Evidence map›Paper›PMID 40124641›Full record

ArticleEthnicity & disease2025

Stroke Incidence and High-Sensitivity C-Reactive Protein Among African Americans: The Jackson Heart Study.

Cellas A Hayes, Roland J Thorpe, Mandip Dhamoon, Elizabeth Heitman, Keith C Norris, Bettina M Beech, Marino Bruce, Benjamin Walker, Jennifer C Reneker

Abstract read
In one paragraph

Article in Ethnicity & disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Cellas A HayesDepartment of Epidemiology and Population Health, Stanford University School of Medicine, Palo Alto, CA.ORCID 0000-0002-6259-9456
Roland J ThorpeProgram for Research on Men's Health, Johns Hopkins Center for Health Disparities Solutions, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Mandip DhamoonDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY.
Elizabeth HeitmanProgram in Ethics in Science and Medicine, University of Texas Southwestern Medical Center, Dallas, TX.
Keith C NorrisProgram for Research on Men's Health, Johns Hopkins Center for Health Disparities Solutions, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Bettina M BeechProgram for Research on Men's Health, Johns Hopkins Center for Health Disparities Solutions, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Marino BruceProgram for Research on Men's Health, Johns Hopkins Center for Health Disparities Solutions, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Benjamin WalkerDepartment of Population Health Science, John D. Bower School of Population Health, University of Mississippi Medical Center, Jackson, MS.
Jennifer C RenekerDepartment of Population Health Science, John D. Bower School of Population Health, University of Mississippi Medical Center, Jackson, MS.

Funding

The Health & Aging Brain Study - Health Disparities (HABS-HD)U19AG078109 · NIA · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI Sid E O'Bryant · 2022 to 2026
$181.1M
Cellular Mechanisms of Insulin-like Growth Factor-1 Neuroprotection with Ischemic StrokeF31NS124302 · NINDS · UNIVERSITY OF MISSISSIPPI · PI HAYES, CELLAS · 2022 to 2022
$28k
NIA NIH HHS U19 AG078109NINDS NIH HHS F31 NS124302
6 · The paper itself

Abstract

Background: Strokes are a leading cause of death and disability among African Americans in the United States. Biological markers to predict stroke remain elusive; thus, our objective was to investigate whether inflammation, as measured by high-sensitivity C-reactive protein (hs-CRP), was associated with stroke incidence among African Americans enrolled in the Jackson Heart Study (JHS). Methods: Baseline hs-CRP levels were categorized in quintiles: quintile 1 (0.0084 mg/L); quintile 2 (0.0085-0.0189 mg/L); quintile 3 (0.0190-0.036 mg/L); quintile 4 (0.037-0.0675 mg/L); quintile 5 (≥0.0676 mg/L). Nonfatal stroke incidence was ascertained from passive community surveillance through annual phone calls and adjudicated via hospital records. At baseline, stroke risk factors/covariates were compared across quintiles using a one-way analysis of variance and a chi-square test. The association between baseline hs-CRP levels and stroke incidence was determined using a Cox regression analysis to estimate hazard ratios (HRs) and 95% confidence intervals (CI). Results: In the unadjusted model, hs-CRP levels in quintile 2 (HR, 1.48; 95% CI, 0.96-2.29), quintile 3 (HR, 1.44; 95% CI, 0.93-2.24), and quintile 4 (HR, 1.09; 95% CI, 0.68-1.74) were not associated with stroke incidence when compared with quintile 1 (reference). However, individuals within quintile 5 (HR, 1.78; 95% CI, 1.17-2.72) exhibited a significantly increased risk for stroke compared with those in the reference quintile. This risk persisted after adjusting for stroke risk factors (demographics, anthropometrics, health condition covariates, health behavioral risk factors, and cardiovascular disease history) for quintile 5 (HR, 1.87; 95% CI, 1.17-2.98) compared with reference quintile 1. Conclusions: An increased and independent risk of nonfatal stroke appears at the highest quintile of hs-CRP values (≥0.0676 mg/L) among JHS participants.

Indexed as

Black or African AmericanC-Reactive ProteinStrokeAdultAgedBiomarkersFemaleHumansIncidenceInflammationMaleMiddle AgedMississippiProportional Hazards ModelsRisk FactorsBiomarkersC-Reactive ProteinAfrican AmericansHigh-sensitivity C-reactive Proteinhs-CRPInflammationJackson Heart StudyStroke

Identifiers

PMID40124641
PMCPMC11928021

What OpenQuestion holds

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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.