曾露露, 冀肖健, 胡立冬, 胡嘉文, 张奕楠, 张家鑫, 刘兴康, 朱剑, 黄烽. 伴与不伴外周关节炎的中轴型脊柱关节炎临床特征及治疗的比较研究[J]. 解放军医学院学报. DOI: 10.12435/j.issn.2095-5227.2023.150
引用本文: 曾露露, 冀肖健, 胡立冬, 胡嘉文, 张奕楠, 张家鑫, 刘兴康, 朱剑, 黄烽. 伴与不伴外周关节炎的中轴型脊柱关节炎临床特征及治疗的比较研究[J]. 解放军医学院学报. DOI: 10.12435/j.issn.2095-5227.2023.150
ZENG Lulu, JI Xiaojian, HU Lidong, HU Jiawen, ZHANG Yinan, ZHANG Jiaxin, LIU Xingkang, ZHU Jian, HUANG Feng. Clinical characteristics and treatment regimes of axial spondyloarthritis complicated with peripheral arthritis[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL. DOI: 10.12435/j.issn.2095-5227.2023.150
Citation: ZENG Lulu, JI Xiaojian, HU Lidong, HU Jiawen, ZHANG Yinan, ZHANG Jiaxin, LIU Xingkang, ZHU Jian, HUANG Feng. Clinical characteristics and treatment regimes of axial spondyloarthritis complicated with peripheral arthritis[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL. DOI: 10.12435/j.issn.2095-5227.2023.150

伴与不伴外周关节炎的中轴型脊柱关节炎临床特征及治疗的比较研究

Clinical characteristics and treatment regimes of axial spondyloarthritis complicated with peripheral arthritis

  • 摘要:
    背景 尽管中轴型脊柱关节炎(axial spondyloarthritis,axSpA)是一种以中轴脊柱受累为主的慢性炎症性疾病,部分患者仍可能出现外周关节炎。国内外关于伴发外周关节炎的axSpA患者的临床特征和治疗选择的研究较少,误诊误治常见。
    目的 比较伴发外周关节炎的axSpA患者与不伴外周关节炎的axSpA患者在临床特征和治疗选择上的差异,以帮助临床医生及早发现与识别。
    方法 本研究为回顾性研究,连续纳入2016年1月至2022年12月于解放军总医院第一医学中心首次就诊的axSpA患者,根据患者是否伴随外周关节炎分为伴外周关节炎组和不伴外周关节炎组。采用倾向性评分匹配均衡就诊时间,对伴外周关节炎组及不伴外周关节炎组进行1∶3匹配,匹配后456例axSpA患者(伴外周关节炎组和不伴外周关节炎组分别为114例和342例)纳入分析,比较两组间临床特征和治疗选择差异。
    结果 456例axSpA患者中,男性357例,女性99例,中位年龄30.0(IQR:25.0 ~ 36.5)岁。相较于不伴外周关节炎的axSpA患者,伴外周关节炎的axSpA患者发病年龄较晚IQR:23.0(18.6 ~ 31.7)岁vs 21.5(17.0 ~ 27.0)岁,P=0.022,病程较短5.7(1.7 ~ 10.5)年vs 7.7(3.5 ~ 11.4)年,P=0.024,身体质量指数(body mass index,BMI)较低Md(IQR):22.3(19.6 ~ 25.3) kg/m2 vs 23.6(20.7 ~ 25.8) kg/m2P=0.01,吸烟比例也更低10.5%(12/114) vs 28.4%(97/342),P < 0.001,也伴随更多的附着点炎和指/趾炎(P均 < 0.05)。此外,伴外周关节炎的axSpA患者的红细胞沉降率及C反应蛋白(C-reactive protein,CRP)更高(P均 < 0.05)。治疗方面,伴外周关节炎的axSpA患者使用中成药44.7%(51/114) vs 59.9%(205/342),P=0.005,更多使用传统抗风湿药(conventional synthetic disease-modifying antirheumatic drugs,csDMARDs)79.8%(91/114) vs 59.9%(205/342),P < 0.001、生物类药物(biologic disease-modifying antirheumatic drugs,bDMARDs)40.4%(46/114) vs 21.3%(73/342),P < 0.001和糖皮质激素9.6%(11/114) vs 0.6%(2/342),P < 0.001,更多地联合使用传统和生物类抗风湿药物 30.7%(35/114) vs 9.4%(32/342),P < 0.001或者两种以上的csDMARDs用药43.0%(49/114) vs 9.9%(34/342),P < 0.001治疗。多因素logistic回归分析结果提示,患者发病年龄较小(OR=0.967,95% CI:0.942 ~ 0.992, P=0.011)、吸烟(OR=1.745,95% CI:1.030 ~ 2.955, P=0.038)、合并葡萄膜炎(OR=2.169,95% CI:1.025 ~ 4.592, P=0.043)/银屑病(OR=20.838,95% CI:2.340 ~ 185.560, P=0.006)、伴外周关节炎(OR=2.482,95% CI:1.423 ~ 4.332, P=0.001)或CRP(OR=1.011,95% CI:1.003 ~ 1.020, P=0.011)升高,医生更倾向于开具有生物类抗风湿药物的处方。
    结论 伴外周关节炎的axSpA患者尽管发病较晚、病程较短,但因为伴随更多的附着点炎、指/趾炎以及较高的炎症指标,这类患者往往需要接受多种药物治疗。

