PMID- 17499233 OWN - NLM STAT- MEDLINE DCOM- 20070817 LR - 20221207 IS - 0009-9120 (Print) IS - 0009-9120 (Linking) VI - 40 IP - 11 DP - 2007 Jul TI - Association of serum levels of glycated albumin, C-reactive protein and tumor necrosis factor-alpha with the severity of coronary artery disease and renal impairment in patients with type 2 diabetes mellitus. PG - 810-6 AB - OBJECTIVES: This study aimed to determine whether elevated serum levels of glycated albumin, high-sensitivity C-reactive protein (hsCRP) and tumor necrosis factor (TNF)-alpha were related to an increased risk for coronary artery disease (CAD) and renal insufficiency in patients with type 2 diabetes mellitus (T2DM). DESIGN AND METHODS: Serum levels of glycated albumin, hsCRP, TNF-alpha and blood glycosylated hemoglobin A1c (HbA1c) were measured in 317 consecutive patients with T2DM and 309 normal controls. Patients with T2DM were grouped based upon coronary angiographic findings (Group I: 151 patients with normal coronary arteries; Group II: 166 patients with significant coronary stenosis [>70% luminal diameter narrowing]) and renal functional status evaluated by estimated creatinine clearance (CrCl) (normal renal function group: 187 patients with CrCl >90 mL/min; mild renal insufficiency group: 103 patients with CrCl 60-90 mL/min; moderate renal insufficiency group: 27 patients with CrCl 30-60 mL/min). Multivariate analysis was performed to determine independent risk factors for CAD and renal insufficiency in patients with T2DM. RESULTS: Serum levels of glycated albumin, hsCRP and TNF-alpha were significantly higher in Group II than in controls (P<0.01) and Group I (P<0.01). A significant difference was found in glycated albumin, hsCRP and TNF-alpha levels among diabetic patients with mild, moderate renal insufficiency and normal renal function (P<0.05). These biochemical measurements correlated significantly with number of diseased coronary vessels (P<0.01) and status of renal function (P<0.05). No difference existed in HbA1c levels between Group II and Group I, and among patients with various CrCL stages. Multivariate analysis revealed that male gender, old age and serum levels of glycated albumin, hsCRP, TNF-alpha and lipoprotein (a) were independent risk factors for CAD, and older age, hypertension and glycated albumin were for CrCl <60 mL/min in diabetes. CONCLUSIONS: Increased serum levels of glycated albumin, hsCRP and TNF-alpha are associated with the presence and severity of CAD and renal impairment in patients with T2DM. FAU - Lu, Lin AU - Lu L AD - Department of Cardiology, Rui Jin Hospital, Jiaotong University School of Medicine, Shanghai, PR China. FAU - Pu, Li Jin AU - Pu LJ FAU - Xu, Xue Wei AU - Xu XW FAU - Zhang, Qi AU - Zhang Q FAU - Zhang, Rui Yan AU - Zhang RY FAU - Zhang, Jian Sheng AU - Zhang JS FAU - Hu, Jian AU - Hu J FAU - Yang, Zheng Kun AU - Yang ZK FAU - Lu, An Kang AU - Lu AK FAU - Ding, Feng Hua AU - Ding FH FAU - Shen, Jie AU - Shen J FAU - Chen, Qiu Jin AU - Chen QJ FAU - Lou, Sheng AU - Lou S FAU - Fang, Dan Hong AU - Fang DH FAU - Shen, Wei Feng AU - Shen WF LA - eng PT - Journal Article DEP - 20070419 PL - United States TA - Clin Biochem JT - Clinical biochemistry JID - 0133660 RN - 0 (Glycated Hemoglobin A) RN - 0 (Glycation End Products, Advanced) RN - 0 (Serum Albumin) RN - 0 (Tumor Necrosis Factor-alpha) RN - 0 (hemoglobin A1c protein, human) RN - 9007-41-4 (C-Reactive Protein) RN - 0 (Glycated Serum Albumin) SB - IM MH - Aged MH - C-Reactive Protein/*metabolism MH - Coronary Artery Disease/*blood/pathology MH - Diabetes Mellitus, Type 2/*blood/pathology MH - Female MH - Glycated Hemoglobin/metabolism MH - Glycation End Products, Advanced MH - Humans MH - Kidney Diseases/*blood/pathology MH - Male MH - Middle Aged MH - Regression Analysis MH - Risk Factors MH - Serum Albumin/*metabolism MH - Tumor Necrosis Factor-alpha/*blood MH - Glycated Serum Albumin EDAT- 2007/05/15 09:00 MHDA- 2007/08/19 09:00 CRDT- 2007/05/15 09:00 PHST- 2007/01/31 00:00 [received] PHST- 2007/03/17 00:00 [revised] PHST- 2007/03/27 00:00 [accepted] PHST- 2007/05/15 09:00 [pubmed] PHST- 2007/08/19 09:00 [medline] PHST- 2007/05/15 09:00 [entrez] AID - S0009-9120(07)00163-4 [pii] AID - 10.1016/j.clinbiochem.2007.03.022 [doi] PST - ppublish SO - Clin Biochem. 2007 Jul;40(11):810-6. doi: 10.1016/j.clinbiochem.2007.03.022. Epub 2007 Apr 19.