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脑瘫患儿铁代谢与炎症的评估

Assessment of Iron Metabolism and Inflammation in Children with Cerebral Palsy.

作者信息

Orhan Ozhan, Gokdemir Gul Sahika

机构信息

Department of Pediatrics, Faculty of Medicine, Mardin Artuklu University, Mardin 47100, Turkey.

Department of Physiology, Faculty of Medicine, Mardin Artuklu University, Mardin 47100, Turkey.

出版信息

J Clin Med. 2024 Dec 26;14(1):61. doi: 10.3390/jcm14010061.

DOI:10.3390/jcm14010061
PMID:39797144
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11721373/
Abstract

Cerebral palsy (CP) is a motor disorder resulting from brain damage that is common in childhood. Iron is vital for the body's basic functions. Iron metabolism disorders and inflammation contribute to the neurological complications seen in CP. The purpose of this research was to ascertain the association and correlation between markers of inflammation and iron metabolism in children with CP. : A total of 181 children diagnosed with CP and 111 typically developing children were retrospectively included in the study. Demographic data, blood parameters, C-reactive protein, iron, total iron binding capacity, and inflammation markers were evaluated. : C-reactive protein (CRP), neutrophil-to-lymphocyte ratio (NLR) and systemic immuno-inflammatory index (SII) levels of CP children were found to be statistically significantly higher than those of control group children ( < 0.05). Iron (Fe) and ferritin levels were lower in the CP group, while total iron binding capacity (TIBC) was higher. Spearman correlation analysis showed significant correlations between iron, ferritin and TIBC and SII. Iron deficiency and chronic inflammation are associated with the pathophysiology of CP in patients with CP, and therefore it is important to monitor markers of iron metabolism and inflammation in these patients.

摘要

脑瘫(CP)是一种由脑损伤导致的运动障碍,在儿童中很常见。铁对身体的基本功能至关重要。铁代谢紊乱和炎症会导致脑瘫中出现的神经并发症。本研究的目的是确定脑瘫患儿炎症标志物与铁代谢之间的关联和相关性。:本研究回顾性纳入了181名被诊断为脑瘫的儿童和111名发育正常的儿童。评估了人口统计学数据、血液参数、C反应蛋白、铁、总铁结合力和炎症标志物。:发现脑瘫患儿的C反应蛋白(CRP)、中性粒细胞与淋巴细胞比值(NLR)和全身免疫炎症指数(SII)水平在统计学上显著高于对照组儿童(<0.05)。脑瘫组的铁(Fe)和铁蛋白水平较低,而总铁结合力(TIBC)较高。Spearman相关性分析显示铁、铁蛋白、TIBC与SII之间存在显著相关性。铁缺乏和慢性炎症与脑瘫患者脑瘫的病理生理学相关,因此监测这些患者的铁代谢和炎症标志物很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48c1/11721373/b2b2ff19a71c/jcm-14-00061-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48c1/11721373/d3fc663aef26/jcm-14-00061-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48c1/11721373/b2b2ff19a71c/jcm-14-00061-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48c1/11721373/d3fc663aef26/jcm-14-00061-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48c1/11721373/b2b2ff19a71c/jcm-14-00061-g002.jpg

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本文引用的文献

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Association between Cu/Zn/Iron/Ca/Mg levels and cerebral palsy: a pooled-analysis.铜/锌/铁/钙/镁水平与脑瘫的关系:荟萃分析。
Sci Rep. 2023 Oct 27;13(1):18427. doi: 10.1038/s41598-023-45697-w.
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A Retrospective Analysis of the Association of Neutrophil-Lymphocyte Ratio (NLR) with Anemia in the Saudi Population.沙特人群中性粒细胞与淋巴细胞比值(NLR)与贫血相关性的回顾性分析
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Paraoxonase-1 and fetuin-A levels in children with cerebral palsy.脑瘫患儿血清对氧磷酶-1 和胎球蛋白 A 水平。
Turk J Med Sci. 2022 Jun;52(3):803-808. doi: 10.55730/1300-0144.5376. Epub 2022 Jun 16.
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Combined Blood Indexes of Systemic Inflammation as a Mirror to Admission to Intensive Care Unit in COVID-19 Patients: A Multicentric Study.全身炎症联合血液指标作为 COVID-19 患者入住重症监护病房的镜子:一项多中心研究。
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Multi-Organ Dysfunction in Cerebral Palsy.脑瘫中的多器官功能障碍
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7
Hepcidin-Ferroportin Interaction Controls Systemic Iron Homeostasis.亚铁转运蛋白与铁调素的相互作用控制着全身铁稳态。
Int J Mol Sci. 2021 Jun 17;22(12):6493. doi: 10.3390/ijms22126493.
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On Iron Metabolism and Its Regulation.关于铁代谢及其调节。
Int J Mol Sci. 2021 Apr 27;22(9):4591. doi: 10.3390/ijms22094591.
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Systematic Review: Quantitative Susceptibility Mapping (QSM) of Brain Iron Profile in Neurodegenerative Diseases.系统评价:神经退行性疾病脑铁分布的定量磁化率成像(QSM)
Front Neurosci. 2021 Feb 18;15:618435. doi: 10.3389/fnins.2021.618435. eCollection 2021.
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Neutrophil-to-lymphocyte ratio predicts the severity of motor impairment in cerebral palsy children living at home and the rehabilitation center: A comparative study.中性粒细胞与淋巴细胞比值可预测居家及康复中心脑瘫患儿运动功能障碍的严重程度:一项对比研究。
Biomed Rep. 2020 Dec;13(6):63. doi: 10.3892/br.2020.1370. Epub 2020 Oct 16.