Weder-Cisneros N D, Téllez-Zenteno J F, Cardiel M H, Guibert-Toledano M, Cabiedes J, Velásquez-Paz A L, García-Ramos G, Cantú C
Department of Neurology and Psychiatry, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Department of Immunology and Rheumatology, INCMNSZ.
Cephalalgia. 2004 Dec;24(12):1031-44. doi: 10.1111/j.1468-2982.2004.00822.x.
Headache is common in systemic lupus erythematosus with reported prevalence as high as 70%. The aims of this study were: to estimate the prevalence and types of headache in a sample of patients with systemic lupus erythematosus comparing it with rheumatoid arthritis, to determine clinical and serological associations. Eighty-one systemic lupus erythematosus and 29 rheumatoid arthritis consecutive patients seen in our outpatient clinic were interviewed. Headache was evaluated using the diagnostic criteria proposed by the International Headache Society. Additional evaluations were carried out in the 81 systemic lupus erythematosus patients including depression, disease activity, lupus damage, function disability, quality of life, and severity degree using a validated scales. We analysed the following autoantibodies: anti-double stranded DNA, anti-nucleosomes, anti-histones, anti-ribosomal P, anti-cardiolipin antibodies, anti-beta2-glycoprotein-I (GPI), and antinuclear antibodies. Forty-one per cent of systemic lupus erythematosus and 17% of rheumatoid arthritis patients suffered from headache (P = 0.02). No significant difference for any primary headache type between the two groups was found. Frequency of headache types in systemic lupus erythematosus patients was: migraine 24%, tensional-type headache 11%, and mixed headache 5%. In systemic lupus erythematosus patients the risk factors associated with headaches were Raynaud's phenomenon (OR 3.6; 95% CI 1.3-9.5; P = 0.009) and beta2GPI antibody positivity (OR 4.5; 95% CI 1.2-16.2; p = 0.016). We conclude that headache is more common in systemic lupus erythematosus than in rheumatoid arthritis patients and was independently associated with Raynaud's phenomenon and beta2GP-I antibodies.
头痛在系统性红斑狼疮中很常见,据报道患病率高达70%。本研究的目的是:估计系统性红斑狼疮患者样本中头痛的患病率和类型,并与类风湿关节炎进行比较,以确定临床和血清学关联。对在我们门诊就诊的81例系统性红斑狼疮患者和29例类风湿关节炎连续患者进行了访谈。使用国际头痛协会提出的诊断标准对头痛进行评估。对81例系统性红斑狼疮患者进行了额外评估,包括使用经过验证的量表评估抑郁、疾病活动度、狼疮损害、功能残疾、生活质量和严重程度。我们分析了以下自身抗体:抗双链DNA、抗核小体、抗组蛋白、抗核糖体P、抗心磷脂抗体、抗β2糖蛋白-I(GPI)和抗核抗体。41%的系统性红斑狼疮患者和17%的类风湿关节炎患者患有头痛(P = 0.02)。两组之间任何原发性头痛类型均未发现显著差异。系统性红斑狼疮患者头痛类型的频率为:偏头痛24%,紧张型头痛11%,混合性头痛5%。在系统性红斑狼疮患者中,与头痛相关的危险因素为雷诺现象(OR 3.6;95% CI 1.3 - 9.5;P = 0.009)和β2GPI抗体阳性(OR 4.5;95% CI 1.2 - 16.2;p = 0.016)。我们得出结论,头痛在系统性红斑狼疮患者中比在类风湿关节炎患者中更常见,并且与雷诺现象和β2GP - I抗体独立相关。