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Increased C-reactive protein is associated with future development of diabetes mellitus in essential hypertensive
Chiung-Mei Weng1, Chang-Hua Chou, Yao-Yi Huang
1Department of Internal Medicine, National Cheng Kung University Hospital Dou-Liou Branch, Taiwan.
Insights
High-sensitivity C-reactive protein (hsCRP) predicts new-onset diabetes mellitus (DM) in patients with essential hypertension. Elevated hsCRP, age, and baseline glucose are key risk factors for developing DM in this population.
Area of Science:
- Cardiology
- Endocrinology
- Inflammation Research
Background:
- Hypertension and diabetes mellitus (DM) significantly increase cardiovascular disease risk.
- Predictors for DM development in patients with essential hypertension are not well understood.
Purpose of the Study:
- To identify factors associated with new-onset DM in patients with essential hypertension.
- To investigate the role of high-sensitivity C-reactive protein (hsCRP) in predicting DM development.
Main Methods:
- Prospective study of 168 essential hypertensive patients without initial DM or complications.
- Baseline evaluation included demographics, blood pressure, BMI, antihypertensive agents, and serum hsCRP.
- Patients were followed for a mean of 32 months for the occurrence of new DM.
Main Results:
- 13.1% of patients developed new DM.
- New DM patients had higher baseline glucose, triglycerides, and hsCRP, with lower HDL.
- Multivariate analysis identified hsCRP, age, and baseline glucose as independent predictors of new DM.
Conclusions:
- High-sensitivity CRP is an independent predictor of future DM in essential hypertensive patients.
- Increased inflammation may play a crucial role in DM pathogenesis in hypertensive individuals.
- Early identification of inflammation markers could aid in DM prevention strategies.
Abstract:
Coexistence of hypertension and diabetes mellitus (DM) increases the risk of cardiovascular disease. However, factors associated with future development of DM have not been well elucidated in patients already having essential hypertension. This study prospectively included 168 patients (mean age 41 +/- 7 years, 112 men) with essential hypertension. All patients did not have DM and vascular or renal complications initially. Baseline demographic data, blood pressure, body mass index, and antihypertensive agents were carefully evaluated and serum high-sensitivity C-reactive protein (hsCRP) was measured at the beginning of the study. All of the patients were followed for at least 6 months. The study endpoint was occurrence of new DM. After a mean follow-up period of 32 +/- 10 months, 22 subjects (13.1%) developed new DM. Patients with new DM had higher baseline glucose (105.2 +/- 11.8 vs 94.2 +/- 8.0 mg/dl, P < 0.001), triglyceride level (213.7 +/- 112.4 vs 155.6 +/- 83.2 mg/dl, P = 0.04), log hsCRP (0.31 +/- 0.44 vs 0.19 +/- 0.25 mg/dl, P = 0.016), and lower high-density lipoprotein (40.2 +/- 7.8 vs 46.6 +/- 14.4 mg/dl, P = 0.045). Total cholesterol, low-density lipoprotein, homeostasis model assessment index, and adiponectin were not different in patients with or without new DM. Among antihypertensive agents, only use of beta-blocker was significantly associated with new DM (P = 0.008). Multivariate Cox regression analysis showed log hsCRP (hazard ratio [HR] 9.77, 95% confidence interval [CI] 2.97-32.10, P < 0.001), age (HR 1.21, 95% CI 1.06-1.38, P = 0.004), and baseline glucose level (HR 1.11, 95% CI 1.06-1.15, P < 0.001) to be independent predictors for occurrence of new DM. High-sensitivity CRP was an independent factor for future development of DM in essential hypertensive patients. Increased inflammation might have a key role in the pathogenesis of DM in hypertension.
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