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胃蛋白酶原I放射免疫测定与血清总胃蛋白酶原比色测定:正常人和消化性溃疡患者的对比研究

Pepsinogen Group I radioimmunoassay and total serum pepsinogen colorimetric determination: a comparative study in normal subjects and in peptic ulcer patients.

作者信息

Plebani M, Di Mario F, Vianello F, Giordano A, Masiero M, Lazzaretto M, Farini R, Ceriotti G, Naccarato R

出版信息

Clin Biochem. 1983 Feb;16(1):20-2. doi: 10.1016/s0009-9120(83)94279-0.

DOI:10.1016/s0009-9120(83)94279-0
PMID:6861334
Abstract

Pepsinogens, proteolytic enzymes produced by peptic cells of the stomach and discharged into the gastric lumen as well as into the blood have been divided into two groups: PG-I, originating from chief cells, and PG-II, mainly from antrum peptic cells. Both total serum pepsinogen (s-Pg) and PG-I have been separately reported as being significantly increased in gastric (GU) and duodenal ulcer (DU) patients and related to maximal acid output. In order to ascertain the relationship between s-Pg measured by means of the colorimetric Uete method, and PG-I determined by RIA method, these were assayed in 72 control subjects, 35 GU and 95 DU patients. s-Pg was found to be significantly increased both in GU and DU patients in comparison with control subjects. Likewise PG-I was significantly enhanced in GU and DU patients as compared with controls. A significant direct correlation between s-Pg and PG-I was found in all the subjects studied (r = 0.732).

摘要

胃蛋白酶原是由胃的主细胞产生并排入胃腔和血液的蛋白水解酶,已被分为两组:PG-I,起源于主细胞;PG-II,主要来自胃窦主细胞。血清总胃蛋白酶原(s-Pg)和PG-I均分别被报道在胃溃疡(GU)和十二指肠溃疡(DU)患者中显著升高,并与最大胃酸分泌量相关。为了确定用比色法Uete法测定的s-Pg与用放射免疫分析法(RIA)测定的PG-I之间的关系,对72名对照受试者、35名GU患者和95名DU患者进行了检测。发现GU和DU患者的s-Pg均较对照受试者显著升高。同样,与对照组相比,GU和DU患者的PG-I也显著升高。在所有研究对象中,s-Pg与PG-I之间存在显著的正相关(r = 0.732)。

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引用本文的文献

1
Pepsin concentration in gastroduodenal biopsy homogenates in chronic ulcer disease.慢性溃疡病患者胃十二指肠活检匀浆中的胃蛋白酶浓度
Dig Dis Sci. 1994 Feb;39(2):301-8. doi: 10.1007/BF02090201.
2
Study of duodenal ulcer disease in 100 families using total serum pepsinogen as a genetic marker.以血清总胃蛋白酶原作为遗传标记对100个家庭的十二指肠溃疡病进行研究。
Gut. 1984 Dec;25(12):1380-3. doi: 10.1136/gut.25.12.1380.