Evaluation of Systemic Sclerosis Primary Heart Involvement and Chronic Heart Failure in the European Scleroderma Trials and Research Cohort
Györfi, Andrea-Hermina; Filla, Tim; Polzin, Amin; Tascilar, Koray; Buch, Maya; Tröbs, Monique; Matei, Alexandru-Emil; Airo, Paolo; Balbir-Gurman, Alexandra; Kuwert, Frederic; Mihai, Carina; Kabala, Anna; Graßhoff, Hanna; Callaghan, Julia; Isomura, Yohei; Mansour, Jennifer; Spierings, Julia; Tennoe, Anders Heiervang; Selvi, Enrico; Riccieri, Valeria; Hoffmann-Vold, Anna-Maria; Bergmann, Christina; Schett, Georg; Hunzelmann, Nicolas; van Laar, Jacob M; Saketkoo, Lesley Ann; Kuwana, Masataka; Siegert, Elise; Riemekasten, Gabriela; Distler, Oliver; du Four, Tessa; Smith, Vanessa; Truchetet, Marie-Elise; Distler, Jörg H W; EUSTAR collaborators
(2025) Journal of the American Heart Association, volume 14, issue 5
(Article)
Abstract
BACKGROUND: Systemic sclerosis (SSc) primary heart involvement (SSc-pHI) is one of the leading causes of mortality in SSc. We aimed to evaluate risk factors for SSc-pHI and its progression and the outcomes in the EUSTAR (European Scleroderma Trials and Research) cohort. METHODS: SSc-pHI was defined according to the World Scleroderma
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Foundation/Heart Failure Association definition. Data from 5741 patients with SSc in the EUSTAR cohort were analyzed. Additional cardiovascular data were collected from a subcohort of 838 patients with SSc. Lasso regression was used for risk factor analyses. Kaplan-Meier estimator was used for survival analyses. Progression of SSc-pHI was evaluated by a study definition developed by rheumatology and cardiology experts. RESULTS: Risk factors for the presence of SSc-pHI comprised skeletal muscle atrophy (odds ratio [OR], 2.00 [95% CI, 1.00-2.68]), age (OR, 1.91 [95% CI, 1.73-2.03]), male sex (OR, 1.77 [95% CI, 1.42-2.05]), swollen joints (OR, 1.70 [95% CI, 1.47-1.98]), skeletal muscle weakness (OR, 1.38 [95% CI, 1.00-1.85]), and tendon friction rubs (OR, 1.46 [95% CI, 1.00-1.77]) (n=3276). Telangiectasia (OR, 2.10 [95% CI, 1.38-2.72]), intestinal symptoms (OR, 1.70 [95% CI, 1.04-2.42]), age (OR, 1.47 [95% CI, 1.21-1.62]), and antitopoisomerase I antibodies (OR, 1.37 [95% CI, 1.00-1.77]) were associated with an increased risk for new onset of SSc-pHI (n=1000). Survival rate was significantly lower in patients with SSc-pHI than in those without (P value <0.0001, n=3768). Patients with SSc-pHI had a lower survival rate than patients with interstitial lung disease (n=3365). Swollen joints were associated with an increased risk of progressive SSc-pHI (OR, 2.49 [95% CI, 1.79-3.52]) (n=595). Tendon friction rubs (OR, 1.21 [95% CI, 0.94-1.90]) increased the risk of heart failure with preserved ejection fraction in patients with SSc-pHI. CONCLUSIONS: We defined progressive SSc-pHI and identified risk factors for new onset and progression of SSc-pHI and for SSc-pHI-associated heart failure with preserved ejection fraction in the largest cohort with SSc. These findings may guide patient stratification for diagnostic workup and therapy.
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Keywords: Journal Article
ISSN: 2047-9980
Publisher: Wiley-Blackwell
Note: Publisher Copyright: © 2012, American Heart Association Inc. All rights reserved.
(Peer reviewed)