4.7 Review

HDL and type 2 diabetes: the chicken or the egg?

Journal

DIABETOLOGIA
Volume 64, Issue 9, Pages 1917-1926

Publisher

SPRINGER
DOI: 10.1007/s00125-021-05509-0

Keywords

High-density lipoprotein; Review; The metabolic syndrome; Type 2 diabetes mellitus

Funding

  1. project 'INSPIRED' under the Action 'Reinforcement of the Research and Innovation Infrastructure' - Operational Program 'Competitiveness, Entrepreneurship and Innovation' (NSRF 2014-2020) [MIS 5002550]

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The level of HDL-C and the functionality of HDL particles are correlated with the pathogenesis and prognosis of type 2 diabetes mellitus. High blood sugar leads to reduced levels of HDL-C and worsened HDL functionality, through various changes in the proteome and lipidome of HDL particles. Decreased levels of HDL-C and impaired HDL functionality impact the performance of key organs related to glucose homeostasis, such as the pancreas and skeletal muscles.
HDL is a complex macromolecular cluster of various components, such as apolipoproteins, enzymes and lipids. Quality evidence from clinical and epidemiological studies led to the principle that HDL-cholesterol (HDL-C) levels are inversely correlated with the risk of CHD. Nevertheless, the failure of many cholesteryl ester transfer protein inhibitors to protect against CVD casts doubts on this principle and highlights the fact that HDL functionality, as dictated by its proteome and lipidome, also plays an important role in protecting against metabolic disorders. Recent data indicate that HDL-C levels and HDL particle functionality are correlated with the pathogenesis and prognosis of type 2 diabetes mellitus, a major risk factor for CVD. Hyperglycaemia leads to reduced HDL-C levels and deteriorated HDL functionality, via various alterations in HDL particles' proteome and lipidome. In turn, reduced HDL-C levels and impaired HDL functionality impact the performance of key organs related to glucose homeostasis, such as pancreas and skeletal muscles. Interestingly, different structural alterations in HDL correlate with distinct metabolic abnormalities, as indicated by recent data evaluating the role of apolipoprotein A1 and lecithin-cholesterol acyltransferase deficiency in glucose homeostasis. While it is becoming evident that not all HDL disturbances are causatively associated with the development and progression of type 2 diabetes, a bidirectional correlation between these two conditions exists, leading to a perpetual self-feeding cycle.

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