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[The association of high-sensitivity C-reactive protein with new-onset hypertension in different age groups]
1Graduate School of North China University of Science and Technology, Tangshan 063000, China.
Insights
Elevated high-sensitivity C-reactive protein (hsCRP) levels increase the risk of developing new-onset hypertension. This association is more pronounced in younger age groups, indicating an age-dependent risk.
Area of Science:
- Cardiovascular Medicine
- Inflammation Biomarkers
- Epidemiology
Context:
- Hypertension is a major global health concern with complex risk factors.
- Inflammation, indicated by high-sensitivity C-reactive protein (hsCRP), is increasingly recognized as a contributor to cardiovascular disease.
- Understanding the relationship between hsCRP and hypertension across different age demographics is crucial for targeted prevention strategies.
Purpose:
- To examine the association between baseline hsCRP levels and the incidence of new-onset hypertension.
- To investigate whether this association varies across different age strata.
- To quantify the risk of developing hypertension associated with elevated hsCRP levels in a prospective cohort.
Summary:
- A prospective cohort study of 51,179 non-hypertensive adults followed for 8.1 years found that higher hsCRP levels were associated with an increased risk of new-onset hypertension.
- The risk of developing hypertension was significantly higher in the high-risk hsCRP group (hsCRP > 3.0 mg/L) compared to the low-risk group (hsCRP < 1.0 mg/L), with a hazard ratio of 1.11.
- This association was age-dependent, with a stronger risk observed in younger age groups (<45, 45-54, 55-64 years) compared to those aged 65 and older.
Impact:
- Identifies hsCRP as a significant, age-dependent risk factor for incident hypertension.
- Suggests that hsCRP levels could aid in risk stratification for hypertension, particularly in middle-aged populations.
- Highlights the need for considering inflammatory markers in hypertension prevention and management strategies, tailored by age.
Abstract:
Objective: To investigate the association between high sensitivity C-reactive protein (hsCRP) level and new-onset hypertension in different age groups. Methods: This was a prospective cohort study involving non-hypertensive population in Kailuan Group community who participated in health examination between 2006 and 2007.Follow-up was conducted every 2 years, and the time of new onset of hypertension was used as the endpoint of follow-up. The endtime of follow-up for patients without hypertension was the time of death or the last follow-up (December 31, 2017).According to the baseline hsCRP level, the participants were divided into low-risk group (hsCRP<1.0 mg/L), medium-risk group (hsCRP ≥1.0 and ≤3.0 mg/L), and high-risk group (hsCRP>3.0 mg/L), and further stratified by age. Kaplan-Meier method was used to calculate the cumulative incidence of hypertension in each group. Multivariate Cox regression model was used to analyze the association between hsCRP level and new-onset hypertension. Results: A total of 51 179 participants were included in this study, including 38 606 males (75.43%) with an average age of (48.1±12.2) years. The baseline hsCRP was 0.64 (0.25, 1.60) mg/L. The baseline hsCRP was 0.30 (0.16, 0.59), 1.57 (1.20, 2.10), 5.17 (3.80, 7.10) mg/L respectively in low-, medium- and high-risk groups. During the follow-up of (8.1±2.2) years, a total of 9 523 (18.60%) patients developed hypertension, and the cumulative incidence rates of low-, medium- and high-risk groups were 17.41%, 20.48% and 20.73%, respectively. The cumulative incidence of hypertension in low-, medium- and high-risk groups of<45, 45-54, 55-64, ≥65 years old were 13.53%, 15.82%, 16.76%; 19.27%, 22.84%, 21.62%; 21.55%, 24.19%, 24.88%;20.20%, 22.35%, 19.11%, respectively. Except for people aged ≥65 years, there were significant differences in the cumulative incidence of hypertension in low-, medium- and high-risk groups (all P<0.05).Multivariate Cox regression analysis showed that the risk of new-onset hypertension in the high risk group was 1.11 times higher than that in the low risk group (HR=1.11, 95%CI 1.05-1.18). The risk of new-onset hypertension in the high-risk group was 1.22 times (HR=1.22, 95%CI 1.08-1.38), 1.14 times (HR=1.14, 95%CI 1.04-1.26), 1.16 times (HR=1.16, 95%CI 1.04-1.30), and 1.02 times (HR=1.02, 95%CI 0.86-1.20) of the low-risk group, in the<45, 45-54, 55-64, and ≥65 years old groups, respectively. Conclusion: Higher hsCRP level is a risk factor for new-onset hypertension, and the risk of developing hypertension caused by elevated hsCRP is age-dependent.
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