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Hematologic setpoints are a stable and patient-specific deep phenotype
The complete blood count is an important screening tool for healthy adults and is the most commonly ordered test at periodic physical exams. However, results are usually interpreted relative to one-size-fits-all reference intervals, undermining the goal of precision medicine to tailor medical care t...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557837/ https://www.ncbi.nlm.nih.gov/pubmed/37808854 http://dx.doi.org/10.1101/2023.09.26.23296146 |
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author | Foy, Brody H Petherbridge, Rachel Roth, Maxwell Mow, Christopher Patel, Hasmukh R Patel, Chhaya H Ho, Samantha N Lam, Evie Karczewski, Konrad J Tozzo, Veronica Higgins, John M |
author_facet | Foy, Brody H Petherbridge, Rachel Roth, Maxwell Mow, Christopher Patel, Hasmukh R Patel, Chhaya H Ho, Samantha N Lam, Evie Karczewski, Konrad J Tozzo, Veronica Higgins, John M |
author_sort | Foy, Brody H |
collection | PubMed |
description | The complete blood count is an important screening tool for healthy adults and is the most commonly ordered test at periodic physical exams. However, results are usually interpreted relative to one-size-fits-all reference intervals, undermining the goal of precision medicine to tailor medical care to the needs of individual patients based on their unique characteristics. Here we show that standard complete blood count indices in healthy adults have robust homeostatic setpoints that are patient-specific and stable, with the typical healthy adult’s set of 9 blood count setpoints distinguishable from 98% of others, and with these differences persisting for decades. These setpoints reflect a deep physiologic phenotype, enabling improved detection of both acquired and genetic determinants of hematologic regulation, including discovery of multiple novel loci via GWAS analyses. Patient-specific reference intervals derived from setpoints enable more accurate personalized risk assessment, and the setpoints themselves are significantly correlated with mortality risk, providing new opportunities to enhance patient-specific screening and early intervention. This study shows complete blood count setpoints are sufficiently stable and patient-specific to help realize the promise of precision medicine for healthy adults. |
format | Online Article Text |
id | pubmed-10557837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105578372023-10-07 Hematologic setpoints are a stable and patient-specific deep phenotype Foy, Brody H Petherbridge, Rachel Roth, Maxwell Mow, Christopher Patel, Hasmukh R Patel, Chhaya H Ho, Samantha N Lam, Evie Karczewski, Konrad J Tozzo, Veronica Higgins, John M medRxiv Article The complete blood count is an important screening tool for healthy adults and is the most commonly ordered test at periodic physical exams. However, results are usually interpreted relative to one-size-fits-all reference intervals, undermining the goal of precision medicine to tailor medical care to the needs of individual patients based on their unique characteristics. Here we show that standard complete blood count indices in healthy adults have robust homeostatic setpoints that are patient-specific and stable, with the typical healthy adult’s set of 9 blood count setpoints distinguishable from 98% of others, and with these differences persisting for decades. These setpoints reflect a deep physiologic phenotype, enabling improved detection of both acquired and genetic determinants of hematologic regulation, including discovery of multiple novel loci via GWAS analyses. Patient-specific reference intervals derived from setpoints enable more accurate personalized risk assessment, and the setpoints themselves are significantly correlated with mortality risk, providing new opportunities to enhance patient-specific screening and early intervention. This study shows complete blood count setpoints are sufficiently stable and patient-specific to help realize the promise of precision medicine for healthy adults. Cold Spring Harbor Laboratory 2023-09-28 /pmc/articles/PMC10557837/ /pubmed/37808854 http://dx.doi.org/10.1101/2023.09.26.23296146 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Foy, Brody H Petherbridge, Rachel Roth, Maxwell Mow, Christopher Patel, Hasmukh R Patel, Chhaya H Ho, Samantha N Lam, Evie Karczewski, Konrad J Tozzo, Veronica Higgins, John M Hematologic setpoints are a stable and patient-specific deep phenotype |
title | Hematologic setpoints are a stable and patient-specific deep phenotype |
title_full | Hematologic setpoints are a stable and patient-specific deep phenotype |
title_fullStr | Hematologic setpoints are a stable and patient-specific deep phenotype |
title_full_unstemmed | Hematologic setpoints are a stable and patient-specific deep phenotype |
title_short | Hematologic setpoints are a stable and patient-specific deep phenotype |
title_sort | hematologic setpoints are a stable and patient-specific deep phenotype |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10557837/ https://www.ncbi.nlm.nih.gov/pubmed/37808854 http://dx.doi.org/10.1101/2023.09.26.23296146 |
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