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Volumn 82, Issue 4, 2007, Pages 379-

Low hepatic cytochrome P450 3A activity is a risk for corticosteroid- induced osteonecrosis [1]

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MARKER; CORTICOSTEROID; CYTOCHROME P450 3A; ERYTHROMYCIN; LIVER ENZYME; MIDAZOLAM;

EID: 34548664602     PISSN: 00099236     EISSN: 15326535     Source Type: Journal    
DOI: 10.1038/sj.clpt.6100105     Document Type: Letter
Times cited : (8)

References (8)
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    • Low hepatic cytochrome P450 3A activity is a risk for corticosteroid-induced osteonecrosis
    • Kaneshiro, Y. et al. Low hepatic cytochrome P450 3A activity is a risk for corticosteroid-induced osteonecrosis. Clin. Pharmacol. Ther. 80, 396-402 (2006).
    • (2006) Clin. Pharmacol. Ther , vol.80 , pp. 396-402
    • Kaneshiro, Y.1
  • 2
    • 85047697278 scopus 로고    scopus 로고
    • Limited sampling strategy to predict AUC of the CYP3A phenotyping probe midazolam in adults: Application to various assay techniques
    • Kim, J.S. et al. Limited sampling strategy to predict AUC of the CYP3A phenotyping probe midazolam in adults: application to various assay techniques. J. Clin. Pharmacol. 42, 376-382 (2002).
    • (2002) J. Clin. Pharmacol , vol.42 , pp. 376-382
    • Kim, J.S.1
  • 3
    • 31344459534 scopus 로고    scopus 로고
    • Limited sampling models for oral midazolam:midazolam plasma concentrations, not the ratio of 1-hydroxymidazolam to midazolam plasma concentrations, accurately predicts AUC as a biomarker of CYP3A activity
    • Lee, L.S., Bertino, J.S. Jr & Nafziger, A.N. Limited sampling models for oral midazolam:midazolam plasma concentrations, not the ratio of 1-hydroxymidazolam to midazolam plasma concentrations, accurately predicts AUC as a biomarker of CYP3A activity. J. Clin. Pharmacol. 46, 229-234 (2006).
    • (2006) J. Clin. Pharmacol , vol.46 , pp. 229-234
    • Lee, L.S.1    Bertino Jr, J.S.2    Nafziger, A.N.3
  • 4
    • 0027985506 scopus 로고
    • Use of midazolam as a human cytochrome P450 3A probe: II. Characterization of inter- and intraindividual hepatic CYP3A variability after liver transplantation
    • Thummel, K.E. et al. Use of midazolam as a human cytochrome P450 3A probe: II. Characterization of inter- and intraindividual hepatic CYP3A variability after liver transplantation. J. Pharmacol. Exp. Ther. 271, 557-566 (1994).
    • (1994) J. Pharmacol. Exp. Ther , vol.271 , pp. 557-566
    • Thummel, K.E.1
  • 5
    • 0036784471 scopus 로고    scopus 로고
    • Single plasma concentrations of 1′-hydroxymidazolam or the ratio of 1′-hydroxymidazolam:midazolam do not predictmidazolamclearance in healthy subjects
    • Rogers, J.F. et al. Single plasma concentrations of 1′-hydroxymidazolam or the ratio of 1′-hydroxymidazolam:midazolam do not predictmidazolamclearance in healthy subjects. J. Clin. Pharmacol. 42, 1079-1082 (2002).
    • (2002) J. Clin. Pharmacol , vol.42 , pp. 1079-1082
    • Rogers, J.F.1
  • 6
    • 0035218021 scopus 로고    scopus 로고
    • In-vivo phenotyping for CYP3A by a single-point determination of midazolam plasma concentration
    • Lin, Y.S. et al. In-vivo phenotyping for CYP3A by a single-point determination of midazolam plasma concentration. Pharmacogenetics 11, 781-791 (2001).
    • (2001) Pharmacogenetics , vol.11 , pp. 781-791
    • Lin, Y.S.1
  • 7
    • 10744232330 scopus 로고    scopus 로고
    • The conduct of in vitro and in vivo drug-drug interaction studies: A Pharmaceutical Research and Manufacturers of America (PhRMA) perspective
    • Bjornsson, T.D. et al. The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective. Drug Metab. Dispos. 31, 815-832 (2003).
    • (2003) Drug Metab. Dispos , vol.31 , pp. 815-832
    • Bjornsson, T.D.1
  • 8
    • 34548703429 scopus 로고    scopus 로고
    • Drug interaction studies - study design, data analysis, and implications for dosing and labeling
    • Food and Drug Administration, ed. Pharmacology C, US Department of Health and Human Services, Food and Drug Administration, Rockville
    • Food and Drug Administration. Drug interaction studies - study design, data analysis, and implications for dosing and labeling. In Guidance for Industry (ed. Pharmacology C.) US Department of Health and Human Services, Food and Drug Administration, Rockville, 2006, pp 1-34.
    • (2006) Guidance for Industry , pp. 1-34


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.