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Exploring the Mechanisms of Neuronal Protection by Glial Cell Line-Derived Neurotrophic Factor in Autism Spectrum
Sarwat Ali Raja1, Amna Batool2, Maryum Sana3,4
1Pharmacy, Yashfeen Education College of Pharmacy & Allied Health, Bhawalpur, PAK.
Cureus
|November 6, 2024
Summary
Glial cell line-derived neurotrophic factor (GDNF) levels are decreased in autism spectrum disorder (ASD), correlating with cognitive deficits. Lower GDNF may indicate reduced neuronal protection in ASD patients.
Area of Science:
- Neuroscience
- Genetics
- Biochemistry
Background:
- Autism spectrum disorder (ASD) is a complex neurological condition characterized by social interaction, communication, and behavioral challenges.
- Genetic factors, including neurotrophic genes like glial cell line-derived neurotrophic factor (GDNF), are implicated in ASD's neural protective mechanisms.
Purpose of the Study:
- To investigate the association between GDNF gene expression and serum levels with cognitive function in ASD patients.
- To evaluate the relationship between GDNF and neuronal protection using Mini-Mental State Examination (MMSE) scores.
Main Methods:
- A case-control study involving 100 ASD patients and 40 healthy controls.
- Analysis of GDNF gene expression using real-time quantitative polymerase chain reaction (qPCR).
- Measurement of serum GDNF levels via enzyme-linked immunosorbent assay (ELISA) and cognitive assessment using MMSE scores.
Main Results:
- ASD patients exhibited significantly lower serum GDNF levels (9.371 ± 2.388 pg/ml) compared to controls (27.1 ± 2.1).
- Lower GDNF levels correlated with more severe cognitive and behavioral deficits, as indicated by lower MMSE scores (13.6 ± 3.5) in ASD patients.
- Relative GDNF gene fold expression was lower in ASD patients (5.51) than in healthy individuals (11.71).
Conclusions:
- A notable decrease in GDNF gene expression and serum levels occurs in individuals with ASD.
- GDNF appears crucial for cognitive performance and neuronal protection in ASD.
- GDNF may serve as a potential biomarker for ASD diagnosis and understanding its molecular underpinnings.
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