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新诊断系统性红斑狼疮的脑磁共振成像

Brain magnetic resonance imaging in newly diagnosed systemic lupus erythematosus.

作者信息

Petri Michelle, Naqibuddin Mohammad, Carson Kathryn A, Wallace Daniel J, Weisman Michael H, Holliday Stephen L, Sampedro Margaret, Narayana Shalini, Fox Peter T, Franklin Crystal, Padilla Patricia A, Brey Robin L

机构信息

Johns Hopkins University, Baltimore, Maryland 21205, USA.

出版信息

J Rheumatol. 2008 Dec;35(12):2348-54. doi: 10.3899/jrheum.071010. Epub 2008 Sep 15.

Abstract

OBJECTIVE

We wished to determine the prevalence of cerebral atrophy and focal lesions in a cohort of patients with newly diagnosed systemic lupus erythematosus (SLE) and the association of these brain abnormalities with clinical characteristics.

METHODS

A total of 97 patients with SLE, within 9 months of diagnosis, with 4 or more American College of Rheumatology classification criteria, were enrolled. Brain magnetic resonance imaging was performed.

RESULTS

The patients were 97% female, mean age 38.1 (SD 12.2) years, education 15.1 (2.8) years; 59 Caucasian, 11 African American, 19 Hispanic, 5 Asian, and 3 other ethnicity. Cerebral atrophy was prevalent in 18% (95% CI 11%-27%): mild in 12%, moderate in 5%. Focal lesions were prevalent in 8% (95% CI 4%-16%): mild in 2%, moderate in 5%, severe in 1%. Patients with cerebral atrophy were more likely to have anxiety disorder (p = 0.04). Patients with focal lesions were more likely to be African American (p = 0.045) and had higher Safety of Estrogens in Lupus Erythematosus National Assessment SLEDAI scores (p = 0.02) and anti-dsDNA (p = 0.05).

CONCLUSION

In this population with newly diagnosed SLE, brain abnormalities were prevalent in 25% of patients. These findings suggest that the brain may be affected extremely early in the course of SLE, even before the clinical diagnosis of SLE is made. Followup of these patients is planned, to determine the reversibility or progression of these abnormalities and their association with and potential predictive value for subsequent neuropsychiatric SLE manifestations.

摘要

目的

我们希望确定一组新诊断的系统性红斑狼疮(SLE)患者中脑萎缩和局灶性病变的患病率,以及这些脑部异常与临床特征之间的关联。

方法

共纳入97例诊断后9个月内、符合4项或更多美国风湿病学会分类标准的SLE患者。进行了脑磁共振成像检查。

结果

患者中97%为女性,平均年龄38.1(标准差12.2)岁,受教育年限15.1(2.8)年;59例为白种人,11例为非裔美国人,19例为西班牙裔,5例为亚洲人,3例为其他种族。脑萎缩患病率为18%(95%可信区间11%-27%):轻度占12%,中度占5%。局灶性病变患病率为8%(95%可信区间4%-16%):轻度占2%,中度占5%,重度占1%。脑萎缩患者更易患焦虑症(p = 0.04)。局灶性病变患者更可能是非裔美国人(p = 0.045),且在狼疮性红斑国家评估SLEDAI评分(p = 0.02)和抗双链DNA水平(p = 0.05)更高。

结论

在这组新诊断的SLE患者中,25%的患者存在脑部异常。这些发现表明,在SLE病程中,脑部可能在极早期就受到影响,甚至在SLE临床诊断之前。计划对这些患者进行随访,以确定这些异常的可逆性或进展情况,以及它们与后续神经精神性SLE表现的关联和潜在预测价值。

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