{"title":"Organ damage profiles and associated factors in juvenile versus adult-onset SLE: a matched analysis from the Japanese ANSWER-SLE cohort.","authors":"Shion Kachi, Hideaki Tsuji, Akira Onishi, Kaori Ishimura, Hirofumi Miyake, Natsuko Esa, Yuri Hiramatsu, Masao Katsushima, Hideki Oka, Shigeru Iwata, Wataru Yamamoto, Koichiro Ohmura, Takao Fujii, Yuji Nozaki, Motomu Hashimoto, Akio Morinobu","doi":"10.1093/rheumatology/keag575","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>To elucidate differences in organ damage in patients with systemic lupus erythematosus (SLE) between juvenile-onset (<18 years) and adult-onset (≥18 years) using the Systemic Lupus International Collaborating Clinics Damage Index (SDI).</p><p><strong>Methods: </strong>Among patients in the multicenter registry, ANSWER-SLE (2019-2023), total-SDI and organ domains of SDI were compared between juvenile- and adult-onset patients after 1:2 matching based on sex and current age. Factors associated with total SDI and organ domains of SDI were analyzed by regression models in the total population.</p><p><strong>Results: </strong>A total of 615 patients were included. Among them, 83 juvenile- and 166 adult-onset patients were matched. Juvenile-onset showed higher total-SDI (juvenile-onset vs. adult-onset, 2.17 vs. 1.16) and higher damage in the ocular, nervous system, renal, cardiovascular, and musculoskeletal domains than adult-onset. In the multivariable negative binomial regression analysis of the total cohort, younger age at onset (incidence rate ratio [IRR] 0.99, p=0.005) and older current age (IRR 1.03, p<0.001) were independently associated with higher total SDI scores. These associations persisted in the matched cohort (IRR 0.96 and IRR 1.03, respectively). In multivariable analyses of organ-specific damage adjusted for sex, current age, and age at onset, younger age at onset was associated with a higher SDI in the cataract, angina/coronary artery bypass, valvular disease, avascular necrosis, skin ulceration, and premature gonadal failure in the total cohort, and additionally with renal domain in the matched cohort.</p><p><strong>Conclusions: </strong>Juvenile-onset SLE is associated with organ damage compared to adult-onset SLE, with prominent ocular, neurological, renal, cardiovascular, and musculoskeletal systems.</p>","PeriodicalId":21255,"journal":{"name":"Rheumatology","volume":" ","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2026-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rheumatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/rheumatology/keag575","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: To elucidate differences in organ damage in patients with systemic lupus erythematosus (SLE) between juvenile-onset (<18 years) and adult-onset (≥18 years) using the Systemic Lupus International Collaborating Clinics Damage Index (SDI).
Methods: Among patients in the multicenter registry, ANSWER-SLE (2019-2023), total-SDI and organ domains of SDI were compared between juvenile- and adult-onset patients after 1:2 matching based on sex and current age. Factors associated with total SDI and organ domains of SDI were analyzed by regression models in the total population.
Results: A total of 615 patients were included. Among them, 83 juvenile- and 166 adult-onset patients were matched. Juvenile-onset showed higher total-SDI (juvenile-onset vs. adult-onset, 2.17 vs. 1.16) and higher damage in the ocular, nervous system, renal, cardiovascular, and musculoskeletal domains than adult-onset. In the multivariable negative binomial regression analysis of the total cohort, younger age at onset (incidence rate ratio [IRR] 0.99, p=0.005) and older current age (IRR 1.03, p<0.001) were independently associated with higher total SDI scores. These associations persisted in the matched cohort (IRR 0.96 and IRR 1.03, respectively). In multivariable analyses of organ-specific damage adjusted for sex, current age, and age at onset, younger age at onset was associated with a higher SDI in the cataract, angina/coronary artery bypass, valvular disease, avascular necrosis, skin ulceration, and premature gonadal failure in the total cohort, and additionally with renal domain in the matched cohort.
Conclusions: Juvenile-onset SLE is associated with organ damage compared to adult-onset SLE, with prominent ocular, neurological, renal, cardiovascular, and musculoskeletal systems.
期刊介绍:
Rheumatology strives to support research and discovery by publishing the highest quality original scientific papers with a focus on basic, clinical and translational research. The journal’s subject areas cover a wide range of paediatric and adult rheumatological conditions from an international perspective. It is an official journal of the British Society for Rheumatology, published by Oxford University Press.
Rheumatology publishes original articles, reviews, editorials, guidelines, concise reports, meta-analyses, original case reports, clinical vignettes, letters and matters arising from published material. The journal takes pride in serving the global rheumatology community, with a focus on high societal impact in the form of podcasts, videos and extended social media presence, and utilizing metrics such as Altmetric. Keep up to date by following the journal on Twitter @RheumJnl.