Literature DB >> 31564022

Health-related quality of life and depressive symptoms in Friedreich ataxia.

Javier Pérez-Flores1, Atteneri Hernández-Torres1, Fernando Montón1,2, Antonieta Nieto3.   

Abstract

PURPOSE: Friedreich ataxia (FRDA) is a chronic, progressive and highly disabling cerebellar degenerative disease. Despite this, little attention has been paid to the health-related quality of life (HRQOL) in this disease. The aim of the present study was to assess FRDA patients' perception of HRQOL and to determine the influence of depression, and demographic and clinical variables.
METHOD: The sample consisted of 62 patients with genetically confirmed FRDA. The SF-36 Health Survey was used to assess HRQOL. Depressive symptoms were evaluated with the Beck Depression Inventory-II.
RESULTS: FRDA patients' mean scores were significantly lower than the values for the Spanish population in all SF36 dimensions. Average z scores ranged from - 5.5 in physical functioning to - 0.48 in mental health. Age and clinical variables were significant predictors of HRQOL in only several dimensions, whereas BDI scores were able to predict a significant percentage of variance in all SF36 dimensions, except physical functioning.
CONCLUSIONS: Our study demonstrates the high impact of Friedreich ataxia on quality of life. This impact does not only occur in those aspects most related to motor disability but it is also present in non-motor dimensions. Depressive symptomatology is the most relevant variable for predicting quality of life.

Entities:  

Keywords:  Cerebellum; Depression; Friedreich ataxia; Neurological diseases; Quality of life

Mesh:

Year:  2019        PMID: 31564022     DOI: 10.1007/s11136-019-02311-9

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  37 in total

1.  [Population reference values of the Spanish version of the Health Questionnaire SF-36].

Authors:  J Alonso; E Regidor; G Barrio; L Prieto; C Rodríguez; L de la Fuente
Journal:  Med Clin (Barc)       Date:  1998-10-10       Impact factor: 1.725

Review 2.  Determinants of health-related quality of life in Parkinson's disease: a systematic review.

Authors:  Sze-Ee Soh; Meg E Morris; Jennifer L McGinley
Journal:  Parkinsonism Relat Disord       Date:  2010-09-15       Impact factor: 4.891

Review 3.  Prevalence gradients of Friedreich's ataxia and R1b haplotype in Europe co-localize, suggesting a common Palaeolithic origin in the Franco-Cantabrian ice age refuge.

Authors:  Pierre Vankan
Journal:  J Neurochem       Date:  2013-08       Impact factor: 5.372

4.  Scale for the assessment and rating of ataxia: development of a new clinical scale.

Authors:  T Schmitz-Hübsch; S Tezenas du Montcel; L Baliko; J Berciano; S Boesch; C Depondt; P Giunti; C Globas; J Infante; J-S Kang; B Kremer; C Mariotti; B Melegh; M Pandolfo; M Rakowicz; P Ribai; R Rola; L Schöls; S Szymanski; B P van de Warrenburg; A Dürr; T Klockgether; Roberto Fancellu
Journal:  Neurology       Date:  2006-06-13       Impact factor: 9.910

5.  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

6.  A longitudinal study of the SF-36 version 2 in Friedreich ataxia.

Authors:  G Tai; L A Corben; E M Yiu; M B Delatycki
Journal:  Acta Neurol Scand       Date:  2016-09-28       Impact factor: 3.209

7.  Friedreich ataxia in Norway - an epidemiological, molecular and clinical study.

Authors:  Iselin Marie Wedding; Mette Kroken; Sandra Pilar Henriksen; Kaja Kristine Selmer; Torunn Fiskerstrand; Per Morten Knappskog; Tone Berge; Chantal M E Tallaksen
Journal:  Orphanet J Rare Dis       Date:  2015-09-04       Impact factor: 4.123

Review 8.  Consensus clinical management guidelines for Friedreich ataxia.

Authors:  Louise A Corben; David Lynch; Massimo Pandolfo; Jörg B Schulz; Martin B Delatycki
Journal:  Orphanet J Rare Dis       Date:  2014-11-30       Impact factor: 4.123

9.  Depressive symptoms in Friedreich ataxia.

Authors:  Antonieta Nieto; Atteneri Hernández-Torres; Javier Pérez-Flores; Fernando Montón
Journal:  Int J Clin Health Psychol       Date:  2017-12-08

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

View more
  2 in total

Review 1.  Friedreich ataxia: clinical features and new developments.

Authors:  Medina Keita; Kellie McIntyre; Layne N Rodden; Kim Schadt; David R Lynch
Journal:  Neurodegener Dis Manag       Date:  2022-06-29

2.  Should Advanced Friedreich's Ataxia Be a Contraindication for Heart Transplantation? A Case Report of a Successful Procedure in a 58-Year-Old Patient.

Authors:  María Jesús Valero; Jose L Muñoz-Blanco; Alejandro Garrido Sanchez; Gregorio Cuerpo; Javier Castrodeza; Paula Navas; Iago Sousa; Adolfo Villa; Francisco Fernández-Avilés; Manuel Martínez-Sellés
Journal:  J Cardiovasc Dev Dis       Date:  2022-03-09
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.