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.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117 World+J+Gastroenterol
2015 ; 21
(44
): 12519-43
Nephropedia Template TP
gab.com Text
Twit Text FOAVip
Twit Text #
English Wikipedia
Update on pathogenesis and predictors of response of therapeutic strategies used
in inflammatory bowel disease
#MMPMID26640330
Quetglas EG
; Mujagic Z
; Wigge S
; Keszthelyi D
; Wachten S
; Masclee A
; Reinisch W
World J Gastroenterol
2015[Nov]; 21
(44
): 12519-43
PMID26640330
show ga
The search for biomarkers that characterize specific aspects of inflammatory
bowel disease (IBD), has received substantial interest in the past years and is
moving forward rapidly with the help of modern technologies. Nevertheless, there
is a direct demand to identify adequate biomarkers for predicting and evaluating
therapeutic response to different therapies. In this subset, pharmacogenetics
deserves more attention as part of the endeavor to provide personalized medicine.
The ultimate goal in this area is the adjustment of medication for a patient's
specific genetic background and thereby to improve drug efficacy and safety
rates. The aim of the following review is to utilize the latest knowledge on
immunopathogenesis of IBD and update the findings on the field of Immunology and
Genetics, to evaluate the response to the different therapies. In the present
article, more than 400 publications were reviewed but finally 287 included based
on design, reproducibility (or expectancy to be reproducible and translationable
into humans) or already measured in humans. A few tests have shown clinical
applicability. Other, i.e., genetic associations for the different therapies in
IBD have not yet shown consistent or robust results. In the close future it is
anticipated that this, cellular and genetic material, as well as the
determination of biomarkers will be implemented in an integrated molecular
diagnostic and prognostic approach to manage IBD patients.
|Animals
[MESH]
|Anti-Inflammatory Agents/adverse effects/pharmacokinetics/*therapeutic use
[MESH]
|Biotransformation/genetics
[MESH]
|Diagnostic Imaging/methods
[MESH]
|Drug Monitoring/*methods
[MESH]
|Gastrointestinal Agents/adverse effects/pharmacokinetics/*therapeutic use
[MESH]