Pharmacokinetics of Orally Administered Cyclosporine in Patients with Crohn's Disease
Cyclosporine pharmacokinetics were reported to be influenced in patients with Crohn's disease. To explore the relationship between Crohn's disease and cyclosporine pharmacokinetics, this investigation was performed in 20 patients with varying Crohn's Disease Activity Index (CDAI). A s...
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Veröffentlicht in: | Journal of clinical pharmacology 1995-07, Vol.35 (7), p.681-687 |
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description | Cyclosporine pharmacokinetics were reported to be influenced in patients with Crohn's disease. To explore the relationship between Crohn's disease and cyclosporine pharmacokinetics, this investigation was performed in 20 patients with varying Crohn's Disease Activity Index (CDAI). A single oral dose of 300 mg of cyclosporine was given and serial blood samples were obtained over 52 hours. Cyclosporine whole blood concentrations were determined by a specific monoclonal radioimmunoassay. Pharmacokinetic parameters were comparable with those of healthy volunteers. No statistically significant difference between the pharmacokinetic parameters of the patients with CDAI values less than 150 and those with CDAI values 150 or greater could be shown. Although several factors associated with the pathology of Crohn's disease theoretically could influence the pharmacokinetics of orally administered cyclosporine, this investigation did not identify statistically significant differences in cyclosporine pharmacokinetics in Crohn's disease patients with different disease activities or different localization of inflammation as compared with healthy volunteers. However, if large parts of the small bowel were removed, a decrease of absorption of cyclosporine could be observed. In any case, it is important to be aware of the clinical variability of Crohn's disease and its potential implications in cyclosporine absorption. |
doi_str_mv | 10.1002/j.1552-4604.1995.tb04108.x |
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To explore the relationship between Crohn's disease and cyclosporine pharmacokinetics, this investigation was performed in 20 patients with varying Crohn's Disease Activity Index (CDAI). A single oral dose of 300 mg of cyclosporine was given and serial blood samples were obtained over 52 hours. Cyclosporine whole blood concentrations were determined by a specific monoclonal radioimmunoassay. Pharmacokinetic parameters were comparable with those of healthy volunteers. No statistically significant difference between the pharmacokinetic parameters of the patients with CDAI values less than 150 and those with CDAI values 150 or greater could be shown. Although several factors associated with the pathology of Crohn's disease theoretically could influence the pharmacokinetics of orally administered cyclosporine, this investigation did not identify statistically significant differences in cyclosporine pharmacokinetics in Crohn's disease patients with different disease activities or different localization of inflammation as compared with healthy volunteers. However, if large parts of the small bowel were removed, a decrease of absorption of cyclosporine could be observed. In any case, it is important to be aware of the clinical variability of Crohn's disease and its potential implications in cyclosporine absorption.</description><identifier>ISSN: 0091-2700</identifier><identifier>EISSN: 1552-4604</identifier><identifier>DOI: 10.1002/j.1552-4604.1995.tb04108.x</identifier><identifier>PMID: 7560248</identifier><identifier>CODEN: JCPCBR</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Administration, Oral ; Adult ; Biological and medical sciences ; Capsules ; Crohn Disease - metabolism ; Crohn Disease - pathology ; Cyclosporine - administration & dosage ; Cyclosporine - blood ; Cyclosporine - pharmacokinetics ; Drug Monitoring ; Female ; Humans ; Immunomodulators ; Immunosuppressive Agents - administration & dosage ; Immunosuppressive Agents - blood ; Immunosuppressive Agents - pharmacokinetics ; Intestinal Absorption ; Male ; Medical sciences ; Middle Aged ; Pharmacology. 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To explore the relationship between Crohn's disease and cyclosporine pharmacokinetics, this investigation was performed in 20 patients with varying Crohn's Disease Activity Index (CDAI). A single oral dose of 300 mg of cyclosporine was given and serial blood samples were obtained over 52 hours. Cyclosporine whole blood concentrations were determined by a specific monoclonal radioimmunoassay. Pharmacokinetic parameters were comparable with those of healthy volunteers. No statistically significant difference between the pharmacokinetic parameters of the patients with CDAI values less than 150 and those with CDAI values 150 or greater could be shown. Although several factors associated with the pathology of Crohn's disease theoretically could influence the pharmacokinetics of orally administered cyclosporine, this investigation did not identify statistically significant differences in cyclosporine pharmacokinetics in Crohn's disease patients with different disease activities or different localization of inflammation as compared with healthy volunteers. However, if large parts of the small bowel were removed, a decrease of absorption of cyclosporine could be observed. In any case, it is important to be aware of the clinical variability of Crohn's disease and its potential implications in cyclosporine absorption.