Literature DB >> 36053339

Comorbidities in Friedreich ataxia: incidence and manifestations from early to advanced disease stages.

Mario Fichera1,2, Anna Castaldo1, Alessia Mongelli1, Gloria Marchini1, Cinzia Gellera1, Lorenzo Nanetti3, Caterina Mariotti1.   

Abstract

OBJECTIVES: Friedreich's ataxia (FA) is the most common hereditary ataxia, characterized by multisystemic manifestations including neurological, cardiological, and skeletal abnormalities. In this study, we aimed to analyze the incidences of disease-related and unrelated comorbidities occurring in different stages of the disease progression.
METHODS: We analyzed longitudinal data from a 10-year prospective observational study in a cohort of 175 FA patients with disease onset < 25 years. We analyzed the time of diagnosis for the most frequently reported medical conditions, with respect to age and disease duration of each patient.
RESULTS: In the early stage of the disease, scoliosis (53.3%), hypertrophic cardiomyopathy (46.7%), and pes cavus (33.3%) were the most frequently diagnosed conditions, sometimes occurring even before the onset of ataxia. Diabetes, bone fractures, and depression have the same incidence at all disease stages. In patients with > 20 years of disease duration, the most frequent complications were hearing and visual loss (20% and 26%), arrhythmias (16%), and psychosis (18%). Thirteen patients presented hallucinations/delusions in the absence of neurological acute events or mental illness predisposing to psychotic manifestations. Six of these patients fulfill the diagnostic criteria for Charles Bonnet syndrome.
CONCLUSIONS: Incidence of FA-related medical conditions varies according to disease duration. In patients with very long disease duration, we observed an unexpectedly high incidence of visual and auditory pseudo-hallucinations that were not previously reported in FA patients. We hypothesized that these late complications may be possibly related to the severe sensory deafferentation syndrome observed in the advanced stages of FA disease.
© 2022. Fondazione Società Italiana di Neurologia.

Entities:  

Keywords:  Charles Bonnet syndrome; Complications; Deafferentation syndrome; Hallucination; Optic neuropathy; Psychosis

Year:  2022        PMID: 36053339     DOI: 10.1007/s10072-022-06360-w

Source DB:  PubMed          Journal:  Neurol Sci        ISSN: 1590-1874            Impact factor:   3.830


  34 in total

1.  Analysis of echocardiograms in a large heterogeneous cohort of patients with friedreich ataxia.

Authors:  Sean R Regner; Sarah J Lagedrost; Ted Plappert; Erin K Paulsen; Lisa S Friedman; Madeline L Snyder; Susan L Perlman; Katherine D Mathews; George R Wilmot; Kimberly A Schadt; Martin St John Sutton; David R Lynch
Journal:  Am J Cardiol       Date:  2011-11-10       Impact factor: 2.778

Review 2.  Clinical features of Friedreich's ataxia: classical and atypical phenotypes.

Authors:  Michael H Parkinson; Sylvia Boesch; Wolfgang Nachbauer; Caterina Mariotti; Paola Giunti
Journal:  J Neurochem       Date:  2013-08       Impact factor: 5.372

3.  FXN methylation predicts expression and clinical outcome in Friedreich ataxia.

Authors:  Marguerite V Evans-Galea; Nissa Carrodus; Simone M Rowley; Louise A Corben; Geneieve Tai; Richard Saffery; John C Galati; Nicholas C Wong; Jeffrey M Craig; David R Lynch; Sean R Regner; Alicia F D Brocht; Susan L Perlman; Khalaf O Bushara; Christopher M Gomez; George R Wilmot; Lingli Li; Elizabeth Varley; Martin B Delatycki; Joseph P Sarsero
Journal:  Ann Neurol       Date:  2012-04       Impact factor: 10.422

4.  Clinical and genetic abnormalities in patients with Friedreich's ataxia.

Authors:  A Dürr; M Cossee; Y Agid; V Campuzano; C Mignard; C Penet; J L Mandel; A Brice; M Koenig
Journal:  N Engl J Med       Date:  1996-10-17       Impact factor: 91.245

5.  A 22-Year Follow-up Study of Long-term Cardiac Outcome and Predictors of Survival in Friedreich Ataxia.

Authors:  Francoise Pousset; Lise Legrand; Marie-Lorraine Monin; Claire Ewenczyk; Perrine Charles; Michel Komajda; Alexis Brice; Massimo Pandolfo; Richard Isnard; Sophie Tezenas du Montcel; Alexandra Durr
Journal:  JAMA Neurol       Date:  2015-11       Impact factor: 18.302

6.  Frataxin gene point mutations in Italian Friedreich ataxia patients.

Authors:  Cinzia Gellera; Barbara Castellotti; Caterina Mariotti; Rossana Mineri; Viviana Seveso; Stefano Didonato; Franco Taroni
Journal:  Neurogenetics       Date:  2007-08-17       Impact factor: 2.660

7.  Scoliosis in Patients With Friedreich Ataxia: Results of a Consecutive Prospective Series.

Authors:  Anne Laure Simon; Jean Meyblum; Bastien Roche; Christophe Vidal; Keyvan Mazda; Isabelle Husson; Brice Ilharreborde
Journal:  Spine Deform       Date:  2019-09

8.  Predictors of loss of ambulation in Friedreich's ataxia.

Authors:  Christian Rummey; Jennifer M Farmer; David R Lynch
Journal:  EClinicalMedicine       Date:  2020-01-08

Review 9.  Friedreich's ataxia: clinical features, pathogenesis and management.

Authors:  A Cook; P Giunti
Journal:  Br Med Bull       Date:  2017-12-01       Impact factor: 4.291

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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