Key result
Hypertension and insulin resistance synergistically increase cardiovascular and diabetes risk via shared inflammatory mechanisms.
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Understanding the shared pathophysiological links between hypertension and insulin resistance is critical for designing therapies and preventive strategies against type 2 diabetes and cardiovascular disease.
Cardiovascular diseases and type 2 diabetes mellitus (T2DM) have risen steadily worldwide, particularly in low-income and developing countries. In the last hundred years, deaths caused by cardiovascular diseases increased rapidly to 35-40%, becoming the most common cause of mortality worldwide. Cardiovascular disease is the leading cause of morbidity and mortality in type 2 diabetes mellitus (T2DM), which is aggravated by hypertension. Hypertension and diabetes are closely interlinked since they have similar risk factors such as endothelial dysfunction, vascular inflammation, arterial remodeling, atherosclerosis, dyslipidemia, and obesity. Patients with high blood pressure often show insulin resistance and have a higher risk of developing diabetes than normotensive individuals. It has been observed that over the last 30 years, the prevalence of insulin resistance (IR) has increased significantly. Accordingly, hypertension and insulin resistance are strongly related to an increased risk of impaired glucose tolerance, diabetes, cardiovascular diseases (CVD), and endocrine disorders. Common mechanisms, for instance, upregulation of the renin-angiotensin-aldosterone system, oxidative stress, inflammation, and activation of the immune system, possibly have a role in the association between diabetes and hypertension. Altogether these abnormalities significantly increase the risk of developing type 2 diabetes.
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Sinha et al. (2022) conducted a review in Hypertension, Insulin Resistance, and Type 2 Diabetes Mellitus. Hypertension and Insulin Resistance was evaluated. Hypertension and insulin resistance share common pathophysiological mechanisms, including oxidative stress, inflammation, and RAAS upregulation, which synergistically increase the risk of cardiovascular disease and type 2 diabetes.
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