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Beta-adrenergic receptor mediated inflammation control by monocytes is associated with blood pressure and risk
Suzi Hong1, Stoyan Dimitrov2, Tiefu Cheng2
1Department of Psychiatry, University of California San Diego, USA; Department of Family Medicine and Public Health, University of California San Diego, USA.
Insights
Prehypertension is linked to reduced beta-adrenergic receptor-mediated inflammation control (BARIC) in monocytes, indicating increased cardiovascular disease risk. This inflammation dysregulation is associated with traditional risk factors, even at lower blood pressure levels.
Area of Science:
- Immunology
- Cardiovascular Science
- Endocrinology
Background:
- Individuals with mildly elevated blood pressure (prehypertension) face significant risks for hypertension and cardiovascular disease (CVD).
- Pathophysiology and clinical outcome mechanisms of prehypertension remain incompletely understood.
- Beta-adrenergic receptor (BAR)-mediated inflammation control (BARIC) in monocytes is a potential biomarker for CVD risk.
Purpose of the Study:
- To investigate BARIC responses in blood monocytes to isoproterenol (Iso) in prehypertensive versus normotensive individuals.
- To examine the relationship between BARIC and cardiovascular disease risk factors, including blood pressure, obesity, mood, and metabolic/lipid profiles.
Main Methods:
- Monocyte intracellular TNF production was measured after lipopolysaccharide stimulation and ex vivo Iso treatment.
- Blood pressure, obesity (BMI), depressive mood (BDI), fasting glucose, lipid panels, and plasma cytokines were assessed.
- BARIC was quantified as the inhibition of TNF production by Iso.
Main Results:
- Prehypertensive participants were older, heavier, and had higher glucose, triglycerides, cholesterol, and TNF levels than normotensive individuals.
- BARIC was significantly attenuated in prehypertensive individuals compared to normotensive controls.
- BARIC was negatively associated with systolic BP, diastolic BP, age, BMI, glucose, lipids, and depressive symptoms across all participants.
Conclusions:
- Attenuated BARIC in prehypertension suggests inflammation dysregulation mediated by sympathoadrenal activation.
- BARIC may serve as a sensitive indicator of vascular inflammatory disease risk, detectable even at lower blood pressure levels.
- Findings highlight the link between inflammation, sympathoadrenal activity, and blood pressure, even in individuals with normal to mildly elevated BP.
Abstract:
Overwhelming data indicate that individuals with even mildly elevated blood pressure (BP) are at great risk for developing clinical hypertension and future cardiovascular disease (CVD). There remains a lack of consensus regarding treatment strategies for mildly elevated BP, termed prehypertension, and the knowledge of pathophysiology and mechanisms of its clinical outcomes remains limited. Our primary aim was to investigate βAR-mediated inflammation control (BARIC) responses of blood monocytes to isoproterenol (Iso) in relation to BP and CVD risk factors, including obesity, depressive mood, fasting glucose, triglycerides, and cholesterol levels in the 64 prehypertensive compared to 84 individuals with normal BP. BARIC was determined by measuring the degree of inhibition in lipopolysaccharides-stimulated monocytic intracellular TNF production by ex vivo Iso treatment (10(-8)M). Depressive mood was assessed by Beck Depression Inventory (BDI). Fasting metabolic and lipid panels were assessed, and plasma levels of inflammatory cytokines TNF, IL-1β, IL-6 were measured in a subset to confirm proinflammatory state of prehypertensive participants. Prehypertensive participants were older, heavier, included more men, and presented higher levels of fasting glucose, triglycerides, cholesterol, and plasma TNF compared to normotensive participants (p's<.05). BARIC was significantly attenuated in the prehypertensive compared to normotensive group (p<.05). BARIC was negatively associated with systolic BP, diastolic BP, age, BMI, fasting glucose, triglycerides, total and low density cholesterol levels, and somatic depressive symptoms in all participants (p's<.0001 to .05). However, among the prehypertensive individuals BARIC was positively associated with SBP even after controlling for the covariates (age, gender, race, BMI, glucose and lipid panel, somatic BDI scores) (p<.05). This differing nature of the BARIC-SBP relationship between the two BP groups may be attributed to moderating factors such as cardiorespiratory fitness or depressive symptoms that could not be clearly deciphered in this current study. Nonetheless, our findings indicate the associations between inflammation dysregulation mediated by sympathoadrenal activation and BP that is observable even among individuals with normal to mildly elevated BP. BARIC may be a useful and sensitive indicator of elevated risk for vascular inflammatory disease that can be detected even at lower BP levels, especially given its associations with traditional CVD risk factors and the critical role of monocytes in atherogenic processes.
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