Shi Fachao, Yang Zhe, Wang Zheng, Wang Long, Fang Caoyang
Department of Cardiology, Ma'anshan People's Hospital,Ma'anshan Hospital Affiliated to Wannan Medical College, Maanshan, 243000, Anhui, China.
Department of Emergency, Division of Life Sciences and Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, 230000, Anhui, China.
Sci Rep. 2025 Jul 1;15(1):20696. doi: 10.1038/s41598-025-07743-7.
The relationship between HGI and mortality in patients with diabetes or prediabetes who have comorbid CVD has not yet been clearly established. Therefore, the aim of this study was to investigate the correlation between baseline HGI and all-cause and cardiovascular mortality in US adults with diabetes or prediabetes and comorbid CVD. This study analyzed data from 1,760 patients with diabetes or prediabetes and comorbid CVD from the NHANES from 1999 to 2018. Three models were constructed considering covariates to evaluate the correlation between HGI and mortality risk. Additionally, we used RCS and threshold effects to analyze the nonlinear relationship. During the follow-up of 1,760 patients with diabetes or prediabetes and comorbid CVD, there were 793 all-cause deaths and 274 cardiovascular-related deaths recorded. Restricted cubic spline analysis results showed that baseline HGI was U-shapedly associated with all-cause and cardiovascular mortality rates. Threshold effect analysis indicated that the turning points of HGI for all-cause and cardiovascular mortality rates were - 0.382 and - 0.380, respectively. Specifically, when baseline HGI was below the turning point, HGI was negatively correlated with all-cause mortality rate (HR: 0.6, 95% CI: 0.5-0.7) and cardiovascular mortality rate (HR: 0.6, 95% CI: 0.4-1.0), while when baseline HGI exceeded the turning point, HGI was positively correlated with all-cause mortality rate (HR: 1.2, 95% CI: 1.1-1.4) and cardiovascular mortality rate (HR: 1.3, 95% CI: 1.1-1.5). We found that in US adults with diabetes or prediabetes and comorbid CVD, baseline HGI was U-shapedly associated with all-cause and cardiovascular mortality rates. Specifically, the turning points for all-cause and cardiovascular mortality rates were - 0.382 and - 0.380, respectively.
在患有合并心血管疾病(CVD)的糖尿病或糖尿病前期患者中,糖化血红蛋白指数(HGI)与死亡率之间的关系尚未明确确立。因此,本研究的目的是调查美国患有糖尿病或糖尿病前期且合并CVD的成年人中,基线HGI与全因死亡率和心血管死亡率之间的相关性。本研究分析了1999年至2018年美国国家健康和营养检查调查(NHANES)中1760例患有糖尿病或糖尿病前期且合并CVD的患者的数据。构建了三个考虑协变量的模型,以评估HGI与死亡风险之间的相关性。此外,我们使用限制立方样条(RCS)和阈值效应来分析非线性关系。在对1760例患有糖尿病或糖尿病前期且合并CVD的患者进行随访期间,记录到793例全因死亡和274例心血管相关死亡。限制立方样条分析结果表明,基线HGI与全因死亡率和心血管死亡率呈U形关联。阈值效应分析表明,全因死亡率和心血管死亡率的HGI转折点分别为-0.382和-0.380。具体而言,当基线HGI低于转折点时,HGI与全因死亡率(风险比:0.6,95%置信区间:0.5-0.7)和心血管死亡率(风险比:0.6,95%置信区间:0.4-1.0)呈负相关,而当基线HGI超过转折点时,HGI与全因死亡率(风险比:1.2,95%置信区间:1.1-1.4)和心血管死亡率(风险比:1.3,95%置信区间:1.1-1.5)呈正相关。我们发现,在美国患有糖尿病或糖尿病前期且合并CVD的成年人中,基线HGI与全因死亡率和心血管死亡率呈U形关联。具体而言,全因死亡率和心血管死亡率的转折点分别为-0.382和-0.380。