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影响 2 型糖尿病合并冠心病患者加速衰老的因素。

Factors influencing accelerated aging in patients with type 2 diabetes mellitus and coronary heart disease.

机构信息

Xuzhou Central Hospital, Affiliated Xuzhou Clinical College of Xuzhou Medical University, Xuzhou, Jiangsu, China.

出版信息

Front Endocrinol (Lausanne). 2024 Jul 31;15:1416234. doi: 10.3389/fendo.2024.1416234. eCollection 2024.

Abstract

OBJECTIVE

To investigate the factors influencing accelerated aging in patients with type 2 diabetes mellitus (T2DM) and coronary heart disease (CHD).

METHODS

A total of 216 patients diagnosed with T2DM and CHD between August 2019 and August 2023 at Xuzhou Central Hospital were selected. Patients were divided into an aging group and a non-aging group, based on the positive or negative values of phenotypic age acceleration (PhenoAgeAccel). Logistic regression analysis was conducted. Variables that had a univariate analysis < 0.05 were included in the multivariate analysis to identify factors influencing aging in patients with T2DM and CHD, and the area under the curve of the model was reported.

RESULTS

This study included 216 patients, with 89 in the accelerated aging group, and 127 in the non-accelerated aging group. The average age of patients was 70.40 (95% CI: 69.10-71.69) years, with 137 males (63.4%). Compared with the non-accelerated aging group, patients in the accelerated aging group were older, with a higher proportion of males, and a higher prevalence of hypertension, stable angina pectoris, and unstable angina pectoris. Multivariate Logistic regression analysis indicated that the absolute value of neutrophils (NEUT#), urea (UREA), adenosine deaminase (ADA), and the triglyceride-glucose index (TyG) were risk factors for accelerated aging, while cholinesterase (CHE) was a protective factor. For each unit increase in NEUT#, UREA, ADA, and TyG, the risk of aging increased by 64%, 48%, 10%, and 789%, respectively. The overall area under the receiver operating characteristic (ROC) curve of the model in the training set was 0.894, with a 95% confidence interval (CI) of 0.851-0.938.

CONCLUSION

NEUT#, CHE, UREA, ADA, and TyG are predictors of accelerated aging in patients with T2DM and CHD, with the model showing favorable overall predictive performance.

摘要

目的

探讨影响 2 型糖尿病(T2DM)合并冠心病(CHD)患者加速衰老的因素。

方法

选取 2019 年 8 月至 2023 年 8 月在徐州市中心医院确诊为 T2DM 合并 CHD 的 216 例患者。根据表型年龄加速(PhenoAgeAccel)的正负值,将患者分为衰老组和非衰老组。采用 logistic 回归分析,将单因素分析<0.05 的变量纳入多因素分析,识别影响 T2DM 合并 CHD 患者衰老的因素,并报告模型的曲线下面积。

结果

本研究共纳入 216 例患者,其中加速衰老组 89 例,非加速衰老组 127 例。患者平均年龄为 70.40 岁(95%CI:69.10-71.69),男性 137 例(63.4%)。与非加速衰老组相比,加速衰老组患者年龄较大,男性比例较高,高血压、稳定性心绞痛和不稳定性心绞痛的患病率较高。多因素 logistic 回归分析表明,中性粒细胞绝对值(NEUT#)、尿素(UREA)、腺苷脱氨酶(ADA)和甘油三酯-葡萄糖指数(TyG)是加速衰老的危险因素,而胆碱酯酶(CHE)是保护因素。NEUT#、UREA、ADA 和 TyG 每增加一个单位,衰老的风险分别增加 64%、48%、10%和 789%。模型在训练集中的整体受试者工作特征(ROC)曲线下面积为 0.894,95%置信区间(CI)为 0.851-0.938。

结论

NEUT#、CHE、UREA、ADA 和 TyG 是 T2DM 合并 CHD 患者加速衰老的预测因子,该模型具有良好的整体预测性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/772d/11322350/856d41b368de/fendo-15-1416234-g001.jpg

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