男性系统性硬化症原发性性腺功能减退的患病率和临床相关性。

IF 1.4 Q3 RHEUMATOLOGY
Sapol Thepwiwatjit, Suranut Charoensri, Wichien Sirithanaphol, Ajanee Mahakkanukrauh, Siraphop Suwannaroj, Chingching Foocharoen
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引用次数: 0

摘要

背景:系统性硬化症可能影响男性和女性的生育能力。据报道,女性系统性硬化症患者卵巢早衰,但尚未研究系统性硬化对男性生育能力的影响。目的:我们旨在确定男性系统性硬化症患者原发性性腺功能减退的患病率和临床相关性。方法:这是一项横断面试点研究,包括30名在开大学硬皮病诊所就诊的成年男性系统性硬化症患者。使用衰老男性症状评定量表、泌尿系统检查和血液测试(总睾酮、游离睾酮、卵泡刺激素和黄体生成素)评估睾酮缺乏症状。我们排除了先天性性腺功能减退症和任何获得性睾丸和生殖器疾病的患者。原发性性腺功能减退症的定义基于国际老龄男性研究协会2015年性腺功能减退诊断标准。结果:7名患者符合原发性性腺功能减退症的定义,患病率为23.3%(95%置信区间:9.9-42.3)。其平均年龄和平均系统性硬化持续时间分别为59.4 ± 11.9和5.5 ± 4.7 年。发病年龄较大、甘油三酯水平较高以及年龄较大开始皮质类固醇治疗与原发性性腺功能减退显著相关(p = 分别为0.02、0.02和0.03)。在泰国男性系统性硬化症患者中,系统性硬化亚群、疾病严重程度和免疫抑制剂的使用与原发性性腺功能减退无关。结论:大约四分之一的男性系统性硬化症患者患有原发性性腺功能减退症。老年人系统性硬化症发作、高甘油三酯血症和晚期皮质类固醇治疗是发展为原发性性腺功能减退症的危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence and clinical associations with primary hypogonadism in male systemic sclerosis.

Background: Systemic sclerosis may affect male and female fertility. Premature ovarian failure has been reported in female systemic sclerosis patients, but the effects on male fertility in systemic sclerosis have not been studied.

Objectives: We aimed to determine the prevalence and clinical associations with primary hypogonadism among male systemic sclerosis patients.

Methods: This was a cross-sectional pilot study, including 30 adult male systemic sclerosis patients attending the Scleroderma Clinic, Khon Kaen University. Testosterone deficiency symptoms were assessed using the Aging Males' Symptoms Rating Scale, urological examination, and blood testing (for total testosterone, free testosterone, follicle-stimulating hormone, and luteinizing hormone). We excluded patients with congenital hypogonadism and any acquired disorders of the testes and genitalia. The definition of primary hypogonadism was based on the International Society for the Study of the Aging Male 2015 diagnostic criteria for hypogonadism.

Results: Seven patients met the definition of primary hypogonadism-a prevalence of 23.3% (95% confidence interval: 9.9-42.3). The respective mean age and mean systemic sclerosis duration was 59.4 ± 11.9 and 5.5 ± 4.7 years. Older age at onset, high triglyceride level, and older age starting corticosteroid treatment were significantly associated with primary hypogonadism (p = 0.02, 0.02, and 0.03, respectively). Systemic sclerosis subset, disease severity, and immunosuppressant use were not associated with primary hypogonadism among Thai male systemic sclerosis patients.

Conclusion: Around one-quarter of male systemic sclerosis patients had primary hypogonadism. Elderly onset of systemic sclerosis, hypertriglyceridemia, and late corticosteroid treatment were risk factors for developing primary hypogonadism.

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