Plasma apoCIII Levels in Relation to Inflammatory Traits and Metabolic Syndrome in Patients not Treated with Lipid-lowering Drugs Undergoing Coronary Angiography.
- Author:
Na Qiong WU
1
;
Sha LI
1
;
Yan ZHANG
1
;
Cheng Gang ZHU
1
;
Yuan Lin GUO
1
;
Ying GAO
1
;
Ping QING
1
;
Jing SUN
1
;
Geng LIU
1
;
Qian DONG
1
;
Jian Jun LI
1
Author Information
- Publication Type:Journal Article
- Keywords: Apolipoprotein CIII; Inflammation; Metabolic syndrome
- MeSH: Adult; Aged; Apolipoprotein C-III; blood; Biomarkers; blood; C-Reactive Protein; metabolism; Coronary Angiography; Cross-Sectional Studies; Female; Humans; Inflammation; blood; Leukocyte Count; Male; Metabolic Syndrome; blood; Middle Aged
- From: Biomedical and Environmental Sciences 2017;30(1):1-9
- CountryChina
- Language:English
-
Abstract:
OBJECTIVEAssessment of the comprehensive relationship among apolipoprotein CIII (apoCIII) levels, inflammation, and metabolic disorders is rare.
METHODSA total of 1455 consecutive patients not treated with lipid-lowering drugs and undergoing coronary angiography were enrolled in this cross-sectional study. A mediation analysis was used to detect the underlying role of apoCIII in the association of inflammation with metabolic syndrome (MetS).
RESULTSPatients with MetS showed higher levels of apoCIII [95.1 (73.1-131.4) vs. 81.7 (58.6-112.4) μg/mL, P < 0.001] and inflammatory markers [high sensitivity C-reactive protein, 1.7 (0.8-3.4) vs. 1.1 (0.5-2.2) mg/L; white blood cell count, (6.48 ± 1.68) vs. (6.11 ± 1.67) × 109/L]. The levels of apoCIII and inflammatory markers increased with the number of metabolic risk components (all P < 0.001). Furthermore, apoCIII levels were associated with virtually all individual MetS risk factors and inflammatory markers (all P < 0.05). Importantly, the prevalence of MetS in each metabolic disorder rose as apoCIII levels increased (all P < 0.05). Mediation analysis showed that apoCIII partially mediated the effect of inflammation on MetS independently from triglycerides.
CONCLUSIONPlasma apoCIII levels were significantly associated with the development and severity of MetS, and a role of apoCIII in the effect of inflammation on the development of MetS was identified.