Literature DB >> 28693754

A comprehensive analysis of mitochondrial genes variants and their association with antipsychotic-induced weight gain.

Kirti Mittal1, Vanessa F Gonçalves2, Ricardo Harripaul3, Ari B Cuperfain1, Brandi Rollins4, Arun K Tiwari1, Clement C Zai1, Malgorzata Maciukiewicz1, Daniel J Müller1, Marquis P Vawter4, James L Kennedy1.   

Abstract

Antipsychotic Induced Weight Gain (AIWG) is a common and severe side effect of many antipsychotic medications. Mitochondria play a vital role for whole-body energy homeostasis and there is increasing evidence that antipsychotics modulate mitochondrial function. This study aimed to examine the role of variants in nuclear-encoded mitochondrial genes and the mitochondrial DNA (mtDNA) in conferring risk for AIWG. We selected 168 European-Caucasian individuals from the CATIE sample based upon meeting criteria of multiple weight measures while taking selected antipsychotics (risperidone, quetiapine or olanzapine). We tested the association of 670 nuclear-encoded mitochondrial genes with weight change (%) using MAGMA software. Thirty of these genes showed nominally significant P-values (<0.05). We were able to replicate the association of three genes, CLPB, PARL, and ACAD10, with weight change (%) in an independent prospectively assessed AIWG sample. We analyzed mtDNA variants in a subset of 74 of these individuals using next-generation sequencing. No common or rare mtDNA variants were found to be significantly associated with weight change (%) in our sample. Additionally, analysis of mitochondrial haplogroups showed no association with weight change (%). In conclusion, our findings suggest nuclear-encoded mitochondrial genes play a role in AIWG. Replication in larger sample is required to validate our initial report of mtDNA variants in AIWG.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Antipsychotic-induced weight gain; Mitochondria; Mitochondrial DNA variants; Next generation sequencing; Nuclear-encoded mitochondrial genes; Schizophrenia

Mesh:

Substances:

Year:  2017        PMID: 28693754      PMCID: PMC5660917          DOI: 10.1016/j.schres.2017.06.046

Source DB:  PubMed          Journal:  Schizophr Res        ISSN: 0920-9964            Impact factor:   4.939


  39 in total

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Journal:  Am J Hum Genet       Date:  2007-07-25       Impact factor: 11.025

4.  The diversity present in 5140 human mitochondrial genomes.

Authors:  Luísa Pereira; Fernando Freitas; Verónica Fernandes; Joana B Pereira; Marta D Costa; Stephanie Costa; Valdemar Máximo; Vincent Macaulay; Ricardo Rocha; David C Samuels
Journal:  Am J Hum Genet       Date:  2009-05-07       Impact factor: 11.025

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Authors:  Daniel J Müller; James L Kennedy
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Review 1.  Pharmacogenetic Correlates of Antipsychotic-Induced Weight Gain in the Chinese Population.

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3.  Extensive analysis of mitochondrial DNA quantity and sequence variation in human cumulus cells and assisted reproduction outcomes.

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Review 4.  Psychiatric drugs impact mitochondrial function in brain and other tissues.

Authors:  Shawna T Chan; Michael J McCarthy; Marquis P Vawter
Journal:  Schizophr Res       Date:  2019-11-16       Impact factor: 4.939

Review 5.  The Complex Interaction of Mitochondrial Genetics and Mitochondrial Pathways in Psychiatric Disease.

Authors:  Ari B Cuperfain; Zhi Lun Zhang; James L Kennedy; Vanessa F Gonçalves
Journal:  Mol Neuropsychiatry       Date:  2018-05-30

6.  Olanzapine Induced Dysmetabolic Changes Involving Tissue Chromium Mobilization in Female Rats.

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Journal:  Int J Mol Sci       Date:  2019-02-01       Impact factor: 5.923

Review 7.  Impact of Psychotropic Medication Effects on Obesity and the Metabolic Syndrome in People With Serious Mental Illness.

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Journal:  Front Endocrinol (Lausanne)       Date:  2020-10-09       Impact factor: 5.555

  7 in total

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