Hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events

Maria Lembo1, Daniela Pacella2, Maria Virginia Manzi1

  • 1Department of Advanced Biomedical Sciences, Federico II University of Naples, Via S. Pansini 5, 80131 Napoli, Italy.

PubMed

Insights

Hypertension-mediated organ damage (HMOD) in multiple sites significantly increases major adverse cardiovascular events (MACE) risk in hypertensive patients. Metabolic dysregulation also contributes to this increased cardiovascular risk.

Area of Science:

  • Cardiology
  • Nephrology
  • Endocrinology

Background:

  • Chronic pressure overload leads to hypertension-mediated organ damage (HMOD) affecting multiple organs.
  • HMOD is a significant contributor to cardiovascular morbidity and mortality in hypertensive individuals.

Purpose of the Study:

  • To evaluate the prognostic impact of HMOD presence and extent on major adverse cardiovascular events (MACE).
  • To assess the role of blood pressure and metabolic control in hypertensive patients with HMOD.

Main Methods:

  • Analysis of 7237 hypertensive patients from the Campania Salute Network Registry.
  • Evaluation of HMOD in left ventricular hypertrophy, carotid plaques, and chronic kidney disease.
  • Utilized Cox multivariate models to assess associations with MACE, adjusting for clinical factors.

Main Results:

  • MACE rates increased with the number of HMOD sites: 2.7% (no HMOD) to 9.8% (three sites).
  • Major adverse cardiovascular events were significantly associated with age, metabolic dysregulation (METS-IR), and multiple HMOD sites.
  • Optimal blood pressure control was achieved in 57.3% of patients.

Conclusions:

  • The risk of MACE escalates with the number of HMOD sites, independent of blood pressure control.
  • Hypertension-mediated organ damage involving multiple sites is an independent risk factor for MACE.
  • Metabolic dysregulation significantly contributes to cardiovascular risk in hypertensive patients with HMOD.
Abstract

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