Nonamyloidogenic TTR gene variants c.76G>A and c.337-18G>C are not associated with idiopathic small-fiber neuropathy.

TTR amyloidosis small‐fiber neuropathy variants

Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
04 Sep 2024
Historique:
revised: 08 08 2024
received: 23 08 2023
accepted: 18 08 2024
medline: 4 9 2024
pubmed: 4 9 2024
entrez: 4 9 2024
Statut: aheadofprint

Résumé

Small-fiber neuropathy (SFN) affects only unmyelinated and thin myelinated fibers. It may be caused by amyloidogenic mutations of the transthyretin (TTR) gene, but not all TTR gene variants are pathogenic. The nonamyloidogenic c.76G>A (rs1800458) and c.337-18G>C (rs36204272) variants of TTR were recently reported to be associated with SFN. We investigated this putative association by analyzing TTR gene sequencing data retrospectively for two cohorts of patients, one with SFN and a control group. In this retrospective single-center study, we analyzed the frequency of the c.76G>A and c.337-18G>C TTR gene variants in a cohort of patients meeting a strict definition of SFN, with or without dysautonomia, a control cohort of patients investigated for nonneurological conditions, and the gnomAD international database. We included 55 SFN patients in this study, 17 of whom had dysautonomia. The allelic frequencies of the two variants in our cohort of 55 SFN patients were 7.27% for c.76G>A TTR and 5.25% for c.337-18G>C. The frequencies of both variants were statistically similar in the 337 control patients and the gnomAD database. The c.76G>A and c.337-18G>C TTR gene variants are not associated with SFN.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
Small-fiber neuropathy (SFN) affects only unmyelinated and thin myelinated fibers. It may be caused by amyloidogenic mutations of the transthyretin (TTR) gene, but not all TTR gene variants are pathogenic. The nonamyloidogenic c.76G>A (rs1800458) and c.337-18G>C (rs36204272) variants of TTR were recently reported to be associated with SFN. We investigated this putative association by analyzing TTR gene sequencing data retrospectively for two cohorts of patients, one with SFN and a control group.
METHODS METHODS
In this retrospective single-center study, we analyzed the frequency of the c.76G>A and c.337-18G>C TTR gene variants in a cohort of patients meeting a strict definition of SFN, with or without dysautonomia, a control cohort of patients investigated for nonneurological conditions, and the gnomAD international database.
RESULTS RESULTS
We included 55 SFN patients in this study, 17 of whom had dysautonomia. The allelic frequencies of the two variants in our cohort of 55 SFN patients were 7.27% for c.76G>A TTR and 5.25% for c.337-18G>C. The frequencies of both variants were statistically similar in the 337 control patients and the gnomAD database.
CONCLUSIONS CONCLUSIONS
The c.76G>A and c.337-18G>C TTR gene variants are not associated with SFN.

Identifiants

pubmed: 39230471
doi: 10.1111/ene.16461
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e16461

Informations de copyright

© 2024 The Author(s). European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.

