Cargando…
Hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events
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 met...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10597657/ https://www.ncbi.nlm.nih.gov/pubmed/37881599 http://dx.doi.org/10.1093/ehjopen/oead102 |
_version_ | 1785125390018150400 |
---|---|
author | Lembo, Maria Pacella, Daniela Manzi, Maria Virginia Morisco, Carmine La Mura, Lucia Mancusi, Costantino Bardi, Luca Trimarco, Valentina Trimarco, Bruno Izzo, Raffaele Esposito, Giovanni |
author_facet | Lembo, Maria Pacella, Daniela Manzi, Maria Virginia Morisco, Carmine La Mura, Lucia Mancusi, Costantino Bardi, Luca Trimarco, Valentina Trimarco, Bruno Izzo, Raffaele Esposito, Giovanni |
author_sort | Lembo, Maria |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10597657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-105976572023-10-25 Hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events Lembo, Maria Pacella, Daniela Manzi, Maria Virginia Morisco, Carmine La Mura, Lucia Mancusi, Costantino Bardi, Luca Trimarco, Valentina Trimarco, Bruno Izzo, Raffaele Esposito, Giovanni Eur Heart J Open Original Article 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. Oxford University Press 2023-10-04 /pmc/articles/PMC10597657/ /pubmed/37881599 http://dx.doi.org/10.1093/ehjopen/oead102 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Article Lembo, Maria Pacella, Daniela Manzi, Maria Virginia Morisco, Carmine La Mura, Lucia Mancusi, Costantino Bardi, Luca Trimarco, Valentina Trimarco, Bruno Izzo, Raffaele Esposito, Giovanni Hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events |
title | Hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events |
title_full | Hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events |
title_fullStr | Hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events |
title_full_unstemmed | Hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events |
title_short | Hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events |
title_sort | hypertension-mediated organ damage involving multiple sites is an independent risk factor for cardiovascular events |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10597657/ https://www.ncbi.nlm.nih.gov/pubmed/37881599 http://dx.doi.org/10.1093/ehjopen/oead102 |
work_keys_str_mv | AT lembomaria hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents AT pacelladaniela hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents AT manzimariavirginia hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents AT moriscocarmine hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents AT lamuralucia hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents AT mancusicostantino hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents AT bardiluca hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents AT trimarcovalentina hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents AT trimarcobruno hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents AT izzoraffaele hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents AT espositogiovanni hypertensionmediatedorgandamageinvolvingmultiplesitesisanindependentriskfactorforcardiovascularevents |