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Published on: November 10, 2023
Association between human blood metabolome and the risk of hypertension
Nannan Dai1, Yujuan Deng2,3, Baishi Wang4
1The Eco-city Hospital of Tianjin Fifth Central Hospital, Tianjin, 300467, China. dairuiaiai@126.com.
Insights
This study identifies key blood metabolites linked to high blood pressure (hypertension). Findings suggest these metabolites could be future targets for developing new hypertension treatments.
Area of Science:
- Metabolomics
- Genetics
- Cardiovascular Health
Background:
- Hypertension (high blood pressure) is a widespread, often asymptomatic condition.
- Understanding the link between metabolites and blood pressure is crucial for intervention.
Purpose of the Study:
- To investigate the causal relationship between blood metabolites and blood pressure (diastolic and systolic).
- To explore the potential of metabolites as therapeutic targets for hypertension.
Main Methods:
- Utilized two-sample Mendelian Randomization (MR) analysis.
- Analyzed genome-wide association study (GWAS) data for 1,091 individuals.
- Examined summary statistics for diastolic blood pressure (DBP) and systolic blood pressure (SBP) from 757,601 participants.
Main Results:
- Identified twelve metabolites associated with DBP and twenty-two with SBP.
- Four metabolites showed robust associations with blood pressure.
- Reverse MR indicated blood pressure influences specific metabolite levels, such as decreasing tricosanoyl sphingomyelin and increasing 2-hydroxyhippurate.
Conclusions:
- Blood metabolites are significantly associated with blood pressure levels.
- These identified metabolites represent potential novel targets for hypertension management and treatment.
Abstract:
Hypertension, commonly referred to as high blood pressure, is a chronic medical condition characterized by persistently elevated blood pressure levels. It is a prevalent global health issue, affecting a significant portion of the population worldwide. Hypertension is often asymptomatic, making it a silent but potentially dangerous condition if left untreated. Genetic instruments for 1,091 were from a recent comprehensive metabolome genome-wide association study (GWAS). Summary statistics of diastolic blood pressure (DBP) and systolic blood pressure (SBP) involving 757,601 sample size were analyzed. Two-sample Mendelian Randomization (MR) was conducted to assess causal effect of metabolites on DBP and SBP risk, and reverse MR analysis was performed to identify the DBP/SBP causal effect on blood metabolites. Twelve and twenty-two metabolites were identified to be associated with DBP and SBP, respectively. Sensitive analysis showed four metabolites had robustness association on BP. Reverse MR demonstrated DBP and SBP could decrease the tricosanoyl sphingomyelin (d18:1/23:0)* level and increase the 2-hydroxyhippurate (salicylurate) level in blood, respectively. Our findings reveal an association between blood metabolites and blood pressure (DBP and SBP), suggesting potential therapeutic targets for hypertension intervention.
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