Cited by 1,787Diabetes, Cardiovascular Risks, and LipoproteinsChronic Kidney Disease and DiabetesBlood Pressure and Hypertension Studies

Diabetes, Hypertension, and Cardiovascular Disease: Clinical Insights and Vascular Mechanisms

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Petrie, John R., Guzik, Tomasz J., Touyz, Rhian M.·2018·Canadian Journal of Cardiology

Abstract

Hypertension and type 2 diabetes are common comorbidities. Hypertension is twice as frequent in patients with diabetes compared with those who do not have diabetes. Moreover, patients with hypertension often exhibit insulin resistance and are at greater risk of diabetes developing than are normotensive individuals. The major cause of morbidity and mortality in diabetes is cardiovascular disease, which is exacerbated by hypertension. Accordingly, diabetes and hypertension are closely interlinked because of similar risk factors, such as endothelial dysfunction, vascular inflammation, arterial remodelling, atherosclerosis, dyslipidemia, and obesity. There is also substantial overlap in the cardiovascular complications of diabetes and hypertension related primarily to microvascular and macrovascular disease. Common mechanisms, such as upregulation of the renin-angiotensin-aldosterone system, oxidative stress, inflammation, and activation of the immune system likely contribute to the close relationship between diabetes and hypertension. In this article we discuss diabetes and hypertension as comorbidities and discuss the pathophysiological features of vascular complications associated with these conditions. We also highlight some vascular mechanisms that predispose to both conditions, focusing on advanced glycation end products, oxidative stress, inflammation, the immune system, and microRNAs. Finally, we provide some insights into current therapies targeting diabetes and cardiovascular complications and introduce some new agents that may have vasoprotective therapeutic potential in diabetes.

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  • Chronic conditions including obesity, cardiovascular disorders, type 2 diabetes, and hypertension are closely interconnected through shared pathological mechanisms such as persistent low-grade inflammation, oxidative stress, and metabolic dysfunction.

    “These chronic conditions are closely interconnected through shared pathological mechanisms such as persistent low-grade inflammation, oxidative stress, and metabolic dysfunction [35].”

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References 122 · Cited by 1,787

Authors
Petrie, J. R., Guzik, T. J., & Touyz, R. M.
Affiliations
University of Glasgow (GB)
Corresponding author
Touyz, Rhian M.
Venue
Canadian Journal of Cardiology
Publisher
Elsevier BV
Published
2018-05
Volume
34
Issue
5
Pages
575-584
ISSN
0828-282X (ISSN-L)
OpenAlex
W2775794168
Cited by
1,787
References
122
Citations by year
2026: 100 · 2025: 265 · 2024: 357 · 2023: 334 · 2022: 272 · 2021: 248 · 2020: 146 · 2019: 52 · 2018: 10 · 2015: 1
FWCI
8.29
Type
journal article
Language
en
Open access
Locations
  • Canadian Journal of Cardiology (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (acceptedVersion, cc-by-sa)
Funders
  • Wellcome Trust
  • British Heart Foundation (RG/13/7/30099, 30099, RE/13/5/30177)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes, Cardiovascular Risks, and Lipoproteins
  • Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Blood Pressure and Hypertension Studies
Keywords
type 2 diabetes, hypertension, cardiovascular disease, comorbidities, insulin resistance, endothelial dysfunction, vascular inflammation, arterial remodeling, atherosclerosis, dyslipidemia, obesity, microangiopathy, macroangiopathy, renin-angiotensin-aldosterone system, oxidative stress, advanced glycation end products, microRNA
MeSH terms
Blood Vessels, Diabetes Mellitus, Type 2, Humans, Hypertension, Inflammation, Oxidative Stress, Disease Management, MicroRNAs

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