Bengtsson Camilla, Malspeis Susan, Orellana Cecilia, Sparks Jeffrey A, Costenbader Karen H, Karlson Elizabeth W
Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Brigham & Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Arthritis Care Res (Hoboken). 2017 Nov;69(11):1676-1684. doi: 10.1002/acr.23194. Epub 2017 Sep 21.
To investigate whether menopausal factors are associated with the development of serologic rheumatoid arthritis (RA) phenotypes.
Data were analyzed from the Nurses' Health Studies (NHS; 1976-2010 and NHSII 1989-2011). A total of 120,700 female nurses ages 30-55 years in the NHS, and a total of 116,430 female nurses ages 25-42 years in the NHSII, were followed via biennial questionnaires on lifestyle and disease outcomes. In total, 1,096 incident RA cases were confirmed by questionnaire and chart review. Seropositive RA was defined as rheumatoid factor positive (RF) or antibodies to citrullinated protein antigen (ACPA) positive, and seronegative RA was defined as RF negative and ACPA negative. We used Cox proportional hazards models to obtain multivariable-adjusted hazard ratios (HRs) with 95% confidence intervals (95% CIs) of seropositive/seronegative RA associated with menopausal status, age at menopause, type of menopause, ovulatory years, and postmenopausal hormone therapy (PMH) use.
Postmenopausal women had a 2-fold increased risk of seronegative RA, compared with premenopausal women (NHS: HR 1.8 [95% CI 1.1-3.0], NHSII: HR 2.4 [95% CI 1.4-3.9], and pooled HR 2.1 [95% CI 1.4-3.0]). Natural menopause at early age (≤44 years) was associated with an increased risk of seronegative RA (pooled HR 2.4 [95% CI 1.5-4.0]). None of the menopausal factors was significantly associated with seropositive RA. We observed no association between PMH use and the risk of seronegative or seropositive RA, except that PMH use of ≥8 years was associated with increased risk of seropositive RA (pooled HR 1.4 [95% CI 1.1-1.9]).
Postmenopause and natural menopause at an early age were strongly associated with seronegative RA, but only marginally with seropositive RA, suggesting potential differences in the etiology of RA subtypes.
探讨绝经因素是否与血清学类风湿关节炎(RA)表型的发生有关。
对护士健康研究(NHS;1976 - 2010年)和护士健康研究II(NHSII;1989 - 2011年)的数据进行分析。NHS中共有120700名年龄在30 - 55岁的女性护士,NHSII中共有116430名年龄在25 - 42岁的女性护士,通过每两年一次关于生活方式和疾病结局的问卷调查进行随访。总共通过问卷和病历审查确认了1096例新发RA病例。血清阳性RA定义为类风湿因子阳性(RF)或抗瓜氨酸化蛋白抗原(ACPA)抗体阳性,血清阴性RA定义为RF阴性且ACPA阴性。我们使用Cox比例风险模型来获得与绝经状态、绝经年龄、绝经类型、排卵年限和绝经后激素治疗(PMH)使用相关的血清阳性/血清阴性RA的多变量调整风险比(HRs)及95%置信区间(95% CIs)。
与绝经前女性相比,绝经后女性患血清阴性RA的风险增加了2倍(NHS:HR 1.8 [95% CI 1.1 - 3.0],NHSII:HR 2.4 [95% CI 1.4 - 3.9],合并HR 2.1 [95% CI 1.4 - 3.0])。早年自然绝经(≤44岁)与血清阴性RA风险增加相关(合并HR 2.4 [95% CI 1.5 - 4.0])。没有任何绝经因素与血清阳性RA显著相关。我们观察到PMH使用与血清阴性或血清阳性RA风险之间无关联,除了使用PMH≥8年与血清阳性RA风险增加相关(合并HR 1.4 [95% CI 1.1 - 1.9])。
绝经后和早年自然绝经与血清阴性RA密切相关,但与血清阳性RA仅存在微弱关联,提示RA亚型病因可能存在差异。