Foocharoen Chingching, Suwannachat Prangsuporn, Netwijitpan Sittichai, Mahakkanukrauh Ajanee, Suwannaroj Siraphop, Nanagara Ratanavadee
Department of Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Int J Rheum Dis. 2016 Mar;19(3):312-20. doi: 10.1111/1756-185X.12492. Epub 2014 Oct 8.
Anti-topoisomerase I antibody (ATA) carries an increased risk of systemic sclerosis (SSc) internal organ involvement. There have been no published comparisons of the clinical characteristics of patients positive and negative for ATA in Thailand, where the positive rate for ATA is higher than among Caucasians.
To define the clinical differences between SSc, positive versus negative, for ATA.
A retrospective cohort study was performed among SSc patients over 18 at Srinagarind Hospital, Khon Kaen University, Thailand, during January 2006-December 2013. SSc-overlap syndrome was excluded.
Two hundred and ninety-four SSc patients were included (female : male 2.5 : 1). The majority (68.6%) were the diffuse cutaneous SSc subset (dcSSc). ATA was positive in 252 patients (85.7%), among whom 71.7% had dcSSc and 28.2% limited cutaneous SSc (lcSSc). Using a multivariate analysis, hand deformity had a significantly positive association with ATA (odds ratio [OR] 7.01; 95% CI 1.02-48.69), whereas being anti-centromere (ACA) positive had a negative association (OR 0.17; 95% CI 0.03-0.92). After doing a subgroup analysis of the SSc subset, the median duration of disease at time of pulmonary fibrosis detection among ATA positive dcSSc was significantly shorter than the ATA negative group (1.05 vs. 6.77 years, P = 0.01). Raynaud's phenomenon (RP) at onset was significantly more frequent in lcSSc sufferers who were ATA negative than those who were ATA positive (90.5% vs. 56.9%, P = 0.005).
A high prevalence of ATA positivity was found among Thai SSc patients and this was associated with a high frequency of hand deformity, ACA negativity, a short duration of pulmonary fibrosis in dcSSc and a lower frequency of RP in lcSSc.
抗拓扑异构酶I抗体(ATA)会增加系统性硬化症(SSc)累及内脏器官的风险。在ATA阳性率高于白种人的泰国,尚未有关于ATA阳性和阴性患者临床特征比较的报道。
明确ATA阳性与阴性的SSc患者之间的临床差异。
对2006年1月至2013年12月期间泰国孔敬大学诗里拉吉医院18岁以上的SSc患者进行回顾性队列研究。排除SSc重叠综合征患者。
纳入294例SSc患者(女性∶男性为2.5∶1)。大多数(68.6%)为弥漫性皮肤型SSc亚组(dcSSc)。252例患者(85.7%)ATA呈阳性,其中71.7%为dcSSc,28.2%为局限性皮肤型SSc(lcSSc)。多因素分析显示,手部畸形与ATA呈显著正相关(比值比[OR]7.01;95%置信区间[CI]1.02 - 48.69),而抗着丝点抗体(ACA)阳性则呈负相关(OR 0.17;95% CI 0.03 - 0.92)。在对SSc亚组进行亚组分析后,ATA阳性的dcSSc患者在检测出肺纤维化时的疾病中位病程显著短于ATA阴性组(1.05年对6.77年,P = 0.01)。ATA阴性的lcSSc患者发病时雷诺现象(RP)的发生率显著高于ATA阳性患者(90.5%对56.9%,P = 0.005)。
泰国SSc患者中ATA阳性率较高,且与手部畸形高发、ACA阴性、dcSSc中肺纤维化病程短以及lcSSc中RP发生率较低相关。