Identifying pathways to cardiovascular mortality by causal graphical models and mediation analysis among hypertensive patients: insights from a prospective study

Abstract Background Many biochemical markers are involved in cardiovascular (CV) prognosis in the hypertensive population, but most findings are derived from a single-exposure setting, and their interaction and potential pathways remain scarce. The aim of this study was to determine the direct cause...

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Main Authors: Simiao Tian, Zhen Li, Yanhong Bi, Xiaoyu Che, Ao Feng, Yiou Wang
Format: Article
Language:English
Published: BMC 2025-06-01
Series:Journal of Translational Medicine
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Online Access:https://doi.org/10.1186/s12967-025-06755-1
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author Simiao Tian
Zhen Li
Yanhong Bi
Xiaoyu Che
Ao Feng
Yiou Wang
author_facet Simiao Tian
Zhen Li
Yanhong Bi
Xiaoyu Che
Ao Feng
Yiou Wang
author_sort Simiao Tian
collection DOAJ
description Abstract Background Many biochemical markers are involved in cardiovascular (CV) prognosis in the hypertensive population, but most findings are derived from a single-exposure setting, and their interaction and potential pathways remain scarce. The aim of this study was to determine the direct cause-effect relationship and the mediating effect of CV mortality to suggest potential pathways. Methods This prospective study analysed a data from 3559 hypertensive individuals from the National Health and Nutrition Examination Survey (1999–2018), with their CV mortality ascertained through linkage to the National Death Index on December 31, 2019. Baseline sociodemographic characteristics, habits, medical history data and serum biochemical markers, including cardiometabolic markers, inflammatory markers, liver enzyme markers, blood-cell based inflammatory and immune markers and kidney and renal markers were recorded. The Mixed Graphical Model-Fast-Causal Inference-Maximum algorithm (MGM-FCI-MAX) was applied to build a causal graphical model (CGM) depicting direct and indirect causes of CV mortality, then pathways were further identified from CGM where mediation analyses were performed. Results Of the total participants, 562 (15.79%, 302 men and 260 women) CV deaths occurred after a median follow-up of 154 months. Survival analysis revealed significant sex- and ethnicity-specific differences in CV mortality rates (log-rank P < 0.01 and P < 0.01, respectively). Based on the resulting CGM, we identified three direct causes, estimated glomerular filtration rate (eGFR), blood urea nitrogen (BUN) and monocytes, of CV mortality, representing direct pathways underlying kidney and renal function and blood-cell based inflammatory function, respectively. BUN significantly mediated 30.29% of the effect of the eGFR on CV mortality, whereas neither the liver enzyme markers nor insulin pathway with the eGFR as a mediator showed a significant tendency towards a mediated effect after adjusting for covariates. Sex and race were significantly (21.73% and 20.96%, respectively) mediated by monocytes and the eGFR for CV mortality. Conclusion By using prospective survey data and background clinical knowledge, CGM retrieved direct and indirect causes of CV prognosis and identified pathways and the associated mediated effects. These insights will be useful in designing clinical protocols and targeting improvements in hypertensive patient management.
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spelling doaj-art-6f4af0b6619141b7894aa8f929a037b72025-08-20T03:22:54ZengBMCJournal of Translational Medicine1479-58762025-06-0123111610.1186/s12967-025-06755-1Identifying pathways to cardiovascular mortality by causal graphical models and mediation analysis among hypertensive patients: insights from a prospective studySimiao Tian0Zhen Li1Yanhong Bi2Xiaoyu Che3Ao Feng4Yiou Wang5Department of Medical Records and Statistics, Affiliated Zhongshan Hospital of Dalian UniversityDepartment of Medical Records and Statistics, Affiliated Zhongshan Hospital of Dalian UniversityDepartment of Research, Affiliated Zhongshan Hospital of Dalian UniversityDepartment of Research, Affiliated Zhongshan Hospital of Dalian UniversityDepartment of Prevention and Healthcare, Affiliated Zhongshan Hospital of Dalian UniversityDepartment of Medical Records and Statistics, Affiliated Zhongshan Hospital of Dalian UniversityAbstract Background Many biochemical markers are involved in cardiovascular (CV) prognosis in the hypertensive population, but most findings are derived from a single-exposure setting, and their interaction and potential pathways remain scarce. The aim of this study was to determine the direct cause-effect relationship and the mediating effect of CV mortality to suggest potential pathways. Methods This prospective study analysed a data from 3559 hypertensive individuals from the National Health and Nutrition Examination Survey (1999–2018), with their CV mortality ascertained through linkage to the National Death Index on December 31, 2019. Baseline sociodemographic characteristics, habits, medical history data and serum biochemical markers, including cardiometabolic markers, inflammatory markers, liver enzyme markers, blood-cell based inflammatory and immune markers and kidney and renal markers were recorded. The Mixed Graphical Model-Fast-Causal Inference-Maximum algorithm (MGM-FCI-MAX) was applied to build a causal graphical model (CGM) depicting direct and indirect causes of CV mortality, then pathways were further identified from CGM where mediation analyses were performed. Results Of the total participants, 562 (15.79%, 302 men and 260 women) CV deaths occurred after a median follow-up of 154 months. Survival analysis revealed significant sex- and ethnicity-specific differences in CV mortality rates (log-rank P < 0.01 and P < 0.01, respectively). Based on the resulting CGM, we identified three direct causes, estimated glomerular filtration rate (eGFR), blood urea nitrogen (BUN) and monocytes, of CV mortality, representing direct pathways underlying kidney and renal function and blood-cell based inflammatory function, respectively. BUN significantly mediated 30.29% of the effect of the eGFR on CV mortality, whereas neither the liver enzyme markers nor insulin pathway with the eGFR as a mediator showed a significant tendency towards a mediated effect after adjusting for covariates. Sex and race were significantly (21.73% and 20.96%, respectively) mediated by monocytes and the eGFR for CV mortality. Conclusion By using prospective survey data and background clinical knowledge, CGM retrieved direct and indirect causes of CV prognosis and identified pathways and the associated mediated effects. These insights will be useful in designing clinical protocols and targeting improvements in hypertensive patient management.https://doi.org/10.1186/s12967-025-06755-1HypertensionCardiovascular mortalityCausal graphical modelsNHANES
spellingShingle Simiao Tian
Zhen Li
Yanhong Bi
Xiaoyu Che
Ao Feng
Yiou Wang
Identifying pathways to cardiovascular mortality by causal graphical models and mediation analysis among hypertensive patients: insights from a prospective study
Journal of Translational Medicine
Hypertension
Cardiovascular mortality
Causal graphical models
NHANES
title Identifying pathways to cardiovascular mortality by causal graphical models and mediation analysis among hypertensive patients: insights from a prospective study
title_full Identifying pathways to cardiovascular mortality by causal graphical models and mediation analysis among hypertensive patients: insights from a prospective study
title_fullStr Identifying pathways to cardiovascular mortality by causal graphical models and mediation analysis among hypertensive patients: insights from a prospective study
title_full_unstemmed Identifying pathways to cardiovascular mortality by causal graphical models and mediation analysis among hypertensive patients: insights from a prospective study
title_short Identifying pathways to cardiovascular mortality by causal graphical models and mediation analysis among hypertensive patients: insights from a prospective study
title_sort identifying pathways to cardiovascular mortality by causal graphical models and mediation analysis among hypertensive patients insights from a prospective study
topic Hypertension
Cardiovascular mortality
Causal graphical models
NHANES
url https://doi.org/10.1186/s12967-025-06755-1
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