Monoclonal gammopathy in systemic lupus erythematosus is associated with distinctive clinical course, malignancy and mortality rate: a single-centre retrospective cohort study.

IF 3.7 2区 医学 Q1 RHEUMATOLOGY
Andzelika Siwiec-Kozlik, Pawel Kozlik-Siwiec, Magdalena Spalkowska, Mariusz Korkosz, Joanna Kosalka-Wegiel
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引用次数: 0

Abstract

Objectives: Rheumatic diseases were previously associated with increased incidence of monoclonal gammopathy (MG) and its malignant transformation. The present study aimed to investigate the prevalence, malignant transformation risk, clinical correlates and prognostic impact of MG in SLE.

Methods: A retrospective cohort study based on the medical records of n=1039 patients with SLE fulfilling the 1997 American College of Rheumatology (ACR), the 2019 European Alliance of Associations for Rheumatology (EULAR)/ACR and/or the 2012 Systemic Lupus International Collaborating Clinics (SLICC) criteria managed at two tertiary care departments of the University Hospital (Krakow, Poland) from January 2012 until November 2019.

Results: SLE+MG cases were older at SLE diagnosis compared with non-MG SLE controls (53±15 years vs 37±15 years, respectively, p<0.01), had higher rates of lymphopenia, anaemia, haemolysis, serous effusions and interstitial lung disease (all p<0.05), and were more frequently treated with cyclophosphamide (57% vs 28%, p<0.01) or rituximab (13% vs 3%, p<0.01). Most MG cases were detected within a year after SLE diagnosis (Q25, Q75: 0, 12 years). With the median follow-up of 11 years (Q25, Q75: 6, 19 years), 34.8% (8 cases) of the SLE+MG cohort were diagnosed with malignancy, compared with 8.1% (82 cases) among the SLE controls (p<0.001). MG was associated with the relative hazard of death of HR 2.99 (95% CI 1.26 to 7.06, p<0.05) and a median survival time from SLE diagnosis to death of 5 years (Q25, Q75: 1, 14; range 0-41) for SLE+MG cases, as compared with 12 years (Q25, Q75: 6, 19; range 0-62) for the controls. The effect was non-independent on antimalarial medication use.

Conclusions: Our study emphasises heightened malignancy and mortality rates in SLE+MG cases. The association between immunosuppression, MG incidence and progression warrants further research.

系统性红斑狼疮中的单克隆丙种球蛋白病与独特的临床过程、恶性肿瘤和死亡率有关:一项单中心回顾性队列研究。
目的:风湿性疾病曾与单克隆丙种球蛋白病(MG)及其恶性转化的发病率增加有关。本研究旨在探讨系统性红斑狼疮中单克隆抗体的患病率、恶性转化风险、临床相关性和对预后的影响:一项回顾性队列研究,以2012年1月至2019年11月期间波兰克拉科夫大学医院两个三级医疗部门管理的符合1997年美国风湿病学会(ACR)、2019年欧洲风湿病学协会联盟(EULAR)/ACR和/或2012年系统性红斑狼疮国际合作诊所(SLICC)标准的1039名系统性红斑狼疮患者的病历为基础:结果:与非MG系统性红斑狼疮对照组相比,系统性红斑狼疮+MG病例在确诊时年龄更大(分别为53±15岁和37±15岁,p):我们的研究强调了系统性红斑狼疮+MG 病例恶性肿瘤和死亡率的升高。免疫抑制、MG发病率和进展之间的关系值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lupus Science & Medicine
Lupus Science & Medicine RHEUMATOLOGY-
CiteScore
5.30
自引率
7.70%
发文量
88
审稿时长
15 weeks
期刊介绍: Lupus Science & Medicine is a global, peer reviewed, open access online journal that provides a central point for publication of basic, clinical, translational, and epidemiological studies of all aspects of lupus and related diseases. It is the first lupus-specific open access journal in the world and was developed in response to the need for a barrier-free forum for publication of groundbreaking studies in lupus. The journal publishes research on lupus from fields including, but not limited to: rheumatology, dermatology, nephrology, immunology, pediatrics, cardiology, hepatology, pulmonology, obstetrics and gynecology, and psychiatry.
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