Orlandi Martina, Giuggioli Dilia, Ferri Clodoveo, De Angelis Rossella, Riccieri Valeria, Cacciapaglia Fabio, Bosello Silvia Laura, Codullo Veronica, Bajocchi Gianluigi, Dagna Lorenzo, Campochiaro Corrado, De Luca Giacomo, Zanframundo Giovanni, Foti Rosario, Cuomo Giovanna, Ariani Alarico, Rosato Edoardo, Girelli Francesco, Zanatta Elisabetta, Cavazzana Ilaria, Ingegnoli Francesca, De Santis Maria, Murdaca Giuseppe, Abignano Giuseppina, Petitti Giorgio, Della Rossa Alessandra, Caminiti Maurizio, Iuliano Anna Maria, Ciano Giovanni, Beretta Lorenzo, Bagnato Gianluca, Lubrano Ennio, De Andres Ilenia, Giollo Alessandro, Saracco Marta, Agnes Cecilia, Cipolletta Edoardo, Lumetti Federica, Spinella Amelia, Magnani Luca, Visalli Elisa, Iandoli Carlo, Gigante Antonietta, Pellegrino Greta, Pigatto Erika, Lazzaroni Maria Grazia, Franceschini Franco, Generali Elena, Mennillo Gianna, Barsotti Simone, Pagano Mariano Giuseppa, Furini Federica, Vultaggio Licia, Parisi Simone, Peroni Clara Lisa, Bianchi Gerolamo, Fusaro Enrico, Sebastiani Gian Domenico, Govoni Marcello, D'Angelo Salvatore, Cozzi Franco, Doria Andrea, Salvarani Carlo, Iannone Florenzo, Guiducci Serena, Bellando-Randone Silvia, Matucci-Cerinic Marco, Bruni Cosimo
Department of Medical and Surgical Sciences for Children and Adults, University Hospital of Modena and Reggio Emilia School of Medicine, Modena, Italy.
Rheumatology Clinic "Madonna dello Scoglio" Cotronei, Crotone, Italy.
Ther Adv Musculoskelet Dis. 2025 Jul 14;17:1759720X251354898. doi: 10.1177/1759720X251354898. eCollection 2025.
Hormonal changes in menopause might interact with the presentation of underlying autoimmune diseases, such as systemic sclerosis (SSc).
Our study aimed to evaluate the association of (1) current menopausal status, (2) early menopause, and (3) disease onset during fertile or post-menopausal age on SSc clinical phenotype in a large SSc cohort from the Italian Systemic sclerosis Progression INvestiGation (SPRING-SIR) registry.
Female SSc patients from the SPRING-SIR registry, fulfilling the American College of Rheumatology (ACR)/European Alliance of Associations for Rheumatology (EULAR) 2013 classification criteria, with data on SSc disease onset, menopausal status, and menopausal age, were eligible. SSc onset was categorized as pre-menopausal if SSc onset happened >1 year before menopause or as post-menopausal onset if it occurred >1 year after menopause. An early menopause was defined by a menopausal age <45 years.
Descriptive statistics and regression models were built to test the association between current menopausal status, pre-menopausal disease onset, and early menopause with SSc-related features.
At baseline, 1157/1538 (75%) patients were in menopause, 632 (50.4%) had a pre-menopausal SSc onset, and 130 (14.4%) reported an early menopause. Post-menopausal patients had more frequent limited cutaneous SSc, anti-centromere antibody positivity, interstitial lung disease, and gastrointestinal manifestations. Pre-menopausal onset cases showed more frequent diffuse cutaneous involvement and peripheral vasculopathy. Patients with early menopause had more frequent peripheral vasculopathy and interstitial lung disease, being early menopause an independent risk factor for digital ulcers and lower diffusing capacity of the lung for carbon monoxide.
Current post-menopausal status and early menopause may impact SSc presentation, being associated with vascular and gastrointestinal manifestations. Menopausal status and age should therefore be thoroughly addressed, aiming at better disease management.
更年期的激素变化可能与潜在自身免疫性疾病的表现相互作用,如系统性硬化症(SSc)。
我们的研究旨在评估(1)当前更年期状态、(2)早发性更年期以及(3)在育龄期或绝经后发病对来自意大利系统性硬化症进展调查(SPRING - SIR)登记处的大型SSc队列中SSc临床表型的影响。
来自SPRING - SIR登记处的女性SSc患者,符合美国风湿病学会(ACR)/欧洲风湿病联盟(EULAR)2013年分类标准,且有SSc疾病发病、更年期状态和绝经年龄数据的患者符合条件。如果SSc发病发生在绝经前1年以上,则分类为绝经前发病;如果发生在绝经后1年以上,则分类为绝经后发病。早发性更年期定义为绝经年龄<45岁。
建立描述性统计和回归模型,以检验当前更年期状态、绝经前疾病发病和早发性更年期与SSc相关特征之间的关联。
基线时,1157/1538(75%)的患者处于更年期,632例(50.4%)有绝经前SSc发病,130例(14.4%)报告有早发性更年期。绝经后患者局限性皮肤型SSc、抗着丝点抗体阳性、间质性肺病和胃肠道表现更为常见。绝经前发病的病例弥漫性皮肤受累和外周血管病变更为常见。早发性更年期患者外周血管病变和间质性肺病更为常见,早发性更年期是指端溃疡和肺一氧化碳弥散能力降低的独立危险因素。
当前的绝经后状态和早发性更年期可能影响SSc的表现,与血管和胃肠道表现相关。因此,应全面考虑更年期状态和年龄,以更好地管理疾病。