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沙特阿拉伯624例系统性红斑狼疮患者的临床和免疫学表现。

Clinical and immunological manifestations in 624 SLE patients in Saudi Arabia.

作者信息

Al Arfaj A S, Khalil N

机构信息

Division of Rheumatology, Department of Medicine, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

出版信息

Lupus. 2009 Apr;18(5):465-73. doi: 10.1177/0961203308100660.

Abstract

Our objective was to study the demographic, clinical, laboratory features, therapy, and outcome of systemic lupus erythematosus (SLE) patients. In this retrospective study, which covered a 27-year period (1980-2006), 624 SLE patients referring to King Khalid University hospital, Riyadh were included. There were 566 females and 58 males (9.8:1) with a mean age of 34.3 (range 8-71) years and mean age at disease onset of 25.3 years (range 0.08-67). The mean disease duration was 9.3 years (range 0.3-30). The most common disease manifestations were hematological abnormalities (82.7%), arthritis (80.4%), and mucocutaneous symptoms (64.3%). The prevalence of malar rash was 47.9%, discoid rash 17.6%, photosensitivity 30.6%, oral ulcers 39.1%, serositis 27.4%, nephritis 47.9%, and neuropsychiatric manifestations 27.6%. Lymphopenia (40.3%), anti-Ro (53.1%), anti-La (26.6%), anti-Sm (41.6%), anticardiolipin IgG (49.7%), and IgM (33.5%) antibodies were highly prevalent. Antinuclear antibodies were detected in 99.7% and anti-DNA in 80.1% patients. Low C3 and C4 were observed in 45.4% and 42.2%, respectively. Therapy included oral steroids (96.2%), IV cyclophosphamide (34.1%) and azathioprine (32.1%) along with other drugs. Long-term remission was achieved in 82.4%, disease was active in 2.6%, renal failure occurred in 4.3% requiring dialysis, 6.7% lost follow up and 4.0% patients died. Infections (48%) and active SLE (36%) were the common causes of death. The 5- and 10-year patient survival rate was 98% and 97%, respectively. This study suggests that, in our patients, SLE manifests with features similar to SLE patients from other Arab countries and Caucasia. In comparison to Caucasians, higher prevalence of anti-Ro antibodies is observed in our study, in some Middle-Eastern and Asian countries; this may likely be due to inter-ethnic variation owing to genetic differences. Our 5-year patient survival rate was similar to that of western countries, while 10-year survival rate was better than that of most places.

摘要

我们的目的是研究系统性红斑狼疮(SLE)患者的人口统计学、临床、实验室特征、治疗方法及预后情况。在这项涵盖27年(1980 - 2006年)的回顾性研究中,纳入了利雅得国王哈立德大学医院的624例SLE患者。其中有566名女性和58名男性(9.8:1),平均年龄为34.3岁(范围8 - 71岁),疾病发病的平均年龄为25.3岁(范围0.08 - 67岁)。平均病程为9.3年(范围0.3 - 30年)。最常见的疾病表现为血液学异常(82.7%)、关节炎(80.4%)和黏膜皮肤症状(64.3%)。颊部红斑的患病率为47.9%,盘状红斑为17.6%,光过敏为30.6%,口腔溃疡为39.1%,浆膜炎为27.4%,肾炎为47.9%,神经精神表现为27.6%。淋巴细胞减少(40.3%)、抗Ro(53.1%)、抗La(26.6%)、抗Sm(41.6%)、抗心磷脂IgG(49.7%)和IgM(33.5%)抗体高度流行。99.7%的患者检测到抗核抗体,80.1%的患者检测到抗DNA抗体。分别有45.4%和42.2%的患者观察到低C3和低C4。治疗包括口服类固醇(96.2%)、静脉注射环磷酰胺(34.1%)和硫唑嘌呤(32.1%)以及其他药物。82.4%的患者实现了长期缓解,2.6%的患者疾病处于活动期,4.3%的患者发生肾衰竭需要透析,6.7%的患者失访,4.0%的患者死亡。感染(48%)和活动性SLE(36%)是常见的死亡原因。患者的5年和10年生存率分别为98%和97%。这项研究表明,在我们的患者中,SLE的表现与其他阿拉伯国家和高加索地区的SLE患者相似。与高加索人相比,在我们的研究以及一些中东和亚洲国家中,抗Ro抗体的患病率更高;这可能是由于遗传差异导致的种族间差异。我们的5年患者生存率与西方国家相似,而10年生存率优于大多数地区。

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