荷尔蒙和妇产风险因素面对面脱臼

E. Makrantonaki
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简介:额部纤维化性脱发(FFA)的发病机制可能涉及自身免疫、激素和环境因素的相互作用。缺乏比较研究证明FFA患者与一般人群相比存在激素背景差异。材料与方法:设计单中心病例对照研究,纳入女性FFA患者104例,对照组208例。对患者和对照组进行了访谈,并记录了有关其妇科和激素背景的大量数据。结果:研究纳入了104例病例和208例年龄匹配的对照。绝经年龄的显著差异为2岁,而对照组的生育寿命平均增加了1.7岁。多因素分析后,我们发现既往摄入他莫昔芬是FFA发生的危险因素(OR 14.89)。唯一确定的保护因素是以前使用过宫内节育器(IUD) (OR 0.22)。结论:提前绝经和摄入他莫昔芬可能促进或维持FFA,而使用宫内节育器可能防止FFA的发生。我们的研究结果支持了先前提出的FFA发病机制中潜在激素机制的假设,并指出低雌激素环境是FFA发展的理想条件。
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Hormonelle und gynäkologische Risikofaktoren bei frontal fibrosierender Alopezie
Introduction: Frontal fibrosing alopecia (FFA) is a condition that likely involves an interplay of autoimmune, hormonal, and environmental factors in its pathogenesis. There is a lack of comparative studies demonstrating the presence of hormonal background differences in FFA patients compared to the general population. Materials and Methods: A single-center case-control study was designed, including 104 female FFA patients and 208 controls. Patients and controls were interviewed, and extensive data regarding their gynecological and hormonal background were recorded. Results: One hundred four cases and 208 age-matched controls were included in the study. A significant difference of 2 years in the age of menopause was detected with a consistent mean increase in fertile life for the control group of 1.7 years. After the multivariate analysis, we found previous intake of tamoxifen to be a risk factor for the development of FFA (OR 14.89). The only protective factor identified was the previous use of an intrauterine device (IUD) (OR 0.22). Conclusions: An earlier menopause and tamoxifen intake might promote or maintain FFA, while the use of an IUD might protect from developing FFA. Our results support the previously proposed hypothesis of an underlying hormonal mechanism in the etiopathogenesis of FFA and point out low-estrogen environments as an ideal condition for FFA development.
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