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Volumn 13, Issue 4, 2014, Pages 373-377

Neonates with cystic fibrosis have a reduced nasal liquid pH; A small pilot study

Author keywords

Airway surface liquid (ASL); Cystic fibrosis; Neonatal screen; Neonates; PH

Indexed keywords

ACIDITY; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; CYSTIC FIBROSIS; FEMALE; HUMAN; MALE; NASAL AIRWAY SURFACE LIQUID PH; NEWBORN; NEWBORN DISEASE; NEWBORN MONITORING; NEWBORN SCREENING; NORMAL VALUE; PEDIATRICS; PH; PH MEASUREMENT; PILOT STUDY; RESPIRATORY TRACT PARAMETERS; ADOLESCENT; BODY FLUID; CHEMISTRY; FOLLOW UP; GENETICS; GENOTYPE; INFANT; METABOLISM; MIDDLE AGED; MUTATION; NOSE MUCOSA; PRESCHOOL CHILD; RETROSPECTIVE STUDY; SECRETION (PROCESS); YOUNG ADULT;

EID: 84902333159     PISSN: 15691993     EISSN: 18735010     Source Type: Journal    
DOI: 10.1016/j.jcf.2013.12.006     Document Type: Article
Times cited : (63)

References (24)
  • 2
    • 0142043977 scopus 로고    scopus 로고
    • Pathophysiology and management of pulmonary infections in cystic fibrosis
    • Gibson R.L., Burns J.L., Ramsey B.W. Pathophysiology and management of pulmonary infections in cystic fibrosis. Am J Respir Crit Care Med 2003, 168(8):918-951.
    • (2003) Am J Respir Crit Care Med , vol.168 , Issue.8 , pp. 918-951
    • Gibson, R.L.1    Burns, J.L.2    Ramsey, B.W.3
  • 3
    • 0028232830 scopus 로고
    • Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator
    • Poulsen J.H., Fischer H., Illek B., Machen T.E. Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator. Proc Natl Acad Sci U S A 1994, 91(12):5340-5344.
    • (1994) Proc Natl Acad Sci U S A , vol.91 , Issue.12 , pp. 5340-5344
    • Poulsen, J.H.1    Fischer, H.2    Illek, B.3    Machen, T.E.4
  • 4
    • 0026645366 scopus 로고
    • CAMP stimulates bicarbonate secretion across normal, but not cystic fibrosis airway epithelia
    • Smith J.J., Welsh M.J. cAMP stimulates bicarbonate secretion across normal, but not cystic fibrosis airway epithelia. J Clin Invest 1992, 89(4):1148-1153.
    • (1992) J Clin Invest , vol.89 , Issue.4 , pp. 1148-1153
    • Smith, J.J.1    Welsh, M.J.2
  • 6
    • 78649915334 scopus 로고    scopus 로고
    • Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia
    • Chen J.H., Stoltz D.A., Karp P.H., Ernst S.E., Pezzulo A.A., Moninger T.O., et al. Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia. Cell 2010, 143(6):911-923.
    • (2010) Cell , vol.143 , Issue.6 , pp. 911-923
    • Chen, J.H.1    Stoltz, D.A.2    Karp, P.H.3    Ernst, S.E.4    Pezzulo, A.A.5    Moninger, T.O.6
  • 8
    • 33645451580 scopus 로고    scopus 로고
    • Hyperacidity of secreted fluid from submucosal glands in early cystic fibrosis
    • Song Y., Salinas D., Nielson D.W., Verkman A.S. Hyperacidity of secreted fluid from submucosal glands in early cystic fibrosis. Am J Physiol Cell Physiol 2006, 290(3):C741-C749.
    • (2006) Am J Physiol Cell Physiol , vol.290 , Issue.3
    • Song, Y.1    Salinas, D.2    Nielson, D.W.3    Verkman, A.S.4
  • 9
    • 84863476402 scopus 로고    scopus 로고
    • Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis lung
    • Pezzulo A.A., Tang X.X., Hoegger M.J., Alaiwa M.H., Ramachandran S., Moninger T.O., et al. Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis lung. Nature 2012, 487(7405):109-113.
    • (2012) Nature , vol.487 , Issue.7405 , pp. 109-113
    • Pezzulo, A.A.1    Tang, X.X.2    Hoegger, M.J.3    Alaiwa, M.H.4    Ramachandran, S.5    Moninger, T.O.6
  • 10
    • 78649647597 scopus 로고    scopus 로고
    • Role of epithelial HCO3(-) transport in mucin secretion: lessons from cystic fibrosis
    • Quinton P.M. Role of epithelial HCO3(-) transport in mucin secretion: lessons from cystic fibrosis. Am J Physiol Cell Physiol 2010, 299(6):C1222-C1233.
    • (2010) Am J Physiol Cell Physiol , vol.299 , Issue.6
    • Quinton, P.M.1
  • 12
    • 0019985202 scopus 로고
    • Measurements of transepithelial electric potential differences in the trachea and bronchi of human subjects in vivo
    • Knowles M.R., Buntin W.H., Bromberg P.A., Gatzy J.T., Boucher R.C. Measurements of transepithelial electric potential differences in the trachea and bronchi of human subjects in vivo. Am Rev Respir Dis 1982, 126(1):108-112.
    • (1982) Am Rev Respir Dis , vol.126 , Issue.1 , pp. 108-112
    • Knowles, M.R.1    Buntin, W.H.2    Bromberg, P.A.3    Gatzy, J.T.4    Boucher, R.C.5
  • 13
    • 0033498170 scopus 로고    scopus 로고
    • Absence of amiloride-sensitive sodium absorption in the airway of an infant with pseudohypoaldosteronism
