Evidence map›Paper›PMID 24925693›Full record

ReviewSeminars in arthritis and rheumatism2014

Impaired response or insufficient dosage? Examining the potential causes of "inadequate response" to allopurinol in the treatment of gout.

Lisa K Stamp, Tony R Merriman, Murray L Barclay, Jasvinder A Singh, Rebecca L Roberts, Daniel F B Wright, Nicola Dalbeth

Abstract readReview
In one paragraph

Review in Seminars in arthritis and rheumatism, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Article
  9. The genetics of gout: translation into clinical practice.Therapeutic advances in musculoskeletal disease · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. An update on the genetics of hyperuricaemia and gout.Nature reviews. Rheumatology · 2018
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Lisa K StampDepartment of Medicine, University of Otago, Christchurch, P.O. Box 4345, Christchurch 8140, New Zealand. Electronic address: lisa.stamp@cdhb.health.nz.
Tony R MerrimanDepartment of Biochemistry, University of Otago, Dunedin, New Zealand.
Murray L BarclayDepartment of Clinical Pharmacology, Christchurch Hospital, Christchurch, New Zealand.
Jasvinder A SinghMedicine Service, Birmingham VA Medical Center, Birmingham, AL; Rheumatology Division, University of Alabama, Birmingham, AL.
Rebecca L RobertsDepartment of Surgical Sciences, University of Otago, Dunedin, New Zealand.
Daniel F B WrightSchool of Pharmacy, University of Otago, Dunedin, New Zealand.
Nicola DalbethDepartment of Medicine, University of Auckland, Auckland, New Zealand.
University of Otago · NZBirmingham VA Medical Center · USChristchurch Hospital · NZUniversity of Auckland · NZ

Funding

Multicenter Osteoarthritis Study (MOST) Second Renewal - UAB Clinical CenterU01AG018947 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LEWIS, CORA E · 2001 to 2020
$13.2M
The Effects of Urate Lowering Therapy on Inflammation, Endothelial function, andP50AR060772 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SAAG, KENNETH G · 2012 to 2021
$12.8M
UAB Deep South Arthritis and Musculoskeletal CERTsU19HS021110 · AHRQ · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SAAG, KENNETH G · 2011 to 2015
$4.1M
ACOSOG Community Clinical Oncology Program (CCOP) Research BaseU10CA149950 · NCI · MAYO CLINIC ROCHESTER · PI NELSON, HEIDI, SLOAN, JEFF A. · 2011 to 2014
$3.9M
Effectiveness of DiscontinuinG bisphosphonatEs Study (EDGE)U34AR062891 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SAAG, KENNETH G · 2013 to 2014
$647k
AHRQ HHS U19 HS021110NCI NIH HHS U10 CA149950NIAMS NIH HHS P50 AR060772NIAMS NIH HHS U34 AR062891NIA NIH HHS U01 AG018947
6 · The paper itself

Abstract

objectivesGout is one of the most common forms of arthritis. It is well established that urate-lowering therapy that aims for a serum urate less than at least 0.36 mmol/l (6 mg/dl) is required for the successful management of gout. Allopurinol, a xanthine oxidase (XO) inhibitor, is the most commonly used urate-lowering therapy. However, many patients fail to achieve the target serum urate on allopurinol; these patients can be considered to have "inadequate response" to allopurinol. Herein, we examine the potential mechanisms and implications of inadequate response to allopurinol.

methodsThe literature was reviewed for potential causes for failure to reach target serum urate in patients receiving allopurinol.

resultsThe two most common causes of inadequate response to allopurinol are poor adherence and under-dosing of allopurinol. Adherent patients who fail to achieve target serum urate on standard doses of allopurinol form a group that could be considered to be "partially resistant" to allopurinol. There are four potential mechanisms for partial allopurinol resistance: decreased conversion of allopurinol to oxypurinol; increased renal excretion of oxypurinol; abnormality in XO structure and/or function such that oxypurinol is rendered less effective and/or drug interactions.

conclusionsIt is important to determine the reasons for failure to achieve treatment targets with allopurinol, particularly as newer agents become available. The knowledge of the mechanisms for inadequate response may help guide the clinician towards making a therapeutic choice that is more likely to result in achieving the serum urate target.

Indexed as

AllopurinolBiomarkersDose-Response Relationship, DrugGoutGout SuppressantsHumansPatient ComplianceTreatment FailureUric AcidAllopurinolBiomarkersGout SuppressantsUric AcidAllopurinolDrug resistanceGoutOxypurinol

Identifiers

PMID24925693
PMCPMC4225179
OpenAlexW2119411321

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.