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.

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