Evidence map›Paper›PMID 42457209›Full record

ArticleRMD open2026

Assessment of markers of primary aldosteronism in systemic sclerosis and their relationships with renal and cardiovascular outcomes.

Aurore Collet, Sébastien Sanges, Stéphanie Espiard, Bodale Djobo, Romain Vankemmel, Sylvain Dubucquoi, Eric Hachulla, Claire Douillard, David Launay, Jun Yang and 1 more

Abstract read
In one paragraph

Article in RMD open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Aurore Collet *INSERM, CHU Lille, Institute for Translational Research in Inflammation (INFINITE), University of Lille, Lille, France.
Sébastien Sanges *INSERM, CHU Lille, Institute for Translational Research in Inflammation (INFINITE), University of Lille, Lille, France.
Stéphanie EspiardDepartment of Endocrinology and Metabolism, CHU Lille, Lille, France.
Bodale DjoboService Hormonologie, Métabolisme, Nutrition, Oncologie, Pôle de Biologie Pathologie Génétique, CHU Lille, Lille, France.
Romain VankemmelService Hormonologie, Métabolisme, Nutrition, Oncologie, Pôle de Biologie Pathologie Génétique, CHU Lille, Lille, France.ORCID http://orcid.org/0009-0009-4923-6587
Sylvain DubucquoiINSERM, CHU Lille, Institute for Translational Research in Inflammation (INFINITE), University of Lille, Lille, France.
Eric HachullaDépartement de Médecine Interne et Immunologie Clinique, CHU Lille, Lille, France.ORCID http://orcid.org/0000-0001-7432-847X
Claire DouillardDepartment of Endocrinology and Metabolism, CHU Lille, Lille, France.
David LaunayINSERM, CHU Lille, Institute for Translational Research in Inflammation (INFINITE), University of Lille, Lille, France.
Jun Yang *Centre for Endocrinology and Reproductive Health, Hudson Institute of Medical Research, Clayton, Victoria, Australia.
Fabien B Vincent *Rheumatology Research Group, Centre for Inflammatory Diseases, Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, Victoria, Australia fabien.vincent@monash.edu.ORCID http://orcid.org/0000-0001-7220-0800

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhether primary aldosteronism (PA), the most common endocrine cause of hypertension (HTN), contributes to HTN and cardiovascular disease burden in systemic sclerosis (SSc) has never been explored. We aimed to assess the prevalence and management of HTN, prevalence of positive PA screening test results and the associations between markers of PA with HTN and SSc-related outcomes in SSc.

methodsData from adult SSc patients and normotensive healthy controls (HC) were analysed in this single-centre study. HTN was defined as blood pressures ≥140/90 mm Hg on two visits or as documented in medical records. PA screening was performed using the aldosterone:renin ratio (ARR). Associations between biomarkers of PA (renin, aldosterone, ARR, hybrid steroid 18-hydroxycortisol (18OHF)) with HTN and SSc-related outcomes were assessed using multivariable regression modelling.

resultsData from 112 SSc patients (median (IQR) age 60 (49, 69) years, 79% female) and 48 HC (median (IQR) age 42.5 (31, 57) years, 52% female) were analysed. At baseline, 41 SSc patients (37%) had HTN, increasing to 52% of the cohort at the last follow-up visit (median follow-up 5.1 years). The prevalence of positive baseline ARR in SSc was 8% (9/112), corresponding to 12% (5/41) in the hypertensive subset. No associations were observed between biomarkers of PA and SSc-related renal and cardiovascular outcomes or HTN at last follow-up visit.

conclusionsHTN was common in this SSc cohort, and prevalence of positive PA screening test was estimated at 12% among hypertensive SSc patients, supporting consideration of PA screening in this population.

Indexed as

BiomarkersCardiovascular DiseasesHyperaldosteronismHypertensionScleroderma, SystemicAdultAgedFemaleHumansMaleMiddle AgedPrevalenceBiomarkersAutoimmune DiseasesBiomarkersCardiovascular DiseasesHypertensionScleroderma, Systemic

Identifiers

PMID42457209
PMCPMC13374450

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.