Table 3.
Disease | Type of Statin | Study Design | Dose/Day | Intestinal Microbial Changes | Results | Reference |
---|---|---|---|---|---|---|
Hypercholesteremia | Atorvastatin | Rat | 10, 15, 20 mg/kg | Proteobacteria increased, Firmicutes decreased | Intestinal microbial diversity increased | [149] |
Human | 20 mg |
Faecalibacterium prausnitzii, Akkermansia muciniphilaa and Oscillospira increased Desufovibrio decreased |
Reduced pro-inflammatory bacteria and taxa associated with atherosclerosis formation and CVD progression | [150] | ||
Ischemic stroke | Atorvastatin | Mice | 20 mg/kg | Firmicutes and Lactobacillus increased, Bacteroidetes decreased | Increased fecal butyrate level, promoted intestinal barrier function | [151] |
Acute coronary syndrome |
Statins | Human | / |
Parabacteroides merdae decreased Bifidobacterium longum subsp. longum, Anaerostipes hadrus and Ruminococcus obeum increased |
Specific changes in bacterial taxa were associated with disease severity or outcomes either directly or by mediating metabolites such as fatty acids and prenol lipids | [152] |
Obesity | Atorvastatin | Mice | 10 mg/kg | Bacteroides, Butyricimonas, and Mucispirillum increased | Statins improved the inflammation associated microbiota in elderly obese mice | [153] |
Rosuvastatin | 3 mg/kg 9.3 mg/kg |
Lachnospiraceae, Rikenella and Coprococcus increased Akkermansiaceae, Proteobacteria decreased |
[153,154] | |||
NASH/NAFLD | Atorvastatin | Mice | 20 mg/kg | Mucispirillum, Desulfovibrio, Anaerotruncus and Desulfovibrionaceae decreased | Increased serum TCA and depleted 3-IPA | [155] |
20 mg/kg | Ruminococcaceae increased | Promoted the formation of deoxycholic acid and lithocholic acid | [156] |
CVD, cardiovascular disease; NASH, nonalcoholic steatohepatitis; NAFLD, nonalcoholic fatty liver disease; TCA, taurocholic acid; IPA, indolepropionic acid.