Open Label Vancomycin in Primary Sclerosing Cholangitis-Inflammatory Bowel Disease: Improved Colonic Disease Activity and Associations With Changes in Host–Microbiome–Metabolomic Signatures - Scorecard - MDSpire

Open Label Vancomycin in Primary Sclerosing Cholangitis-Inflammatory Bowel Disease: Improved Colonic Disease Activity and Associations With Changes in Host–Microbiome–Metabolomic Signatures

  • By

  • Mohammed Nabil Quraishi

  • Jonathan Cheesbrough

  • Peter Rimmer

  • Benjamin H Mullish

  • Naveen Sharma

  • Elena Efstathiou

  • Animesh Acharjee

  • Georgios Gkoutus

  • Arzoo Patel

  • Julian R Marchesi

  • Stephane Camuzeaux

  • Katie Chappell

  • Maria A Valdivia-Garcia

  • James Ferguson

  • Matthew J Brookes

  • Martine Walmsley

  • Amanda E Rossiter

  • Willem van Schaik

  • Ross S McInnes

  • Rachel Cooney

  • Michael Trauner

  • Andrew D Beggs

  • Tariq H Iqbal

  • Palak J Trivedi

  • December 14, 2024

  • 0 min

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Clinical Scorecard: Efficacy of Oral Vancomycin in Patients with Primary Sclerosing Cholangitis-Related Inflammatory Bowel Disease: Enhanced Colonic Disease Activity and Correlations with Host-Microbiome-Metabolomic Changes

At a Glance

CategoryDetail
ConditionPrimary sclerosing cholangitis-associated inflammatory bowel disease (PSC-IBD)
Key MechanismsGut microbial alterations, bile acid homeostasis disruption, immune dysregulation including IL-17 responses
Target PopulationAdults (≥18 years) with PSC and active pancolonic IBD
Care SettingSpecialist gastroenterology and hepatology centers with capacity for endoscopic surveillance

Key Highlights

  • Oral vancomycin (125 mg QID for 4 weeks) induced clinical remission in 12 of 15 PSC-IBD patients with active colitis.
  • Treatment was associated with reduced fecal calprotectin and significant shifts in gut microbiota composition, including decreased Lachnospiraceae and increased Enterobacteriaceae.
  • Vancomycin modulated host mucosal gene expression, downregulating inflammatory and antimicrobial pathways and upregulating extracellular matrix repair genes.

Guideline-Based Recommendations

Diagnosis

  • Confirm PSC diagnosis with clinical, biochemical, and imaging criteria.
  • Assess IBD activity using partial Mayo colitis score and fecal calprotectin.
  • Exclude infectious causes of diarrhea prior to antibiotic therapy.

Management

  • Consider oral vancomycin as an induction therapy for active colitis in PSC-IBD patients.
  • Administer oral vancomycin at 125 mg four times daily for 4 weeks.
  • Monitor for clinical remission and biochemical markers such as fecal calprotectin.

Monitoring & Follow-up

  • Perform colonoscopic assessment and collect colonic biopsies at baseline and after treatment.
  • Monitor fecal calprotectin and clinical symptoms at baseline, 2, 4, and 8 weeks.
  • Observe for relapse of colitis activity following vancomycin withdrawal.

Risks

  • Potential relapse of colitis activity after cessation of vancomycin.
  • Alterations in gut microbiota diversity and composition with unknown long-term effects.
  • Contraindications include vancomycin intolerance and recent antibiotic or immunomodulator use.

Patient & Prescribing Data

Adults with PSC and mild to moderately active pancolonic IBD without recent antibiotic or immunomodulator changes.

Oral vancomycin effectively induces remission in PSC-IBD colitis, with associated microbiome and metabolomic changes; relapse may occur after treatment withdrawal.

Clinical Best Practices

  • Screen for and exclude infectious diarrhea before initiating oral vancomycin.
  • Use oral vancomycin as a short-term induction agent with close monitoring of clinical and biochemical response.
  • Incorporate multi-omic assessments where available to understand host-microbiome interactions.
  • Maintain regular colonoscopic surveillance due to increased colorectal cancer risk in PSC-IBD.
  • Consider liver transplant status and recurrent PSC in treatment planning.

References

Original Source(s)

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