Global transcript profiles of fat in monozygotic twins discordant for BMI: pathways behind acquired obesity.

<h4>Background</h4>The acquired component of complex traits is difficult to dissect in humans. Obesity represents such a trait, in which the metabolic and molecular consequences emerge from complex interactions of genes and environment. With the substantial morbidity associated with obes...

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Autores principales: Kirsi H Pietiläinen, Jussi Naukkarinen, Aila Rissanen, Juha Saharinen, Pekka Ellonen, Heli Keränen, Anu Suomalainen, Alexandra Götz, Tapani Suortti, Hannele Yki-Järvinen, Matej Oresic, Jaakko Kaprio, Leena Peltonen
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Publicado: Public Library of Science (PLoS) 2008
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spelling oai:doaj.org-article:9c1d27490def4fc7ae999f3a5beb2ce12021-11-25T05:37:03ZGlobal transcript profiles of fat in monozygotic twins discordant for BMI: pathways behind acquired obesity.1549-12771549-167610.1371/journal.pmed.0050051https://doaj.org/article/9c1d27490def4fc7ae999f3a5beb2ce12008-03-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/18336063/?tool=EBIhttps://doaj.org/toc/1549-1277https://doaj.org/toc/1549-1676<h4>Background</h4>The acquired component of complex traits is difficult to dissect in humans. Obesity represents such a trait, in which the metabolic and molecular consequences emerge from complex interactions of genes and environment. With the substantial morbidity associated with obesity, a deeper understanding of the concurrent metabolic changes is of considerable importance. The goal of this study was to investigate this important acquired component and expose obesity-induced changes in biological pathways in an identical genetic background.<h4>Methods and findings</h4>We used a special study design of "clonal controls," rare monozygotic twins discordant for obesity identified through a national registry of 2,453 young, healthy twin pairs. A total of 14 pairs were studied (eight male, six female; white), with a mean +/- standard deviation (SD) age 25.8 +/- 1.4 y and a body mass index (BMI) difference 5.2 +/- 1.8 kg/m(2). Sequence analyses of mitochondrial DNA (mtDNA) in subcutaneous fat and peripheral leukocytes revealed no aberrant heteroplasmy between the co-twins. However, mtDNA copy number was reduced by 47% in the obese co-twin's fat. In addition, novel pathway analyses of the adipose tissue transcription profiles exposed significant down-regulation of mitochondrial branched-chain amino acid (BCAA) catabolism (p < 0.0001). In line with this finding, serum levels of insulin secretion-enhancing BCAAs were increased in obese male co-twins (9% increase, p = 0.025). Lending clinical relevance to the findings, in both sexes the observed aberrations in mitochondrial amino acid metabolism pathways in fat correlated closely with liver fat accumulation, insulin resistance, and hyperinsulinemia, early aberrations of acquired obesity in these healthy young adults.<h4>Conclusions</h4>Our findings emphasize a substantial role of mitochondrial energy- and amino acid metabolism in obesity and development of insulin resistance.Kirsi H PietiläinenJussi NaukkarinenAila RissanenJuha SaharinenPekka EllonenHeli KeränenAnu SuomalainenAlexandra GötzTapani SuorttiHannele Yki-JärvinenMatej OresicJaakko KaprioLeena PeltonenPublic Library of Science (PLoS)articleMedicineRENPLoS Medicine, Vol 5, Iss 3, p e51 (2008)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
spellingShingle Medicine
R
Kirsi H Pietiläinen
Jussi Naukkarinen
Aila Rissanen
Juha Saharinen
Pekka Ellonen
Heli Keränen
Anu Suomalainen
Alexandra Götz
Tapani Suortti
Hannele Yki-Järvinen
Matej Oresic
Jaakko Kaprio
Leena Peltonen
Global transcript profiles of fat in monozygotic twins discordant for BMI: pathways behind acquired obesity.
description <h4>Background</h4>The acquired component of complex traits is difficult to dissect in humans. Obesity represents such a trait, in which the metabolic and molecular consequences emerge from complex interactions of genes and environment. With the substantial morbidity associated with obesity, a deeper understanding of the concurrent metabolic changes is of considerable importance. The goal of this study was to investigate this important acquired component and expose obesity-induced changes in biological pathways in an identical genetic background.<h4>Methods and findings</h4>We used a special study design of "clonal controls," rare monozygotic twins discordant for obesity identified through a national registry of 2,453 young, healthy twin pairs. A total of 14 pairs were studied (eight male, six female; white), with a mean +/- standard deviation (SD) age 25.8 +/- 1.4 y and a body mass index (BMI) difference 5.2 +/- 1.8 kg/m(2). Sequence analyses of mitochondrial DNA (mtDNA) in subcutaneous fat and peripheral leukocytes revealed no aberrant heteroplasmy between the co-twins. However, mtDNA copy number was reduced by 47% in the obese co-twin's fat. In addition, novel pathway analyses of the adipose tissue transcription profiles exposed significant down-regulation of mitochondrial branched-chain amino acid (BCAA) catabolism (p < 0.0001). In line with this finding, serum levels of insulin secretion-enhancing BCAAs were increased in obese male co-twins (9% increase, p = 0.025). Lending clinical relevance to the findings, in both sexes the observed aberrations in mitochondrial amino acid metabolism pathways in fat correlated closely with liver fat accumulation, insulin resistance, and hyperinsulinemia, early aberrations of acquired obesity in these healthy young adults.<h4>Conclusions</h4>Our findings emphasize a substantial role of mitochondrial energy- and amino acid metabolism in obesity and development of insulin resistance.
format article
author Kirsi H Pietiläinen
Jussi Naukkarinen
Aila Rissanen
Juha Saharinen
Pekka Ellonen
Heli Keränen
Anu Suomalainen
Alexandra Götz
Tapani Suortti
Hannele Yki-Järvinen
Matej Oresic
Jaakko Kaprio
Leena Peltonen
author_facet Kirsi H Pietiläinen
Jussi Naukkarinen
Aila Rissanen
Juha Saharinen
Pekka Ellonen
Heli Keränen
Anu Suomalainen
Alexandra Götz
Tapani Suortti
Hannele Yki-Järvinen
Matej Oresic
Jaakko Kaprio
Leena Peltonen
author_sort Kirsi H Pietiläinen
title Global transcript profiles of fat in monozygotic twins discordant for BMI: pathways behind acquired obesity.
title_short Global transcript profiles of fat in monozygotic twins discordant for BMI: pathways behind acquired obesity.
title_full Global transcript profiles of fat in monozygotic twins discordant for BMI: pathways behind acquired obesity.
title_fullStr Global transcript profiles of fat in monozygotic twins discordant for BMI: pathways behind acquired obesity.
title_full_unstemmed Global transcript profiles of fat in monozygotic twins discordant for BMI: pathways behind acquired obesity.
title_sort global transcript profiles of fat in monozygotic twins discordant for bmi: pathways behind acquired obesity.
publisher Public Library of Science (PLoS)
publishDate 2008
url https://doaj.org/article/9c1d27490def4fc7ae999f3a5beb2ce1
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