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评估 SIRT1 作为伴有肢体威胁性缺血的糖尿病患者心血管结局的预测因子。

Evaluation of sirtuin 1 as a predictor of cardiovascular outcomes in diabetic patients with limb-threatening ischemia.

机构信息

Cardiovascular Internal Medicine , Fondazione Policlinico Universitario A. Gemelli IRCCS , Largo Agostino Gemelli 8, 00168, Roma, Italy.

Università Cattolica del Sacro Cuore, Largo Francesco Vito 1, 00168, Roma, Italy.

出版信息

Sci Rep. 2024 Nov 6;14(1):26940. doi: 10.1038/s41598-024-78576-z.

DOI:10.1038/s41598-024-78576-z
PMID:39506067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11542011/
Abstract

Chronic limb-threatening ischemia (CLTI) significantly increases the risk of major adverse limb events (MALE) and major adverse cardiac events (MACE) after lower extremity revascularization (LER). This study aims to identify novel biomarkers that help to further reduce the risk of postoperative cardiovascular complications. In this prospective, nonrandomized, observational study, baseline serum levels of sirtuin 1 (SIRT1) were assessed in 147 diabetic patients scheduled for LER due to CLTI, and participants were followed for the occurrence of MALE and MACE over 12 months. Fifty-three patients experienced MALE, and 33 experienced MACE within the follow-up period. Lower baseline SIRT1 levels were significantly associated with an increased risk of MALE and MACE, independent of other risk factors. The ROC curve analysis identified a SIRT1 cutoff of 3.79 ng/mL for predicting the risk of MALE. Moreover, incorporating SIRT1 into predictive models significantly enhanced the accuracy of predicting adverse outcomes. Results suggest serum SIRT1 is a potential independent marker for predicting MALE and MACE in diabetic patients with CLTI undergoing LER. Further research is needed to clarify the mechanistic pathways in which SIRT1 may influence cardiovascular outcomes, and the role of this novel biomarker in the management of PAD and CLTI among patients with diabetes.

摘要

慢性肢体威胁性缺血 (CLTI) 会显著增加下肢血运重建 (LER) 后主要不良肢体事件 (MALE) 和主要不良心脏事件 (MACE) 的风险。本研究旨在确定有助于进一步降低术后心血管并发症风险的新型生物标志物。在这项前瞻性、非随机、观察性研究中,评估了 147 例因 CLTI 而计划接受 LER 的糖尿病患者的基线血清 SIRT1 水平,并对患者在 12 个月内发生 MALE 和 MACE 的情况进行了随访。53 例患者发生 MALE,33 例患者发生 MACE。较低的基线 SIRT1 水平与 MALE 和 MACE 的风险增加显著相关,独立于其他危险因素。ROC 曲线分析确定了 3.79ng/mL 的 SIRT1 截断值,用于预测 MALE 的风险。此外,将 SIRT1 纳入预测模型显著提高了预测不良结局的准确性。结果表明,血清 SIRT1 是预测糖尿病合并 CLTI 患者接受 LER 后发生 MALE 和 MACE 的潜在独立标志物。需要进一步研究阐明 SIRT1 可能影响心血管结局的机制途径,以及该新型生物标志物在糖尿病患者的 PAD 和 CLTI 管理中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da3/11542011/663b7c2587a0/41598_2024_78576_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da3/11542011/1c2bdda401b9/41598_2024_78576_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da3/11542011/663b7c2587a0/41598_2024_78576_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da3/11542011/1c2bdda401b9/41598_2024_78576_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5da3/11542011/663b7c2587a0/41598_2024_78576_Fig2_HTML.jpg

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