Lami F, Callegari C, Miglioli M, Barbara L
Am J Gastroenterol. 1984 Sep;79(9):697-700.
An investigation of fecal chymotrypsin activity on spot fecal specimens was carried out in three groups of subjects, divided as follows: 45 healthy controls (group C); 36 patients with gastroenterological diseases of extrapancreatic origin (group VP); and 42 patients with chronic pancreatitis (group CP). Nineteen patients of group CP underwent pancreozymin-secretin and NBT-PABA tests. The following results, expressed as mg of chymotrypsin/g of feces, were obtained: C = 0.610 +/- 0.203; CP = 0.291 +/- 0.154, p less than 0.001; VP = 0.560 +/- 0.234. FCT showed a sensitivity rate of 78.5% and a specificity rate of 71.6%. The fecal output of chymotrypsin correlated well with the pancreatic secretion of chymotrypsin (r = 0.59, p less than 0.01) and with the percentage of recovery of urinary PABA (r = 0.44, p less than 0.05). We conclude that chymotrypsin assay by the described method on spot stool specimens is a simple, reliable technique which may be considered a good screening test for pancreatic insufficiency. The test will not detect minimal pancreatic disease or minimal pancreatic dysfunction.
对三组受试者的粪便标本进行了粪糜蛋白酶活性检测,分组如下:45名健康对照者(C组);36名胰腺外源性胃肠疾病患者(VP组);42名慢性胰腺炎患者(CP组)。CP组的19名患者接受了胰泌素-促胰液素和NBT-PABA检测。得到以下结果,以每克粪便中糜蛋白酶的毫克数表示:C组 = 0.610±0.203;CP组 = 0.291±0.154,p<0.001;VP组 = 0.560±0.234。粪糜蛋白酶检测的灵敏度为78.5%,特异度为71.6%。粪便中糜蛋白酶的排出量与胰腺分泌的糜蛋白酶密切相关(r = 0.59,p<0.01),与尿中PABA的回收率也密切相关(r = 0.44,p<0.05)。我们得出结论,用所述方法对即时粪便标本进行糜蛋白酶检测是一种简单、可靠的技术,可被视为胰腺功能不全的良好筛查试验。该试验无法检测出轻微的胰腺疾病或轻微的胰腺功能障碍。