Diabetes, Hypertension, and Cardiovascular Disease: Clinical Insights and Vascular Mechanisms
Open accessAbstract
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].”
From Navigating the potential of algal peptides: health effects, market applications, and scientific challenges (2026) · cites this paper as [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)
- PMC
- PMC5953551
- 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
- hybrid
- doi.org
- 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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