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The Difference of Gut Microbiota and Their Correlations With Urinary Organic Acids Between Autistic Children With and Without Atopic Dermatitis
被引:3
|作者:
Hong, Ru-ping
[1
]
Hou, Yue-ying
[1
]
Xu, Xin-jie
[2
]
Lang, Ji-dong
[3
]
Jin, Yun-feng
[4
]
Zeng, Xiao-feng
[1
,5
,6
]
Zhang, Xuan
[1
,5
,6
]
Tian, Geng
[3
]
You, Xin
[1
,5
,6
,7
]
机构:
[1] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Rheumatol & Clin Immunol, Beijing, Peoples R China
[2] Peking Union Med Coll Hosp, Med Sci Res Ctr, Res Ctr Translat Med, Dept Sci Res, Beijing, Peoples R China
[3] Geneis Beijing Co Ltd, Beijing, Peoples R China
[4] Beijing Herun Clin, Beijing, Peoples R China
[5] Minist Educ, Key Lab Rheumatol & Clin Immunol, Beijing, Peoples R China
[6] Natl Clin Res Ctr Dermatol & Immunol Dis NCRC DID, Beijing, Peoples R China
[7] Peking Union Med Fdn, Autism Special Fund, Beijing, Peoples R China
来源:
关键词:
autism;
atopic dermatitis;
gut microbiota;
organic acids;
mitochondrial dysfunction;
CHAIN FATTY-ACIDS;
OMICRON-HYDROXYHIPPURIC ACID;
AKKERMANSIA-MUCINIPHILA;
SPECTRUM DISORDER;
GASTROINTESTINAL SYMPTOMS;
METABOLIC SYNDROME;
CELIAC-DISEASE;
RECEPTOR;
INFLAMMATION;
COMORBIDITY;
D O I:
10.3389/fcimb.2022.886196
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Autism is a kind of biologically based neurodevelopmental condition, and the coexistence of atopic dermatitis (AD) is not uncommon. Given that the gut microbiota plays an important role in the development of both diseases, we aimed to explore the differences of gut microbiota and their correlations with urinary organic acids between autistic children with and without AD. We enrolled 61 autistic children including 36 with AD and 25 without AD. The gut microbiota was sequenced by metagenomic shotgun sequencing, and the diversity, compositions, and functional pathways were analyzed further. Urinary organic acids were assayed by gas chromatography-mass spectrometry, and univariate/multivariate analyses were applied. Spearman correlation analysis was conducted to explore their relationships. In our study, AD individuals had more prominent gastrointestinal disorders. The alpha diversity of the gut microbiota was lower in the AD group. LEfSe analysis showed a higher abundance of Anaerostipes caccae, Eubacterium hallii, and Bifidobacterium bifidum in AD individuals, with Akkermansia muciniphila, Roseburia intestinalis, Haemophilus parainfluenzae, and Rothia mucilaginosa in controls. Meanwhile, functional profiles showed that the pathway of lipid metabolism had a higher proportion in the AD group, and the pathway of xenobiotics biodegradation was abundant in controls. Among urinary organic acids, adipic acid, 3-hydroxyglutaric acid, tartaric acid, homovanillic acid, 2-hydroxyphenylacetic acid, aconitic acid, and 2-hydroxyhippuric acid were richer in the AD group. However, only adipic acid remained significant in the multivariate analysis (OR = 1.513, 95% CI [1.042, 2.198], P = 0.030). In the correlation analysis, Roseburia intestinalis had a negative correlation with aconitic acid (r = -0.14, P = 0.02), and the latter was positively correlated with adipic acid (r = 0.41, P = 0.006). Besides, the pathway of xenobiotics biodegradation seems to inversely correlate with adipic acid (r = -0.42, P = 0.18). The gut microbiota plays an important role in the development of AD in autistic children, and more well-designed studies are warranted to explore the underlying mechanism.
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