Health- and Vision-Related Quality of Life in a Randomized Controlled Trial Comparing Methotrexate and Mycophenolate Mofetil for Uveitis

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Abstract

Purpose: To evaluate changes in health-related and vision-related quality of life (VRQoL) among patients with noninfectious uveitis who were treated with antimetabolites. Design: Secondary analysis of a randomized controlled trial. Participants: Patients with noninfectious uveitis from India, the United States, Australia, Saudi Arabia, and Mexico. Methods: From 2013 through 2017, 216 participants were randomized to receive 25 mg weekly oral methotrexate or 1.5 g twice daily oral mycophenolate mofetil. Median changes in quality of life (QoL) were measured using Wilcoxon signed-rank tests, and differences between treatment groups were measured using linear mixed models, adjusting for baseline QoL score, age, gender, and site. Among Indian patients, VRQoL scores from a general scale (the National Eye Institute Visual Function Questionnaire [NEI-VFQ]) and a culturally specific scale (the Indian Visual Function Questionnaire [IND-VFQ]) were compared using Pearson correlation tests. Main Outcome Measures: Vision-related QoL (NEI-VFQ and IND-VFQ) and health-related QoL (HRQoL; physical component score [PCS] and mental component score [MCS] of the Medical Outcomes Study 36-Item Short Form Survey [SF-36v2]) were measured at baseline, the primary end point (6 months or treatment failure before 6 months), and the secondary end point (12 months or treatment failure between 6 and 12 months). Results: Among 193 participants who reached the primary end point, VRQoL increased from baseline by a median of 12.0 points (interquartile range [IQR], 1.0–26.1, NEI-VFQ scale), physical HRQoL increased by a median of 3.6 points (IQR, –1.4 to 14.9, PCS SF-36v2), and mental HRQoL increased by a median of 3.0 points (IQR, –3.7 to 11.9, MCS SF-36v2). These improvements in NEI-VFQ, SF-36v2 PCS, and SF-36v2 MCS scores all were significant (P < 0.01). The linear mixed models showed that QoL did not differ between treatment groups for each QoL assessment (NEI-VFQ, IND-VFQ, PCS SF-36v2, and MCS SF-36v2; P > 0.05 for all). The NEI-VFQ and IND-VFQ scores for Indian participants were correlated highly at baseline and the primary and secondary end points (correlation coefficients, 0.87, 0.80, and 0.90, respectively). Conclusions: Among patients treated with methotrexate or mycophenolate mofetil for uveitis, VRQoL and HRQoL improved significantly over the course of 1 year and did not differ by treatment allocation. These findings suggest that antimetabolites could improve overall patient well-being and daily functioning.

Original languageEnglish (US)
Pages (from-to)1337-1345
Number of pages9
JournalOphthalmology
Volume128
Issue number9
DOIs
StatePublished - Sep 2021

Funding

Supported by the National Eye Institute , National Institutes of Health , Bethesda, Maryland (grant nos.: U10 EY021125 and EY06190 ); Research to Prevent Blindness , Inc., New York, New York (unrestricted grant to the Department of Ophthalmology at UCSF ); and That Man May See Foundation. The sponsors had no role in the design or conduct of this research. Supported by the National Eye Institute, National Institutes of Health, Bethesda, Maryland (grant nos.: U10 EY021125 and EY06190); Research to Prevent Blindness, Inc., New York, New York (unrestricted grant to the Department of Ophthalmology at UCSF); and That Man May See Foundation. The sponsors had no role in the design or conduct of this research. The author(s) have made the following disclosure(s): A.K.: Nonfinancial support ? F. I. Proctor Foundation. L.L.L.: Consultant ? Allergan, Novotech; Advisory board ? Allergan; Financial support ? Bayer. E.B.S.: Financial support ? AbbVie, Aldeyra, Clearside, Eyegate, Eyepoint, Gilead, Eyevensys Obtained funding: Lim, Suhler

Keywords

  • Antimetabolites
  • Quality of life
  • uveitis

ASJC Scopus subject areas

  • Ophthalmology

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