메뉴 건너뛰기




Volumn 8, Issue 8, 1996, Pages 755-759

Exocrine pancreatic function in cystic fibrosis

Author keywords

Cystic fibrosis; Dysfunction; Exocrine pancreas; Genotype

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR; TRYPSIN;

EID: 0029792590     PISSN: 0954691X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (15)

References (35)
  • 1
    • 0000471085 scopus 로고
    • Cystic fibrosis of the pancreas and its relation to celiac disease: A clinical and pathologic study
    • Andersen DH: Cystic fibrosis of the pancreas and its relation to celiac disease: a clinical and pathologic study. Am J Dis Child 1938, 56:344-399.
    • (1938) Am J Dis Child , vol.56 , pp. 344-399
    • Andersen, D.H.1
  • 2
    • 0024453308 scopus 로고
    • Identification of the cystic fibrosis gene: Chromosomes walking and jumping
    • Rommens JM, Iannuzzi MC, Kerem BS, Drumm ML, Melmer G, Dean M, et al: Identification of the cystic fibrosis gene: chromosomes walking and jumping. Science 1989, 245:1059-1065.
    • (1989) Science , vol.245 , pp. 1059-1065
    • Rommens, J.M.1    Iannuzzi, M.C.2    Kerem, B.S.3    Drumm, M.L.4    Melmer, G.5    Dean, M.6
  • 3
    • 0024424270 scopus 로고
    • Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
    • Riordan JR, Rommens JM, Kerem BS, Alon N, Rozmahel R, Grzelczak Z, et al.: Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 1989, 245:1066-1072.
    • (1989) Science , vol.245 , pp. 1066-1072
    • Riordan, J.R.1    Rommens, J.M.2    Kerem, B.S.3    Alon, N.4    Rozmahel, R.5    Grzelczak, Z.6
  • 5
    • 0022913087 scopus 로고
    • Prenatal diagnosis in 200 pregnancies with a 1-in-4 risk of cystic fibrosis
    • Boué A, Muller F, Nezeloff C, Oury JF, Duchatel F, Dumez Y, et al.: Prenatal diagnosis in 200 pregnancies with a 1-in-4 risk of cystic fibrosis. Hum Genet 1986, 74:288-297.
    • (1986) Hum Genet , vol.74 , pp. 288-297
    • Boué, A.1    Muller, F.2    Nezeloff, C.3    Oury, J.F.4    Duchatel, F.5    Dumez, Y.6
  • 6
    • 0026533779 scopus 로고
    • Levels and molecular forms of immunoreactive trypsin and chymotrypsin in amniotic fluids from normal and cystic fibrosis fetus: Evidence for a lack of activation of proteolytic zymogens in cystic fibrosis fetus
    • Carrère J, Muller F, Boué A, Guy-Crotte O, Figarella C: Levels and molecular forms of immunoreactive trypsin and chymotrypsin in amniotic fluids from normal and cystic fibrosis fetus: evidence for a lack of activation of proteolytic zymogens in cystic fibrosis fetus. J Pediatr Gastroenterol Nutr 1992, 14:198-203.
    • (1992) J Pediatr Gastroenterol Nutr , vol.14 , pp. 198-203
    • Carrère, J.1    Muller, F.2    Boué, A.3    Guy-Crotte, O.4    Figarella, C.5
  • 7
    • 0026656560 scopus 로고
    • The neonatal detection of cystic fibrosis by measurement of immunoreactive trypsin in blood
    • Heeley AF, Bangert SK: The neonatal detection of cystic fibrosis by measurement of immunoreactive trypsin in blood. Ann Clin Biochem 1992, 29:361-376.
    • (1992) Ann Clin Biochem , vol.29 , pp. 361-376
    • Heeley, A.F.1    Bangert, S.K.2
  • 8
    • 0026667231 scopus 로고
    • Quelle approche pour le dépistage néonatal de la mucoviscidose?
    • Figarella C: Quelle approche pour le dépistage néonatal de la mucoviscidose? Immunoanal Biol Spec 1992, 33:77-81. Assays of serum immunoreactive trypsin must be optimized and remain the best neonatal screening of cystic fibrosis.
    • (1992) Immunoanal Biol Spec , vol.33 , pp. 77-81
    • Figarella, C.1
  • 9
    • 0018769118 scopus 로고
    • Dried blood spot screening for cystic fibrosis in the newborn
    • Crossley JR, Elliot RP, Smith PA: Dried blood spot screening for cystic fibrosis in the newborn. Lancet 1979, i:472-474
    • (1979) Lancet , vol.1 , pp. 472-474
    • Crossley, J.R.1    Elliot, R.P.2    Smith, P.A.3
  • 10
