Literature DB >> 31685286

An integrative analysis of transcriptome-wide association study and mRNA expression profile identified candidate genes for attention-deficit/hyperactivity disorder.

Xin Qi1, Sen Wang1, Lu Zhang1, Li Liu1, Yan Wen1, Mei Ma1, Shiqiang Cheng1, Ping Li1, Bolun Cheng1, Yanan Du1, Xiao Liang1, Yan Zhao1, Miao Ding1, Feng Zhang2.   

Abstract

BACKGROUND: Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, but the genetic mechanism of ADHD remains elusive now.
METHODS: Tissue specific transcriptome-wide association study (TWAS) of ADHD was performed by FUSION utilizing a genome-wide association study (GWAS) dataset of ADHD (including 20,183 ADHD cases and 35,191 healthy controls) and gene expression reference from brain and blood. Furthermore, the genes identified by TWAS were compared with the differently expressed genes detected by mRNA expression profiles of ADHD rat model and autism spectrum disorders (ASD) patients. Functional enrichment and annotation analysis of the identified genes were performed by DAVID and FUMAGWAS tool.
RESULTS: For brain tissue, TWAS identified 148 genes with P value < 0.05, such as TDO2 (PTWAS=4.01×10-2), CHD1L (PTWAS=9.64×10-3) and KIAA0319L (PTWAS=4.05×10-4). Further 11 common genes were examined in the mRNA expression datasets, such as ACSM5 (PTWAS=3.62×10-2, PmRNA=0.005), CCDC24 (PTWAS=1.49×10-2, PmRNA=2.35×10-3) and MVP (PTWAS=5.55×10-3, PmRNA=5.40×10-3). Pathway enrichment analysis of the genes identified by TWAS detected 3 pathways for ADHD, including Other glycan degradation (P value=0.021), Viral myocarditis (P value=0.034) and Endocytosis (P value=0.041).
CONCLUSIONS: Through integrating GWAS and mRNA expression data, we identified a group of ADHD-associated genes and pathways, providing novel clues for understanding the genetic mechanism of ADHD.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Attention-deficit/hyperactivity disorder (ADHD); Gene ontology (GO); Genome-wide association study (GWAS); Pathway; Transcriptome-wide association study (TWAS)

Mesh:

Substances:

Year:  2019        PMID: 31685286     DOI: 10.1016/j.psychres.2019.112639

Source DB:  PubMed          Journal:  Psychiatry Res        ISSN: 0165-1781            Impact factor:   3.222


  5 in total

Review 1.  Systematic review of mitochondrial genetic variation in attention-deficit/hyperactivity disorder.

Authors:  Stavroula V Giannoulis; Daniel Müller; James L Kennedy; Vanessa Gonçalves
Journal:  Eur Child Adolesc Psychiatry       Date:  2022-07-07       Impact factor: 4.785

2.  Non-genetic risk and protective factors and biomarkers for neurological disorders: a meta-umbrella systematic review of umbrella reviews.

Authors:  Alexios-Fotios A Mentis; Efthimios Dardiotis; Vasiliki Efthymiou; George P Chrousos
Journal:  BMC Med       Date:  2021-01-13       Impact factor: 8.775

3.  Integrative analysis of genome-wide DNA methylation and single-nucleotide polymorphism identified ACSM5 as a suppressor of lumbar ligamentum flavum hypertrophy.

Authors:  Yanlin Cao; Yenan Zhan; Sujun Qiu; Zhong Chen; Kaiqin Gong; Songjia Ni; Yang Duan
Journal:  Arthritis Res Ther       Date:  2021-09-30       Impact factor: 5.156

4.  DNA methylation signatures in human neonatal blood following maternal antenatal corticosteroid treatment.

Authors:  Bona Kim; Aya Sasaki; Kellie Murphy; Stephen G Matthews
Journal:  Transl Psychiatry       Date:  2022-03-31       Impact factor: 6.222

5.  The PH Domain and C-Terminal polyD Motif of Phafin2 Exhibit a Unique Concurrence in Animals.

Authors:  Mahmudul Hasan; Daniel G S Capelluto
Journal:  Membranes (Basel)       Date:  2022-07-07
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.