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慢性肾脏病中的软组织钙化——血管系统之外

Soft tissue calcifications in chronic kidney disease-beyond the vasculature.

作者信息

Fajol Abul, Faul Christian

机构信息

Section of Mineral Metabolism, Division of Nephrology, Department of Medicine, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

Pflugers Arch. 2025 Jun 5. doi: 10.1007/s00424-025-03098-0.

Abstract

Inappropriate mineralization of soft tissues, also called ectopic calcification, is a well-known pathology in chronic kidney disease (CKD) that is associated with increases in systemic phosphate levels. Vascular calcification is a major contributor to cardiovascular injury and high mortality rates in CKD patients. Therefore, most animal and human studies have focused on the vasculature when describing ectopic calcifications and on the pathologic actions of elevated phosphate on vascular smooth muscle cells in this process. The extent of calcifications within soft tissues beyond the vasculature is not well described, and the involvement of cell types other than vascular smooth muscle cells is not clear. Here we provide a summary of CKD-associated extravascular calcifications in various tissues, which includes the lung, the gastrointestinal system, the liver, the skin, and the brain. Since phosphate elevations and widespread ectopic calcifications do not only occur in the context of CKD, but also in rare genetic disorders that affect the regulators of phosphate metabolism, the cellular transporters of phosphate and the factors protecting from mineral depositions outside of bone, we also discuss these pathologic scenarios. We describe different types of ectopic calcification to flesh out common aspects as well as differences in the potential mechanisms and target cell types. We postulate that phosphate elevations might act in various ways and on various tissues, which together causes a wide spectrum of phosphate-induced pathologies in CKD.

摘要

软组织的异常矿化,也称为异位钙化,是慢性肾脏病(CKD)中一种众所周知的病理现象,与全身磷酸盐水平升高有关。血管钙化是CKD患者心血管损伤和高死亡率的主要原因。因此,大多数动物和人体研究在描述异位钙化时都集中在脉管系统,以及在此过程中磷酸盐升高对血管平滑肌细胞的病理作用。脉管系统以外软组织内的钙化程度描述得并不充分,除血管平滑肌细胞外其他细胞类型的参与情况也不清楚。在这里,我们总结了CKD相关的各种组织中的血管外钙化,包括肺、胃肠道系统、肝脏、皮肤和大脑。由于磷酸盐升高和广泛的异位钙化不仅发生在CKD的情况下,也发生在影响磷酸盐代谢调节因子、磷酸盐细胞转运体以及防止骨外矿物质沉积的因子的罕见遗传疾病中,我们也讨论了这些病理情况。我们描述了不同类型的异位钙化,以阐明潜在机制和靶细胞类型的共同方面以及差异。我们推测,磷酸盐升高可能以多种方式作用于各种组织,共同导致CKD中一系列由磷酸盐引起的病理状况。

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