Physiologically Based Pharmacokinetic Modeling of Metformin in Children and Adolescents With Obesity

被引:14
作者
Ford, Jennifer Lynn [1 ]
Gerhart, Jacqueline G. [1 ]
Edginton, Andrea N. [2 ]
Yanovski, Jack A. [3 ]
Hon, Yuen Yi [4 ]
Gonzalez, Daniel [1 ]
机构
[1] Univ N Carolina, Div Pharmacotherapy & Expt Therapeut, UNC Eshelman Sch Pharm, Chapel Hill, NC 27515 USA
[2] Univ Waterloo, Sch Pharm, Waterloo, ON, Canada
[3] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Sect Growth & Obes, Program Dev Endocrinol & Genet, NIH, Bethesda, MD USA
[4] NIH, Clin Pharmacokinet Res Lab, Clin Ctr, Pharm Dept, Bldg 10, Bethesda, MD 20892 USA
关键词
adolescents; children; metformin; obesity; PBPK modeling; pharmacokinetics; CLINICAL PHARMACOKINETICS; PHARMACOLOGY; ABSORPTION; INFANTS;
D O I
10.1002/jcph.2034
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Childhood obesity continues to rise in the United States and, with it, the off-label use of metformin for weight loss. The influence of age and obesity on the drug's disposition and exposure has not previously been studied using a mechanistic framework. Here, an adult physiologically based pharmacokinetic (PBPK) model of metformin was scaled to pediatric populations without obesity, with overweight/obesity, and with severe obesity; a published virtual population of children and adolescents with obesity was leveraged during model evaluation. When the pediatric model was simulated in groups aged 10 to 18 years, oral clearance following 1000 mg of metformin was higher (approximate to 1200 mL/min) in those with obesity and severe obesity compared to the groups without and with overweight (approximate to 1000 mL/min). In addition, simulated area under the concentration-time curve in older children and adolescents with obesity and severe obesity was comparable to that in adults with a similar dose-exposure relationship. Overall, simulations using the pediatric PBPK model support the use of adult doses of metformin in older children and adolescents with obesity. Moreover, the virtual population of children and adolescents with obesity offers a valuable tool to facilitate development of pediatric PBPK models for studying populations with obesity and, in turn, contribute information to inform drug labeling in this special population.
引用
收藏
页码:960 / 969
页数:10
相关论文
共 28 条
  • [21] Effects of SLC22A1 Polymorphisms on Metformin-Induced Reductions in Adiposity and Metformin Pharmacokinetics in Obese Children With Insulin Resistance
    Sam, Wai Johnn
    Roza, Orsolya
    Hon, Yuen Yi
    Alfaro, Raul M.
    Calis, Karim A.
    Reynolds, James C.
    Yanovski, Jack A.
    [J]. JOURNAL OF CLINICAL PHARMACOLOGY, 2017, 57 (02) : 219 - 229
  • [22] Food intake and dosage level, but not tablet vs solution dosage form, affect the absorption of metformin HCl in man
    Sambol, NC
    Brookes, LG
    Chiang, J
    Goodman, AM
    Lin, ET
    Liu, CY
    Benet, LZ
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 42 (04) : 510 - 512
  • [23] Pharmacokinetics of Metformin in Girls Aged 9 Years
    Sanchez-Infantes, David
    Diaz, Marta
    Lopez-Bermejo, Abel
    Victoria Marcos, Maria
    de Zegher, Francis
    Ibanez, Lourdes
    [J]. CLINICAL PHARMACOKINETICS, 2011, 50 (11) : 735 - 738
  • [24] Clinical pharmacokinetics of metformin
    Scheen, AJ
    [J]. CLINICAL PHARMACOKINETICS, 1996, 30 (05) : 359 - 371
  • [25] Obesity and drug pharmacology: a review of the influence of obesity on pharmacokinetic and pharmacodynamic parameters
    Smit, Cornelis
    De Hoogd, Sjoerd
    Bruggemann, Roger J. M.
    Knibbe, Catherijne A. J.
    [J]. EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2018, 14 (03) : 275 - 285
  • [27] Increased Metformin Clearance in Overweight and Obese Adolescents: A Pharmacokinetic Substudy of a Randomized Controlled Trial
    van Rongen, Anne
    van der Aa, Marloes P.
    Matic, Maja
    van Schaik, Ron H. N.
    Deneer, Vera H. M.
    van der Vorst, Marja M.
    Knibbe, Catherijne A. J.
    [J]. PEDIATRIC DRUGS, 2018, 20 (04) : 365 - 374
  • [28] Zisowsky Jochen, 2010, Pharmaceutics, V2, P364, DOI 10.3390/pharmaceutics2040364