TY - JOUR
T1 - Quantitative systems pharmacology and the personalized drug-microbiota-diet axis
AU - Thiele, Ines
AU - Clancy, Catherine M.
AU - Heinken, Almut
AU - Fleming, Ronan M.T.
N1 - Publisher Copyright:
© 2017 The Authors.
PY - 2017/8
Y1 - 2017/8
N2 - Precision medicine is an emerging paradigm that aims at maximizing the benefits and minimizing the adverse effects of drugs. Realistic mechanistic models are needed to understand and limit heterogeneity in drug responses. While pharmacokinetic models describe in detail a drug's absorption and metabolism, they generally do not account for individual variations in response to environmental influences, in addition to genetic variation. For instance, the human gut microbiota metabolizes drugs and is modulated by diet, and it exhibits significant variation among individuals. However, the influence of the gut microbiota on drug failure or drug side effects is under-researched. Here, we review recent advances in computational modeling approaches that could contribute to a better, mechanism-based understanding of drug-microbiota-diet interactions and their contribution to individual drug responses. By integrating systems biology and quantitative systems pharmacology with microbiology and nutrition, the conceptually and technologically demand for novel approaches could be met to enable the study of individual variability, thereby providing breakthrough support for progress in precision medicine.
AB - Precision medicine is an emerging paradigm that aims at maximizing the benefits and minimizing the adverse effects of drugs. Realistic mechanistic models are needed to understand and limit heterogeneity in drug responses. While pharmacokinetic models describe in detail a drug's absorption and metabolism, they generally do not account for individual variations in response to environmental influences, in addition to genetic variation. For instance, the human gut microbiota metabolizes drugs and is modulated by diet, and it exhibits significant variation among individuals. However, the influence of the gut microbiota on drug failure or drug side effects is under-researched. Here, we review recent advances in computational modeling approaches that could contribute to a better, mechanism-based understanding of drug-microbiota-diet interactions and their contribution to individual drug responses. By integrating systems biology and quantitative systems pharmacology with microbiology and nutrition, the conceptually and technologically demand for novel approaches could be met to enable the study of individual variability, thereby providing breakthrough support for progress in precision medicine.
KW - Constraint-based modeling
KW - Drug metabolism
KW - Gut microbiota
KW - Pharmacokinetic modeling
KW - Precision medicine
UR - https://www.scopus.com/pages/publications/85045297392
U2 - 10.1016/j.coisb.2017.06.001
DO - 10.1016/j.coisb.2017.06.001
M3 - Review article
SN - 2452-3100
VL - 4
SP - 43
EP - 52
JO - Current Opinion in Systems Biology
JF - Current Opinion in Systems Biology
ER -