Rheumatology Unit, University of Messina, Italy.
L'altra Statistica Consultancy and Training, Biostatistics Office, Roma, Italy.
Clin Exp Rheumatol. 2020 Jan-Feb;38 Suppl 123(1):31-39. Epub 2020 Feb 11.
The primary aim of this study was to compare the prevalence of clinical and particularly ultrasonographic signs of enthesitis in patients with psoriatic arthritis (PsA), fibromyalgia (FM), or both. The secondary aim was to assess the impact of FM on disease activity and clinimetric scores.
This single-centre, observational cross-sectional study involved 101 consenting patients: 39 with PsA (CASPAR criteria), 23 with FM (2016 criteria), and 39 with both. Standard PsA and FM clinical, laboratory and clinimetric data were recorded, and entheses were assessed using the Leeds Enthesitis Index (LEI) and the Maastricht Ankylosing Spondylitis Enthesitis Score (MASES). All of the patients underwent B mode (grey scale) and Power Doppler (PD) ultrasonography bilaterally at the insertions of the quadriceps tendons, the proximal and distal patellar tendons, the Achilles tendons, and the plantar fascia insertions of the calcaneus, to evaluate the thickness of entheses, the hypoechogenicity, the presence of bony erosions, the enthesophytes, and the bursitis. The US findings were scored using the Glasgow Ultrasound Enthesitis Scoring System (GUESS). The data were statistically analysed using univariate and multivariate analyses, and receiver-operating characteristic (ROC) curves, concentrating on the shared clinical features of the two condition.
The mean age of the patients as a whole was 53.6±9.47 years. Females accounted for 64.1% of the PsA patients (disease duration 9.13 years), 95.6% of the FM patients (disease duration 5.09 years), and 92.3% of the patients with PsA-FM (disease duration 7.9 years). There were no between-group differences in the patients' body mass index (BMI). In accordance with the study inclusion criteria, none of the FM subjects had PsA or reported any personal or family history of psoriasis. The mean Psoriasis Area and Severity Index was 2.3±3.1 in the PsA group, and 1.2±2.45 in the PsA-FM group. Clinical evidence of enthesopathy was found in 43% of the patients with PsA, 51.3% of those with PsA-FM, and 50.8% of those with FM, while US entheseal abnormalities were detected in respectively 77%, 74% and 35%. The median Bath Ankylosing Spondylitis Disease Activity Index was significantly higher in the patients with PsA-FM than in those with PsA (7.7 [IQR 2.1] vs. 5.0 [IQR 3.8]; p<0.001), as was the median ESR-assessed Ankylosing Spondylitis Disease Activity Score (3.69 [IQR 1.00] vs. 2.82 [IQR 1.55; p=0.004), or CRP- assessed (median 3.27 [IQR 1.07] vs. 2.66 [IQR 1.26]; p=0.006). There was a correlation between GUESS scores and disease duration in the patients with PsA (rho=0.37; p=0.019, 95% CI 0.10-0.61) or PsA-FM (rho=0.38; p=0.016, 95% CI 0.10-0.61), but not in the FM group, and GUESS scores correlated with BMI (rho=0.2; p=0.05, 95% CI 0.00-0.37) and dyslipidemia (rho=0.34; p=0.006, 95% CI 0.11-0.58) in all three groups.
The use of a clinical examination and clinimetric scores alone may overestimate active enthesitis in FM patients. As US was more frequently positive in patients with PsA and PsA-FM than in those with FM, it may be useful in differentiating pain due to enthesitis from entheseal pain due to FM.
本研究的主要目的是比较患有银屑病关节炎 (PsA)、纤维肌痛 (FM) 或两者并存患者的临床和特别是超声影像学附着点炎的患病率。次要目的是评估 FM 对疾病活动度和临床计量评分的影响。
这项单中心、观察性横断面研究纳入了 101 名同意参与的患者:39 名患有 PsA(CASPAR 标准)、23 名患有 FM(2016 标准)和 39 名同时患有两种疾病。记录了标准的 PsA 和 FM 临床、实验室和临床计量数据,并使用利兹附着点炎指数 (LEI) 和马斯特里赫特强直性脊柱炎附着点炎评分 (MASES) 评估附着点。所有患者均接受双侧股四头肌肌腱、近端和远端髌腱、跟腱以及跟骨底筋膜附着处的 B 模式(灰阶)和功率多普勒 (PD) 超声检查,以评估附着点的厚度、低回声、骨侵蚀、附着点骨赘和滑囊炎。使用格拉斯哥超声附着点炎评分系统 (GUESS) 对 US 结果进行评分。使用单变量和多变量分析以及接收者操作特征 (ROC) 曲线对数据进行统计分析,重点关注两种疾病的共同临床特征。
患者的平均年龄为 53.6±9.47 岁。女性占 PsA 患者的 64.1%(疾病病程 9.13 年)、FM 患者的 95.6%(疾病病程 5.09 年)和 PsA-FM 患者的 92.3%(疾病病程 7.9 年)。三组患者的体重指数(BMI)无组间差异。根据研究纳入标准,FM 组中没有任何患者患有 PsA 或报告任何个人或家族银屑病史。PsA 组的银屑病面积和严重程度指数(PASI)平均为 2.3±3.1,PsA-FM 组为 1.2±2.45。临床证据表明附着点病发生在 43%的 PsA 患者、51.3%的 PsA-FM 患者和 50.8%的 FM 患者中,而超声影像学附着点异常分别在 77%、74%和 35%的患者中被发现。PsA-FM 患者的巴斯强直性脊柱炎疾病活动指数(BASDAI)中位数明显高于 PsA 患者(7.7[IQR 2.1] vs. 5.0[IQR 3.8];p<0.001),血沉评估的强直性脊柱炎疾病活动评分(ESR-ASDAS)中位数(3.69[IQR 1.00] vs. 2.82[IQR 1.55];p=0.004)或 C 反应蛋白评估的(CRP-ASDAS)中位数(3.27[IQR 1.07] vs. 2.66[IQR 1.26];p=0.006)也更高。在 PsA(rho=0.37;p=0.019,95%CI 0.10-0.61)或 PsA-FM(rho=0.38;p=0.016,95%CI 0.10-0.61)患者中,GUESS 评分与疾病病程之间存在相关性,但在 FM 患者中无相关性,并且 GUESS 评分与 BMI(rho=0.2;p=0.05,95%CI 0.00-0.37)和血脂异常(rho=0.34;p=0.006,95%CI 0.11-0.58)相关。
仅使用临床检查和临床计量评分可能会高估 FM 患者的活动性附着点炎。由于 PsA 和 PsA-FM 患者的 US 阳性率高于 FM 患者,因此 US 可能有助于区分由附着点炎引起的疼痛和由 FM 引起的附着点疼痛。