Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/112258
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Type: Journal article
Title: Investigation of short tandem repeats in major depression using whole-genome sequencing data
Author: Yu, C.
Baune, B.
Wong, M.
Licinio, J.
Citation: Journal of Affective Disorders, 2018; 232:305-309
Publisher: Elsevier BV
Issue Date: 2018
ISSN: 0165-0327
1573-2517
Statement of
Responsibility: 
Chenglong Yu, Bernhard T. Baune, Ma-Li Wong, Julio Licinio
Abstract: Background: Major depressive disorder (MDD) is a leading contributor to global disease burden. Recent studies have shown that genetic factors play significant roles in the susceptibility to this condition; however, the underlying genetic basis currently remains largely unknown. Short tandem repeat (STR) has been proposed as an explanatory factor in the “missing heritability” of complex diseases or traits. Methods: We investigated STR variations from 15 MDD patients and 10 ethnically matched healthy controls based on their deep whole-genome sequencing (WGS) data. The lobSTR software was used to computationally determine STRs. Results: The results of the Mexican-American sample showed that STRs are significantly richer in healthy controls than in MDD cases on each of the 23 chromosomes (all false discovery rates, FDR P-values< 0.0062); while for the Australian of European-ancestry sample, there was no statistically significant STRs difference between MDD cases and controls. Limitations: High quality WGS costs limited obtaining larger datasets. Conclusions: This preliminary work is the first study that STR variations are applied to investigate MDD based on WGS data. The results on Mexican-American population may imply that within the same ancestry, targeted sequencing on a specific chromosome or region of genome would be sufficient for examining the relationship between STR and MDD. Further studies should examine larger sequencing datasets on other ethnic groups.
Keywords: Major depressive disorder; Heritability; Psychiatric genetics; Whole-genome sequencing; Genetic marker
Description: Available online 24 February 2018
Rights: © 2018 Elsevier B.V. All rights reserved.
RMID: 0030083354
DOI: 10.1016/j.jad.2018.02.046
Grant ID: http://purl.org/au-research/grants/nhmrc/1051931
http://purl.org/au-research/grants/nhmrc/1060524
Appears in Collections:Psychiatry publications

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