ArticleJournal of medical genetics1993
Five year study of prenatal testing for Huntington's disease: demand, attitudes, and psychological assessment.
Article in Journal of medical genetics, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
17 citing papers in PubMed, 1 synthesis or guideline pooled it, 109 citations in OpenAlex.
- Methodology in longitudinal studies on psychological effects of predictive DNA testing: a review.Journal of medical genetics · 2004Pooled it
- Proceed with care: direct predictive testing for Huntington disease.American journal of human genetics · 1994Trial
- Factors influencing patient decision-making on a multimodal precision medicine algorithm for depression: a qualitative European multicentre study of the PROMPT consortium.Frontiers in psychiatry · 2025Article
- A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practice.European journal of human genetics : EJHG · 2019Review
- Prenatal testing in Huntington disease: after the test, choices recommence.European journal of human genetics : EJHG · 2016Article
- Couples at risk for spinocerebellar ataxia type 2: the Cuban prenatal diagnosis experience.Journal of community genetics · 2013Article
- Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.European journal of human genetics : EJHG · 2012Article
- A comprehensive review of spinocerebellar ataxia type 2 in Cuba.Cerebellum (London, England) · 2011Review
- Attitudes toward genetic testing in childhood and reproductive decision-making for familial adenomatous polyposis.European journal of human genetics : EJHG · 2010Article
- Attitude towards pre-implantation genetic diagnosis for hereditary cancer.Familial cancer · 2009Article
- Decision-making about reproductive choices among individuals at-risk for Huntington's disease.Journal of genetic counseling · 2007Article
- Attitudes to predictive DNA testing in familial adenomatous polyposis.Journal of medical genetics · 1996Article
- Attitudes towards bipolar disorder and predictive genetic testing among patients and providers.Journal of medical genetics · 1996Article
- Presymptomatic testing for genetic diseases of later life. Pharmacoepidemiological considerations.Drugs & aging · 1995Review
- The prenatal exclusion test for Huntington's disease: experience in the west of Scotland, 1986-1993.Journal of medical genetics · 1995Article
- Emotional reactions to predictive testing in Alzheimer's disease and other inherited dementias.American journal of Alzheimer's disease and other dementiasArticle
- The words community dwelling, Spanish-preferring Mexican/Mexican American adults use to talk about Alzheimer's disease and genetic testing: Implications for education and outreach.Alzheimer's & dementia (New York, N. Y.)Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Adult predictive and prenatal testing programmes for Huntington's disease (HD) in Canada have been available since 1986. However, the demand for prenatal testing and the reasons why some people choose not to have the prenatal test for this late onset disorder have not been well documented. In addition, the knowledge and attitudes of adult predictive testing candidates and their partners about prenatal testing are not well known nor are the psychological effects of prenatal testing well understood. As of September 1991, 425 subjects had entered the Canadian Collaborative Study of Predictive Testing and, of these, 47 subjects or their partners had become pregnant. Of this group, 14 (30%) couples requested prenatal testing, 24 (51%) couples did not want prenatal testing, and nine (19%) at risk subjects had already received a decreased risk through adult predictive testing and, therefore, were not eligible for the prenatal test. Of the 14 couples who initially requested prenatal testing, seven withdrew. Thus, demand for the prenatal test by eligible candidates was 7/38 or 18%, which is much lower than the 32 to 65% expected based on early survey data. The most frequently cited reason for declining prenatal testing was the hope that a cure would be found in time for their children. While the majority of adult predictive testing candidates (71%) in our study had accurate information about definitive prenatal testing, many (63%) did not have a correct understanding of exclusion prenatal testing. Although no serious adverse events such as suicide planning or admission to psychiatric hospital have occurred, a particular need for careful counselling was identified for those at risk candidates and their partners who have one prenatal test and feel compelled to use the test again in future pregnancies. Even though prenatal testing for HD is not requested as often originally expected, it still remains a desired option for some at risk persons and their partners.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.