Evidence map›Paper›PMID 34014961›Full record

ArticlePloS one2021

Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study.

Nicholette D Palmer, Lingyi Lu, Thomas C Register, Leon Lenchik, J Jeffrey Carr, Pamela J Hicks, S Carrie Smith, Jianzhao Xu, Latchezar Dimitrov, Jacob Keaton and 11 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. 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

21 authors at 6 institutions in 2 countries.

Nicholette D PalmerDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.ORCID 0000-0001-8883-2511
Lingyi LuDivision of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Thomas C RegisterDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Leon LenchikDepartment of Radiology, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
J Jeffrey CarrDepartment of Radiology, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
Pamela J HicksDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
S Carrie SmithDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Jianzhao XuCenter for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Latchezar DimitrovCenter for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Jacob KeatonCenter for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Meijian GuanCenter for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Maggie C Y NgDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Yii-der I ChenDepartment of Pediatrics, The Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, United States of America.
Anthony J HanleyDepartment of Nutritional Sciences, University of Toronto, Toronto, Ontario, Canada.
Corinne D EngelmanDepartment of Population Health Sciences, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States of America.
Jill M NorrisDepartment of Epidemiology, Colorado School of Public Health, Aurora, CO, United States of America.
Carl D LangefeldDepartment of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Lynne E WagenknechtDivision of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Donald W BowdenDepartment of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Barry I FreedmanCenter for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Jasmin DiversDepartment of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.
Wake Forest University · USColorado School of Public Health · USUCLA Medical Center · USUniversity of Toronto · CAUniversity of Wisconsin–Madison · USVanderbilt University · US

Funding

Understanding Obesity In Relation to the Built EnvironmentP20MD006899 · NIMHD · JACKSON STATE UNIVERSITY · PI ANTOINE-LAVIGNE, DONNA A · 2012 to 2016
$5.3M
Subclinical CVD in African American Type 2 DiabeticsR01DK071891 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FREEDMAN, BARRY IRA · 2007 to 2016
$4.5M
Epidemiology of cardiovascular disease in diabetesR01HL067348 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BOWDEN, DONALD W · 2001 to 2004
$4.3M
Metabolomics of Neurocognitive Risk for Dementia in DiabetesR01AG058921 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ALLRED, NICHOLETTE D. · 2019 to 2023
$3.8M
Genetics of Bone and Vascular Calcium in Type 2 DiabetesR01AR048797 · NIAMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CARR, JOHN JEFFREY · 2001 to 2004
$1.3M
NHLBI NIH HHS R01 HL067348NIAMS NIH HHS R01 AR048797NIA NIH HHS R01 AG058921NIDDK NIH HHS R01 DK071891NIMHD NIH HHS P20 MD006899
6 · The paper itself

Abstract

Relative to European Americans, African Americans have lower 25-hydroxyvitamin D (25OHD) and vitamin D binding protein (VDBP) concentrations, higher 1,25-dihydroxyvitamin D (1,25(OH)2D3) concentrations and bone mineral density (BMD), and paradoxically reduced burdens of calcified atherosclerotic plaque (subclinical atherosclerosis). To identify genetic factors contributing to vitamin D and BMD measures, association analysis of >14M variants was conducted in a maximum of 697 African American-Diabetes Heart Study participants with type 2 diabetes (T2D). The most significant association signals were detected for VDBP on chromosome 4; variants rs7041 (β = 0.44, SE = 0.019, P = 9.4x10-86) and rs4588 (β = 0.17, SE = 0.021, P = 3.5x10-08) in the group-specific component (vitamin D binding protein) gene (GC). These variants were found to be independently associated. In addition, rs7041 was also associated with bioavailable vitamin D (BAVD; β = 0.16, SE = 0.02, P = 3.3x10-19). Six rare variants were significantly associated with 25OHD, including a non-synonymous variant in HSPG2 (rs116788687; β = -1.07, SE = 0.17, P = 2.2x10-10) and an intronic variant in TNIK (rs143555701; β = -1.01, SE = 0.18, P = 9.0x10-10), both biologically related to bone development. Variants associated with 25OHD failed to replicate in African Americans from the Insulin Resistance Atherosclerosis Family Study (IRASFS). Evaluation of vitamin D metabolism and bone mineral density phenotypes in an African American population enriched for T2D could provide insight into ethnic specific differences in vitamin D metabolism and bone mineral density.

Indexed as

Bone DensityAgedBlack or African AmericanDiabetes Mellitus, Type 2FemaleGenome-Wide Association StudyHumansMaleMiddle AgedPolymorphism, GeneticVitamin DVitamin D-Binding Protein1,25-dihydroxyvitamin D25-hydroxyvitamin DVitamin DVitamin D-Binding Protein

Identifiers

PMID34014961
PMCPMC8136717
OpenAlexW3161499865

What OpenQuestion holds

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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.