Abstract
Objectives: Gastroesophageal reflux disease (GERD) occurs frequently in patients with SSc. We investigated whether the presence of GERD and/or the use of anti-Acid therapy, specifically proton-pump inhibitors (PPIs), are associated with long-Term outcomes, especially in SSc-Associated interstitial lung disease (SSc-ILD). Methods: We retrospectively analysed patients with SSc and SSc-ILD from the German Network for Systemic Sclerosis (DNSS) database (2003 onwards). Kaplan-Meier analysis compared overall survival (OS) and progression-free survival (PFS) in patients with GERD vs without GERD (SSc and SSc-ILD), and PPI vs no PPI use (SSc-ILD only). Progression was defined as a decrease in either percentage predicted forced vital capacity of ≥10% or single-breath diffusing capacity for carbon monoxide of ≥15%, or death. Results: It was found that 2693/4306 (63%) registered patients with SSc and 1204/1931 (62%) with SSc-ILD had GERD. GERD was not associated with decreased OS or decreased PFS in patients in either cohort. In SSc-ILD, PPI use was associated with improved OS vs no PPI use after 1 year [98.4% (95% CI: 97.6, 99.3); n = 760 vs 90.8% (87.9-93.8); n = 290] and after 5 years [91.4% (89.2-93.8); n = 357 vs 70.9% (65.2-77.1); n = 106; P < 0.0001]. PPI use was also associated with improved PFS vs no PPI use after 1 year [95.9% (94.6-97.3); n = 745 vs 86.4% (82.9-90.1); n = 278] and after 5 years [66.8% (63.0-70.8); n = 286 vs 45.9% (39.6-53.2); n = 69; P < 0.0001]. Conclusion: GERD had no effect on survival in SSc or SSc-ILD. PPIs improved survival in patients with SSc-ILD. Controlled, prospective trials are needed to confirm this finding.
| Original language | English |
|---|---|
| Journal | Rheumatology (United Kingdom) |
| Volume | 62 |
| Issue number | 9 |
| Pages (from-to) | 3067-3074 |
| Number of pages | 8 |
| ISSN | 1462-0324 |
| DOIs | |
| Publication status | Published - 01.09.2023 |
Funding
Analysis of ILD-related data was supported by Boehringer Ingelheim International GmbH. No author received payment for the development of this manuscript. Writing support was provided by Chester Trinick and Helen Keyworth of Nucleus Global, which was contracted and funded by Boehringer Ingelheim.
Research Areas and Centers
- Academic Focus: Center for Infection and Inflammation Research (ZIEL)
DFG Research Classification Scheme
- 2.22-18 Rheumatology
- 2.21-05 Immunology