Patient-reported gastrointestinal involvement is associated with reduced quality of life and disability in systemic sclerosis.

IF 1.4 Q3 RHEUMATOLOGY
Patrik Kéringer, Katalin T Kovács, Gabriella Nagy, Ágnes Ágoston-Szabó, Kristóf Filipánits, Franciska Ilona Kiss, Attila Szabó, Gábor Kumánovics
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Abstract

Objectives: To investigate the impact of gastrointestinal involvement in systemic sclerosis affecting the quality of life and systemic sclerosis-related disability using patient-reported outcome measurements (PROMs).

Methods: Data from 160 consecutive systemic sclerosis patients were collected, including clinical characteristics and self-assessment questionnaires. The severity of gastrointestinal involvement was determined by the University of California Los Angeles Scleroderma Clinical Trials Consortium gastrointestinal tract 2.0 (UCLA-GIT 2.0): patients were classified as having "none-to-mild" symptoms (total score = 0.00-0.49: Group A), "moderate" symptoms (Group B), and "severe-to-very severe" symptoms (Group C). All investigations were repeated following 1 year to check the reliability (n = 149).

Results: Quality of life (EuroQol-5 Dimension anxiety/depression, Physical Component Summary, and Mental Component Summary of Short-Form Health Survey-36) and disability questionnaires (Health Assessment Questionnaire Disability Index, Scleroderma Health Assessment Questionnaire), Scleroderma Impact of Disease showed moderate significant correlation with UCLA-GIT 2.0 (rho: 0.400, -0.484, -0.468, 0.400, 0.436, 0.646, respectively). These correlations remained significant when tested in the two main subgroups (limited and diffuse cutaneous systemic sclerosis). Disease duration and UCLA-GIT 2.0 score did not show any correlation (rho: .055, p = 0.488). The average gastrointestinal involvement complaint of early systemic sclerosis (disease duration < 3 years, n = 24) subgroup measured by the UCLA-GIT 2.0 was not different from the rest of the cases (0.13 (0.03-0.46) vs 0.22 (0.08-0.45), p = 0.280). All investigated PROMs regarding quality of life and disability showed worse results in Group B when compared with patients in Group A. Similarly, patients in Group C have worse results compared to Group B. These correlations with the UCLA-GIT 2.0 score were confirmed during the 1-year follow-up.

Conclusion: Moderate/severe gastrointestinal involvement symptoms based on the UCLA-GIT 2.0 are associated with worse quality of life and disability. This correlation holds for both systemic sclerosis subgroups and independent of disease duration: moderate/severe gastrointestinal involvement complaints develop early in systemic sclerosis parallel with early onset of decreased quality of life and disability.

患者报告的胃肠道受累与系统性硬化症患者的生活质量下降和残疾有关。
目的:利用患者报告的结果测量(PROMs)研究胃肠道受累对系统性硬化症患者生活质量和系统性硬化症相关残疾的影响。方法:收集160例连续系统性硬化症患者的临床资料和自评问卷。胃肠受累的严重程度由加州大学洛杉矶分校硬皮病临床试验联盟胃肠道2.0 (UCLA-GIT 2.0)确定:患者分为“无至轻度”症状(总分= 0.00-0.49:A组)、“中度”症状(B组)和“重度至极重度”症状(C组)。1年后再次进行调查以检验信度(n = 149)。结果:生活质量(EuroQol-5维度焦虑/抑郁、短表健康调查-36的身体成分摘要和精神成分摘要)和残疾问卷(健康评估问卷残疾指数、硬皮病健康评估问卷)、硬皮病疾病影响与UCLA-GIT 2.0存在中度显著相关(rho分别为0.400、-0.484、-0.468、0.400、0.436、0.646)。当在两个主要亚组(局限性和弥漫性皮肤系统性硬化症)中进行测试时,这些相关性仍然显著。病程与UCLA-GIT 2.0评分无相关性(rho: 0.055, p = 0.488)。结论:基于UCLA-GIT 2.0的中度/重度胃肠道受累症状与较差的生活质量和残疾相关。这种相关性适用于系统性硬化症亚组,且与病程无关:在系统性硬化症中,中度/重度胃肠道受累的主诉出现得较早,与早发性生活质量下降和残疾平行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
4.10
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