Sexual Dysfunction in Systemic Autoimmune Rheumatic Diseases: Prevalence, Impact, and Management Strategies.

IF 2.1 Q4 Medicine
Mediterranean Journal of Rheumatology Pub Date : 2025-08-18 eCollection Date: 2025-09-01 DOI:10.31138/mjr.170225.iap
Monisha In, Nilanjana Dutta, Harshwardhan Patil, Mahabaleshwar Mamadapur, Veerendra Arakalavadi Guruswamy, Pavan Kumar M R
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引用次数: 0

Abstract

Background: Systemic autoimmune rheumatic diseases (SARDs) profoundly impact patients' quality of life (QoL) including sexual health, yet sexual dysfunction (SD) remains underrecognised in clinical care. Contributing factors include chronic pain, fatigue, joint stiffness, hormonal imbalances and psychological distress.

Objective: This review evaluates the prevalence, impact, and management of SD in patients with systemic autoimmune rheumatic diseases (SARDs), including Systemic Lupus Erythematosus (SLE), Rheumatoid Arthritis (RA), Ankylosing Spondylitis (AS), Sjögren's disease (SjD), and Systemic Sclerosis (SSc), as well as the related chronic condition Fibromyalgia Syndrome (FMS).

Methods: A systematic literature review was conducted using PubMed, Web of Science, and Scopus with relevant MeSH terms. Studies reporting SD in SARDs were included, with sexual function commonly assessed via the Female Sexual Function Index (FSFI) and International Index of Erectile Function (IIEF).

Results: SD prevalence ranged from 30% to 90%, varying by disease and gender. Up to 90% of women with SLE reported reduced desire and arousal. RA affected 30-70% of patients, with pain and depression as key drivers. In AS, erectile dysfunction affected 41-58% of men, influenced by age and disease duration. Over 56% of women with SjD experienced SD, often linked to vaginal dryness. SSc-induced fibrosis led to erectile dysfunction in 80% of men. FMS showed a 63% SD rate, associated with chronic pain and psychological burden.

Conclusion: SD is highly prevalent yet underaddressed in SARDs. A multidisciplinary approach combining pain management, psychological support, hormonal therapy, and patient education is essential.

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系统性自身免疫性风湿病的性功能障碍:患病率、影响和管理策略。
背景:系统性自身免疫性风湿病(SARDs)深刻影响患者的生活质量(QoL),包括性健康,但性功能障碍(SD)在临床护理中仍未得到充分认识。诱发因素包括慢性疼痛、疲劳、关节僵硬、荷尔蒙失衡和心理困扰。目的:本综述评估系统性自身免疫性风湿性疾病(SARDs)患者SD的患病率、影响和管理,包括系统性红斑狼疮(SLE)、类风湿性关节炎(RA)、强直性脊柱炎(AS)、Sjögren病(SjD)和系统性硬化症(SSc),以及相关的慢性疾病纤维肌痛综合征(FMS)。方法:系统查阅PubMed、Web of Science、Scopus等相关MeSH术语的文献。研究报告了sard中的SD,性功能通常通过女性性功能指数(FSFI)和国际勃起功能指数(IIEF)进行评估。结果:SD患病率从30%到90%不等,因疾病和性别而异。高达90%的SLE女性报告性欲和性唤起降低。RA影响了30-70%的患者,疼痛和抑郁是主要驱动因素。在AS患者中,41-58%的男性存在勃起功能障碍,受年龄和疾病持续时间的影响。超过56%的女性患有性功能障碍,通常与阴道干燥有关。ssc诱导的纤维化导致80%的男性勃起功能障碍。FMS显示63%的SD率,与慢性疼痛和心理负担有关。结论:SD在SARDs中非常普遍,但未得到充分重视。结合疼痛管理、心理支持、激素治疗和患者教育的多学科方法是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
42
审稿时长
8 weeks
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