Wu Na Qiong, Li Sha, Zhang Yan, Zhu Cheng Gang, Guo Yuan Lin, Gao Ying, Qing Ping, Sun Jing, Liu Geng, Dong Qian, Li Jian Jun
Division of Dyslipidemia, State Key Laboratory of Cardiovascular Disease, Fu Wai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100037, China.
Biomed Environ Sci. 2017 Jan;30(1):1-9. doi: 10.3967/bes2017.001.
Assessment of the comprehensive relationship among apolipoprotein CIII (apoCIII) levels, inflammation, and metabolic disorders is rare.
A 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).
Patients 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.
Plasma 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.
载脂蛋白CIII(apoCIII)水平、炎症与代谢紊乱之间的综合关系评估较为少见。
本横断面研究纳入了1455例未接受降脂药物治疗且正在接受冠状动脉造影的连续患者。采用中介分析来检测apoCIII在炎症与代谢综合征(MetS)关联中的潜在作用。
患有MetS的患者显示出较高的apoCIII水平[95.1(73.1 - 131.4)对81.7(58.6 - 112.4)μg/mL,P < 0.001]和炎症标志物[高敏C反应蛋白,1.7(0.8 - 3.4)对1.1(0.5 - 2.2)mg/L;白细胞计数,(6.48 ± 1.68)对(6.11 ± 1.67)×10⁹/L]。apoCIII和炎症标志物水平随着代谢风险成分数量的增加而升高(所有P < 0.001)。此外,apoCIII水平几乎与所有个体MetS风险因素和炎症标志物相关(所有P < 0.05)。重要的是,随着apoCIII水平升高,每种代谢紊乱中MetS的患病率上升(所有P < 0.05)。中介分析表明,apoCIII独立于甘油三酯部分介导了炎症对MetS的影响。
血浆apoCIII水平与MetS的发生和严重程度显著相关,并且确定了apoCIII在炎症对MetS发生影响中的作用。