dc.contributor.author |
Adam, Lyla
|
|
dc.contributor.author |
Phulukdaree, Alisa
|
|
dc.contributor.author |
Soma, Prashilla
|
|
dc.date.accessioned |
2018-02-23T10:13:46Z |
|
dc.date.issued |
2018-04 |
|
dc.description.abstract |
Azathioprine (AZA) is a well-known immunosuppressant used for many years for its ability to ensure long term disease remission in inflammatory bowel diseases (IBD) at an affordable cost to the public. However, the side effect profile has raised many concerns with numerous investigations into the risk, cause and prevention of these effects. Much of the side effect profile of AZA can be linked to a single nucleotide polymorphism (SNP) in the thiopurine methyltransferase (TPMT) gene which ensures the breakdown and efficacy of AZA. Mutated TPMT alleles result in low or deficient TPMT levels which directly correlate to cytotoxity. This is a review of the role of AZA in the treatment of IBD. Knowing a patient's TPMT status allows the prescribing doctor to make an informed decision about dosage and be more alert to the signs of cytotoxicity. It is essential to include "early warning" SNP testing into common practice to ensure therapeutic efficacy. |
en_ZA |
dc.description.department |
Pharmacology |
en_ZA |
dc.description.department |
Physiology |
en_ZA |
dc.description.embargo |
2019-04-30 |
|
dc.description.librarian |
hj2018 |
en_ZA |
dc.description.sponsorship |
The Research Development Programme, South Africa [grant number A0Z859]. |
en_ZA |
dc.description.uri |
http://www.elsevier.com/locate/biopha |
en_ZA |
dc.identifier.citation |
Adam, L., Phulukdaree, A. & Soma, P. 2018, 'Effective long-term solution to therapeutic remission in inflammatory bowel disease : role of azathioprine', Biomedicine and Pharmacotherapy, vol. 100, pp. 8-14. |
en_ZA |
dc.identifier.issn |
0753-3322 (print) |
|
dc.identifier.issn |
1950-6007 (online) |
|
dc.identifier.other |
10.1016/j.biopha.2018.01.152 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/64072 |
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dc.language.iso |
en |
en_ZA |
dc.publisher |
Elsevier |
en_ZA |
dc.rights |
© 2018 Elsevier Masson SAS. All rights reserved. Notice : this is the author’s version of a work that was accepted for publication in Biomedicine and Pharmacotherapy. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. A definitive version was subsequently published in Biomedicine and Pharmacotherapy, vol. 100, pp. 8-14, 2018. doi : 10.1016/j.biopha.2018.01.152. |
en_ZA |
dc.subject |
Azathioprine (AZA) |
en_ZA |
dc.subject |
Inflammatory bowel diseases (IBD) |
en_ZA |
dc.subject |
Single nucleotide polymorphism (SNP) |
en_ZA |
dc.subject |
Thiopurine methyltransferase (TPMT) |
en_ZA |
dc.subject |
Inosine Triphosphatase (ITPase) |
en_ZA |
dc.subject |
Drug efficacy |
en_ZA |
dc.subject |
Drug mechanism |
en_ZA |
dc.subject |
Immunosuppressant |
en_ZA |
dc.subject |
Immunosuppressive therapy |
en_ZA |
dc.subject |
Long term care |
en_ZA |
dc.subject |
Pharmacogenetics |
en_ZA |
dc.title |
Effective long-term solution to therapeutic remission in inflammatory bowel disease : role of azathioprine |
en_ZA |
dc.type |
Postprint Article |
en_ZA |