Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA 02115.
Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA 02115.
Semin Arthritis Rheum. 2017 Dec;47(3):376-383. doi: 10.1016/j.semarthrit.2017.05.011. Epub 2017 May 25.
Obesity is increasingly prevalent and related to increased risk of several autoimmune diseases, likely via generation of inflammatory adipokines. Prior studies have not evaluated obesity in relation to systemic lupus erythematosus (SLE) risk. We prospectively evaluated whether obesity was associated with increased SLE risk among women in the U.S. Nurses' Health Study cohorts.
We conducted a prospective cohort study among 238,130 women in the Nurses' Health Studies (NHS, 1976-2012; NHSII, 1989-2013). Incident SLE was confirmed by American College of Rheumatology 1997 criteria and validated through medical record review. Body mass index (BMI, kg/m) was calculated at baseline and on biennial questionnaires. Cox proportional hazards models estimated HRs (95% CIs) for SLE by cumulative average BMI category {18.5 to <25 [normal (reference)], 25 to <30 (overweight), ≥30 (obese)}, adjusting for potential time-varying confounders. Models were performed separately in each cohort; results were meta-analyzed. Sensitivity analyses used simple time-varying BMI, a 4-year lag between exposure and SLE risk window to address potential reverse causation, and evaluated BMI at age 18 and weight change since age 18. A secondary analysis started follow-up in both cohorts at similar calendar years when the prevalence of obesity in the U.S. increased most dramatically [1988 (NHS)/1989 (NHSII)].
We identified 153 NHS incident SLE cases and 115 incident NHSII cases during 5,602,653 person-years of follow-up. At baseline, 8.4% of women in NHS and 11.8% in NHSII were obese. Mean age at enrollment was 42.5 (SD 7.2) years in NHS and 34.4 (SD 4.7) years in NHSII. Cumulative average obesity was significantly associated with SLE risk in NHSII [HR = 1.85 (1.17-2.91)], but not in NHS [HR = 1.11 (0.65-1.87)] compared to normal BMI. In the meta-analysis of both cohorts, obesity was not significantly associated with increased risk of SLE [HR = 1.46 (0.88-2.40)]. Simple time-varying BMI and lagging the exposure window by 4 years produced similar findings to the primary analysis. In NHSII, a 4.54 kg gain between age 18 and enrollment slightly increased SLE risk [HR = 1.09 (1.02-1.18)]. In the secondary analysis starting follow-up of both cohorts at similar calendar years, the point estimate for obesity in NHS was higher than the primary analysis [HR = 1.67 (0.81-3.45)].
We observed an 85% significantly increased risk of SLE among obese compared to normal BMI women in the more recent NHSII cohort, but no association was observed in the earlier NHS cohort. Secular trends in obesity may account for the differences between the two birth cohorts.
肥胖症的发病率日益增高,与多种自身免疫性疾病的风险增加有关,可能是通过产生炎症性脂肪因子导致的。先前的研究并未评估肥胖症与系统性红斑狼疮(SLE)风险之间的关系。我们前瞻性地评估了肥胖症是否与美国护士健康研究队列中女性的 SLE 风险增加有关。
我们对参加护士健康研究(NHS,1976-2012 年;NHSII,1989-2013 年)的 238130 名女性进行了前瞻性队列研究。通过美国风湿病学会 1997 年标准确诊 SLE,并通过病历回顾进行验证。体重指数(BMI,kg/m)在基线和每两年一次的调查问卷中进行计算。Cox 比例风险模型估计了 SLE 的 HR(95%CI),按累积平均 BMI 类别{18.5 至<25(正常[参考]),25 至<30(超重),≥30(肥胖)},调整了潜在的时间变化混杂因素。在每个队列中分别进行了模型分析;结果进行了荟萃分析。敏感性分析使用了简单的时间变化 BMI、暴露和 SLE 风险窗口期之间的 4 年滞后,以解决潜在的反向因果关系,并评估了 18 岁时的 BMI 和 18 岁以来的体重变化。二次分析从美国肥胖症患病率急剧增加的相似历年开始在两个队列中进行随访[1988 年(NHS)/1989 年(NHSII)]。
我们在 5602653 人年的随访中发现了 153 例 NHS 新发 SLE 病例和 115 例 NHSII 新发 SLE 病例。NHS 中有 8.4%的女性和 NHSII 中有 11.8%的女性肥胖。NHS 的入组平均年龄为 42.5(SD 7.2)岁,NHSII 的入组平均年龄为 34.4(SD 4.7)岁。累积平均肥胖与 NHSII 中的 SLE 风险显著相关[HR = 1.85(1.17-2.91)],但与 NHS 中的肥胖与 SLE 风险无显著相关性[HR = 1.11(0.65-1.87)]。在两个队列的荟萃分析中,肥胖与 SLE 风险增加无显著相关性[HR = 1.46(0.88-2.40)]。简单的时间变化 BMI 和将暴露窗口期滞后 4 年的结果与主要分析相似。在 NHSII 中,18 岁至入组时体重增加 4.54 公斤略微增加了 SLE 风险[HR = 1.09(1.02-1.18)]。在从相似历年开始对两个队列进行随访的二次分析中,NHS 中肥胖的点估计值高于主要分析[HR = 1.67(0.81-3.45)]。
我们观察到,与正常 BMI 的女性相比,NHSII 中肥胖的女性患 SLE 的风险增加了 85%,但在较早的 NHS 队列中没有观察到这种关联。肥胖症的流行趋势可能是这两个出生队列之间差异的原因。