Literature DB >> 23709094

Two decades of Huntington disease testing: patient's demographics and reproductive choices.

Rebekah C Krukenberg1, Daniel L Koller, David D Weaver, Jennifer N Dickerson, Kimberly A Quaid.   

Abstract

Predictive testing for Huntington disease (HD) has been available in the United States (US) since 1987, and the Indiana University Predictive Testing Program has been providing this testing since 1990. To date there has been no published description of those who present for such testing in the US. Here we describe demographics of 141 individuals and reproductive decision making of a subset of 16 of those individuals who underwent predictive HD testing between 1990 and 2010 at one site in the US. This study is a retrospective chart review of the "Personal History Questionnaire" participants completed prior to testing. As seen in other studies, most participants were female (64.5 %), in their mid-30s (mean = 34), and had at least one child prior to testing (54 %). Multiple demographic datum points are described, and the reproductive decision making of these at-risk individuals was analyzed using Fisher's Exact Tests. Of those women who had children before learning of their risk to inherit HD, those who attended church more frequently, had three or more children total, or whose mother was affected with HD were more likely to be comfortable with their choice to have children. We conclude that these demographic factors influence the reproductive decision-making of individuals at risk for HD. Psychologists, clinical geneticists, and genetic counselors may be able to use this information to help counsel at-risk patients regarding current or past reproductive decision making.

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Year:  2013        PMID: 23709094     DOI: 10.1007/s10897-013-9596-0

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  28 in total

Review 1.  The clinical and genetic features of Huntington disease.

Authors:  Aaron Sturrock; Blair R Leavitt
Journal:  J Geriatr Psychiatry Neurol       Date:  2010-10-05       Impact factor: 2.680

2.  One hundred requests for predictive testing for Huntington's disease.

Authors:  S A Simpson; J Besson; D Alexander; K Allan; A W Johnston
Journal:  Clin Genet       Date:  1992-06       Impact factor: 4.438

3.  Personal factors associated with reported benefits of Huntington disease family history or genetic testing.

Authors:  Janet K Williams; Cheryl Erwin; Andrew Juhl; James Mills; Bradley Brossman; Jane S Paulsen
Journal:  Genet Test Mol Biomarkers       Date:  2010-08-19

4.  Young people's experiences of growing up in a family affected by Huntington's disease.

Authors:  K Forrest Keenan; Z Miedzybrodzka; E van Teijlingen; L McKee; S A Simpson
Journal:  Clin Genet       Date:  2007-02       Impact factor: 4.438

Review 5.  Huntington's Disease.

Authors:  Francis O Walker
Journal:  Semin Neurol       Date:  2007-04       Impact factor: 3.420

6.  Differences in duration of Huntington's disease based on age at onset.

Authors:  T Foroud; J Gray; J Ivashina; P M Conneally
Journal:  J Neurol Neurosurg Psychiatry       Date:  1999-01       Impact factor: 10.154

7.  Huntington's disease in Greece: the experience of 14 years.

Authors:  M Panas; G Karadima; E Vassos; N Kalfakis; A Kladi; K Christodoulou; D Vassilopoulos
Journal:  Clin Genet       Date:  2010-12-20       Impact factor: 4.438

8.  Attachment in families with Huntington's disease. A paradigm in clinical genetics.

Authors:  Lucienne Van der Meer; Reinier Timman; Wim Trijsburg; Marleen Duisterhof; Ruud Erdman; Thérèse Van Elderen; Aad Tibben
Journal:  Patient Educ Couns       Date:  2006-01-20

9.  Ten years of presymptomatic testing for Huntington's disease: the experience of the UK Huntington's Disease Prediction Consortium.

Authors:  P S Harper; C Lim; D Craufurd
Journal:  J Med Genet       Date:  2000-08       Impact factor: 6.318

10.  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
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  3 in total

1.  Impact of Huntington Disease Gene-Positive Status on Pre-Symptomatic Young Adults and Recommendations for Genetic Counselors.

Authors:  Ping Gong; Joanna H Fanos; Lauren Korty; Carly E Siskind; Andrea K Hanson-Kahn
Journal:  J Genet Couns       Date:  2016-04-22       Impact factor: 2.537

2.  Genetic testing preferences in families containing multiple individuals with epilepsy.

Authors:  Janice O Okeke; Virginia E Tangel; Shawn T Sorge; Dale C Hesdorffer; Melodie R Winawer; Jeff Goldsmith; Jo C Phelan; Wendy K Chung; Sara Shostak; Ruth Ottman
Journal:  Epilepsia       Date:  2014-09-29       Impact factor: 5.864

3.  Predictive testing for Huntington disease over 24 years: Evolution of the profile of the participants and analysis of symptoms.

Authors:  Francis Ramond; Isabelle Quadrio; Laurence Le Vavasseur; Hélène Chaumet; Fabrice Boyer; Muriel Bost; Elisabeth Ollagnon-Roman
Journal:  Mol Genet Genomic Med       Date:  2019-08-22       Impact factor: 2.183

  3 in total

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