Departments of Dermatology and Cutaneous Biology, and Biochemistry and Molecular Biology, Jefferson Medical College, and Jefferson Institute of Molecular Medicine, Thomas Jefferson University, 233 South 10th Street, Suite 450 BLSB, Philadelphia, PA, 19107, USA.
J Mol Med (Berl). 2013 Oct;91(10):1177-84. doi: 10.1007/s00109-013-1066-5. Epub 2013 Jun 27.
Pseudoxanthoma elasticum (PXE), a multisystem heritable disorder with aberrant mineralization of arterial blood vessels, is caused by mutations in the ABCC6 gene. Previous studies have suggested that carriers of the ABCC6 mutations, particularly of p.R1141X, are at increased risk for coronary artery disease. In this study, we used Abcc6 (tm1Jfk) knock-out mice to determine the serum lipid profiles and examine the effects of atorvastatin on the aberrant mineralization in this model of PXE. First, serum lipid profiles at 12 weeks of age, after overnight fasting, revealed a statistically significant increase in total cholesterol and triglyceride levels in Abcc6 (tm1Jfk) mice compared to their wild-type littermates. Placing these mice at 4 weeks of age for 20 weeks on atorvastatin, either 0.01 % or 0.04 % of the diet (low statin and high statin groups, respectively), reduced the total triglyceride and cholesterol levels, which was accompanied with significantly reduced mineralization of the dermal sheath of vibrissae, a biomarker of the aberrant mineralization process in these mice. However, if the mice were placed on atorvastatin for 12 weeks at 12 weeks of age, at which time point significant mineralization had already taken place, no difference in the amount of mineralization was noted. These observations suggest that statins, particularly atorvastatin, can prevent, but not reverse, aberrant mineralization in this mouse model of PXE. For a clinical perspective, a survey of 1,747 patients with PXE was conducted regarding their present or past use of statins. The results indicated that about one third of all PXE patients are currently or have previously been on cholesterol-lowering drugs. Thus, a sizable number of patients with PXE could be subject to modulation of their mineralization processes by concomitant statin treatment.
The Abcc6 (-/-) mice serve as a model system for PXE, an ectopic mineralization disorder Abcc6 (-/-) mice were shown to have elevated serum cholesterol and triglyceride levels Feeding of the Abcc6 (-/-) mice with atorvastatin prevented connective tissue mineralization A third of patients with PXE was found to be on cholesterol-lowering therapy Atorvastatin may potentially be beneficial for patients with PXE.
弹性假黄瘤(PXE)是一种多系统遗传性疾病,其特征为动脉血管的异常矿化,由 ABCC6 基因突变引起。先前的研究表明,ABCC6 基因突变的携带者,特别是 p.R1141X 突变,患冠状动脉疾病的风险增加。在这项研究中,我们使用 Abcc6(tm1Jfk)敲除小鼠来确定血清脂质谱,并研究阿托伐他汀对这种 PXE 模型中异常矿化的影响。首先,在禁食一夜后 12 周龄时,Abcc6(tm1Jfk)小鼠的总胆固醇和甘油三酯水平显著升高。将这些小鼠在 4 周龄时置于阿托伐他汀饮食中 20 周,分别为 0.01%或 0.04%(低他汀组和高他汀组),降低了总甘油三酯和胆固醇水平,同时显著减少了触须真皮鞘的矿化,这是这些小鼠异常矿化过程的生物标志物。然而,如果在 12 周龄时将小鼠置于阿托伐他汀治疗 12 周,此时已经发生了明显的矿化,则没有注意到矿化量的差异。这些观察结果表明,他汀类药物,特别是阿托伐他汀,可以预防,但不能逆转,这种 PXE 小鼠模型中的异常矿化。从临床角度来看,对 1747 例 PXE 患者进行了一项关于他们目前或过去使用他汀类药物的调查。结果表明,大约三分之一的所有 PXE 患者目前或以前都在服用降胆固醇药物。因此,相当数量的 PXE 患者可能会受到伴随的他汀类药物治疗对其矿化过程的调节。
Abcc6(-/-)小鼠可作为 PXE 的模型系统,这是一种异位矿化疾病 Abcc6(-/-)小鼠的血清胆固醇和甘油三酯水平升高 用阿托伐他汀喂养 Abcc6(-/-)小鼠可防止结缔组织矿化 三分之一的 PXE 患者正在接受降胆固醇治疗 阿托伐他汀可能对 PXE 患者有益。