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系统性红斑狼疮患者发生骨坏死的预测因素:一项前瞻性队列研究。

Predictors of Osteonecrosis in Systemic Lupus Erythematosus: A Prospective Cohort Study.

机构信息

Johns Hopkins University School of Medicine, Baltimore, Maryland.

出版信息

Arthritis Care Res (Hoboken). 2022 Jul;74(7):1122-1132. doi: 10.1002/acr.24541. Epub 2022 Apr 20.

Abstract

OBJECTIVE

We aimed at determining the predictors of osteonecrosis (ON) in a longitudinal lupus cohort.

METHODS

Data were reviewed from the initiation of the cohort in 1987 until October 2019. In total, 2,428 patients were included in the analysis based on 224,295 person-months of follow-up. We used pooled logistic regression to assess the relationship between risk factors and rates of ON events. After identifying a set of variables related to ON incidence, we fit a final multivariable model to identify the most important risk factors for incident ON.

RESULTS

In 18,691 person-years of follow-up after cohort entry, 122 incident ON events were observed (rate = 6.5/1,000 person-years). In the multivariable analysis, African American patients were at twice the risk for ON compared to White patients. Male patients and smokers had an increased risk for ON of ~80% and 50% compared to female patients and nonsmokers, respectively. For every 10-year increase in the age at diagnosis, there was a 20% reduced risk for ON. Patients diagnosed after the 1990s had a 50% reduced risk of ON compared to those diagnosed before the 1990s. A highest daily dosage of prednisone of 40 mg or higher, even when administered for a month or less, significantly increased the risk of ON. Use of pulse methylprednisolone or intramuscular triamcinolone was not associated with an increased risk of ON.

CONCLUSION

African American patients with systemic lupus erythematosus are at double the risk of experiencing ON compared to White patients. Oral prednisone at 20-39 mg for more than 1 month, or 40 mg daily for even 1 month, at any point in the disease course, remained the most important glucocorticoid predictor of ON.

摘要

目的

我们旨在确定狼疮队列的纵向研究中骨坏死(ON)的预测因素。

方法

对该队列于 1987 年开始至 2019 年 10 月的数据进行了回顾。总共纳入了 2428 例患者,基于 224295 人月的随访,对其进行了分析。我们使用汇总逻辑回归来评估危险因素与 ON 事件发生率之间的关系。在确定与 ON 发病相关的一组变量后,我们拟合了一个最终的多变量模型,以确定发生 ON 的最重要危险因素。

结果

在队列进入后 18691 人年的随访中,观察到 122 例新发 ON 事件(发生率为 6.5/1000 人年)。在多变量分析中,与白人患者相比,非裔美国患者发生 ON 的风险是其两倍。与女性患者和非吸烟者相比,男性患者和吸烟者发生 ON 的风险分别增加了约 80%和 50%。诊断年龄每增加 10 岁,ON 的风险降低 20%。与 1990 年代前诊断的患者相比,1990 年代后诊断的患者发生 ON 的风险降低了 50%。即使泼尼松的最高日剂量为 40mg 或更低,且使用时间为 1 个月或更短,也会显著增加发生 ON 的风险。使用脉冲甲基强的松龙或肌内曲安奈德与发生 ON 的风险增加无关。

结论

与白人患者相比,系统性红斑狼疮的非裔美国患者发生 ON 的风险增加了一倍。在疾病过程中的任何时候,泼尼松的剂量为 20-39mg,持续使用 1 个月以上,或剂量为 40mg,每日使用,即使使用 1 个月,仍是发生 ON 的最重要的糖皮质激素预测因素。

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