Literature DB >> 17380059

Knowledge of and attitudes about Alzheimer disease genetics: report of a pilot survey and two focus groups.

T J Moscarillo1, H Holt, M Perman, S Goldberg, L Cortellini, J M Stoler, W DeJong, B J Miles, M S Albert, R C P Go, D Blacker.   

Abstract

OBJECTIVES: In preparation for the development of an educational intervention on Alzheimer disease (AD) genetics, we undertook a pilot survey of knowledge in this area and attitudes toward genetic testing for AD among individuals with a family history of AD.
METHODS: For the pilot study, we administered a 30-min questionnaire to 57 unaffected individuals from a genetic linkage study. For the focus groups, we interviewed two groups of subjects, ages 44-70 years, with a family history of AD, one of 10 Caucasians and the other of 6 African-Americans.
RESULTS: The pilot study showed that there was limited knowledge of genetics overall and AD genetics in particular, considerable concern about personal risk, and little knowledge of or interest in genetic testing for the disease. The focus groups reinforced and fleshed out these impressions and highlighted the importance of caregiving experience in the attitudes toward personal risk for AD.
CONCLUSIONS: These results underscore the value of genetics education for this and other complex diseases and suggest specific foci for educational interventions. Copyright 2007 S. Karger AG, Basel.

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Year:  2007        PMID: 17380059     DOI: 10.1159/000099087

Source DB:  PubMed          Journal:  Community Genet        ISSN: 1422-2795


  7 in total

1.  Knowledge and attitudes towards genetic testing in those affected with Parkinson's disease.

Authors:  Tracey M Scuffham; Aideen McInerny-Leo; Shu-Kay Ng; George Mellick
Journal:  J Community Genet       Date:  2013-09-10

2.  Differences between African American and White research volunteers in their attitudes, beliefs and knowledge regarding genetic testing for Alzheimer's disease.

Authors:  Ibidapo Akinleye; J Scott Roberts; Charmaine D M Royal; Erin Linnenbringer; Thomas O Obisesan; Grace-Ann Fasaye; Robert C Green
Journal:  J Genet Couns       Date:  2011-06-09       Impact factor: 2.537

Review 3.  Public perceptions about risk and protective factors for cognitive health and impairment: a review of the literature.

Authors:  Daniela B Friedman; Katie Becofsky; Lynda A Anderson; Lucinda L Bryant; Rebecca H Hunter; Susan L Ivey; Basia Belza; Rebecca G Logsdon; Sarah Brannon; Ann E Vandenberg; Shih-Yin Lin
Journal:  Int Psychogeriatr       Date:  2015-01-16       Impact factor: 3.878

4.  Genetic counselling in sickle cell disease: views of single young adults in Ghana.

Authors:  Stella Appiah; Kwadwo Ameyaw Korsah; Charles AmpongAdjei; Osei Evans Appiah
Journal:  J Community Genet       Date:  2020-07-01

5.  Genetic testing and Parkinson disease: assessment of patient knowledge, attitudes, and interest.

Authors:  Dana Clay Falcone; Elisabeth McCarty Wood; Sharon X Xie; Andrew Siderowf; Vivianna M Van Deerlin
Journal:  J Genet Couns       Date:  2011-04-08       Impact factor: 2.537

6.  Caregiving by teens for family members with Huntington disease.

Authors:  Janet K Williams; Lioness Ayres; Janet Specht; Kathleen Sparbel; Mary Lou Klimek
Journal:  J Fam Nurs       Date:  2009-05-22       Impact factor: 3.818

7.  Effectiveness of a condensed protocol for disclosing APOE genotype and providing risk education for Alzheimer disease.

Authors:  J Scott Roberts; Clara A Chen; Wendy R Uhlmann; Robert C Green
Journal:  Genet Med       Date:  2012-04-12       Impact factor: 8.822

  7 in total

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