Diagnostic Accuracy of a Short Endoscopic Secretin Test in Patients With Cystic Fibrosis

被引:17
作者
Engjom, Trond [1 ,2 ]
Erchinger, Friedemann [1 ,3 ]
Laerum, Birger Norderud [4 ,5 ]
Tjora, Erling [5 ,6 ]
Aksnes, Lage [2 ,5 ,6 ]
Gilja, Odd Helge [1 ,7 ]
Dimcevski, Georg [1 ,2 ]
机构
[1] Univ Bergen, Dept Clin Med, N-5020 Bergen, Norway
[2] Haukeland Hosp, Dept Med, N-5021 Bergen, Norway
[3] Voss Hosp, Dept Med, Voss, Norway
[4] Haukeland Hosp, Dept Thorac Med, N-5021 Bergen, Norway
[5] Univ Bergen, Dept Clin Sci, Bergen, Norway
[6] Haukeland Hosp, Dept Pediat, N-5021 Bergen, Norway
[7] Haukeland Hosp, Natl Ctr Ultrasound Gastroenterol, N-5021 Bergen, Norway
关键词
pancreas; cystic fibrosis; exocrine pancreatic function; secretin; endoscopy; EXOCRINE PANCREATIC-FUNCTION; FECAL ELASTASE-1; CFTR GENE; IDENTIFICATION; GUIDELINES; MUTATIONS; DISEASE; SUFFICIENCY; CROSSOVER; GENOTYPE;
D O I
10.1097/MPA.0000000000000425
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective: Short endoscopic secretin tests for exocrine pancreatic function are not properly evaluated in cystic fibrosis (CF). Methods: Patients with CF and healthy controls (HCs) underwent endoscopic collection of duodenal juice between 30 and 45 minutes after secretin stimulation. Duodenal juice was analyzed for HCO3- concentration and pancreatic enzyme activities. Stool was analyzed for fecal elastase. Results: Thirty-one patients with CF and 25 HCs were tested. Patients were classified as exocrine pancreatic sufficient (n = 13) or insufficient (n = 18). Both bicarbonate concentrations and enzyme activities in duodenal juice differentiated patients with CFI from patients with CFS and HC (P < 0.001). The population displays strong correlation between severe CF genotype in both alleles and pancreatic insufficient phenotype (P < 0.001). Conclusions: Pancreatic exocrine insufficient CF patients could be differentiated from exocrine sufficient patients and HCs using short endoscopic secretin test.
引用
收藏
页码:1266 / 1272
页数:7
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