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The need for polygenic score reporting standards in evidence-based practice: lipid genetics use case
Polygenic scores (PGS) are used to quantify the genetic predisposition for heritable traits, with hypothesized utility for personalized risk assessments. Lipid PGS are primed for clinical translation, but evidence-based practice changes will require rigorous PGS standards to ensure reproducibility a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962796/ https://www.ncbi.nlm.nih.gov/pubmed/33538426 http://dx.doi.org/10.1097/MOL.0000000000000733 |
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author | Wand, Hannah Knowles, Joshua W. Clarke, Shoa L. |
author_facet | Wand, Hannah Knowles, Joshua W. Clarke, Shoa L. |
author_sort | Wand, Hannah |
collection | PubMed |
description | Polygenic scores (PGS) are used to quantify the genetic predisposition for heritable traits, with hypothesized utility for personalized risk assessments. Lipid PGS are primed for clinical translation, but evidence-based practice changes will require rigorous PGS standards to ensure reproducibility and generalizability. Here we review applicable reporting and technical standards for dyslipidemia PGS translation along phases of the ACCE (Analytical validity, Clinical validity, Clinical utility, Ethical considerations) framework for evaluating genetic tests. RECENT FINDINGS: New guidance suggests existing standards for study designs incorporating the ACCE framework are applicable to PGS and should be adopted. One recent example is the Clinical Genomics Resource (ClinGen) and Polygenic Score Catalog's PRS reporting standards, which define minimal requirements for describing rationale for score development, study population definitions and data parameters, risk model development and application, risk model evaluation, and translational considerations, such as generalizability beyond the target population studied. SUMMARY: Lipid PGS are likely to be integrated into clinical practice in the future. Clinicians will need to be prepared to determine if and when lipid PGS is useful and valid. This decision-making will depend on the quality of evidence for the clinical use of PGS. Establishing reporting standards for PGS will help facilitate data sharing and transparency for critical evaluation, ultimately benefiting the efficiency of evidence-based practice. |
format | Online Article Text |
id | pubmed-7962796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-79627962021-03-29 The need for polygenic score reporting standards in evidence-based practice: lipid genetics use case Wand, Hannah Knowles, Joshua W. Clarke, Shoa L. Curr Opin Lipidol GENETICS AND MOLECULAR BIOLOGY: Edited by Robert A. Hegele Polygenic scores (PGS) are used to quantify the genetic predisposition for heritable traits, with hypothesized utility for personalized risk assessments. Lipid PGS are primed for clinical translation, but evidence-based practice changes will require rigorous PGS standards to ensure reproducibility and generalizability. Here we review applicable reporting and technical standards for dyslipidemia PGS translation along phases of the ACCE (Analytical validity, Clinical validity, Clinical utility, Ethical considerations) framework for evaluating genetic tests. RECENT FINDINGS: New guidance suggests existing standards for study designs incorporating the ACCE framework are applicable to PGS and should be adopted. One recent example is the Clinical Genomics Resource (ClinGen) and Polygenic Score Catalog's PRS reporting standards, which define minimal requirements for describing rationale for score development, study population definitions and data parameters, risk model development and application, risk model evaluation, and translational considerations, such as generalizability beyond the target population studied. SUMMARY: Lipid PGS are likely to be integrated into clinical practice in the future. Clinicians will need to be prepared to determine if and when lipid PGS is useful and valid. This decision-making will depend on the quality of evidence for the clinical use of PGS. Establishing reporting standards for PGS will help facilitate data sharing and transparency for critical evaluation, ultimately benefiting the efficiency of evidence-based practice. Lippincott Williams & Wilkins 2021-04 2021-02-03 /pmc/articles/PMC7962796/ /pubmed/33538426 http://dx.doi.org/10.1097/MOL.0000000000000733 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | GENETICS AND MOLECULAR BIOLOGY: Edited by Robert A. Hegele Wand, Hannah Knowles, Joshua W. Clarke, Shoa L. The need for polygenic score reporting standards in evidence-based practice: lipid genetics use case |
title | The need for polygenic score reporting standards in evidence-based practice: lipid genetics use case |
title_full | The need for polygenic score reporting standards in evidence-based practice: lipid genetics use case |
title_fullStr | The need for polygenic score reporting standards in evidence-based practice: lipid genetics use case |
title_full_unstemmed | The need for polygenic score reporting standards in evidence-based practice: lipid genetics use case |
title_short | The need for polygenic score reporting standards in evidence-based practice: lipid genetics use case |
title_sort | need for polygenic score reporting standards in evidence-based practice: lipid genetics use case |
topic | GENETICS AND MOLECULAR BIOLOGY: Edited by Robert A. Hegele |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962796/ https://www.ncbi.nlm.nih.gov/pubmed/33538426 http://dx.doi.org/10.1097/MOL.0000000000000733 |
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