    • 0022491917 scopus 로고
    • Physiologically elevated concentration of serum trypsin-like immunoreactivity in newborns. Comparison with lipase
    • Carrère J, Estevenon JP, Guy-Crotte O, Thouvenot JP, Figarella C: Physiologically elevated concentration of serum trypsin-like immunoreactivity in newborns. Comparison with lipase. Biol Neonate 1986, 49:113-120.
    • (1986) Biol Neonate , vol.49 , pp. 113-120
    • Carrère, J.1    Estevenon, J.P.2    Guy-Crotte, O.3    Thouvenot, J.P.4    Figarella, C.5
  • 11
    • 0018421282 scopus 로고
    • Quantitative evaluation of the development of the exocrine pancreas in cystic fibrosis and control infants
    • Imrie JR, Fagan DG, Sturgess JM: Quantitative evaluation of the development of the exocrine pancreas in cystic fibrosis and control infants. Am J Pathol 1979, 95:697-708.
    • (1979) Am J Pathol , vol.95 , pp. 697-708
    • Imrie, J.R.1    Fagan, D.G.2    Sturgess, J.M.3
  • 12
    • 9444269647 scopus 로고
    • 1-proteinase inhibitor in meconium from healthy infants and infants with cystic fibrosis
    • Edited by Arnaud P, Bienvenu J, Laurent P. Berlin: Walter de Gruyter
    • 1-proteinase inhibitor in meconium from healthy infants and infants with cystic fibrosis. In Marker Proteins in Inflammation. Edited by Arnaud P, Bienvenu J, Laurent P. Berlin: Walter de Gruyter; 1984:251-254.
    • (1984) Marker Proteins in Inflammation , pp. 251-254
    • Lafont, P.1    Barbier, Y.2    Mathian, J.3    Boisson, R.C.4    Garcia, I.5    Gilly, R.6
  • 13
    • 0023874980 scopus 로고
    • Proteinase inhibitor and defective proteolysis in cystic fibrosis
    • Hsieh M, Berry HK: Proteinase inhibitor and defective proteolysis in cystic fibrosis. Dig Dis Sci 1988, 33:282-288.
    • (1988) Dig Dis Sci , vol.33 , pp. 282-288
    • Hsieh, M.1    Berry, H.K.2
  • 14
    • 0000507886 scopus 로고
    • The evolution of pancreatic disease in cystic fibrosis
    • Edited by Dodge JA, Brock DJH, Widdicombe JH. Chichester: John Wiley
    • Figarella C: The evolution of pancreatic disease in cystic fibrosis. In Cystic Fibrosis - Current Topics, vol 2. Edited by Dodge JA, Brock DJH, Widdicombe JH. Chichester: John Wiley; 1994:255-275.
    • (1994) Cystic Fibrosis - Current Topics , vol.2 , pp. 255-275
    • Figarella, C.1
  • 15
    • 0015929760 scopus 로고
    • Relations between pancreatic enzyme outputs and malabsorption in severe pancreatic insufficiency
    • DiMagno EP, Co VLW, Summerskill WH: Relations between pancreatic enzyme outputs and malabsorption in severe pancreatic insufficiency. N Engl J Med 1973, 288:813-815.
    • (1973) N Engl J Med , vol.288 , pp. 813-815
    • DiMagno, E.P.1    Co, V.L.W.2    Summerskill, W.H.3
  • 16
    • 0021369735 scopus 로고
    • Colipase and lipase secretion in childhood onset pancreatic insufficiency. Delineation of patients with steatorrhea secondary to relative colipase deficiency
    • Gaskin KJ, Durie PR, Lee L, Hill R, Forstner G: Colipase and lipase secretion in childhood onset pancreatic insufficiency. Delineation of patients with steatorrhea secondary to relative colipase deficiency. Gastroenterology 1984, 86:1-7.
    • (1984) Gastroenterology , vol.86 , pp. 1-7
    • Gaskin, K.J.1    Durie, P.R.2    Lee, L.3    Hill, R.4    Forstner, G.5
  • 17
    • 0025181586 scopus 로고
    • Pancreatic function in infants identified as having cystic fibrosis in a neonatal screening program
    • Waters DL, Dorney S, Gaskin KJ, Gruca MA, O'Halloran M, Wicken B: Pancreatic function in infants identified as having cystic fibrosis in a neonatal screening program. N Engl J Med 1990, 332:303-308.
    • (1990) N Engl J Med , vol.332 , pp. 303-308
    • Waters, D.L.1    Dorney, S.2    Gaskin, K.J.3    Gruca, M.A.4    O'Halloran, M.5    Wicken, B.6
  • 20
    • 0022644083 scopus 로고
