PMID- 31425951 OWN - NLM STAT- MEDLINE DCOM- 20200212 LR - 20200212 IS - 1878-0334 (Electronic) IS - 1871-4021 (Linking) VI - 13 IP - 5 DP - 2019 Sep-Oct TI - Effects of vitamin D supplementation on circulatory YKL-40 and MCP-1 biomarkers associated with vascular diabetic complications: A randomized, placebo-controlled, double-blind clinical trial. PG - 2873-2877 LID - S1871-4021(19)30449-7 [pii] LID - 10.1016/j.dsx.2019.07.047 [doi] AB - AIM: Diabetic patients predispose to vascular diseases such as nephropathy, and retinopathy. Poor adherence to medical treatment and dietary recommendations in uncontrolled diabetes leads to vascular damages. Vitamin D has been extensively studied and found to be protective against diabetes mellitus. YKL-40 and Monocyte chemoattractant protein-1 (MCP-1) are considered to exert crucial role in diabetes and its complications. Therefore, this study was designed to investigate effects of vitamin D supplementation on serum levels of YKL-40 and MCP-1 involved in the development of diabetic complications. METHODS: For 12 weeks, 48 type 2 diabetic patients enrolled in the trial and randomly were divided into two groups (n = 24 per group), receiving one of the following: 100 mug (4000 IU) vitamin D or placebo. Before and after intervention, serumYKL-40, MCP-1, insulin, IL-6, TNF-alpha, 25- (OH) vitamin D and HbA1c were measured. RESULTS: Our results revealed that serum levels of 25 (OH) vitamin D significantly increased in vitamin D group (p < 0.001). Vitamin D supplementation also significantly reduced serum YKL-40 levels (-22.7 vs. -2.4 ng/ml; (p-value = 0.003)). There was a significant decline in MCP-1 concentration in intervention group at the end of the study (-45.7 vs. -0.9 pg/ml; (p = 0.001)). Furthermore, there was a significant decrease in IL-6, fasting insulin and HOMA-IR in intervention group after 3 months supplementation. CONCLUSIONS: Daily vitamin D supplementation effectively reduced circulatory YKL-40 and MCP-1 levels in patients with type-2 diabetes and vitamin D deficiency. Vitamin D might contribute in reducing diabetic complications via modulating YKL-40 and MCP-1 signaling pathways. CI - Copyright (c) 2019. Published by Elsevier Ltd. FAU - Omidian, Mahsa AU - Omidian M AD - Department of Cellular and Molecular Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran. FAU - Mahmoudi, Maryam AU - Mahmoudi M AD - Department of Cellular and Molecular Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran. FAU - Javanbakht, Mohammad Hassan AU - Javanbakht MH AD - Department of Cellular and Molecular Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran. FAU - Eshraghian, Mohammad Reza AU - Eshraghian MR AD - Department of Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran. FAU - Abshirini, Maryam AU - Abshirini M AD - Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran. FAU - Daneshzad, Elnaz AU - Daneshzad E AD - Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran. FAU - Hasani, Hossein AU - Hasani H AD - Department of Community Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran. FAU - Alvandi, Ehsan AU - Alvandi E AD - Department of Cellular and Molecular Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran. FAU - Djalali, Mahmoud AU - Djalali M AD - Department of Cellular and Molecular Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran. Electronic address: Jalalikh@sina.tums.ac.ir. LA - eng PT - Journal Article PT - Randomized Controlled Trial DEP - 20190729 PL - Netherlands TA - Diabetes Metab Syndr JT - Diabetes & metabolic syndrome JID - 101462250 RN - 0 (Biomarkers) RN - 0 (CCL2 protein, human) RN - 0 (CHI3L1 protein, human) RN - 0 (Chemokine CCL2) RN - 0 (Chitinase-3-Like Protein 1) RN - 0 (Vitamins) RN - 1406-16-2 (Vitamin D) SB - IM MH - Adult MH - Biomarkers/*blood MH - Chemokine CCL2/*blood MH - Chitinase-3-Like Protein 1/*blood MH - Diabetes Mellitus, Type 2/*complications MH - Diabetic Angiopathies/*blood/drug therapy/etiology MH - Dietary Supplements MH - Double-Blind Method MH - Female MH - Follow-Up Studies MH - Humans MH - Male MH - Middle Aged MH - Prognosis MH - Vitamin D/*administration & dosage MH - Vitamin D Deficiency/blood/*drug therapy/physiopathology MH - Vitamins/administration & dosage OTO - NOTNLM OT - Diabetic complications OT - Inflammation OT - Monocyte chemoattractant protein-1 OT - Vitamin D OT - YKL-40 EDAT- 2019/08/20 06:00 MHDA- 2020/02/13 06:00 CRDT- 2019/08/20 06:00 PHST- 2019/06/30 00:00 [received] PHST- 2019/07/29 00:00 [accepted] PHST- 2019/08/20 06:00 [pubmed] PHST- 2020/02/13 06:00 [medline] PHST- 2019/08/20 06:00 [entrez] AID - S1871-4021(19)30449-7 [pii] AID - 10.1016/j.dsx.2019.07.047 [doi] PST - ppublish SO - Diabetes Metab Syndr. 2019 Sep-Oct;13(5):2873-2877. doi: 10.1016/j.dsx.2019.07.047. Epub 2019 Jul 29.