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. 2022 Sep 24;14(19):3967. doi: 10.3390/nu14193967

Table 1.

Changes in microbiome composition, its metabolic status, and influence on host homeostasis and metabolome in AD and PD.

Alzheimer’s Disease
Microbiome Quantitative and Qualitative Changes Changes in Microbiome Metabolome Changes in Human Metabolome Systemic Effects Citation
Eubacterium deficiency; Escherichia, Shigella abundance Increased LPS Increased β-amyloid levels
Increased plasma LPS levels
Increased inflammatory state [74,93]
H. pylori infection Increased levels of H2O2 Increased levels of homocysteine Disrupted BBB integrity [98]
Increased abundance of: Escherichia coli, Bacillus subtilis, Klebsiella pneumoniae, Mycobacterium and Salmonella species, Staphylococcus aureus, and Streptococcus spp. Increased production of Aβ-amyloid plaques Increased overall Aβ-amyloid plaques deposits Disruption of proteostasis via molecular mimicry mechanism [95]
Reduced: Clostridium sporogenes and Ruminococcus gnavus Reduced levels of tryptamine Reduced release of serotonin by enterochromaffin cells Reduced levels of serotonin in gut [48]
Not specified Increased amount of secondary bile acids (deoxycholic acid, glycodeoxycholic acid, taurodeoxycholic acid or glycolithocholic acid) Increased ratio between secondary bile acids and primary bile acids Positive correlation between increased levels of secondary BAs, and hallmarks of AD [91,100]
Parkinson’s disease
Increased levels of Akkermansia muciniphila and Bilophila wadsworthia Increased levels of S2-and SO3-
Increased degradation of taurine-conjugated bile acids
Disrupted transsulfuration pathways
Reduced levels of glutathione
Increased oxidative stress peripheral and neuroinflammation [135,139]
Reduced levels of Prevotellaceae, Faecalibacterium, and Lachnospiraceae Reduced SCFAs production, increased proteolytic activity (production of p-cresol or phenylacetylglutamine) Increased SCFAs concentration in plasma
Possibly connected to lower levels of methionine in serum
Impaired gut-barrier function, increasing the risk of infection with enteric pathogens and boosting the α-synuclein formation [119,122,123]