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Pre-heparin lipoprotein lipase mass as a potential mediator in the association between adiponectin and HDL-cholesterol in type 2 diabetes

Authors :
Raelene E. Maser
P. Babu Balagopal
Ryan T. Pohlig
M. James Lenhard
Source :
Journal of Clinical & Translational Endocrinology, Journal of Clinical & Translational Endocrinology, Vol 7, Iss C, Pp 7-11 (2017)
Publication Year :
2016

Abstract

Highlights • We examined pre-heparin LPL mass in type 2 diabetes mellitus (T2DM). • Association of adiponectin, pre-heparin LPL mass, and HDL-C was examined in T2DM. • Pre-heparin LPL mass may mediate the adiponectin and HDL-C association in T2DM.<br />Aim Lipoprotein lipase (LPL) is a major enzyme in lipid metabolism. Dyslipidemia, characterized by decreased high-density lipoprotein cholesterol (HDL-C), is prevalent in persons with type 2 diabetes mellitus (T2DM). The aim of this study was to determine whether pre-heparin LPL mass mediates the association between adiponectin and HDL-C in individuals with T2DM. Methods Pre-heparin LPL mass was measured via an enzyme-linked immunosorbent assay, adiponectin by radioimmunoassay, and HDL-C was determined enzymatically. Participants’ (n = 50) demographics, HbA1c, adiposity, homeostasis model assessment for insulin resistance (HOMA-IR), serum creatinine, and lipids were measured. Path analysis was utilized to test whether pre-heparin LPL mass is a mediator in the relationship between adiponectin and HDL-C. Results All four criteria for mediation were satisfied in the path analysis. The indirect effect of adiponectin on HDL-C through pre-heparin LPL mass was significant, p = 0.001, whereas the direct effect of adiponectin on HDL-C was not significant, p = 0.074. These results remained consistent even after adjustments for age, gender, body mass index, HOMA-IR, and serum creatinine in the model. Conclusion The findings in this study suggest that pre-heparin LPL mass may mediate the association between adiponectin and HDL-C in T2DM. This relationship for measures of HDL-C functionality requires future investigation.

Details

ISSN :
22146237
Volume :
7
Database :
OpenAIRE
Journal :
Journal of clinicaltranslational endocrinology
Accession number :
edsair.doi.dedup.....a9d98303ce1527f3fc7bd884cc534018