TY - JOUR
T1 - A potential pathogenic association between periodontal disease and Crohn's disease
AU - Imai, Jin
AU - Ichikawa, Hitoshi
AU - Kitamoto, Sho
AU - Golob, Jonathan L.
AU - Kaneko, Motoki
AU - Nagata, Junko
AU - Takahashi, Miho
AU - Gillilland, Merritt G.
AU - Tanaka, Rika
AU - Nagao-Kitamoto, Hiroko
AU - Hayashi, Atsushi
AU - Sugihara, Kohei
AU - Bishu, Shrinivas
AU - Tsuda, Shingo
AU - Ito, Hiroyuki
AU - Kojima, Seiichiro
AU - Karakida, Kazunari
AU - Matsushima, Masashi
AU - Suzuki, Takayoshi
AU - Hozumi, Katsuto
AU - Watanabe, Norihito
AU - Giannobile, William V.
AU - Shirai, Takayuki
AU - Suzuki, Hidekazu
AU - Kamada, Nobuhiko
N1 - Funding Information:
We dedicate this paper to the memory of Haruo Sakamoto, who passed away while we were conducting this research. The authors wish to thank the University of Michigan Center for Gastrointestinal Research (NIH 5P30DK034933) and the Host Microbiome Initiative at the University of Michigan. The authors also wish to thank the Support Center for Medical Research and Education at Tokai University. This work was supported by NIH grants DK119219 and AI142047 (to NK), Department of Defense grant CA191087 (to S. Kitamoto), Japan Society for the Promotion of Science grant 19K17413 (to JI), and Takeda Japan Medical Office Funded Research Grant 2019 (to JI).
Publisher Copyright:
© 2021, Imai et al.
PY - 2021/12/8
Y1 - 2021/12/8
N2 - Oral conditions are relatively common in patients with inflammatory bowel disease (IBD). However, the contribution of oral maladies to gut inflammation remains unexplored. Here, we investigated the effect of periodontitis on disease phenotypes of patients with IBD. In all, 60 patients with IBD (42 with ulcerative colitis [UC] and 18 with Crohn's disease [CD]) and 45 healthy controls (HCs) without IBD were recruited for this clinical investigation. The effects of incipient periodontitis on the oral and gut microbiome as well as IBD characteristics were examined. In addition, patients were prospectively monitored for up to 12 months after enrollment. We found that, in both patients with UC and those with CD, the gut microbiome was significantly more similar to the oral microbiome than in HCs, suggesting that ectopic gut colonization by oral bacteria is increased in patients with IBD. Incipient periodontitis did not further enhance gut colonization by oral bacteria. The presence of incipient periodontitis did not significantly affect the clinical outcomes of patients with UC and CD. However, the short CD activity index increased in patients with CD with incipient periodontitis but declined or was unchanged during the study period in patients without periodontitis. Thus, early periodontitis may associate with worse clinically symptoms in some patients with CD.
AB - Oral conditions are relatively common in patients with inflammatory bowel disease (IBD). However, the contribution of oral maladies to gut inflammation remains unexplored. Here, we investigated the effect of periodontitis on disease phenotypes of patients with IBD. In all, 60 patients with IBD (42 with ulcerative colitis [UC] and 18 with Crohn's disease [CD]) and 45 healthy controls (HCs) without IBD were recruited for this clinical investigation. The effects of incipient periodontitis on the oral and gut microbiome as well as IBD characteristics were examined. In addition, patients were prospectively monitored for up to 12 months after enrollment. We found that, in both patients with UC and those with CD, the gut microbiome was significantly more similar to the oral microbiome than in HCs, suggesting that ectopic gut colonization by oral bacteria is increased in patients with IBD. Incipient periodontitis did not further enhance gut colonization by oral bacteria. The presence of incipient periodontitis did not significantly affect the clinical outcomes of patients with UC and CD. However, the short CD activity index increased in patients with CD with incipient periodontitis but declined or was unchanged during the study period in patients without periodontitis. Thus, early periodontitis may associate with worse clinically symptoms in some patients with CD.
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U2 - 10.1172/jci.insight.148543
DO - 10.1172/jci.insight.148543
M3 - Article
C2 - 34710061
AN - SCOPUS:85120868150
SN - 2379-3708
VL - 6
JO - JCI insight
JF - JCI insight
IS - 23
M1 - e148543
ER -