Your browser doesn't support javascript.
loading
The impact of diuretic use and ABCG2 genotype on the predictive performance of a published allopurinol dosing tool.
Wright, Daniel F B; Dalbeth, Nicola; Phipps-Green, Amanda J; Merriman, Tony R; Barclay, Murray L; Drake, Jill; Tan, Paul; Horne, Anne; Stamp, Lisa K.
Affiliation
  • Wright DFB; School of Pharmacy, University of Otago, Dunedin, New Zealand.
  • Dalbeth N; Department of Medicine, University of Auckland, Auckland, New Zealand.
  • Phipps-Green AJ; Department of Biochemistry, University of Otago, Dunedin, New Zealand.
  • Merriman TR; Department of Biochemistry, University of Otago, Dunedin, New Zealand.
  • Barclay ML; Department of Medicine, University of Otago, Christchurch, New Zealand.
  • Drake J; Department of Clinical Pharmacology, Christchurch Hospital, Christchurch, New Zealand.
  • Tan P; Department of Medicine, University of Otago, Christchurch, New Zealand.
  • Horne A; Department of Medicine, University of Auckland, Auckland, New Zealand.
  • Stamp LK; Department of Medicine, University of Auckland, Auckland, New Zealand.
Br J Clin Pharmacol ; 84(5): 937-943, 2018 05.
Article in En | MEDLINE | ID: mdl-29341237
ABSTRACT

AIM:

This research aims to evaluate the predictive performance of a published allopurinol dosing tool.

METHODS:

Allopurinol dose predictions were compared to the actual dose required to achieve serum urate (SU) <0.36 mmol l-1 using mean prediction error. The influence of patient factors on dose predictions was explored using multilinear regression.

RESULTS:

Allopurinol doses were overpredicted by the dosing tool; however, this was minimal in patients without diuretic therapy (MPE 63 mg day-1 , 95% CI 40-87) compared to those receiving diuretics (MPE 295 mg day-1 , 95% CI 260-330, P < 0.0001). ABCG2 genotype (rs2231142, G>T) had an important impact on the dose predictions (MPE 201, 107, 15 mg day-1 for GG, GT and TT, respectively, P < 0.0001). Diuretic use and ABCG2 genotype explained 53% of the variability in prediction error (R2  = 0.53, P = 0.0004).

CONCLUSIONS:

The dosing tool produced acceptable maintenance dose predictions for patients not taking diuretics. Inclusion of ABCG2 genotype and a revised adjustment for diuretics would further improve the performance of the dosing tool.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Allopurinol / Decision Support Techniques / Diuretics / ATP Binding Cassette Transporter, Subfamily G, Member 2 / Neoplasm Proteins Type of study: Clinical_trials / Evaluation_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Br J Clin Pharmacol Year: 2018 Document type: Article Affiliation country: New Zealand

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Allopurinol / Decision Support Techniques / Diuretics / ATP Binding Cassette Transporter, Subfamily G, Member 2 / Neoplasm Proteins Type of study: Clinical_trials / Evaluation_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Br J Clin Pharmacol Year: 2018 Document type: Article Affiliation country: New Zealand