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   <subfield code="a">The association between genetic variants of RUNX2 , ADIPOQ and vertebral fracture in Korean postmenopausal women</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Kyong-Chol Kim, Hyejin Chun, ChaoQiang Lai, Laurence Parnell, Yangsoo Jang, Jongho Lee, Jose. Ordovas]</subfield>
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   <subfield code="a">Contrary to the traditional belief that obesity acts as a protective factor for bone, recent epidemiologic studies have shown that body fat might be a risk factor for osteoporosis and bone fracture. Accordingly, we evaluated the association between the phenotypes of osteoporosis or vertebral fracture and variants of obesity-related genes, peroxisome proliferator-activated receptor-gamma (PPARG), runt-related transcription factor 2 (RUNX2), leptin receptor (LEPR), and adiponectin (ADIPOQ). In total, 907 postmenopausal healthy women, aged 60-79years, were included in this study. BMD and biomarkers of bone health and adiposity were measured. We genotyped for four single nucleotide polymorphisms (SNPs) from four genes (PPARG, RUNX2, LEPR, ADIPOQ). A general linear model for continuous dependent variables and a logistic regression model for categorical dependent variables were used to analyze the statistical differences among genotype groups. Compared with the TT subjects at rs7771980 in RUNX2, C-carrier (TC+CC) subjects had a lower vertebral fracture risk after adjusting for age, smoking, alcohol, total calorie intake, total energy expenditure, total calcium intake, total fat intake, weight, body fat. Odds ratio (OR) and 95% interval (CI) for the vertebral fracture risk was 0.55 (95% CI 0.32-0.94). After adjusting for multiple variables, the prevalence of vertebral fracture was highest in GG subjects at rs1501299 in ADIPOQ (p=0.0473). A high calcium intake (&gt;1000mg/day) contributed to a high bone mineral density (BMD) in GT+TT subjects at rs1501299 in ADIPOQ (p for interaction=0.0295). Even if the mechanisms between obesity-related genes and bone health are not fully established, the results of our study revealed the association of certain SNPs from obesity-related genes with BMD or vertebral fracture risk in postmenopausal Korean women.</subfield>
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   <subfield code="a">The Japanese Society for Bone and Mineral Research and Springer Japan, 2014</subfield>
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   <subfield code="a">Polymorphisms</subfield>
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   <subfield code="a">Runt-related transcription factor 2 ( RUNX2 )</subfield>
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   <subfield code="a">Adiponectin ( ADIPOQ)</subfield>
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   <subfield code="a">Kim</subfield>
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   <subfield code="u">Department of Family Medicine, Chaum Hospital, Cha University, Seoul, Korea</subfield>
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   <subfield code="u">Health Promotion Center, Ewha Woman's University Mokdong Hospital Ewha Woman's University School of Medicine, Seoul, Korea</subfield>
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   <subfield code="a">Lai</subfield>
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   <subfield code="u">Nutritional Genomics Lab, Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA</subfield>
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   <subfield code="u">Graduate Program in Science for Aging, Yonsei University, Seoul, Korea</subfield>
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   <subfield code="a">Lee</subfield>
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   <subfield code="t">Journal of Bone and Mineral Metabolism</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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