Key result
Baseline hs-CRP was associated with an increased risk of CHD events (HR 1.028; 95% CI 1.024-1.032) per standard deviation increment in patients with type 2 diabetes.
Why the study?
Does baseline hs-CRP predict coronary heart disease events and microvascular complications in patients with type 2 diabetes mellitus?
Cohort (n=1,301)
Does baseline hs-CRP predict coronary heart disease events and microvascular complications in patients with type 2 diabetes mellitus?
Hazard Ratio: 1.028 (95% CI 1.024–1.032)
Baseline hs-CRP improves risk discrimination and reclassification for both macrovascular and microvascular complications in patients with type 2 diabetes when added to traditional risk factors.
hs-CRP may refine CHD risk stratification in type 2 diabetes; leaves open causal effects and microvascular utility.
BACKGROUND/AIMS: This prospective study is aimed at examining the predictive value of high-sensitivity C-reactive protein (hs-CRP) for coronary heart disease (CHD) events and microvascular complications of type 2 diabetes mellitus (T2DM). METHODS: A population-based study (NCT02958579) was conducted on 1,301 participants with T2DM (mean follow-up of 7.5 years). Risk assessment for vascular events was done at baseline, and serum hs-CRP was measured. End points of this study include CHD events, diabetic retinopathy, neuropathy, and diabetic kidney disease. Individuals with unavailable data or hs-CRP >20 mg/L were excluded. The discrimination and reclassification improvement of study end points were tested after addition of hs-CRP to traditional risk factors. RESULTS: Median serum hs-CRP was 2.00 ranging from 0.1 to 17 mg/L. Hazards ratio of each SD increment in baseline hs-CRP was 1.028 (1.024-1.032) for CHD, 1.025 (1.021-1.029) for diabetic neuropathy, 1.037 (1.030-1.043) for diabetic retinopathy, and 1.035 (1.027-1.043) for diabetic kidney disease. The addition of hs-CRP to traditional risk factors of vascular complications of T2DM improved discrimination of all end points (p < 0.001). Net reclassification improvement ranged from 8% for diabetic neuropathy to 31% for diabetic kidney disease (p < 0.05). CONCLUSION: Baseline hs-CRP predicts both of CHD events and microvascular complications of patients with T2D.
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Aryan et al. (2018) conducted a cohort in Type 2 diabetes mellitus (n=1,301). Baseline high-sensitivity C-reactive protein (hs-CRP) was evaluated on CHD events (HR 1.028, 95% CI 1.024-1.032). Baseline hs-CRP was associated with an increased risk of CHD events (HR 1.028; 95% CI 1.024-1.032) per standard deviation increment in patients with type 2 diabetes.
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