Literature DB >> 18565098

Predictive testing for Huntington disease in a developing country.

M J Futter1, J M Heckmann, L J Greenberg.   

Abstract

Predictive testing for Huntington disease (HD), by means of direct mutation analysis, has been offered at the Division of Human Genetics, University of Cape Town, from 1995. The aim of this study was to compile a comprehensive profile of the participants who had undergone predictive testing in the Western Cape from 1995 to 2005. The sociodemographic data, uptake and outcome of tests were analyzed to inform changes to improve the current genetic counseling services. A retrospective cross-sectional design using a 'multi-method' approach of both qualitative and quantitative methods was used. Data were gathered from the participants' hospital files and genetic database. Psychosocial data were obtained by face-to-face interviews with the participants in their homes or venues of choice. A total of 36 predictive tests were performed. The uptake for predictive testing was approximately 4.5% of the estimated at-risk population. The cohort of 27 individuals comprised 16 females and 11 males. Their mean age was 35.3 years; 6 were mixed ancestry and 21 were White people (European ancestry); 11 tested gene positive, 15 gene negative and 1 was in the reduced penetrance range. The most important issue identified was that the uptake of individuals classified as mixed ancestry was substantially lower than that of the White people possibly due to limited access to the predictive testing program because of the low levels of income and education in the general population of families with HD. Strategies to address these aspects have been incorporated into the program and will be reassessed after 1 year.

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Year:  2008        PMID: 18565098     DOI: 10.1111/j.1399-0004.2008.01044.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  9 in total

1.  Genetics Health Professionals' Views on Quality of Genetic Counseling Service Provision for Presymptomatic Testing in Late-Onset Neurological Diseases in Portugal: Core Components, Specific Challenges and the Need for Assessment Tools.

Authors:  M Paneque; Á Mendes; L Guimarães; J Sequeiros; H Skirton
Journal:  J Genet Couns       Date:  2014-11-04       Impact factor: 2.537

2.  Genetic testing and counseling for hereditary neurological diseases in Mali.

Authors:  Katherine Gloria Meilleur; Souleymane Coulibaly; Moussa Traoré; Guida Landouré; Alison La Pean; Modibo Sangaré; Fanny Mochel; Siona Traoré; Kenneth H Fischbeck; Hae-Ra Han
Journal:  J Community Genet       Date:  2011-02-22

3.  Huntington disease: who seeks presymptomatic genetic testing, why and what are the outcomes?

Authors:  Tracey M Scuffham; John C MacMillan
Journal:  J Genet Couns       Date:  2014-01-08       Impact factor: 2.537

4.  Couples at risk for spinocerebellar ataxia type 2: the Cuban prenatal diagnosis experience.

Authors:  Tania Cruz-Mariño; Luis Velázquez-Pérez; Yanetza González-Zaldivar; Raúl Aguilera-Rodríguez; Miguel Velázquez-Santos; Yaimé Vázquez-Mojena; Annelié Estupiñán-Rodríguez; Rubén Reynaldo-Armiñán; Luis Enrique Almaguer-Mederos; José Miguel Laffita-Mesa; Victor Tamayo-Chiang; Milena Paneque
Journal:  J Community Genet       Date:  2013-05-15

5.  Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes.

Authors:  Fiona K Baine; Chris Kay; Maria E Ketelaar; Jennifer A Collins; Alicia Semaka; Crystal N Doty; Amanda Krause; L Jacquie Greenberg; Michael R Hayden
Journal:  Eur J Hum Genet       Date:  2013-03-06       Impact factor: 4.246

6.  Ethical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: a systematic review.

Authors:  Adrina Zhong; Benedict Darren; Bethina Loiseau; Li Qun Betty He; Trillium Chang; Jessica Hill; Helen Dimaras
Journal:  Genet Med       Date:  2018-08-03       Impact factor: 8.822

7.  Ethical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: protocol for a systematic review.

Authors:  Adrina Zhong; Benedict Darren; Helen Dimaras
Journal:  Syst Rev       Date:  2017-07-11

Review 8.  Genetic counseling and testing practices for late-onset neurodegenerative disease: a systematic review.

Authors:  Ashley Crook; Chris Jacobs; Toby Newton-John; Rosie O'Shea; Alison McEwen
Journal:  J Neurol       Date:  2021-03-01       Impact factor: 6.682

9.  Participants' Preferences and Reasons for Wanting Feedback of Individual Genetic Research Results From an HIV-TB Genomic Study: A Case Study From Botswana.

Authors:  Dimpho Ralefala; Mary Kasule; Olivia P Matshabane; Ambroise Wonkam; Mogomotsi Matshaba; Jantina de Vries
Journal:  J Empir Res Hum Res Ethics       Date:  2021-12       Impact factor: 1.742

  9 in total

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