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Capsules</subject><subject>Crohn Disease - metabolism</subject><subject>Crohn Disease - pathology</subject><subject>Cyclosporine - administration & dosage</subject><subject>Cyclosporine - blood</subject><subject>Cyclosporine - pharmacokinetics</subject><subject>Drug Monitoring</subject><subject>Female</subject><subject>Humans</subject><subject>Immunomodulators</subject><subject>Immunosuppressive Agents - administration & dosage</subject><subject>Immunosuppressive Agents - blood</subject><subject>Immunosuppressive Agents - pharmacokinetics</subject><subject>Intestinal Absorption</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><issn>0091-2700</issn><issn>1552-4604</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkV1v0zAUhi0EGmXwE5AihOAq4TjxR8LVpsA2xrT1ggmJG-vUOVHd5aPYqdb-exI16j1Xtvw-57X1mLEPHBIOkH7ZJFzKNBYKRMKLQibDCgSHPNm_YItT9JItAAoepxrgNXsTwgaAKyH5GTvTUkEq8gV7XK7Rt2j7J9fR4GyI-jp68Ng0h-iyal3nwkCeqqg82KYP296PXOS6aImDo24I0bMb1lHp-3X3OUTfXCAM9Ja9qrEJ9G5ez9nj1fdf5U1893D9o7y8i61QWR6vkKy2iKpQStb5eAhaVBKLSguhFSkopKJCFShVhcgljKhGwQUR1cizc_bp2Lv1_d8dhcG0LlhqGuyo3wWjtUo5qAn8egSt70PwVJutdy36g-FgJqdmYyZxZhJnJqdmdmr24_D7-ZbdqqXqNDpLHPOPc47BYlN77KwLJyyTuQAJI3ZxxJ5dQ4f_eIC5LZc303asiI8V06_sTxXon4zSmZbm9_21Ubd5efXnJ5j77B-bCaNh</recordid><startdate>199507</startdate><enddate>199507</enddate><creator>Flückiger, Simone S.</creator><creator>Schmidt, Christoph</creator><creator>Meyer, Ansgar</creator><creator>Kallay, Zoltan</creator><creator>Johnston, Atholl</creator><creator>Kutz, Klaus</creator><general>Blackwell Publishing Ltd</general><general>Sage Science</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199507</creationdate><title>Pharmacokinetics of Orally Administered Cyclosporine in Patients with Crohn's Disease</title><author>Flückiger, Simone S. ; Schmidt, Christoph ; Meyer, Ansgar ; Kallay, Zoltan ; Johnston, Atholl ; Kutz, Klaus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4638-baec7caa69665f8c46074d5a9d74476e60956e969a56daa150a697a414eeefa13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Administration, Oral</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Capsules</topic><topic>Crohn Disease - metabolism</topic><topic>Crohn Disease - pathology</topic><topic>Cyclosporine - administration & dosage</topic><topic>Cyclosporine - blood</topic><topic>Cyclosporine - pharmacokinetics</topic><topic>Drug Monitoring</topic><topic>Female</topic><topic>Humans</topic><topic>Immunomodulators</topic><topic>Immunosuppressive Agents - administration & dosage</topic><topic>Immunosuppressive Agents - blood</topic><topic>Immunosuppressive Agents - pharmacokinetics</topic><topic>Intestinal Absorption</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Flückiger, Simone S.</creatorcontrib><creatorcontrib>Schmidt, Christoph</creatorcontrib><creatorcontrib>Meyer, Ansgar</creatorcontrib><creatorcontrib>Kallay, Zoltan</creatorcontrib><creatorcontrib>Johnston, Atholl</creatorcontrib><creatorcontrib>Kutz, Klaus</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Flückiger, Simone S.</au><au>Schmidt, Christoph</au><au>Meyer, Ansgar</au><au>Kallay, Zoltan</au><au>Johnston, Atholl</au><au>Kutz, Klaus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacokinetics of Orally Administered Cyclosporine in Patients with Crohn's Disease</atitle><jtitle>Journal of clinical pharmacology</jtitle><addtitle>J Clin Pharmacol</addtitle><date>1995-07</date><risdate>1995</risdate><volume>35</volume><issue>7</issue><spage>681</spage><epage>687</epage><pages>681-687</pages><issn>0091-2700</issn><eissn>1552-4604</eissn><coden>JCPCBR</coden><abstract>Cyclosporine pharmacokinetics were reported to be influenced in patients with Crohn's disease. To explore the relationship between Crohn's disease and cyclosporine pharmacokinetics, this investigation was performed in 20 patients with varying Crohn's Disease Activity Index (CDAI). A single oral dose of 300 mg of cyclosporine was given and serial blood samples were obtained over 52 hours. Cyclosporine whole blood concentrations were determined by a specific monoclonal radioimmunoassay. Pharmacokinetic parameters were comparable with those of healthy volunteers. No statistically significant difference between the pharmacokinetic parameters of the patients with CDAI values less than 150 and those with CDAI values 150 or greater could be shown. Although several factors associated with the pathology of Crohn's disease theoretically could influence the pharmacokinetics of orally administered cyclosporine, this investigation did not identify statistically significant differences in cyclosporine pharmacokinetics in Crohn's disease patients with different disease activities or different localization of inflammation as compared with healthy volunteers. However, if large parts of the small bowel were removed, a decrease of absorption of cyclosporine could be observed. In any case, it is important to be aware of the clinical variability of Crohn's disease and its potential implications in cyclosporine absorption.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>7560248</pmid><doi>10.1002/j.1552-4604.1995.tb04108.x</doi><tpages>7</tpages></addata></record> |
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subjects | Administration, Oral Adult Biological and medical sciences Capsules Crohn Disease - metabolism Crohn Disease - pathology Cyclosporine - administration & dosage Cyclosporine - blood Cyclosporine - pharmacokinetics Drug Monitoring Female Humans Immunomodulators Immunosuppressive Agents - administration & dosage Immunosuppressive Agents - blood Immunosuppressive Agents - pharmacokinetics Intestinal Absorption Male Medical sciences Middle Aged Pharmacology. Drug treatments |
title | Pharmacokinetics of Orally Administered Cyclosporine in Patients with Crohn's Disease |
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