    • Age-related alterations of immunoreaclive pancreatic cationic trypsinogen in sera from cystic fibrosis patients with and without pancreatic sufficiency
    • Durie PR, Forstner GG, Gaskin KJ, Moore DJ, Cleghorn GJ, Wong SS, et al.: Age-related alterations of immunoreaclive pancreatic cationic trypsinogen in sera from cystic fibrosis patients with and without pancreatic sufficiency. Pediatr Res 1986, 20:209-213.
    • (1986) Pediatr Res , vol.20 , pp. 209-213
    • Durie, P.R.1    Forstner, G.G.2    Gaskin, K.J.3    Moore, D.J.4    Cleghorn, G.J.5    Wong, S.S.6
  • 21
    • 0029121023 scopus 로고
    • Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic sufficient patients with cystic fibrosis
    • Couper RTL, Corey M, Durie PR, Forstner GG, Moore DJ: Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic sufficient patients with cystic fibrosis. J Pediatr 1995, 127:408-413. 329 patients with CF aged 3 days to 40 years had serum levels of trypsinogen measured on 2 to 12 occasions for period ranging from 1 week to 7 years. The results show that serial measurement of serum trypsinogen is a valuable tool for monitoring the pancreatic status of patients with cystic fibrosis.
    • (1995) J Pediatr , vol.127 , pp. 408-413
    • Couper, R.T.L.1    Corey, M.2    Durie, P.R.3    Forstner, G.G.4    Moore, D.J.5
  • 22
    • 0026753701 scopus 로고
    • Decline of exocrine pancreatic function in cystic fibrosis patients with pancreatic sufficiency
    • Couper RTL, Corey M, Moore DJ, Fisher LJ, Forstner, GG, Durie PR: Decline of exocrine pancreatic function in cystic fibrosis patients with pancreatic sufficiency. Pediatr Res 1992, 32:179-182.
    • (1992) Pediatr Res , vol.32 , pp. 179-182
    • Couper, R.T.L.1    Corey, M.2    Moore, D.J.3    Fisher, L.J.4    Forstner, G.G.5    Durie, P.R.6
  • 23
    • 0027195534 scopus 로고
    • Cell-specific localization of CFTR mRNA shows developmentally regulated expression in human fetal tissues
    • Tizzano EF, Chitayat D, Buchwald M: Cell-specific localization of CFTR mRNA shows developmentally regulated expression in human fetal tissues. Hum Mol Genet 1993, 2:219-224. The expression of CFTR in human fetal tissues was studied at different gestational ages, 10 to 33 weeks gestation, using in-situ hybridization. The detection of CFTR transcript is consistent with the clinical manifestation of CF and the function of CFTR as a chloride channel early in development.
    • (1993) Hum Mol Genet , vol.2 , pp. 219-224
    • Tizzano, E.F.1    Chitayat, D.2    Buchwald, M.3
  • 24
    • 0027207509 scopus 로고
    • Expression of the cystic fibrosis gene in human foetal tissues
    • Trezise AEO, Chambers IA, Wardle CJ, Gould S, Harris A: Expression of the cystic fibrosis gene in human foetal tissues. Hum Mol Genet 1993, 2:213-218. The expression of CFTR has been examined in mid-trimester human fetal tissues by in-situ hybridization. CFTR mRNA was detected in the epithelia of pancreatic ducts, small intestine, colon, genital ducts, lung and trachea.
    • (1993) Hum Mol Genet , vol.2 , pp. 213-218
    • Trezise, A.E.O.1    Chambers, I.A.2    Wardle, C.J.3    Gould, S.4    Harris, A.5
  • 26
    • 0025241696 scopus 로고
    • The relation between genotype and phenotype in cystic fibrosis: Analysis of the most common mutation (ΔF 508)
    • Kerem E, Corey M, Kerem BS, Rommens J, Markiewicz D, Levison H, et al.: The relation between genotype and phenotype in cystic fibrosis: analysis of the most common mutation (ΔF 508). N Engl J Med 1990, 323:1517-1522.
    • (1990) N Engl J Med , vol.323 , pp. 1517-1522
    • Kerem, E.1    Corey, M.2    Kerem, B.S.3    Rommens, J.4    Markiewicz, D.5    Levison, H.6
  • 27
    • 0026734588 scopus 로고
    • Genetic determination of exocrine pancreatic function in cystic fibrosis
