Clinical, molecular, physiologic, and therapeutic feature of patients with CHRNA4 and CHRNB2 deficiency: A systematic review

Author:

Jalaiei Abbas1,Asadi Mohammad Reza1,Daneshmandpour Yousef1,Rezazadeh Maryam1,Ghafouri‐Fard Soudeh2ORCID

Affiliation:

1. Department of Medical Genetics Faculty of Medicine Tabriz University of Medical Sciences Tabriz Iran

2. Department of Medical Genetics Faculty of Medicine Shahid Beheshti University of Medical Sciences Tehran Iran

Abstract

AbstractThe α4β2 nAChRs are crucial ion channels that control neurotransmitter release and play a role in various physiologic and pathologic processes. CHRNA4 encodes the α4‐nAChRs, while CHRNB2 encodes the β2‐nAChRs. Recent studies have found different variants of α4β2‐nAChRs in individuals with conditions such as AD, ADHD, ALS, PD, and brain abnormalities. We conducted a scoping review following a six‐stage methodology structure and adhering to PRISMA guidelines. We systematically reviewed articles using relevant keywords up to October 2, 2023. In this summary, we cover the clinical symptoms reported, the genes and protein structure of CHRNA4 and CHRNB2, mutations in these genes, inheritance patterns, the functional impact of mutations and polymorphisms in CHRNA4 and CHRNB2, and the epidemiology of these diseases. Recent research indicates that nAChRs may play a significant role in neurodegenerative disorders, possibly impacting neuronal function through yet undiscovered regulatory pathways. Studying how nAChRs interact with disease‐related aggregates in neurodegenerative conditions may lead to new treatment options for these disorders.image

Publisher

Wiley

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