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泼尼松低或中剂量对系统性红斑狼疮患者胰岛素抵抗的影响。

Effects of low or medium-dose of prednisone on insulin resistance in patients with systemic lupus erythematosus.

机构信息

Systemic Autoimmune Diseases Unit, Internal Medicine Service, Virgen de las Nieves University Hospital, Granada, Spain.

出版信息

Clin Exp Rheumatol. 2010 Jul-Aug;28(4):483-9. Epub 2010 Aug 30.

PMID:20497628
Abstract

OBJECTIVES

To determine the effect of low (< or =7.5 mg/day; LD-PRD group) or medium (>7.5 mg/day; MD-PRD group) doses of prednisone over the past 4 months on insulin levels and insulin resistance (IR) in SLE patients.

METHODS

SLE patients were categorised in prednisone non-users (No PRD) (n=41), LD-PRD (n=71) and MD-PRD (n=16) users. We compared insulin levels, presence of increased IR using homeostasis model assessment (HOMA index), metabolic syndrome (MetS), and other clinical, metabolic and inflammatory parameters in the 3 groups. A Spearman's rho test was used to identify independent associations between daily prednisone dose, HOMA index and insulin levels and other parameters, after adjusting for confounders.

RESULTS

No differences in increased IR, HOMA index and insulin between No PRD and LD-PRD were found. In contrast, the MD-PRD group was younger (p=0.001) and had higher insulin (p=0.015), higher HOMA index (p=0.019) and increased IR (OR 5.8, 95% CI (1.7-20), p=0.007) in comparison with the LD-PRD group. The HOMA index strongly correlated with body mass index (BMI) (rs=0.460, p<0.001) but not with clinical activity or inflammatory state after adjusting for confounders. Prednisone dose correlated with the HOMA index and insulin but not with inflammatory parameters (erythrocyte sedimentation rate p=0.075) after adjusting for confounder.

CONCLUSIONS

Daily medium-dose prednisone use (>7.5 mg/d) but not low-dose (< or =7.5 mg/d) use increased insulin levels and IR in SLE, which may contribute to increased CV risk experienced by these patients.

摘要

目的

确定过去 4 个月中低剂量(≤7.5 毫克/天;LD-PRD 组)或中剂量(>7.5 毫克/天;MD-PRD 组)泼尼松对 SLE 患者胰岛素水平和胰岛素抵抗(IR)的影响。

方法

将 SLE 患者分为泼尼松未使用者(No PRD)(n=41)、LD-PRD(n=71)和 MD-PRD(n=16)使用者。我们比较了 3 组患者的胰岛素水平、使用稳态模型评估(HOMA 指数)的 IR 升高情况、代谢综合征(MetS)以及其他临床、代谢和炎症参数。在调整混杂因素后,使用 Spearman 秩相关检验来确定每日泼尼松剂量、HOMA 指数和胰岛素水平与其他参数之间的独立关联。

结果

No PRD 和 LD-PRD 组之间的 IR 升高、HOMA 指数和胰岛素水平无差异。相比之下,MD-PRD 组更年轻(p=0.001),胰岛素(p=0.015)、HOMA 指数(p=0.019)和 IR 更高(OR 5.8,95%CI(1.7-20),p=0.007)与 LD-PRD 组相比。在调整混杂因素后,HOMA 指数与体重指数(BMI)强烈相关(rs=0.460,p<0.001),但与临床活动或炎症状态无关。在调整混杂因素后,泼尼松剂量与 HOMA 指数和胰岛素相关,但与炎症参数(红细胞沉降率 p=0.075)无关。

结论

每日中剂量(>7.5 毫克/天)泼尼松的使用而不是低剂量(≤7.5 毫克/天)的使用增加了 SLE 患者的胰岛素水平和 IR,这可能导致这些患者的 CV 风险增加。

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