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Causal relationship and shared genes between air pollutants and amyotrophic lateral sclerosis: A large-scale genetic analysis.
Li, Zhihao; Wen, Jie; Wu, Wantao; Dai, Ziyu; Liang, Xisong; Zhang, Nan; Cheng, Quan; Zhang, Hao.
Afiliação
  • Li Z; Department of Neurosurgery, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.
  • Wen J; Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
  • Wu W; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.
  • Dai Z; Department of Oncology, Xiangya Hospital, Central South University, Changsha, China.
  • Liang X; Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
  • Zhang N; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.
  • Cheng Q; Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
  • Zhang H; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.
CNS Neurosci Ther ; 30(7): e14812, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38970158
ABSTRACT

OBJECTIVE:

Air pollutants have been reported to have a potential relationship with amyotrophic lateral sclerosis (ALS). The causality and underlying mechanism remained unknown despite several existing observational studies. We aimed to investigate the potential causality between air pollutants (PM2.5, NOX, and NO2) and the risk of ALS and elucidate the underlying mechanisms associated with this relationship.

METHODS:

The data utilized in our study were obtained from publicly available genome-wide association study data sets, in which single nucleotide polymorphisms (SNPs) were employed as the instrumental variantswith three principles. Two-sample Mendelian randomization and transcriptome-wide association (TWAS) analyses were conducted to evaluate the effects of air pollutants on ALS and identify genes associated with both pollutants and ALS, followed by regulatory network prediction.

RESULTS:

We observed that exposure to a high level of PM2.5 (OR 2.40 [95% CI 1.26-4.57], p = 7.46E-3) and NOx (OR 2.35 [95% CI 1.32-4.17], p = 3.65E-3) genetically increased the incidence of ALS in MR analysis, while the effects of NO2 showed a similar trend but without sufficient significance. In the TWAS analysis, TMEM175 and USP35 turned out to be the genes shared between PM2.5 and ALS in the same direction.

CONCLUSION:

Higher exposure to PM2.5 and NOX might causally increase the risk of ALS. Avoiding exposure to air pollutants and air cleaning might be necessary for ALS prevention.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Poluentes Atmosféricos / Estudo de Associação Genômica Ampla / Análise da Randomização Mendeliana / Esclerose Lateral Amiotrófica Limite: Humans Idioma: En Revista: CNS Neurosci Ther Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Poluentes Atmosféricos / Estudo de Associação Genômica Ampla / Análise da Randomização Mendeliana / Esclerose Lateral Amiotrófica Limite: Humans Idioma: En Revista: CNS Neurosci Ther Ano de publicação: 2024 Tipo de documento: Article