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Published on: October 22, 2014
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.
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.
Aims:
Chronic pressure overload determines functional and structural alterations, leading to hypertension-mediated organ damage (HMOD), affecting multiple districts. We aim at evaluating the prognostic impact of the absence vs. presence of HMOD in one or more sites and of blood pressure (BP) and metabolic control in hypertensive patients.
Methods And Results:
The study included 7237 hypertensive patients from the Campania Salute Network Registry, followed up for 5.3 ± 4.5 years. As HMOD, we analysed the presence of left ventricular hypertrophy, carotid plaques, and chronic kidney disease (CKD-EPI ≥3 stage) and evaluated the impact of zero vs. one vs. two vs. three sites of HMOD on the occurrence of major adverse cardiovascular events (MACEs). Blood pressure control and Metabolic Score for Insulin Resistance (METS-IR) were also considered. Optimal BP control was achieved in 57.3% patients. Major adverse cardiovascular events occurred in 351 (4.8%) patients. The MACE rate in patients without HMOD was 2.7%, whereas it was 4.7, 7.9, and 9.8% in patients with one, two, and three sites with HMOD, respectively. By using Cox multivariate models, adjusted for age, BP control, mean heart rate, mean METS-IR, number of HMOD sites, and drugs, MACE was found to be significantly associated with ageing, mean METS-IR, anti-platelet therapy, and multiple sites with HMOD, whereas a negative association was found with renin-angiotensin system inhibitor drugs.
Conclusion:
In hypertensive patients, the risk of MACE increases with the incremental number of districts involved by HMOD, independent of BP control and despite the significant impact of metabolic dysregulation. Hypertension-mediated organ damage involving multiple sites is the deleterious consequence of hypertension and dysmetabolism but, when established, it represents an independent cardiovascular risk factor for MACE occurrence.
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