Literature DB >> 31848916

HINT1 gene pathogenic variants: the most common cause of recessive hereditary motor and sensory neuropathies in Russian patients.

O A Shchagina1, T B Milovidova2, A F Murtazina3, G E Rudenskaya4, S S Nikitin5, E L Dadali4, A V Polyakov2.   

Abstract

Pathogenic variants in the HINT1 gene lead to hereditary axonopathy with neuromyotonia. However, many studies show that neuromyotonia may remain undiagnosed, while axonopathy is the major clinical finding. The most common cause of neuromyotonia and axonopathy, especially in patients of Slavic origin, is a c.110G>C (p.Arg37Pro) pathogenic variant in homozygous or compound heterozygous state. In this study, we analyzed a peripheral neuropathy caused by pathogenic variants in the HINT1 gene and evaluated its contribution to the hereditary neuropathy structure. The studied group included 1596 non-related families diagnosed with hereditary motor and sensory neuropathy (HMSN). The results show that HINT1 gene pathogenic variants make a significant contribution to the hereditary neuropathy epidemiology in Russian patients. They account for at least 1.9% of all HMSN cases and 9% of axonopathy cases. The most common HINT1 pathogenic variant in Russian patients is the c.110G>C (p.Arg37Pro) substitution. Its allelic frequency is 0.2% (95% CI 0.19-0.21%), carrier frequency is 1 in 250 people in Russian Federation, and the estimated disease incidence is 1 in 234,000 individuals. It was determined that the cause of this pathogenic variant's prevalence is the founder effect.

Entities:  

Keywords:  Axonopathy; Charcot–Marie–Tooth disease; Distal motor neuropathy; HINT1 gene; Hereditary motor and sensory neuropathy; Neuromyotonia

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Year:  2019        PMID: 31848916     DOI: 10.1007/s11033-019-05238-z

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  6 in total

1.  Epidemiology of Rare Hereditary Diseases in the European Part of Russia: Point and Cumulative Prevalence.

Authors:  Rena A Zinchenko; Eugeny K Ginter; Andrey V Marakhonov; Nika V Petrova; Vitaly V Kadyshev; Tatyana P Vasilyeva; Oksana U Alexandrova; Alexander V Polyakov; Sergey I Kutsev
Journal:  Front Genet       Date:  2021-08-30       Impact factor: 4.772

2.  HINT1 neuropathy in Norway: clinical, genetic and functional profiling.

Authors:  Silvia Amor-Barris; Helle Høyer; Albena Jordanova; Geir J Braathen; Kristien Peeters; Lin V Brauteset; Els De Vriendt; Linda Strand
Journal:  Orphanet J Rare Dis       Date:  2021-03-04       Impact factor: 4.123

3.  Protein network analysis to prioritize key genes in amyotrophic lateral sclerosis.

Authors:  Rupesh Kumar; Shazia Haider
Journal:  IBRO Neurosci Rep       Date:  2021-12-07

4.  HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling.

Authors:  Matilde Malcorps; Silvia Amor-Barris; Birute Burnyte; Albena Jordanova; Kristien Peeters; Ramune Vilimiene; Camila Armirola-Ricaurte; Kristina Grigalioniene; Alexandra Ekshteyn; Ausra Morkuniene; Arunas Vaitkevicius; Els De Vriendt; Jonathan Baets; Steven S Scherer; Laima Ambrozaityte; Algirdas Utkus
Journal:  Orphanet J Rare Dis       Date:  2022-10-14       Impact factor: 4.303

5.  Rare among Rare: Phenotypes of Uncommon CMT Genotypes.

Authors:  Luca Gentile; Massimo Russo; Federica Taioli; Moreno Ferrarini; M'Hammed Aguennouz; Carmelo Rodolico; Antonio Toscano; Gian Maria Fabrizi; Anna Mazzeo
Journal:  Brain Sci       Date:  2021-12-08

6.  HINT1 founder mutation causing axonal neuropathy with neuromyotonia in South America: A case report.

Authors:  Bianca de Aguiar Coelho Silva Madeiro; Kristien Peeters; Elker Lene Santos de Lima; Silvia Amor-Barris; Els De Vriendt; Albena Jordanova; Maria Tereza Cartaxo Muniz; Carolina da Cunha Correia
Journal:  Mol Genet Genomic Med       Date:  2021-09-25       Impact factor: 2.183

  6 in total

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