Comorbidity clusters and their relationship with severity and outcomes of index diseases, in a large multicentre systemic lupus erythematosus cohort.

IF 3.7 2区 医学 Q1 RHEUMATOLOGY
Iñigo Rua-Figueroa, Natalia Pérez-Veiga, Esther Rodríguez-Almaraz, María Galindo-Izquierdo, Celia Erausquin, Antonio Fernandez-Nebro, Esther Uriarte Itzazelaia, Belén Serrano-Benavente, Jaime Calvo Alén, Sara Manrique-Arija, Jose M Senabre, Jose A Bernal, Javier Narvaez, Eva Tomero, Elena Aurrecoechea, Mónica Ibáñez-Barceló, Vicente Torrente Segarra, Clara Sangüesa, Mercedes Freire-González, María Jesús García-Villanueva, Víctor Martínez Taboada, Marta Arevalo, Claudia Moriano Morales, Carlota Iñiguez, Ana Perez, Eva Salgado, Irene Carrión-Barberà, Jose L Andreu, Tatiana Cobo, Loreto Horcada, Gema Bonilla, Nuria Lozano-Rivas, Lorena Exposito, Carlos Montilla, Francisco J Toyos, Oihane Ibarguengoitia-Barrena, Elia Valls Pascual, Javier Nóvoa Medina, Raúl Menor-Almagro, Jose Andrés Roman Ivorra, Alejandro Muñoz Jiménez, Joan M Nolla, Jose Maria Pego-Reigosa
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Abstract

Objective: Patients with SLE have a well-known increased risk of major comorbidities, although they are also very heterogeneous in terms of the prevalence of comorbid conditions. The relationships of such comorbidities with the outcomes and the severity of index diseases are less known. We aimed to evaluate the interactions between comorbid conditions, in a large multicentre SLE cohort, and their impact on severity and outcomes, using a cluster analysis.

Methods: Data on 14 cumulative comorbidities were derived from patients with SLE (American College of Rheumatology (ACR)-97 criteria) who had been included in the retrospective phase of the RELESSER (Spanish Society of Rheumatology National Register of SLE). The Severity Katz Index and the SLICC/ACR Damage Index were calculated. Unsupervised cluster analysis was performed to better characterise the relationships between comorbidities in a large multicentre cohort of patients with SLE. For intercluster differences testing, analysis of variance and Tukey tests were used to compare continuous numerical variables; a Kruskal-Wallis test to discrete variables and the χ² (or Fisher's exact test) were used for categorical ones.

Results: A total of 3658 patients with SLE were included. Men accounted for 9.6% of patients. The mean (SD) age was 45.9 years, and 93% were Caucasian. Four clusters, with markedly different comorbidity profiles and outcomes, were identified: in cluster 2 (n=516), patients were grouped around depression (100% of the cases); in cluster 3 (n=418) around serious infections (100%); and in cluster 4 (n=388) around cardiovascular events (also 100%). However, in cluster 1, the largest one (n=2336), no patient had any of the three defining comorbidities of the other clusters, and this cluster was associated with the best outcomes.

Conclusions: Cluster analysis identifies well-differentiated subsets of patients with SLE in terms of their comorbidities. The most relevant comorbidities in SLE tend to aggregate in the most severe patient subsets.

在一个大型多中心系统性红斑狼疮队列中,共病集群及其与严重程度和指标疾病结局的关系
目的:众所周知,SLE患者发生主要合并症的风险增加,尽管他们在合并症的患病率方面也非常不同。这些合并症与预后和指数疾病严重程度的关系尚不清楚。我们的目的是通过聚类分析,在一个大型多中心SLE队列中评估合并症之间的相互作用,以及它们对严重程度和结局的影响。方法:14项累积合并症的数据来自SLE患者(美国风湿病学会(ACR)-97标准),这些患者已纳入RELESSER(西班牙风湿病学会国家SLE登记)的回顾性阶段。计算了严重程度Katz指数和SLICC/ACR损伤指数。在一个大型多中心SLE患者队列中进行无监督聚类分析,以更好地描述合并症之间的关系。聚类间差异检验采用方差分析和Tukey检验对连续数值变量进行比较;离散变量使用Kruskal-Wallis检验,分类变量使用χ 2(或Fisher精确检验)。结果:共纳入3658例SLE患者。男性占9.6%。平均(SD)年龄为45.9岁,93%为白种人。共病概况和结果明显不同的四组患者被确定:在第2组(n=516)中,患者按抑郁症分组(100%的病例);在第3类(n=418)严重感染周围(100%);在第4组(n=388)中,心血管事件的发生率也是100%。然而,在最大的第1组(n=2336)中,没有患者出现其他组中定义的三种合并症中的任何一种,并且该组与最佳结果相关。结论:聚类分析在合并症方面确定了SLE患者的良好分化亚群。SLE中最相关的合并症往往聚集在最严重的患者亚群中。
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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