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Published on: May 17, 2024
Comparative Study of Metabolite Changes After Antihypertensive Therapy With Calcium Channel Blockers or Angiotensin
Jieyu Lu1, Yunfan Tian, Jia Gu
1Department of Cardiology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Insights
This study explored how calcium channel blockers (CCBs) and angiotensin receptor blockers (ARBs) affect serum metabolites in hypertension patients. Specific metabolic pathways changed with ARB and CCB treatments, offering potential biomarkers for monitoring drug effects.
Area of Science:
- Cardiovascular Medicine
- Metabolomics
- Pharmacology
Background:
- Hypertension is a major global health issue, increasing cardiovascular disease risk.
- Calcium channel blockers (CCBs) and angiotensin type 1 receptor blockers (ARBs) are common hypertension treatments.
- The impact of CCBs and ARBs on serum metabolites is largely unknown.
Purpose of the Study:
- To investigate serum metabolite alterations following single-drug therapy with CCBs or ARBs in newly diagnosed hypertension patients.
- To identify potential metabolic biomarkers associated with antihypertensive treatment response.
Main Methods:
- Employed untargeted metabolomics to analyze 625 serum metabolites in 33 patients after 4 weeks of CCB or ARB monotherapy.
- Utilized statistical screening (P < 0.05, fold change, variable importance) to identify differential metabolites.
Main Results:
- Identified 63 differential metabolites.
- ARBs affected cysteine and methionine, phenylalanine, taurine and hypotaurine, and tyrosine metabolism.
- CCBs uniquely impacted taurine and hypotaurine metabolism.
- Homocitrulline and glucosamine-6-phosphate levels correlated with achieving target blood pressure reduction.
Conclusions:
- Serum metabolite changes, particularly in specific pathways, are associated with CCB and ARB antihypertensive therapies.
- Identified metabolites may serve as potential markers for monitoring the efficacy and safety of antihypertensive drugs.
Abstract:
The high prevalence of hypertension contributes to an increased global burden of cardiovascular diseases. Calcium channel blockers (CCBs) and angiotensin type 1 receptor blockers (ARBs) are the most widely used antihypertensive drugs, and the effects of these drugs on serum metabolites remain unknown. Untargeted metabolomics has been proved to be a powerful approach for the detection of biomarkers and new compounds. In this study, we aimed to determine the changes in metabolites after single-drug therapy with a CCB or ARB in patients newly diagnosed with mild to moderate primary hypertension. We enrolled 33 patients and used an untargeted metabolomics approach to measure 625 metabolites associated with the response to a 4-week treatment of antihypertensive drugs. After screening based on P < 0.05, fold change > 1.2 or fold change < 0.83, and variable importance in projection > 1, 63 differential metabolites were collected. Four metabolic pathways-cysteine and methionine metabolism, phenylalanine metabolism, taurine and hypotaurine metabolism, and tyrosine metabolism-were identified in participants treated with ARBs. Only taurine and hypotaurine metabolism were identified in participants treated with CCBs. Furthermore, homocitrulline and glucosamine-6-phosphate were relevant to whether the blood pressure reduction achieved the target blood pressure (P < 0.05). Our study provides some evidence that changes in certain metabolites may be a potential marker for the dynamic monitoring of the protective effects and side effects of antihypertensive drugs.
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