Evidence map›Paper›PMID 40640959›Full record

ArticleGenome biology2025

Protein quantitative trait locus analysis in African American and non-Hispanic White individuals.

Yanwei Cai, Mari Johnson, Jeffrey Haessler, Aaron J Molstad, Shih-Jen Hwang, Roby Joehanes, Joanne M Murabito, Usman A Tahir, Nora Franceschini, Robert E Gerszten and 6 more

Abstract read
In one paragraph

Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Plasma proteomics link menopause timing to brain aging and dementia risk.medRxiv : the preprint server for health sciences · 2026
    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

16 authors.

Yanwei CaiPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, USA.
Mari JohnsonPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, USA.
Jeffrey HaesslerPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, USA.
Aaron J MolstadSchool of Statistics, University of Minnesota, Minneapolis, USA.
Shih-Jen HwangPopulation Sciences Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, USA.
Roby JoehanesPopulation Sciences Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, USA.
Joanne M MurabitoDepartment of Medicine, Boston University Chobanian and Avedisian School of Medicine, Boston, USA.
Usman A TahirDivision of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, USA.
Nora FranceschiniDepartment of Epidemiology, Gillings School of Public Health, University of North Carolina at Chapel Hill, Chapel Hill, USA.
Robert E GersztenDivision of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, USA.
Wei SunPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, USA.
Daniel LevyPopulation Sciences Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, USA.
Laura M RaffieldDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, USA.
Charles KooperbergPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, USA.
Li HsuPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, USA.
Alexander P ReinerPublic Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, USA. apreiner@uw.edu.

Funding

Proteomics of Cardiometabolic and Renal Traits in African AmericansR01HL133870 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI ROBERT E GERSZTEN · 2017 to 2026
$6.7M
Polygenic risk scores for cardiometabolic disorders: the role of blood cells immune response and evolutionary adaptationU01HG011720 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Yun Li, ALEXANDER P REINER · 2021 to 2026
$5.4M
Integrative Genomics into Genetic Association Studies of Blood Pressure and Stroke in African AmericansR01HL152439 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HSU, LI, KOOPERBERG, CHARLES L · 2021 to 2024
$2.8M
The Role of SECTM1 in Monocyte Biology and AtherosclerosisK08HL161445 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Usman A. Tahir · 2022 to 2026
$822k
NHGRI NIH HHS U01 HG011720NHGRI NIH HHS U01-HG011720NHLBI NIH HHS K08 HL161445NHLBI NIH HHS R01 HL133870NHLBI NIH HHS R01 HL152439NIH HHS HHSN268201600034I, HL133870NIH HHS K08 HL161445-01A1
6 · The paper itself

Abstract

backgroundSubstantial efforts have been dedicated to exploring the link between genetic regulation and the proteome, informing studies of complex trait mechanisms. Most of these efforts have been limited to populations of European ancestry.

resultsWe conduct an Olink protein quantitative trait locus (pQTL) analysis on 1245 proteins involving 1033 self-identified African American (AA) and 1764 non-Hispanic White (NHW) participants from the Women's Health Initiative and Framingham Heart Study. For replication of candidate pQTLs, we use data from 534 self-identified AA adults from the Jackson Heart Study and protein genome-wide association analysis statistics from the UK Biobank Pharma Proteomics Project, including 54,219 participants, of whom 931 are of African ancestry. In total, we identify and validate 5103 pQTLs (4496 or 88% cis- and 602 or 12% trans-pQTLs) for 983 proteins. Among these, 195 are previously unreported, with most (166 or 85%) identified in our AA sample, many of which were essentially monomorphic in European reference populations. Several of these newly identified African ancestry-specific pQTLs have been reported in ClinVar; our results suggest impact on circulating protein levels, potentially bolstering evidence for clinical significance. We identify a "cis pQTL hotspot" within the leukocyte receptor gene cluster on human chromosome 19q13.4. We also provide examples where a particular cis-pQTL, identified through conditional analysis, offers biological insights into an overlapping GWAS signal for disease susceptibility.

conclusionsThe identification of previously undescribed African ancestry-specific pQTLs contributes to understanding protein genetic regulation and highlights the significance of proteomic analysis in diverse populations.

Indexed as

Black or African AmericanQuantitative Trait LociWhiteAdultFemaleGenome-Wide Association StudyHumansMaleMiddle AgedPolymorphism, Single NucleotideOlinkProteomicsWhole genome sequencing

Identifiers

PMID40640959
PMCPMC12243311

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.