Evidence map›Paper›PMID 42733468›Full record

ArticleAmerican heart journal plus : cardiology research and practice2026

C-reactive protein and incidence of symptomatic peripheral vascular disease (sPVD): Findings from the multi-ethnic study of atherosclerosis (MESA).

Atef Akoum, Christopher Wang, Bahaa El Deen Wehbeh, Yugene Y Guo, Lee Bockus, Joey Chiang, Kai Chen, Younghoon Kwon, Honghuang Lin, Rajeev Malhotra and 2 more

Abstract read
In one paragraph

Article in American heart journal plus : cardiology research and practice, 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
–field-weighted citation impact
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

12 authors.

Atef AkoumDepartment of Medicine, Hennepin Healthcare, Minneapolis, MN, United States of America.
Christopher WangDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX, United States of America.
Bahaa El Deen WehbehAmerican University of Beirut Medical Center.
Yugene Y GuoDivision of Cardiology, Heart & Vascular Institute, Boston, MA, United States of America.
Lee BockusDivision of Cardiology, Department of Medicine, University of Washington, Seattle, WA, United States of America.
Joey ChiangDepartment of Medicine, University of Washington, Seattle, WA, United States of America.
Kai ChenDivision of Cardiology, Department of Medicine, UMass Chan Medical School, Worcester, MA, United States of America.
Younghoon KwonDivision of Cardiology, Department of Medicine, University of Washington, Seattle, WA, United States of America.
Honghuang LinDivision of Health System Science, Department of Medicine, UMass Chan Medical School Worcester, MA.
Rajeev MalhotraDivision of Cardiology, Heart & Vascular Institute, Boston, MA, United States of America.
Allan WalkeyDivision of Health System Science, Department of Medicine, UMass Chan Medical School Worcester, MA.
Jason P LiDivision of Cardiology, Department of Medicine, UMass Chan Medical School, Worcester, MA, United States of America.

Funding

The Role of Arylsulfatase in Vascular CalcificationR01HL162928 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI PAUL STEFAN DE VRIES, Rajeev Malhotra · 2023 to 2026
$2.6M
Characterization of Functional Iron Deficiency and Repletion in Heart Failure with Preserved Ejection FractionR01HL159514 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI LEWIS, GREGORY DYER, MALHOTRA, RAJEEV · 2021 to 2024
$2.5M
NHLBI NIH HHS R01 HL159514NHLBI NIH HHS R01 HL162928
6 · The paper itself

Abstract

Early identification of individuals at risk for symptomatic peripheral vascular disease (sPVD), including abdominal aortic aneurysm (AAA) and peripheral artery disease (PAD), is essential to reduce the substantial burden of associated morbidity and mortality. Given the central role of systemic inflammation in the pathogenesis and progression of atherosclerosis, we prospectively evaluated high sensitivity C-reactive protein (CRP) as a potential predictive biomarker for the long-term development of these specific vascular conditions within a large, population-based cohort free of baseline cardiovascular disease. Among 6161 participants followed over a median of 10.0 years, elevated CRP at or above 2.0 mg/L was independently associated with a more than two-fold higher incidence of sPVD after adjustment for traditional risk factors (HR 2.70; 95% CI 1.64 to 4.43; p < 0.001). Collectively, these findings suggest that elevated CRP might be an independent marker of long-term peripheral vascular risk and support further investigation of its role in primary prevention risk stratification.

Indexed as

Abdominal aortic aneurysmC-reactive proteinInflammationPeripheral artery diseaseSubclinical atherosclerosisSymptomatic peripheral vascular disease

Identifiers

PMID42733468
PMCPMC13571112

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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.