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Comparative effects of biological and targeted synthetic DMARDs on incident chronic kidney disease in patients with rheumatoid arthritis
Rheumatology ( IF 4.7 ) Pub Date : 2024-10-30 , DOI: 10.1093/rheumatology/keae603 Nozomi Nishimura, Akira Onishi, Wataru Yamamoto, Koji Nagai, Hideyuki Shiba, Yasutaka Okita, Yonsu Son, Hideki Amuro, Takaichi Okano, Yo Ueda, Ryota Hara, Masaki Katayama, Shinsuke Yamada, Motomu Hashimoto, Yuichi Maeda, Hideo Onizawa, Takayuki Fujii, Koichi Murata, Kosaku Murakami, Masao Tanaka, Shuichi Matsuda, Akio Morinobu
Rheumatology ( IF 4.7 ) Pub Date : 2024-10-30 , DOI: 10.1093/rheumatology/keae603 Nozomi Nishimura, Akira Onishi, Wataru Yamamoto, Koji Nagai, Hideyuki Shiba, Yasutaka Okita, Yonsu Son, Hideki Amuro, Takaichi Okano, Yo Ueda, Ryota Hara, Masaki Katayama, Shinsuke Yamada, Motomu Hashimoto, Yuichi Maeda, Hideo Onizawa, Takayuki Fujii, Koichi Murata, Kosaku Murakami, Masao Tanaka, Shuichi Matsuda, Akio Morinobu
Objectives The impact of individual biological/targeted synthetic disease-modifying anti-rheumatic drug (b/tsDMARD) on kidney function in patients with rheumatoid arthritis (RA) remains unclear. This study aimed to determine the comparative effects of b/tsDMARDs on chronic kidney disease (CKD) incidence in patients with RA. Methods This multicentre cohort study included patients with RA who had baseline estimated glomerular filtration rate (eGFR) of ≥ 60 mL/min/1.73 m2 and started a tumor necrosis factor inhibitor (TNFi), cytotoxic T lymphocyte-associated antigen-4-Ig (CTLA4-Ig), interleukin-6 receptor inhibitor (IL-6Ri), or Janus kinase inhibitor (JAKi) in Japan. Multiple propensity score-based inverse probability weighting (IPW) was used to adjust confounders. The incidence of CKD was compared among b/tsDMARDs using IPW mixed-effect Cox proportional hazards models and linear mixed-effect models with IPW examined trajectories of eGFR. Results Among 2187 patients with 3068 treatment courses and up to 11 years of follow-up, CKD occurred in 275 cases. Compared with the CTLA4-Ig group, the TNFi group had a significantly lower CKD incidence (hazard ratio [HR] 0.67, 95% confidence interval [CI] 0.46–0.97, p= 0.04), whereas the JAKi group had a significantly higher incidence (HR 2.16, 95% CI 1.23–3.79, p= 0.01). The trajectory of eGFR was significantly greater in the JAKi group than in the CTLA4-Ig group (CTLA4-Ig: −1.28 mL/min/1.73 m2/year, JAKi: −2.29 mL/min/1.73 m2/year, p< 0.001). Conclusions TNFi use was associated with reduced CKD incidence, whereas JAKi showed a less protective association for kidney function in patients with RA.
中文翻译:
生物和靶向合成 DMARD 对类风湿性关节炎患者慢性肾病发病率的比较影响
目的 个体生物/靶向合成疾病缓解抗风湿药 (b/tsDMARD) 对类风湿性关节炎 (RA) 患者肾功能的影响仍不清楚。本研究旨在确定 b/tsDMARDs 对 RA 患者慢性肾脏病 (CKD) 发病率的比较影响。方法 这项多中心队列研究纳入了基线估计肾小球滤过率 (eGFR) 为 ≥ 60 mL/min/1.73 m2 并开始使用肿瘤坏死因子抑制剂 (TNFi) 、细胞毒性 T 淋巴细胞相关抗原-4-Ig (CTLA4-Ig)、白细胞介素-6 受体抑制剂 (IL-6Ri) 或 Janus 激酶抑制剂 (JAKi) 的 RA 患者在日本。使用基于多倾向得分的逆概率加权 (IPW) 来调整混杂因素。使用 IPW 混合效应 Cox 比例风险模型和线性混合效应模型比较 b/tsDMARD 的 CKD 发生率,其中 IPW 检查 eGFR 的轨迹。结果 2187 例患者,3068 个疗程,随访长达 11 年,其中 275 例发生 CKD。与 CTLA4-Ig 组相比,TNFi 组的 CKD 发生率显著降低 (风险比 [HR] 0.67,95% 置信区间 [CI] 0.46-0.97,p = 0.04),而 JAKi 组的发生率显著较高 (HR 2.16,95% CI 1.23-3.79,p = 0.01)。JAKi 组的 eGFR 轨迹显著大于 CTLA4-Ig 组 (CTLA4-Ig: -1.28 mL/min/1.73 m2/年,JAKi:-2.29 mL/min/1.73 m2/年,p< 0.001)。结论 TNFi 使用与 CKD 发生率降低相关,而 JAKi 对 RA 患者肾功能的保护性关联较小。
更新日期:2024-10-30
中文翻译:
生物和靶向合成 DMARD 对类风湿性关节炎患者慢性肾病发病率的比较影响
目的 个体生物/靶向合成疾病缓解抗风湿药 (b/tsDMARD) 对类风湿性关节炎 (RA) 患者肾功能的影响仍不清楚。本研究旨在确定 b/tsDMARDs 对 RA 患者慢性肾脏病 (CKD) 发病率的比较影响。方法 这项多中心队列研究纳入了基线估计肾小球滤过率 (eGFR) 为 ≥ 60 mL/min/1.73 m2 并开始使用肿瘤坏死因子抑制剂 (TNFi) 、细胞毒性 T 淋巴细胞相关抗原-4-Ig (CTLA4-Ig)、白细胞介素-6 受体抑制剂 (IL-6Ri) 或 Janus 激酶抑制剂 (JAKi) 的 RA 患者在日本。使用基于多倾向得分的逆概率加权 (IPW) 来调整混杂因素。使用 IPW 混合效应 Cox 比例风险模型和线性混合效应模型比较 b/tsDMARD 的 CKD 发生率,其中 IPW 检查 eGFR 的轨迹。结果 2187 例患者,3068 个疗程,随访长达 11 年,其中 275 例发生 CKD。与 CTLA4-Ig 组相比,TNFi 组的 CKD 发生率显著降低 (风险比 [HR] 0.67,95% 置信区间 [CI] 0.46-0.97,p = 0.04),而 JAKi 组的发生率显著较高 (HR 2.16,95% CI 1.23-3.79,p = 0.01)。JAKi 组的 eGFR 轨迹显著大于 CTLA4-Ig 组 (CTLA4-Ig: -1.28 mL/min/1.73 m2/年,JAKi:-2.29 mL/min/1.73 m2/年,p< 0.001)。结论 TNFi 使用与 CKD 发生率降低相关,而 JAKi 对 RA 患者肾功能的保护性关联较小。