糖尿病和慢性心力衰竭伴中度射血分数降低患者炎症生物标志物与碳水化合物和脂质代谢的相互作用

L. S. Efremova, L. V. Vasilieva, E. Gosteva
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引用次数: 0

摘要

目的:研究脂蛋白相关磷脂酶A2 (LP-PLA2)炎症生物标志物和肿瘤坏死因子α (TNF-α)与碳水化合物和脂质代谢指标在糖尿病(DM)慢性心力衰竭伴中度射血分数降低(HFmrEF)进展中的关系。材料和方法。对78例确诊为DM和HFmrEF (EF = 41-49%),根据NYHA检查CHF I和II功能分级(FC)的患者进行检查。检查患者的碳水化合物和脂质代谢,血清LP-PLA2和TNF-a水平。将患者分为两组:第一组合并心肌梗死(MI)的HFmrEF和DM患者37例(47.4%),第二组合并HFmrEF和DM患者41例(52.6%)。结果。随着CHF FC的增加,LP-PLA2和TNF-a的含量增加。1组患者炎症标志物、胰岛素、HOMA-IR、总胆固醇、低密度脂蛋白水平均明显高于2组。LP-PLA2和TNF-a水平与糖脂代谢参数呈正相关。结论。随着CHF FC的增加,DM和HFmrEF的进展伴随着慢性炎症的增加和Lp-PLA2和TNF-a含量的增加。炎症生物标志物水平升高与碳水化合物和脂质代谢的关联是HFmrEF在DM患者中进展的另一个因素。与HFmrEF和DM患者相比,心肌梗死的HFmrEF和DM患者血清炎症生物标志物水平升高,使得使用LP-PLA2和TNF-a诊断DM和HFmrEF患者的并发症成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interaction between inflammatory biomarkers and carbohydrate and lipid metabolism in patients with diabetes mellitus and chronic heart failure with moderately reduced ejection fraction
The purpose — to study the association of lipoprotein-associated phospholipase A2 (LP-PLA2) inflammatory biomarkers and tumor necrosis factor-alpha (TNF-α) with indicators of carbohydrate and lipid metabolism in the progression of chronic heart failure with moderately reduced ejection fraction (HFmrEF) in patients with diabetes mellitus (DM). Material and methods. 78 patients with established diagnosis of DM and HFmrEF (EF = 41–49%), functional class (FC) of CHF I and II according to NYHA were examined. The patients underwent examination of carbohydrate and lipid metabolism, serum levels of LP-PLA2 and TNF-a. Two groups of patients were formed: the 1st group — patients with HFmrEF and DM who had myocardial infarction (MI), 37 people (47.4%), the 2nd group — patients with HFmrEFand DM, 41 people (52.6%). Results. An increase in the content of LP-PLA2 and TNF-a with an increase in CHF FC was revealed. In the 1st group, the levels of inflammation biomarkers, insulin, HOMA-IR, total cholesterol, low density lipoproteins significantly exceeded those in the 2nd group. A positive correlation was found between the levels of LP-PLA2 and TNF-a and the parameters of carbohydrate and lipid metabolism. Conclusion. The progression of DM and HFmrEF is accompanied by an increase in chronic inflammation and an increase in the content of Lp-PLA2 and TNF-a with an increase in CHF FC. The association of elevated levels of inflammatory biomarkers with carbohydrate and lipid metabolism is an additional factor of HFmrEF progression in patients with DM. An increase in the serum levels of inflammatory biomarkers in patients with HFmrEF and DM who underwent MI, compared with patients with HFmrEF and DM, makes it possible to use LP-PLA2 and TNF-a for diagnosing complications in patients with DM and HFmrEF.
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