PMID- 30816670 OWN - NLM STAT- MEDLINE DCOM- 20190308 LR - 20190308 IS - 1421-9778 (Electronic) IS - 1015-8987 (Linking) VI - 52 IP - 2 DP - 2019 TI - The Effects of Adiponectin and Adiponectin Receptor 1 Levels on Macrovascular Complications Among Patients with Type 2 Diabetes Mellitus. PG - 225-231 LID - 10.33594/000000016 [doi] AB - BACKGROUND/AIMS: The present study aimed to investigate the serum levels of adiponectin (APN) and adiponectin receptor 1 (AdipoR1) in patients with type 2 diabetes mellitus (T2DM) combined with macrovascular complications (MVC), as well as their correlation with clinical parameters. METHODS: A total of 60 T2DM patients were divided into 2 groups according to the presence of MVC: T2DM + MVC group (n=30) and T2DM group (n=30). Additionally, 30 healthy people were selected as control group (NC group). Clinical data and biological parameters were detected and recorded. T test was performed to compare the differences between two groups, and the results were corrected using Bonferroni method. Meanwhile, the correlation analysis and multiple stepwise regression analysis were used to analyze the association of APN and AdipoR1 with clinical factors. RESULTS: The levels of APN and AdipoR1 were significantly decreased in T2DM group and T2DM + MVC group compared with NC group, with the lowest value in T2DM + MVC group (all P<0.01). Serum APN levels were positively correlated with FINS and TG (r = 0.412, 0.316, respectively; both P<0.05), and negatively correlated with SBP, DBP and LDL-C (r = -0.292, -0.383, -0.334, respectively; all P<0.05). Serum levels of AdipoR1 were positively correlated with APN (r = 0.726, P<0.01), and negatively correlated with BMI, SBP, DBP, FBG, TC and LDL-C (r = -0.440, -0.446, -0.374, -0.444, -0.344, -0.709, respectively; all P<0.01). CONCLUSION: Serum levels of APN and AdipoR1 are significantly lower in T2DM group and T2DM + MVC group, showing lowest value in T2DM + MVC group. APN and AdipoR1 levels may influence glucose and lipid metabolism in T2DM patients. CI - (c) Copyright by the Author(s). Published by Cell Physiol Biochem Press. FAU - Su, Na AU - Su N AD - Department of Second Endocrinology, Cangzhou Central Hospital, Cangzhou, China, sdourirr@163.com. FAU - Zhao, Nairui AU - Zhao N AD - Department of Second Endocrinology, Cangzhou Central Hospital, Cangzhou, China. FAU - Wang, Guangya AU - Wang G AD - Department of Second Endocrinology, Cangzhou Central Hospital, Cangzhou, China. FAU - Wang, Linxia AU - Wang L AD - Department of Second Endocrinology, Cangzhou Central Hospital, Cangzhou, China. FAU - Zhang, Yunna AU - Zhang Y AD - Department of Second Endocrinology, Cangzhou Central Hospital, Cangzhou, China. FAU - Li, Ruijie AU - Li R AD - Department of Second Endocrinology, Cangzhou Central Hospital, Cangzhou, China. FAU - Liu, Ying AU - Liu Y AD - Department of Second Ultrasound, Cangzhou Central Hospital, Cangzhou, China. FAU - Yang, Xinxin AU - Yang X AD - Department of Second Endocrinology, Cangzhou Central Hospital, Cangzhou, China. FAU - Li, Cuiliu AU - Li C AD - Department of Second Endocrinology, Cangzhou Central Hospital, Cangzhou, China. FAU - Hou, Mingming AU - Hou M AD - Department of Medical Records, Cangzhou Central Hospital, Cangzhou, China. LA - eng PT - Comparative Study PT - Journal Article PT - Randomized Controlled Trial DEP - 20190228 PL - Germany TA - Cell Physiol Biochem JT - Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology JID - 9113221 RN - 0 (ADIPOQ protein, human) RN - 0 (ADIPOR1 protein, human) RN - 0 (Adiponectin) RN - 0 (Blood Glucose) RN - 0 (Receptors, Adiponectin) SB - IM MH - Adiponectin/*blood MH - Blood Glucose/*metabolism MH - Diabetes Mellitus, Type 2/*blood MH - Diabetic Angiopathies/*blood MH - Female MH - Humans MH - *Lipid Metabolism MH - Male MH - Middle Aged MH - Receptors, Adiponectin/*blood OTO - NOTNLM OT - Adiponectin OT - Adiponectin receptor 1 OT - Macrovascular complications OT - Type 2 diabetes mellitus COIS- The authors declare to have no competing interests. EDAT- 2019/03/01 06:00 MHDA- 2019/03/09 06:00 CRDT- 2019/03/01 06:00 PHST- 2018/01/06 00:00 [received] PHST- 2019/02/22 00:00 [accepted] PHST- 2019/03/01 06:00 [entrez] PHST- 2019/03/01 06:00 [pubmed] PHST- 2019/03/09 06:00 [medline] AID - 10.33594/000000016 [doi] PST - ppublish SO - Cell Physiol Biochem. 2019;52(2):225-231. doi: 10.33594/000000016. Epub 2019 Feb 28.