Plebani M, Di Mario F, Vianello F, Farini R, Piccoli A, Lazzaretto L, Perobelli L, Naccarato R, Burlina A
Clin Biochem. 1983 Oct;16(5):310-2. doi: 10.1016/s0009-9120(83)94151-6.
The role of serum PG I in screening patients with chronic atrophic gastritis and gastric cancer, and in detecting peptic ulcer patients with high relapse risk, was ascertained in 276 subjects. Although not diagnostic per se, PG I was found to be under 20 micrograms/L in patients with chronic atrophic gastritis and in some gastric cancer or partially gastrectomized patients. In patients presenting with relapsing duodenal ulcer, PG I values were significantly higher than in the non-relapsing ones, but a satisfactory identification of all the duodenal ulcer patients with high relapse risk was not possible on this basis. Even the correlation between PG I and MAO was not accurate in every subject considered. These results suggest that the value of PG I is limited to assessing patients with upper gastrointestinal diseases in which a reduction of peptic secretion, and therefore of PG I in serum, is present.
在276名受试者中确定了血清胃蛋白酶原I(PG I)在筛查慢性萎缩性胃炎和胃癌患者以及检测具有高复发风险的消化性溃疡患者中的作用。尽管PG I本身并非诊断性指标,但发现慢性萎缩性胃炎患者以及一些胃癌或部分胃切除患者的PG I低于20微克/升。在复发性十二指肠溃疡患者中,PG I值显著高于非复发性患者,但仅基于此无法令人满意地识别所有具有高复发风险的十二指肠溃疡患者。即使在所有考虑的受试者中,PG I与最大胃酸分泌量(MAO)之间的相关性也不准确。这些结果表明,PG I的价值仅限于评估存在胃酸分泌减少,进而血清中PG I减少的上消化道疾病患者。