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Associations between Variation in CHRNA5-CHRNA3-CHRNB4, Body Mass Index and Blood Pressure in the Northern Finland Birth Cohort 1966

Title: Associations between Variation in CHRNA5-CHRNA3-CHRNB4, Body Mass Index and Blood Pressure in the Northern Finland Birth Cohort 1966
Authors: Kaakinen, M
Ducci, F
Sillanpaa, MJ
Laara, E
Jarvelin, M-R
Item Type: Journal Article
Abstract: Background: The CHRNA5-CHRNA3-CHRNB4 gene cluster on 15q25 has consistently been associated with smoking quantity, nicotine dependence and lung cancer. Recent research also points towards its involvement in cardiovascular homeostasis, but studies in large human samples are lacking, especially on the role of the gene cluster in blood pressure regulation. Methodology/Principal Findings: We studied the associations between 18 single nucleotide polymorphisms (SNPs) in CHRNA5-CHRNA3-CHRNB4 and systolic blood pressure (SBP), diastolic blood pressure (DBP), and body mass index (BMI) in 5402 young adults from the Northern Finland Birth Cohort 1966. We observed some evidence for associations between two SNPs and SBP and between six SNPs and BMI; the evidence for associations with DBP was weaker. The associations with the three phenotypes were driven by different loci with low linkage disequilibrium with each other. The associations appeared more pronounced in smokers, such that the smoking-increasing alleles would predict lower SBP and BMI. Each additional copy of the rs1948 G-allele and the rs950776 A-allele reduced SBP on average by −1.21 (95% CI −2.01, −0.40) mmHg in smokers. The variants associated with BMI included rs2036534, rs6495309, rs1996371, rs6495314, rs4887077 and rs11638372 and had an average effect size of −0.38 (−0.68, −0.08) kg/m2 per an additional copy of the risk allele in smokers. Formal assessments of interactions provided weaker support for these findings, especially after adjustment for multiple testing. Conclusions: Variation at 15q25 appears to interact with smoking status in influencing SBP and BMI. The genetic loci associated with SBP were in low linkage disequilibrium with those associated with BMI suggesting that the gene cluster might regulate SBP through biological mechanisms that partly differ from those regulating BMI. Further studies in larger samples are needed for more precise evaluation of the possible interactions, and to understand the mechanisms behind.
Issue Date: 27-Sep-2012
Date of Acceptance: 1-Sep-2012
URI: http://hdl.handle.net/10044/1/48630
DOI: https://dx.doi.org/10.1371/journal.pone.0046557
ISSN: 1932-6203
Publisher: Public Library of Science
Journal / Book Title: PLOS One
Volume: 7
Issue: 9
Copyright Statement: © 2012 Kaakinen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Sponsor/Funder: Medical Research Council (MRC)
Funder's Grant Number: G0801056B
Keywords: Science & Technology
Multidisciplinary Sciences
Science & Technology - Other Topics
MULTIDISCIPLINARY SCIENCES
GENOME-WIDE ASSOCIATION
NICOTINE DEPENDENCE
LUNG-CANCER
ENVIRONMENT INTERACTIONS
SUSCEPTIBILITY LOCUS
EUROPEAN-AMERICANS
PERMUTATION TESTS
GENE-ENVIRONMENT
HEAVY SMOKING
WHOLE-GENOME
Blood Pressure
Body Mass Index
Cohort Studies
Female
Finland
Genetic Association Studies
Humans
Linkage Disequilibrium
Male
Middle Aged
Multigene Family
Nerve Tissue Proteins
Phenotype
Polymorphism, Single Nucleotide
Principal Component Analysis
Receptors, Nicotinic
Smoking
Tobacco Use Disorder
General Science & Technology
MD Multidisciplinary
Publication Status: Published
Article Number: ARTN e46557
Appears in Collections:Department of Medicine (up to 2019)