Shikata Kentaro, Ninomiya Toshiharu, Yonemoto Koji, Ikeda Fumie, Hata Jun, Doi Yasufumi, Fukuhara Masayo, Matsumoto Takayuki, Iida Mitsuo, Kitazono Takanari, Kiyohara Yutaka
Department of Environmental Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Scand J Gastroenterol. 2012 Jun;47(6):669-75. doi: 10.3109/00365521.2012.658855. Epub 2012 Mar 20.
Serum pepsinogen (sPG) levels have been established as a good marker of chronic atrophic gastritis and the sequential occurrence of gastric cancer. However, there have been few prospective investigations which investigated the predictive performance of sPG for future gastric cancer incidence.
We prospectively followed-up a total of 2446 community-dwelling Japanese aged ≥ 40 years for 10 years and used the Youden's index to determine the cutoff values of the pepsinogen I level and pepsinogen I/II ratio to accurately discriminate gastric cancer events. Predictive performance of sPG was assessed by ROC curve.
During the follow-up, 69 subjects developed gastric cancer. The most predictive sPG test criteria were determined to be a pepsinogen I level ≤ 59 ng/ml and pepsinogen I/II ratio ≤ 3.9. The sensitivity and specificity of these criteria to discriminate the actual occurrence of gastric cancer were 71.0% and 69.2%, respectively. The area under the ROC curve for gastric cancer occurrence increased significantly by adding the sPG test to the model that included the status of Helicobater pylori infection and other potential risk factors (from 0.742 to 0.809; p for difference in the area < 0.001).
This study determined the optimal sPG test criteria for predicting gastric cancer occurrence over 10 years in a general Japanese population. These criteria would be effective to screen for individuals at high risk of this disease.
血清胃蛋白酶原(sPG)水平已被确立为慢性萎缩性胃炎及胃癌相继发生的良好标志物。然而,很少有前瞻性研究调查sPG对未来胃癌发病率的预测性能。
我们对总共2446名年龄≥40岁的日本社区居民进行了为期10年的前瞻性随访,并使用约登指数来确定胃蛋白酶原I水平和胃蛋白酶原I/II比值的临界值,以准确区分胃癌事件。通过ROC曲线评估sPG的预测性能。
在随访期间,69名受试者患上了胃癌。最具预测性的sPG检测标准被确定为胃蛋白酶原I水平≤59 ng/ml和胃蛋白酶原I/II比值≤3.9。这些标准区分实际发生的胃癌的敏感性和特异性分别为71.0%和69.2%。通过将sPG检测添加到包含幽门螺杆菌感染状况和其他潜在风险因素的模型中,胃癌发生的ROC曲线下面积显著增加(从0.742增加到0.809;面积差异的p值<0.001)。
本研究确定了在一般日本人群中预测10年内胃癌发生的最佳sPG检测标准。这些标准将有效地筛查出该疾病的高危个体。