Profiles of subgingival microbiomes and gingival crevicular metabolic signatures in patients with amnestic mild cognitive impairment and Alzheimer's disease

被引:12
作者
Qiu, Che [1 ,2 ,3 ,4 ,5 ,6 ]
Zhou, Wei [3 ,4 ,5 ,6 ,7 ,8 ]
Shen, Hui [1 ,2 ,3 ,4 ,5 ,6 ]
Wang, Jintao [9 ,10 ]
Tang, Ran [9 ,10 ]
Wang, Tao [11 ,12 ]
Xie, Xinyi [1 ,2 ,3 ,4 ,5 ,6 ]
Hong, Bo [11 ,12 ]
Ren, Rujing [9 ,10 ]
Wang, Gang [9 ,10 ]
Song, Zhongchen [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Sch Med, Dept Periodontol, Zhizaoju Rd 639, Shanghai 200011, Peoples R China
[2] Shanghai Jiao Tong Univ, Coll Stomatol, Zhizaoju Rd 639, Shanghai 200011, Peoples R China
[3] Natl Ctr Stomatol, Shanghai 200011, Peoples R China
[4] Natl Clin Res Ctr Oral Dis, Zhizaoju Rd 639, Shanghai 200011, Peoples R China
[5] Shanghai Key Lab Stomatol, Zhizaoju Rd 639, Shanghai 200011, Peoples R China
[6] Shanghai Res Inst Stomatol, Zhizaoju Rd 639, Shanghai 200011, Peoples R China
[7] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Sch Med, Lab Oral Microbiota & Syst Dis, Jinzun Road 115, Shanghai 200125, Peoples R China
[8] Shanghai Jiao Tong Univ, Coll Stomatol, Jinzun Rd 115, Shanghai 200125, Peoples R China
[9] Shanghai Jiao Tong Univ, Sch Med, Dept Neurol, Ruijin Hosp, Ruijin 2nd Rd 197, Shanghai 200025, Peoples R China
[10] Shanghai Jiao Tong Univ, Ruijin Hosp, Inst Neurol, Sch Med, Ruijin 2nd Rd 197, Shanghai 200025, Peoples R China
[11] Shanghai Jiao Tong Univ, Shanghai Mental Hlth Ctr, Sch Med, Dept Geriatr Psychiat, South Wanping Rd 600, Shanghai 200030, Peoples R China
[12] Shanghai Jiao Tong Univ, Alzheimers Dis & Related Disorders Ctr, South Wanping Rd 600, Shanghai 200030, Peoples R China
基金
中国国家自然科学基金;
关键词
Microbiome; Metabolome; Multiomics; Alzheimer's disease; Mild cognitive impairment; Periodontitis; PERIODONTAL-DISEASE; CLASSIFICATION; HEALTH; GALACTOSE; DEMENTIA;
D O I
10.1186/s13195-024-01402-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundThe relationship between periodontitis and Alzheimer's disease (AD) has attracted more attention recently, whereas profiles of subgingival microbiomes and gingival crevicular fluid (GCF) metabolic signatures in AD patients have rarely been characterized; thus, little evidence exists to support the oral-brain axis hypothesis. Therefore, our study aimed to characterize both the microbial community of subgingival plaque and the metabolomic profiles of GCF in patients with AD and amnestic mild cognitive impairment (aMCI) for the first time.MethodsThis was a cross-sectional study. Clinical examinations were performed on all participants. The microbial community of subgingival plaque and the metabolomic profiles of GCF were characterized using the 16S ribosomal RNA (rRNA) gene high-throughput sequencing and liquid chromatography linked to tandem mass spectrometry (LC-MS/MS) analysis, respectively.ResultsThirty-two patients with AD, 32 patients with aMCI, and 32 cognitively normal people were enrolled. The severity of periodontitis was significantly increased in AD patients compared with aMCI patients and cognitively normal people. The 16S rRNA gene sequencing results showed that the relative abundances of 16 species in subgingival plaque were significantly correlated with cognitive function, and LC-MS/MS analysis identified a total of 165 differentially abundant metabolites in GCF. Moreover, multiomics Data Integration Analysis for Biomarker discovery using Latent cOmponents (DIABLO) analysis revealed that 19 differentially abundant metabolites were significantly correlated with Veillonella parvula, Dialister pneumosintes, Leptotrichia buccalis, Pseudoleptotrichia goodfellowii, and Actinomyces massiliensis, in which galactinol, sn-glycerol 3-phosphoethanolamine, D-mannitol, 1 h-indole-1-pentanoic acid, 3-(1-naphthalenylcarbonyl)- and L-iditol yielded satisfactory accuracy for the predictive diagnosis of AD progression.ConclusionsThis is the first combined subgingival microbiome and GCF metabolome study in patients with AD and aMCI, which revealed that periodontal microbial dysbiosis and metabolic disorders may be involved in the etiology and progression of AD, and the differential abundance of the microbiota and metabolites may be useful as potential markers for AD in the future.
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页数:17
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