Li Qiaoli, Sundberg John P, Levine Michael A, Terry Sharon F, Uitto Jouni
a Department of Dermatology and Cutaneous Biology; Sidney Kimmel Medical College ; Thomas Jefferson University ; Philadelphia , PA USA.
Cell Cycle. 2015;14(7):1082-9. doi: 10.1080/15384101.2015.1007809.
Pseudoxanthoma elasticum (PXE) and generalized arterial calcification of infancy (GACI) are heritable ectopic mineralization disorders. Most cases of PXE and many cases of GACI harbor mutations in the ABCC6 gene. There is no effective treatment for these disorders. We explored the potential efficacy of bisphosphonates to prevent ectopic calcification caused by ABCC6 mutations by feeding Abcc6(-/-) mice with diet containing etidronate disodium (ETD) or alendronate sodium trihydrate (AST) in quantities corresponding to 1x, 5x, or 12x of the doses used to treat osteoporosis in humans. The mice were placed on diet at 4 weeks of age, and the degree of mineralization was assessed at 12 weeks by quantitation of the calcium deposits in the dermal sheath of vibrissae, a progressive biomarker of the mineralization, by computerized morphometry of histopathologic sections and by direct chemical assay of calcium. We found that ETD, but not AST, at the 12x dosage, significantly reduced mineralization, suggesting that selected bisphosphonates may be helpful for prevention of mineral deposits in PXE and GACI caused by mutations in the ABCC6 gene, when combined with careful monitoring of efficacy and potential side-effects.
弹性假黄瘤(PXE)和婴儿期全身性动脉钙化(GACI)是遗传性异位矿化疾病。大多数PXE病例以及许多GACI病例在ABCC6基因中存在突变。这些疾病尚无有效治疗方法。我们通过给Abcc6(-/-)小鼠喂食含有依替膦酸二钠(ETD)或阿仑膦酸钠三水合物(AST)的饮食,剂量相当于用于治疗人类骨质疏松症剂量的1倍、5倍或12倍,来探索双膦酸盐预防由ABCC6突变引起的异位钙化的潜在疗效。小鼠在4周龄时开始喂食该饮食,并在12周时通过对触须真皮鞘中钙沉积进行定量(矿化的一种进展性生物标志物)、对组织病理学切片进行计算机形态测量以及直接化学测定钙来评估矿化程度。我们发现,12倍剂量的ETD而非AST能显著减少矿化,这表明当结合仔细监测疗效和潜在副作用时,选定的双膦酸盐可能有助于预防由ABCC6基因突变导致的PXE和GACI中的矿物质沉积。