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

被引:2
作者
Goren, Idan [1 ,2 ]
Fischler, Tali Sharar [1 ]
Yanai, Henit [1 ]
Pal, Partha [3 ]
Adigopula, Bhargavi [3 ]
Pendyala, Sushmitha [3 ]
Ganesh, Girish [3 ]
Vishnubhotla, Ravikanth [4 ,5 ]
Rabinowitz, Keren Masha [1 ,6 ]
Barda, Efrat Shaham [1 ,6 ]
Yadamreddy, Durga [4 ,5 ]
Godny, Lihi [1 ]
Peleg, Noam [1 ]
Banerjee, Rupa [3 ]
Dotan, Iris [1 ]
机构
[1] Tel Aviv Univ, Rabin Med Ctr, IBD Ctr, Div Gastroenterol,Sackler Fac Med, IL-49100 Petah Tiqwa, Israel
[2] Cleveland Clin, Dept Inflammat & Immun, Lerner Res Inst, Cleveland, OH 44195 USA
[3] Asian Inst Gastroenterol, Dept Gastroenterol, Hyderabad 501301, India
[4] Asian Inst Gastroenterol, Dept Genom & Mol Biol, Inst Translat Res, Hyderabad 500032, India
[5] AIG Hosp, Hyderabad 500032, India
[6] Tel Aviv Univ, Beilinson Hosp, Felsenstein Med Res Ctr, Rabin Med Ctr,Sackler Fac Med, IL-49414 Petah Tiqwa, Israel
关键词
Crohn's disease; inception cohort; India; complication; serology; prediction; genetic; East-West; INFLAMMATORY-BOWEL-DISEASE; SACCHAROMYCES-CEREVISIAE ANTIBODY; ASSOCIATION; ASIA; PROGRESSION; GENOTYPE; BEHAVIOR; ASCA; SUSCEPTIBILITY; PREVALENCE;
D O I
10.3390/jcm11236899
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 < 0.001). Complicated phenotype at diagnosis was observed in 48% of Indian and 30% of Israeli patients (p = 0.003). Complicated phenotype was associated with higher anti-Saccharomyces cerevisiae antibody (ASCA) seropositivity rate among Israeli patients (p < 0.001), but not among Indian patients. Antiglycan serology did not correlate with the tested genetic variants. Early complicated course occurred in 28 (18%) Israeli and 13 (12.5%) Indian patients. The time from diagnosis to complication was comparable (log rank 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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页数:14
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