/l 的 SHBG 被认为是最佳阈值,其敏感性为 73.3%,特异性为 70.7%。为了验证 SHBG 作为可能与 NAFLD 存在相关的代谢损伤标志物,我们在队列 2 中测试了该阈值。SHBG<33.4 nmol/l 的 FSD 女性的代谢参数比 SHBG≥33.4 nmol/l 的女性更差,并且即使在调整混杂因素后,NAFLD-LFS 也显著更高(B=4.18 [2.05; 6.31],p=0.001)。总之,本研究为 NAFLD 的诊断过程提供了新的证据,表明在为可能的 PCOS 就诊的女性进行常规检查时测量 SHBG 可以识别代谢风险更高的女性,从而发现那些可能需要进一步针对性诊断评估的女性。