Peschken C A, Esdaile J M
Department of Medicine, University of Manitoba, Winnipeg, Canada.
J Rheumatol. 2000 Aug;27(8):1884-91.
To evaluate the prevalence, disease course, and survival of patients with systemic lupus erythematosus (SLE) in a population of over 120,000 North American Indians (NAI), and contrast the results to those in the non-Indian population.
The regional arthritis center database and the medical records of all rheumatologists, hematologists, nephrologists, and general internists with > 1 patient with SLE were searched for cases of SLE diagnosed between 1980 and 1996. A random survey of 20% of family physicians serving this population suggested that > 85% of all SLE cases were identified. Demographics, SLE Disease Activity Index (SLEDAI) scores, Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) damage scores. clinical manifestations, and therapy for NAI were contrasted with the results in Caucasians (CAUC).
We identified 257 cases meeting the ACR criteria for SLE diagnosed between 1980 and 1996. There were 49 NAI cases, resulting in a prevalence of 42.3/100,000, compared to a prevalence of 20.6/100,000 for the remainder of the population. NAI patients were younger at diagnosis, had higher SLEDAI scores at diagnosis, and had more frequent vasculitis, proteinuria and cellular casts. There were no treatment differences at diagnosis or at 2 years, but NAI patients were significantly more likely to receive treatment with prednisone or immunosuppressives at the last clinic visit. The NAI patients had similar damage scores at diagnosis, but significantly higher scores at 2 years and at the last clinic visit. NAI ethnicity increased the likelihood of death more than 4-fold.
The prevalence of SLE was increased 2-fold in the NAI population. NAI patients had higher SLEDAI scores at diagnosis and more frequent vasculitis and renal involvement, required more treatment later in the disease course, accumulated more damage following diagnosis, and had increased fatality.
评估北美印第安人(NAI)超过120,000人群中系统性红斑狼疮(SLE)患者的患病率、病程及生存率,并将结果与非印第安人群进行对比。
检索地区关节炎中心数据库以及所有诊治过1例以上SLE患者的风湿病学家、血液学家、肾脏病学家和普通内科医生的病历,查找1980年至1996年间确诊的SLE病例。对服务于该人群的20%家庭医生进行随机调查,结果显示已识别出超过85%的SLE病例。将NAI患者的人口统计学资料、SLE疾病活动指数(SLEDAI)评分、系统性红斑狼疮国际协作诊所/美国风湿病学会(SLICC/ACR)损伤评分、临床表现及治疗情况与高加索人(CAUC)的结果进行对比。
我们识别出1980年至1996年间确诊的符合ACR标准的257例SLE病例。其中有49例NAI患者,患病率为42.3/10万,而其余人群的患病率为20.6/10万。NAI患者诊断时年龄更小,诊断时SLEDAI评分更高,血管炎、蛋白尿和细胞管型更常见。诊断时及2年时治疗情况无差异,但在最后一次门诊就诊时,NAI患者接受泼尼松或免疫抑制剂治疗的可能性显著更高。NAI患者诊断时损伤评分相似,但2年时及最后一次门诊就诊时评分显著更高。NAI族裔使死亡可能性增加4倍多。
NAI人群中SLE患病率增加了2倍。NAI患者诊断时SLEDAI评分更高,血管炎和肾脏受累更常见,病程后期需要更多治疗,诊断后累积损伤更多,且死亡率增加。