Li Guowei, Adachi Jonathan D, Cheng Ji, Thabane Lehana, Hudson Marie, Fritzler Marvin J, Lorenzi Steven, Baron Murray, Larché Maggie
Department of Clinical Epidemiology & Biostatistics, McMaster University, Hamilton; and St. Joseph's Healthcare Hamilton, ON, Canada.
St. Joseph's Healthcare Hamilton, ON; and Division of Rheumatology, Department of Medicine, McMaster University, Hamilton, ON, Canada.
Clin Exp Rheumatol. 2017 Sep-Oct;35 Suppl 106(4):56-60. Epub 2017 Jan 31.
Recent experimental evidence suggests that calcium channel blockers (CCBs) may have anti-fibrotic effects on liver and pulmonary fibrosis. We aimed to investigate whether use of CCBs was associated with the skin fibrosis in patients with systemic sclerosis (SSc).
Based on the 5-year follow-up data from the Canadian Scleroderma Research Group registry, we used the generalised estimating equations (GEE) model to assess the relationship between use of CCBs and the primary outcome of skin fibrosis measured by the modified Rodnan skin score (mRSS). We also used GEE models to explore the associations between use of CCBs and risk of secondary outcomes including digital ulcers, pulmonary fibrosis, calcinosis, and scleroderma renal crisis.
There were 1547 patients (1330 females) with SSc included in this study. Their mean age was 55.5 years and there were 606 patients taking CCBs at baseline. No significant difference in mRSS between the use versus non-use of CCBs was found in the multivariable analysis: mean difference = -0.19 (95% confidence interval: -0.62, 0.23), p-value = 0.37. Use of CCBs was not significantly related to risk of secondary outcomes, with an odds ratio (OR) of 1.13 for digital ulcers, 0.94 for pulmonary fibrosis, 0.90 for calcinosis and 1.69 for scleroderma renal crisis, respectively.
No significant associations between use of CCBs and skin fibrosis, digital ulcers, pulmonary fibrosis, calcinosis and scleroderma renal crisis were found in patients with SSc. More evidence from other well-designed studies would be required to confirm these findings.
近期实验证据表明,钙通道阻滞剂(CCB)可能对肝纤维化和肺纤维化具有抗纤维化作用。我们旨在研究CCB的使用是否与系统性硬化症(SSc)患者的皮肤纤维化相关。
基于加拿大硬皮病研究组登记处的5年随访数据,我们使用广义估计方程(GEE)模型评估CCB的使用与通过改良Rodnan皮肤评分(mRSS)测量的皮肤纤维化主要结局之间的关系。我们还使用GEE模型探讨CCB的使用与包括指端溃疡、肺纤维化、钙质沉着和硬皮病肾危象等次要结局风险之间的关联。
本研究纳入了1547例SSc患者(1330例女性)。他们的平均年龄为55.5岁,基线时有606例患者服用CCB。在多变量分析中,未发现使用CCB与未使用CCB之间的mRSS有显著差异:平均差异=-0.19(95%置信区间:-0.62,0.23),p值=0.37。CCB的使用与次要结局风险无显著相关性,指端溃疡的比值比(OR)为1.13,肺纤维化的OR为0.94,钙质沉着的OR为0.90,硬皮病肾危象的OR为1.69。
在SSc患者中,未发现CCB的使用与皮肤纤维化、指端溃疡、肺纤维化、钙质沉着和硬皮病肾危象之间存在显著关联。需要其他精心设计研究的更多证据来证实这些发现。