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Pleiotropic Associations of Allelic Variants in a 2q22 Region with Risks of Major Human Diseases and Mortality.

Publication ,  Journal Article
Kulminski, AM; He, L; Culminskaya, I; Loika, Y; Kernogitski, Y; Arbeev, KG; Loiko, E; Arbeeva, L; Bagley, O; Duan, M; Yashkin, A; Fang, F ...
Published in: PLoS genetics
November 2016

Gaining insights into genetic predisposition to age-related diseases and lifespan is a challenging task complicated by the elusive role of evolution in these phenotypes. To gain more insights, we combined methods of genome-wide and candidate-gene studies. Genome-wide scan in the Atherosclerosis Risk in Communities (ARIC) Study (N = 9,573) was used to pre-select promising loci. Candidate-gene methods were used to comprehensively analyze associations of novel uncommon variants in Caucasians (minor allele frequency~2.5%) located in band 2q22.3 with risks of coronary heart disease (CHD), heart failure (HF), stroke, diabetes, cancer, neurodegenerative diseases (ND), and mortality in the ARIC study, the Framingham Heart Study (N = 4,434), and the Health and Retirement Study (N = 9,676). We leveraged the analyses of pleiotropy, age-related heterogeneity, and causal inferences. Meta-analysis of the results from these comprehensive analyses shows that the minor allele increases risks of death by about 50% (p = 4.6×10-9), CHD by 35% (p = 8.9×10-6), HF by 55% (p = 9.7×10-5), stroke by 25% (p = 4.0×10-2), and ND by 100% (p = 1.3×10-3). This allele also significantly influences each of two diseases, diabetes and cancer, in antagonistic fashion in different populations. Combined significance of the pleiotropic effects was p = 6.6×10-21. Causal mediation analyses show that endophenotypes explained only small fractions of these effects. This locus harbors an evolutionary conserved gene-desert region with non-coding intergenic sequences likely involved in regulation of protein-coding flanking genes ZEB2 and ACVR2A. This region is intensively studied for mutations causing severe developmental/genetic disorders. Our analyses indicate a promising target region for interventions aimed to reduce risks of many major human diseases and mortality.

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Published In

PLoS genetics

DOI

EISSN

1553-7404

ISSN

1553-7390

Publication Date

November 2016

Volume

12

Issue

11

Start / End Page

e1006314

Related Subject Headings

  • Zinc Finger E-box Binding Homeobox 2
  • Stroke
  • Risk Factors
  • Repressor Proteins
  • Male
  • Humans
  • Homeodomain Proteins
  • Heart Failure
  • Genome-Wide Association Study
  • Genetic Predisposition to Disease
 

Citation

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Kulminski, A. M., He, L., Culminskaya, I., Loika, Y., Kernogitski, Y., Arbeev, K. G., … Yashin, A. I. (2016). Pleiotropic Associations of Allelic Variants in a 2q22 Region with Risks of Major Human Diseases and Mortality. PLoS Genetics, 12(11), e1006314. https://doi.org/10.1371/journal.pgen.1006314
Kulminski, Alexander M., Liang He, Irina Culminskaya, Yury Loika, Yelena Kernogitski, Konstantin G. Arbeev, Elena Loiko, et al. “Pleiotropic Associations of Allelic Variants in a 2q22 Region with Risks of Major Human Diseases and Mortality.PLoS Genetics 12, no. 11 (November 2016): e1006314. https://doi.org/10.1371/journal.pgen.1006314.
Kulminski AM, He L, Culminskaya I, Loika Y, Kernogitski Y, Arbeev KG, et al. Pleiotropic Associations of Allelic Variants in a 2q22 Region with Risks of Major Human Diseases and Mortality. PLoS genetics. 2016 Nov;12(11):e1006314.
Kulminski, Alexander M., et al. “Pleiotropic Associations of Allelic Variants in a 2q22 Region with Risks of Major Human Diseases and Mortality.PLoS Genetics, vol. 12, no. 11, Nov. 2016, p. e1006314. Epmc, doi:10.1371/journal.pgen.1006314.
Kulminski AM, He L, Culminskaya I, Loika Y, Kernogitski Y, Arbeev KG, Loiko E, Arbeeva L, Bagley O, Duan M, Yashkin A, Fang F, Kovtun M, Ukraintseva SV, Wu D, Yashin AI. Pleiotropic Associations of Allelic Variants in a 2q22 Region with Risks of Major Human Diseases and Mortality. PLoS genetics. 2016 Nov;12(11):e1006314.

Published In

PLoS genetics

DOI

EISSN

1553-7404

ISSN

1553-7390

Publication Date

November 2016

Volume

12

Issue

11

Start / End Page

e1006314

Related Subject Headings

  • Zinc Finger E-box Binding Homeobox 2
  • Stroke
  • Risk Factors
  • Repressor Proteins
  • Male
  • Humans
  • Homeodomain Proteins
  • Heart Failure
  • Genome-Wide Association Study
  • Genetic Predisposition to Disease