Literature DB >> 30153683

Epidemiology of Transthyretin Familial Amyloid Polyneuropathy in Portugal: A Nationwide Study.

Mónica Inês1, Teresa Coelho2,3, Isabel Conceição4,5, Filipa Duarte-Ramos6, Mamede de Carvalho4,5, João Costa4,7.   

Abstract

BACKGROUND: Transthyretin-associated familial amyloid polyneuropathy (TTR-FAP) is a rare, hereditary, progressive and neurodegenerative disease. We aimed to study -TTR-FAP epidemiology in Portugal.
METHODS: National, observational, prospective and retrospective, case identification of adults with TTR-FAP. Countrywide patient multiple identification sources included reference centers registries and centralized medical electronic prescription database. Crude rates were reported per 100,000 adult inhabitants.
RESULTS: Over 2010-2016 period, mean incidence rates was 0.87/100,000 (95% CI 0.68-1.10) corresponding to 71 new patients yearly, that has decreased 31% in the last 7 years. The proportion of late-onset cases (age ≥50 years) among incident cases was 28.7%. Estimated crude 2016 prevalence was 22.93/100,000 adult inhabitants (95% CI 21.90-23.99) corresponding to 1,865 TTR-FAP individuals in Portugal (45.8% male; mean age: 52.3 ± 15.4 years). In 2016, the Portuguese region with the highest TTR-FAP prevalence shows a 16% prevalence increase over the last 25 years.
CONCLUSIONS: In Portugal, TTR-FAP affects both genders and mainly young adults. TTR-FAP incidence appears to be decreasing while prevalence is increasing. In comparison to previous studies, there is an increased representativeness of late-onset patients. This epidemiological setting poses future and complex challenges for the social and healthcare system, strengthening the relevance of regular epidemiologic surveillance.
© 2018 S. Karger AG, Basel.

Entities:  

Keywords:  Amyloidosis; Epidemiology; Incidence; Portugal; Prevalence; Transthyretin familial amyloid polyneuropathy

Mesh:

Year:  2018        PMID: 30153683     DOI: 10.1159/000490553

Source DB:  PubMed          Journal:  Neuroepidemiology        ISSN: 0251-5350            Impact factor:   3.282


  10 in total

Review 1.  Novel approaches to diagnosis and management of hereditary transthyretin amyloidosis.

Authors:  Antonia Carroll; P James Dyck; Mamede de Carvalho; Marina Kennerson; Mary M Reilly; Matthew C Kiernan; Steve Vucic
Journal:  J Neurol Neurosurg Psychiatry       Date:  2022-03-07       Impact factor: 13.654

Review 2.  RNA-targeting and gene editing therapies for transthyretin amyloidosis.

Authors:  Alberto Aimo; Vincenzo Castiglione; Claudio Rapezzi; Maria Franzini; Giorgia Panichella; Giuseppe Vergaro; Julian Gillmore; Marianna Fontana; Claudio Passino; Michele Emdin
Journal:  Nat Rev Cardiol       Date:  2022-03-23       Impact factor: 49.421

Review 3.  Epidemiological and clinical characteristics of symptomatic hereditary transthyretin amyloid polyneuropathy: a global case series.

Authors:  Márcia Waddington-Cruz; Hartmut Schmidt; Marc F Botteman; John A Carter; Michelle Stewart; Markay Hopps; Shari Fallet; Leslie Amass
Journal:  Orphanet J Rare Dis       Date:  2019-02-08       Impact factor: 4.123

4.  Gait Characterization and Analysis of Hereditary Amyloidosis Associated with Transthyretin Patients: A Case Series.

Authors:  Maria do Carmo Vilas-Boas; Pedro Filipe Pereira Fonseca; Inês Martins Sousa; Márcio Neves Cardoso; João Paulo Silva Cunha; Teresa Coelho
Journal:  J Clin Med       Date:  2022-07-07       Impact factor: 4.964

5.  Benefits and Risks of Sharing Genomic Data for Research: Comparing the Views of Rare Disease Patients, Informal Carers and Healthcare Professionals.

Authors:  Mariana Amorim; Susana Silva; Helena Machado; Elisa Leão Teles; Maria João Baptista; Tiago Maia; Ngozi Nwebonyi; Cláudia de Freitas
Journal:  Int J Environ Res Public Health       Date:  2022-07-19       Impact factor: 4.614

6.  High Hereditary Transthyretin-Related Amyloidosis Prevalence in Crete: Genetic Heterogeneity and Distinct Phenotypes.

Authors:  Minas Tzagournissakis; Emmanouil Foukarakis; Dimitrios Samonakis; Miltiadis Tsilimbaris; Kleita Michaelidou; Lambros Mathioudakis; Anastasios Marinis; Emmanouil Giannakoudakis; Cleanthe Spanaki; Irene Skoula; Sofia Erimaki; Georgios Amoiridis; Georgios Koutsis; Sofia Koukouraki; Kostas Stylianou; Andreas Plaitakis; Panayiotis D Mitsias; Ioannis Zaganas
Journal:  Neurol Genet       Date:  2022-09-09

7.  Health-related quality of life in hereditary transthyretin amyloidosis polyneuropathy: a prospective, observational study.

Authors:  Mónica Inês; Teresa Coelho; Isabel Conceição; Lara Ferreira; Mamede de Carvalho; João Costa
Journal:  Orphanet J Rare Dis       Date:  2020-03-06       Impact factor: 4.123

8.  Clinical 3-D Gait Assessment of Patients With Polyneuropathy Associated With Hereditary Transthyretin Amyloidosis.

Authors:  Maria do Carmo Vilas-Boas; Ana Patrícia Rocha; Márcio Neves Cardoso; José Maria Fernandes; Teresa Coelho; João Paulo Silva Cunha
Journal:  Front Neurol       Date:  2020-11-23       Impact factor: 4.086

9.  Chance or challenge, spoilt for choice? New recommendations on diagnostic and therapeutic considerations in hereditary transthyretin amyloidosis with polyneuropathy: the German/Austrian position and review of the literature.

Authors:  Maike F Dohrn; Michaela Auer-Grumbach; Ralf Baron; Frank Birklein; Fabiola Escolano-Lozano; Christian Geber; Nicolai Grether; Tim Hagenacker; Ernst Hund; Juliane Sachau; Matthias Schilling; Jens Schmidt; Wilhelm Schulte-Mattler; Claudia Sommer; Markus Weiler; Gilbert Wunderlich; Katrin Hahn
Journal:  J Neurol       Date:  2020-06-04       Impact factor: 4.849

Review 10.  Effective tools for RNA-derived therapeutics: siRNA interference or miRNA mimicry.

Authors:  Peipei Wang; Yue Zhou; Arthur M Richards
Journal:  Theranostics       Date:  2021-08-11       Impact factor: 11.556

  10 in total

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