摘要 14 - 新加坡放射学轴性脊柱关节炎与非放射学脊柱关节炎的 ASAS 健康指数比较

Y. Kwan, Ting Hui Woon, C. Wang, Warren Fong
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Sociodemographic variables, clinical variables and patient-reported outcomes were collected. Univariable and multivariable linear regression were performed to identify variables associated with ASAS HI scores. Variables with p-value of <0.10 were included in the multivariable regression. A p-value of <0.05 was considered significant. Results Of the 331 patients, 265 (80.0%) and 66 (20.0%) had r-axSpA and nr-axSpA respectively. The median (IQR) age in r-axSpA was [40.0 (30.0-53.0) years], higher than nr-axSpA [34.0 (25.0-47.0) years], p<0.01. There was a higher proportion of males in r-axSpA (80.4%) than nr-axSpA (65.2%), p=0.01. Patients with r-axSpA had a longer disease duration [6.8 (1.8-14.0) years] than nr-axSpA [1.1 (0.2-5.4) years], p<0.01. More patients with r-axSpA (90.2%) were positive for HLA-B27 than nr-axSpA (69.7%), p<0.01. Differences in ASAS HI scores were not statistically significant between r-axSpA and nr-axSpA [4.0 (2.0-6.8) vs 5.5 (1.1-8.5), p=0.12]. Post multivariable regression, nr-axSpA ([Formula: see text]: 0.70, 95% CI: 0.09, 1.32, p=0.02), BASDAI ([Formula: see text]: 0.18, 95% CI: 0.01, 0.35, p=0.04), BASFI ([Formula: see text]: 0.47, 95% CI: 0.30, 0.65, p<0.01) and HADS-Depression scores ([Formula: see text]: 0.11, 95% CI: 0.01, 0.21, p=0.04) were positively associated with ASAS HI. Higher SF36-PCS ([Formula: see text]: −0.11, 95% CI: −0.14, −0.08, p<0.01) and SF36-MCS ([Formula: see text]: −0.07, 95% CI: −0.10, −0.04, p<0.01) were negatively associated with ASAS HI (Table 1). Conclusion Patients with nr-axSpA were associated with poorer overall health and functioning as compared to r-axSpA. 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Univariable and multivariable linear regression were performed to identify variables associated with ASAS HI scores. Variables with p-value of <0.10 were included in the multivariable regression. A p-value of <0.05 was considered significant. Results Of the 331 patients, 265 (80.0%) and 66 (20.0%) had r-axSpA and nr-axSpA respectively. The median (IQR) age in r-axSpA was [40.0 (30.0-53.0) years], higher than nr-axSpA [34.0 (25.0-47.0) years], p<0.01. There was a higher proportion of males in r-axSpA (80.4%) than nr-axSpA (65.2%), p=0.01. Patients with r-axSpA had a longer disease duration [6.8 (1.8-14.0) years] than nr-axSpA [1.1 (0.2-5.4) years], p<0.01. More patients with r-axSpA (90.2%) were positive for HLA-B27 than nr-axSpA (69.7%), p<0.01. Differences in ASAS HI scores were not statistically significant between r-axSpA and nr-axSpA [4.0 (2.0-6.8) vs 5.5 (1.1-8.5), p=0.12]. Post multivariable regression, nr-axSpA ([Formula: see text]: 0.70, 95% CI: 0.09, 1.32, p=0.02), BASDAI ([Formula: see text]: 0.18, 95% CI: 0.01, 0.35, p=0.04), BASFI ([Formula: see text]: 0.47, 95% CI: 0.30, 0.65, p<0.01) and HADS-Depression scores ([Formula: see text]: 0.11, 95% CI: 0.01, 0.21, p=0.04) were positively associated with ASAS HI. Higher SF36-PCS ([Formula: see text]: −0.11, 95% CI: −0.14, −0.08, p<0.01) and SF36-MCS ([Formula: see text]: −0.07, 95% CI: −0.10, −0.04, p<0.01) were negatively associated with ASAS HI (Table 1). Conclusion Patients with nr-axSpA were associated with poorer overall health and functioning as compared to r-axSpA. 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引用次数: 0

