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Pharmacogenetics of Biological Agents Used in Inflammatory Bowel Disease: A Systematic Review
- Source :
- Biomedicines, Vol 9, Iss 1748, p 1748 (2021), Biomedicines
- Publication Year :
- 2021
- Publisher :
- MDPI AG, 2021.
-
Abstract
- Inflammatory Bowel Disease (IBD) comprises a group of disorders, in particular Crohn’s disease (CD) and ulcerative colitis (UC), characterized by chronic inflammation affecting the gastrointestinal tract. The treatment of these conditions is primarily based on anti-inflammatory drugs, although the use of biological drugs with lower side effects quickly increased in the last decade. However, the presence of certain polymorphisms in the population may determine a different outcome in response to therapy, reflecting the heterogeneity of the efficacy in patients. Considering that several studies showed important correlations between genetic polymorphisms and response to biological treatments in IBD patients, this systematic review aims to summarize the pharmacogenetics of biologicals approved for IBD, thus highlighting a possible association between some polymorphisms and drug response. With this purpose, we reviewed PubMed papers published over the past 21 years (2000–2021), using as the search term “drug name and IBD or CD or UC and polymorphisms” to underline the role of pharmacogenetic tests in approaching the disease with a targeted therapy.
- Subjects :
- Crohn’s disease
QH301-705.5
medicine.medical_treatment
Population
Medicine (miscellaneous)
Disease
Bioinformatics
Inflammatory bowel disease
Vedolizumab
General Biochemistry, Genetics and Molecular Biology
Targeted therapy
Adalimumab
Inflammatory Bowel Disease
Infliximab
Polymorphism
Ulcerative colitis
Ustekinumab
medicine
Biology (General)
education
Crohn's disease
education.field_of_study
business.industry
medicine.disease
digestive system diseases
Systematic Review
business
Pharmacogenetics
medicine.drug
Subjects
Details
- ISSN :
- 22279059
- Volume :
- 9
- Database :
- OpenAIRE
- Journal :
- Biomedicines
- Accession number :
- edsair.doi.dedup.....dd893b805b506a443180c97c960400a6