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CKD-MBD: from the Pathogenesis to the Identification and Development of Potential Novel Therapeutic Targets

  • Kidney and Bone (I Salusky and T Nickolas, Section Editors)
  • Published:
Current Osteoporosis Reports Aims and scope Submit manuscript

Abstract

Purpose of Review

Although we have seen tremendous advances in the comprehension of CKD-MBD pathophysiology during the last few years, this was not accompanied by a significant change in mortality rate and quality of life. This review will address the traditional and updated pathophysiology of CKD-MBD along with the therapeutic limitations that affect CKD-MBD and proposed alternative treatment targets.

Recent Findings

An innovative concept brings the osteocyte to the center of CKD-MBD pathophysiology, in contrast to the traditional view of the skeleton as a target organ for disturbances in calcium, phosphate, parathyroid hormone, and vitamin D. Osteocytes, through the synthesis of FGF-23, sclerostin, among others, are able to interact with other organs, making bone an endocrine organ. Thus, osteocyte dysregulation might be an early event during the course of CKD.

Summary

This review will revisit general concepts on the pathophysiology of CKD-MBD and discuss new perspectives for its treatment.

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Authors and Affiliations

  1. Universidade Nove de Julho, UNINOVE, Rua Iperoig, 690 ap 121, São Paulo, SP, 05016-000, Brazil

    Rosilene Motta Elias, Maria Aparecida Dalboni & Rosa M. A. Moysés

  2. Nephrology Division, HCFCMUSP, Universidade de São Paulo, São Paulo, Brazil

    Rosilene Motta Elias & Rosa M. A. Moysés

  3. Nephrology Division, Universidade Estadual Paulista, UNESP, São Paulo, Brazil

    Ana Carolina E. Coelho

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  1. Rosilene Motta Elias
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  2. Maria Aparecida Dalboni
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  3. Ana Carolina E. Coelho
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  4. Rosa M. A. Moysés
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Correspondence to Rosa M. A. Moysés.

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Rosilene Motta Elias, Maria Aparecida Dalboni, Ana Carolina Coelho, and Rosa MA Moysés declare no conflict of interest.

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Elias, R.M., Dalboni, M.A., Coelho, A.C.E. et al. CKD-MBD: from the Pathogenesis to the Identification and Development of Potential Novel Therapeutic Targets. Curr Osteoporos Rep 16, 693–702 (2018). https://doi.org/10.1007/s11914-018-0486-0

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