Literature DB >> 35588347

Application of a custom NGS gene panel revealed a high diagnostic utility for molecular testing of hereditary ataxias.

Wiktoria Radziwonik1, Ewelina Elert-Dobkowska1, Aleksandra Klimkowicz-Mrowiec2, Karolina Ziora-Jakutowicz1, Iwona Stepniak1, Jacek Zaremba1, Anna Sulek3.   

Abstract

Hereditary ataxias (HA) are a rare group of heterogeneous disorders. Here, we present the results of molecular testing of a group of ataxia patients using a custom-designed next-generation sequencing (NGS) panel. Due to the genetic and clinical overlapping of hereditary ataxias and spastic paraplegias (HSP), the panel encompasses together HA and HSP genes. The NGS libraries, comprising coding sequences for 152 genes, were performed using KAPA HyperPlus and HyperCap Target Enrichment Kit, sequenced on the MiSeq instrument. The results were analyzed using the BaseSpace Variant Interpreter and Integrative Genomics Viewer. All pathogenic and likely pathogenic variants were confirmed using Sanger sequencing. A total of 29 patients with hereditary ataxias were enrolled in the NGS testing, and 16 patients had a confirmed molecular diagnosis with diagnostic accuracy rate of 55.2%. Pathogenic or likely pathogenic mutations were identified in 10 different genes: POLG (PEOA1, n = 3; SCAE, n = 2), CACNA1A (EA2, n = 2), SACS (ARSACS, n = 2), SLC33A1 (SPG42, n = 2), STUB1 (SCA48, n = 1), SPTBN2 (SCA5, n = 1), TGM6 (SCA35, n = 1), SETX (AOA2, n = 1), ANO10 (SCAR10, n = 1), and SPAST (SPG4, n = 1). We demonstrated that an approach based on the targeted use of the NGS panel can be highly effective and a useful tool in the molecular diagnosis of ataxia patients. Furthermore, we highlight the fact that a sequencing panel targeting both ataxias and HSP genes increases the diagnostic success level.
© 2022. The Author(s), under exclusive licence to Institute of Plant Genetics Polish Academy of Sciences.

Entities:  

Keywords:  Hereditary ataxias; Hereditary spastic paraplegias; Neurodegenerative diseases; Next-generation sequencing; Rare genetic variants

Mesh:

Substances:

Year:  2022        PMID: 35588347     DOI: 10.1007/s13353-022-00701-3

Source DB:  PubMed          Journal:  J Appl Genet        ISSN: 1234-1983            Impact factor:   2.653


  14 in total

Review 1.  Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond.

Authors:  Alexandra Durr
Journal:  Lancet Neurol       Date:  2010-09       Impact factor: 44.182

2.  Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.

Authors:  Peter Huppke; Cornelia Brendel; Vera Kalscheuer; Georg Christoph Korenke; Iris Marquardt; Peter Freisinger; John Christodoulou; Merle Hillebrand; Gaele Pitelet; Callum Wilson; Ursula Gruber-Sedlmayr; Reinhard Ullmann; Stefan Haas; Orly Elpeleg; Gudrun Nürnberg; Peter Nürnberg; Shzeena Dad; Lisbeth Birk Møller; Stephen G Kaler; Jutta Gärtner
Journal:  Am J Hum Genet       Date:  2012-01-13       Impact factor: 11.025

3.  Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia.

Authors:  Brent L Fogel; Hane Lee; Joshua L Deignan; Samuel P Strom; Sibel Kantarci; Xizhe Wang; Fabiola Quintero-Rivera; Eric Vilain; Wayne W Grody; Susan Perlman; Daniel H Geschwind; Stanley F Nelson
Journal:  JAMA Neurol       Date:  2014-10       Impact factor: 18.302

4.  High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.

Authors:  C Denier; A Ducros; K Vahedi; A Joutel; P Thierry; A Ritz; G Castelnovo; T Deonna; P Gérard; J L Devoize; A Gayou; B Perrouty; T Soisson; A Autret; J M Warter; A Vighetto; P Van Bogaert; S Alamowitch; E Roullet; E Tournier-Lasserve
Journal:  Neurology       Date:  1999-06-10       Impact factor: 9.910

5.  The correlation between carbamazepine and valproic acid monotherapy with serum adiponectin and carnitine.

Authors:  Fatma Şimşek; Mustafa Ceylan; Ahmet Kızıltunç; İbrahim İyigün
Journal:  Acta Neurol Belg       Date:  2020-11-26       Impact factor: 2.396

6.  Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.

Authors:  Yosr Bouhlal; Mourad Zouari; Mounir Kefi; Christiane Ben Hamida; Fayçal Hentati; Rim Amouri
Journal:  J Neurogenet       Date:  2008       Impact factor: 1.250

7.  Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variant.

Authors:  Chloé Angelini; Julien Van Gils; Antoine Bigourdan; Pierre-Simon Jouk; Didier Lacombe; Patrice Menegon; Sébastien Moutton; Florence Riant; Guilhem Sole; Elisabeth Tournier-Lasserve; Aurélien Trimouille; Marie Vincent; Cyril Goizet
Journal:  Eur J Med Genet       Date:  2018-08-22       Impact factor: 2.708

8.  Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.

Authors:  Alfredo Brusco; Cinzia Gellera; Claudia Cagnoli; Alessandro Saluto; Alessia Castucci; Chiara Michielotto; Vincenza Fetoni; Caterina Mariotti; Nicola Migone; Stefano Di Donato; Franco Taroni
Journal:  Arch Neurol       Date:  2004-05

9.  A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42).

Authors:  Pengfei Lin; Jianwei Li; Qiji Liu; Fei Mao; Jisheng Li; Rongfang Qiu; Huili Hu; Yang Song; Yang Yang; Guimin Gao; Chuanzhu Yan; Wanling Yang; Changshun Shao; Yaoqin Gong
Journal:  Am J Hum Genet       Date:  2008-12       Impact factor: 11.025

10.  Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes.

Authors:  Ewelina Elert-Dobkowska; Iwona Stepniak; Wioletta Krysa; Karolina Ziora-Jakutowicz; Maria Rakowicz; Anna Sobanska; Jacek Pilch; Dorota Antczak-Marach; Jacek Zaremba; Anna Sulek
Journal:  Neurogenetics       Date:  2019-02-19       Impact factor: 2.660

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