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©2012 Baishideng Publishing Group Co.
World J Gastroenterol. May 28, 2012; 18(20): 2511-2516
Published online May 28, 2012. doi: 10.3748/wjg.v18.i20.2511
Published online May 28, 2012. doi: 10.3748/wjg.v18.i20.2511
Low1 EmA and TG2-ab, n = 40 | High EmA or TG2-ab, n = 17 | |
Baseline | ||
Age, median (range), yr | 39 (5-68) | 39 (6-70) |
Females, n (%) | 30 (75) | 11 (65) |
Age below 18 yr | 7 (18) | 7 (41) |
Gastrointestinal symptoms | 28 (70) | 12 (71) |
Extraintestinal symptoms | 2 (5) | 4 (23) |
Screen-detected subjects | 10 (25) | 1 (6) |
EmA, median (range), titer | 1:50 (1:5-1:200) | 1:500 (1:5-1:2000) |
TG2-ab, median (range), U/L | 6.3 (0-24.8) | 45.5 (13.9-> 100) |
HLA DQ2 or DQ8, n (%) | 33/33 (100) | 16/16 (100) |
Marsh 0 | 9 (23) | 3 (18) |
MarshI-II | 31 (77) | 14 (82) |
Follow-up | ||
Celiac disease diagnosis | 29 (73) | 16 (94) |
Villous atrophy later2 | 12 (30) | 8 (47) |
Positive response to GFD | 17 (43) | 8 (47) |
Gluten, no villous atrophy | 2 (5) | 0 |
Lost to follow-up | 9 (22) | 1 (6) |
- Citation: Kurppa K, Räsänen T, Collin P, Iltanen S, Huhtala H, Ashorn M, Saavalainen P, Haimila K, Partanen J, Mäki M, Kaukinen K. Endomysial antibodies predict celiac disease irrespective of the titers or clinical presentation. World J Gastroenterol 2012; 18(20): 2511-2516
- URL: https://www.wjgnet.com/1007-9327/full/v18/i20/2511.htm
- DOI: https://dx.doi.org/10.3748/wjg.v18.i20.2511