메뉴 건너뛰기




Volumn 188, Issue 1, 2013, Pages 83-89

Inhalation treatment with glutathione in patients with cystic fibrosis: A randomized clinical trial

(25)  Griese, Matthias a   Kappler, Matthias a   Eismann, Claudia a   Ballmann, Manfred b   Junge, Sibylle b   Rietschel, Ernst c   Van Koningsbruggen Rietschel, Silke c   Staab, Doris d   Rolinck Werninghaus, Claudia d   Mellies, Uwe e   Köhnlein, Thomas b   Wagner, Thomas f   König, Susanne g   Teschler, Helmut h   Heuer, Hans Eberhard i   Kopp, Matthias j   Heyder, Susanne k   Hammermann, Jutta l   Küster, Peter m   Honer, Marguerite n   more..


Author keywords

Antioxidant; Clinical trial; Cystic fibrosis; Glutathione; Inhaled therapy

Indexed keywords

GLUTATHIONE; LIPID; PLACEBO;

EID: 84880170145     PISSN: 1073449X     EISSN: 15354970     Source Type: Journal    
DOI: 10.1164/rccm.201303-0427OC     Document Type: Article
Times cited : (73)

References (29)
  • 4
    • 33751580475 scopus 로고    scopus 로고
    • Antioxidants in cystic fibrosis. Conclusions from the CF Antioxidant Workshop, Bethesda, Maryland, November 11-12, 2003
    • DOI 10.1016/j.freeradbiomed.2006.09.022, PII S0891584906005983
    • Cantin AM, White TB, Cross CE, Forman HJ, Sokol RJ, Borowitz D. Antioxidants in cystic fibrosis: conclusions from the CF Antioxidant Workshop, Bethesda, Maryland, November 11-12, 2003. Free Radic Biol Med 2007;42:15-31. (Pubitemid 44842010)
    • (2007) Free Radical Biology and Medicine , vol.42 , Issue.1 , pp. 15-31
    • Cantin, A.M.1    White, T.B.2    Cross, C.E.3    Forman, H.J.4    Sokol, R.J.5    Borowitz, D.6
  • 8
    • 0035876878 scopus 로고    scopus 로고
    • Rethinking cystic fibrosis pathology: The critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation
    • DOI 10.1016/S0891-5849(01)00530-5, PII S0891584901005305
    • Hudson VM. Rethinking cystic fibrosis pathology: the critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation. Free Radic Biol Med 2001;30:1440-1461. (Pubitemid 32522959)
    • (2001) Free Radical Biology and Medicine , vol.30 , Issue.12 , pp. 1440-1461
    • Hudson, V.M.1
  • 9
    • 0030802906 scopus 로고    scopus 로고
    • Pulmonary oxidative stress response in young children with cystic fibrosis
    • Hull J, Vervaart P, Grimwood K, Phelan P. Pulmonary oxidative stress response in young children with cystic fibrosis. Thorax 1997;52:557-560. (Pubitemid 27298509)
    • (1997) Thorax , vol.52 , Issue.6 , pp. 557-560
    • Hull, J.1    Vervaart, P.2    Grimwood, K.3    Phelan, P.4
  • 10
  • 12
    • 79551607386 scopus 로고    scopus 로고
    • Hypertonic saline increases lung epithelial lining fluid glutathione and thiocyanate: Two protective CFTR-dependent thiols against oxidative injury
    • Gould NS, Gauthier S, Kariya CT, Min E, Huang J, Brian DJ. Hypertonic saline increases lung epithelial lining fluid glutathione and thiocyanate: two protective CFTR-dependent thiols against oxidative injury. Respir Res 2010;11:119.
    • (2010) Respir Res , vol.11 , pp. 119
    • Gould, N.S.1    Gauthier, S.2    Kariya, C.T.3    Min, E.4    Huang, J.5    Brian, D.J.6
  • 13
    • 3343004752 scopus 로고    scopus 로고
    • Glutathione and glutathione peroxidase in sputum samples of adult patients with cystic fibrosis
    • DOI 10.1016/j.jcf.2004.03.005, PII S156919930400044X
    • Dauletbaev N, Viel K, Buhl R, Wagner TO, Bargon J. Glutathione and glutathione peroxidase in sputum samples of adult patients with cystic fibrosis. J Cyst Fibros 2004;3:119-124. (Pubitemid 38987022)
    • (2004) Journal of Cystic Fibrosis , vol.3 , Issue.2 , pp. 119-124
    • Dauletbaev, N.1    Viel, K.2    Buhl, R.3    Wagner, T.O.F.4    Bargon, J.5
  • 14
    • 13844322148 scopus 로고    scopus 로고
    • A pilot study of the effect of inhaled buffered reduced glutathione on the clinical status of patients with cystic fibrosis
    • DOI 10.1378/chest.127.1.308
    • Bishop C, Hudson VM, Hilton SC, Wilde C. A pilot study of the effect of inhaled buffered reduced glutathione on the clinical status of patients with cystic fibrosis. Chest 2005;127:308-317. (Pubitemid 41724591)
    • (2005) Chest , vol.127 , Issue.1 , pp. 308-317
    • Bishop, C.1    Hudson, V.M.2    Hilton, S.C.3    Wilde, C.4
