Dynamic contrast-enhanced MRI in determining disease activity in perianal fistulizing Crohn disease: a pilot study

Manon L W Ziech1, Cristina Lavini, Shandra Bipat

  • 1Department of Radiology, Academic Medical Center, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands. m.l.ziech@amc.uva.nl

Abstract

Insights

Dynamic contrast-enhanced MRI effectively assesses Crohn disease activity. Key metrics like maximum enhancement and initial slope correlate with disease severity, while K(trans) indicates therapeutic response to anti-tumor necrosis factor α therapy.

Area of Science:

  • Gastroenterology
  • Radiology
  • Medical Imaging

Background:

  • Perianal fistulizing Crohn disease (PFCD) presents diagnostic challenges.
  • Accurate assessment of disease activity and treatment response is crucial for patient management.

Purpose of the Study:

  • To evaluate dynamic contrast-enhanced MRI (DCE-MRI) for semiquantitative analysis of disease activity in PFCD.
  • To assess the utility of DCE-MRI parameters in predicting therapeutic response to anti-tumor necrosis factor α (anti-TNF-α) therapy.

Main Methods:

  • Pelvic MRI with a 3 T DCE sequence was performed on 16 patients with PFCD.
  • Quantitative parameters including maximum enhancement, initial slope, K(trans), and V e were calculated.
  • Disease activity was assessed using Perianal Disease Activity Index, C-reactive protein, and an MRI-based score.
  • Six patients underwent follow-up MRI after 6 weeks of anti-TNF-α treatment.

Main Results:

  • Maximum enhancement and initial slope of increase showed moderate correlation with disease activity indices.
  • Volume of enhancing pixels strongly correlated with disease activity and MRI-based scores.
  • K(trans) values significantly decreased after 6 weeks of anti-TNF-α therapy, suggesting treatment efficacy.

Conclusions:

  • DCE-MRI parameters, particularly maximum enhancement and initial slope, are valuable for assessing disease activity in PFCD.
  • K(trans) shows promise as a biomarker for monitoring therapeutic response to anti-TNF-α treatment in PFCD.

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