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Independent associations of TOMM40 and APOE variants with body mass index

The TOMM40‐APOE variants are known for their strong, antagonistic associations with Alzheimer's disease and body weight. While a stronger role of the APOE than TOMM40 variants in Alzheimer's disease was suggested, comparative contribution of the TOMM40‐APOE variants in the regulation of bo...

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Autores principales: Kulminski, Alexander M., Loika, Yury, Culminskaya, Irina, Huang, Jian, Arbeev, Konstantin G., Bagley, Olivia, Feitosa, Mary F., Zmuda, Joseph M., Christensen, Kaare, Yashin, Anatoliy I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351823/
https://www.ncbi.nlm.nih.gov/pubmed/30462377
http://dx.doi.org/10.1111/acel.12869
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author Kulminski, Alexander M.
Loika, Yury
Culminskaya, Irina
Huang, Jian
Arbeev, Konstantin G.
Bagley, Olivia
Feitosa, Mary F.
Zmuda, Joseph M.
Christensen, Kaare
Yashin, Anatoliy I.
author_facet Kulminski, Alexander M.
Loika, Yury
Culminskaya, Irina
Huang, Jian
Arbeev, Konstantin G.
Bagley, Olivia
Feitosa, Mary F.
Zmuda, Joseph M.
Christensen, Kaare
Yashin, Anatoliy I.
author_sort Kulminski, Alexander M.
collection PubMed
description The TOMM40‐APOE variants are known for their strong, antagonistic associations with Alzheimer's disease and body weight. While a stronger role of the APOE than TOMM40 variants in Alzheimer's disease was suggested, comparative contribution of the TOMM40‐APOE variants in the regulation of body weight remains elusive. We examined additive effects of rs2075650 and rs157580 TOMM40 variants and rs429358 and rs7412 APOE variants coding the ε2/ε3/ε4 polymorphism on body mass index (BMI) in age‐aggregated and age‐stratified cohort‐specific and cohort‐pooled analysis of 27,863 Caucasians aged 20–100 years from seven longitudinal studies. Minor alleles of rs2075650, rs429358, and rs7412 were individually associated with BMI (β = −1.29, p = 3.97 × 10(−9); β = −1.38, p = 2.78 × 10(−10); and β = 0.58, p = 3.04 × 10(−2), respectively). Conditional analysis with rs2075650 and rs429358 identified independent BMI‐lowering associations for minor alleles (β = −0.63, p = 3.99 × 10(−2) and β = −0.94, p = 2.17 × 10(−3), respectively). Polygenic mega‐analysis identified additive effects of the rs2075650 and rs429358 heterozygotes (β = −1.68, p = 3.00 × 10(−9)), and the strongest BMI‐lowering association for the rs2075650 heterozygous and rs429358 minor allele homozygous carriers (β = −4.11, p = 2.78 × 10(−3)). Conditional analysis with four polymorphisms identified independent BMI‐lowering (rs2075650, rs157580, and rs429358) and BMI‐increasing (rs7412) associations of heterozygous genotypes with BMI. Age‐stratified conditional analysis revealed well‐powered support for a differential and independent association of the rs429358 heterozygote with BMI in younger and older individuals, β = 0.58, 95% confidence interval (CI) = −1.18, 2.35, p = 5.18 × 10(−1) for 3,068 individuals aged ≤30 years and β = −4.28, CI = −5.65, −2.92, p = 7.71 × 10(−10) for 6,052 individuals aged >80 years. TOMM40 and APOE variants are independently and additively associated with BMI. The APOE ε4‐coding rs429358 polymorphism is associated with BMI in older individuals but not in younger individuals.
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spelling pubmed-63518232019-02-07 Independent associations of TOMM40 and APOE variants with body mass index Kulminski, Alexander M. Loika, Yury Culminskaya, Irina Huang, Jian Arbeev, Konstantin G. Bagley, Olivia Feitosa, Mary F. Zmuda, Joseph M. Christensen, Kaare Yashin, Anatoliy I. Aging Cell Original Papers The TOMM40‐APOE variants are known for their strong, antagonistic associations with Alzheimer's disease and body weight. While a stronger role of the APOE than TOMM40 variants in Alzheimer's disease was suggested, comparative contribution of the TOMM40‐APOE variants in the regulation of body weight remains elusive. We examined additive effects of rs2075650 and rs157580 TOMM40 variants and rs429358 and rs7412 APOE variants coding the ε2/ε3/ε4 polymorphism on body mass index (BMI) in age‐aggregated and age‐stratified cohort‐specific and cohort‐pooled analysis of 27,863 Caucasians aged 20–100 years from seven longitudinal studies. Minor alleles of rs2075650, rs429358, and rs7412 were individually associated with BMI (β = −1.29, p = 3.97 × 10(−9); β = −1.38, p = 2.78 × 10(−10); and β = 0.58, p = 3.04 × 10(−2), respectively). Conditional analysis with rs2075650 and rs429358 identified independent BMI‐lowering associations for minor alleles (β = −0.63, p = 3.99 × 10(−2) and β = −0.94, p = 2.17 × 10(−3), respectively). Polygenic mega‐analysis identified additive effects of the rs2075650 and rs429358 heterozygotes (β = −1.68, p = 3.00 × 10(−9)), and the strongest BMI‐lowering association for the rs2075650 heterozygous and rs429358 minor allele homozygous carriers (β = −4.11, p = 2.78 × 10(−3)). Conditional analysis with four polymorphisms identified independent BMI‐lowering (rs2075650, rs157580, and rs429358) and BMI‐increasing (rs7412) associations of heterozygous genotypes with BMI. Age‐stratified conditional analysis revealed well‐powered support for a differential and independent association of the rs429358 heterozygote with BMI in younger and older individuals, β = 0.58, 95% confidence interval (CI) = −1.18, 2.35, p = 5.18 × 10(−1) for 3,068 individuals aged ≤30 years and β = −4.28, CI = −5.65, −2.92, p = 7.71 × 10(−10) for 6,052 individuals aged >80 years. TOMM40 and APOE variants are independently and additively associated with BMI. The APOE ε4‐coding rs429358 polymorphism is associated with BMI in older individuals but not in younger individuals. John Wiley and Sons Inc. 2018-11-21 2019-02 /pmc/articles/PMC6351823/ /pubmed/30462377 http://dx.doi.org/10.1111/acel.12869 Text en © 2018 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Kulminski, Alexander M.
Loika, Yury
Culminskaya, Irina
Huang, Jian
Arbeev, Konstantin G.
Bagley, Olivia
Feitosa, Mary F.
Zmuda, Joseph M.
Christensen, Kaare
Yashin, Anatoliy I.
Independent associations of TOMM40 and APOE variants with body mass index
title Independent associations of TOMM40 and APOE variants with body mass index
title_full Independent associations of TOMM40 and APOE variants with body mass index
title_fullStr Independent associations of TOMM40 and APOE variants with body mass index
title_full_unstemmed Independent associations of TOMM40 and APOE variants with body mass index
title_short Independent associations of TOMM40 and APOE variants with body mass index
title_sort independent associations of tomm40 and apoe variants with body mass index
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351823/
https://www.ncbi.nlm.nih.gov/pubmed/30462377
http://dx.doi.org/10.1111/acel.12869
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