Worse cardiovascular and renal outcome in male SLE patients.
Détails
Télécharger: 37903784_BIB_6E0F97DEE154.pdf (973.70 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY 4.0
Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_6E0F97DEE154
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Worse cardiovascular and renal outcome in male SLE patients.
Périodique
Scientific reports
Collaborateur⸱rice⸱s
Swiss Systemic Lupus Erythematosus Cohort Study Group (SSCS)
Contributeur⸱rice⸱s
Comte D., Eisenberger U., Hauser T., Roux-Lombard P., Rubbert-Roth A., Steiner U.
ISSN
2045-2322 (Electronic)
ISSN-L
2045-2322
Statut éditorial
Publié
Date de publication
30/10/2023
Peer-reviewed
Oui
Editeur⸱rice scientifique
Comte D., Eisenberger U., Hauser T., Roux-Lombard P., Rubbert-Roth A., Steiner U.
Volume
13
Numéro
1
Pages
18628
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Publication Status: epublish
Résumé
Systemic lupus erythematosus (SLE) in males is rare and poorly understood. Thus, still little is known about sex differences in SLE. We set out to identify sex differences regarding clinical manifestations as well as renal and cardiovascular outcomes of SLE. We analyzed patient data from the Swiss SLE Cohort Study. Cumulative clinical manifestations according to the updated American College of Rheumatology criteria were recorded at inclusion. Cardiovascular events were recorded within Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SLICC-SDI). Renal failure was defined as eGFR < 15 ml/min/1.73 m <sup>2</sup> , initiation of renal replacement therapy or doubling of serum creatinine which were all assessed yearly or documented as end stage renal disease in SLICC-SDI. Risk differences were calculated using logistic regression and cox regression models. We analyzed 93 men and 529 women with a median follow up time of 2 years. Males were significantly older at diagnosis (44.4 versus 33.1 years, p < 0.001) and had less often arthritis (57% versus 74%, p = 0.001) and dermatological disorders (61% versus 76%, p < 0.01). In multivariate analysis female sex remained a significantly associated with arthritis and dermatological disorders. In multivariate analysis men had a significantly higher hazard ratio of 2.3 for renal failure (95% confidence interval (95%-CI) 1.1-5.2, p < 0.04). Total SLICC-SDI Score was comparable. Men had significantly more coronary artery disease (CAD) (17% versus 4%, p < 0.001) and myocardial infarction (10% versus 2%, p < 0.01). In multivariate analysis, male sex remained a significant risk factor for CAD (odds ratio (OR) 5.6, 95%-CI 2.3-13.7, p < 0.001) and myocardial infarction (OR 8.3, 95%-CI 2.1-32.6, p = 0.002). This first sex study in a western European population demonstrates significant sex differences in SLE. Male sex is a risk factor for cardiovascular events and renal failure in SLE. Potential etiological pathomechanisms such as hormonal or X-chromosomal factors remain to be further investigated.
Mots-clé
Humans, Female, Male, Cohort Studies, Lupus Erythematosus, Systemic/complications, Lupus Erythematosus, Systemic/epidemiology, Lupus Erythematosus, Systemic/diagnosis, Myocardial Infarction/complications, Kidney Failure, Chronic/etiology, Kidney Failure, Chronic/complications, Arthritis/complications, Severity of Illness Index
Pubmed
Web of science
Open Access
Oui
Création de la notice
06/11/2023 13:55
Dernière modification de la notice
08/08/2024 6:35