Metabolic Syndrome, Kidney-Related Adiposity, and Kidney Microcirculation: Unraveling the Damage
Metabolic syndrome (MetS) is a cluster of interrelated risk factors, including insulin resistance, hypertension, dyslipidemia, and visceral adiposity, all of which contribute to kidney microvascular injury and the progression of chronic kidney disease (CKD). However, the specific impact of each comp...
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MDPI AG
2024-11-01
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author | Kyu Won Jang Jin Hur Dong Won Lee Seo Rin Kim |
author_facet | Kyu Won Jang Jin Hur Dong Won Lee Seo Rin Kim |
author_sort | Kyu Won Jang |
collection | DOAJ |
description | Metabolic syndrome (MetS) is a cluster of interrelated risk factors, including insulin resistance, hypertension, dyslipidemia, and visceral adiposity, all of which contribute to kidney microvascular injury and the progression of chronic kidney disease (CKD). However, the specific impact of each component of MetS on kidney microcirculation remains unclear. Given the increasing prevalence of obesity, understanding how visceral fat—particularly fat surrounding the kidneys—affects kidney microcirculation is critical. This review examines the consequences of visceral obesity and other components of MetS on renal microcirculation. These kidney-related fat deposits can contribute to the mechanical compression of renal vasculature, promote inflammation and oxidative stress, and induce endothelial dysfunction, all of which accelerate kidney damage. Each factor of MetS initiates a series of hemodynamic and metabolic disturbances that impair kidney microcirculation, leading to vascular remodeling and microvascular rarefaction. The review concludes by discussing therapeutic strategies targeting the individual components of MetS, which have shown promise in alleviating inflammation and oxidative stress. Integrated approaches that address both of the components of MetS and kidney-related adiposity may improve renal outcomes and slow the progression of CKD. |
format | Article |
id | doaj-art-db71a7f93dbc44d686df688850b78d06 |
institution | Kabale University |
issn | 2227-9059 |
language | English |
publishDate | 2024-11-01 |
publisher | MDPI AG |
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series | Biomedicines |
spelling | doaj-art-db71a7f93dbc44d686df688850b78d062024-12-27T14:12:35ZengMDPI AGBiomedicines2227-90592024-11-011212270610.3390/biomedicines12122706Metabolic Syndrome, Kidney-Related Adiposity, and Kidney Microcirculation: Unraveling the DamageKyu Won Jang0Jin Hur1Dong Won Lee2Seo Rin Kim3Division of Nephrology and Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Republic of KoreaDivision of Nephrology and Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Republic of KoreaDivision of Nephrology and Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Republic of KoreaDivision of Nephrology and Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Yangsan 50612, Republic of KoreaMetabolic syndrome (MetS) is a cluster of interrelated risk factors, including insulin resistance, hypertension, dyslipidemia, and visceral adiposity, all of which contribute to kidney microvascular injury and the progression of chronic kidney disease (CKD). However, the specific impact of each component of MetS on kidney microcirculation remains unclear. Given the increasing prevalence of obesity, understanding how visceral fat—particularly fat surrounding the kidneys—affects kidney microcirculation is critical. This review examines the consequences of visceral obesity and other components of MetS on renal microcirculation. These kidney-related fat deposits can contribute to the mechanical compression of renal vasculature, promote inflammation and oxidative stress, and induce endothelial dysfunction, all of which accelerate kidney damage. Each factor of MetS initiates a series of hemodynamic and metabolic disturbances that impair kidney microcirculation, leading to vascular remodeling and microvascular rarefaction. The review concludes by discussing therapeutic strategies targeting the individual components of MetS, which have shown promise in alleviating inflammation and oxidative stress. Integrated approaches that address both of the components of MetS and kidney-related adiposity may improve renal outcomes and slow the progression of CKD.https://www.mdpi.com/2227-9059/12/12/2706metabolic syndromekidney microcirculationvisceral adipositykidney-related fat |
spellingShingle | Kyu Won Jang Jin Hur Dong Won Lee Seo Rin Kim Metabolic Syndrome, Kidney-Related Adiposity, and Kidney Microcirculation: Unraveling the Damage Biomedicines metabolic syndrome kidney microcirculation visceral adiposity kidney-related fat |
title | Metabolic Syndrome, Kidney-Related Adiposity, and Kidney Microcirculation: Unraveling the Damage |
title_full | Metabolic Syndrome, Kidney-Related Adiposity, and Kidney Microcirculation: Unraveling the Damage |
title_fullStr | Metabolic Syndrome, Kidney-Related Adiposity, and Kidney Microcirculation: Unraveling the Damage |
title_full_unstemmed | Metabolic Syndrome, Kidney-Related Adiposity, and Kidney Microcirculation: Unraveling the Damage |
title_short | Metabolic Syndrome, Kidney-Related Adiposity, and Kidney Microcirculation: Unraveling the Damage |
title_sort | metabolic syndrome kidney related adiposity and kidney microcirculation unraveling the damage |
topic | metabolic syndrome kidney microcirculation visceral adiposity kidney-related fat |
url | https://www.mdpi.com/2227-9059/12/12/2706 |
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