Time-dependent changes in RPILD and mortality risk in anti-MDA5+ DM patients: a cohort study of 272 cases in China

医学 比例危险模型 内科学 队列 队列研究 疾病 死亡率
作者
Hanxiao You,Lei Wang,Jiajia Wang,Chengyin Lv,Lingxiao Xu,Fenghong Yuan,Ju Li,Min Wu,Shiliang Zhou,Zhanyun Da,Jie Qian,Hua Wei,Wei Yan,Lei Zhou,Yan Wang,Shi Yin,Dongmei Zhou,Jian Wu,Yan Lü,Dinglei Su,Zhichun Liu,Lin Liu,Longxin Ma,Xiaoyan Xu,Yinshan Zang,Huijie Liu,Tao Ren,Fang Wang,Miaojia Zhang,Wenfeng Tan
出处
期刊:Rheumatology [Oxford University Press]
卷期号:62 (3): 1216-1226 被引量:17
标识
DOI:10.1093/rheumatology/keac450
摘要

Abstract Objectives Anti-melanoma differentiation-associated gene 5 positive (anti-MDA5+) DM has a close relationship with rapidly progressive interstitial lung disease (RPILD) and is associated with high mortality. However, data regarding the time-dependent risk of RPILD and deaths during disease progression are limited. We conducted this study to investigate whether the risk of RPILD and death were time-dependent or not in anti-MDA5+ DM. Methods We assessed a cohort of 272 patients with anti-MDA5+ DM. The clinical characteristics of patients with anti-MDA5+ were collected, and COX regression was used to analyse independent risk factors for RPILD and death. We also described changes in risk of RPILD and death over time and their potential clinical implications. Results There were 272 anti-MDA5+ DM patients enrolled in this study. According to the multivariate cox regression analysis, short disease course, high CRP level, anti-Ro52 positive and anti-MDA5 titre (++∼+++) were independent risk factors of RPILD. High creatine kinase level, high CRP level and RPILD were independent risk factors for death, and >90% RPILD and 84% mortality occurred in the first 6 months after disease onset. Notably, the first 3 months is a particularly high-risk period, with 50% of RPILD and 46% of deaths occurring. Hazards regarding RPILD and mortality diminished over time during a median follow-up of 12 months. Conclusion These results suggest significant, time-dependent changes in RPILD and mortality risk in anti-MDA5+ DM patients, providing a cut-off time window to estimate disease progression and poor prognosis.
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