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超重儿科受试者白细胞中O-连接N-乙酰葡糖胺化增加:一项初步研究。

Increased O-GlcNAcylation in Leukocytes from Overweight Pediatric Subjects: A Pilot Study.

作者信息

Remigante Alessia, Spinelli Sara, Rizzo Gianluca, Caruso Daniele, Marino Angela, Straface Elisabetta, Dossena Silvia, Morabito Rossana

机构信息

Department of Biomedical, Dental and Morphological and Functional Imaging, University of Messina, 98125 Messina, Italy.

Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, 98125 Messina, Italy.

出版信息

Int J Mol Sci. 2025 Jun 13;26(12):5665. doi: 10.3390/ijms26125665.

DOI:10.3390/ijms26125665
PMID:40565129
Abstract

Type II diabetes mellitus (T2D) is a metabolic disorder. Childhood overweight or obesity raises the risk for developing T2D later in life. Early identification of at-risk individuals is fundamental for disease prevention and patient management. The scope of this pilot study was to explore whether leukocyte protein O-GlcNAc modification is elevated in an overweight pediatric cohort. Eight overweight and eight normal-weight children aged 3-13 years were recruited at the Papardo General Hospital (Messina, Italy). Physical exams, complete blood tests, and determination of leukocyte protein O-GlcNAcylation were carried out. Protein O-GlcNAcylation was higher in leucocytes from overweight children compared to normal-weight children, and was significantly correlated with BMI, metabolic markers (LDL-cholesterol/triglycerides), and the inflammatory marker CRP. This study suggests that leukocyte protein O-GlcNAcylation may represent a novel biomarker for the early detection of metabolic abnormalities that may lead to the development of pre-diabetes or T2D later in life.

摘要

2型糖尿病(T2D)是一种代谢紊乱疾病。儿童期超重或肥胖会增加日后患2型糖尿病的风险。早期识别高危个体是疾病预防和患者管理的基础。这项初步研究的目的是探讨在超重的儿科队列中白细胞蛋白O-连接N-乙酰葡糖胺修饰是否升高。在意大利墨西拿的帕帕尔多综合医院招募了8名超重和8名体重正常的3至13岁儿童。进行了体格检查、全血细胞检测以及白细胞蛋白O-连接N-乙酰葡糖胺化的测定。与体重正常的儿童相比,超重儿童白细胞中的蛋白O-连接N-乙酰葡糖胺化水平更高,并且与体重指数、代谢标志物(低密度脂蛋白胆固醇/甘油三酯)以及炎症标志物CRP显著相关。这项研究表明,白细胞蛋白O-连接N-乙酰葡糖胺化可能代表一种新型生物标志物,用于早期检测可能导致日后发生糖尿病前期或2型糖尿病的代谢异常。

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本文引用的文献

1
Crosstalk between O-GlcNAcylation and phosphorylation in metabolism: regulation and mechanism.代谢中O-连接的N-乙酰葡糖胺化与磷酸化之间的相互作用:调控与机制
Cell Death Differ. 2025 Mar 5. doi: 10.1038/s41418-025-01473-z.
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The post-translational modification O-GlcNAc is a sensor and regulator of metabolism.翻译后的文本:O-GlcNAc 是一种代谢的传感器和调节剂。
Open Biol. 2024 Oct;14(10):240209. doi: 10.1098/rsob.240209. Epub 2024 Oct 30.
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Population-based prevalence of self-reported pediatric diabetes and screening for undiagnosed type 2 diabetes in Chinese children in years 2017-2019, a cross-sectional study.
2017 - 2019年中国儿童自我报告的儿科糖尿病患病率及未诊断的2型糖尿病筛查:一项横断面研究
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The Interplay of Mitochondrial Dysfunction in Oral Diseases: Recent Updates in Pathogenesis and Therapeutic Implications.线粒体功能障碍在口腔疾病中的相互作用:发病机制和治疗意义的最新研究进展。
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A nexus of lipid and Glcnac metabolism in physiology and disease.脂质和 Glcnac 代谢在生理和疾病中的联系。
Front Endocrinol (Lausanne). 2022 Aug 30;13:943576. doi: 10.3389/fendo.2022.943576. eCollection 2022.
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-GlcNAcylation Suppresses the Ion Current IClswell by Preventing the Binding of the Protein ICln to α-Integrin.N-乙酰葡糖胺化通过阻止蛋白质ICln与α-整合素结合来抑制肿胀激活氯离子电流(IClswell) 。
Front Cell Dev Biol. 2020 Nov 19;8:607080. doi: 10.3389/fcell.2020.607080. eCollection 2020.
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Causes, consequences, and treatment of metabolically unhealthy fat distribution.代谢不健康的脂肪分布的原因、后果和治疗。
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Adolescent Obesity and Early-Onset Type 2 Diabetes.青少年肥胖与 2 型糖尿病早发
Diabetes Care. 2020 Jul;43(7):1487-1495. doi: 10.2337/dc19-1988. Epub 2020 Apr 22.
9
O-GlcNAc transferase inhibits visceral fat lipolysis and promotes diet-induced obesity.O-GlcNAc 转移酶抑制内脏脂肪脂解,促进饮食诱导的肥胖。
Nat Commun. 2020 Jan 10;11(1):181. doi: 10.1038/s41467-019-13914-8.
10
Rapid progression of type 2 diabetes and related complications in children and young people-A literature review.儿童和青少年 2 型糖尿病及其相关并发症的快速进展——文献综述。
Pediatr Diabetes. 2020 Mar;21(2):158-172. doi: 10.1111/pedi.12953. Epub 2020 Jan 10.