Journal of Clinical Medicine (Nov 2022)

Newly Diagnosed Crohn’s Disease Patients in India and Israel Display Distinct Presentations and Serological Markers: Insights from Prospective Cohorts

  • Idan Goren,
  • Tali Sharar Fischler,
  • Henit Yanai,
  • Partha Pal,
  • Bhargavi Adigopula,
  • Sushmitha Pendyala,
  • Girish Ganesh,
  • Ravikanth Vishnubhotla,
  • Keren Masha Rabinowitz,
  • Efrat Shaham Barda,
  • Durga Yadamreddy,
  • Lihi Godny,
  • Noam Peleg,
  • Rupa Banerjee,
  • Iris Dotan

DOI
https://doi.org/10.3390/jcm11236899
Journal volume & issue
Vol. 11, no. 23
p. 6899

Abstract

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Background: Crohn’s disease (CD) incidence is rising in India. However, features of newly diagnosed patients with CD in this population are largely unknown. The Indo-Israeli IBD GastroEnterology paRtnership (TiiiGER) aimed to investigate differences in presentation among patients with newly diagnosed CD in India and Israel, and to explore phenotype–serotype correlations. Methods: A prospective observational cohort study of consecutive adults (>18 years) conducted in two large referral centers in India and Israel (2014–2018). Clinical data, an antiglycan serological panel, and 20 CD-associated genetic variants were analyzed. Outcomes: complicated phenotype at diagnosis and early complicated course (hospitalizations/surgeries) within 2 years of diagnosis. Results: We included 260 patients (104, Indian (65.4%, male; age, 37.8); 156 Israeli (49.4%, male; 31.8, age)). Median lag time from symptoms onset to diagnosis was 10.5 (IQR 3–38) vs. 3 (IQR 1–8) months in Indian vs. Israeli patients (p p = 0.003). Complicated phenotype was associated with higher anti-Saccharomyces cerevisiae antibody (ASCA) seropositivity rate among Israeli patients (p p = 0.152). Antiglycan serology did not correlate with a complicated early course in either cohort. Conclusions: There are significant differences in patients presenting with newly diagnosed CD in India and Israel, including phenotype and distinct biomarkers at diagnosis. These differences suggest different genetic and environmental disease modifiers.

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