Background:: Focally enhanced gastritis has been described in association with Crohn's disease and ulcerative colitis, but is rare in the general population. The study aim was to test whether idiopathic colitis in macaques was associated with any characteristic changes of the gastric mucosa resembling similar changes in humans.
Methods:: The presence or absence of idiopathic colitis was established by gross and microscopic examination of the colons of rhesus macaques (Macaca mulatta), which died at the Oregon National Primate Research Center. Gastric tissue specimens were compared between a case population of 26 macaques with idiopathic colitis and a control population of 21 macaques without colitis. The specimens were histologically assessed by two independent pathologists blinded to the presence or absence of idiopathic colitis. Differences between cases and controls were compared using a two‐sided Fisher's exact test.
Results:: Of the 26 cases of macaques with colitis, 11 animals (42%) harbored signs of chronic gastritis. Of the 21 control macaques without colitis, nine animals (43%) harbored signs of chronic gastritis, P = 1.0000. Of all animals with gastritis, 1/11 animals with colitis and 2/9 control animals showed rare active gastritis as evidenced by the presence of neutrophils, P = 0.5658. Lymphocytic infiltrates of the gastric mucosa were seen in 4/11 colitis cases and 0/9 controls, P = 0.0942. No gastric specimens with focally enhanced gastritis were found among any of the case or control animals.
Conclusions:: Unlike chronic inflammatory bowel disease in humans, idiopathic colitis in macaques is not associated with focally enhanced gastritis or any other type of specific gastritis.
1 Portland VA Medical Center, Portland, Oregon
2 Oregon Health & Science University, Portland, Oregon
3 University of Texas Southwestern Medical Center, Dallas, Texas
4 Caris Diagnostics, Dallas, Texas
5 Dallas VA Medical Center, Dallas, Texas
6 Oregon National Primate Research Center, Portland, Oregon
*Reprints: Gastroenterology, Portland VA Medical Center P3‐GI, 3710 SW U.S. Veterans Hospital Road, Portland, Oregon 97239
Received 26 January 2011; Accepted 31 January 2011
Published online 18 March 2011 in Wiley Online Library (wileyonlinelibrary.com).
The authors have no potential conflicts of interest to declare. Amnon Sonnenberg has been supported by a grant from Takeda Pharmaceuticals. Anne D. Lewis has been supported by the Oregon National Primate Research Center NCRR base grant RR000163.