Literature DB >> 23654213

Predictive gene testing for Huntington disease and other neurodegenerative disorders.

S Wedderburn1, P K Panegyres, S Andrew, J Goldblatt, T Liebeck, F McGrath, M Wiltshire, C Pestell, J Lee, J Beilby.   

Abstract

BACKGROUND: Controversies exist around predictive testing (PT) programmes in neurodegenerative disorders. AIMS: This study sets out to answer the following questions relating to Huntington disease (HD) and other neurodegenerative disorders: differences between these patients in their PT journeys, why and when individuals withdraw from PT, and decision-making processes regarding reproductive genetic testing.
METHODS: A case series analysis of patients having PT from the multidisciplinary Western Australian centre for PT over the past 20 years was performed using internationally recognised guidelines for predictive gene testing in neurodegenerative disorders.
RESULTS: Of 740 at-risk patients, 518 applied for PT: 466 at risk of HD, 52 at risk of other neurodegenerative disorders - spinocerebellar ataxias, hereditary prion disease and familial Alzheimer disease. Thirteen percent withdrew from PT - 80.32% of withdrawals occurred during counselling stages. Major withdrawal reasons related to timing in the patients' lives or unknown as the patient did not disclose the reason. Thirty-eight HD individuals had reproductive genetic testing: 34 initiated prenatal testing (of which eight withdrew from the process) and four initiated pre-implantation genetic diagnosis. There was no recorded or other evidence of major psychological reactions or suicides during PT.
CONCLUSIONS: People withdrew from PT in relation to life stages and reasons that are unknown. Our findings emphasise the importance of: (i) adherence to internationally recommended guidelines for PT; (ii) the role of the multidisciplinary team in risk minimisation; and (iii) patient selection.
© 2013 The Authors; Internal Medicine Journal © 2013 Royal Australasian College of Physicians.

Entities:  

Keywords:  Huntington disease; neurodegenerative disorder; predictive gene testing

Mesh:

Year:  2013        PMID: 23654213     DOI: 10.1111/imj.12176

Source DB:  PubMed          Journal:  Intern Med J        ISSN: 1444-0903            Impact factor:   2.048


  5 in total

Review 1.  A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practice.

Authors:  Felicity Wadrup; Simon Holden; Rhona MacLeod; Zosia Miedzybrodzka; Andrea H Németh; Shan Owens; Sara Pasalodos; Oliver Quarrell; Angus J Clarke
Journal:  Eur J Hum Genet       Date:  2019-03-19       Impact factor: 4.246

2.  Prospective Evaluation of Predictive DNA Testing for Huntington's Disease in a Large German Center.

Authors:  Aysegül Ibisler; Sebastian Ocklenburg; Susanne Stemmler; Larissa Arning; Jörg T Epplen; Carsten Saft; Sabine Hoffjan
Journal:  J Genet Couns       Date:  2017-03-30       Impact factor: 2.537

3.  Public perceptions of presymptomatic testing for Alzheimer disease.

Authors:  Richard J Caselli; Jessica Langbaum; Gary E Marchant; Rachel A Lindor; Katherine S Hunt; Bruce R Henslin; Amylou C Dueck; Jason S Robert
Journal:  Mayo Clin Proc       Date:  2014-08-26       Impact factor: 7.616

4.  1993-2014: two decades of predictive testing for Huntington's disease at the Medical Genetics Unit of the University of Genoa.

Authors:  Paola Mandich; Merit Lamp; Fabio Gotta; Rossella Gulli; Ariela Iacometti; Roberta Marchese; Emilia Bellone; Giovanni Abbruzzese; Giovanna Ferrandes
Journal:  Mol Genet Genomic Med       Date:  2017-06-17       Impact factor: 2.183

5.  Presentation and care of a family with Huntington disease in a resource-limited community.

Authors:  Jarmal Charles; Lindyann Lessey; Jennifer Rooney; Ingmar Prokop; Katherine Yearwood; Hazel Da Breo; Patrick Rooney; Ruth H Walker; Andrew K Sobering
Journal:  J Clin Mov Disord       Date:  2017-04-12
  5 in total

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