    • Kristidis P, Bozon D, Corey M, Markiewicz D, Rommens J, Tsui LC, et al.: Genetic determination of exocrine pancreatic function in cystic fibrosis. Am J Hum Genet 1992, 50:1178-1184. The genomic DNA of 538 CF patients with well documented pancreatic function were analysed for a series of known mutations in their CFTR gene. The data showed that each genotype was associated only with PI or only with PS but not with both. This result is consistent with the hypothesis that PI and PS in CF are predisposed by the genotype at the CFTR locus.
    • (1992) Am J Hum Genet , vol.50 , pp. 1178-1184
    • Kristidis, P.1    Bozon, D.2    Corey, M.3    Markiewicz, D.4    Rommens, J.5    Tsui, L.C.6
  • 28
    • 0028929909 scopus 로고
    • Mechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiency
    • - current and suggest that the residual function is sufficient to confer a milder clinical phenotype.
    • (1995) EMBO J , vol.14 , pp. 876-883
    • Sheppard, D.N.1    Ostedgaard, L.S.2    Winter, M.C.3    Welsh, M.J.4
  • 29
    • 0029126565 scopus 로고
    • Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: Detection of 90% of molecular defects and identification of three novel mutations
    • Brancolini V, Cremonesi L, Belloni E, Pappalardo E, Bardoni R, Seia M, et al.: Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutations. Hum Genet 1995, 96:312-318. 31 CF patients with pancreatic sufficiency and an unidentified mutation on at least one chromosome were screened for mutations. Three new and 19 previously described mutations were detected. Among them, 17 presumed mild mutations can be considered responsible for pancreatic sufficiency.
    • (1995) Hum Genet , vol.96 , pp. 312-318
    • Brancolini, V.1    Cremonesi, L.2    Belloni, E.3    Pappalardo, E.4    Bardoni, R.5    Seia, M.6
  • 30
    • 0024313506 scopus 로고
    • 1,-proteinase inhibitor complex in some cystic fibrosis patients
    • 1,-proteinase inhibitor complex in some cystic fibrosis patients. Biochim Biophys Acta 1989, 993:137-142. This study shows that active trypsin has been released in blood in some sera of CF patients, suggesting that subclinical attacks of acute pancre-atitis may occur in CF patients.
    • (1989) Biochim Biophys Acta , vol.993 , pp. 137-142
    • Carrère, J.1    Chazalette, J.P.2    Figarella, C.3
  • 31
    • 0016835773 scopus 로고
    • Recurrent acute pancreatitis in patients with cystic fibrosis with normal pancreatic enzymes
    • Shwachman H, Lebenthal E, Khaw K: Recurrent acute pancreatitis in patients with cystic fibrosis with normal pancreatic enzymes. Pediatrics 1975, 55:86-94.
    • (1975) Pediatrics , vol.55 , pp. 86-94
    • Shwachman, H.1    Lebenthal, E.2    Khaw, K.3
  • 33
    • 0029054747 scopus 로고
    • Chronic pancreatitis in a patient with cystic fibrosis and clinical pancreatic insufficiency
    • Fernando del Rosario J, Putnam PE, Orenstein DM: Chronic pancreatitis in a patient with cystic fibrosis and clinical pancreatic insufficiency. J Pediatr 1995, 126:951-952.
    • (1995) J Pediatr , vol.126 , pp. 951-952
    • Fernando Del Rosario, J.1    Putnam, P.E.2    Orenstein, D.M.3
  • 34
    • 0029160442 scopus 로고
    • CFTR expression and organ damage in cystic fibrosis
    • Tizzano EF, Buchwald M: CFTR expression and organ damage in cystic fibrosis. Ann Intern Med 1995, 123:305-308.
    • (1995) Ann Intern Med , vol.123 , pp. 305-308
    • Tizzano, E.F.1    Buchwald, M.2
  • 35
    • 13344282728 scopus 로고    scopus 로고
    • Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor
    • Rozmahel R, Wilschanski M, Matin A, Plyte S, Oliver M, Auerbach W, et al.: Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor. Nature Genet 1996 12:280-287.
    • (1996) Nature Genet , vol.12 , pp. 280-287
    • Rozmahel, R.1    Wilschanski, M.2    Matin, A.3    Plyte, S.4    Oliver, M.5    Auerbach, W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.