摘要

背景 以前的研究报告显示,放射性轴性脊柱关节炎(r-axSpA)和非放射性轴性脊柱关节炎(nr-axSpA)之间的脊柱关节炎评估(ASAS)健康指数(HI)得分存在差异,结果相互矛盾。此外,还观察到疾病活动性的国家级差异。因此,本研究旨在比较新加坡 r-axSpA 和 nr-axSpA 的 ASAS HI 评分,并确定与较差 ASAS HI 评分相关的因素。方法 这是一项对新加坡中央医院前瞻性队列研究基线数据的横断面评估,时间为 2018 年 1 月至 2023 年 3 月。根据 2009 年 ASAS 标准临床诊断为轴性脊柱关节炎(axSpA)的 21 岁及以上患者被纳入研究。研究人员收集了社会人口学变量、临床变量和患者报告的结果。通过单变量和多变量线性回归来确定与 ASAS HI 评分相关的变量。P 值小于 0.10 的变量被纳入多变量回归。P值<0.05为显著。结果 331 名患者中,分别有 265 人(80.0%)和 66 人(20.0%)患有 r-axSpA 和 nr-axSpA。r-axSpA患者的年龄中位数(IQR)为[40.0(30.0-53.0)岁],高于nr-axSpA患者的[34.0(25.0-47.0)岁],P<0.01。男性在 r-axSpA 中的比例(80.4%)高于 nr-axSpA(65.2%),P=0.01。r-axSpA患者的病程[6.8(1.8-14.0)年]长于nr-axSpA[1.1(0.2-5.4)年],P<0.01。HLA-B27阳性的 r-axSpA 患者(90.2%)多于 nr-axSpA 患者(69.7%),P<0.01。r-axSpA和nr-axSpA的ASAS HI评分差异无统计学意义[4.0 (2.0-6.8) vs 5.5 (1.1-8.5),p=0.12]。多变量回归后,nr-axSpA([公式:见正文]:0.70,95% CI:0.09,1.32,P=0.02)、BASDAI([公式:见正文]:0.18,95% CI:0.01,0.35,P=0.04)、BASFI([计算公式:见正文]:0.47,95% CI:0.30,0.65,p<0.01)和 HADS 抑郁评分([计算公式:见正文]:0.11,95% CI:0.01,0.21,p=0.04)与 ASAS HI 呈正相关。较高的 SF36-PCS ([计算公式:见正文]:-0.11,95% CI:-0.14,-0.08,p<0.01)和 SF36-MCS ([计算公式:见正文]:-0.07,95% CI:-0.10,-0.04,p<0.01)与 ASAS HI 呈负相关(表 1)。结论 与 r-axSpA 相比,nr-axSpA 患者的整体健康和功能较差。较高的疾病活动度、较差的身体功能、较差的心理健康状况和较多的抑郁症状与较差的健康和功能相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 14 — Comparison of the ASAS Health Index Between Radiographic Axial Spondyloarthritis and Non-Radiographic Spondyloarthritis in Singapore
Background Prior studies reported conflicting results regarding differences in Assessment of SpondyloArthritis (ASAS) Health Index (HI) scores between radiographic axial spondyloarthritis (r-axSpA) and non-radiographic axial spondyloarthritis (nr-axSpA). Country-level variations in disease activity were also observed. Hence, this study aimed to compare the ASAS HI scores between r-axSpA and nr-axSpA in Singapore, and determine factors associated with poorer ASAS HI scores. Methods This was a cross-sectional evaluation of baseline data from a prospective cohort study in Singapore General Hospital, from January 2018 to March 2023. Patients aged 21 years and above who were clinically diagnosed with axial spondyloarthritis (axSpA) based on the 2009 ASAS criteria were included. Sociodemographic variables, clinical variables and patient-reported outcomes were collected. Univariable and multivariable linear regression were performed to identify variables associated with ASAS HI scores. Variables with p-value of <0.10 were included in the multivariable regression. A p-value of <0.05 was considered significant. Results Of the 331 patients, 265 (80.0%) and 66 (20.0%) had r-axSpA and nr-axSpA respectively. The median (IQR) age in r-axSpA was [40.0 (30.0-53.0) years], higher than nr-axSpA [34.0 (25.0-47.0) years], p<0.01. There was a higher proportion of males in r-axSpA (80.4%) than nr-axSpA (65.2%), p=0.01. Patients with r-axSpA had a longer disease duration [6.8 (1.8-14.0) years] than nr-axSpA [1.1 (0.2-5.4) years], p<0.01. More patients with r-axSpA (90.2%) were positive for HLA-B27 than nr-axSpA (69.7%), p<0.01. Differences in ASAS HI scores were not statistically significant between r-axSpA and nr-axSpA [4.0 (2.0-6.8) vs 5.5 (1.1-8.5), p=0.12]. Post multivariable regression, nr-axSpA ([Formula: see text]: 0.70, 95% CI: 0.09, 1.32, p=0.02), BASDAI ([Formula: see text]: 0.18, 95% CI: 0.01, 0.35, p=0.04), BASFI ([Formula: see text]: 0.47, 95% CI: 0.30, 0.65, p<0.01) and HADS-Depression scores ([Formula: see text]: 0.11, 95% CI: 0.01, 0.21, p=0.04) were positively associated with ASAS HI. Higher SF36-PCS ([Formula: see text]: −0.11, 95% CI: −0.14, −0.08, p<0.01) and SF36-MCS ([Formula: see text]: −0.07, 95% CI: −0.10, −0.04, p<0.01) were negatively associated with ASAS HI (Table 1). Conclusion Patients with nr-axSpA were associated with poorer overall health and functioning as compared to r-axSpA. Higher disease activity, poorer physical function, poorer mental health status and more depressive symptoms were associated with worse health and functioning.
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