Cytokines, C-Reactive Protein, and Risk of Incident Hypertension in the REGARDS Study

Author:

Plante Timothy B.1ORCID,Juraschek Stephen P.2ORCID,Howard George3ORCID,Howard Virginia J.4ORCID,Tracy Russell P.5ORCID,Olson Nels C.5ORCID,Judd Suzanne E.3ORCID,Kamin Mukaz Debora1ORCID,Zakai Neil A.15ORCID,Long D. Leann6ORCID,Cushman Mary15ORCID

Affiliation:

1. Departments of Medicine (T.B.P., D.K.M., N.A.Z., M.C.), Larner College of Medicine at the University of Vermont, Burlington, VT.

2. Department of Medicine, Beth Israel Lahey Clinic/Harvard Medical School, Boston, MA (S.P.J).

3. Departments of Biostatistics (G.H., S.E.J.), School of Public Health, University of Alabama at Birmingham, Birmingham, AL.

4. Epidemiology (V.J.H.), School of Public Health, University of Alabama at Birmingham, Birmingham, AL.

5. Pathology and Laboratory Medicine (R.P.T., N.C.O., N.A.Z., M.C.), Larner College of Medicine at the University of Vermont, Burlington, VT.

6. Department of Biostatistics and Data Science, Wake Forest University School of Medicine, Winston-Salem, NC (D.L.L.).

Abstract

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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