Heritability and Genetics of Serum Dickkopf 1 Levels in African Ancestry Families

被引:0
作者
Allison L. Kuipers
Shibing Yu
Candace M. Kammerer
Cara S. Nestlerode
Clareann H. Bunker
Alan L. Patrick
Victor W. Wheeler
Yingze Zhang
Joseph M. Zmuda
机构
[1] University of Pittsburgh,Department of Epidemiology, Graduate School of Public Health
[2] University of Pittsburgh,Department of Medicine, School of Medicine
[3] University of Pittsburgh,Department of Human Genetics, Graduate School of Public Health
[4] Tobago Health Studies Office,Department of Epidemiology, Graduate School of Public Health
[5] University of Pittsburgh,undefined
来源
Calcified Tissue International | 2015年 / 96卷
关键词
Dickkopf-1; Heritability; Single nucleotide polymorphism; Gene expression; African ancestry;
D O I
暂无
中图分类号
学科分类号
摘要
The aim of the study was to determine the heritability of serum dickkopf-1 (DKK1) and its association with DKK1 polymorphisms in African ancestry subjects. Serum DKK1 was measured in 422 Afro–Caribbean men and women aged 18+ from 7 large, multi-generational families (mean family size: 60; 3,215 relative pairs). Twenty-four common single nucleotide polymorphisms (SNPs) were genotyped within an 80 kilobase-pair region encompassing the DKK1 gene. Heritability was estimated and SNPs were tested for association with serum DKK1 using variance components analysis. DKK1 mRNA expression was tested in peripheral blood of 16 individuals from each of the rs7069912 genotypes. Mean serum DKK1 was 1724.1 pg/mL and was significantly lower in women than men (P = 0.043). Residual genetic heritability of serum DKK1 was 0.4460 (P < 0.0001). Six SNPs reached nominal significance with DKK1, with rs7069912 being significant after adjustment for multiple comparisons. Two of these six SNPs represented independent association signals (rs7069912 and rs16928725), which accounted for 4.6 % of the phenotypic variation in DKK1. Additionally, carriers of the rs7069912 variant had significantly greater DKK1 expression than non-carriers (P = 0.036). Serum DKK1 levels are highly heritable in the African ancestry families. Two SNPs within the DKK1 region accounted for nearly 5 % of the variation in serum DKK1.
引用
收藏
页码:155 / 159
页数:4
相关论文
共 112 条
[1]  
Kawano Y(2003)Secreted antagonists of the Wnt signalling pathway J Cell Sci 116 2627-2634
[2]  
Kypta R(2013)The relationship between inhibitors of the Wnt signalling pathway (Dickkopf-1(DKK1) and sclerostin), bone mineral density, vascular calcification and arterial stiffness in post-menopausal women Bone 56 42-47
[3]  
Hampson G(2012)Circulating sclerostin and Dickkopf-1 (DKK1) in predialysis chronic kidney disease (CKD): relationship with bone density and arterial stiffness Calcif Tissue Int 90 473-480
[4]  
Edwards S(2012)Sclerostin and DKK1 in postmenopausal osteoporosis treated with denosumab J Bone Miner Res 27 2259-2263
[5]  
Conroy S(2011)The role of Dkk1 in bone mass regulation: correlating serum Dkk1 expression with bone mineral density J Orthop Res 29 414-418
[6]  
Blake GM(2011)A novel biomarker of coronary atherosclerosis: serum DKK1 concentration correlates with coronary artery calcification and atherosclerotic plaques J Korean Med Sci 26 1178-1184
[7]  
Fogelman I(2012)Secreted Wnt modulators in symptomatic aortic stenosis J Am Heart Assoc 1 e002261-237
[8]  
Frost ML(2011)Circulating Dickkopf-1 in acute ischemic stroke and clinically stable cerebrovascular disease Atherosclerosis 218 233-1760
[9]  
Thambiah S(2012)Clinical significance of serum and tissue Dickkopf-1 levels in patients with gastric cancer Clin Chim Acta 413 1753-826
[10]  
Roplekar R(2012)Serum DKK1 as a protein biomarker for the diagnosis of hepatocellular carcinoma: a large-scale, multicentre study Lancet Oncol 13 817-234