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Genetic Risk of Alzheimer’s Disease: Three Wishes Now That the Genie is Out of the Bottle
The availability and increasing popularity of direct-to-consumer genetic testing for the presence of an APOE4 allelle led the Alzheimer’s Foundation of America Medical, Scientific and Memory Screening Advisory Board to identify three critical areas for attention: 1) ensure consumer understanding of...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218128/ https://www.ncbi.nlm.nih.gov/pubmed/30282369 http://dx.doi.org/10.3233/JAD-180629 |
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author | Frank, Lori Wesson Ashford, J. Bayley, Peter J. Borson, Soo Buschke, Herman Cohen, Donna Cummings, Jeffrey L. Davies, Peter Dean, Margaret Finkel, Sanford I. Hyer, Lee Perry, George Powers, Richard E. Schmitt, Frederick |
author_facet | Frank, Lori Wesson Ashford, J. Bayley, Peter J. Borson, Soo Buschke, Herman Cohen, Donna Cummings, Jeffrey L. Davies, Peter Dean, Margaret Finkel, Sanford I. Hyer, Lee Perry, George Powers, Richard E. Schmitt, Frederick |
author_sort | Frank, Lori |
collection | PubMed |
description | The availability and increasing popularity of direct-to-consumer genetic testing for the presence of an APOE4 allelle led the Alzheimer’s Foundation of America Medical, Scientific and Memory Screening Advisory Board to identify three critical areas for attention: 1) ensure consumer understanding of test results; 2) address and limit potential negative consequences of acquiring this information; and 3) support linking results with positive health behaviors, including potential clinical trial participation. Improving access to appropriate sources of genetic counseling as part of the testing process is critical and requires action from clinicians and the genetic testing industry. Standardizing information and resources across the industry should start now, with the input of consumers and experts in genetic risk and health information disclosure. Direct-to-consumer testing companies and clinicians should assist consumers by facilitating consultation with genetic counselors and facilitating pursuit of accurate information about testing. |
format | Online Article Text |
id | pubmed-6218128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62181282018-11-07 Genetic Risk of Alzheimer’s Disease: Three Wishes Now That the Genie is Out of the Bottle Frank, Lori Wesson Ashford, J. Bayley, Peter J. Borson, Soo Buschke, Herman Cohen, Donna Cummings, Jeffrey L. Davies, Peter Dean, Margaret Finkel, Sanford I. Hyer, Lee Perry, George Powers, Richard E. Schmitt, Frederick J Alzheimers Dis Editorial The availability and increasing popularity of direct-to-consumer genetic testing for the presence of an APOE4 allelle led the Alzheimer’s Foundation of America Medical, Scientific and Memory Screening Advisory Board to identify three critical areas for attention: 1) ensure consumer understanding of test results; 2) address and limit potential negative consequences of acquiring this information; and 3) support linking results with positive health behaviors, including potential clinical trial participation. Improving access to appropriate sources of genetic counseling as part of the testing process is critical and requires action from clinicians and the genetic testing industry. Standardizing information and resources across the industry should start now, with the input of consumers and experts in genetic risk and health information disclosure. Direct-to-consumer testing companies and clinicians should assist consumers by facilitating consultation with genetic counselors and facilitating pursuit of accurate information about testing. IOS Press 2018-10-30 /pmc/articles/PMC6218128/ /pubmed/30282369 http://dx.doi.org/10.3233/JAD-180629 Text en © 2018 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Editorial Frank, Lori Wesson Ashford, J. Bayley, Peter J. Borson, Soo Buschke, Herman Cohen, Donna Cummings, Jeffrey L. Davies, Peter Dean, Margaret Finkel, Sanford I. Hyer, Lee Perry, George Powers, Richard E. Schmitt, Frederick Genetic Risk of Alzheimer’s Disease: Three Wishes Now That the Genie is Out of the Bottle |
title | Genetic Risk of Alzheimer’s Disease: Three Wishes Now That the Genie is Out of the Bottle |
title_full | Genetic Risk of Alzheimer’s Disease: Three Wishes Now That the Genie is Out of the Bottle |
title_fullStr | Genetic Risk of Alzheimer’s Disease: Three Wishes Now That the Genie is Out of the Bottle |
title_full_unstemmed | Genetic Risk of Alzheimer’s Disease: Three Wishes Now That the Genie is Out of the Bottle |
title_short | Genetic Risk of Alzheimer’s Disease: Three Wishes Now That the Genie is Out of the Bottle |
title_sort | genetic risk of alzheimer’s disease: three wishes now that the genie is out of the bottle |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218128/ https://www.ncbi.nlm.nih.gov/pubmed/30282369 http://dx.doi.org/10.3233/JAD-180629 |
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