PMID- 27581838 OWN - NLM STAT- MEDLINE DCOM- 20170327 LR - 20181113 IS - 1476-511X (Electronic) IS - 1476-511X (Linking) VI - 15 IP - 1 DP - 2016 Aug 31 TI - Plasma phospholipid transfer protein activity is inversely associated with betaine in diabetic and non-diabetic subjects. PG - 143 LID - 10.1186/s12944-016-0313-5 [doi] LID - 143 AB - BACKGROUND: The choline metabolite, betaine, plays a role in lipid metabolism, and may predict the development of cardiovascular disease and type 2 diabetes mellitus (T2DM). Phospholipid transfer protein (PLTP) and lecithin:cholesterol acyltransferase (LCAT) require phosphatidylcholine as substrate, raising the possibility that there is an intricate relationship of these protein factors with choline metabolism. Here we determined the relationships of PLTP and LCAT activity with betaine in subjects with and without T2DM. METHODS: Plasma betaine (nuclear magnetic resonance spectroscopy), PLTP activity (liposome-vesicle HDL system), LCAT activity (exogenous substrate assay) and (apo)lipoproteins were measured in 65 type 2 diabetic (T2DM) and in 55 non-diabetic subjects. RESULTS: PLTP and LCAT activity were elevated in T2DM (p < 0.05), whereas the difference in betaine was not significant. In age-, sex- and diabetes status-controlled correlation analysis, betaine was inversely correlated with triglycerides and positively with HDL cholesterol (p < 0.05 to 0.01). PLTP and LCAT activity were positively correlated with triglycerides and inversely with HDL cholesterol (p < 0.05 to 0.001). PLTP (r = -0.245, p = 0.006) and LCAT activity (r = -0.195, p = 0.035) were correlated inversely with betaine. The inverse association of PLTP activity with betaine remained significant after additional adjustment for body mass index and lipoprotein variables (beta = -0.179, p = 0.034), whereas its association with LCAT activity lost significance (beta = -0.056, p = 0.44). CONCLUSIONS: Betaine may influence lipoprotein metabolism via an effect on PLTP activity. FAU - Dullaart, R P F AU - Dullaart RP AD - Department of Endocrinology, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, Groningen, 9700 RB, The Netherlands. r.p.f.dullaart@umcg.nl. FAU - Garcia, Erwin AU - Garcia E AD - LipoScience, Laboratory Corporation of America(R) Holdings, Raleigh, NC, USA. FAU - Jeyarajah, Elias AU - Jeyarajah E AD - LipoScience, Laboratory Corporation of America(R) Holdings, Raleigh, NC, USA. FAU - Gruppen, Eke G AU - Gruppen EG AD - Departments of Endocrinology and Nephrology, University of Groningen and University Medical Center Groningen, Groningen, The Netherlands. FAU - Connelly, Margery A AU - Connelly MA AD - LipoScience, Laboratory Corporation of America(R) Holdings, Raleigh, NC, USA. LA - eng PT - Journal Article DEP - 20160831 PL - England TA - Lipids Health Dis JT - Lipids in health and disease JID - 101147696 RN - 0 (Blood Glucose) RN - 0 (Cholesterol, HDL) RN - 0 (Phospholipid Transfer Proteins) RN - 0 (Triglycerides) RN - 3SCV180C9W (Betaine) RN - EC 2.3.1.43 (Phosphatidylcholine-Sterol O-Acyltransferase) SB - IM MH - Age Factors MH - Aged MH - Betaine/*blood MH - Blood Glucose/analysis MH - Cholesterol, HDL/blood MH - Diabetes Mellitus, Type 2/*blood MH - Female MH - Humans MH - Male MH - Middle Aged MH - Phosphatidylcholine-Sterol O-Acyltransferase/blood MH - Phospholipid Transfer Proteins/*blood MH - Triglycerides/blood PMC - PMC5007837 OTO - NOTNLM OT - Betaine OT - Lecithin:cholesterol acyltransferase OT - Lipoproteins OT - Phospholipid transfer protein OT - Type 2 diabetes mellitus EDAT- 2016/09/02 06:00 MHDA- 2017/03/28 06:00 PMCR- 2016/08/31 CRDT- 2016/09/02 06:00 PHST- 2016/07/15 00:00 [received] PHST- 2016/08/23 00:00 [accepted] PHST- 2016/09/02 06:00 [entrez] PHST- 2016/09/02 06:00 [pubmed] PHST- 2017/03/28 06:00 [medline] PHST- 2016/08/31 00:00 [pmc-release] AID - 10.1186/s12944-016-0313-5 [pii] AID - 313 [pii] AID - 10.1186/s12944-016-0313-5 [doi] PST - epublish SO - Lipids Health Dis. 2016 Aug 31;15(1):143. doi: 10.1186/s12944-016-0313-5.