Références

Devigili G, Cazzato D, Lauria G. Clinical diagnosis and management of small fiber neuropathy: an update on best practice. Expert Rev Neurother. 2020;20(9):967‐980.
Lauria G, Hsieh ST, Johansson O, et al. European Federation of Neurological Societies/Peripheral Nerve Society guideline on the use of skin biopsy in the diagnosis of small fiber neuropathy. Report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society. Eur J Neurol. 2010;17(7):903.
Devigili G, Tugnoli V, Penza P, et al. The diagnostic criteria for small fibre neuropathy: from symptoms to neuropathology. Brain J Neurol. 2008;131(Pt 7):1912‐1925.
Lefaucheur JP, Wahab A, Planté‐Bordeneuve V, et al. Diagnosis of small fiber neuropathy: a comparative study of five neurophysiological tests. Neurophysiol Clin. 2015;45(6):445‐455.
Blackmore D, Siddiqi ZA. Diagnostic criteria for small fiber neuropathy. J Clin Neuromuscul Dis. 2017;18(3):125‐131.
Brouwer BA, Bakkers M, Hoeijmakers JGJ, Faber CG, Merkies ISJ. Improving assessment in small fiber neuropathy. J Peripher Nerv Syst. 2015;20(3):333‐340.
Lauria G, Merkies ISJ, Faber CG. Small fibre neuropathy. Curr Opin Neurol. 2012;25(5):542‐549.
Lauria G, Faber CG, Cornblath DR. Skin biopsy and small fibre neuropathies: facts and thoughts 30 years later. J Neurol Neurosurg Psychiatry. 2022;93(9):915‐918.
Terkelsen AJ, Karlsson P, Lauria G, Freeman R, Finnerup NB, Jensen TS. The diagnostic challenge of small fibre neuropathy: clinical presentations, evaluations, and causes. Lancet Neurol. 2017;16(11):934‐944.
Adams D, Koike H, Slama M, Coelho T. Hereditary transthyretin amyloidosis: a model of medical progress for a fatal disease. Nat Rev Neurol. 2019;15(7):387‐404.
Richards S, Aziz N, Bale S, et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015;17(5):405‐424.
Rowczenio DM, Noor I, Gillmore JD, et al. Online registry for mutations in hereditary amyloidosis including nomenclature recommendations. Hum Mutat. 2014;35(9):E2403‐E2412.
Levine TD, Bland RJ. Incidence of nonamyloidogenic mutations in the transthyretin gene in patients with autonomic and small fiber neuropathy. Muscle Nerve. 2018;57(1):140‐142.
Thimm A, Bolz S, Fleischer M, et al. Prevalence of hereditary transthyretin amyloid polyneuropathy in idiopathic progressive neuropathy in conurban areas. Neurol Res Pract. 2019;1:30.
Provitera V, Gibbons CH, Wendelschafer‐Crabb G, et al. A multi‐center, multinational age‐ and gender‐adjusted normative dataset for immunofluorescent intraepidermal nerve fiber density at the distal leg. Eur J Neurol. 2015;23:333‐338.
Joint Task Force of the EFNS and the PNS. European Federation of Neurological Societies/Peripheral Nerve Society guideline on the use of skin biopsy in the diagnosis of small fiber neuropathy. Report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society. J Peripher Nerv Syst. 2010;15(2):79‐92.
Karczewski KJ, Francioli LC, Tiao G, et al. The mutational constraint spectrum quantified from variation in 141,456 humans. Nature. 2020;581(7809):434‐443.
Devigili G, Rinaldo S, Lombardi R, et al. Diagnostic criteria for small fibre neuropathy in clinical practice and research. Brain. 2019;142(12):3728‐3736.
Fabry V, Gerdelat A, Acket B, et al. Which method for diagnosing small fiber neuropathy? Front Neurol. 2020;11:342.
Leonardi L, Adam C, Beaudonnet G, et al. Skin amyloid deposits and nerve fiber loss as markers of neuropathy onset and progression in hereditary transthyretin amyloidosis. Eur J Neurol. 2022;29(5):1477‐1487.

Auteurs

Céline Konecki (C)

Génétique Moléculaire Pharmacogénétique et Hormonologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Bruno Francou (B)

Génétique Moléculaire Pharmacogénétique et Hormonologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Kenneth Chappell (K)

Génétique Moléculaire Pharmacogénétique et Hormonologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Lucie Augey (L)

Génétique Moléculaire Pharmacogénétique et Hormonologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Guillemette Beaudonnet (G)

Referral Center for Familial Amyloid Polyneuropathy and Other Rare Peripheral Neuropathies and Department of Neurology, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Cécile Cauquil (C)

Referral Center for Familial Amyloid Polyneuropathy and Other Rare Peripheral Neuropathies and Department of Neurology, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.
Service de Neurologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Dalia Dimitri-Boulos (D)

Service de Neurologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Adeline Not (A)

Service de Neurologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Clovis Adam (C)

Referral Center for Familial Amyloid Polyneuropathy and Other Rare Peripheral Neuropathies and Department of Neurology, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Vianney Poinsignon (V)

Génétique Moléculaire Pharmacogénétique et Hormonologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Céline Verstuyft (C)

Génétique Moléculaire Pharmacogénétique et Hormonologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

David Adams (D)

Referral Center for Familial Amyloid Polyneuropathy and Other Rare Peripheral Neuropathies and Department of Neurology, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.
Service de Neurologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Andoni Echaniz-Laguna (A)

Referral Center for Familial Amyloid Polyneuropathy and Other Rare Peripheral Neuropathies and Department of Neurology, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.
Service de Neurologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Céline Labeyrie (C)

Referral Center for Familial Amyloid Polyneuropathy and Other Rare Peripheral Neuropathies and Department of Neurology, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.
Service de Neurologie, Bicêtre University Hospital, Public Hospital Network of Paris, Le Kremlin-Bicêtre, France.

Classifications MeSH