Department of Periodontology, Academic Centre for Dentistry Amsterdam (ACTA), University of Amsterdam and Vrije Universiteit Amsterdam, Gustav Mahlerlaan 3004, 1081 LA Amsterdam, The Netherlands.
Center for Bone Quality Department of Internal Medicine division of Endocrinology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Int J Mol Sci. 2021 Feb 11;22(4):1810. doi: 10.3390/ijms22041810.
Pycnodysostosis, a rare autosomal recessive skeletal dysplasia, is caused by a deficiency of cathepsin K. Patients have impaired bone resorption in the presence of normal or increased numbers of multinucleated, but dysfunctional, osteoclasts. Cathepsin K degrades collagen type I and generates N-telopeptide (NTX) and the C-telopeptide (CTX) that can be quantified. Levels of these telopeptides are increased in lactating women and are associated with increased bone resorption. Nothing is known about the consequences of cathepsin K deficiency in lactating women. Here we present for the first time normalized blood and CTX measurements in a patient with pycnodysostosis, exclusively related to the lactation period. In vitro studies using osteoclasts derived from blood monocytes during lactation and after weaning further show consistent bone resorption before and after lactation. Increased expression of cathepsins L and S in osteoclasts derived from the lactating patient suggests that other proteinases could compensate for the lack of cathepsin K during the lactation period of pycnodysostosis patients.
原发性骨脆症是一种罕见的常染色体隐性骨骼发育不良,由组织蛋白酶 K 缺乏引起。患者在存在正常或增加数量的多核、但功能失调的破骨细胞的情况下,骨吸收受损。组织蛋白酶 K 降解 I 型胶原并产生 N-末端肽 (NTX) 和 C-末端肽 (CTX),这些肽可以被定量。这些末端肽的水平在哺乳期妇女中增加,与骨吸收增加有关。目前尚不清楚原发性骨脆症患者在哺乳期时组织蛋白酶 K 缺乏的后果。在这里,我们首次在一名原发性骨脆症患者中报告了与哺乳期相关的正常血液和 CTX 测量结果。在哺乳期和断奶后从血液单核细胞中获得的破骨细胞进行的体外研究进一步表明,在哺乳期前后骨吸收一致。来自哺乳期患者的破骨细胞中组织蛋白酶 L 和 S 的表达增加表明,在原发性骨脆症患者的哺乳期期间,其他蛋白酶可能会代偿组织蛋白酶 K 的缺乏。