Brito-Zerón P, Ramos-Casals M, Bove A, Sentis J, Font J
Department of Autoimmune Diseases, School of Medicine, University of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Hospital Clínic, Barcelona, Spain.
Rheumatology (Oxford). 2007 Aug;46(8):1359-62. doi: 10.1093/rheumatology/kem079. Epub 2007 Jun 14.
To identify features present at diagnosis that were prospectively associated with adverse outcomes in a large cohort of patients with primary Sjögren's syndrome (SS).
Two hundred and sixty-six patients diagnosed with primary SS in our department between 1984 and 2002 were consecutively included and followed up. Outcomes measured were vasculitis, B-cell lymphoma and death. Cox regression analysis was used to evaluate the effect of variables at diagnosis on outcomes.
Twenty-five (9%) patients developed vasculitis. Multivariate analysis identified parotid scintigraphy grades III or IV (HR 3.55, P = 0.05) and C4 levels <0.11 g/l (HR 8.26, P < 0.001) as variables predicting the development of vasculitis. Nine (3%) patients developed B-cell lymphoma. Multivariate analysis identified C3 levels <0.82 g/l (HR 7.54, P = 0.016) as a predictive factor of lymphoma development. Twenty-five (9%) patients died during follow-up. Systemic involvement (HR 4.51, P = 0.022), vasculitis (HR 4.58, P = 0.042), C4 levels <0.11 g/l (HR 5.47, P = 0.027) and cryoglobulins (HR 4.58, P = 0.013) were independently associated with death. The presence of at least two of the above-mentioned predictive factors (parotid scintigraphy, vasculitis, hypocomplementaemia and cryoglobulinaemia) was associated with a lower survival in comparison with patients with no factor (log rank and Breslow tests <0.001).
The main prognostic factors for an adverse outcome identified in our cohort of patients with primary SS were vasculitis, severe involvement in parotid scintigraphy, hypocomplementaemia and/or cryoglobulins at diagnosis. Patients with at least two of these factors need a closer follow-up.
确定在一大群原发性干燥综合征(SS)患者诊断时存在的、与不良预后相关的特征。
连续纳入并随访了1984年至2002年间在我科诊断为原发性SS的266例患者。测量的结局包括血管炎、B细胞淋巴瘤和死亡。采用Cox回归分析评估诊断时各变量对结局的影响。
25例(9%)患者发生血管炎。多因素分析确定腮腺闪烁显像分级为III级或IV级(风险比[HR] 3.55,P = 0.05)和C4水平<0.11 g/l(HR 8.26,P < 0.001)为预测血管炎发生的变量。9例(3%)患者发生B细胞淋巴瘤。多因素分析确定C3水平<0.82 g/l(HR 7.54,P = 0.016)为淋巴瘤发生的预测因素。25例(9%)患者在随访期间死亡。全身受累(HR 4.51,P = 0.022)、血管炎(HR 4.58,P = 0.042)、C4水平<0.11 g/l(HR 5.47,P = 0.027)和冷球蛋白(HR 4.58,P = 0.013)与死亡独立相关。与无上述因素的患者相比,存在至少两种上述预测因素(腮腺闪烁显像、血管炎、低补体血症和冷球蛋白血症)与较低的生存率相关(对数秩检验和Breslow检验<0.001)。
在我们的原发性SS患者队列中确定的不良预后主要预测因素为血管炎、腮腺闪烁显像严重受累、诊断时低补体血症和/或冷球蛋白血症。具有至少两种这些因素的患者需要密切随访。