# The Association Between Short-Term Blood Pressure Variability and Inflammation in Healthy Young Adults

## TL;DR

This study finds that diastolic blood pressure variability is linked to inflammation markers in healthy young adults, suggesting early cardiovascular risk.

## Contribution

The study identifies diastolic BPV as a novel marker of low-grade inflammation in young, healthy populations.

## Key findings

- Diastolic BPV is significantly associated with higher hs-CRP and TNF-α levels in young adults.
- No associations were found between BPV and IL-6 or IFN-γ markers.
- Both daytime and nighttime diastolic BPV show significant links to inflammation markers.

## Abstract

Blood pressure variability (BPV) is linked to cardiovascular disease (CVD) and systemic inflammation in adults, but its relevance in young, healthy populations remains unclear. This study examined the association between short-term BPV and inflammatory markers in 447 normotensive participants (mean age, 22.9 years) from the Georgia Stress and Heart (GSH) study, a cohort of Non-Hispanic Black and White individuals. Participants underwent 24 h ambulatory blood pressure monitoring and assessment of serum inflammatory markers, including hs-CRP, IFN-γ, IL-6, and TNF-α. BPV was quantified using average real variability (ARV), and generalized estimating equations (GEEs) were used to evaluate associations, adjusting for age, sex, race, and mean blood pressure. Diastolic BPV was significantly, positively associated with hs-CRP and TNF-α, whereas systolic BPV was not associated with any inflammatory marker. Specifically, 24 h diastolic BPV was positively associated with hs-CRP (p = 0.001) and TNF-α (p = 0.015), while daytime diastolic BPV was positively associated with hs-CRP (p = 0.002). Nighttime diastolic BPV was positively associated with both hs-CRP (p = 0.020) and TNF-α (p = 0.007). No significant associations were found between BPV and IL-6 or IFN-γ. These findings suggest diastolic BPV may be a marker of low-grade inflammation in healthy young adults and could represent an early cardiovascular risk factor that warrants longitudinal study.