Suzon Benoit, Louis-Sidney Fabienne, Aglaé Cédric, Henry Kim, Bagoée Cécile, Wolff Sophie, Moinet Florence, Emal-Aglaé Violaine, Polomat Katlyne, DeBandt Michel, Deligny Christophe, Couturier Aymeric
Department of Internal Medicine, Martinique University Hospital, CEDEX CS, 90632 Fort-de-France, Martinique, France.
Department of Rheumatology, Martinique University Hospital, CEDEX CS, 90632 Fort-de-France, Martinique, France.
J Clin Med. 2022 Aug 19;11(16):4860. doi: 10.3390/jcm11164860.
Lupus nephritis (LN) has been described as having worse survival and renal outcomes in African-descent patients than Caucasians. We aimed to provide long-term population-based data in an Afro-descendant cohort of LN with high income and easy and free access to specialized healthcare.
We performed a retrospective population-based analysis using data from 2002-2015 of 1140 renal biopsies at the University Hospital of Martinique (French West Indies). All systemic lupus erythematosus patients with a diagnosis of LN followed for at least 12 months in Martinique or who died during this period were included.
A total of 89 patients were included, of whom 68 (76.4%) had proliferative (class III or IV), 17 (19.1%) had membranous (class V), and 4 (4.5%) had class I or II lupus nephritis according to the ISN/RPS classification. At a mean follow-up of 118.3 months, 51.7% of patients were still in remission. The rates of end-stage renal disease were 13.5%, 19.1%, and 21.3% at 10, 15, and 20 years of follow-up, respectively, and mortality rates were 4.5%, 5.6%, and 7.9% at 10, 15, and 20 years of follow-up, respectively.
The good survival of our Afro-descendant LN patients, similar to that observed in Caucasians, shades the burden of ethnicity but rather emphasizes and reinforces the importance of optimizing all modifiable factors associated with poor outcome, especially socioeconomics.
狼疮性肾炎(LN)在非洲裔患者中的生存率和肾脏预后被描述为比白种人更差。我们旨在提供一个高收入且能轻松免费获得专科医疗服务的非洲裔LN队列的长期基于人群的数据。
我们使用了马提尼克大学医院(法属西印度群岛)2002年至2015年期间1140例肾活检的数据进行回顾性人群分析。纳入所有在马提尼克被诊断为LN且随访至少12个月或在此期间死亡的系统性红斑狼疮患者。
共纳入89例患者,根据国际肾脏病学会/肾脏病理学会(ISN/RPS)分类,其中68例(76.4%)为增殖性(III或IV级),17例(19.1%)为膜性(V级),4例(4.5%)为I或II级狼疮性肾炎。平均随访118.3个月时,51.7%的患者仍处于缓解期。随访10年、15年和20年时的终末期肾病发生率分别为13.5%、19.1%和21.3%,死亡率分别为4.5%、5.6%和7.9%。
我们非洲裔LN患者的良好生存率与白种人相似,淡化了种族负担,而是强调并强化了优化所有与不良预后相关的可改变因素的重要性,尤其是社会经济因素。