TY - JOUR
T1 - Relationship Between Plasma Lipopolysaccharides, Gut Microbiota, and Dementia
T2 - A Cross-Sectional Study
AU - Saji, Naoki
AU - Saito, Yoshihiro
AU - Yamashita, Tomoya
AU - Murotani, Kenta
AU - Tsuduki, Tsuyoshi
AU - Hisada, Takayoshi
AU - Sugimoto, Taiki
AU - Niida, Shumpei
AU - Toba, Kenji
AU - Sakurai, Takashi
N1 - Funding Information:
This study was supported by a Grant-in-Aid for Scientific Research (C), JSPS KAKENHI (20k07 861), grants from the Research Funding of Longevity Sciences from the NCGG (19-24), the NARO Bio-Oriented Technology Research Advancement Institution Project (Advanced Integration Research for Agriculture and Interdisciplinary Fields), the Danone Institute of Japan Foundation, the Honjo International Scholarship Foundation (to Dr. Saji), and the PRIME from the Japan Agency for Medical Research and Development (AMED) under Grant Number 18069370 (to Dr.Yamashita).Wewould like to thank Yukie Ohsaki, Maki Yamamoto, Hana Saito, and Ayaka Suzuki (NCGG) for their technical and secretarial assistance. We also thank the BioBank and NCGG for quality control of the clinical samples and data. Finally, we thank Sarina Iwabuchi, PhD, from Edanz (https://jp.edanz.com/ac) for editing a draft of this manuscript.
Funding Information:
This study was supported by a Grant-in-Aid for Scientific Research (C), JSPS KAKENHI (20k07 861), grants from the Research Funding of Longevity Sciences from the NCGG (19–24), the NARO Bio-Oriented Technology Research Advancement Institution Project (Advanced Integration Research for Agriculture and Interdisciplinary Fields), the Danone Institute of Japan Foundation, the Honjo International Scholarship Foundation (to Dr. Saji), and the PRIME from the Japan Agency for Medical Research and Development (AMED) under Grant Number 18069370 (to Dr. Yamashita). We would like to thank Yukie Ohsaki, Maki Yamamoto, Hana Saito, and Ayaka Suzuki (NCGG) for their technical and secretarial assistance. We also thank the BioBank and NCGG for quality control of the clinical samples and data. Finally, we thank Sarina Iwabuchi, PhD,
Publisher Copyright:
© 2022 The authors.
PY - 2022
Y1 - 2022
N2 - Background: Previous studies have demonstrated associations between gut microbiota, microbial metabolites, and cognitive decline. However, relationships between these factors and lipopolysaccharides (LPS; molecules of the outer membrane of gram-negative bacteria) remain controversial. Objective: To evaluate associations between plasma LPS, gut microbiota, and cognitive function. Methods: We performed a cross-sectional sub-analysis of data of 127 participants (women: 58%, mean age: 76 years) from our prospective cohort study regarding the relationship between gut microbiota and cognitive function. We enrolled patients who visited our memory clinic and assessed demographics, dementia-related risk factors, cognitive function, brain imaging, gut microbiomes, and microbial metabolites. We evaluated relationships between cognitive decline and plasma LPS using multivariable logistic regression analyses. Results: Plasma LPS concentration increased with increasing degree of cognitive decline and total cerebral small vessel disease (SVD) score (Kruskal-Wallis test; p = 0.016 and 0.007, respectively). Participants with high plasma LPS concentrations tended to have lower concentrations of gut microbial metabolites, such as lactic acid and acetic acid, and were less likely to consume fish and shellfish (44.7% versus 69.6%, p = 0.027) than those with low plasma LPS concentrations. Multivariable analyses revealed that plasma LPS concentration was independently associated with the presence of mild cognitive impairment in participants without dementia (odds ratio: 2.09, 95% confidence interval: 1.14-3.84, p = 0.007). Conclusion: In this preliminary study, plasma LPS concentration was associated with both cognitive decline and cerebral SVD and significantly correlated with beneficial gut microbial metabolites. Plasma LPS may be a risk factor for cognitive decline.
AB - Background: Previous studies have demonstrated associations between gut microbiota, microbial metabolites, and cognitive decline. However, relationships between these factors and lipopolysaccharides (LPS; molecules of the outer membrane of gram-negative bacteria) remain controversial. Objective: To evaluate associations between plasma LPS, gut microbiota, and cognitive function. Methods: We performed a cross-sectional sub-analysis of data of 127 participants (women: 58%, mean age: 76 years) from our prospective cohort study regarding the relationship between gut microbiota and cognitive function. We enrolled patients who visited our memory clinic and assessed demographics, dementia-related risk factors, cognitive function, brain imaging, gut microbiomes, and microbial metabolites. We evaluated relationships between cognitive decline and plasma LPS using multivariable logistic regression analyses. Results: Plasma LPS concentration increased with increasing degree of cognitive decline and total cerebral small vessel disease (SVD) score (Kruskal-Wallis test; p = 0.016 and 0.007, respectively). Participants with high plasma LPS concentrations tended to have lower concentrations of gut microbial metabolites, such as lactic acid and acetic acid, and were less likely to consume fish and shellfish (44.7% versus 69.6%, p = 0.027) than those with low plasma LPS concentrations. Multivariable analyses revealed that plasma LPS concentration was independently associated with the presence of mild cognitive impairment in participants without dementia (odds ratio: 2.09, 95% confidence interval: 1.14-3.84, p = 0.007). Conclusion: In this preliminary study, plasma LPS concentration was associated with both cognitive decline and cerebral SVD and significantly correlated with beneficial gut microbial metabolites. Plasma LPS may be a risk factor for cognitive decline.
KW - Biomarkers
KW - cerebral small vessel disease
KW - cognitive decline
KW - dementia
KW - gut microbiota
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U2 - 10.3233/JAD-215653
DO - 10.3233/JAD-215653
M3 - Article
C2 - 35213381
AN - SCOPUS:85129321173
SN - 1387-2877
VL - 86
SP - 1947
EP - 1957
JO - Journal of Alzheimer's Disease
JF - Journal of Alzheimer's Disease
IS - 4
ER -