TY - JOUR
T1 - The association between objective tongue color and endoscopic findings
T2 - Results from the Kyushu and Okinawa population study (KOPS)
AU - Kainuma, Mosaburo
AU - Furusyo, Norihiro
AU - Urita, Yoshihisa
AU - Nagata, Masaharu
AU - Ihara, Takeshi
AU - Oji, Takeshi
AU - Nakaguchi, Toshiya
AU - Namiki, Takao
AU - Hayashi, Jun
N1 - Funding Information:
This study was supported, in part, by JSPS KAKENHI Grant Number 12103377 and by the Foundation for Total Health Promotion. We greatly thank Drs. IKEZAKI Hiroaki, HARADA Yuji, URA Kazuya and EIRAKU Kunimitsu of our department for their assistance in this research. Also, we greatly thank Drs. SUGIMOTO Motonobu, NAKAJIMA Hitoshi, and WATANABE Toshiyasu from the Department of General Medicine and Emergency Care, Toho University School of Medicine Omori Hospital, Tokyo, Japan, for their technical assistance.
Publisher Copyright:
© 2015 Kainuma et al.
PY - 2015/10/16
Y1 - 2015/10/16
N2 - Background: The relation between tongue color and gastroesophageal disease is unclear. This study was done to investigate the associations between tongue color (TC), endoscopic findings, Helicobacter.pylori infection status, and serological atrophic gastritis (SAG). Methods: The participants were 896 residents of Ishigaki Island, Okinawa, aged 28-86 years. The tongue was photographed, esophagogastroduodenoscopy was done, and serum antibody to H.pylori was measured. SAG was defined as a serum Pepsinogen (PG)Ilevel ≥70ng/ml and a PGI/IIratio ≥3.0. TC was measured by the device-independent international commission on Illumination 1976L*a*b* color space standards at four points: (1) edge, (2) posterior, (3) middle, and (4) apex. We also calculated the ratio of the tongue edge to the three other measured points to examine the association between the coating of the tongue and the endoscopic and laboratory findings. Results: Participants were excluded who had two or more endoscopic findings (n = 315) or who had SAG without seropositivity to H.pylori (n = 33). The remaining 548 participants were divided into three groups: SAG and seropositive to H.pylori (n = 67), seropositive to H.pylori alone (n = 56), and without SAG and seronegative for H.pylori (n = 425). We divided 425 residents into a single endoscopic finding positive group (n = 207) and a negative group, which served as a control (n = 218). The most frequent single endoscopic finding was esophageal hernia (n = 110), followed by erosive esophagitis (n = 35) and erosive gastritis (EG) (n = 45). EH was significantly associated with TC (2b*/1b*) (P < 0.05). EG was significantly associated with TC (3a*, 3b*) (P < 0.05). Seropositivity to H.pylori was significantly associated with TC (3L*, 3L*/1L*) (P < 0.05, <0.01), and seropositivity to both H.pylori and SAG was significantly associated with TC (3L*/1L*) (P < 0.05). Multivariate analysis extracted TC (3a*, 3b*) as an independent factor associated with a differential diagnosis of EG (Odds ratio (OR) 2.66 P = 0.008, OR 2.17 P = 0.045). Conclusions: The tongue body color of the middle area reflects acute change of gastric mucosa, such as erosive gastritis. Tongue diagnosis would be a useful, non-invasive screening tool for EG.
AB - Background: The relation between tongue color and gastroesophageal disease is unclear. This study was done to investigate the associations between tongue color (TC), endoscopic findings, Helicobacter.pylori infection status, and serological atrophic gastritis (SAG). Methods: The participants were 896 residents of Ishigaki Island, Okinawa, aged 28-86 years. The tongue was photographed, esophagogastroduodenoscopy was done, and serum antibody to H.pylori was measured. SAG was defined as a serum Pepsinogen (PG)Ilevel ≥70ng/ml and a PGI/IIratio ≥3.0. TC was measured by the device-independent international commission on Illumination 1976L*a*b* color space standards at four points: (1) edge, (2) posterior, (3) middle, and (4) apex. We also calculated the ratio of the tongue edge to the three other measured points to examine the association between the coating of the tongue and the endoscopic and laboratory findings. Results: Participants were excluded who had two or more endoscopic findings (n = 315) or who had SAG without seropositivity to H.pylori (n = 33). The remaining 548 participants were divided into three groups: SAG and seropositive to H.pylori (n = 67), seropositive to H.pylori alone (n = 56), and without SAG and seronegative for H.pylori (n = 425). We divided 425 residents into a single endoscopic finding positive group (n = 207) and a negative group, which served as a control (n = 218). The most frequent single endoscopic finding was esophageal hernia (n = 110), followed by erosive esophagitis (n = 35) and erosive gastritis (EG) (n = 45). EH was significantly associated with TC (2b*/1b*) (P < 0.05). EG was significantly associated with TC (3a*, 3b*) (P < 0.05). Seropositivity to H.pylori was significantly associated with TC (3L*, 3L*/1L*) (P < 0.05, <0.01), and seropositivity to both H.pylori and SAG was significantly associated with TC (3L*/1L*) (P < 0.05). Multivariate analysis extracted TC (3a*, 3b*) as an independent factor associated with a differential diagnosis of EG (Odds ratio (OR) 2.66 P = 0.008, OR 2.17 P = 0.045). Conclusions: The tongue body color of the middle area reflects acute change of gastric mucosa, such as erosive gastritis. Tongue diagnosis would be a useful, non-invasive screening tool for EG.
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U2 - 10.1186/s12906-015-0904-0
DO - 10.1186/s12906-015-0904-0
M3 - Article
C2 - 26474972
AN - SCOPUS:84944474495
SN - 1472-6882
VL - 15
JO - BMC Complementary and Alternative Medicine
JF - BMC Complementary and Alternative Medicine
IS - 1
M1 - 372
ER -