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Differential Patterns of Gut and Oral Microbiomes in Hispanic Individuals with Cognitive Impairment
by
Wadop, Yannick N.
, Kautz, Tiffany F.
, Vasquez, Erin L.
, Maestre, Gladys
, Fongang, Bernard
, Seshadri, Sudha
, Satizabal, Claudia L.
, Gonzales, Mitzi M.
, Tanner, Jeremy
, Fonteh, Alfred N.
, Mathews, Julia J.
, Muhammad, Jazmyn A. S.
, Pirela Mavarez, Rosa
in
Abundance
/ Alzheimer's disease
/ Analysis
/ Anti-inflammatory agents
/ anti-inflammatory properties
/ Brain research
/ Cognitive ability
/ cognitive impairment
/ Creatinine
/ Dementia
/ Dementia disorders
/ Dysbacteriosis
/ Ethics
/ Gene sequencing
/ Genes
/ Genomes
/ Gingivitis
/ Gum disease
/ gut microbiome
/ Gut microbiota
/ Hispanic Americans
/ Homocysteine
/ Impairment
/ Intestinal microflora
/ KEGG pathways
/ Medical laboratories
/ Microbiomes
/ Neurodegenerative diseases
/ oral microbiome
/ Pathogenesis
/ Periodontal diseases
/ Phylogenetics
/ Physiology
/ RNA
/ rRNA 16S
/ Saliva
/ Synergistic effect
2025
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Differential Patterns of Gut and Oral Microbiomes in Hispanic Individuals with Cognitive Impairment
by
Wadop, Yannick N.
, Kautz, Tiffany F.
, Vasquez, Erin L.
, Maestre, Gladys
, Fongang, Bernard
, Seshadri, Sudha
, Satizabal, Claudia L.
, Gonzales, Mitzi M.
, Tanner, Jeremy
, Fonteh, Alfred N.
, Mathews, Julia J.
, Muhammad, Jazmyn A. S.
, Pirela Mavarez, Rosa
in
Abundance
/ Alzheimer's disease
/ Analysis
/ Anti-inflammatory agents
/ anti-inflammatory properties
/ Brain research
/ Cognitive ability
/ cognitive impairment
/ Creatinine
/ Dementia
/ Dementia disorders
/ Dysbacteriosis
/ Ethics
/ Gene sequencing
/ Genes
/ Genomes
/ Gingivitis
/ Gum disease
/ gut microbiome
/ Gut microbiota
/ Hispanic Americans
/ Homocysteine
/ Impairment
/ Intestinal microflora
/ KEGG pathways
/ Medical laboratories
/ Microbiomes
/ Neurodegenerative diseases
/ oral microbiome
/ Pathogenesis
/ Periodontal diseases
/ Phylogenetics
/ Physiology
/ RNA
/ rRNA 16S
/ Saliva
/ Synergistic effect
2025
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Do you wish to request the book?
Differential Patterns of Gut and Oral Microbiomes in Hispanic Individuals with Cognitive Impairment
by
Wadop, Yannick N.
, Kautz, Tiffany F.
, Vasquez, Erin L.
, Maestre, Gladys
, Fongang, Bernard
, Seshadri, Sudha
, Satizabal, Claudia L.
, Gonzales, Mitzi M.
, Tanner, Jeremy
, Fonteh, Alfred N.
, Mathews, Julia J.
, Muhammad, Jazmyn A. S.
, Pirela Mavarez, Rosa
in
Abundance
/ Alzheimer's disease
/ Analysis
/ Anti-inflammatory agents
/ anti-inflammatory properties
/ Brain research
/ Cognitive ability
/ cognitive impairment
/ Creatinine
/ Dementia
/ Dementia disorders
/ Dysbacteriosis
/ Ethics
/ Gene sequencing
/ Genes
/ Genomes
/ Gingivitis
/ Gum disease
/ gut microbiome
/ Gut microbiota
/ Hispanic Americans
/ Homocysteine
/ Impairment
/ Intestinal microflora
/ KEGG pathways
/ Medical laboratories
/ Microbiomes
/ Neurodegenerative diseases
/ oral microbiome
/ Pathogenesis
/ Periodontal diseases
/ Phylogenetics
/ Physiology
/ RNA
/ rRNA 16S
/ Saliva
/ Synergistic effect
2025
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Differential Patterns of Gut and Oral Microbiomes in Hispanic Individuals with Cognitive Impairment
Journal Article
Differential Patterns of Gut and Oral Microbiomes in Hispanic Individuals with Cognitive Impairment
2025
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Overview
Alterations in both oral and gut microbiomes have been associated with Alzheimer’s disease and related dementia (ADRD). While extensive research has focused on the role of gut dysbiosis in ADRD, the contribution of the oral microbiome remains relatively understudied. This study aims to evaluate distinct patterns and potential synergistic effects of oral and gut microbiomes in a cohort of predominantly Hispanic individuals with cognitive impairment (CI) and without cognitive impairment (NC). We conducted 16S rRNA gene sequencing on stool and saliva samples from 32 participants (17 CI, 15 NC; 62.5% female, mean age = 70.4 ± 6.2 years) recruited in San Antonio, Texas, USA. Differential abundance analysis evaluated taxa with significant differences between both groups. While diversity metrics showed no significant differences between CI and NC groups, differential abundance analysis revealed an increased presence of oral genera such as Dialister, Fretibacterium, and Mycoplasma in CI participants. Conversely, CI individuals exhibited a decreased abundance of gut genera, including Shuttleworthia, Holdemania, and Subdoligranulum, which are known for their anti-inflammatory properties. No evidence was found for synergistic contributions between oral and gut microbiomes in the context of CI. Our findings suggest that like the gut microbiome, the oral microbiome of CI participants undergoes significant modifications. Notably, the identified oral microbes have been previously associated with periodontal diseases and gingivitis. These results underscore the necessity for further investigations with larger sample sizes to validate our findings and elucidate the complex interplay between oral and gut microbiomes in ADRD pathogenesis.
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