The causal relationship between blood cell traits and aging: a Mendelian randomization study

Abstract Background The global population is aging rapidly, raising significant concerns about public health issues. Routine blood tests, which assess blood cell traits, are commonly performed clinical laboratory tests. Understanding the intricate relationship between blood cell traits and aging is...

Full description

Saved in:
Bibliographic Details
Main Authors: Peng Chen, Yi-Hang Zhou, Xin Wei, Hua-Gui Wei, Bo Li, Ling Ou-Yang
Format: Article
Language:English
Published: BMC 2025-05-01
Series:BMC Geriatrics
Subjects:
Online Access:https://doi.org/10.1186/s12877-025-06051-z
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850242920089649152
author Peng Chen
Yi-Hang Zhou
Xin Wei
Hua-Gui Wei
Bo Li
Ling Ou-Yang
author_facet Peng Chen
Yi-Hang Zhou
Xin Wei
Hua-Gui Wei
Bo Li
Ling Ou-Yang
author_sort Peng Chen
collection DOAJ
description Abstract Background The global population is aging rapidly, raising significant concerns about public health issues. Routine blood tests, which assess blood cell traits, are commonly performed clinical laboratory tests. Understanding the intricate relationship between blood cell traits and aging is vital for identifying individuals at risk of early decline in health. Methods This study employed bidirectional Mendelian randomization (MR) to explore causal links between 36 blood cell traits and aging indicators, including frailty index (FI), telomere length (TL), and epigenetic aging clocks. Univariate MR analysis primarily used inverse variance weighted, MR-Egger, weighted median, and weighted mode methods. Multivariate MR was applied to investigate independent effects of each blood cell trait on aging utilizing multivariable inverse variance-weighted techniques. Furthermore, the mediating effects of nine potential mediators, such as 25-hydroxyvitamin D, C-reactive protein, and cholesterol levels on the causal relationship between blood cell traits and aging were examined by a mediation analysis. Results The study revealed significant causal associations: eosinophil counts were positively associated with FI (odds ratio (OR) = 1.063, p = 1.4e-07). Mean corpuscular volume (MCV) was linked to telomere length (OR = 0.978, p = 0.0001). Lymphocyte counts showed causal connections with epigenetic aging clocks (GrimAge acceleration: OR = 0.614, p = 7.0e-08; Hannum age acceleration: OR = 0.519, p = 5.4e-11; and PhenoAge acceleration: OR = 0.519, p = 5.4e-11). Conclusion This MR study uncovered significant causal relationships between blood cell traits such as eosinophil counts, MCV, and lymphocyte counts, with aging indicators. Monitoring these traits in routine blood tests can provide valuable insights for assessing age-related health risks and promoting healthy aging.
format Article
id doaj-art-9b5cc83b99574abaaa3decb6bf950528
institution OA Journals
issn 1471-2318
language English
publishDate 2025-05-01
publisher BMC
record_format Article
series BMC Geriatrics
spelling doaj-art-9b5cc83b99574abaaa3decb6bf9505282025-08-20T02:00:09ZengBMCBMC Geriatrics1471-23182025-05-0125111410.1186/s12877-025-06051-zThe causal relationship between blood cell traits and aging: a Mendelian randomization studyPeng Chen0Yi-Hang Zhou1Xin Wei2Hua-Gui Wei3Bo Li4Ling Ou-Yang5Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical UniversityDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical UniversityDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical UniversityDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical UniversityDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical UniversityDepartment of Obstetrics and Gynecology, Shengjing Hospital of China Medical UniversityAbstract Background The global population is aging rapidly, raising significant concerns about public health issues. Routine blood tests, which assess blood cell traits, are commonly performed clinical laboratory tests. Understanding the intricate relationship between blood cell traits and aging is vital for identifying individuals at risk of early decline in health. Methods This study employed bidirectional Mendelian randomization (MR) to explore causal links between 36 blood cell traits and aging indicators, including frailty index (FI), telomere length (TL), and epigenetic aging clocks. Univariate MR analysis primarily used inverse variance weighted, MR-Egger, weighted median, and weighted mode methods. Multivariate MR was applied to investigate independent effects of each blood cell trait on aging utilizing multivariable inverse variance-weighted techniques. Furthermore, the mediating effects of nine potential mediators, such as 25-hydroxyvitamin D, C-reactive protein, and cholesterol levels on the causal relationship between blood cell traits and aging were examined by a mediation analysis. Results The study revealed significant causal associations: eosinophil counts were positively associated with FI (odds ratio (OR) = 1.063, p = 1.4e-07). Mean corpuscular volume (MCV) was linked to telomere length (OR = 0.978, p = 0.0001). Lymphocyte counts showed causal connections with epigenetic aging clocks (GrimAge acceleration: OR = 0.614, p = 7.0e-08; Hannum age acceleration: OR = 0.519, p = 5.4e-11; and PhenoAge acceleration: OR = 0.519, p = 5.4e-11). Conclusion This MR study uncovered significant causal relationships between blood cell traits such as eosinophil counts, MCV, and lymphocyte counts, with aging indicators. Monitoring these traits in routine blood tests can provide valuable insights for assessing age-related health risks and promoting healthy aging.https://doi.org/10.1186/s12877-025-06051-zBlood cellFrailty indexMendelian randomizationEpigenetic clockTelomere lengthAging
spellingShingle Peng Chen
Yi-Hang Zhou
Xin Wei
Hua-Gui Wei
Bo Li
Ling Ou-Yang
The causal relationship between blood cell traits and aging: a Mendelian randomization study
BMC Geriatrics
Blood cell
Frailty index
Mendelian randomization
Epigenetic clock
Telomere length
Aging
title The causal relationship between blood cell traits and aging: a Mendelian randomization study
title_full The causal relationship between blood cell traits and aging: a Mendelian randomization study
title_fullStr The causal relationship between blood cell traits and aging: a Mendelian randomization study
title_full_unstemmed The causal relationship between blood cell traits and aging: a Mendelian randomization study
title_short The causal relationship between blood cell traits and aging: a Mendelian randomization study
title_sort causal relationship between blood cell traits and aging a mendelian randomization study
topic Blood cell
Frailty index
Mendelian randomization
Epigenetic clock
Telomere length
Aging
url https://doi.org/10.1186/s12877-025-06051-z
work_keys_str_mv AT pengchen thecausalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT yihangzhou thecausalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT xinwei thecausalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT huaguiwei thecausalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT boli thecausalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT lingouyang thecausalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT pengchen causalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT yihangzhou causalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT xinwei causalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT huaguiwei causalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT boli causalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy
AT lingouyang causalrelationshipbetweenbloodcelltraitsandagingamendelianrandomizationstudy