Dataset Information

A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.

ABSTRACT: Apolipoprotein A-IV (apoA-IV) is a major component of HDL and chylomicron particles and is involved in reverse cholesterol transport. It is an early marker of impaired renal function. We aimed to identify genetic loci associated with apoA-IV concentrations and to investigate relationships with known susceptibility loci for kidney function and lipids. A genome-wide association meta-analysis on apoA-IV concentrations was conducted in five population-based cohorts (n?=?13,813) followed by two additional replication studies (n?=?2,267) including approximately 10 M SNPs. Three independent SNPs from two genomic regions were significantly associated with apoA-IV concentrations: rs1729407 near APOA4 (P?=?6.77?×?10?-? 44), rs5104 in APOA4 (P?=?1.79?×?10-24) and rs4241819 in KLKB1 (P?=?5.6?×?10-14). Additionally, a look-up of the replicated SNPs in downloadable GWAS meta-analysis results was performed on kidney function (defined by eGFR), HDL-cholesterol and triglycerides. From these three SNPs mentioned above, only rs1729407 showed an association with HDL-cholesterol (P?=?7.1?×?10?-? 07). Moreover, weighted SNP-scores were built involving known susceptibility loci for the aforementioned traits (53, 70 and 38 SNPs, respectively) and were associated with apoA-IV concentrations. This analysis revealed a significant and an inverse association for kidney function with apoA-IV concentrations (P?=?5.5?×?10-05). Furthermore, an increase of triglyceride-increasing alleles was found to decrease apoA-IV concentrations (P?=?0.0078). In summary, we identified two independent SNPs located in or next the APOA4 gene and one SNP in KLKB1 The association of KLKB1 with apoA-IV suggests an involvement of apoA-IV in renal metabolism and/or an interaction within HDL particles. Analyses of SNP-scores indicate potential causal effects of kidney function and by lesser extent triglycerides on apoA-IV concentrations.

SUBMITTER: Lamina C

PROVIDER: S-EPMC5179953 | biostudies-literature | 2016 Aug

REPOSITORIES: biostudies-literature

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A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.

Lamina Claudia C Friedel Salome S Coassin Stefan S Rueedi Rico R Yousri Noha A NA Seppälä Ilkka I Gieger Christian C Schönherr Sebastian S Forer Lukas L Erhart Gertraud G Kollerits Barbara B Marques-Vidal Pedro P Ried Janina J Waeber Gerard G Bergmann Sven S Dähnhardt Doreen D Stöckl Andrea A Kiechl Stefan S Raitakari Olli T OT Kähönen Mika M Willeit Johann J Kedenko Ludmilla L Paulweber Bernhard B Peters Annette A Meitinger Thomas T Strauch Konstantin K Lehtimäki Terho T Hunt Steven C SC Vollenweider Peter P Kronenberg Florian F

Human molecular genetics 20160712 16

Apolipoprotein A-IV (apoA-IV) is a major component of HDL and chylomicron particles and is involved in reverse cholesterol transport. It is an early marker of impaired renal function. We aimed to identify genetic loci associated with apoA-IV concentrations and to investigate relationships with known susceptibility loci for kidney function and lipids. A genome-wide association meta-analysis on apoA-IV concentrations was conducted in five population-based cohorts (n = 13,813) followed by two addit ...[more]

PMID: 27412012

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Project description:Poor vitamin K status is linked to greater risk of several chronic diseases. Age, sex, and diet are determinants of circulating vitamin K; however, there is still large unexplained interindividual variability in vitamin K status. Although a strong genetic component has been hypothesized, this has yet to be examined by a genome-wide association (GWA) study.The objective was to identify common genetic variants associated with concentrations of circulating phylloquinone, the primary circulating form of vitamin K.We conducted a 2-stage GWA meta-analysis of circulating phylloquinone in 2 populations of European descent from the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium Nutrition Working Group. Circulating phylloquinone was measured by using reversed-phase high-performance liquid chromatography. Results from adjusted cohort-specific discovery GWA analyses were meta-analyzed with inverse variance weights (n = 2138). Associations with circulating phylloquinone at P < 1 × 10(-6) were then evaluated in a second-stage analysis consisting of one independent cohort (n = 265).No significant association was observed for circulating phylloquinone at the genome-wide significance level of 5 × 10(-8). However, from the discovery GWA, there were 11 single-nucleotide polymorphism (SNP) associations with circulating phylloquinone at P < 1 × 10(-6), including a functional variant previously associated with warfarin dose and altered phylloquinone metabolism. These SNPs are on 5 independent loci on 11q23.3, 8q24.3, 5q22.3, 2p12, and 19p13.12, and they fall within or near the candidate genes APOA1/C3/A4/A5 cluster (involved in lipoprotein metabolism), COL22A1, CDO1, CTNAA2, and CYP4F2 (a phylloquinone oxidase), respectively. Second-stage analysis in an independent cohort further suggests the association of the 5q22.3 locus with circulating phylloquinone (P < 0.05).Multiple candidate genes related to lipoprotein and vitamin K metabolism were identified as potential determinants of circulating phylloquinone. Further investigation with a larger sample is warranted to verify our initial findings and identify other loci contributing to circulating phylloquinone. Trials related to this study were registered at clinicaltrials.gov as NCT00005121 (Framingham Offspring Study) and NCT00005487 (Multi-Ethnic Study of Atherosclerosis).

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Dataset Information

A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.

Publications

A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.

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