Evidence map›Paper›PMID 24465435›Full record

ArticlePloS one2014

Possible race and gender divergence in association of genetic variations with plasma von Willebrand factor: a study of ARIC and 1000 genome cohorts.

Zhou Zhou, Fuli Yu, Ashley Buchanan, Yuanyuan Fu, Marco Campos, Kenneth K Wu, Lloyd E Chambless, Aaron R Folsom, Eric Boerwinkle, Jing-fei Dong

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Phenotypic and Genotypic Signatures ofInternational journal of general medicine · 2022
    Article
  4. Article
  5. The commonBlood advances · 2018
    Article
  6. Article
  7. Article
  8. What have we learned from large population studies of von Willebrand disease?Hematology. American Society of Hematology. Education Program · 2016
    Review
  9. Article
  10. The ABO Histo-Blood Group and AKI in Critically Ill Patients with Trauma or Sepsis.Clinical journal of the American Society of Nephrology : CJASN · 2015
    Article
  11. Article
  12. Article
  13. Coagulation Status and Venous Thromboembolism Risk in African Americans: A Potential Risk Factor in COVID-19.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

10 authors at 8 institutions in 3 countries.

Zhou ZhouState Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Diseases, Fuwai Hospital, CAMS & PUMC, Beijing, China.
Fuli YuHuman Genome Sequencing Center, Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, Texas, United States of America ; Institute of Neurology, Tianjin Medical University General Hospital, Tianjin, China.
Ashley BuchananDepartment of Biostatistics, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Yuanyuan FuState Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Diseases, Fuwai Hospital, CAMS & PUMC, Beijing, China.
Marco CamposSection of Cardiology, Department of Medicine, Baylor College of Medicine, Houston, Texas, United States of America.
Kenneth K WuNational Health Research Institutes, Taipei, Taiwan.
Lloyd E ChamblessDepartment of Biostatistics, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Aaron R FolsomDivision of Epidemiology & Community Health, School of Public Health, University of Minnesota, Minneapolis, Minnesota, United States of America.
Eric BoerwinkleHuman Genetic Center, University of Texas School of Public Health, Houston, Texas, United States of America.
Jing-fei DongPuget Sound Blood Research Institute, Puget Sound Blood Center, Seattle, Washington, United States of America ; Division of Hematology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, United States of America.
Baylor College of Medicine · USUniversity of North Carolina at Chapel Hill · USChinese Academy of Medical Sciences & Peking Union Medical College · CNNational Health Research Institutes · TWState Key Laboratory of Cardiovascular DiseaseThe University of Texas Health Science Center at Houston · USUniversity of Minnesota · USUniversity of Washington · US

Funding

The Human Genome Sequencing CenterU54HG003273 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A · 2004 to 2015
$341.3M
Ultra-Large VWF and Thrombotic MicroangiopathyR01HL071895 · NHLBI · BLOODWORKS · PI DONG, JING-FEI · 2003 to 2012
$3.4M
Proteolysis of ultralarge von Willebrand factor and metabolic syndrome-diabetesR01HL085769 · NHLBI · BLOODWORKS · PI DONG, JING-FEI · 2008 to 2011
$1.5M
COMMUNITY AND COHORT SURVEILLANCE PROGRAMS-N01HC55015N01HC055015 · HC · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI CHAMBLESS, LLOYD E · 1985 to 2006
$1.1M
COMMUNITY AND COHORT SURVEILLANCE PROGRAMN01HC055016 · HC · BAYLOR COLLEGE OF MEDICINE · PI BALLANTYNE, CHRISTIE M · 1985 to 2000
$785k
FIELD CENTER FOR CCSPN01HC055019 · HC · UNIVERSITY OF MINNESOTA TWIN CITIES · PI FOLSOM, AARON R · 1985 to 2000
$748k
FIELD CENTERN01HC055021 · HC · UNIVERSITY OF MISSISSIPPI MEDICAL CENTER · PI JONES, DANIEL W · 1985 to 2000
$617k
CCSP-FIELD CENTERN01HC055020 · HC · JOHNS HOPKINS UNIVERSITY · PI NIETO, F JAVIER · 1985 to 2000
$334k
CENTRAL HEMOSTATIS LABORATORY FOR CCSPN01HC055022 · HC · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WU, KENNETH K · 1985 to 2000
$264k
CCSP--FIELD CENTER AND ULTRASOUND READING CENTERN01HC055018 · HC · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI HEISS, GERARDO · 1985 to 2000
$104k
NHGRI NIH HHS U54 HG003273NHLBI NIH HHS HL085769NHLBI NIH HHS HL71895NHLBI NIH HHS N01 HC055015NHLBI NIH HHS N01 HC055016NHLBI NIH HHS N01 HC055018NHLBI NIH HHS N01 HC055019NHLBI NIH HHS N01 HC055020NHLBI NIH HHS N01 HC055021NHLBI NIH HHS N01 HC055022NHLBI NIH HHS N01-HC-55015NHLBI NIH HHS N01-HC-55016NHLBI NIH HHS N01-HC-55018NHLBI NIH HHS N01-HC-55019NHLBI NIH HHS N01-HC-55020NHLBI NIH HHS N01-HC-55021NHLBI NIH HHS N01-HC-55022NHLBI NIH HHS R01 HL071895NHLBI NIH HHS R01 HL085769
6 · The paper itself

Abstract

The synthesis, secretion and clearance of von Willebrand factor (VWF) are regulated by genetic variations in coding and promoter regions of the VWF gene. We have previously identified 19 single nucleotide polymorphisms (SNPs), primarily in introns that are associated with VWF antigen levels in subjects of European descent. In this study, we conducted race by gender analyses to compare the association of VWF SNPs with VWF antigen among 10,434 healthy Americans of European (EA) or African (AA) descent from the Atherosclerosis Risk in Communities (ARIC) study. Among 75 SNPs analyzed, 13 and 10 SNPs were associated with VWF antigen levels in EA male and EA female subjects, respectively. However, only one SNP (RS1063857) was significantly associated with VWF antigen in AA females and none was in AA males. Haplotype analysis of the ARIC samples and studying racial diversities in the VWF gene from the 1000 genomes database suggest a greater degree of variations in the VWF gene in AA subjects as compared to EA subjects. Together, these data suggest potential race and gender divergence in regulating VWF expression by genetic variations.

Indexed as

Genetic VariationSex CharacteristicsAtherosclerosisBlack PeopleCohort StudiesDemographyFemaleGene FrequencyGenome, HumanHaplotypesHumansMalePolymorphism, Single Nucleotidevon Willebrand FactorWhite Peoplevon Willebrand Factor

Identifiers

PMID24465435
PMCPMC3894939
OpenAlexW1982096415

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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.