Meta-analysis of Oro-cecal Transit Time in Fasting Subjects

被引:5
|
作者
Kokubo, Tohru [1 ,3 ]
Matsui, Shigeyuki [1 ,2 ]
Ishiguro, Makio [1 ,2 ]
机构
[1] Grad Univ Adv Studies, Hayama, Kanagawa 2400193, Japan
[2] Inst Stat Math, Tachikawa, Tokyo 1908562, Japan
[3] Qualicaps Co Inc, Yamatokoriyama City, Nara 6391032, Japan
基金
日本学术振兴会;
关键词
computer simulation; gastrointestinal tract; lactulose hydrogen breath test; meta-analysis; oro-cecal transit time; HYDROGEN BREATH TEST; SMALL-INTESTINAL TRANSIT; SMALL-BOWEL TRANSIT; TO-CECUM TRANSIT; MORPHINE-INDUCED DELAY; GASTROINTESTINAL MOTILITY; PATIENT-LEVEL; LACTULOSE; METHYLNALTREXONE; MOUTH;
D O I
10.1007/s11095-012-0882-6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Computer simulations are utilized during pharmaceutical development in order to design appropriate formulation based on the absorption, distribution, metabolism, and excretion (ADME) and physicochemical properties of target compounds, so that adequate prescriptions are offered to patients. Oro-cecal transit time (OCTT) is an important factor affecting these simulations because the absorption of drug that administered orally and the resultant pharmacokinetic profile are expressed as a function of time. Given the large intra- and inter-individual variance in OCTT, it is unsurprising that an accurate model has not yet been proposed. We conducted a meta-analysis using subject-level data to construct a statistical model that predicted OCTT. Literature that utilized lactulose to measure OCTT was identified and analyzed using a mixed-effects model. The OCTTs of fasting healthy subjects were expressed using a linear model, with the amount of lactulose as the single significant explanatory factor. We found that this model could statistically distinguish the OCTTs of subjects with altered physical status from those of healthy people. Specifically, cystic fibrosis and celiac disease most significantly affected OCTT. The OCTT models developed herein incorporate inter-subject variations and can contribute to providing more accurate predictions of drug pharmacokinetic profiles.
引用
收藏
页码:402 / 411
页数:10
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