Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
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
_version_ 1785117157761220608
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
work_keys_str_mv AT foybrodyh hematologicsetpointsareastableandpatientspecificdeepphenotype
AT petherbridgerachel hematologicsetpointsareastableandpatientspecificdeepphenotype
AT rothmaxwell hematologicsetpointsareastableandpatientspecificdeepphenotype
AT mowchristopher hematologicsetpointsareastableandpatientspecificdeepphenotype
AT patelhasmukhr hematologicsetpointsareastableandpatientspecificdeepphenotype
AT patelchhayah hematologicsetpointsareastableandpatientspecificdeepphenotype
AT hosamanthan hematologicsetpointsareastableandpatientspecificdeepphenotype
AT lamevie hematologicsetpointsareastableandpatientspecificdeepphenotype
AT karczewskikonradj hematologicsetpointsareastableandpatientspecificdeepphenotype
AT tozzoveronica hematologicsetpointsareastableandpatientspecificdeepphenotype
AT higginsjohnm hematologicsetpointsareastableandpatientspecificdeepphenotype