Author
Listed:
- Brody H. Foy
(Massachusetts General Hospital
Massachusetts General Hospital
Harvard Medical School
University of Washington)
- Rachel Petherbridge
(Massachusetts General Hospital
Massachusetts General Hospital
Harvard Medical School)
- Maxwell T. Roth
(Massachusetts General Hospital
Massachusetts General Hospital)
- Cindy Zhang
(University of Washington)
- Daniel C. De Souza
(Massachusetts General Hospital
Massachusetts General Hospital
Harvard Medical School)
- Christopher Mow
(Massachusetts General Hospital
Mass General Brigham Enterprise Research IS)
- Hasmukh R. Patel
(Massachusetts General Hospital
Massachusetts General Hospital)
- Chhaya H. Patel
(Massachusetts General Hospital
Massachusetts General Hospital)
- Samantha N. Ho
(Massachusetts General Hospital
Massachusetts General Hospital)
- Evie Lam
(Massachusetts General Hospital
Massachusetts General Hospital)
- Camille E. Powe
(Massachusetts General Hospital
Harvard Medical School
Massachusetts General Hospital and Harvard Medical School
Broad Institute of MIT and Harvard)
- Robert P. Hasserjian
(Massachusetts General Hospital)
- Konrad J. Karczewski
(Broad Institute of MIT and Harvard
Massachusetts General Hospital
Broad Institute of MIT and Harvard)
- Veronica Tozzo
(Massachusetts General Hospital
Massachusetts General Hospital
Harvard Medical School
David Geffen School of Medicine at UCLA)
- John M. Higgins
(Massachusetts General Hospital
Massachusetts General Hospital
Harvard Medical School)
Abstract
The complete blood count (CBC) is an important screening tool for healthy adults and a common test at periodic exams. However, results are usually interpreted relative to one-size-fits-all reference intervals1,2, undermining the precision medicine goal to tailor care for patients on the basis of their unique characteristics3,4. Here we study thousands of diverse patients at an academic medical centre and show that routine CBC indices fluctuate around stable values or setpoints5, and setpoints are patient-specific, with the typical healthy adult’s nine CBC setpoints distinguishable as a group from those of 98% of other healthy adults, and setpoint differences persist for at least 20 years. Haematological setpoints reflect a deep physiologic phenotype enabling investigation of acquired and genetic determinants of haematological regulation and its variation among healthy adults. Setpoints in apparently healthy adults were associated with significant variation in clinical risk: absolute risk of some common diseases and morbidities varied by more than 2% (heart attack and stroke, diabetes, kidney disease, osteoporosis), and absolute risk of all-cause 10 year mortality varied by more than 5%. Setpoints also define patient-specific reference intervals and personalize the interpretation of subsequent test results. In retrospective analysis, setpoints improved sensitivity and specificity for evaluation of some common conditions including diabetes, kidney disease, thyroid dysfunction, iron deficiency and myeloproliferative neoplasms. This study shows CBC setpoints are sufficiently stable and patient-specific to help realize the promise of precision medicine for healthy adults.
Suggested Citation
Brody H. Foy & Rachel Petherbridge & Maxwell T. Roth & Cindy Zhang & Daniel C. De Souza & Christopher Mow & Hasmukh R. Patel & Chhaya H. Patel & Samantha N. Ho & Evie Lam & Camille E. Powe & Robert P., 2025.
"Haematological setpoints are a stable and patient-specific deep phenotype,"
Nature, Nature, vol. 637(8045), pages 430-438, January.
Handle:
RePEc:nat:nature:v:637:y:2025:i:8045:d:10.1038_s41586-024-08264-5
DOI: 10.1038/s41586-024-08264-5
Download full text from publisher
As the access to this document is restricted, you may want to search for a different version of it.
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:637:y:2025:i:8045:d:10.1038_s41586-024-08264-5. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.