The association between genetic variants of RUNX2 , ADIPOQ and vertebral fracture in Korean postmenopausal women

Verfasser / Beitragende:
[Kyong-Chol Kim, Hyejin Chun, ChaoQiang Lai, Laurence Parnell, Yangsoo Jang, Jongho Lee, Jose. Ordovas]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Bone and Mineral Metabolism, 33/2(2015-03-01), 173-179
Format:
Artikel (online)
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024 7 0 |a 10.1007/s00774-014-0570-1  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00774-014-0570-1 
245 0 4 |a The association between genetic variants of RUNX2 , ADIPOQ and vertebral fracture in Korean postmenopausal women  |h [Elektronische Daten]  |c [Kyong-Chol Kim, Hyejin Chun, ChaoQiang Lai, Laurence Parnell, Yangsoo Jang, Jongho Lee, Jose. Ordovas] 
520 3 |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 (>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. 
540 |a The Japanese Society for Bone and Mineral Research and Springer Japan, 2014 
690 7 |a Polymorphisms  |2 nationallicence 
690 7 |a Runt-related transcription factor 2 ( RUNX2 )  |2 nationallicence 
690 7 |a Adiponectin ( ADIPOQ)  |2 nationallicence 
690 7 |a Osteoporosis  |2 nationallicence 
690 7 |a Vertebral fracture  |2 nationallicence 
700 1 |a Kim  |D Kyong-Chol  |u Department of Family Medicine, Chaum Hospital, Cha University, Seoul, Korea  |4 aut 
700 1 |a Chun  |D Hyejin  |u Health Promotion Center, Ewha Woman's University Mokdong Hospital Ewha Woman's University School of Medicine, Seoul, Korea  |4 aut 
700 1 |a Lai  |D ChaoQiang  |u Nutritional Genomics Lab, Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA  |4 aut 
700 1 |a Parnell  |D Laurence  |u Nutritional Genomics Lab, Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA  |4 aut 
700 1 |a Jang  |D Yangsoo  |u Graduate Program in Science for Aging, Yonsei University, Seoul, Korea  |4 aut 
700 1 |a Lee  |D Jongho  |u Graduate Program in Science for Aging, Yonsei University, Seoul, Korea  |4 aut 
700 1 |a Ordovas  |D Jose  |u Nutritional Genomics Lab, Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA  |4 aut 
773 0 |t Journal of Bone and Mineral Metabolism  |d Springer Japan  |g 33/2(2015-03-01), 173-179  |x 0914-8779  |q 33:2<173  |1 2015  |2 33  |o 774 
856 4 0 |u https://doi.org/10.1007/s00774-014-0570-1  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00774-014-0570-1  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kim  |D Kyong-Chol  |u Department of Family Medicine, Chaum Hospital, Cha University, Seoul, Korea  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Chun  |D Hyejin  |u Health Promotion Center, Ewha Woman's University Mokdong Hospital Ewha Woman's University School of Medicine, Seoul, Korea  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Lai  |D ChaoQiang  |u Nutritional Genomics Lab, Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Parnell  |D Laurence  |u Nutritional Genomics Lab, Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Jang  |D Yangsoo  |u Graduate Program in Science for Aging, Yonsei University, Seoul, Korea  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Lee  |D Jongho  |u Graduate Program in Science for Aging, Yonsei University, Seoul, Korea  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ordovas  |D Jose  |u Nutritional Genomics Lab, Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Journal of Bone and Mineral Metabolism  |d Springer Japan  |g 33/2(2015-03-01), 173-179  |x 0914-8779  |q 33:2<173  |1 2015  |2 33  |o 774