临汾市人民医院儿童保健科 临汾 041000
张德全 硕士 副主任医师;研究方向:儿童保健(生长发育、营养、言语行为发育,E-mail: zdq15333089993@163.com
收稿:2025-04-24,
纸质出版:2025-09-15
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张德全.肠道菌群-神经生理因素交互作用对孤独症谱系障碍儿童语言发育的影响[J].中国听力语言康复科学杂志,2025,23(05):542-547.
ZHANG De-quan.Analysis of the Influence of Interaction between Intestinal Flora and Neurophysiological Factors on Language Development in Children with Autism[J].Chinese Scientific Journal of Hearing and Speech Rehabilitation,2025,23(05):542-547.
张德全.肠道菌群-神经生理因素交互作用对孤独症谱系障碍儿童语言发育的影响[J].中国听力语言康复科学杂志,2025,23(05):542-547. DOI: 10.3969/j.issn.1672-4933.2025.05.022.
ZHANG De-quan.Analysis of the Influence of Interaction between Intestinal Flora and Neurophysiological Factors on Language Development in Children with Autism[J].Chinese Scientific Journal of Hearing and Speech Rehabilitation,2025,23(05):542-547. DOI: 10.3969/j.issn.1672-4933.2025.05.022.
目的
2
探讨肠道菌群与神经生理因素的交互作用对孤独症谱系障碍(ASD)儿童语言发育的影响,揭示其潜在的肠-脑轴调控机制。
方法
2
采用回顾性队列研究设计,纳入82例3~8岁ASD患儿,根据临床评估语言基础量表(clinical evaluation of language fundamentals-fifth edition, CELF-5)分为语言发育迟缓组(n=52)与语言发育正常组(n=30)。通过16S rRNA测序分析肠道菌群多样性及物种组成,静息态fMRI和脑电频谱评估语言网络功能连接,酶联免疫吸附测定(enzyme-linked immunosorbent assay, ELISA)检测血清5-羟色胺(5-hydroxytryptamine, 5-HT)、脑源性神经营养因子(brain-derived neurotrophic factor, BDNF)及短链脂肪酸(short-chain fatty acids, SCFAs)水平。
结果
2
语言发育迟缓组呈现肠道菌群α多样性降低(Shannon指数:3.82±0.51 vs 4.25±0.63,
P
=0.001),厚壁菌门(Firmicutes, LDA=4.32,
P
=0.002)及产气荚膜梭菌(Clostridium perfringens,丰度提高3.1倍)显著富集,而语言发育正常组拟杆菌属(Bacteroidales, LDA=3.78,
P
=0.008)和普雷沃菌属(
Prevotella
, LDA=3.92,
P
=0.004)占优。神经生理层面,语言发育迟缓组γ频段功能连接强度降低29.3%(0.29±0.09 vs. 0.41±0.11,
P
<
0.001),血清5-HT水平升高25.3%(182.62±35.42 vs. 145.86±28.71 ng/mL,
P
<
0.001),BDNF和SCFAs水平分别降低23.4%和16.0%(
P
<
0.05)。
结论
2
ASD语言发育迟缓与肠道菌群(梭菌属富集)、神经递质(5-HT/BDNF)失衡及神经生理(γ频段振荡受损)特征相关,其中普雷沃菌属可能通过SCFAs-迷走神经通路增强语言网络功能连接。尽管跨系统异常提示肠-脑轴存在潜在关联,但三者间的直接级联因果关系尚未明确。
Objective
2
To explore the effect of the interaction between intestinal flora and neurophysiological factors on language development in children with autism spectrum disorder (ASD)
and to reveal the potential "gut-brain axis" regulation mechanism.
Methods
2
A retrospective cohort study was designed to include 82 children aged 3-8 years with ASD
who were divided into language retardation group (n=52) and normal language development group (n=30) according to Clinical Evaluation of Language Fundamentals-Fifth Edition (CELF-5). The diversity and species composition of intestinal flora were analyzed by 16S rRNA sequencing. The functional connectivity of language network was evaluated by resting state fMRI and EEG spectrum
and 5-Hydroxytrypt
amine (5-HT). Brain-Derived Neurotrophic Factor (BDNF) and Short-Chain Fatty Acids (SCFAs) were detected by Enzyme-Linked Immunosorbent Assay(ELISA)
.
Results
2
The language development delay group showed a decreased alpha diversity of the gut microbiota (Shannon index:) 3.82±0.51 vs 4.25±0.63
P
=0.001)
Firmicutes (LDA=4.32
P
=0.002) and Clostridium perfringens (abundance increased by 3.1 times) were significantly enriched. In the normal language development group
Bacteroidales (LDA=3.78
P
=0.008) and Prevotella (LDA=3.92
P
=0.004) were dominant. At the neurophysiological level
the functional connectivity intensity of the γ band in the language development delay group decreased by 29.3% (0.29±0.09 vs. 0.41±0.11
P
<
0.001)
and the serum 5-HT level increased by 25.3% (182.62±35.42 vs. 145.86±28.71 ng/mL) (
P
<
0.001)
the levels of BDNF and SCFAs decreased by 23.4% and 16.0% respectively (
P
<
0.05).
Conclusion
2
TASD language development delay is associated with intestinal microbiota (Clostridium enrichment)
neurotransmitters (5-HT/BDNF imbalance)
and neurophysiological characteristics (impaired γ band oscillations). Among them
Prevotella may enhance the functional connectivity of the language network through the SCFas-vagus nerve pathway
although cross-system abnormalities suggest a potential association with the "gut-brain axis". However
the direct cascading causal relationship among the three remains unclear.
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