Literature DB >> 25893506

SCA2 predictive testing in Cuba: challenging concepts and protocol evolution.

Tania Cruz-Mariño1, Yaimeé Vázquez-Mojena, Luis Velázquez-Pérez, Yanetza González-Zaldívar, Raúl Aguilera-Rodríguez, Miguel Velázquez-Santos, Annelié Estupiñán-Rodríguez, José Miguel Laffita-Mesa, Luis E Almaguer-Mederos, Milena Paneque.   

Abstract

Spinocerebellar ataxia type 2 (SCA2) is a neurodegenerative disease caused by a CAG repeat expansion in the ATXN2 gene. Cuba has the highest prevalence (6.57 cases/10(5) inhabitants) of SCA2 in the world. The existence of 753 affected individuals and 7173 relatives at risk prompted the development in 2001 of the first predictive testing program in the country. The medical records of over 1193 individuals, who requested the test within a 13-year period, were analyzed retrospectively. The presymptomatic and the prenatal tests had uptake rates of 43.4 and 23.9 %, respectively. Several ethical challenges resulted from this program. These include the following: (1) withdrawal due to the initial protocol's length; (2) the request to participate by 16 at-risk adolescents; (3) the decision made by ten out of 33 couples with a test-positive fetus to carry the pregnancy to term, leading to de facto predictive testing of minors; (4) the elevated frequency of the ATXN2 gene large normal alleles (≥23 to 31 repeats) in the reference population. These issues have led to major changes in the guidelines of the predictive testing protocol: (1) the protocol length was shortened; (2) the inclusion criteria were expanded to reach at-risk adolescents with an interest in prenatal diagnosis; (3) interdisciplinary follow-up was offered to families in which test-positive fetuses were not aborted; (4) prenatal testing was made available to carriers of large normal alleles with ≥27 CAG repeats. The profiles of the participants were similar to those reported for other predictive testing programs for conditions like Huntington disease and familial adenomatous polyposis. The genetic counseling practices at the community level, the ample health education provided to the at-risk population, together with multidisciplinary and specialized attention to the affected families, are lessons from the Cuban experience that can be relevant for other international teams conducting predictive testing for other late-onset neurodegenerative disorders.

Entities:  

Year:  2015        PMID: 25893506      PMCID: PMC4524837          DOI: 10.1007/s12687-015-0226-4

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  40 in total

1.  Lessons from predictive testing for Huntington disease: 25 years on.

Authors:  Alice K Hawkins; Anita Ho; Michael R Hayden
Journal:  J Med Genet       Date:  2011-10       Impact factor: 6.318

2.  Presymptomatic testing for neurogenetic diseases in Brazil: assessing who seeks and who follows through with testing.

Authors:  Caroline Santa Maria Rodrigues; Viviane Ziebell de Oliveira; Gabriela Camargo; Claudio Maria da Silva Osório; Raphael Machado de Castilhos; Maria Luiza Saraiva-Pereira; Lavínia Schuler-Faccini; Laura Bannach Jardim
Journal:  J Genet Couns       Date:  2011-06-30       Impact factor: 2.537

3.  Prenatal testing for Huntington's disease: a European collaborative study.

Authors:  Sheila A Simpson; Moniek W Zoeteweij; Kurt Nys; Peter Harper; Alexandra Dürr; Gioia Jacopini; Christos Yapijakis; Gerry Evers-Kiebooms
Journal:  Eur J Hum Genet       Date:  2002-11       Impact factor: 4.246

4.  What counts as effective genetic counselling for presymptomatic testing in late-onset disorders? A study of the consultand's perspective.

Authors:  Lídia Guimarães; Jorge Sequeiros; Heather Skirton; Milena Paneque
Journal:  J Genet Couns       Date:  2013-01-07       Impact factor: 2.537

5.  Comprehensive study of early features in spinocerebellar ataxia 2: delineating the prodromal stage of the disease.

Authors:  Luis Velázquez-Pérez; Roberto Rodríguez-Labrada; Edilia M Cruz-Rivas; Juan Fernández-Ruiz; Israel Vaca-Palomares; Jandy Lilia-Campins; Bulmaro Cisneros; Arnoy Peña-Acosta; Yaimeé Vázquez-Mojena; Rosalinda Diaz; Jonathan J Magaña-Aguirre; Tania Cruz-Mariño; Annelié Estupiñán-Rodríguez; José M Laffita-Mesa; Rigoberto González-Piña; Nalia Canales-Ochoa; Yanetza González-Zaldivar
Journal:  Cerebellum       Date:  2014-10       Impact factor: 3.847

6.  The Cuban program for predictive testing of SCA2: 11 years and 768 individuals to learn from.

Authors:  T Cruz-Mariño; L Velázquez-Pérez; Y González-Zaldivar; R Aguilera-Rodríguez; M Velázquez-Santos; Y Vázquez-Mojena; A Estupiñán-Rodríguez; J M Laffita-Mesa; R Reynaldo-Armiñán; L E Almaguer-Mederos; M Paneque
Journal:  Clin Genet       Date:  2013-06       Impact factor: 4.438

7.  Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2.

Authors:  L Velázquez-Pérez; C Seifried; M Abele; F Wirjatijasa; R Rodríguez-Labrada; N Santos-Falcón; G Sánchez-Cruz; L Almaguer-Mederos; R Tejeda; N Canales-Ochoa; M Fetter; U Ziemann; T Klockgether; J Medrano-Montero; J Rodríguez-Díaz; J M Laffita-Mesa; G Auburger
Journal:  Clin Neurophysiol       Date:  2009-02-07       Impact factor: 3.708

8.  Presymptomatic diagnosis in Huntington's disease: the Mexican experience.

Authors:  Maria Elisa Alonso; Adriana Ochoa; Ana Luisa Sosa; Yaneth Rodríguez; Mireya Chávez; Catherine Boll; Petra Yescas; Rosario Macías; Astrid Rasmussen
Journal:  Genet Test Mol Biomarkers       Date:  2009-12

9.  Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population.

Authors:  G Auburger; G O Diaz; R F Capote; S G Sanchez; M P Perez; M E del Cueto; M G Meneses; M Farrall; R Williamson; S Chamberlain
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

10.  Ethical and social issues in presymptomatic testing for Huntington's disease: a European Community collaborative study. European Community Huntington's Disease Collaborative Study Group.

Authors: 
Journal:  J Med Genet       Date:  1993-12       Impact factor: 6.318

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  3 in total

Review 1.  Ethical issues in neurogenetics.

Authors:  Wendy R Uhlmann; J Scott Roberts
Journal:  Handb Clin Neurol       Date:  2018

2.  RNA Toxicity and Perturbation of rRNA Processing in Spinocerebellar Ataxia Type 2.

Authors:  Pan P Li; Roumita Moulick; Hongxuan Feng; Xin Sun; Nicolas Arbez; Jing Jin; Leonard O Marque; Erin Hedglen; H Y Edwin Chan; Christopher A Ross; Stefan M Pulst; Russell L Margolis; Sarah Woodson; Dobrila D Rudnicki
Journal:  Mov Disord       Date:  2021-08-14       Impact factor: 9.698

Review 3.  Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches.

Authors:  Luis C Velázquez-Pérez; Roberto Rodríguez-Labrada; Juan Fernandez-Ruiz
Journal:  Front Neurol       Date:  2017-09-11       Impact factor: 4.003

  3 in total

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