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既往和新发糖尿病对心力衰竭患者临床结局的影响。

Effects of preexisting and new-onset diabetes mellitus on clinical outcomes of patients with heart failure.

作者信息

Chen Ching-Pei, Chien Szu-Chi, Kor Chew-Teng, Hsu Che-Ming

机构信息

Post-Baccalaureate Medicine, College of Medicine, National Chung Hsing University, Taichung, Taiwan.

Division of Cardiology, Department of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan.

出版信息

Ann Med. 2025 Dec;57(1):2514088. doi: 10.1080/07853890.2025.2514088. Epub 2025 Jun 5.

DOI:10.1080/07853890.2025.2514088
PMID:40470769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12143004/
Abstract

BACKGROUND

Diabetes mellitus (DM) is a common comorbidity in heart failure (HF), but the impact of new-onset DM on HF outcomes remains unclear. This study evaluated the effects of DM status on hospitalization for HF (HHF), major adverse cardiac events (MACEs), and mortality in HF patients.

METHODS

We conducted a retrospective cohort study of patients newly diagnosed HF at Changhua Christian Hospital, Taiwan, from 2011 to 2021. Patients were grouped as non-DM ( = 1477), preexisting DM ( = 1488), and new-onset DM ( = 328). Inverse propensity score weighting was applied to balance covariates.

RESULTS

Compared to the non-DM group, the preexisting DM was associated with higher risks of HHF [hazard ratio (HR), 1.13; 95% confidence interval (CI), 1.02-1.25], MACEs (HR, 1.22; 95% CI, 1.00-1.49), all-cause mortality (HR, 1.17; 95% CI, 1.01-1.36), and cardiovascular death (HR, 1.54; 95% CI, 1.15-2.06). The new-onset DM group showed a significantly higher risk of HHF (HR, 1.24; 95% CI, 1.01-1.51) and MACEs (HR, 1.22; 95% CI, 1.00-1.49), with nonsignificant trends toward increased all-cause mortality (HR, 1.08; 95% CI, 0.79-1.48) and cardiovascular death (HR, 1.36; 95% CI, 0.74-2.48).

CONCLUSION

In HF patients, preexisting DM is associated with worse outcomes across multiple endpoints. New-onset DM also elevates risks of HHF and MACE, though its effect on mortality is less clear. Although our study, utilizing electronic medical record data, revealed a different pattern compared to the Danish registry, the findings emphasize the need for individualized management strategies based on DM status in HF care.

摘要

背景

糖尿病(DM)是心力衰竭(HF)常见的合并症,但新发糖尿病对心力衰竭预后的影响仍不明确。本研究评估了糖尿病状态对心力衰竭患者因心力衰竭住院(HHF)、主要不良心脏事件(MACE)和死亡率的影响。

方法

我们对2011年至2021年在台湾彰化基督教医院新诊断为心力衰竭的患者进行了一项回顾性队列研究。患者分为非糖尿病组(n = 1477)、既往糖尿病组(n = 1488)和新发糖尿病组(n = 328)。应用逆倾向评分加权来平衡协变量。

结果

与非糖尿病组相比,既往糖尿病组发生HHF的风险更高[风险比(HR),1.13;95%置信区间(CI),1.02 - 1.25]、MACE(HR,1.22;95% CI,1.00 - 1.49)、全因死亡率(HR,1.17;95% CI,1.01 - 1.36)和心血管死亡(HR,1.54;95% CI,1.15 - 2.06)。新发糖尿病组发生HHF(HR,1.24;95% CI,1.01 - 1.51)和MACE(HR,1.22;95% CI,1.00 - 1.49)的风险显著更高,全因死亡率(HR,1.08;95% CI,0.79 - 1.48)和心血管死亡(HR,1.36;95% CI,0.74 - 2.48)呈非显著上升趋势。

结论

在心力衰竭患者中,既往糖尿病与多个终点的不良预后相关。新发糖尿病也会增加HHF和MACE的风险,尽管其对死亡率的影响尚不清楚。尽管我们利用电子病历数据的研究与丹麦登记处的结果不同,但研究结果强调了在心力衰竭治疗中基于糖尿病状态制定个体化管理策略的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077a/12143004/80aa1b43b988/IANN_A_2514088_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077a/12143004/40ebdb7ab464/IANN_A_2514088_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077a/12143004/80aa1b43b988/IANN_A_2514088_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077a/12143004/40ebdb7ab464/IANN_A_2514088_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077a/12143004/80aa1b43b988/IANN_A_2514088_F0002_C.jpg

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本文引用的文献

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Association of Evaluated Glomerular Filtration Rate and Incident Diabetes Mellitus: A Secondary Retrospective Analysis Based on a Chinese Cohort Study.评估的肾小球滤过率与新发糖尿病的关联:基于一项中国队列研究的二次回顾性分析。
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Prevalence and clinical outcome of main echocardiographic and hemodynamic heart failure phenotypes in a population of hospitalized patients 70 years old and older.70 岁及以上住院患者中心力衰竭主要超声心动图和血液动力学表型的患病率和临床转归。
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Diabetes Mellitus and Heart Failure.
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Diabetes Mellitus Is an Independent Predictor for the Development of Heart Failure: A Population Study.糖尿病是心力衰竭发展的独立预测因素:一项人群研究。
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Cardiovasc Diabetol. 2019 Jun 12;18(1):79. doi: 10.1186/s12933-019-0883-4.
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Circ Res. 2019 Jan 4;124(1):121-141. doi: 10.1161/CIRCRESAHA.118.311371.
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