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探索胶质细胞源性神经营养因子在自闭症谱系障碍中发挥神经元保护作用的机制。

Exploring the Mechanisms of Neuronal Protection by Glial Cell Line-Derived Neurotrophic Factor in Autism Spectrum Disorder.

作者信息

Ali Raja Sarwat, Batool Amna, Sana Maryum, Khaliq Hafiz Muhammad Haseeb, Choudhry Faiza, Devi Durga

机构信息

Pharmacy, Yashfeen Education College of Pharmacy & Allied Health, Bhawalpur, PAK.

Surgery, Fatima Memorial Hospital, Lahore, PAK.

出版信息

Cureus. 2024 Oct 5;16(10):e70913. doi: 10.7759/cureus.70913. eCollection 2024 Oct.

Abstract

BACKGROUND

A complicated neurological disease known as autism spectrum disorder (ASD) is typified by issues with social interaction, communication, and repetitive behavior. The neural protective mechanisms in ASD are thought to be influenced by genetic variables, including the expression of neurotrophic genes such as glial cell line-derived neurotrophic factor (GDNF).

OBJECTIVE

The aim was to examine the relationship between neuronal protection and cognitive functioning by crosslinking GDNF gene expression and serum levels in individuals with relation to Mini-Mental State Examination (MMSE) scores in ASD patients.

MATERIALS AND METHODS

After getting study approval and informed consent of patients, this case-control study experimental study was conducted for six months between July 2023 and December 2023. The blood samples (5 ml each) were drawn from the study population (n = 140), including 100 ASD patients with a disease course of 30 months based on patients' reports data and 40 healthy controls from four major clinical and hospital settings in Lahore, Karachi, and Bahawalpur from Pakistan. The analytical procedures included nucleic acid extraction, primer design and optimization, and GDNF-targeted real-time quantitative polymerase chain reaction expression analysis. To measure cognitive and behavioral deficits, enzyme-linked immunosorbent assay-based serum GDNF levels (pg/ml) and MMSE scores were compared, concluding the neuronal protection potential of GDNF.

RESULTS

In patients with ASD, lower serum levels of GDNF (9.371 ± 2.388 pg/ml) were linked to more severe behavioral and cognitive deficits confirmed by MMSE scores (13.6 ± 3.5) of ASD patients in comparison with the control group (27.1 ± 2.1). Healthy individuals showed higher relative gene fold expression (11.71) compared to the ASD patients (5.51).

CONCLUSION

There is a notable decrease in GDNF gene expression in people with ASD, which raises the possibility that GDNF is important for both cognitive performance and neuronal protection in these people. GDNF may be a useful biomarker for identifying ASD and comprehending its molecular causes, opening the door for focused treatment approaches.

摘要

背景

自闭症谱系障碍(ASD)是一种复杂的神经疾病,其特征是社交互动、沟通和重复行为存在问题。ASD中的神经保护机制被认为受遗传变量影响,包括神经营养基因如胶质细胞源性神经营养因子(GDNF)的表达。

目的

通过将GDNF基因表达和血清水平与ASD患者的简易精神状态检查表(MMSE)评分相关联,研究神经元保护与认知功能之间的关系。

材料与方法

在获得研究批准并征得患者知情同意后,于2023年7月至2023年12月进行了为期六个月的病例对照研究实验。从研究人群(n = 140)中采集血样(每份5 ml),包括100名根据患者报告数据病程为30个月的ASD患者,以及来自巴基斯坦拉合尔、卡拉奇和巴哈瓦尔布尔四个主要临床和医院机构的40名健康对照。分析程序包括核酸提取、引物设计与优化以及针对GDNF的实时定量聚合酶链反应表达分析。为测量认知和行为缺陷,比较了基于酶联免疫吸附测定的血清GDNF水平(pg/ml)和MMSE评分,得出GDNF的神经元保护潜力。

结果

与对照组(27.1 ± 2.1)相比,ASD患者中较低的血清GDNF水平(9.371 ± 2.388 pg/ml)与更严重的行为和认知缺陷相关,这由ASD患者的MMSE评分(13.6 ± 3.5)证实。与ASD患者(5.51)相比,健康个体显示出更高的相对基因折叠表达(11.71)。

结论

ASD患者中GDNF基因表达显著降低,这增加了GDNF对这些患者的认知表现和神经元保护都很重要的可能性。GDNF可能是用于识别ASD并理解其分子病因的有用生物标志物,为针对性治疗方法打开了大门。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbfc/11535394/b6d905f72cbc/cureus-0016-00000070913-i01.jpg

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