Evidence map›Paper›PMID 36093178›Full record

ArticleFrontiers in cellular and infection microbiology2022

A comparison of the composition and functions of the oral and gut microbiotas in Alzheimer's patients.

Lili Chen, Xinhua Xu, Xiaoqi Wu, Huizhen Cao, Xiuli Li, Zhaoyi Hou, Bixia Wang, Jinxiu Liu, Xinli Ji, Ping Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
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  4. Intersections of gastrointestinal dysbiosis of the gut microbiome and aging.World journal of gastrointestinal pathophysiology · 2026
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  13. Open medicine (Warsaw, Poland) · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Lili ChenThe School of Nursing, Fujian Medical University, Fuzhou, China.
Xinhua XuThe School of Nursing, Fujian Medical University, Fuzhou, China.
Xiaoqi WuCollege of Traditional Chinese Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, China.
Huizhen CaoThe School of Nursing, Fujian Medical University, Fuzhou, China.
Xiuli LiThe School of Nursing, Fujian Medical University, Fuzhou, China.
Zhaoyi HouThe School of Nursing, Fujian Medical University, Fuzhou, China.
Bixia WangThe School of Nursing, Fujian Medical University, Fuzhou, China.
Jinxiu LiuThe School of Nursing, Fujian Medical University, Fuzhou, China.
Xinli JiThe School of Nursing, Fujian Medical University, Fuzhou, China.
Ping ZhangThe School of Nursing, Fujian Medical University, Fuzhou, China.
Hong LiThe School of Nursing, Fujian Medical University, Fuzhou, China.
Fujian Medical University · CNFujian Provincial Hospital · CNFujian University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Alterations in the oral or gut microbiotas have been reported in patients with subjective and mild cognitive impairment or AD dementia. However, whether these microbiotas change with the severity of the AD spectrum (mild, moderate, and severe AD) remains unknown. Thus, we compared alterations in the composition and gene functions of the oral and gut microbiota between different phases of AD. Methods: We recruited 172 individuals and classified these into three groups: healthy controls (n = 40), a mild AD group (n = 43) and a moderate AD group (n = 89). Subgingival plaques and fecal samples were collected from all individuals. Then, we conducted 16S ribosomal RNA. sequencing to analyze the microbiotas. Results: In order of the severity of cognition impairment (from normal to mild and to moderate AD), the oral abundances of the phyla Firmicutes and Fusobacteria showed a gradual upwards trend, while the abundance of the Proteobacteria phylum gradually decreased. In contrast, the abundance of the Firmicutes and Bacteroidetes phyla in the gut decreased progressively, while that of the Proteobacteria, Verrucomicrobia and Actinobacteria phyla increased gradually. Key differences were identified in the microbiomes when compared between the mild AD and moderate AD groups when applying the linear discriminant analysis effect size (LEfSe) algorithm. LEfSe analysis revealed alterations that were similar to those described above; furthermore, different bacterial taxa were associated with MMSE scores and age. KEGG analysis showed that the functional pathways associated with the oral microbiota were mainly involved in membrane transport and carbohydrate metabolism, while the gene functions of the fecal microbiota related to metabolism of amino acids, energy, cofactors and vitamins; identified significant differences among the three groups. Venn diagram analysis revealed that the number of genera that were present in both the oral and gut microbiota increased progressively from NC to mild AD and then to moderate AD. Conclusions: This study is the first to report a comparative analysis of the oral and fecal microbiota of patients with mild and moderate AD. The compositions and functions of the oral and gut microbiotas differed when compared between different stages of AD.

Indexed as

Alzheimer DiseaseGastrointestinal MicrobiomeBacillotaFecesHumansProteobacteriaRNA, Ribosomal, 16SVerrucomicrobiaRNA, Ribosomal, 16S16S ribosomal RNAAlzheimer’s diseasegut microbiomeoral-gut-brain axisoral microbiome

Identifiers

PMID36093178
PMCPMC9448892
OpenAlexW4292878181

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.