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Cytokines, C-Reactive Protein, and Risk of Incident Hypertension in the REGARDS Study
Timothy B Plante1, Stephen P Juraschek2, George Howard3
1Departments of Medicine (T.B.P., D.K.M., N.A.Z., M.C.), Larner College of Medicine at the University of Vermont, Burlington, VT.
Insights
Higher levels of interleukin-1β, tumor necrosis factor-α, and interferon-γ are linked to increased hypertension risk. These inflammatory markers may predict future high blood pressure development.
Area of Science:
- Cardiovascular Disease Epidemiology
- Inflammatory Biomarkers and Hypertension
- Public Health and Chronic Disease Prevention
Background:
- Hypertension is a major cardiovascular disease risk factor.
- Inflammation is implicated in hypertension development.
- The specific relationship between inflammatory cytokines and hypertension risk is not fully understood.
Purpose of the Study:
- To investigate the association between elevated levels of specific inflammatory cytokines and the risk of developing hypertension.
- To examine whether interleukin (IL)-1β, IL-6, tumor necrosis factor (TNF)-α, interferon (IFN)-γ, IL-17A, and C-reactive protein (CRP) predict incident hypertension.
Main Methods:
- Prospective cohort study (REGARDS) with 1866 participants without prevalent hypertension.
- Follow-up assessment approximately 9 years after baseline.
- Poisson regression used to estimate risk ratios for incident hypertension based on inflammatory biomarker levels.
Main Results:
- Higher levels of IL-1β were associated with increased hypertension risk in White participants.
- Elevated TNF-α and IFN-γ levels were associated with a greater risk of incident hypertension in all participants.
- No significant association was found between IL-6, IL-17A, or CRP levels and the risk of developing hypertension.
Conclusions:
- Elevated levels of IL-1β, TNF-α, and IFN-γ precede hypertension development, indicating distinct inflammatory pathways.
- These findings suggest potential biomarkers for hypertension risk prediction.
- Further research is needed to determine if targeting these cytokines can reduce hypertension incidence.
Background:
Hypertension is a highly prevalent cardiovascular disease risk factor that may be related to inflammation. Whether adverse levels of specific inflammatory cytokines relate to hypertension is unknown. The present study sought to determine whether higher levels of IL (interleukin)-1β, IL-6, TNF (tumor necrosis factor)-α, IFN (interferon)-γ, IL-17A, and CRP (C-reactive protein) are associated with a greater risk of incident hypertension.
Methods:
The REGARDS study (Reasons for Geographic and Racial Difference in Stroke) is a prospective cohort study that recruited 30 239 community-dwelling Black and White adults from the contiguous United States in 2003 to 2007 (visit 1), with follow-up 9 years later in 2013 to 2016 (visit 2). We included participants without prevalent hypertension who attended follow-up 9 years later and had available laboratory measures and covariates of interest. Poisson regression estimated the risk ratio of incident hypertension by level of inflammatory biomarkers.
Results:
Among 1866 included participants (mean [SD] aged of 62 [8] years, 25% Black participants, 55% women), 36% developed hypertension. In fully adjusted models comparing the third to first tertile of each biomarker, there was a greater risk of incident hypertension for higher IL-1β among White (1.24 [95% CI, 1.01-1.53]) but not Black participants (1.01 [95% CI, 0.83-1.23]) and higher TNF-α (1.20 [95% CI, 1.02-1.41]) and IFN-γ (1.22 [95% CI, 1.04-1.42]) among all participants. There was no increased risk with IL-6, IL-17A, or CRP.
Conclusions:
Higher levels of IL-1β, TNF-α, and IFN-γ, representing distinct inflammatory pathways, are elevated in advance of hypertension development. Whether modifying these cytokines will reduce incident hypertension is unknown.
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