Abstract:
:High-density lipoprotein (HDL) particles comprising heterogeneous subclasses of different functions exert anti-inflammatory effects by interacting with immune-response cells. However, the relationship of HDL subclasses with immune-response cells in metabolic unhealth/obesity has not been defined clearly. The purpose of this study was to delineate the relational changes of HDL subclasses with immune cells and inflammatory markers in metabolic unhealth/obesity to understand the role of anti-inflammatory HDL subclasses. A total of 316 participants were classified by metabolic health. HDL subclasses were detected by microfluidic chip electrophoresis. White blood cell (WBC) counts and lymphocytes were assessed using automatic haematology analyser. Levels of high-sensitivity C-reactive protein (hs-CRP) and interleukin 6 (IL-6) were measured. In our study, not only the distribution of HDL subclasses, but also HDL-related structural proteins changed with the deterioration of metabolic disease. Moreover, lymphocytes and inflammation factors significantly gradually increased. The level of HDL2b was negatively associated with WBC, lymphocytes and hs-CRP in multivariable linear regression analysis. In multinomial logistic regression analysis, high levels of HDL3 and low levels of HDL2b increased the probability of having an unfavourable metabolic unhealth/obesity status. We supposed that HDL2b particles may play anti-inflammation by negatively regulating lymphocytes activation. HDL2b may be a therapeutic target for future metabolic disease due to the anti-inflammatory effects.
journal_name
Artif Cells Nanomed Biotechnoljournal_title
Artificial cells, nanomedicine, and biotechnologyauthors
Tang H,Xiang Z,Li L,Shao X,Zhou Q,You X,Xiong C,Ning J,Chen T,Deng D,Zou Hdoi
10.1080/21691401.2021.1961798keywords:
[" immune-response cells","HDL subclasses","inflammation","metabolic unhealth","microfluidic electrophoresis","obesity"]subject
Has Abstractpub_date
2021-12-01 00:00:00pages
565-575issue
1eissn
2169-1401issn
2169-141Xjournal_volume
49pub_type
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