改良型强直性脊柱炎患者中轴性脊柱炎影像学进展与累积TNF抑制剂剂量的关系

IF 4.1 2区 医学 Q2 RHEUMATOLOGY
Therapeutic Advances in Musculoskeletal Disease Pub Date : 2025-07-27 eCollection Date: 2025-01-01 DOI:10.1177/1759720X251358022
Tae-Hwan Kim, Seo Young Park, Ji Hui Shin, Seunghun Lee, Kyung Bin Joo, Bon San Koo
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引用次数: 0

摘要

背景:肿瘤坏死因子抑制剂(Tumor necrosis factor inhibitors, TNFi)能有效治疗影像学上的轴性脊柱炎(axial spondyloarthritis, SpA),对于病情稳定的患者,常采用减量治疗。然而,其对影像学进展的长期影响尚不清楚。目的:分析影像学中轴位SpA累积TNFi剂量与影像学进展的相关性。设计:单中心回顾性图表回顾。方法:筛选2001年1月至2018年12月x线轴向SpA患者的电子病历。TNFi百分比剂量计算为总规定剂量除以2年间隔的标准剂量。采用线性混合模型评估TNFi百分比剂量与改良Stokes强直性脊柱炎脊柱评分(mSASSS)变化之间的关系,将其分为三个基线mSASSS组:mSASSS≥24,mSASSS >≥24,mSASSS >≥48。结果:在最初的线性混合模型中,在三个基线mSASSS组中检查了放射学进展,定义为两年间隔内mSASSS的变化。在基线mSASSS≥24组中,累积TNFi剂量与影像学进展呈负相关(β = -0.888, 95%可信区间(CI): -1.793 ~ 0.017, p = 0.055)。p = 0.379)。同样,对于基线mSASSS bbb48组,没有发现显著相关(β = 0.182, 95% CI: -0.832至1.196,p = 0.715)。在经年龄和性别调整的基线mSASSS≥24组的多变量模型中,累积TNFi剂量与mSASSS变化呈负相关(β = -1.871, 95% CI: -1.871 ~ -0.059, p = 0.037)。结论:在影像学轴向SpA和基线mSASSS≥24的患者中,累积TNFi剂量与影像学进展呈负相关。维持标准剂量的TNFi可能会减缓早期SpA脊柱结构改变的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association between cumulative TNF inhibitor dose and spinal radiographic progression in radiographic axial spondyloarthritis in patients with modified stoke ankylosing spondylitis spinal score ⩽24.

Association between cumulative TNF inhibitor dose and spinal radiographic progression in radiographic axial spondyloarthritis in patients with modified stoke ankylosing spondylitis spinal score ⩽24.

Association between cumulative TNF inhibitor dose and spinal radiographic progression in radiographic axial spondyloarthritis in patients with modified stoke ankylosing spondylitis spinal score ⩽24.

Association between cumulative TNF inhibitor dose and spinal radiographic progression in radiographic axial spondyloarthritis in patients with modified stoke ankylosing spondylitis spinal score ⩽24.

Background: Tumor necrosis factor inhibitors (TNFi) effectively manage radiographic axial spondyloarthritis (SpA), and dose reduction is often used for stable patients. However, its long-term impact on radiographic progression remains unclear.

Objective: To analyze the correlation between cumulative TNFi dose and radiographic progression in radiographic axial SpA.

Design: Single-center retrospective chart review.

Methods: Electronic medical records of patients with radiographic axial SpA from January 2001 to December 2018 were screened. The TNFi percentage dose was calculated as the total prescribed dose divided by the standard dose at 2-year intervals. The relationship between TNFi percentage dose and modified Stokes Ankylosing Spondylitis Spinal Score (mSASSS) changes was assessed using linear mixed models, separated into three baseline mSASSS groups: mSASSS ⩽24, mSASSS >24 to ⩽48, and mSASSS >48.

Results: In the initial linear mixed model, radiographic progression, defined as the change in mSASSS over 2-year intervals, was examined in three baseline mSASSS groups. In the baseline mSASSS ⩽24 group, the cumulative TNFi dose showed a negative correlation with radiographic progression (β = -0.888, 95% confidence interval (CI): -1.793 to 0.017, p = 0.055). In the group with 24 < baseline mSASSS ⩽ 48, a positive but nonsignificant association was observed (β = 1.688, 95% CI: -2.119 to 5.495, p = 0.379). Similarly, for the baseline mSASSS >48 group, no significant correlation was found (β = 0.182, 95% CI: -0.832 to 1.196, p = 0.715). In the multivariable model of the baseline mSASSS ⩽24 group adjusted for age and sex, the cumulative TNFi dose was negatively correlated with the mSASSS change (beta = -1.871, 95% CI: -1.871 to -0.059, p = 0.037).

Conclusion: In patients with radiographic axial SpA and baseline mSASSS ⩽24, the cumulative TNFi dose was negatively correlated with radiographic progression. Maintaining a standard TNFi dose may slow the progression of spinal structural changes in early stage SpA.

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来源期刊
CiteScore
6.80
自引率
4.80%
发文量
132
审稿时长
18 weeks
期刊介绍: Therapeutic Advances in Musculoskeletal Disease delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of musculoskeletal disease.
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