Fukui Sho, Winkelmayer Wolfgang C, Tedeschi Sara K, Marrugo Javier, Guan Hongshu, Harrold Leslie, Litman Heather J, Shinozaki Tomohiro, Solomon Daniel H
Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA; Department of Emergency and General Medicine, Kyorin University, Tokyo, Japan; Immuno-Rheumatology Center, St. Luke's International Hospital, Tokyo, Japan.
Selzman Institute for Kidney Health, Section of Nephrology, Baylor College of Medicine, Houston, Texas, USA.
Ann Rheum Dis. 2025 Feb;84(2):201-209. doi: 10.1136/ard-2024-226156. Epub 2025 Jan 2.
Chronic kidney disease (CKD) is a common comorbidity of rheumatoid arthritis (RA). The association of longitudinal RA disease activity with long-term kidney function has remained uncertain.
We analysed a multicentre prospective RA registry in the USA from 2001 to 2022. The exposure was updated time-averaged Clinical Disease Activity Index (TA-CDAI) categories from study enrolment. The primary outcome was a longitudinal estimated glomerular filtration rate (eGFR) change. Secondary outcomes included developments of CKD stage G3a (eGFR<60 mL/min/1.73 m) and stage G3b (eGFR<45 mL/min/1.73 m). Results were adjusted for relevant time-fixed and time-varying covariates.
31 129 patients (median age: 58.0 years, female: 76.3%, median eGFR: 90.7 mL/min/1.73 m) contributed 234 973 visits and 146 778 person-years of follow-up. Multivariable mixed-effect linear model showed an average annual eGFR decline during follow-up in the TA-CDAI-remission group of -0.83 mL/min/1.73 m and estimated additional annual declines (95% CI) of -0.09 (-0.15 to -0.03) in low, -0.17 (-0.23 to -0.10) in moderate and -0.18 (-0.27 to -0.08) mL/min/1.73 m in high disease activity patients. Compared with TA-CDAI remission, adjusted HRs (95% CI) for CKD stage G3a during follow-up were 1.15 (1.01 to 1.30) in low, 1.22 (1.06 to 1.40) in moderate and 1.27 (1.05 to 1.52) in high disease activity; for CKD stage G3b, 1.22 (0.84 to 1.76) in low, 1.66 (1.12 to 2.45) in moderate and 1.93 (1.16 to 3.20) in high disease activity.
Higher RA disease activity was associated with accelerated eGFR decline and increased risk of clinically relevant kidney dysfunction. Future intervention studies should attempt to replicate the association between RA disease activity and eGFR.
慢性肾脏病(CKD)是类风湿关节炎(RA)常见的合并症。RA疾病活动的纵向变化与长期肾功能之间的关联尚不确定。
我们分析了美国2001年至2022年的一项多中心前瞻性RA登记研究。暴露因素为自研究入组起更新的时间平均临床疾病活动指数(TA-CDAI)类别。主要结局是纵向估计肾小球滤过率(eGFR)的变化。次要结局包括CKD 3a期(eGFR<60 mL/min/1.73 m²)和3b期(eGFR<45 mL/min/1.73 m²)的发生情况。对结果进行了相关时间固定和时间变化协变量的校正。
31129例患者(中位年龄:58.0岁,女性:76.3%,中位eGFR:90.7 mL/min/1.73 m²)贡献了234973次就诊和146778人年的随访。多变量混合效应线性模型显示,TA-CDAI缓解组在随访期间eGFR平均每年下降0.83 mL/min/1.73 m²,低疾病活动度患者估计每年额外下降(95%CI)为-0.09(-0.15至-0.03),中度为-0.17(-0.23至-0.10),高疾病活动度患者为-0.18(-0.27至-0.08)mL/min/1.73 m²。与TA-CDAI缓解相比,随访期间CKD 3a期的校正风险比(95%CI)在低疾病活动度时为1.15(1.01至1.30),中度为1.22(1.06至1.40),高疾病活动度时为1.27(1.05至1.52);CKD 3b期,低疾病活动度时为1.22(0.84至1.76),中度为1.66(1.12至2.45),高疾病活动度时为1.93(1.16至3.20)。
较高的RA疾病活动度与eGFR加速下降及临床相关肾功能障碍风险增加相关。未来的干预研究应尝试重现RA疾病活动度与eGFR之间的关联。