Uncoupling protein 2 haplotype does not affect human brain structure and function in a sample of community-dwelling older adults.

Uncoupling protein 2 (UCP2) is a mitochondrial membrane protein that plays a role in uncoupling electron transport from adenosine triphosphate (ATP) formation. Polymorphisms of the UCP2 gene in humans affect protein expression and function and have been linked to survival into old age. Since UCP2 is...

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Main Authors: Verena Heise, Enikő Zsoldos, Sana Suri, Claire Sexton, Anya Topiwala, Nicola Filippini, Abda Mahmood, Charlotte L Allan, Archana Singh-Manoux, Mika Kivimäki, Clare E Mackay, Klaus P Ebmeier
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0181392
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author Verena Heise
Enikő Zsoldos
Sana Suri
Claire Sexton
Anya Topiwala
Nicola Filippini
Abda Mahmood
Charlotte L Allan
Archana Singh-Manoux
Mika Kivimäki
Clare E Mackay
Klaus P Ebmeier
author_facet Verena Heise
Enikő Zsoldos
Sana Suri
Claire Sexton
Anya Topiwala
Nicola Filippini
Abda Mahmood
Charlotte L Allan
Archana Singh-Manoux
Mika Kivimäki
Clare E Mackay
Klaus P Ebmeier
author_sort Verena Heise
collection DOAJ
description Uncoupling protein 2 (UCP2) is a mitochondrial membrane protein that plays a role in uncoupling electron transport from adenosine triphosphate (ATP) formation. Polymorphisms of the UCP2 gene in humans affect protein expression and function and have been linked to survival into old age. Since UCP2 is expressed in several brain regions, we investigated in this study whether UCP2 polymorphisms might 1) affect occurrence of neurodegenerative or mental health disorders and 2) affect measures of brain structure and function. We used structural magnetic resonance imaging (MRI), diffusion-weighted MRI and resting-state functional MRI in the neuroimaging sub-study of the Whitehall II cohort. Data from 536 individuals aged 60 to 83 years were analyzed. No association of UCP2 polymorphisms with the occurrence of neurodegenerative disorders or grey and white matter structure or resting-state functional connectivity was observed. However, there was a significant effect on occurrence of mood disorders in men with the minor alleles of -866G>A (rs659366) and Ala55Val (rs660339)) being associated with increasing odds of lifetime occurrence of mood disorders in a dose dependent manner. This result was not accompanied by effects of UCP2 polymorphisms on brain structure and function, which might either indicate that the sample investigated here was too small and underpowered to find any significant effects, or that potential effects of UCP2 polymorphisms on the brain are too subtle to be picked up by any of the neuroimaging measures used.
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spelling doaj.art-9e3be38c69064b699eb1d4188b7d91c52022-12-22T04:06:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01128e018139210.1371/journal.pone.0181392Uncoupling protein 2 haplotype does not affect human brain structure and function in a sample of community-dwelling older adults.Verena HeiseEnikő ZsoldosSana SuriClaire SextonAnya TopiwalaNicola FilippiniAbda MahmoodCharlotte L AllanArchana Singh-ManouxMika KivimäkiClare E MackayKlaus P EbmeierUncoupling protein 2 (UCP2) is a mitochondrial membrane protein that plays a role in uncoupling electron transport from adenosine triphosphate (ATP) formation. Polymorphisms of the UCP2 gene in humans affect protein expression and function and have been linked to survival into old age. Since UCP2 is expressed in several brain regions, we investigated in this study whether UCP2 polymorphisms might 1) affect occurrence of neurodegenerative or mental health disorders and 2) affect measures of brain structure and function. We used structural magnetic resonance imaging (MRI), diffusion-weighted MRI and resting-state functional MRI in the neuroimaging sub-study of the Whitehall II cohort. Data from 536 individuals aged 60 to 83 years were analyzed. No association of UCP2 polymorphisms with the occurrence of neurodegenerative disorders or grey and white matter structure or resting-state functional connectivity was observed. However, there was a significant effect on occurrence of mood disorders in men with the minor alleles of -866G>A (rs659366) and Ala55Val (rs660339)) being associated with increasing odds of lifetime occurrence of mood disorders in a dose dependent manner. This result was not accompanied by effects of UCP2 polymorphisms on brain structure and function, which might either indicate that the sample investigated here was too small and underpowered to find any significant effects, or that potential effects of UCP2 polymorphisms on the brain are too subtle to be picked up by any of the neuroimaging measures used.https://doi.org/10.1371/journal.pone.0181392
spellingShingle Verena Heise
Enikő Zsoldos
Sana Suri
Claire Sexton
Anya Topiwala
Nicola Filippini
Abda Mahmood
Charlotte L Allan
Archana Singh-Manoux
Mika Kivimäki
Clare E Mackay
Klaus P Ebmeier
Uncoupling protein 2 haplotype does not affect human brain structure and function in a sample of community-dwelling older adults.
PLoS ONE
title Uncoupling protein 2 haplotype does not affect human brain structure and function in a sample of community-dwelling older adults.
title_full Uncoupling protein 2 haplotype does not affect human brain structure and function in a sample of community-dwelling older adults.
title_fullStr Uncoupling protein 2 haplotype does not affect human brain structure and function in a sample of community-dwelling older adults.
title_full_unstemmed Uncoupling protein 2 haplotype does not affect human brain structure and function in a sample of community-dwelling older adults.
title_short Uncoupling protein 2 haplotype does not affect human brain structure and function in a sample of community-dwelling older adults.
title_sort uncoupling protein 2 haplotype does not affect human brain structure and function in a sample of community dwelling older adults
url https://doi.org/10.1371/journal.pone.0181392
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