医学
狼疮性肾炎
队列
内科学
来复枪
比例危险模型
系统性红斑狼疮
疾病
考古
历史
作者
Shirley Chiu Wai Chan,Yongfei Wang,Desmond Y. H. Yap,Tak Mao Chan,YL Lau,Pamela Lee,Wai Ming Lai,Shirley King Yee Ying,Niko Kei Chiu Tse,Moon Ho Leung,Chi Chiu Mok,Ka Lai Lee,Teresa W. L. Li,Helen Hoi Lun Tsang,Winnie Wan Yin Yeung,Carmen Ho,Raymond Woon Sing Wong,Wanling Yang,Chak Sing Lau,Philip H. Li
标识
DOI:10.3389/fimmu.2023.1200732
摘要
Objectives Lupus nephritis (LN) remains one of the most severe manifestations in patients with systemic lupus erythematosus (SLE). Onset and overall LN risk among SLE patients remains considerably difficult to predict. Utilizing a territory-wide longitudinal cohort of over 10 years serial follow-up data, we developed and validated a risk stratification strategy to predict LN risk among Chinese SLE patients – Risk and Factors associated with disease manifestations in systemic Lupus Erythematosus – Lupus Nephritis (RIFLE-LN). Methods Demographic and longitudinal data including autoantibody profiles, clinical manifestations, major organ involvement, LN biopsy results and outcomes were documented. Association analysis was performed to identify factors associated with LN. Regression modelling was used to develop a prediction model for 10-year risk of LN and thereafter validated. Results A total of 1652 patients were recruited: 1382 patients were assigned for training and validation of the RIFLE-LN model; while 270 were assigned for testing. The median follow-up duration was 21 years. In the training and validation cohort, 845 (61%) of SLE patients developed LN. Cox regression and log rank test showed significant positive association between male sex, age of SLE onset and anti-dsDNA positivity. These factors were thereafter used to develop RIFLE-LN. The algorithm was tested in 270 independent patients and showed good performance (AUC = 0·70). Conclusion By using male sex, anti-dsDNA positivity, age of SLE onset and SLE duration; RIFLE-LN can predict LN among Chinese SLE patients with good performance. We advocate its potential utility in guiding clinical management and disease monitoring. Further validation studies in independent cohorts are required.
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