Correlation between insulin resistance and coronary collateral circulation in patients with chronic total coronary occlusion
10.12122/j.issn.1673-4254.2024.04.21
- VernacularTitle:冠状动脉慢性完全闭塞病变侧支循环的建立与胰岛素抵抗的相关性
- Author:
Sigan HU
1
;
Zengwei CHENG
;
Min LI
;
Shiyi GAO
;
Dasheng GAO
;
Pinfang KANG
Author Information
1. 蚌埠医科大学第一附属医院心血管科,安徽 蚌埠 233004
- Keywords:
coronary heart disease;
insulin resistance;
collateral circulation;
chronic total occlusion;
metabolomics
- From:
Journal of Southern Medical University
2024;44(4):780-786
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the impact of diabetes on collateral circulation (CC) development in patients with chronic total coronary occlusion (CTO) and the underlying regulatory mechanism. Methods This study was conducted among 87 patients with coronary heart disease (CHD), who had CTO in at least one vessel as confirmed by coronary angiography. Among them 42 patients were found to have a low CC level (Cohen-Rentrop grades 0-1) and 45 had a high CC level (grades 2-3). In the 39 patients with comorbid diabetes mellitus and 48 non-diabetic patients, insulin resistance (IR) levels were compared between the subgroups with different CC levels. The steady-state mode evaluation method was employed for calculating the homeostatic model assessment for insulin resistance index (HOMA-IR) using a mathematical model. During the interventional procedures, collateral and peripheral blood samples were collected from 22 patients for comparison of the metabolites using non-targeted metabolomics analysis. Results NT-proBNP levels and LVEF differed significantly between the patients with different CC levels (P<0.05). In non-diabetic patients, HOMA-IR was higher in low CC level group than in high CC level groups. Compared with the non-diabetic patients, the diabetic patients showed 63 upregulated and 48 downregulated metabolites in the collateral blood and 23 upregulated and 14 downregulated metabolites in the peripheral blood. The differential metabolites in the collateral blood were involved in aromatic compound degradation, fatty acid biosynthesis, and steroid degradation pathways; those in the peripheral blood were related with pentose phosphate metabolism, bacterial chemotaxis, hexanoyl-CoA degradation, glycerophospholipid metabolism, and lysine degradation pathways. Conclusion The non-diabetic patients with a low level of CC had significant insulin resistance. The degradation pathways of aromatic compounds, fatty acid biosynthesis, and steroid degradation are closely correlated with the development of CC.
