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Mitochondrial DNA Variants in Obesity

Heritability estimates for body mass index (BMI) variation are high. For mothers and their offspring higher BMI correlations have been described than for fathers. Variation(s) in the exclusively maternally inherited mitochondrial DNA (mtDNA) might contribute to this parental effect. Thirty-two to 40...

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Autores principales: Knoll, Nadja, Jarick, Ivonne, Volckmar, Anna-Lena, Klingenspor, Martin, Illig, Thomas, Grallert, Harald, Gieger, Christian, Wichmann, Heinz-Erich, Peters, Annette, Wiegand, Susanna, Biebermann, Heike, Fischer-Posovszky, Pamela, Wabitsch, Martin, Völzke, Henry, Nauck, Matthias, Teumer, Alexander, Rosskopf, Dieter, Rimmbach, Christian, Schreiber, Stefan, Jacobs, Gunnar, Lieb, Wolfgang, Franke, Andre, Hebebrand, Johannes, Hinney, Anke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008486/
https://www.ncbi.nlm.nih.gov/pubmed/24788344
http://dx.doi.org/10.1371/journal.pone.0094882
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author Knoll, Nadja
Jarick, Ivonne
Volckmar, Anna-Lena
Klingenspor, Martin
Illig, Thomas
Grallert, Harald
Gieger, Christian
Wichmann, Heinz-Erich
Peters, Annette
Wiegand, Susanna
Biebermann, Heike
Fischer-Posovszky, Pamela
Wabitsch, Martin
Völzke, Henry
Nauck, Matthias
Teumer, Alexander
Rosskopf, Dieter
Rimmbach, Christian
Schreiber, Stefan
Jacobs, Gunnar
Lieb, Wolfgang
Franke, Andre
Hebebrand, Johannes
Hinney, Anke
author_facet Knoll, Nadja
Jarick, Ivonne
Volckmar, Anna-Lena
Klingenspor, Martin
Illig, Thomas
Grallert, Harald
Gieger, Christian
Wichmann, Heinz-Erich
Peters, Annette
Wiegand, Susanna
Biebermann, Heike
Fischer-Posovszky, Pamela
Wabitsch, Martin
Völzke, Henry
Nauck, Matthias
Teumer, Alexander
Rosskopf, Dieter
Rimmbach, Christian
Schreiber, Stefan
Jacobs, Gunnar
Lieb, Wolfgang
Franke, Andre
Hebebrand, Johannes
Hinney, Anke
author_sort Knoll, Nadja
collection PubMed
description Heritability estimates for body mass index (BMI) variation are high. For mothers and their offspring higher BMI correlations have been described than for fathers. Variation(s) in the exclusively maternally inherited mitochondrial DNA (mtDNA) might contribute to this parental effect. Thirty-two to 40 mtDNA single nucleotide polymorphisms (SNPs) were available from genome-wide association study SNP arrays (Affymetrix 6.0). For discovery, we analyzed association in a case-control (CC) sample of 1,158 extremely obese children and adolescents and 435 lean adult controls. For independent confirmation, 7,014 population-based adults were analyzed as CC sample of n = 1,697 obese cases (BMI≥30 kg/m(2)) and n = 2,373 normal weight and lean controls (BMI<25 kg/m(2)). SNPs were analyzed as single SNPs and haplogroups determined by HaploGrep. Fisher's two-sided exact test was used for association testing. Moreover, the D-loop was re-sequenced (Sanger) in 192 extremely obese children and adolescents and 192 lean adult controls. Association testing of detected variants was performed using Fisher's two-sided exact test. For discovery, nominal association with obesity was found for the frequent allele G of m.8994G/A (rs28358887, p = 0.002) located in ATP6. Haplogroup W was nominally overrepresented in the controls (p = 0.039). These findings could not be confirmed independently. For two of the 252 identified D-loop variants nominal association was detected (m.16292C/T, p = 0.007, m.16189T/C, p = 0.048). Only eight controls carried the m.16292T allele, five of whom belonged to haplogroup W that was initially enriched among these controls. m.16189T/C might create an uninterrupted poly-C tract located near a regulatory element involved in replication of mtDNA. Though follow-up of some D-loop variants still is conceivable, our hypothesis of a contribution of variation in the exclusively maternally inherited mtDNA to the observed larger correlations for BMI between mothers and their offspring could not be substantiated by the findings of the present study.
