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本文引用的文献

1
Type 2 Diabetes Mellitus: A Comprehensive Review of Pathophysiology, Comorbidities, and Emerging Therapies.2型糖尿病:病理生理学、合并症及新兴疗法的全面综述
Compr Physiol. 2025 Feb;15(1):e70003. doi: 10.1002/cph4.70003.
2
Protective Influence of SGLT-2 Inhibitors Against Heart Failure in Type 2 Diabetes Mellitus Through Longitudinal Clinical Database Analysis.通过纵向临床数据库分析探讨SGLT-2抑制剂对2型糖尿病患者心力衰竭的保护作用
J Clin Med. 2024 Nov 24;13(23):7093. doi: 10.3390/jcm13237093.
3
Comparative estimate of glucose-lowering therapies on risk of incident pneumonia and severe sepsis: an analysis of real-world cohort data.降糖疗法对新发肺炎和严重脓毒症风险的比较评估:一项真实世界队列数据分析
Thorax. 2024 Dec 23;80(1):32-41. doi: 10.1136/thorax-2024-221906.
4
Worldwide trends in diabetes prevalence and treatment from 1990 to 2022: a pooled analysis of 1108 population-representative studies with 141 million participants.全球糖尿病患病率和治疗趋势 1990 年至 2022 年:基于 14100 万参与者的 1108 项人群代表性研究的汇总分析。
Lancet. 2024 Nov 23;404(10467):2077-2093. doi: 10.1016/S0140-6736(24)02317-1. Epub 2024 Nov 13.
5
Comparative risk of infection of medications used for type 2 diabetes.用于 2 型糖尿病的药物的感染比较风险。
Expert Opin Drug Saf. 2024 Sep;23(9):1079-1091. doi: 10.1080/14740338.2024.2401024. Epub 2024 Sep 11.
6
Evaluation of Cardiovascular Disease Risk in Patients with Type 2 Diabetes Mellitus Using Clinical Laboratory Markers.使用临床实验室指标评估2型糖尿病患者的心血管疾病风险
J Clin Med. 2024 Jun 18;13(12):3561. doi: 10.3390/jcm13123561.
7
Sodium Glucose Cotransporter-2 Inhibitors in Non-Diabetic Kidney Disease: Evidence in Experimental Models.非糖尿病肾病中钠-葡萄糖协同转运蛋白2抑制剂:实验模型中的证据
Pharmaceuticals (Basel). 2024 Mar 11;17(3):362. doi: 10.3390/ph17030362.
8
The effect of sodium-glucose cotransporter 2 inhibitors in patients with chronic kidney disease with or without type 2 diabetes mellitus on cardiovascular and renal outcomes: A systematic review and meta-analysis.钠-葡萄糖共转运蛋白 2 抑制剂在伴有或不伴有 2 型糖尿病的慢性肾脏病患者中的心血管和肾脏结局影响:系统评价和荟萃分析。
PLoS One. 2023 Nov 29;18(11):e0295059. doi: 10.1371/journal.pone.0295059. eCollection 2023.
9
Anti‑inflammatory effect of metformin against an experimental model of LPS‑induced cytokine storm.二甲双胍对脂多糖诱导的细胞因子风暴实验模型的抗炎作用。
Exp Ther Med. 2023 Jul 13;26(3):415. doi: 10.3892/etm.2023.12114. eCollection 2023 Sep.
10
Prevalent diabetes and long-term cardiovascular outcomes in adult sepsis survivors: a population-based cohort study.成年脓毒症幸存者中常见的糖尿病与长期心血管结局:一项基于人群的队列研究。
Crit Care. 2023 Jul 31;27(1):302. doi: 10.1186/s13054-023-04586-4.

抗糖尿病药物使用对2型糖尿病患者脓毒症风险的影响:一项多变量分析

Effect of Anti-Diabetic Medication Use on Sepsis Risk in Type 2 Diabetes Mellitus: A Multivariate Analysis.