     

    Abstract:
    Background Although axial spondyloarthritis (axSpA) is a chronic inflammatory disease primarily affecting the axial spine, some patients may also present with peripheral arthritis. There is limited research on the clinical characteristics and treatment options for axSpA patients with peripheral arthritis, both domestically and internationally, leading to frequent misdiagnosis and mistreatment.
    Objective To compare the clinical characteristics and treatment options between two groups of axSpA patients with or without peripheral arthritis, in order to assist clinicians in early detection and identification.
    Methods This was a retrospective study. axSpA patients who admitted to Chinese PLA General Hospital firstly from January 2016 to December 2022 were consecutively included. Patients were divided into the group with peripheral arthritis and the group without peripheral arthritis. A propensity score matching was performed to balance the baseline characteristics between the two groups using the visit time as a matching factor in a 1:3 ratio. After matching, 456 patients with axSpA (114 with peripheral arthritis and 342 without peripheral arthritis) were included in the analysis. The clinical characteristics and differences in treatment choices between the two groups were compared.
    Results Of the 456 patients with axSpA, there were 357 males and 99 females with a median age of 30.0 (25.0,36.5) years. Compared to axSpA patients without peripheral arthritis, axSpA patients with peripheral arthritis had a later onset of disease (MdIQR:23.0 18.6, 31.7 years vs 21.5 17.0, 27.0 years, P=0.022), a shorter disease duration (MdIQR:5.7 1.7, 10.5 years vs 7.7 3.5, 11.4 years, P=0.024), a lower body mass index (BMI) (MdIQR:22.3 19.6, 25.3 kg/m2 vs 23.6 20.7, 25.8kg/m2, P=0.01), a lower smoking rate (10.5% 12/114 vs 28.4% 97/342, P < 0.001), and a higher prevalence of enthesitis and dactylitis (P < 0.05 for both). Moreover, axSpA patients with peripheral arthritis had higher erythrocyte sedimentation rate and C-reactive protein (CRP) (P < 0.05 for both).. In terms of treatment, patients with peripheral arthritis had less usage of traditional Chinese medicine (44.7% 51/114 vs 59.9% 205/342, P=0.005), while higher usage of conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) (79.8% 91/114 vs 59.9% 205/342, P < 0.001), biologic disease-modifying antirheumatic drugs (bDMARDs) (40.4% 46/114 vs 21.3% 73/342, P < 0.001), and glucocorticoids (9.6% 11/114 vs 0.6% 2/342, P < 0.001), and were more often treated with a combination of csDMARDs and bDMARDs (30.7% 35/114 vs 9.4% 32/342, P < 0.001) or two or more csDMARDs (43.0% 49/114 vs 9.9% 34/342, P < 0.001). The results of the logistic regression analysis of factors indicate that younger age at onset (OR=0.967, 95% CI: 0.942 ~ 0.992, P=0.011), smoking (OR=1.745, 95% CI: 1.030 ~ 2.955, P=0.038), presence of uveitis (OR=2.169, 95% CI: 1.025 ~ 4.592, P=0.043) / psoriasis (OR=20.838, 95% CI: 2.340 ~ 185.560, P=0.006), peripheral arthritis (OR=2.482, 95% CI: 1.423 ~ 4.332, P=0.001), or elevated CRP levels (OR=1.011, 95% CI: 1.003 ~ 1.020, P=0.011) are associated with the use of bDMARDs in axSpA patients.
    Conclusion Patients with peripheral arthritis, despite having a later onset and shorter disease duration, often require multiple drug therapies due to the presence of more enthesitis, dactylitis, and higher inflammatory markers.

     

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