PMID- 25409499 OWN - NLM STAT- MEDLINE DCOM- 20150713 LR - 20220409 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 9 IP - 11 DP - 2014 TI - Low serum cartonectin/CTRP3 concentrations in newly diagnosed type 2 diabetes mellitus: in vivo regulation of cartonectin by glucose. PG - e112931 LID - 10.1371/journal.pone.0112931 [doi] LID - e112931 AB - OBJECTIVES: Cartonectin is a novel adipokine of the C1q complement/TNF-related protein (CTRP) superfamily, with glucose lowering effects, anti-inflammatory and cardio-protective properties. We sought to investigate circulating cartonectin concentrations in subjects with type 2 diabetes mellitus (T2DM) as well as age and BMI matched control subjects. We also examined the effects of a 2 hour 75 g oral glucose tolerance test (OGTT) on serum cartonectin concentrations in T2DM subjects. DESIGN: Cross-sectional study [newly diagnosed (first discovery, not on any treatments) T2DM (n = 47) and control (n = 63) subjects]. Serum cartonectin was measured by ELISA. RESULTS: Serum cartonectin concentrations were significantly lower in patients with T2DM compared to controls (P<0.05). Furthermore, serum cartonectin was significantly negatively correlated with glucose and CRP, and significantly positively correlated with leptin, in all subjects (n = 110). When subjected to multiple regression analysis, none of these variables were predictive of serum cartonectin (P>0.05). There were no significant correlations in T2DM subjects (n = 47). In control subjects (n = 63), serum cartonectin was significantly negatively correlated with CRP, and significantly positively correlated with insulin, HOMA-IR and leptin. However, when subjected to multiple regression analysis, none of these variables were predictive of serum cartonectin (P>0.05). Finally, serum cartonectin concentrations were significantly lower in T2DM subjects after a 2 hour 75 g OGTT (P<0.01). CONCLUSIONS: Cartonectin may serve as a novel biomarker for the prediction and early diagnosis of T2DM patients. Furthermore, cartonectin and/or pharmacological agents that increase circulating cartonectin levels can represent a new therapeutic field in the treatment of T2DM patients. Further research is needed to clarify these points. FAU - Ban, Bo AU - Ban B AD - Department of Endocrine and Metabolic Diseases, Jining Medical College Affiliated Hospital, Jining Medical University, Jining, Shandong, P.R. of China. FAU - Bai, Bo AU - Bai B AD - Neurobiology Institute, Jining Medical University, Jining, Shandong, P.R. of China. FAU - Zhang, Manman AU - Zhang M AD - Department of Endocrine and Metabolic Diseases, Jining Medical College Affiliated Hospital, Jining Medical University, Jining, Shandong, P.R. of China; School of Medicine, Shandong University, Jinan, Shandong, P.R. of China. FAU - Hu, Jiamiao AU - Hu J AD - Warwick Medical School, University of Warwick, Coventry, West Midlands, United Kingdom. FAU - Ramanjaneya, Manjunath AU - Ramanjaneya M AD - Warwick Medical School, University of Warwick, Coventry, West Midlands, United Kingdom. FAU - Tan, Bee K AU - Tan BK AD - Warwick Medical School, University of Warwick, Coventry, West Midlands, United Kingdom; Department of Obstetrics and Gynaecology, Birmingham Heartlands and Solihull Hospitals, Heart of England NHS Foundation Trust, Birmingham, West Midlands, United Kingdom. FAU - Chen, Jing AU - Chen J AD - Neurobiology Institute, Jining Medical University, Jining, Shandong, P.R. of China; Warwick Medical School, University of Warwick, Coventry, West Midlands, United Kingdom. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20141119 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Biomarkers) RN - 0 (C1QTNF3 protein, human) RN - 0 (Tumor Necrosis Factors) RN - IY9XDZ35W2 (Glucose) SB - IM MH - Adult MH - Biomarkers/*blood MH - Cross-Sectional Studies MH - Diabetes Mellitus, Type 2/*blood/diagnosis MH - Female MH - Glucose/administration & dosage/*metabolism MH - Glucose Tolerance Test MH - Humans MH - Male MH - Middle Aged MH - Tumor Necrosis Factors/*blood PMC - PMC4237345 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2014/11/20 06:00 MHDA- 2015/07/15 06:00 PMCR- 2014/11/19 CRDT- 2014/11/20 06:00 PHST- 2014/06/12 00:00 [received] PHST- 2014/10/16 00:00 [accepted] PHST- 2014/11/20 06:00 [entrez] PHST- 2014/11/20 06:00 [pubmed] PHST- 2015/07/15 06:00 [medline] PHST- 2014/11/19 00:00 [pmc-release] AID - PONE-D-14-26284 [pii] AID - 10.1371/journal.pone.0112931 [doi] PST - epublish SO - PLoS One. 2014 Nov 19;9(11):e112931. doi: 10.1371/journal.pone.0112931. eCollection 2014.