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Title: | Association of serum high-sensitivity C-reactive protein with metabolic control and diabetic chronic vascular complications in patients with type 2 diabetes |
Authors: | Chuengsamarn S. Rattanamongkolgul S. Sittithumcharee G. Jirawatnotai S. |
Keywords: | C reactive protein glucose hemoglobin A1c high density lipoprotein cholesterol low density lipoprotein cholesterol triacylglycerol C reactive protein glycosylated hemoglobin hemoglobin A1c protein, human triacylglycerol adult Article cerebrovascular disease cholesterol blood level cohort analysis coronary artery disease diabetic nephropathy diabetic neuropathy diabetic patient diabetic retinopathy female glucose blood level hemoglobin blood level human laboratory test major clinical study male metabolic regulation middle aged non insulin dependent diabetes mellitus peripheral neuropathy priority journal triacylglycerol blood level aged blood complication diabetic angiopathy metabolism non insulin dependent diabetes mellitus Adult Aged Blood Glucose C-Reactive Protein Cohort Studies Diabetes Mellitus, Type 2 Diabetic Angiopathies Female Glycated Hemoglobin A Humans Male Middle Aged Triglycerides |
Issue Date: | 2017 |
Abstract: | Aims To determine an association between hs-CRP and metabolic control/diabetic chronic vascular complications (DCVCCxs) in the patients with type 2 diabetes (DM). In addition, the possibility of using hs-CRP levels to predict risk of DCVCCxs will also be validated. Methods This cohort study randomly enrolled 608 patients with DM during the 2007–2008 study period. We also recorded basic laboratory findings at baseline and at one year, to include fasting plasma glucose, HbA1c, triglyceride, total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and hs-CRP. Results Logistic regressions of odds ratios between hs-CRP and DCVCCxs (coronary arterial disease, cerebrovascular disease, diabetic nephropathy, diabetic retinopathy, and diabetic peripheral neuropathy) showed significant correlations, except for cerebrovascular disease, as follows 0.2 (0.11–0.38), 0.09 (0.01–0.77), 0.06 (0.02–0.16), 0.31 (0.12–0.82), and 0.17 (0.07–0.43), respectively. Linear regression for changes in hs-CRP were significantly correlated with HbA1c (r = 0.38), fasting plasma glucose (r = 0.40), triglyceride (r = 0.20), low-density lipoprotein cholesterol (r = 0.12), and high-density lipoprotein cholesterol (r = −0.12). No correlation was found for total cholesterol (r = 0.06). Based on receiver operating characteristic (ROC) analysis, the cut-off points for hs-CRP levels for prediction of DCVCCxs were 2.89, 2.25, 2.10, 2.25, and 2.82 mg/L, for coronary arterial disease, cerebrovascular disease, diabetic nephropathy, diabetic retinopathy, and diabetic peripheral neuropathy, respectively. Conclusions Our data showed that DCVCCxs were associated with hs-CRP in patients with DM. The cut-off point for hs-CRP can be used to predict association with DCVCCxs. Well-controlled metabolic components in diabetic patients, especially HbA1c, fasting plasma glucose, and triglyceride may reduce the level of hs-CRP. © 2016 Diabetes India |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/13106 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85008627653&doi=10.1016%2fj.dsx.2016.08.012&partnerID=40&md5=dc7e4bc70fe517b0c4cc10bc3e0ab2c0 |
ISSN: | 18714021 |
Appears in Collections: | Scopus 1983-2021 |
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