Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Aug 6;23(1):34.
doi: 10.1007/s11914-025-00928-z.

A Fragile Phosphate/Pyrophosphate Balance: From Essential Mineralization to Rare Calcifying Diseases

Affiliations
Review

A Fragile Phosphate/Pyrophosphate Balance: From Essential Mineralization to Rare Calcifying Diseases

Elodie Baptista et al. Curr Osteoporos Rep. .

Abstract

Purpose of review: Calcification, the deposition of phosphate-calcium crystals, is essential for the development and function of mineralized tissues. When dysregulated, it can cause harmful effects. This review focuses on the critical role of the balance between phosphate (Pi) and pyrophosphate (PPi) in maintaining healthy mineralization and explains how disruptions in this balance contribute to rare calcifying disorders.

Recent findings: Studies have identified key regulators of PPi production and Pi generation. Recent research on rare calcifying diseases and animal models has revealed how Pi/PPi imbalances lead to ectopic calcification in soft tissues, driving disease progression. The balance of Pi/PPi is vital for bone health and preventing pathological calcification. Disruptions in this equilibrium contribute to rare diseases. Understanding these mechanisms, supported by preclinical models, opens potential therapeutic avenues to restore balance and mitigate the impact of these diseases.

Keywords: Phosphate; Pyrophosphate, mineralization, ectopic calcification; Rare diseases; Therapeutic strategy.

PubMed Disclaimer

Conflict of interest statement

Declarations. Competing Interests: The authors declare no competing interests.

Similar articles

References

    1. Reznikov N, Hoac B, Buss DJ, Addison WN, Barros NMT, McKee MD. Biological stenciling of mineralization in the skeleton: local enzymatic removal of inhibitors in the extracellular matrix. Bone. 2020;138:115447. - PubMed
    1. McKee MD, Buss DJ, Reznikov N. Mineral tessellation in bone and the stenciling principle for extracellular matrix mineralization. J Struct Biol. 2022;214:107823. - PubMed
    1. Zhang J, Ma Z, Yan K, Wang Y, Yang Y, Wu X. Matrix Gla protein promotes the bone formation by up-regulating Wnt/β-Catenin signaling pathway. Front Endocrinol. 2019;10:891.
    1. Zhang Y, Zhao L, Wang N, Li J, He F, Li X, et al. Unexpected role of matrix Gla protein in osteoclasts: inhibiting osteoclast differentiation and bone resorption. Mol Cell Biol. 2019;39:e00012–19. - PubMed - PMC
    1. Si J, Wang C, Zhang D, Wang B, Zhou Y. Osteopontin in bone metabolism and bone diseases. Med Sci Monit. 2020;26:e919159.

LinkOut - more resources