Literature DB >> 20545631

A homozygous genetic variant of mitochondrial uncoupling protein 4 affects the occurrence of leukoaraiosis.

Z Szolnoki1, A Kondacs, Y Mandi, A Bodor, F Somogyvari.   

Abstract

OBJECTIVES: We hypothesized that an appropriate balance of the mitochondrial energy production is essential in the maintenance of the glia cells in the brain. The aim of this study was to examine the roles of the rs10807344 and rs2270450 genetic variants of mitochondrial uncoupling protein 4 in the development of vascular demyelinization of the white matter of the brain, referred to as leukoaraiosis (LA). The mUCPs are presumed to be of great importance in the regulation of the mitochondrial membrane potential (MMP) and the cellular energy metabolism.
MATERIALS AND METHODS: An analysis was performed on the clinical and genetic data on 401 LA patients without infarction and on 451 neuroimaging alteration-free subjects. After univariate statistical approaches, logistic regression models were also used to adjust differences in significant clinical factors between the patients and controls.
RESULTS: The rs10807344 CC genotype proved to exert a protective effect on the occurrence of LA (neuroimaging alteration-free controls: 57.7%, LA group: 44.9%, P < 0.0002; adjusted OR: 0.41, 95% CI: 0.2-0.68, P < 0.005).
CONCLUSION: The present findings indirectly raise the possibility that a shift or imbalance in the finely regulated MMP may play a role in the development of LA.
© 2010 John Wiley & Sons A/S.

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Year:  2011        PMID: 20545631     DOI: 10.1111/j.1600-0404.2010.01391.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  5 in total

1.  Tumor necrosis factor-α impairs oligodendroglial differentiation through a mitochondria-dependent process.

Authors:  M Bonora; E De Marchi; S Patergnani; J M Suski; F Celsi; A Bononi; C Giorgi; S Marchi; A Rimessi; J Duszyński; T Pozzan; M R Wieckowski; P Pinton
Journal:  Cell Death Differ       Date:  2014-03-21       Impact factor: 15.828

2.  Caenorhabditis elegans UCP4 protein controls complex II-mediated oxidative phosphorylation through succinate transport.

Authors:  Matthew Pfeiffer; Ernst-Bernhard Kayzer; Xianmei Yang; Ellen Abramson; M Alexander Kenaston; Cory U Lago; Herng-Hsiang Lo; Margaret M Sedensky; Adam Lunceford; Catherine F Clarke; Sarah J Wu; Chris McLeod; Toren Finkel; Philip G Morgan; Edward M Mills
Journal:  J Biol Chem       Date:  2011-08-23       Impact factor: 5.486

3.  Further support to the uncoupling-to-survive theory: the genetic variation of human UCP genes is associated with longevity.

Authors:  Giuseppina Rose; Paolina Crocco; Francesco De Rango; Alberto Montesanto; Giuseppe Passarino
Journal:  PLoS One       Date:  2011-12-27       Impact factor: 3.240

4.  Uncoupling protein-4 (UCP4) increases ATP supply by interacting with mitochondrial Complex II in neuroblastoma cells.

Authors:  Philip Wing-Lok Ho; Jessica Wing-Man Ho; Ho-Man Tse; Danny Hon-Fai So; David Chi-Wai Yiu; Hui-Fang Liu; Koon-Ho Chan; Michelle Hiu-Wai Kung; David Boyer Ramsden; Shu-Leong Ho
Journal:  PLoS One       Date:  2012-02-29       Impact factor: 3.240

5.  Human neuronal uncoupling proteins 4 and 5 (UCP4 and UCP5): structural properties, regulation, and physiological role in protection against oxidative stress and mitochondrial dysfunction.

Authors:  David B Ramsden; Philip W-L Ho; Jessica W-M Ho; Hui-Fang Liu; Danny H-F So; Ho-Man Tse; Koon-Ho Chan; Shu-Leong Ho
Journal:  Brain Behav       Date:  2012-07       Impact factor: 2.708

  5 in total

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