Effects of Allopurinol Dose Escalation on Bone Erosion and Urate Volume in Gout: A Dual-Energy Computed Tomography Imaging Study Within a Randomized, Controlled Trial.

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dc.contributor.author Dalbeth, Nicola en
dc.contributor.author Billington, Karen en
dc.contributor.author Doyle, Anthony en
dc.contributor.author Frampton, Christopher en
dc.contributor.author Tan, Paul en
dc.contributor.author Aati, Opetaia en
dc.contributor.author Allan, Jordyn en
dc.contributor.author Drake, Jill en
dc.contributor.author Horne, Anne en
dc.contributor.author Stamp, Lisa K en
dc.date.accessioned 2019-10-02T00:55:20Z en
dc.date.issued 2019-10 en
dc.identifier.issn 2326-5191 en
dc.identifier.uri http://hdl.handle.net/2292/48348 en
dc.description.abstract OBJECTIVE:To examine whether allopurinol dose escalation to achieve serum urate (SU) target can influence bone erosion or monosodium urate (MSU) crystal deposition, as measured by dual-energy computed tomography (DECT) in patients with gout. METHODS:We conducted an imaging study of a 2-year randomized clinical trial that compared immediate allopurinol dose escalation to SU target with conventional dosing for 1 year followed by dose escalation to target, in gout patients who were receiving allopurinol and who had an SU level of ≥0.36 mmoles/liter. DECT scans of feet and radiographs of hands and feet were obtained at baseline, year 1, and year 2 visits. DECT scans were scored for bone erosion and urate volume. RESULTS:Paired imaging data were available for 87 patients (42 in the dose-escalation group and 45 in the control group). At year 2, the progression in the CT erosion score was higher in the control group than in the dose-escalation group (+7.8% versus +1.4%; P = 0.015). Changes in plain radiography erosion or narrowing scores did not differ between groups. Reductions in DECT urate volume were observed in both groups. At year 2, patients in the control group who had an SU level of <0.36 mmoles/liter and patients in the dose-escalation group had reduced DECT urate volume (-27.6 to -28.3%), whereas reduction in DECT urate volume was not observed in control group patients with an SU level of ≥0.36 mmoles/liter (+1.5%) (P = 0.023). CONCLUSION:These findings provide evidence that long-term urate-lowering therapy using a treat-to-SU-target strategy can influence structural damage and reduce urate crystal deposition in gout. en
dc.format.medium Print-Electronic en
dc.language eng en
dc.relation.ispartofseries Arthritis & rheumatology (Hoboken, N.J.) en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.subject Foot Bones en
dc.subject Foot Joints en
dc.subject Humans en
dc.subject Bone Resorption en
dc.subject Gout en
dc.subject Allopurinol en
dc.subject Uric Acid en
dc.subject Gout Suppressants en
dc.subject Tomography, X-Ray Computed en
dc.subject Treatment Outcome en
dc.subject Dose-Response Relationship, Drug en
dc.subject Aged en
dc.subject Middle Aged en
dc.subject Female en
dc.subject Male en
dc.subject Hand Bones en
dc.subject Hand Joints en
dc.title Effects of Allopurinol Dose Escalation on Bone Erosion and Urate Volume in Gout: A Dual-Energy Computed Tomography Imaging Study Within a Randomized, Controlled Trial. en
dc.type Journal Article en
dc.identifier.doi 10.1002/art.40929 en
pubs.issue 10 en
pubs.begin-page 1739 en
pubs.volume 71 en
dc.rights.holder Copyright: The author en
pubs.end-page 1746 en
pubs.publication-status Published en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Research Support, Non-U.S. Gov't en
pubs.subtype Randomized Controlled Trial en
pubs.subtype Journal Article en
pubs.elements-id 779645 en
pubs.org-id Medical and Health Sciences en
pubs.org-id Medical Sciences en
pubs.org-id Anatomy and Medical Imaging en
pubs.org-id School of Medicine en
pubs.org-id Medicine Department en
dc.identifier.eissn 2326-5205 en
pubs.record-created-at-source-date 2019-05-14 en
pubs.dimensions-id 31081595 en


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