4.5 Article

Analysis of Salivary Microbiome in Patients with Alzheimer's Disease

期刊

JOURNAL OF ALZHEIMERS DISEASE
卷 72, 期 2, 页码 633-640

出版社

IOS PRESS
DOI: 10.3233/JAD-190587

关键词

Alzheimer's disease; APOE; oral microbiome; 16S rRNA

资金

  1. National Natural Science Foundation of China [81671075, 81701134]
  2. National Key R&D Program of China [2017YFC0840100, 2017YFC0840104]
  3. Xiangya Hospital Youth Scientific Research Fund [2016Q01]

向作者/读者索取更多资源

Recent studies found that poor oral hygiene was associated with increased risk of dementia, and the number of oral bacteria significantly increased in the brain tissues of patients with Alzheimer's disease (AD), suggesting that the oral microbiota may play an important role in the pathogenesis of AD. However, the actual composition of oral bacteria communities in patients with AD and whether these oral bacteria are associated with disease severity remain largely unknown. Also, the APOE epsilon 4 polymorphism is a strong risk factor for sporadic AD, and it would be pertinent to see if the bacterial flora was different in those patients who were APOE epsilon 4 positive. A total of 78 subjects were recruited in this study, including 39 patients with AD and 39 healthy controls. Saliva was collected from each subject. 16S ribosomal RNA(16S rRNA) sequencing was conducted to analyze the salivary microbiota, and Sanger sequencing was performed to analyze the APOE genotype. There was a significantly lower richness and diversity of saliva microbiota detected in AD patients than healthy controls. The relative abundance of Moraxella, Leptotrichia, and Sphaerochaeta in the saliva of AD patients greatly increased, whereas that of Rothia was significantly reduced. Compared with APOE epsilon 4 (-) patients, the level of Abiotrophia and Desulfomicrobium was comparatively abundant, while Actinobacillus and Actinomyces decreased significantly in patients carrying the APOE epsilon 4. No bacteria were found to be associated with the severity of AD. This is the first study to analyze the salivary microorganisms in patients with AD, and we discovered that the composition of salivary microbiome was altered in AD, providing further support for the role of the oral microbiome in AD development.

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