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Bifidobacterium longum with fructo-oligosaccharide (FOS) treatment in minimal hepatic encephalopathy: a randomized,

Mariano Malaguarnera1, Filippo Greco, Gloria Barone

  • 1Department of Senescence, Urological and Neurological Sciences, University of Catania, Viale Andrea Doria 69, 95126, Catania, Italy. malaguar@unict.it

Insights

This study found that Bifidobacterium longum plus fructo-oligosaccharides (FOS) significantly improved cognitive function and reduced ammonia levels in patients with minimal hepatic encephalopathy (MHE). These findings suggest a potential therapeutic benefit for this probiotic and prebiotic combination in managing MHE.

Area of Science:

  • Gastroenterology and Hepatology
  • Neuroscience
  • Microbiology

Background:

  • Minimal hepatic encephalopathy (MHE) affects patients with chronic liver disease, characterized by cognitive deficits despite the absence of overt clinical symptoms.
  • The exact pathogenesis of hepatic encephalopathy is unclear, but elevated ammonia levels and gut-derived toxins are implicated in cerebral dysfunction.
  • Intestinal ammonia production is linked to bacterial urease activity and the generation of other metabolites like mercaptans.

Purpose of the Study:

  • To evaluate the clinical efficacy of Bifidobacterium longum combined with fructo-oligosaccharides (FOS) in treating minimal hepatic encephalopathy (MHE).

Main Methods:

  • A randomized controlled trial involving 60 cirrhotic patients diagnosed with MHE.
  • Participants were equally divided into two groups: one receiving Bifidobacterium+FOS, the other receiving a placebo.
  • Assessments included clinical evaluations, laboratory tests (serum ammonia), psychometric tests (Trail Making Test A & B, Symbol Digit Modalities Test, Block Design, MMSE), and automated EEG analysis.

Main Results:

  • The Bifidobacterium+FOS group showed a significant reduction in fasting serum ammonia levels (P=0.003).
  • Cognitive function significantly improved in the treatment group, with decreased scores on Trail Making Test A (P=0.000) and Trail Making Test B (P=0.000), indicating better executive function and processing speed.
  • Significant improvements were also observed in the Symbol Digit Modalities Test (P<0.05), Block Design (P=0.000), and Mini-Mental State Examination (MMSE) (P=0.000).

Conclusions:

  • Treatment with Bifidobacterium longum plus FOS led to significant improvements in both biochemical markers (serum ammonia) and neuropsychological test performance in MHE patients.
  • The combination of Bifidobacterium longum and FOS demonstrates promising therapeutic potential for managing minimal hepatic encephalopathy.
  • Further research is warranted to closely examine these beneficial effects and their long-term implications.

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