2型糖尿病与肺炎克雷伯菌定植的关系:nomogram模型的建立。

IF 1.7 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
American journal of translational research Pub Date : 2024-12-15 eCollection Date: 2024-01-01 DOI:10.62347/DZKV8669
Xiaoying Li, Hui Zhang, Huili Hu, Xiaolei Song, Beizheng Leng
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引用次数: 0

摘要

目的:探讨2型糖尿病(T2DM)患者基本特征和临床特征与肺炎克雷伯菌(KPC)易感性的关系。此外,我们还建立了一个临床预测模型来识别KPC的高危患者。方法:回顾性收集2020年12月至2022年12月在上海市第五人民医院就诊的486例T2DM患者的资料。根据肺炎克雷伯菌检测结果将患者分为KPC组和正常组。采用t检验和卡方检验分析两组间差异。采用Logistic回归分析T2DM患者KPC易感性的影响因素,并计算优势比(or)。采用nomogram构建临床预测模型,并通过受试者工作特征曲线下面积(AUC)、Hosmer-Lemeshow检验、校准曲线和决策曲线分析(DCA)进行评估。结果:486例T2DM患者中,发现KPC 124例,定植率为25.51%。Logistic回归分析显示,近6个月内住院、白细胞计数升高、血红蛋白降低、铁蛋白水平升高是KPC的独立危险因素。甲状腺和肝功能指标也与KPC易感性相关。临床预测模型的AUC为0.74 (95% CI: 0.68-0.80)。校正曲线显示实测值与预测值无显著差异,表明该模型可有效识别KPC高危患者。结论:T2DM患者继发KPC的风险增高。确定T2DM患者KPC的关键危险因素对早期识别、有针对性的干预和个性化的治疗策略具有重要的临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between type 2 diabetes mellitus and Klebsiella pneumoniae colonization: construction of nomogram model.

Objective: To investigate the association between the basic and clinical characteristics of patients with type 2 diabetes mellitus (T2DM) and their susceptibility to Klebsiella pneumoniae colonization (KPC). Additionally, a clinical prediction model was developed to identify high-risk patients for KPC.

Methods: Data from 486 T2DM patients who visited Shanghai Fifth People's Hospital from December 2020 to December 2022 were retrospectively collected. Patients were classified into the KPC group and normal group based on their Klebsiella pneumoniae test results. Differences between the two groups were analyzed using t-test and chi-square test. Logistic regression was performed to identify factors influencing KPC susceptibility in T2DM patients, with odds ratios (ORs) calculated. A clinical prediction model was constructed using a nomogram and evaluated through the area under the receiver operating characteristic (ROC) curve (AUC), Hosmer-Lemeshow test, calibration curve, and decision curve analysis (DCA).

Results: Of the 486 T2DM patients, 124 were found to have KPC, with a colonization rate of 25.51%. Logistic regression analysis revealed that hospitalization within the past six months, elevated white blood cell count, decreased hemoglobin, and elevated ferritin levels were independent risk factors for KPC. Thyroid and liver function indicators were also associated with KPC susceptibility. The clinical prediction model achieved an AUC of 0.74 (95% CI: 0.68-0.80). The calibration curve indicated no significant differences between observed and predicted values, suggesting that the model effectively identifies high-risk KPC patients.

Conclusion: T2DM patients are at an increased risk of secondary KPC. Identifying key risk factors for KPC in T2DM patients has significant clinical implications for early identification, targeted interventions, and individualized treatment strategies.

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American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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