Department of Medicine, Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, 60 Fenwood Road, #6016U, Boston, MA, 02115, USA.
Harvard Medical School, Boston, MA, USA.
Clin Rheumatol. 2019 Jan;38(1):243-250. doi: 10.1007/s10067-018-4261-5. Epub 2018 Aug 14.
Our objective was to investigate whether a dietary pattern derived using inflammatory biomarkers is associated with rheumatoid arthritis (RA) risk. We prospectively followed 79,988 women in the Nurses' Health Study (NHS, 1984-2014) and 93,572 women in the NHSII (1991-2013); incident RA was confirmed by medical records. Food frequency questionnaires (FFQ) were completed at baseline and approximately every 4 years. Inflammatory dietary pattern was assessed from FFQ data using the Empirical Dietary Inflammatory Pattern (EDIP), including 18 anti-/pro-inflammatory food/beverage groups weighted by correlations with plasma inflammatory biomarkers (interleukin-6, C-reactive protein, and tumor necrosis factor-α receptor 2). We investigated associations between EDIP and RA using Cox regression. We identified 1185 incident RA cases over 4,425,434 person-years. EDIP was not associated with overall RA risk (p trend = 0.21 across EDIP quartiles). Among women ≤ 55 years, increasing EDIP was associated with increased overall RA risk; HRs (95% CIs) across EDIP quartiles were 1.00 (reference), 1.14 (0.86-1.51), 1.35 (1.03-1.77), and 1.38 (1.05-1.83; p for trend = 0.01). Adjusting for BMI attenuated this association. Increasing EDIP was associated with increased seropositive RA risk among women ≤ 55 years (p for trend = 0.04). There was no association between EDIP and RA among women > 55 years (EDIP-age interaction, p = 0.03). An inflammatory dietary pattern was associated with increased seropositive RA risk with onset ≤ 55 years old, and this association may be partially mediated through BMI.
我们的目的是探究基于炎症生物标志物构建的饮食模式是否与类风湿关节炎(RA)风险相关。我们前瞻性地随访了护士健康研究(NHS,1984-2014 年)中的 79988 名女性和 NHSII(1991-2013 年)中的 93572 名女性;通过医疗记录确诊 RA。在基线和大约每 4 年时完成食物频率问卷(FFQ)。使用经验性饮食炎症模式(EDIP),根据与炎症生物标志物(白细胞介素-6、C 反应蛋白和肿瘤坏死因子-α受体 2)相关性的权重,对 FFQ 数据进行了炎症饮食模式的评估,其中包含 18 种抗/促炎食物/饮料组。我们使用 Cox 回归分析 EDIP 与 RA 之间的关联。我们在 4425434 人年中发现了 1185 例 RA 新发病例。EDIP 与总体 RA 风险无关(p 趋势=0.21,四分位数之间)。在≤55 岁的女性中,随着 EDIP 的增加,总体 RA 风险增加;EDIP 四分位数之间的 HR(95%CI)分别为 1.00(参考)、1.14(0.86-1.51)、1.35(1.03-1.77)和 1.38(1.05-1.83;p 趋势=0.01)。调整 BMI 后,该关联减弱。在≤55 岁的女性中,随着 EDIP 的增加,血清阳性 RA 风险增加(p 趋势=0.04)。在>55 岁的女性中,EDIP 与 RA 之间没有关联(EDIP-年龄交互作用,p=0.03)。在≤55 岁发病的女性中,炎症饮食模式与血清阳性 RA 风险增加相关,这种关联可能部分通过 BMI 介导。