作者信息

Ulambayar Battamir, Ghanem Amr Sayed, Nagy Attila Csaba

机构信息

Department of Health Informatics, Faculty of Health Sciences, University of Debrecen, 4032 Debrecen, Hungary.

Coordinating Centre for Epidemiology, University of Debrecen Clinical Centre, 4032 Debrecen, Hungary.

出版信息

Geriatrics (Basel). 2025 Aug 7;10(4):108. doi: 10.3390/geriatrics10040108.

DOI:10.3390/geriatrics10040108
PMID:40863575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12385283/
Abstract

Type 2 diabetes mellitus (T2DM) increases sepsis risk due to immune dysfunction and chronic inflammation. Antidiabetic medications, while primarily used for glycemic control, may modulate sepsis susceptibility through immune and inflammatory pathways. This study investigates the association between antidiabetic medication use and sepsis risk in T2DM patients. A longitudinal cohort study was conducted using clinical registry data from 5009 T2DM patients at the University Hospital, Debrecen, Hungary (2016-2020). Sepsis cases were identified via ICD-10 code A41, and antidiabetic medication use was categorized using ATC codes. Baseline comorbidities and laboratory parameters were extracted. Chi-square and Wilcoxon rank-sum tests assessed associations between sepsis and categorical/numerical variables, respectively. Time-adjusted multivariate logistic regression evaluated predictors of sepsis risk, with odds ratios (ORs) and 95% confidence intervals (CIs) reported. Age, hypertension, ischemic heart disease, nephropathy, elevated blood glucose, C-reactive protein, and creatinine also independently increased sepsis risk. Insulin use was associated with a 2.6-fold increased sepsis risk (OR = 2.6, 95% CI: 2.09-3.34, < 0.001), while SGLT2 inhibitors (OR = 0.56, 95% CI: 0.34-0.91, = 0.02) and GLP-1 receptor agonists (OR = 0.39, 95% CI: 0.19-0.79, = 0.009) were protective. Insulin-treated patients may require closer infection monitoring, while SGLT2 inhibitors and GLP-1 RAs could be prioritized in high-risk individuals. These findings highlight the potential to inform risk stratification and guide personalized antidiabetic therapy to reduce sepsis risk in T2DM.

摘要

2型糖尿病(T2DM)由于免疫功能障碍和慢性炎症而增加了脓毒症风险。抗糖尿病药物虽然主要用于控制血糖,但可能通过免疫和炎症途径调节脓毒症易感性。本研究调查了T2DM患者使用抗糖尿病药物与脓毒症风险之间的关联。利用匈牙利德布勒森大学医院5009例T2DM患者的临床登记数据(2016 - 2020年)进行了一项纵向队列研究。通过ICD - 10编码A41识别脓毒症病例,并使用ATC编码对抗糖尿病药物的使用进行分类。提取基线合并症和实验室参数。卡方检验和Wilcoxon秩和检验分别评估脓毒症与分类/数值变量之间的关联。时间调整的多变量逻辑回归评估脓毒症风险的预测因素,并报告比值比(OR)和95%置信区间(CI)。年龄、高血压、缺血性心脏病、肾病、血糖升高、C反应蛋白和肌酐也独立增加脓毒症风险。使用胰岛素与脓毒症风险增加2.6倍相关(OR = 2.6,95% CI:2.09 - 3.34,<0.001),而钠 - 葡萄糖协同转运蛋白2(SGLT2)抑制剂(OR = 0.56,95% CI:0.34 - 0.91,P = 0.02)和胰高血糖素样肽 - 1(GLP - 1)受体激动剂(OR = 0.39,95% CI:0.19 - 0.79,P = 0.009)具有保护作用。接受胰岛素治疗的患者可能需要更密切的感染监测,而SGLT2抑制剂和GLP - 1受体激动剂可在高危个体中优先使用。这些发现凸显了为风险分层提供信息并指导个性化抗糖尿病治疗以降低T2DM患者脓毒症风险的潜力。