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High Comorbidity Burden in Patients with SLE: Data from the Community-Based Lupus Registry of Crete

Comorbidities and multimorbidity, often complicating the disease course of patients with chronic inflammatory rheumatic diseases, may be influenced by disease-intrinsic and extrinsic determinants including regional and social factors. We analyzed the frequency and co-segregation of self-reported com...

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Autores principales: Gergianaki, Irini, Garantziotis, Panagiotis, Adamichou, Christina, Saridakis, Ioannis, Spyrou, Georgios, Sidiropoulos, Prodromos, Bertsias, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957898/
https://www.ncbi.nlm.nih.gov/pubmed/33801229
http://dx.doi.org/10.3390/jcm10050998
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author Gergianaki, Irini
Garantziotis, Panagiotis
Adamichou, Christina
Saridakis, Ioannis
Spyrou, Georgios
Sidiropoulos, Prodromos
Bertsias, George
author_facet Gergianaki, Irini
Garantziotis, Panagiotis
Adamichou, Christina
Saridakis, Ioannis
Spyrou, Georgios
Sidiropoulos, Prodromos
Bertsias, George
author_sort Gergianaki, Irini
collection PubMed
description Comorbidities and multimorbidity, often complicating the disease course of patients with chronic inflammatory rheumatic diseases, may be influenced by disease-intrinsic and extrinsic determinants including regional and social factors. We analyzed the frequency and co-segregation of self-reported comorbid diseases in a community-based Mediterranean registry of patients (n = 399) with systemic lupus erythematosus (SLE). Predictors for multimorbidity were identified by multivariable logistic regression, strongly-associated pairs of comorbidities by the Cramer’s V-statistic, and comorbidities clusters by hierarchical agglomerative clustering. Among the most prevalent comorbidities were thyroid (45.6%) and metabolic disorders (hypertension: 24.6%, dyslipidemia: 33.3%, obesity: 35.3%), followed by osteoporosis (22.3%), cardiovascular (20.8%), and allergic (20.6%) disorders. Mental comorbidities were also common, particularly depression (26.7%) and generalized anxiety disorder (10.7%). Notably, 51.0% of patients had ≥3 physical and 33.1% had ≥2 mental comorbidities, with a large fraction (n = 86) displaying multimorbidity from both domains. Sociodemographic (education level, marital status) and clinical (disease severity, neurological involvement) were independently associated with physical or mental comorbidity. Patients were grouped into five distinct clusters of variably prevalent comorbid diseases from different organs and domains, which correlated with SLE severity patterns. Conclusively, our results suggest a high multimorbidity burden in patients with SLE at the community, advocating for integrated care to optimize outcomes.
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spelling pubmed-79578982021-03-16 High Comorbidity Burden in Patients with SLE: Data from the Community-Based Lupus Registry of Crete Gergianaki, Irini Garantziotis, Panagiotis Adamichou, Christina Saridakis, Ioannis Spyrou, Georgios Sidiropoulos, Prodromos Bertsias, George J Clin Med Article Comorbidities and multimorbidity, often complicating the disease course of patients with chronic inflammatory rheumatic diseases, may be influenced by disease-intrinsic and extrinsic determinants including regional and social factors. We analyzed the frequency and co-segregation of self-reported comorbid diseases in a community-based Mediterranean registry of patients (n = 399) with systemic lupus erythematosus (SLE). Predictors for multimorbidity were identified by multivariable logistic regression, strongly-associated pairs of comorbidities by the Cramer’s V-statistic, and comorbidities clusters by hierarchical agglomerative clustering. Among the most prevalent comorbidities were thyroid (45.6%) and metabolic disorders (hypertension: 24.6%, dyslipidemia: 33.3%, obesity: 35.3%), followed by osteoporosis (22.3%), cardiovascular (20.8%), and allergic (20.6%) disorders. Mental comorbidities were also common, particularly depression (26.7%) and generalized anxiety disorder (10.7%). Notably, 51.0% of patients had ≥3 physical and 33.1% had ≥2 mental comorbidities, with a large fraction (n = 86) displaying multimorbidity from both domains. Sociodemographic (education level, marital status) and clinical (disease severity, neurological involvement) were independently associated with physical or mental comorbidity. Patients were grouped into five distinct clusters of variably prevalent comorbid diseases from different organs and domains, which correlated with SLE severity patterns. Conclusively, our results suggest a high multimorbidity burden in patients with SLE at the community, advocating for integrated care to optimize outcomes. MDPI 2021-03-02 /pmc/articles/PMC7957898/ /pubmed/33801229 http://dx.doi.org/10.3390/jcm10050998 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gergianaki, Irini
Garantziotis, Panagiotis
Adamichou, Christina
Saridakis, Ioannis
Spyrou, Georgios
Sidiropoulos, Prodromos
Bertsias, George
High Comorbidity Burden in Patients with SLE: Data from the Community-Based Lupus Registry of Crete
title High Comorbidity Burden in Patients with SLE: Data from the Community-Based Lupus Registry of Crete
title_full High Comorbidity Burden in Patients with SLE: Data from the Community-Based Lupus Registry of Crete
title_fullStr High Comorbidity Burden in Patients with SLE: Data from the Community-Based Lupus Registry of Crete
title_full_unstemmed High Comorbidity Burden in Patients with SLE: Data from the Community-Based Lupus Registry of Crete
title_short High Comorbidity Burden in Patients with SLE: Data from the Community-Based Lupus Registry of Crete
title_sort high comorbidity burden in patients with sle: data from the community-based lupus registry of crete
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957898/
https://www.ncbi.nlm.nih.gov/pubmed/33801229
http://dx.doi.org/10.3390/jcm10050998
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