Journal article
Genome-Wide Association Analysis of Longitudinal Bone Mineral Content Data From the Iowa Bone Development Study
Journal of clinical densitometry, Vol.24(1), pp.44-54
01/2021
DOI: 10.1016/j.jocd.2019.09.005
PMCID: PMC7098844
PMID: 31668963
Abstract
The foundation for osteoporosis risk is, in part, established during childhood, adolescence, and young adulthood, all periods of development when bone mass is acquired rapidly. The relative quantity of bone mass accrued is influenced by both lifestyle and genetic factors, although the genetic component is not yet well understood. The purpose of this study was to use a genome-wide association (GWA) analysis to discover single nucleotide polymorphisms (SNPs) associated with: (1) the sex-specific hip bone mineral content at approximately the age of 19 when the amount of bone accrued is near its peak; and (2) the sex-specific rate of hip bone mineral content accrual during the adolescent growth spurt. The Iowa Bone Development Study, a longitudinal cohort study exploring bone health in children, adolescents, and young adults was the source of data. From this cohort, n = 364 (190 females, 174 males) participants were included in GWA analyses to address (1) and n = 258 participants (125 females and 133 males) were included in GWA analyses to address (2). Twenty SNPS were detected having p < 1.0 × 10−5. Of most biologic relevance were 2 suggestive SNPs (rs2051756 and rs2866908) detected in an intron of the DKK2 gene through the GWA analysis that explored peak bone mass in females.
Details
- Title: Subtitle
- Genome-Wide Association Analysis of Longitudinal Bone Mineral Content Data From the Iowa Bone Development Study
- Creators
- Camden P Bay - Center for Clinical Investigation, Brigham & Women's Hospital, Boston, MA, USASteven M Levy - Department of Preventive and Community Dentistry, University of Iowa College of Dentistry, Iowa City, IA, USAKathleen F Janz - Department of Health and Human Physiology, College of Liberal Arts and Sciences, University of Iowa, Iowa City, IA, USABrian J Smith - Holden Comprehensive Cancer Center, University of Iowa Hospitals and Clinics, Iowa City, IA, USAJohn R Shaffer - Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, USAMary L Marazita - Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USATrudy L Burns - Department of Epidemiology, University of Iowa College of Public Health, Iowa City, IA, USA
- Resource Type
- Journal article
- Publication Details
- Journal of clinical densitometry, Vol.24(1), pp.44-54
- DOI
- 10.1016/j.jocd.2019.09.005
- PMID
- 31668963
- PMCID
- PMC7098844
- NLM abbreviation
- J Clin Densitom
- ISSN
- 1094-6950
- eISSN
- 1559-0747
- Publisher
- Elsevier Inc
- Grant note
- DOI: 10.13039/100000002, name: National Institutes of Health
- Language
- English
- Date published
- 01/2021
- Academic Unit
- Preventive and Community Dentistry; Health Management and Policy; Epidemiology; Biostatistics; Fraternal Order of Eagles Diabetes Research Center; Holden Comprehensive Cancer Center; Health, Sport, and Human Physiology
- Record Identifier
- 9984214849002771
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