Lee Ju Yup, Kim Nayoung, Lee Hye Seung, Oh Jane C, Kwon Yong Hwan, Choi Yoon Jin, Yoon Ki Chul, Hwang Jae Jin, Lee Hyun Joo, Lee AeRa, Jeong Yeonsang, Jo Hyun Jin, Yoon Hyuk, Shin Cheol Min, Park Young Soo, Lee Dong Ho
Departments of Internal Medicine, Seoul National University Bundang Hospital, Seoungnam.
Departments of Internal Medicine, Seoul National University Bundang Hospital, Seoungnam ; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul.
J Cancer Prev. 2014 Mar;19(1):47-55. doi: 10.15430/jcp.2014.19.1.47.
Atrophic gastritis is a precancerous condition, which can be diagnosed by several methods. However, there is no consensus for the standard method. The aim of this study was to evaluate the correlations among endoscopic, histologic, and serologic findings for the diagnosis of atrophic gastritis.
From March 2003 to August 2013, a total of 2,558 subjects were enrolled. Endoscopic atrophic gastritis was graded by Kimura-Takemoto classification and histological atrophic gastritis was assessed by updated Sydney system. Serological assessment of atrophic gastritis was based on serum pepsinogen test.
The serum pepsinogen I/II ratio showed a significant decreasing nature when the extent of atrophy increased (R(2)=0.837, P<0.001) and the cut-off value for distinguishing between presence and absence of endoscopic atrophic gastritis was 3.2. The serum pepsinogen I and pepsinogen I/II ratio were significantly lower when the histological atrophic gastritis progressed and the cut-off value was 3.0 for a diagnosis of histological atrophic gastritis. A significant correlation between endoscopic and histological atrophic gastritis was noted and the sensitivity and specificity of endoscopic diagnosis were 65.9% and 58.0% for antrum, 71.3% and 53.7% for corpus, respectively.
The endoscopic, histological, and serological atrophic gastritis showed relatively good correlations. However, as these three methods have a limitation, a multifactorial assessment might be needed to ameliorate the diagnostic accuracy of atrophic gastritis.
萎缩性胃炎是一种癌前状态,可通过多种方法进行诊断。然而,对于标准诊断方法尚无共识。本研究的目的是评估内镜、组织学和血清学检查结果在萎缩性胃炎诊断中的相关性。
2003年3月至2013年8月,共纳入2558名受试者。内镜下萎缩性胃炎采用木村-竹本分类法进行分级,组织学萎缩性胃炎采用更新后的悉尼系统进行评估。萎缩性胃炎的血清学评估基于血清胃蛋白酶原检测。
随着萎缩程度的增加,血清胃蛋白酶原I/II比值呈显著下降趋势(R² = 0.837,P < 0.001),区分内镜下萎缩性胃炎有无的临界值为3.2。组织学萎缩性胃炎进展时,血清胃蛋白酶原I和胃蛋白酶原I/II比值显著降低,诊断组织学萎缩性胃炎的临界值为3.0。内镜下和组织学萎缩性胃炎之间存在显著相关性,内镜诊断胃窦部的敏感性和特异性分别为65.9%和58.0%,胃体部分别为71.3%和53.7%。
内镜、组织学和血清学萎缩性胃炎表现出相对较好的相关性。然而,由于这三种方法都有局限性,可能需要进行多因素评估以提高萎缩性胃炎的诊断准确性。