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A common polymorphism rs1800247 in osteocalcin gene is associated with hypertension and diastolic blood pressure levels: the Shanghai Changfeng study
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نویسنده
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Ling Y ,Gao X ,Lin H ,Ma H ,Pan B ,Gao J
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منبع
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journal of human hypertension - 2016 - دوره : 30 - شماره : 11 - صفحه:679 -684
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چکیده
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Osteocalcin may have a role in hypertension due to its close relationship with energy metabolism and insulin sensitivity. the aim of this study was to evaluate the association of a common polymorphism rs1800247 in osteocalcin gene with hypertension and related traits. this was a population-based cross-sectional study including 5647 individuals. baseline information was collected. body mass index (bmi), waist circumference, blood pressure, glucose and lipids were determined. homeostasis model assessment for insulin resistance (homa-ir) was used to estimate insulin sensitivity. genotyping was performed by matrix-assisted laser desorption/ionization time-of-flight mass spectroscopy. the carriers of c allele of rs1800247 were associated with a decreased odds of hypertension compared with the carriers of t allele adjusted for age, sex and bmi (odds ratio (or)=0.89, 95% confidence interval (ci) 0.81–0.97, p=0.01). the carriers of c allele were also associated with a lower diastolic blood pressure (dbp) level adjusted for age, sex and bmi in normotensive individuals (β=−0.55, 95% ci −0.99 to −0.10, p=0.02), but its association with systolic blood pressure levels was not significant. the interaction between rs1800247 and homa-ir on hypertension was significant (p<0.001). in the stratified analysis by the median of homa-ir (1.93), rs1800247 was significantly associated with hypertension in the subgroup with homa-ir⩽1.93 (or=0.82, 95% ci 0.71–0.94, p=0.005), but this association was not significant in the subgroup with homa-ir >1.93. we demonstrated that a common polymorphism rs1800247 in osteocalcin gene was associated with hypertension and dbp levels. the association of rs1800247 with hypertension was affected by its interaction with homa-ir.
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آدرس
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Fudan University, Department of Endocrinology and Metabolism, China, Fudan University, Department of Endocrinology and Metabolism, China, Fudan University, Department of Endocrinology and Metabolism, China, Fudan University, Department of Geriatrics, China, Fudan University, Department of Laboratory Medicine, China, Fudan University, China
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Authors
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