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

被引:0
|
作者
Jalaiei, Abbas [1 ]
Asadi, Mohammad Reza [1 ]
Daneshmandpour, Yousef [1 ]
Rezazadeh, Maryam [1 ]
Ghafouri-Fard, Soudeh [2 ]
机构
[1] Tabriz Univ Med Sci, Fac Med, Dept Med Genet, Tabriz, Iran
[2] Shahid Beheshti Univ Med Sci, Fac Med, Dept Med Genet, Tehran, Iran
关键词
CHRNA4; CHRNB2; nAChRs; neurodegenerative diseases; NICOTINIC ACETYLCHOLINE-RECEPTOR; FRONTAL-LOBE EPILEPSY; AMYOTROPHIC-LATERAL-SCLEROSIS; DE-NOVO MUTATION; ALPHA-4; SUBUNIT; CHOLINERGIC-RECEPTOR; ALZHEIMERS-DISEASE; GENE CHRNA4; MISSENSE MUTATION; NORWEGIAN FAMILY;
D O I
10.1111/jnc.16200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The alpha 4 beta 2 nAChRs are crucial ion channels that control neurotransmitter release and play a role in various physiologic and pathologic processes. CHRNA4 encodes the alpha 4-nAChRs, while CHRNB2 encodes the beta 2-nAChRs. Recent studies have found different variants of alpha 4 beta 2-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
引用
收藏
页数:23
相关论文
共 4 条
  • [1] Variants in CHRNB2 and CHRNA4 Identified in Patients with Insular Epilepsy
    Cadieux-Dion, Maxime
    Meneghini, Simone
    Villa, Chiara
    Toffa, Denahin Hinnoutondji
    Wickstrom, Ronny
    Bouthillier, Alain
    Sandvik, Ulrika
    Gustavsson, Bengt
    Mohamed, Ismail
    Cossette, Patrick
    Combi, Romina
    Becchetti, Andrea
    Nguyen, Dang Khoa
    CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 2020, 47 (06) : 800 - 809
  • [2] Mutation screening of the CHRNA4 and CHRNB2 nicotinic cholinergic receptor genes in Alzheimer's disease
    Steinlein, OK
    Stoodt, J
    de Vos, RAI
    Steur, ENHJ
    Wevers, A
    Schütz, U
    Schröder, H
    NEUROREPORT, 1999, 10 (14) : 2919 - 2922
  • [3] Mutational analysis of CHRNB2, CHRNA2 and CHRNA4 genes in Chinese population with autosomal dominant nocturnal frontal lobe epilepsy
    Chen, Zhihong
    Wang, Lingan
    Wang, Chun
    Chen, Qian
    Zhai, Qiongxiang
    Guo, Yuxiong
    Zhang, Yuxin
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2015, 8 (06): : 9063 - 9070
  • [4] Candidate gene association studies of the α4 (CHRNA4) and β2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease
    Cook, LJ
    Ho, LW
    Taylor, AE
    Brayne, C
    Evans, JG
    Xuereb, J
    Cairns, NJ
    Pritchard, A
    Lemmon, H
    Mann, D
    Clair, DS
    Turic, D
    Hollingworth, P
    Moore, PJ
    Jehu, L
    Archer, N
    Walter, S
    Foy, C
    Edmondson, A
    Powell, J
    Lovestone, S
    Owen, MJ
    Williams, J
    Lendon, C
    Rubinsztein, DC
    NEUROSCIENCE LETTERS, 2004, 358 (02) : 142 - 146