 |
 |

Thioguanine Nucleotides and Thiopurine Methyltransferase in Immunobullous DiseasesOptimal Levels as Adjunctive Tools for Azathioprine Monitoring
Rokea A. el-Azhary, MD, PhD;
Sara A. Farmer, BS;
Lisa A. Drage, MD;
Roy S. Rogers III, MD;
Marian T. McEvoy, MD;
Mark D. P. Davis, MD;
Alina G. Bridges, MD;
Lawrence E. Gibson, MD
Arch Dermatol. 2009;145(6):644-652.
Objective To prospectively determine optimal levels of 6-thioguanine nucleotide for disease remission in patients with immunobullous disease treated with azathioprine.
Design Prospective, longitudinal study. Laboratory tests and clinical evaluations were performed monthly for 6 months and then every 2 to 3 months (median follow-up, 13.4 months).
Setting Tertiary care medical center.
Patients Twenty-seven patients with immunobullous disease treated with azathioprine were enrolled during a 2-year period. Twelve met the criteria for evaluation of optimal levels of 6-thioguanine nucleotide.
Main Outcome Measures Blood levels of 6-thioguanine nucleotide, 6-methylmercaptopurine, and thiopurine methyltransferase by polymerase chain reaction and enzyme activity were measured longitudinally during treatment.
Results The range of 6-thioguanine nucleotide was 48 to 457 pmol/8 x 108 red blood cells (RBCs), with an average optimal level of 190.7 pmol/8 x 108 RBCs for all patients. The mean optimal levels were 179.4 and 205.6 pmol/8 x 108 RBCs for pemphigus and pemphigoid, respectively. Limited disease required less 6-thioguanine, with a mean of 145.3 pmol/8 x 108 RBCs. Longitudinal induction of thiopurine methyltransferase activity was observed during treatment. Patients with recalcitrant disease showed higher induction of enzyme activity (with an increase of 9.1 to 23.6 U/mL of RBCs above baseline) than did those with responsive disease.
Conclusions Optimal levels of 6-thioguanine nucleotide metabolites for disease remission in dermatology patients are 150 to 300 pmol/8 x 108 RBCs. High levels of the inactive metabolite 6-methylmercaptopurine and induction of thiopurine methyltransferase are associated with recalcitrant disease.
Author Affiliations: Department of Dermatology (Drs el-Azhary, Drage, Rogers, McEvoy, Davis, Bridges, and Gibson) and Division of Biostatistics (Ms Farmer), Mayo Clinic, Rochester, Minnesota.
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
RELATED ARTICLES
This Month in Archives of Dermatology
Arch Dermatol. 2009;145(6):631.
FULL TEXT
Optimizing Clinical Use of Azathioprine With Newer Pharmacogenetic Data
Stephen E. Wolverton
Arch Dermatol. 2009;145(6):707-710.
EXTRACT
| FULL TEXT
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
Optimizing Clinical Use of Azathioprine With Newer Pharmacogenetic Data
Wolverton
Arch Dermatol 2009;145:707-710.
FULL TEXT
|