Evidence map›Paper›PMID 25745061›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2015

Genetic ancestry is associated with measures of subclinical atherosclerosis in African Americans: the Jackson Heart Study.

Samson Y Gebreab, Pia Riestra, Rumana J Khan, Ruihua Xu, Solomon K Musani, Fasil Tekola-Ayele, Adolfo Correa, James G Wilson, Charles N Rotimi, Sharon K Davis

Erratum issuedOpen access · greenAbstract readComparative Study
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Observational
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Leveraging genetic ancestry to study health disparities.American journal of physical anthropology · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Systems Biology and Noninvasive Imaging of Atherosclerosis.Arteriosclerosis, thrombosis, and vascular biology · 2016
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Samson Y GebreabFrom the National Human Genome Research Institute, Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, Bethesda, MD (S.Y.G., P.R., R.J.K., R.X., F.T.-A., C.N.R., S.K.D.); and Jackson Heart Study (S.K.M., A.C.), and Department of Physiology & Biophysics (J.G.W.), University of Mississippi Medical Center, Jackson. samson.gebreab@nih.gov.
Pia RiestraFrom the National Human Genome Research Institute, Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, Bethesda, MD (S.Y.G., P.R., R.J.K., R.X., F.T.-A., C.N.R., S.K.D.); and Jackson Heart Study (S.K.M., A.C.), and Department of Physiology & Biophysics (J.G.W.), University of Mississippi Medical Center, Jackson.
Rumana J KhanFrom the National Human Genome Research Institute, Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, Bethesda, MD (S.Y.G., P.R., R.J.K., R.X., F.T.-A., C.N.R., S.K.D.); and Jackson Heart Study (S.K.M., A.C.), and Department of Physiology & Biophysics (J.G.W.), University of Mississippi Medical Center, Jackson.
Ruihua XuFrom the National Human Genome Research Institute, Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, Bethesda, MD (S.Y.G., P.R., R.J.K., R.X., F.T.-A., C.N.R., S.K.D.); and Jackson Heart Study (S.K.M., A.C.), and Department of Physiology & Biophysics (J.G.W.), University of Mississippi Medical Center, Jackson.
Solomon K MusaniFrom the National Human Genome Research Institute, Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, Bethesda, MD (S.Y.G., P.R., R.J.K., R.X., F.T.-A., C.N.R., S.K.D.); and Jackson Heart Study (S.K.M., A.C.), and Department of Physiology & Biophysics (J.G.W.), University of Mississippi Medical Center, Jackson.
Fasil Tekola-AyeleFrom the National Human Genome Research Institute, Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, Bethesda, MD (S.Y.G., P.R., R.J.K., R.X., F.T.-A., C.N.R., S.K.D.); and Jackson Heart Study (S.K.M., A.C.), and Department of Physiology & Biophysics (J.G.W.), University of Mississippi Medical Center, Jackson.
Adolfo CorreaFrom the National Human Genome Research Institute, Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, Bethesda, MD (S.Y.G., P.R., R.J.K., R.X., F.T.-A., C.N.R., S.K.D.); and Jackson Heart Study (S.K.M., A.C.), and Department of Physiology & Biophysics (J.G.W.), University of Mississippi Medical Center, Jackson.
James G WilsonFrom the National Human Genome Research Institute, Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, Bethesda, MD (S.Y.G., P.R., R.J.K., R.X., F.T.-A., C.N.R., S.K.D.); and Jackson Heart Study (S.K.M., A.C.), and Department of Physiology & Biophysics (J.G.W.), University of Mississippi Medical Center, Jackson.
Charles N RotimiFrom the National Human Genome Research Institute, Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, Bethesda, MD (S.Y.G., P.R., R.J.K., R.X., F.T.-A., C.N.R., S.K.D.); and Jackson Heart Study (S.K.M., A.C.), and Department of Physiology & Biophysics (J.G.W.), University of Mississippi Medical Center, Jackson.
Sharon K DavisFrom the National Human Genome Research Institute, Metabolic, Cardiovascular and Inflammatory Disease Genomics Branch, Bethesda, MD (S.Y.G., P.R., R.J.K., R.X., F.T.-A., C.N.R., S.K.D.); and Jackson Heart Study (S.K.M., A.C.), and Department of Physiology & Biophysics (J.G.W.), University of Mississippi Medical Center, Jackson.
University of Mississippi Medical Center · US

Funding

Genetic epidemiology of complex diseasesZIAHG200362 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI ROTIMI, CHARLES · 2009 to 2025
$54.7M
Social Exposures and Genetics of Cardiovascular DiseaseZIAHG200393 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI GIBBONS, GARY · 2014 to 2019
$13.1M
Understanding Obesity In Relation to the Built EnvironmentP20MD006899 · NIMHD · JACKSON STATE UNIVERSITY · PI ANTOINE-LAVIGNE, DONNA A · 2012 to 2016
$5.3M
Intramural NIH HHS Z99 HG999999NHLBI NIH HHS HHSN268201300046CNHLBI NIH HHS HHSN268201300047CNHLBI NIH HHS HHSN268201300048CNHLBI NIH HHS HHSN268201300049CNHLBI NIH HHS HHSN268201300050CNIMHD NIH HHS P20 MD006899
6 · The paper itself

Abstract

objectiveTo determine whether genetic ancestry was associated with subclinical atherosclerosis measures after adjustment for traditional cardiovascular disease risk factors, inflammatory marker, socioeconomic status, and psychosocial factors in a large admixed African American population. APPROACH AND

resultsParticipants were drawn from the Jackson Heart Study. Participant's percent of European ancestry (PEA) was estimated based on 1747 genetic markers using HAPMIX. Association of PEA with peripheral arterial disease and common carotid intima-media thickness were investigated among 2168 participants and with coronary artery calcification >0 and abdominal aortic calcification >0 among 1139 participants. The associations were evaluated using multivariable regression models. Our results showed that a 1 SD increase in PEA was associated with a lower peripheral arterial disease prevalence after adjusting for age and sex (prevalence ratio=0.90 [95% CI, 0.82-0.99]; P=0.036). Adjustments for traditional cardiovascular disease risk factors, socioeconomic status, and psychosocial factors attenuated this association (prevalence ratio=0.91 [0.82-1.00]; P=0.046). There was also a nonlinear association between PEA and coronary artery calcification and abdominal aortic calcification. The lowest PEA was associated with a lower coronary artery calcification (prevalence ratio=0.75 [0.58-0.96]; P=0.022) and a lower abdominal aortic calcification [prevalence ratio=0.80 [0.67-0.96]; P=0.016) compared with the reference group (10th-90th percentile) after adjusting for traditional cardiovascular disease risk factors, inflammatory marker, socioeconomic status, and psychosocial factors. However, we found no significant association between PEA and common carotid intima-media thickness.

conclusionsOverall, our findings indicate that genetic ancestry was associated with subclinical atherosclerosis, suggesting unmeasured risk factors and interactions with genetic factors might contribute to the distribution of subclinical atherosclerosis among African Americans.

Indexed as

AgedAge DistributionAtherosclerosisBlack or African AmericanCardiovascular DiseasesCarotid Intima-Media ThicknessCohort StudiesFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedMississippiMultivariate AnalysisPeripheral Arterial DiseasePrevalenceAfrican Americanscardiovascular diseaseepidemiologygenetic ancestrysubclinical atherosclerosis

Identifiers

PMID25745061
PMCPMC4523273
OpenAlexW2620941071

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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.