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Vitamin D levels in systemic sclerosis patients: a meta-analysis
Lin An1, Ming-Hui Sun1, Feng Chen1
1Department of Dermatology, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
Systemic sclerosis (SSc) patients have lower vitamin D levels than healthy individuals, with diffused-type SSc showing even lower levels. However, vitamin D deficiency does not appear to worsen SSc clinical features.
Area of Science:
- Endocrinology
- Rheumatology
- Nutritional Science
Background:
- Systemic sclerosis (SSc) is an autoimmune disease characterized by fibrosis and vascular abnormalities.
- Vitamin D plays a crucial role in immune function and bone metabolism, and its deficiency is implicated in various autoimmune conditions.
Purpose of the Study:
- To meta-analyze the association between vitamin D levels and systemic sclerosis.
- To compare vitamin D levels between SSc patients and healthy controls.
- To investigate differences in vitamin D levels between diffused- and limited-type SSc and their correlation with clinical manifestations.
Main Methods:
- A comprehensive literature search was conducted up to June 12, 2017.
- Pooled standardized mean difference (SMD) was calculated to compare vitamin D levels.
- Pooled risk ratios (RRs) with 95% confidence intervals (CIs) assessed the impact of vitamin D on clinical characteristics.
Main Results:
- Six studies involving 554 SSc patients and 321 controls revealed significantly lower vitamin D levels in SSc patients (SMD = -8.72 ng/mL).
- Diffused-type SSc patients had lower vitamin D levels compared to limited-type SSc patients (SMD = -4.71 ng/mL).
- No significant association was found between vitamin D levels and SSc severity markers like Rodnan score, pulmonary pressure, gastrointestinal ulcers, or pulmonary involvement.
Conclusions:
- Systemic sclerosis patients exhibit reduced vitamin D levels compared to healthy controls.
- Vitamin D deficiency is more pronounced in diffused-type SSc.
- The extent of vitamin D deficit does not correlate with the severity of clinical features in SSc, suggesting it may not be a primary driver of disease progression.
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