Literature DB >> 22055258

High-sensitivity C-reactive protein: a novel cardiovascular risk predictor in type 2 diabetics with normal lipid profile.

Shilpa B Asegaonkar1, Amruta Marathe, Mangesh L Tekade, Laxmikant Cherekar, Jayashree Bavikar, Jayashree Bardapurkar, Rote Ajay.   

Abstract

BACKGROUND: India is the diabetic capital of the world. Coronary heart disease is a major cause of morbidity and mortality among diabetics. Type 2 diabetes mellitus and atherosclerosis are complex diseases sharing common antecedents like inflammation. High-sensitivity C-reactive protein (hs-CRP), an acute phase reactant protein, is a proinflammatory atherogenic circulating marker which can prove to be an independent cardiac risk predictor. AIM: The aim of the present study was to evaluate the role of hs-CRP as an independent cardiovascular risk marker among Indians with type 2 diabetes with normal lipid profile. SETTINGS AND
DESIGN: This was a case control study including 60 type 2 diabetics with normal lipid profile and 60 age- and sex-matched healthy controls.
MATERIALS AND METHODS: Twelve-hour fasting blood samples were collected from all the participants. Serum was assayed for hs-CRP and lipid profile. STATISTICAL ANALYSIS: Results were analyzed by unpaired t test.
RESULTS: We found elevated hs-CRP levels (4.8 ± 0.2, P < .0001) among cases compared to controls (0.9 ± 0.1). According to hs-CRP levels, seven cases were in the low-risk (< 1 mg/l), 32 in the moderate-risk (1-3 mg/l), and 21 in the high-risk (3-10 mg/l) group with mean values of hs-CRP of 0.7 ± 0.2, 1.75 ± 0.7, and 5.8 ± 1.4, respectively. Relative risk was 4.75 with odds ratio of 10.23 (95% confidence interval 8.8-11.23).
CONCLUSION: The study suggests that hs-CRP is an independent cardiac risk predictor even with normal lipid profile and can help measure additional risk. The American Heart Association stated that patients in the intermediate- and high-risk group may benefit from therapeutic lifestyle change and that cardiovascular event may be prevented.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 22055258     DOI: 10.1016/j.jdiacomp.2011.10.001

Source DB:  PubMed          Journal:  J Diabetes Complications        ISSN: 1056-8727            Impact factor:   2.852


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