The statistical challenge of analysing changes in dual energy computed tomography (DECT) urate volumes in people with gout.

Semin Arthritis Rheum

Department of Medicine, Faculty of Medical and Health Sciences, University of Auckland, 85 Park Road, Grafton, Auckland 1023, New Zealand.

Published: December 2023

AI Article Synopsis

  • DECT and Gout
  • : Dual energy computed tomography (DECT) helps visualize monosodium urate crystals in gout, but its volume data is often skewed, complicating statistical analysis in longitudinal studies.
  • Methodology
  • : The study created simulated datasets and tested five data transformation methods to normalize DECT urate volumes, followed by linear regression analysis to assess changes over one year.
  • Findings
  • : None of the transformation methods effectively normalized the data; however, significant reductions in DECT urate volumes were observed from baseline to Year 1 across all methods, indicating challenges in accurately analyzing skewed data distributions.

Article Abstract

Background: Dual energy computed tomography (DECT) allows direct visualization of monosodium urate crystal deposition in gout. However, DECT urate volume data are often highly skewed (mostly small volumes with the remainder considerably larger), making statistical analyses challenging in longitudinal research. The aim of this study was to explore the ability of various analysis methods to normalise DECT urate volume data and determine change in DECT urate volumes over time.

Methods: Simulated datasets containing baseline and year 1 DECT urate volumes for 100 people with gout were created from two randomised controlled trials. Five methods were used to transform the DECT urate volume data prior to analysis: log-transformation, Box-Cox transformation, log(X-(min(X)-1)) transformation; inverse hyperbolic sine transformation, and rank order. Linear regression analyses were undertaken to determine the change in DECT urate volume between baseline and year 1. Cohen's d were calculated as a measure of effect size for each data treatment method. These analyses were then tested in a validation clinical trial dataset containing baseline and year 1 DECT urate volumes from 91 people with gout.

Results: No data treatment method successfully normalised the distribution of DECT urate volumes. For both simulated and validation data sets, significant reductions in DECT urate volumes were observed between baseline and Year 1 across all data treatment methods and there were no significant differences in Cohen's d effect sizes.

Conclusions: Normalising highly skewed DECT urate volume data is challenging. Adopting commonly used transformation techniques may not significantly improve the ability to determine differences in measures of central tendency when comparing the change in DECT urate volumes over time.

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Source
http://dx.doi.org/10.1016/j.semarthrit.2023.152303DOI Listing

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