PMID- 27397060 OWN - NLM STAT- MEDLINE DCOM- 20170614 LR - 20181202 IS - 1880-3873 (Electronic) IS - 1340-3478 (Print) IS - 1340-3478 (Linking) VI - 24 IP - 2 DP - 2017 Feb 1 TI - Effect of Glycemic Control on Chylomicron Metabolism and Correlation between Postprandial Metabolism of Plasma Glucose and Chylomicron in Patients with Type 2 Diabetes Treated with Basal-bolus Insulin Therapy with or without Vildagliptin. PG - 157-168 LID - 10.5551/jat.32409 [doi] AB - AIM: Glucagon-like peptide-1 can reduce both postprandial plasma glucose (PG) and chylomicron (CM) levels in patients with type 2 diabetes. However, there have been no reports regarding the relationship between the postprandial metabolism of PG and CM. METHODS: Patients with type 2 diabetes who were admitted for glycemic control were randomized to insulin alone (Ins; n=16) or insulin plus vildagliptin 100 mg (InsV; n=16) groups. The insulin dose was adjusted to maintain normal blood glucose levels. The daily profiles of serum TG, remnant lipoprotein cholesterol (RemL-C), and apolipoprotein B48 (ApoB48) were estimated by frequent blood collection on admission and before discharge, and the daily glucose fluctuation profile was also estimated using continuous glucose monitoring (CGM) before discharge. RESULTS: The daily profiles of serum TG and RemL-C indicated a significant decrease before discharge compared with on admission; however, no significant changes in serum ApoB48 levels were observed in either group. At discharge, daily glucose fluctuation profile and the change in the serum ApoB48 level from fasting to the peak of the daily profile was significantly smaller in the InsV group than in the Ins group. The increment of serum ApoB48 level was significantly correlated with the mean amplitude of glycemic excursions calculated using CGM data only in the Ins group (R(2)= 0.5242,P<0.001). CONCLUSIONS: Short-term glycemic control decreased serum TG and RemL-C levels, but not ApoB48 levels, and the postprandial metabolism of PG and CM might be regulated by the same mechanism except GLP-1 effect. FAU - Okajima, Fumitaka AU - Okajima F AD - Division of Endocrinology, Department of Medicine, Chiba-Hokusoh Hospital, Nippon Medical School. FAU - Emoto, Naoya AU - Emoto N FAU - Kato, Katsuhito AU - Kato K FAU - Sugihara, Hitoshi AU - Sugihara H LA - eng PT - Comparative Study PT - Journal Article PT - Randomized Controlled Trial DEP - 20160708 PL - Japan TA - J Atheroscler Thromb JT - Journal of atherosclerosis and thrombosis JID - 9506298 RN - 0 (Apolipoprotein B-48) RN - 0 (Biomarkers) RN - 0 (Blood Glucose) RN - 0 (Chylomicrons) RN - 0 (Dipeptidyl-Peptidase IV Inhibitors) RN - 0 (Hypoglycemic Agents) RN - 0 (Insulin) RN - 0 (Lipoproteins) RN - 0 (Nitriles) RN - 0 (Pyrrolidines) RN - 0 (Triglycerides) RN - 0 (lipoprotein cholesterol) RN - 97C5T2UQ7J (Cholesterol) RN - I6B4B2U96P (Vildagliptin) RN - PJY633525U (Adamantane) SB - IM MH - Adamantane/*analogs & derivatives/pharmacology MH - Adult MH - Aged MH - Apolipoprotein B-48/metabolism MH - Biomarkers/*blood MH - Blood Glucose/*metabolism MH - Cholesterol/metabolism MH - Chylomicrons/*metabolism MH - Diabetes Mellitus, Type 2/drug therapy/*metabolism MH - Dipeptidyl-Peptidase IV Inhibitors/pharmacology MH - Drug Therapy, Combination MH - Fasting MH - Female MH - Follow-Up Studies MH - Glycemic Index MH - Humans MH - Hypoglycemic Agents/pharmacology MH - Insulin/*pharmacology MH - Lipoproteins/metabolism MH - Male MH - Middle Aged MH - Nitriles/*pharmacology MH - *Postprandial Period MH - Prognosis MH - Pyrrolidines/*pharmacology MH - Triglycerides/metabolism MH - Vildagliptin MH - Young Adult PMC - PMC5305676 COIS- All authors declare no conflict of interest. EDAT- 2016/07/12 06:00 MHDA- 2017/06/15 06:00 PMCR- 2017/02/01 CRDT- 2016/07/12 06:00 PHST- 2016/07/12 06:00 [pubmed] PHST- 2017/06/15 06:00 [medline] PHST- 2016/07/12 06:00 [entrez] PHST- 2017/02/01 00:00 [pmc-release] AID - 10.5551/jat.32409 [doi] PST - ppublish SO - J Atheroscler Thromb. 2017 Feb 1;24(2):157-168. doi: 10.5551/jat.32409. Epub 2016 Jul 8.