系统性红斑狼疮患者血清维生素D水平与疾病活动性。

IF 1.3 Q3 MEDICINE, GENERAL & INTERNAL
Cureus Pub Date : 2025-10-05 eCollection Date: 2025-10-01 DOI:10.7759/cureus.93853
Aye Thin Zar Oo, Wint Thandar Oo, Kyaw L Tun, Aung K Myint, May Thu Zar Aye, Nandar E Khin, Khin Pyae Sone, Pyae Sonn
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引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,具有多种临床表现和疾病活动性。越来越多的证据表明,维生素D可能在免疫调节和疾病发病机制中发挥作用。本研究旨在调查曼德勒总医院SLE患者血清维生素D水平与疾病活动度之间的关系。方法:对60例SLE患者进行横断面研究。疾病活动性采用系统性狼疮活动性测量(SLAM)评分进行评估。在曼德勒国家卫生实验室使用酶联免疫吸附试验(ELISA)测量血清维生素D水平。根据SLAM评分将患者分为活动性和非活动性两组,并进行组间比较。结果:60例患者中,年龄以21 ~ 30岁为主(43.3%),平均±SD年龄25.77±7.98岁。女性患者居多(98.3%,男女比例59:1)。平均SLAM评分为9.25±2.94。常见的临床特征包括贫血(56.7%)、皮疹(33.3%)、粘膜溃疡(16.7%)、关节炎(16.7%)、浆液炎(11.7%)、血管炎(11.7%)和神经精神性狼疮(5%)。活动性疾病患者血清维生素D水平(12.2±1.36 ng/mL)明显低于非活动性疾病患者(26.1±10.22 ng/mL, t = 5.55, p < 0.0001)。SLAM评分与维生素D水平之间存在中度负相关(Pearson’s r = -0.51, p < 0.0001),表明维生素D水平降低与疾病活动性升高之间存在有临床意义的关联。结论:本研究表明血清维生素D水平与SLE疾病活动性之间存在中度反比关系。这些发现表明维生素D可能作为疾病监测的潜在生物标志物。然而,由于横断面设计和相对较小的样本量,无法建立因果关系。建议进行进一步的纵向研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum Vitamin D Level and Disease Activity in Patients With Systemic Lupus Erythematosus.

Introduction: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with variable clinical manifestations and disease activity. Emerging evidence suggests that vitamin D may play a role in immune regulation and disease pathogenesis. This study aimed to investigate the association between serum vitamin D levels and disease activity in patients with SLE at Mandalay General Hospital.

Methods: A cross-sectional study was conducted involving 60 patients diagnosed with SLE. Disease activity was assessed using the Systemic Lupus Activity Measure (SLAM) score. Serum vitamin D levels were measured using the enzyme-linked immunosorbent assay (ELISA) at the National Health Laboratory, Mandalay. Patients were categorized into active and inactive disease groups based on SLAM scores, and intergroup comparisons were made.

Results: Among the 60 patients, the majority (43.3%) were aged 21-30 years, with a mean ± SD age of 25.77 ± 7.98 years. Female patients predominated (98.3%; female-to-male ratio 59:1). The mean SLAM score was 9.25 ± 2.94. Common clinical features included anaemia (56.7%), skin rash (33.3%), mucosal ulcers (16.7%), arthritis (16.7%), serositis (11.7%), vasculitis (11.7%), and neuropsychiatric lupus (5%). Patients with active disease had significantly lower serum vitamin D levels (12.2 ± 1.36 ng/mL) compared to those with inactive disease (26.1 ± 10.22 ng/mL; t = 5.55, p < 0.0001). A moderate inverse correlation was observed between SLAM scores and vitamin D levels (Pearson's r = -0.51, p < 0.0001), suggesting a clinically meaningful association between lower vitamin D levels and higher disease activity.

Conclusion: This study demonstrates a moderate inverse relationship between serum vitamin D levels and SLE disease activity. These findings suggest that vitamin D may serve as a potential biomarker for disease monitoring. However, due to the cross-sectional design and relatively small sample size, causality cannot be established. Further longitudinal studies are recommended.

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