Evidence map›Paper›PMID 26226985›Full record

ArticleMolecular biology and evolution2015

BMD Loci Contribute to Ethnic and Developmental Differences in Skeletal Fragility across Populations: Assessment of Evolutionary Selection Pressures.

Carolina Medina-Gómez, Alessandra Chesi, Denise H M Heppe, Babette S Zemel, Jia-Lian Yin, Heidi J Kalkwarf, Albert Hofman, Joan M Lappe, Andrea Kelly, Manfred Kayser and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology and evolution, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. A Meta-Analysis of the Transferability of Bone Mineral Density Genetic Loci Associations From European to African Ancestry Populations.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Pooled it
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  17. Antagonistic Pleiotropy in Human Disease.Journal of molecular evolution · 2020
    Review
  18. Article
  19. Ancestry and dental development: A geographic and genetic perspective.American journal of physical anthropology · 2018
    Article
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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

18 authors at 7 institutions in 2 countries.

Carolina Medina-GómezDepartment of Internal Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands The Generation R Study Group, Erasmus University Medical Center, Rotterdam, The Netherlands Department of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Alessandra ChesiDivision of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA.
Denise H M HeppeThe Generation R Study Group, Erasmus University Medical Center, Rotterdam, The Netherlands Department of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands Department of Pediatrics, Erasmus University Medical Center, Rotterdam, The Netherlands.
Babette S ZemelDivision of GI, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania.
Jia-Lian YinDepartment of Internal Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands The Generation R Study Group, Erasmus University Medical Center, Rotterdam, The Netherlands Department of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Heidi J KalkwarfDivision of General and Community Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Albert HofmanThe Generation R Study Group, Erasmus University Medical Center, Rotterdam, The Netherlands Department of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Joan M LappeDivision of Endocrinology, Creighton University, Omaha, NE.
Andrea KellyDivision of GI, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA.
Manfred KayserDepartment of Genetic Identification, Erasmus University Medical Center, Rotterdam, The Netherlands.
Sharon E OberfieldDivision of Pediatric Endocrinology, Diabetes, and Metabolism, Department of Pediatrics, Columbia University Medical Center, New York, NY.
Vicente GilsanzDepartment of Radiology, Children's Hospital Los Angeles, Los Angeles, CA.
André G UitterlindenDepartment of Internal Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands The Generation R Study Group, Erasmus University Medical Center, Rotterdam, The Netherlands Department of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands.
John A ShepherdDepartment of Radiology and Biomedical Imaging, University of California, San Francisco.
Vincent W V JaddoeThe Generation R Study Group, Erasmus University Medical Center, Rotterdam, The Netherlands Department of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands Department of Pediatrics, Erasmus University Medical Center, Rotterdam, The Netherlands.
Struan F A GrantDivision of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA.
Oscar LaoDepartment of Genetic Identification, Erasmus University Medical Center, Rotterdam, The Netherlands.
Fernando RivadeneiraDepartment of Internal Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands The Generation R Study Group, Erasmus University Medical Center, Rotterdam, The Netherlands Department of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands f.rivadeneira@erasmusmc.nl.
Erasmus MC · NLChildren's Hospital of Philadelphia · USChildren's Hospital of Los Angeles · USCincinnati Children's Hospital Medical Center · USColumbia University Irving Medical Center · USCreighton University · USUniversity of California, San Francisco · US

Funding

LCenter for Clinical and Translational Science and TrainingUL1TR001425 · NCATS · UNIVERSITY OF CINCINNATI · PI MEINZEN-DERR, JAREEN, STRAWN, JEFFREY ROBERT · 2015 to 2024
$37.5M
ZIDOVUDINE VS 2',3'DIDEHYDRO-3'DEOXYTHYMIDINE IN CHILDRENM01RR000240 · NCRR · CHILDREN'S HOSP OF PHILADELPHIA · PI ALTSCHULER, STEVEN M · 1985 to 2006
$15.3M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR026314 · NCRR · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2009 to 2011
$14.3M
Genome Wide Association Study of Bone Mineral Accretion During ChildhoodR01HD058886 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI GRANT, STRUAN F A, ZEMEL, BABETTE S · 2010 to 2013
$3.1M
BONE MINERAL DENSITY IN CHILDHOOD STUDY-CLINICAL CENTER-275013332-275013332N01HD013332 · NICHD · COLUMBIA UNIV. NEW YORK · PI HORLICK, MARY · 2002 to 2006
–
BONE MINERAL DENSITY IN CHILDHOOD STUDY--CLINICAL CENTER-275013330-275013330N01HD013330 · NICHD · CREIGHTON UNIVERSITY · PI LAPPE, JOAN · 2002 to 2006
–
BONE MINERAL DENSITY IN CHILDHOOD STUDY-CLINICAL CENTER-275013329-275013329N01HD013329 · NICHD · CHILDREN'S HOSP. MED CTR · PI KALKWARF, HEIDI J · 2002 to 2006
–
BONE MINERAL DENSITY IN CHILDHOOD STUDY--CLINICAL CENTER-275013333-275013333N01HD013333 · NICHD · CHILDRENS HOSPITAL LOS ANGELES · PI GILSANZ, VICENTE · 2002 to 2006
–
BONE MINERAL DENSITY IN CHILDHOOD STUDY--CLINICAL CENTER-275013331-275013331N01HD013331 · NICHD · CHILDREN'S HOSP. PHILADELPHIA · PI ZEMEL, BABETTE S · 2002 to 2006
–
NCATS NIH HHS UL1 TR001425NCRR NIH HHS 5-M01-RR-00240NCRR NIH HHS M01 RR000240NCRR NIH HHS UL1 RR-026314NCRR NIH HHS UL1 RR026314NICHD NIH HHS N01-HD-1-3228NICHD NIH HHS N01-HD-1-3329NICHD NIH HHS N01-HD-1-3330NICHD NIH HHS N01-HD-1-3331NICHD NIH HHS N01-HD-1-3332NICHD NIH HHS N01-HD-1-3333NICHD NIH HHS R01 HD058886
6 · The paper itself

Abstract

Bone mineral density (BMD) is a highly heritable trait used both for the diagnosis of osteoporosis in adults and to assess bone health in children. Ethnic differences in BMD have been documented, with markedly higher levels in individuals of African descent, which partially explain disparity in osteoporosis risk across populations. To date, 63 independent genetic variants have been associated with BMD in adults of Northern-European ancestry. Here, we demonstrate that at least 61 of these variants are predictive of BMD early in life by studying their compound effect within two multiethnic pediatric cohorts. Furthermore, we show that within these cohorts and across populations worldwide the frequency of those alleles associated with increased BMD is systematically elevated in individuals of Sub-Saharan African ancestry. The amount of differentiation in the BMD genetic scores among Sub-Saharan and non-Sub-Saharan populations together with neutrality tests, suggest that these allelic differences are compatible with the hypothesis of selective pressures acting on the genetic determinants of BMD. These findings constitute an explorative contribution to the role of selection on ethnic BMD differences and likely a new example of polygenic adaptation acting on a human trait.

Indexed as

AdultAllelesAsian PeopleBiological EvolutionBlack PeopleBone DensityChildEvolution, MolecularFemaleGenetic Association StudiesGenetic LociGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleOsteoporosisadaptationbone mineral densityethnic differencesgenome-wide association studiespolygenicselective pressures

Identifiers

PMID26226985
PMCPMC4651235
OpenAlexW2218581746

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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.