Trends in pharmacogenomics of drugs used in the treatment of asthma
Pharmacological Research, ISSN: 1043-6618, Vol: 49, Issue: 4, Page: 343-349
2004
- 36Citations
- 18Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations36
- Citation Indexes35
- 35
- CrossRef16
- Policy Citations1
- Policy Citation1
- Captures18
- Readers18
- 18
Article Description
Pharmacogenetic studies of drugs used in the treatment of asthma have produced a few examples of reduced response in patients carrying specific genotypes in genes involved in the action of beta-2 agonists or leukotriene modifiers. Other candidate genes related to these drugs, as well as glucocorticoids, theophilline, anticholinergics, antihistaminics, and drug-metabolizing enzymes, may be proposed. Statistical power and population stratification may be issues of importance in case-control association studies. Future developments include expanded gene knowledge from asthma genetic and genomic studies, the development of new preventive and curative treatments, multiple contemporary genotyping methods for pharmacogenetically important genes in a given individual, and the construction of asthma functional pharmacogenomic profiles. In conclusion, it seems that asthma pharmacogenetic studies need to be replicated in prospective clinical trials in different populations with a large number of subjects being genotyped. It is suggested that large clinical trials which are proposed for asthma drugs experimentation should include a pharmacogenetic study as well.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S104366180300358X; http://dx.doi.org/10.1016/j.phrs.2003.04.002; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0842307212&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/15202513; https://linkinghub.elsevier.com/retrieve/pii/S104366180300358X; https://dx.doi.org/10.1016/j.phrs.2003.04.002
Elsevier BV
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