Cargando…

Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden

BACKGROUND: Hereditary transthyretin (TTR) amyloidosis (ATTRv) is a heterogeneous disease with a clinical presentation that varies according to geographical area and TTR mutation. The symptoms of Val50Met-ATTRv are mainly neuropathic and progress to complete disability and death in most untreated pa...

Descripción completa

Detalles Bibliográficos
Autores principales: González-Moreno, Juan, Gaya-Barroso, Aina, Losada-López, Inés, Rodríguez, Adrián, Bosch-Rovira, Teresa, Ripoll-Vera, Tomás, Usón, Mercedes, Figuerola, Antoni, Descals, Cristina, Montalà, Carles, Ferrer-Nadal, María Asunción, Cisneros-Barroso, Eugenia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191011/
https://www.ncbi.nlm.nih.gov/pubmed/34112225
http://dx.doi.org/10.1186/s13023-021-01910-5
_version_ 1783705792436764672
author González-Moreno, Juan
Gaya-Barroso, Aina
Losada-López, Inés
Rodríguez, Adrián
Bosch-Rovira, Teresa
Ripoll-Vera, Tomás
Usón, Mercedes
Figuerola, Antoni
Descals, Cristina
Montalà, Carles
Ferrer-Nadal, María Asunción
Cisneros-Barroso, Eugenia
author_facet González-Moreno, Juan
Gaya-Barroso, Aina
Losada-López, Inés
Rodríguez, Adrián
Bosch-Rovira, Teresa
Ripoll-Vera, Tomás
Usón, Mercedes
Figuerola, Antoni
Descals, Cristina
Montalà, Carles
Ferrer-Nadal, María Asunción
Cisneros-Barroso, Eugenia
author_sort González-Moreno, Juan
collection PubMed
description BACKGROUND: Hereditary transthyretin (TTR) amyloidosis (ATTRv) is a heterogeneous disease with a clinical presentation that varies according to geographical area and TTR mutation. The symptoms of Val50Met-ATTRv are mainly neuropathic and progress to complete disability and death in most untreated patients within 10 to 15 years of diagnosis. The neurological effects may also be accompanied by gastrointestinal impairment, cardiomyopathy, nephropathy and/or ocular deposition. The disease is thus associated with a high degree of patient disability. Accordingly, we aimed to describe the psychosocial burden associated with ATTRv in a group of patients, asymptomatic Val50Met carriers, relatives and caregivers in the endemic focus of the disease in Majorca via a survey addressing various aspects related to psychosocial burden. We performed a an observational, descriptive, cross-sectional and multicentre study in order to analyze the prevalence of self-reported impact of ATTRv disease upon their daily life. In addition to the self-knowledge, fear and burden related to the disease. The survey was disseminated during the regular follow up at the outpatient clinic of the Hospital Universitario Son Llàtzer and during the meetings organized by the Andrade’s Disease patients’ advocacy group from the Balearic Islands. These meetings were attended also by subjects followed up by the Hospital Universitario Son Espases and their caregivers and relatives. Survey was self-administrated. No intervention was done by the investigators. 85 subjects completed the survey: 61 carrying the TTR-V50M variant and 24 caregivers or relatives. RESULTS: Our study revealed that, although most of the population studied had had prior contact with ATTRv through affected relatives, there was still a lack of information regarding disease diagnosis. Fear of the genetic test result and psychological issues were common in our population. Moreover, the disease had a stronger impact on the daily life of our patients than that of our asymptomatic carriers. Autonomic symptoms were the main source of burden for relatives and caregivers. CONCLUSION: Our survey results show high psychosocial burden associated with Val50Met-ATTRv in our area. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-021-01910-5.
format Online
Article
Text
id pubmed-8191011
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-81910112021-06-10 Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden González-Moreno, Juan Gaya-Barroso, Aina Losada-López, Inés Rodríguez, Adrián Bosch-Rovira, Teresa Ripoll-Vera, Tomás Usón, Mercedes Figuerola, Antoni Descals, Cristina Montalà, Carles Ferrer-Nadal, María Asunción Cisneros-Barroso, Eugenia Orphanet J Rare Dis Research BACKGROUND: Hereditary transthyretin (TTR) amyloidosis (ATTRv) is a heterogeneous disease with a clinical presentation that varies according to geographical area and TTR mutation. The symptoms of Val50Met-ATTRv are mainly neuropathic and progress to complete disability and death in most untreated patients within 10 to 15 years of diagnosis. The neurological effects may also be accompanied by gastrointestinal impairment, cardiomyopathy, nephropathy and/or ocular deposition. The disease is thus associated with a high degree of patient disability. Accordingly, we aimed to describe the psychosocial burden associated with ATTRv in a group of patients, asymptomatic Val50Met carriers, relatives and caregivers in the endemic focus of the disease in Majorca via a survey addressing various aspects related to psychosocial burden. We performed a an observational, descriptive, cross-sectional and multicentre study in order to analyze the prevalence of self-reported impact of ATTRv disease upon their daily life. In addition to the self-knowledge, fear and burden related to the disease. The survey was disseminated during the regular follow up at the outpatient clinic of the Hospital Universitario Son Llàtzer and during the meetings organized by the Andrade’s Disease patients’ advocacy group from the Balearic Islands. These meetings were attended also by subjects followed up by the Hospital Universitario Son Espases and their caregivers and relatives. Survey was self-administrated. No intervention was done by the investigators. 85 subjects completed the survey: 61 carrying the TTR-V50M variant and 24 caregivers or relatives. RESULTS: Our study revealed that, although most of the population studied had had prior contact with ATTRv through affected relatives, there was still a lack of information regarding disease diagnosis. Fear of the genetic test result and psychological issues were common in our population. Moreover, the disease had a stronger impact on the daily life of our patients than that of our asymptomatic carriers. Autonomic symptoms were the main source of burden for relatives and caregivers. CONCLUSION: Our survey results show high psychosocial burden associated with Val50Met-ATTRv in our area. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-021-01910-5. BioMed Central 2021-06-10 /pmc/articles/PMC8191011/ /pubmed/34112225 http://dx.doi.org/10.1186/s13023-021-01910-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
González-Moreno, Juan
Gaya-Barroso, Aina
Losada-López, Inés
Rodríguez, Adrián
Bosch-Rovira, Teresa
Ripoll-Vera, Tomás
Usón, Mercedes
Figuerola, Antoni
Descals, Cristina
Montalà, Carles
Ferrer-Nadal, María Asunción
Cisneros-Barroso, Eugenia
Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden
title Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden
title_full Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden
title_fullStr Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden
title_full_unstemmed Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden
title_short Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden
title_sort val50met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191011/
https://www.ncbi.nlm.nih.gov/pubmed/34112225
http://dx.doi.org/10.1186/s13023-021-01910-5
work_keys_str_mv AT gonzalezmorenojuan val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT gayabarrosoaina val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT losadalopezines val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT rodriguezadrian val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT boschrovirateresa val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT ripollveratomas val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT usonmercedes val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT figuerolaantoni val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT descalscristina val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT montalacarles val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT ferrernadalmariaasuncion val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden
AT cisnerosbarrosoeugenia val50methereditarytransthyretinamyloidosisnotjustamedicalproblembutapsychosocialburden