Left ventricular diastolic dysfunction in systemic sclerosis : Clinical, immunological and survival differences in the Spanish RESCLE registry

Copyright © 2022. Published by Elsevier Inc..

OBJECTIVES: Left ventricular diastolic dysfunction (LVDD) remains poorly studied in Systemic Sclerosis (SSc). To determine the prevalence and to define factors associated with LVDD and survival in a large cohort of patients with SSc.

METHODS: An observational study was conducted with data from the multicentre Spanish Scleroderma Registry (RESCLE) to identify factors associated with LVDD and estimate survival.

RESULTS: Out of 1517 patients, 319 (21.0%) had LVDD. The subset of sine scleroderma SSc was associated to LVDD (14.7% vs. 10.6%, p =0.048), whilst diffuse cutaneous SSc was more prevalent in non-LVDD (16.0 % vs. 21.2%, p =0.041). Multivariable analysis identified that LVDD was associated with older age at diagnosis of SSc (OR 1.05; 95% CI 1.04 to 1.06), longer time from diagnosis (OR 1.04; 95% CI 1.03 to 1.06), presence of telangiectasia (OR 1.42; 95% CI 1.08 to 1.88), treatment with calcium channel blockers (CCB) (OR 1.51; 95% CI 1.16 to 1.96), and inversely related to angiotensin-converting-enzyme inhibitors (ACEi) use (OR 0.59; 95% CI 0.44 to 0.80). SSc patients with LVDD had increased mortality (23.8 vs. 17.4%, p =0.010) and shortened survival from the first SSc symptom (p =0.040), even though it was not found to be an independent risk factor for death.

CONCLUSIONS: LVDD is relatively common in SSc patients, and it is associated with worst prognosis, older age, longer time from diagnosis of SSc, presence of telangiectasia and vasodilator treatment.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:55

Enthalten in:

Seminars in arthritis and rheumatism - 55(2022) vom: 15. Aug., Seite 152033

Sprache:

Englisch

Beteiligte Personen:

González García, Andrés [VerfasserIn]
Fabregate, Martin [VerfasserIn]
Manzano, Luis [VerfasserIn]
Guillén Del Castillo, Alfredo [VerfasserIn]
Rubio Rivas, Manuel [VerfasserIn]
Argibay, Ana [VerfasserIn]
Marín Ballvé, Adela [VerfasserIn]
Rodríguez Pintó, Ignasi [VerfasserIn]
Pla Salas, Xavier [VerfasserIn]
Marí-Alfonso, Begoña [VerfasserIn]
Callejas Moraga, Eduardo [VerfasserIn]
Colunga Argüelles, Dolores [VerfasserIn]
Sáez Comet, Luis [VerfasserIn]
González-Echávarri, Cristina [VerfasserIn]
Ortego-Centeno, Norberto [VerfasserIn]
Vargas Hitos, José Antonio [VerfasserIn]
Todolí Parra, José Antonio [VerfasserIn]
Trapiella Martínez, Luis [VerfasserIn]
Herranz Marín, María Teresa [VerfasserIn]
Freire, Mayka [VerfasserIn]
Chamorro, Antonio-J [VerfasserIn]
Perales Fraile, Isabel [VerfasserIn]
Madroñero Vuelta, Ana Belén [VerfasserIn]
Sánchez Trigo, Sabela [VerfasserIn]
Tolosa Vilella, Carles [VerfasserIn]
Fonollosa Pla, Vicent [VerfasserIn]
Simeón Aznar, Carmen Pilar [VerfasserIn]
RESCLE Investigators, Systemic Autoimmune Diseases Study Group (GEAS) [VerfasserIn]

Links:

Volltext

Themen:

Anticentromere
Antinuclear antibodies, Diffuse scleroderma, Limited scleroderma
Interstitial pneumonia
Journal Article
Observational Study
Pulmonary hypertension
Research Support, Non-U.S. Gov't
Systemic sclerosis

Anmerkungen:

Date Completed 08.07.2022

Date Revised 01.08.2022

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.semarthrit.2022.152033

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM342128752