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Proteomic alterations of HDL in youth with type 1 diabetes and their associations with glycemic control: a case–control study

Authors :
Nehal N. Mehta
Junfeng Ma
Radoslav Goldman
Martin P. Playford
Scott M. Gordon
Evgenia Gourgari
Alan T. Remaley
Source :
Cardiovascular Diabetology, Vol 18, Iss 1, Pp 1-11 (2019), Cardiovascular Diabetology
Publication Year :
2019
Publisher :
BMC, 2019.

Abstract

Background Patients with type 1 diabetes (T1DM) typically have normal or even elevated plasma high density lipoprotein (HDL) cholesterol concentrations; however, HDL protein composition can be altered without a change in cholesterol content. Alteration of the HDL proteome can result in dysfunctional HDL particles with reduced ability to protect against cardiovascular disease (CVD). The objective of this study was to compare the HDL proteomes of youth with T1DM and healthy controls (HC) and to evaluate the influence of glycemic control on HDL protein composition. Methods This was a cross-sectional case–control study. Blood samples were obtained from patients with T1DM and HC. HDL was isolated from plasma by size-exclusion chromatography and further purified using a lipid binding resin. The HDL proteome was analyzed by mass spectrometry using label-free SWATH peptide quantification. Results Samples from 26 patients with T1DM and 13 HC were analyzed and 78 HDL-bound proteins were measured. Youth with T1DM had significantly increased amounts of complement factor H related protein 2 (FHR2; adjusted P Conclusions Youth with T1DM have proteomic alterations of their HDL compared to HC, despite similar concentration of HDL cholesterol. The influence of these compositional changes on HDL function are not yet known. Future efforts should focus on investigating the role of these HDL associated proteins in regard to HDL function and their role in CVD risk in patients with T1DM. Trial registration NCT02275091

Details

Language :
English
ISSN :
14752840
Volume :
18
Issue :
1
Database :
OpenAIRE
Journal :
Cardiovascular Diabetology
Accession number :
edsair.doi.dedup.....f60af0831211dac78da7974074fd9eb0