OC-015 The Influence of Gender and Haemoglobin on TPMT Activity. (4th June 2013)
- Record Type:
- Journal Article
- Title:
- OC-015 The Influence of Gender and Haemoglobin on TPMT Activity. (4th June 2013)
- Main Title:
- OC-015 The Influence of Gender and Haemoglobin on TPMT Activity
- Authors:
- Blaker, P A
Kariyawasam, V C
Patel, K V
Goel, R M
Ward, M G
Irving, P M
Marinaki, A M
Sanderson, J D - Abstract:
- Abstract : Introduction: Pre-treatment measurement of red blood cell (RBC) thiopurine- S- methyltransferase (TPMT) activity is recommended to guide initial dosing of azathioprine (AZA) and mercaptopurine (MP). TPMT exhibits a trimodal distribution, with low and intermediate activities predicting myelotoxicity at standard drug doses. There is a high concordance between TPMT genotype and normal or low enzyme activity (93–100%); however the relationship is poor in the intermediate range (53–100%) [1] . Furthermore, there are few explanations for the wide variation in inter-individual TPMT activities in the wild-type range. Bioavailability of the cofactor S -adenosylmethionine (SAM) and RBC age may play a role. The aim of this study was to determine if gender or anaemia influences RBC TPMT activity. Methods: We analysed a retrospective cohort of 6, 496 RBC TPMT samples (n = 3804 females, n = 2692 males) measured in the PRL since 2004 and correlated enzyme activity with gender and haemoglobin concentrations. Results: A greater portion of females exhibited intermediate TPMT activity (13.46%) as compared to males (11.07%). The mean TPMT activity was also significantly lower in females (32.94 pmol/mg Hb/h) versus males (34.13 pmol/mg Hb/h; p = < 0.0001, 95% CI 0.7950–1.589). When separated by low, intermediate or normal TPMT activity, this relationship only remained in patients with normal TPMT activity. TPMT activity was significantly higher in female patients with an Hb < 10g/dlAbstract : Introduction: Pre-treatment measurement of red blood cell (RBC) thiopurine- S- methyltransferase (TPMT) activity is recommended to guide initial dosing of azathioprine (AZA) and mercaptopurine (MP). TPMT exhibits a trimodal distribution, with low and intermediate activities predicting myelotoxicity at standard drug doses. There is a high concordance between TPMT genotype and normal or low enzyme activity (93–100%); however the relationship is poor in the intermediate range (53–100%) [1] . Furthermore, there are few explanations for the wide variation in inter-individual TPMT activities in the wild-type range. Bioavailability of the cofactor S -adenosylmethionine (SAM) and RBC age may play a role. The aim of this study was to determine if gender or anaemia influences RBC TPMT activity. Methods: We analysed a retrospective cohort of 6, 496 RBC TPMT samples (n = 3804 females, n = 2692 males) measured in the PRL since 2004 and correlated enzyme activity with gender and haemoglobin concentrations. Results: A greater portion of females exhibited intermediate TPMT activity (13.46%) as compared to males (11.07%). The mean TPMT activity was also significantly lower in females (32.94 pmol/mg Hb/h) versus males (34.13 pmol/mg Hb/h; p = < 0.0001, 95% CI 0.7950–1.589). When separated by low, intermediate or normal TPMT activity, this relationship only remained in patients with normal TPMT activity. TPMT activity was significantly higher in female patients with an Hb < 10g/dl (n = 250, mean TPMT 38.06 pmol/mg Hb/h) versus females with an Hb > 12g/dl (n = 2192, mean TPMT 32.46 pmol/mg Hb/h; p = < 0.0001). Similarly TPMT activity was significantly higher in male patients with an Hb < 10g/dl (n = 123, mean TPMT 38.14) versus males with an Hb > 12g/dl (n = 1901, mean TPMT 33.76; p = < 0.0001). Conclusion: TPMT activity in the wild-type range is lower in females than males, suggesting a post-translational influence on TPMT activity related to gender. Lower levels of SAM have been reported in females, which may explain this observation[2]. Re-appraisal of the concordance between TPMT genotype and phenotype, adjusting for gender is therefore indicated. The finding of higher TPMT activity with anaemia may be due to a younger red cell population in this group. The difference in TPMT activities between patients with or without anaemia is clinically relevant, particularly where the TPMT activity is around the cut-off between intermediate (10–25 pmol/mg Hb/h) and normal (≥26 pmol/mg Hb/h) ranges. TPMT genotyping should be considered in such patients. Disclosure of Interest: None Declared References: Karas-Kuzelicki, et al. Pharmacogenomics 2009. 10:1309–22. Poirier, et al. Cancer epidemiology, biomarkers & prevention 2001. 10:649–655. … (more)
- Is Part Of:
- Gut. Volume 62(2013)Supplement 1
- Journal:
- Gut
- Issue:
- Volume 62(2013)Supplement 1
- Issue Display:
- Volume 62, Issue 1 (2013)
- Year:
- 2013
- Volume:
- 62
- Issue:
- 1
- Issue Sort Value:
- 2013-0062-0001-0000
- Page Start:
- A6
- Page End:
- A7
- Publication Date:
- 2013-06-04
- Subjects:
- Gastroenterology -- Periodicals
616.33 - Journal URLs:
- http://gut.bmjjournals.com ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/gutjnl-2013-304907.015 ↗
- Languages:
- English
- ISSNs:
- 0017-5749
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18580.xml