  • 15
    • 51549090573 scopus 로고    scopus 로고
    • Improvement in clinical markers in CF patients using a reduced glutathione regimen: An uncontrolled, observational study
    • Visca A, Bishop CT, Hilton SC, Hudson VM. Improvement in clinical markers in CF patients using a reduced glutathione regimen: an uncontrolled, observational study. J Cyst Fibros 2008;7:433-436.
    • (2008) J Cyst Fibros , vol.7 , pp. 433-436
    • Visca, A.1    Bishop, C.T.2    Hilton, S.C.3    Hudson, V.M.4
  • 18
    • 77958025778 scopus 로고    scopus 로고
    • Novel method to process cystic fibrosis sputum for determination of oxidative state
    • Hector A, Jonas F, Kappler M, Feilcke M, Hartl D, Griese M. Novel method to process cystic fibrosis sputum for determination of oxidative state. Respiration 2010;80:393-400.
    • (2010) Respiration , vol.80 , pp. 393-400
    • Hector, A.1    Jonas, F.2    Kappler, M.3    Feilcke, M.4    Hartl, D.5    Griese, M.6
  • 19
    • 0035922668 scopus 로고    scopus 로고
    • Comparison of hypertonic saline and alternate-day or daily recombinant human deoxyribonuclease in children with cystic fibrosis: A randomised trial
    • DOI 10.1016/S0140-6736(01)06412-1
    • Suri R, Metcalfe C, Lees B, Grieve R, Flather M, Normand C, Thompson S, Bush A, Wallis C. Comparison of hypertonic saline and alternate-day or daily recombinant human deoxyribonuclease in children with cystic fibrosis: a randomised trial. Lancet 2001;358:1316-1321. (Pubitemid 33016495)
    • (2001) Lancet , vol.358 , Issue.9290 , pp. 1316-1321
    • Suri, R.1    Metcalfe, C.2    Lees, B.3    Grieve, R.4    Flather, M.5    Normand, C.6    Thompson, S.7    Bush, A.8    Wallis, C.9
  • 20
  • 21
    • 59449101370 scopus 로고    scopus 로고
    • Cystic fibrosis: Evolution from a fatal disease of infancy with a clear phenotype to a chronic disease of adulthood with diverse manifestations
    • Ren CL. Cystic fibrosis: evolution from a fatal disease of infancy with a clear phenotype to a chronic disease of adulthood with diverse manifestations. Clin Rev Allergy Immunol 2008;35:97-99.
    • (2008) Clin Rev Allergy Immunol , vol.35 , pp. 97-99
    • Ren, C.L.1
  • 25
    • 79958257149 scopus 로고    scopus 로고
    • Accurate assessment of adherence: Self-report and clinician report vs electronic monitoring of nebulizers
    • Daniels T, Goodacre L, Sutton C, Pollard K, Conway S, Peckham D. Accurate assessment of adherence: self-report and clinician report vs electronic monitoring of nebulizers. Chest 2011;140:425-432.
    • (2011) Chest , vol.140 , pp. 425-432
    • Daniels, T.1    Goodacre, L.2    Sutton, C.3    Pollard, K.4    Conway, S.5    Peckham, D.6
  • 26
    • 84880175786 scopus 로고    scopus 로고
    • Use of patient monitoring systems in clinical trials to generate objective information on patients' drug adherence of inhaled medications [abstract]
    • Fuchs C, Eismann C, Griese M, Seemann S, Knoch M. Use of patient monitoring systems in clinical trials to generate objective information on patients' drug adherence of inhaled medications [abstract]. J Cyst Fibros 2011;10:S91.
    • (2011) J Cyst Fibros , vol.10
    • Fuchs, C.1    Eismann, C.2    Griese, M.3    Seemann, S.4    Knoch, M.5
  • 27
    • 0004932287 scopus 로고
    • Reversal of the glutathione deficiency in the lower respiratory tract of HIVseropositive individuals by gutathione aerosol therapy
    • Buhl R, Holroyd K, Borok Z, Roum J, Bokser A, Grimes G. Reversal of the glutathione deficiency in the lower respiratory tract of HIVseropositive individuals by gutathione aerosol therapy. Abstr Clin Res 1990;38:596A.
    • (1990) Abstr Clin Res , vol.38
    • Buhl, R.1    Holroyd, K.2    Borok, Z.3    Roum, J.4    Bokser, A.5    Grimes, G.6
  • 29
    • 12744273488 scopus 로고    scopus 로고
    • New insights into the pathogenesis of cystic fibrosis: Pivotal role of glutathione system dysfunction and implications for therapy
    • Hudson VM. New insights into the pathogenesis of cystic fibrosis: pivotal role of glutathione system dysfunction and implications for therapy. Treat Respir Med 2004;3:353-363.
    • (2004) Treat Respir Med , vol.3 , pp. 353-363
    • Hudson, V.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.