Evidence map›Paper›PMID 32209135›Full record

ArticleArthritis research & therapy2020

ACE inhibitors in SSc patients display a risk factor for scleroderma renal crisis-a EUSTAR analysis.

Lukas Bütikofer, Pierre A Varisco, O Distler, O Kowal-Bielecka, Y Allanore, G Riemekasten, P M Villiger, S Adler, EUSTAR collaborators

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
6.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Review
  3. Novel Compounds in Targeting the α1-adrenoceptor for Antihypertensive Therapy.Cardiovascular & hematological agents in medicinal chemistry · 2026
    Review
  4. Authors' Reply: Chronic Lesions in Scleroderma Renal Crisis: A Protective Clue?Journal of the American Society of Nephrology : JASN · 2026
    Article
  5. Chronic Lesions in Scleroderma Renal Crisis: A Protective Clue?Journal of the American Society of Nephrology : JASN · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Emergencies in inflammatory rheumatic diseases.Rheumatology international · 2024
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Systemic sclerosis.Lancet (London, England) · 2023
    Review
  18. Review
  19. Diagnosis and treatment of thrombotic microangiopathy.International journal of laboratory hematology · 2022
    Review
  20. Kidney Involvement in Systemic Sclerosis.Journal of personalized medicine · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 4 countries.

Lukas BütikoferCTU Bern and Institute of Social and Preventive Medicine (ISPM), University of Bern, Bern, Switzerland.
Pierre A VariscoSwiss Health Insurance Service, Bern, Switzerland.
O DistlerDepartment of Rheumatology, University Hospital Zurich, Zurich, Switzerland.
O Kowal-BieleckaMedical University of Bialystok, Jana Kilińskiego 1, 15-089, Białystok, Poland.
Y AllanoreWarsaw Medical University, Warsaw, Poland.
G RiemekastenCochin Hospital, Paris, France.
P M VilligerUniversity Hospital Schleswig-Holstein, Lübeck, Germany.
S AdlerUniversity Hospital Schleswig-Holstein, Lübeck, Germany. sabine.adler@helios-gesundheit.de.ORCID 0000-0002-4194-9146
EUSTAR collaborators
University of Bern · CHMedical University of Białystok · PLHôpital Cochin · FRMedical University of Warsaw · PLUniversity Hospital of Zurich · CH

Funding

research funds division of rheumatology, university hospital bern not applicable
6 · The paper itself

Abstract

objectivesTo investigate the effect of ACE inhibitors (ACEi) on the incidence of scleroderma renal crisis (SRC) when given prior to SRC in the prospectively collected cohort from the European Scleroderma Trial and Research Group (EUSTAR).

methodsSSc patients without prior SRC and at least one follow-up visit were included and analyzed regarding SRC, arterial hypertension, and medication focusing on antihypertensive medication and glucocorticoids (GC).

resultsOut of 14,524 patients in the database, we identified 7648 patients with at least one follow-up. In 27,450 person-years (py), 102 patients developed SRC representing an incidence of 3.72 (3.06-4.51) per 1000 py. In a multivariable time-to-event analysis adjusted for age, sex, disease severity, and onset, 88 of 6521 patients developed SRC. The use of ACEi displayed an increased risk for the development of SRC with a hazard ratio (HR) of 2.55 (95% confidence interval (CI) 1.65-3.95). Adjusting for arterial hypertension resulted in a HR of 2.04 (95%CI 1.29-3.24). There was no evidence for an interaction of ACEi and arterial hypertension (HR 0.83, 95%CI 0.32-2.13, p = 0.69). Calcium channel blockers (CCB), angiotensin receptor blockers (ARB), endothelin receptor antagonists, and GC-mostly in daily dosages below 15 mg of prednisolone-did not influence the hazard for SRC.

conclusionsACEi in SSc patients with concomitant arterial hypertension display an independent risk factor for the development of SRC but are still first choice in SRC treatment. ARBs might be a safe alternative, yet the overall safety of alternative antihypertensive drugs in SSc patients needs to be further studied.

Indexed as

Acute Kidney InjuryAgedAngiotensin-Converting Enzyme InhibitorsEuropeFemaleHumansHypertension, RenalIncidenceMaleMiddle AgedPopulation SurveillanceProspective StudiesRisk FactorsScleroderma, SystemicTreatment OutcomeAngiotensin-Converting Enzyme InhibitorsACE inhibitorsAntihypertensive drugsArterial hypertensionOutcomeScleroderma renal crisis

Identifiers

PMID32209135
PMCPMC7093969
OpenAlexW3013011989

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.