    • Prince L.S., Launspach J.L., Geller D.S., Lifton R.P., Pratt J.H., Zabner J., et al. Absence of amiloride-sensitive sodium absorption in the airway of an infant with pseudohypoaldosteronism. J Pediatr 1999, 135(6):786-789.
    • (1999) J Pediatr , vol.135 , Issue.6 , pp. 786-789
    • Prince, L.S.1    Launspach, J.L.2    Geller, D.S.3    Lifton, R.P.4    Pratt, J.H.5    Zabner, J.6
  • 14
    • 20944434002 scopus 로고    scopus 로고
    • Potential difference measurements in the lower airway of children with and without cystic fibrosis
    • Davies J.C., Davies M., McShane D., Smith S., Chadwick S., Jaffe A., et al. Potential difference measurements in the lower airway of children with and without cystic fibrosis. Am J Respir Crit Care Med 2005, 171(9):1015-1019.
    • (2005) Am J Respir Crit Care Med , vol.171 , Issue.9 , pp. 1015-1019
    • Davies, J.C.1    Davies, M.2    McShane, D.3    Smith, S.4    Chadwick, S.5    Jaffe, A.6
  • 15
    • 0025854202 scopus 로고
    • Neonatal screening strategy for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis
    • Ranieri E., Ryall R.G., Morris C.P., Nelson P.V., Carey W.F., Pollard A.C., et al. Neonatal screening strategy for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis. BMJ 1991, 302(6787):1237-1240.
    • (1991) BMJ , vol.302 , Issue.6787 , pp. 1237-1240
    • Ranieri, E.1    Ryall, R.G.2    Morris, C.P.3    Nelson, P.V.4    Carey, W.F.5    Pollard, A.C.6
  • 17
    • 0025133518 scopus 로고
    • Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene
    • Kerem B.S., Zielenski J., Markiewicz D., Bozon D., Gazit E., Yahav J., et al. Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene. Proc Natl Acad Sci U S A 1990, 87(21):8447-8451.
    • (1990) Proc Natl Acad Sci U S A , vol.87 , Issue.21 , pp. 8447-8451
    • Kerem, B.S.1    Zielenski, J.2    Markiewicz, D.3    Bozon, D.4    Gazit, E.5    Yahav, J.6
  • 19
    • 0035132659 scopus 로고    scopus 로고
    • Noninvasive in vivo fluorescence measurement of airway-surface liquid depth, salt concentration, and pH
    • Jayaraman S., Song Y., Vetrivel L., Shankar L., Verkman A.S. Noninvasive in vivo fluorescence measurement of airway-surface liquid depth, salt concentration, and pH. J Clin Invest 2001, 107(3):317-324.
    • (2001) J Clin Invest , vol.107 , Issue.3 , pp. 317-324
    • Jayaraman, S.1    Song, Y.2    Vetrivel, L.3    Shankar, L.4    Verkman, A.S.5
  • 20
    • 0000065457 scopus 로고
    • Significance of the nasal pH of nasal secretions in situ
    • Fabricant N.D. Significance of the nasal pH of nasal secretions in situ. Arch Otolaryngol 1941, 33:150-163.
    • (1941) Arch Otolaryngol , vol.33 , pp. 150-163
    • Fabricant, N.D.1
  • 21
    • 0032972269 scopus 로고    scopus 로고
    • Nasal pH measurement: a reliable and repeatable parameter
    • England R.J.A., Homer J.J., Knight L.C., Ell S.R. Nasal pH measurement: a reliable and repeatable parameter. Clin Otolaryngol 1999, 24(1):67-68.
    • (1999) Clin Otolaryngol , vol.24 , Issue.1 , pp. 67-68
    • England, R.J.A.1    Homer, J.J.2    Knight, L.C.3    Ell, S.R.4
  • 22
    • 54249153391 scopus 로고    scopus 로고
    • Biomarkers in exhaled breath condensate indicate presence and severity of cystic fibrosis in children
    • Robroeks C.M., Rosias P.P., van Vliet D., Jobsis Q., Yntema J.B., Brackel H.J., et al. Biomarkers in exhaled breath condensate indicate presence and severity of cystic fibrosis in children. Pediatr Allergy Immunol 2008, 19(7):652-659.
    • (2008) Pediatr Allergy Immunol , vol.19 , Issue.7 , pp. 652-659
    • Robroeks, C.M.1    Rosias, P.P.2    van Vliet, D.3    Jobsis, Q.4    Yntema, J.B.5    Brackel, H.J.6
  • 23
    • 69749128729 scopus 로고    scopus 로고
    • Exhaled breath condensate pH and ammonia in cystic fibrosis and response to treatment of acute pulmonary exacerbations
    • Newport S., Amin N., Dozor A.J. Exhaled breath condensate pH and ammonia in cystic fibrosis and response to treatment of acute pulmonary exacerbations. Pediatr Pulmonol 2009, 44(9):866-872.
    • (2009) Pediatr Pulmonol , vol.44 , Issue.9 , pp. 866-872
    • Newport, S.1    Amin, N.2    Dozor, A.J.3
  • 24
    • 84867397129 scopus 로고    scopus 로고
    • Exhaled breath condensate pH in patients with cystic fibrosis
    • Antus B., Barta I., Csiszer E., Kelemen K. Exhaled breath condensate pH in patients with cystic fibrosis. Inflamm Res 2012, 61(10):1141-1147.
    • (2012) Inflamm Res , vol.61 , Issue.10 , pp. 1141-1147
    • Antus, B.1    Barta, I.2    Csiszer, E.3    Kelemen, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.