Literature DB >> 33354116

Efficacy and Tolerability of Interferon Gamma in Treatment of Friedreich's Ataxia: Retrospective Study.

Mehmet Fatih Yetkİn1, Murat GÜltekİn1.   

Abstract

Friedreich's Ataxia (FRDA) is the most common form of autosomal recessive ataxia. The disease primarily results from a GAA trinucleotide repeat expansion within the FXN gene in up to 97% of patients. The clinical presentation begins approximately between the ages of 5 and 15. The major clinical findings of FRDA are progressive extremity and gait ataxia. Although it is known that the disease is caused by low levels of functional protein in the target tissues, there is no effective treatment available for this pathology. However, significant improvements have been achieved in the research into pharmacological treatments for FRDA in recent years. Interferon-gamma (IFN-γ) has been shown to induce frataxin production in many cell types. In this study, the clinical features, tolerability, and the prognosis of individuals with FRDA to whom IFN-γ was administered in a university hospital were evaluated retrospectively and the results were discussed. To the best of our knowledge, this is the first study conducted in our country to evaluate the effect of IFN gamma on this patient group. Copyright:
© 2020 Turkish Neuropsychiatric Society.

Entities:  

Keywords:  Ataxia; Friedreich’s ataxia; interferon gamma

Year:  2020        PMID: 33354116      PMCID: PMC7735154          DOI: 10.29399/npa.25047

Source DB:  PubMed          Journal:  Noro Psikiyatr Ars        ISSN: 1300-0667            Impact factor:   1.339


  22 in total

1.  GIFT-1, a phase IIa clinical trial to test the safety and efficacy of IFNγ administration in FRDA patients.

Authors:  Christian Marcotulli; Silvia Fortuni; Gaetano Arcuri; Barbara Tomassini; Luca Leonardi; Francesco Pierelli; Roberto Testi; Carlo Casali
Journal:  Neurol Sci       Date:  2015-11-30       Impact factor: 3.307

2.  Determination of Genotypic and Phenotypic Characteristics of Friedreich's Ataxia and Autosomal Dominant Spinocerebellar Ataxia Types 1, 2, 3, and 6.

Authors:  Pınar Bengi Boz; Filiz Koç; Sabriye Kocatürk Sel; Ali İrfan Güzel; Halil Kasap
Journal:  Noro Psikiyatr Ars       Date:  2016-06-01       Impact factor: 1.339

3.  Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 2 year cohort study.

Authors:  Kathrin Reetz; Imis Dogan; Ralf-Dieter Hilgers; Paola Giunti; Caterina Mariotti; Alexandra Durr; Sylvia Boesch; Thomas Klopstock; Francisco Javier Rodriguez de Rivera; Ludger Schöls; Thomas Klockgether; Katrin Bürk; Myriam Rai; Massimo Pandolfo; Jörg B Schulz
Journal:  Lancet Neurol       Date:  2016-12       Impact factor: 44.182

4.  A double-blind cross-over trial of amantadine hydrochloride in Friedreich's ataxia.

Authors:  A Filla; G De Michele; G Orefice; F Santorelli; L Trombetta; S Banfi; F Squitieri; G Napolitano; D Puma; G Campanella
Journal:  Can J Neurol Sci       Date:  1993-02       Impact factor: 2.104

Review 5.  Parkinsonism & related disorders. Ataxias.

Authors:  Thomas Klockgether
Journal:  Parkinsonism Relat Disord       Date:  2007       Impact factor: 4.891

6.  Epigenetic and neurological effects and safety of high-dose nicotinamide in patients with Friedreich's ataxia: an exploratory, open-label, dose-escalation study.

Authors:  Vincenzo Libri; Cihangir Yandim; Stavros Athanasopoulos; Naomi Loyse; Theona Natisvili; Pui Pik Law; Ping Kei Chan; Tariq Mohammad; Marta Mauri; Kin Tung Tam; James Leiper; Sophie Piper; Aravind Ramesh; Michael H Parkinson; Les Huson; Paola Giunti; Richard Festenstein
Journal:  Lancet       Date:  2014-04-30       Impact factor: 79.321

7.  Oral mobility reflects rate of progression in advanced Friedreich's ataxia.

Authors:  Stéphanie Borel; Peggy Gatignol; Mustapha Smail; Marie-Lorraine Monin; Claire Ewenczyk; Didier Bouccara; Alexandra Durr
Journal:  Ann Clin Transl Neurol       Date:  2019-08-25       Impact factor: 4.511

8.  Randomized, double-blind, placebo-controlled study of interferon-γ 1b in Friedreich Ataxia.

Authors:  David R Lynch; Lauren Hauser; Ashley McCormick; McKenzie Wells; Yi Na Dong; Shana McCormack; Kim Schadt; Susan Perlman; Sub H Subramony; Katherine D Mathews; Alicia Brocht; Julie Ball; Renee Perdok; Amy Grahn; Tom Vescio; Jeffrey W Sherman; Jennifer M Farmer
Journal:  Ann Clin Transl Neurol       Date:  2019-02-27       Impact factor: 4.511

9.  Rating scales for rare neurological diseases: What are we learning from Friedreich ataxia?

Authors:  Massimo Pandolfo
Journal:  Neurol Genet       Date:  2019-11-25

10.  Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.

Authors:  V Campuzano; L Montermini; M D Moltò; L Pianese; M Cossée; F Cavalcanti; E Monros; F Rodius; F Duclos; A Monticelli; F Zara; J Cañizares; H Koutnikova; S I Bidichandani; C Gellera; A Brice; P Trouillas; G De Michele; A Filla; R De Frutos; F Palau; P I Patel; S Di Donato; J L Mandel; S Cocozza; M Koenig; M Pandolfo
Journal:  Science       Date:  1996-03-08       Impact factor: 47.728

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