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spelling pubmed-40084862014-05-09 Mitochondrial DNA Variants in Obesity Knoll, Nadja Jarick, Ivonne Volckmar, Anna-Lena Klingenspor, Martin Illig, Thomas Grallert, Harald Gieger, Christian Wichmann, Heinz-Erich Peters, Annette Wiegand, Susanna Biebermann, Heike Fischer-Posovszky, Pamela Wabitsch, Martin Völzke, Henry Nauck, Matthias Teumer, Alexander Rosskopf, Dieter Rimmbach, Christian Schreiber, Stefan Jacobs, Gunnar Lieb, Wolfgang Franke, Andre Hebebrand, Johannes Hinney, Anke PLoS One Research Article Heritability estimates for body mass index (BMI) variation are high. For mothers and their offspring higher BMI correlations have been described than for fathers. Variation(s) in the exclusively maternally inherited mitochondrial DNA (mtDNA) might contribute to this parental effect. Thirty-two to 40 mtDNA single nucleotide polymorphisms (SNPs) were available from genome-wide association study SNP arrays (Affymetrix 6.0). For discovery, we analyzed association in a case-control (CC) sample of 1,158 extremely obese children and adolescents and 435 lean adult controls. For independent confirmation, 7,014 population-based adults were analyzed as CC sample of n = 1,697 obese cases (BMI≥30 kg/m(2)) and n = 2,373 normal weight and lean controls (BMI<25 kg/m(2)). SNPs were analyzed as single SNPs and haplogroups determined by HaploGrep. Fisher's two-sided exact test was used for association testing. Moreover, the D-loop was re-sequenced (Sanger) in 192 extremely obese children and adolescents and 192 lean adult controls. Association testing of detected variants was performed using Fisher's two-sided exact test. For discovery, nominal association with obesity was found for the frequent allele G of m.8994G/A (rs28358887, p = 0.002) located in ATP6. Haplogroup W was nominally overrepresented in the controls (p = 0.039). These findings could not be confirmed independently. For two of the 252 identified D-loop variants nominal association was detected (m.16292C/T, p = 0.007, m.16189T/C, p = 0.048). Only eight controls carried the m.16292T allele, five of whom belonged to haplogroup W that was initially enriched among these controls. m.16189T/C might create an uninterrupted poly-C tract located near a regulatory element involved in replication of mtDNA. Though follow-up of some D-loop variants still is conceivable, our hypothesis of a contribution of variation in the exclusively maternally inherited mtDNA to the observed larger correlations for BMI between mothers and their offspring could not be substantiated by the findings of the present study. Public Library of Science 2014-05-02 /pmc/articles/PMC4008486/ /pubmed/24788344 http://dx.doi.org/10.1371/journal.pone.0094882 Text en © 2014 Knoll et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Knoll, Nadja
Jarick, Ivonne
Volckmar, Anna-Lena
Klingenspor, Martin
Illig, Thomas
Grallert, Harald
Gieger, Christian
Wichmann, Heinz-Erich
Peters, Annette
Wiegand, Susanna
Biebermann, Heike
Fischer-Posovszky, Pamela
Wabitsch, Martin
Völzke, Henry
Nauck, Matthias
Teumer, Alexander
Rosskopf, Dieter
Rimmbach, Christian
Schreiber, Stefan
Jacobs, Gunnar
Lieb, Wolfgang
Franke, Andre
Hebebrand, Johannes
Hinney, Anke
Mitochondrial DNA Variants in Obesity
title Mitochondrial DNA Variants in Obesity
title_full Mitochondrial DNA Variants in Obesity
title_fullStr Mitochondrial DNA Variants in Obesity
title_full_unstemmed Mitochondrial DNA Variants in Obesity
title_short Mitochondrial DNA Variants in Obesity
title_sort mitochondrial dna variants in obesity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008486/
https://www.ncbi.nlm.nih.gov/pubmed/24788344
http://dx.doi.org/10.1371/journal.pone.0094882
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