Jiao Xiaojuan, Zhang Qin, Peng Ping, Shen Yunfeng
Department of Endocrinology and Metabolism, The Second Affiliated Hospital of Nanchang University, No. 1, Minde Road, Donghu District, Nanchang, 330006, China.
Branch of National Clinical Research Center for Metabolic Diseases, Nanchang, 330006, China.
Diabetol Metab Syndr. 2023 Mar 20;15(1):50. doi: 10.1186/s13098-023-01015-y.
Coronary heart disease (CHD) is not only a macrovascular complication of type 2 diabetes mellitus (T2DM). Cardiovascular disease (CVD) is one of the leading causes of mortality among individuals with T2DM. Reducing the risk of adverse cardiovascular events (MACE) is crucial for the management of patients with CHD. This study aimed to investigate the effect of glycemic control on CHD severity and 3-point MACE (3p-MACE) risk in patients with T2DM and CHD.
681 patients with both T2DM and CHD throughout October 2017 and October 2021 who were hospitalized in the second affiliated hospital of Nanchang university were included. A total of 300 patients were eventually enrolled in this retrospective cohort research. The severity of CHD in these patients was assessed, and the primary outcome during follow-up was recorded, with the primary result being the 3-point major adverse cardiovascular event (3p-MACE). The correlation between baseline glycated hemoglobin A1c (b-HbA1c) and the severity of CHD was evaluated by logistic regression analysis. The effect of b-HbA1c and follow-up HbA1c (f-HbA1c) levels on the risk of 3p-MACE were investigated by cox regression analysis.
b-HbA1c was positively correlated with the severity of CHD (r = 0.207, p = 0.001), and patients with b-HbA1c > 9% were more likely to have severe CHD. The HRs for b-HbA1c and f-HbA1c on the risk of 3p-MACE were 1.24 (95% CI 0.94-1.64, p = 0.123) and 1.32 (95% CI 1.02-1.72, p = 0.036), respectively. Patients with f-HbA1c ≥8.6% had a higher risk of 3p-MACE than f-HbA1c < 8.6% (HR = 1.79, 95% CI 1.16-2.79, p = 0.009).
In patients with both T2DM and CHD, b-HbA1c was an independent predictive factor of severe CHD. f-HbA1c was an independent predictive factor of 3p-MACE. Having the f-HbA1c below 8.6% significantly reduced the risk of 3p-MACE.
冠心病(CHD)不仅是2型糖尿病(T2DM)的大血管并发症。心血管疾病(CVD)是T2DM患者死亡的主要原因之一。降低不良心血管事件(MACE)风险对于冠心病患者的管理至关重要。本研究旨在探讨血糖控制对T2DM合并CHD患者CHD严重程度和3点MACE(3p-MACE)风险的影响。
纳入2017年10月至2021年10月在南昌大学第二附属医院住院的681例T2DM合并CHD患者。最终共有300例患者纳入这项回顾性队列研究。评估这些患者的CHD严重程度,并记录随访期间的主要结局,主要结果为3点主要不良心血管事件(3p-MACE)。通过逻辑回归分析评估基线糖化血红蛋白A1c(b-HbA1c)与CHD严重程度之间的相关性。通过Cox回归分析研究b-HbA1c和随访糖化血红蛋白A1c(f-HbA1c)水平对3p-MACE风险的影响。
b-HbA1c与CHD严重程度呈正相关(r = 0.207,p = 0.001),b-HbA1c>9%的患者更易发生严重CHD。b-HbA1c和f-HbA1c对3p-MACE风险的HR分别为1.24(95%CI 0.94-1.64,p = 0.123)和1.32(95%CI 1.02-1.72,p = 0.036)。f-HbA1c≥8.6%的患者发生3p-MACE的风险高于f-HbA1c<8.6%的患者(HR = 1.79,95%CI 1.16-2.79,p = 0.009)。
在T2DM合并CHD患者中,b-HbA1c是严重CHD的独立预测因素。f-HbA1c是3p-MACE的独立预测因素。将f-HbA1c控制在8.6%以下可显著降低3p-MACE风险。