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Lay understandings of drug‐gene interactions: The right medication, the right dose, at the right time, but what are the right words?
As pharmacogenomic (PGx) testing increases in popularity, lay concepts of drug‐gene interactions set the stage for shared decision making in precision medicine. Few studies explore what recipients of PGx results think is happening in their bodies when a drug‐gene interaction is discovered. To charac...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932688/ https://www.ncbi.nlm.nih.gov/pubmed/34755460 http://dx.doi.org/10.1111/cts.13193 |
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author | Meagher, Karen M. Stuttgen Finn, Kelsey Curtis, Susan H. Borucki, Jack Beck, Annika T. Cheema, Amal W. Sharp, Richard R. |
author_facet | Meagher, Karen M. Stuttgen Finn, Kelsey Curtis, Susan H. Borucki, Jack Beck, Annika T. Cheema, Amal W. Sharp, Richard R. |
author_sort | Meagher, Karen M. |
collection | PubMed |
description | As pharmacogenomic (PGx) testing increases in popularity, lay concepts of drug‐gene interactions set the stage for shared decision making in precision medicine. Few studies explore what recipients of PGx results think is happening in their bodies when a drug‐gene interaction is discovered. To characterize biobank participants’ understanding of PGx research results, we conducted a focus group study, which took place after PGx variants conferring increased risk of dihydropyrimidine dehydrogenase (DPD) deficiency were disclosed to biobank contributors. DPD deficiency confers an increased risk of adverse reaction to commonly used cancer chemotherapeutics. Ten focus groups were conducted, ranging from two to eight participants. Fifty‐four individuals participated in focus groups. A framework approach was used for descriptive and explanatory analysis. Descriptive themes included participants’ efforts to make sense of PGx findings as they related to: (1) health implications, (2) drugs, and (3) genetics. Explanatory analysis supplied a functional framework of how participant word choices can perform different purposes in PGx communication. Results bear three main implications for PGx research‐related disclosure. First, participants’ use of various terms suggest participants generally understanding their PGx results, including how positive PGx results differ from positive disease susceptibility genetic results. Second, PGx disclosure in biobanking can involve participant conflation of drug‐gene interactions with allergies or other types of medical reactions. Third, the functional framework suggests a need to move beyond a deficit model of genetic literacy in PGx communication. Together, findings provide an initial evidence base for supporting bidirectional expert‐recipient PGx results communication. |
format | Online Article Text |
id | pubmed-8932688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89326882022-03-24 Lay understandings of drug‐gene interactions: The right medication, the right dose, at the right time, but what are the right words? Meagher, Karen M. Stuttgen Finn, Kelsey Curtis, Susan H. Borucki, Jack Beck, Annika T. Cheema, Amal W. Sharp, Richard R. Clin Transl Sci Research As pharmacogenomic (PGx) testing increases in popularity, lay concepts of drug‐gene interactions set the stage for shared decision making in precision medicine. Few studies explore what recipients of PGx results think is happening in their bodies when a drug‐gene interaction is discovered. To characterize biobank participants’ understanding of PGx research results, we conducted a focus group study, which took place after PGx variants conferring increased risk of dihydropyrimidine dehydrogenase (DPD) deficiency were disclosed to biobank contributors. DPD deficiency confers an increased risk of adverse reaction to commonly used cancer chemotherapeutics. Ten focus groups were conducted, ranging from two to eight participants. Fifty‐four individuals participated in focus groups. A framework approach was used for descriptive and explanatory analysis. Descriptive themes included participants’ efforts to make sense of PGx findings as they related to: (1) health implications, (2) drugs, and (3) genetics. Explanatory analysis supplied a functional framework of how participant word choices can perform different purposes in PGx communication. Results bear three main implications for PGx research‐related disclosure. First, participants’ use of various terms suggest participants generally understanding their PGx results, including how positive PGx results differ from positive disease susceptibility genetic results. Second, PGx disclosure in biobanking can involve participant conflation of drug‐gene interactions with allergies or other types of medical reactions. Third, the functional framework suggests a need to move beyond a deficit model of genetic literacy in PGx communication. Together, findings provide an initial evidence base for supporting bidirectional expert‐recipient PGx results communication. John Wiley and Sons Inc. 2021-11-25 2022-03 /pmc/articles/PMC8932688/ /pubmed/34755460 http://dx.doi.org/10.1111/cts.13193 Text en © 2021 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Meagher, Karen M. Stuttgen Finn, Kelsey Curtis, Susan H. Borucki, Jack Beck, Annika T. Cheema, Amal W. Sharp, Richard R. Lay understandings of drug‐gene interactions: The right medication, the right dose, at the right time, but what are the right words? |
title | Lay understandings of drug‐gene interactions: The right medication, the right dose, at the right time, but what are the right words? |
title_full | Lay understandings of drug‐gene interactions: The right medication, the right dose, at the right time, but what are the right words? |
title_fullStr | Lay understandings of drug‐gene interactions: The right medication, the right dose, at the right time, but what are the right words? |
title_full_unstemmed | Lay understandings of drug‐gene interactions: The right medication, the right dose, at the right time, but what are the right words? |
title_short | Lay understandings of drug‐gene interactions: The right medication, the right dose, at the right time, but what are the right words? |
title_sort | lay understandings of drug‐gene interactions: the right medication, the right dose, at the right time, but what are the right words? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8932688/ https://www.ncbi.nlm.nih.gov/pubmed/34755460 http://dx.doi.org/10.1111/cts.13193 |
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