Evidence map›Paper›PMID 42750005›Full record

ArticleBMC cardiovascular disorders2026

Bone morphogenetic protein 10 and one-year outcomes after open revascularisation in symptomatic peripheral arterial disease or carotid stenosis.

Sofia Skröder, Dritan Poci, Daniel Robert Smith, Mats Dreifaldt, Allan Sirsjö, Espen Fengsrud, Anna Björkenheim, Liza Ljungberg

Abstract read
In one paragraph

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

8 authors.

Sofia SkröderSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden. sofia.skroder@oru.se.ORCID http://orcid.org/0000-0002-6360-1167
Dritan PociSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID http://orcid.org/0000-0001-7618-4377
Daniel Robert SmithClinical Epidemiology and Biostatistics, Faculty of Medicine and Health, School of Medical Sciences, Örebro University, Örebro, 70182, Sweden.ORCID http://orcid.org/0000-0002-3916-8041
Mats DreifaldtDepartment of Cardiothoracic Surgery, Örebro University Hospital and University Health Care Research Centre, Örebro, 70182, Sweden.ORCID http://orcid.org/0000-0001-5585-1783
Allan SirsjöSchool of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID http://orcid.org/0000-0002-0278-4510
Espen FengsrudDepartment of Cardiology, Faculty of Medicine and Health, Örebro University, Örebro, 70182, Sweden.ORCID http://orcid.org/0000-0002-2654-9427
Anna Björkenheim *Department of Cardiology, Faculty of Medicine and Health, Örebro University, Örebro, 70182, Sweden.ORCID http://orcid.org/0000-0002-4288-3310
Liza Ljungberg *School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.ORCID http://orcid.org/0000-0003-4253-3369

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBone morphogenetic protein 10 (BMP10) has atrial-specific and vascular properties and may reflect both atrial and vascular pathophysiology. We investigated whether BMP10 levels were associated with new-onset atrial fibrillation (AF), major adverse cardiovascular events (MACE), and all-cause mortality after open revascularisation for symptomatic peripheral arterial disease (PAD) or carotid stenosis (CS).

methodsPatients scheduled for endarterectomy for symptomatic PAD or CS were enrolled. BMP10 concentrations were measured using a multiplex immunoassay. Clinical outcomes were obtained from medical records during one-year follow-up. Associations between BMP10 and outcomes were assessed using Cox proportional hazards regression.

resultsA total of 210 patients were included (63% men; 61% underwent surgery for PAD). Women were older than men and had higher BMP10 levels. Forty patients had known preoperative AF. During one-year follow-up, 26 patients experienced MACE and 13 died. Among 170 patients without AF at baseline, 10 developed new-onset AF. In unadjusted Cox regression, higher BMP10 levels were associated with MACE (HR 1.01, 95% CI 1.00-1.03; p = 0.047) and all-cause mortality (HR 1.03, 95% CI 1.01-1.04; p < 0.001), but not with new-onset AF (HR 1.00, 95% CI 0.97-1.03; p = 0.80). Effect estimates were similar after adjustment for age and sex. Model-based point estimates of one-year cumulative incidence were numerically higher at higher BMP10 concentrations for MACE and all-cause mortality, although confidence intervals were wide; no corresponding pattern was observed for new-onset AF.

conclusionsIn this exploratory cohort, higher BMP10 levels were associated with MACE and all-cause mortality after endarterectomy for symptomatic PAD or CS. Women had higher BMP10 levels than men. These findings should be interpreted cautiously and considered hypothesis-generating; larger studies are required to validate the observed associations.

Indexed as

Bone Morphogenetic ProteinsCarotid StenosisEndarterectomy, CarotidPeripheral Arterial DiseaseAgedAged, 80 and overAtrial FibrillationBiomarkersFemaleHumansMaleMiddle AgedProportional Hazards ModelsRisk FactorsTime FactorsTreatment OutcomeBiomarkersBMP10 protein, humanBone Morphogenetic ProteinsAtherosclerosisAtrial fibrillationBiomarkerBone morphogenetic proteinsCardiovascular disease

Identifiers

PMID42750005
PMCPMC13579758

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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 OpenQuestion graph.