Exposure to ACE inhibitors prior to the onset of scleroderma renal crisis-results from the international scleroderma renal crisis survey
- Marie Hudson(corresponding author),
- Murray Baron,
- Solène Tatibouet,
- Daniel E. Furst,
- Dinesh Khanna,
- Laura Hummers
- McGill University,
- University of California at Los Angeles,
- University of Michigan, Ann Arbor,
- Johns Hopkins University,
- Universite Lille Nord de France,
- University of Pittsburgh
Abstract
Objective: To determine whether exposure to angiotensin-converting enzyme (ACE) inhibitors prior to the onset of scleroderma renal crisis (SRC) leads to worse outcomes of SRC. Methods: Prospective cohort study of incident SRC subjects. The exposure of interest was ACE inhibitors prior to the onset of SRC. The outcomes of interest were death or dialysis during the first year after the onset of SRC. Results: A total of 87 subjects with incident SRC were identified and 1-year follow-up data were obtained in 75 (86%) subjects. Overall, 27 (36%) subjects died within the first year and an additional 19 (25%) remained on dialysis 1 year after the onset of SRC. In adjusted analyses, exposure to ACE inhibitors prior to the onset of SRC was associated with an increased risk of death (hazard ratio 2.42, 95% CI 1.02, 5.75, p < 0.05 in the primary analysis and 2.17, 95% CI 0.88, 5.33, p = 0.09 after post-hoc adjustment for pre-existing hypertension). Conclusion: Overall, the 1-year outcomes of SRC were poor. Prior exposure to ACE inhibitors was associated with an increased risk of death after the onset of SRC, although there was uncertainty around the magnitude of the risk and the possibility of residual confounding could not be ruled out. Further studies will be needed to confirm these findings.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 666-672 (7 pages)Journal (Volume, Issue Number)
Seminars in Arthritis and Rheumatism (Volume 43, Issue 5)Publication milestones
- Published - 04/2014
Publication status
ISSN
0049-0172Publication IDs
- Scopus: 84898780891
- PubMed: 24176729
