CYP3A activity in severe liver cirrhosis correlates with Child–Pugh and model for end‐stage liver disease (MELD) scores. (January 2014)
- Record Type:
- Journal Article
- Title:
- CYP3A activity in severe liver cirrhosis correlates with Child–Pugh and model for end‐stage liver disease (MELD) scores. (January 2014)
- Main Title:
- CYP3A activity in severe liver cirrhosis correlates with Child–Pugh and model for end‐stage liver disease (MELD) scores
- Authors:
- Albarmawi, Albader
Czock, David
Gauss, Annika
Ehehalt, Robert
Lorenzo Bermejo, Justo
Burhenne, Jürgen
Ganten, Tom M.
Sauer, Peter
Haefeli, Walter E. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="bcp12182-sec-0001" sec-type="section"> <title>Aims</title> <p>Impaired liver function often necessitates drug dose adjustment to avoid excessive drug accumulation and adverse events, but a marker for the extent of the required adjustment is lacking. The aim of this study was to investigate whether Child–Pugh (CP) and model for end‐stage liver disease (MELD) scores correlate with drug clearance.</p> </sec> <sec id="bcp12182-sec-0002" sec-type="section"> <title>Methods</title> <p>Midazolam was used as a CYP3A probe and its pharmacokinetics were analyzed in 24 patients with mild to severe liver cirrhosis (<italic>n</italic> = 4, 10 and 10 with CP class A, B and C, respectively) and six patients without liver disease.</p> </sec> <sec id="bcp12182-sec-0003" sec-type="section"> <title>Results</title> <p>Both scores correlated well with unbound midazolam clearance (CL<sub>u</sub>), unbound midazolam fraction and half‐life (all <italic>P</italic> &lt; 0.01), whereas the unbound steady‐state volume of distribution was not significantly changed. In patients with severe liver cirrhosis unbound midazolam clearance was only 14% of controls (CP C: CL<sub>u</sub> = 843 ± 346 l h<sup>−1</sup>, MELD ≥ 15: CL<sub>u</sub> = 805 ± 474 l h<sup>−1</sup>, controls: CL<sub>u</sub> = 5815 ± 2649 l h<sup>−1</sup>, <italic>P</italic> &lt; 0.01).</p> </sec> <sec id="bcp12182-sec-0004" sec-type="section"><abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="bcp12182-sec-0001" sec-type="section"> <title>Aims</title> <p>Impaired liver function often necessitates drug dose adjustment to avoid excessive drug accumulation and adverse events, but a marker for the extent of the required adjustment is lacking. The aim of this study was to investigate whether Child–Pugh (CP) and model for end‐stage liver disease (MELD) scores correlate with drug clearance.</p> </sec> <sec id="bcp12182-sec-0002" sec-type="section"> <title>Methods</title> <p>Midazolam was used as a CYP3A probe and its pharmacokinetics were analyzed in 24 patients with mild to severe liver cirrhosis (<italic>n</italic> = 4, 10 and 10 with CP class A, B and C, respectively) and six patients without liver disease.</p> </sec> <sec id="bcp12182-sec-0003" sec-type="section"> <title>Results</title> <p>Both scores correlated well with unbound midazolam clearance (CL<sub>u</sub>), unbound midazolam fraction and half‐life (all <italic>P</italic> &lt; 0.01), whereas the unbound steady‐state volume of distribution was not significantly changed. In patients with severe liver cirrhosis unbound midazolam clearance was only 14% of controls (CP C: CL<sub>u</sub> = 843 ± 346 l h<sup>−1</sup>, MELD ≥ 15: CL<sub>u</sub> = 805 ± 474 l h<sup>−1</sup>, controls: CL<sub>u</sub> = 5815 ± 2649 l h<sup>−1</sup>, <italic>P</italic> &lt; 0.01).</p> </sec> <sec id="bcp12182-sec-0004" sec-type="section"> <title>Conclusion</title> <p>The correlation with unbound midazolam clearance suggests that either score predicts the metabolic capacity of CYP3A, the most relevant drug metabolizing enzyme subfamily in humans.</p> </sec> </abstract> … (more)
- Is Part Of:
- British journal of clinical pharmacology. Volume 77:Number 1(2014:Jan.)
- Journal:
- British journal of clinical pharmacology
- Issue:
- Volume 77:Number 1(2014:Jan.)
- Issue Display:
- Volume 77, Issue 1 (2014)
- Year:
- 2014
- Volume:
- 77
- Issue:
- 1
- Issue Sort Value:
- 2014-0077-0001-0000
- Page Start:
- 160
- Page End:
- 169
- Publication Date:
- 2014-01
- Subjects:
- Pharmacology -- Periodicals
Drugs -- Periodicals
615.1 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2125 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bcp.12182 ↗
- Languages:
- English
- ISSNs:
- 0306-5251
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2307.180000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3876.xml