» Articles » PMID: 33388898

Inflammation, Oxidative Stress, and Bone in Chronic Kidney Disease in the Osteoimmunology Era

Overview
Specialty Pathology
Date 2021 Jan 3
PMID 33388898
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Bone is not only a mineralized and apparently non-vital structure that provides support for locomotion and protection to inner organs. An increasing number of studies are unveiling new biologic functions and connections to other systems, giving the rise to new fields of research, such as osteoimmunology. The bone marrow niche, a new entity in bone physiology, seems to represent the site where a complex crosstalk between bone and immune/inflammatory responses takes place. An impressive interplay with the immune system is realized in bone marrow, with reciprocal influences between bone cells and haematopoietic cells. In this way, systemic chronic inflammatory diseases realize a crosstalk with bone, resulting in bone disease. Thus, pathogenetic links between chronic kidney disease-mineral bone disorders and osteoporosis, cardiovascular disease, and ageing are common. The aim of this narrative review is to provide a general view of the progresses in the field of bone research and their potential clinical implications, with emphasis on the links with inflammation and the connections to osteoimmunology and chemokines.

Citing Articles

Prediction of Osteoporotic Hip Fracture Outcome: Comparative Accuracy of 27 Immune-Inflammatory-Metabolic Markers and Related Conceptual Issues.

Fisher A, Fisher L, Srikusalanukul W J Clin Med. 2024; 13(13).

PMID: 38999533 PMC: 11242639. DOI: 10.3390/jcm13133969.


The relationship between dietary inflammatory index and osteoporosis among chronic kidney disease population.

Meng X, Sha W, Lou X, Chen J Sci Rep. 2023; 13(1):22867.

PMID: 38129528 PMC: 10739725. DOI: 10.1038/s41598-023-49824-5.


The Impact of Tannic Acid Consumption on Bone Mineralization.

Winiarska-Mieczan A, Muszynski S, Tomaszewska E, Kwiecien M, Donaldson J, Tomczyk-Warunek A Metabolites. 2023; 13(10).

PMID: 37887397 PMC: 10609055. DOI: 10.3390/metabo13101072.


Bone marrow-derived exosomes promote inflammation and osteoclast differentiation in high-turnover renal osteodystrophy.

Fu R, Meng K, Zhang R, Du X, Jiao J Ren Fail. 2023; 45(2):2264396.

PMID: 37870853 PMC: 11001343. DOI: 10.1080/0886022X.2023.2264396.


Transcription factor HNF4α2 promotes osteogenesis and prevents bone abnormalities in mice with renal osteodystrophy.

Martinez-Calle M, Courbon G, Hunt-Tobey B, Francis C, Spindler J, Wang X J Clin Invest. 2023; 133(11).

PMID: 37079387 PMC: 10231994. DOI: 10.1172/JCI159928.


References
1.
Ha C, Park S, Choi Y, Jeong J, Oh C, Bae K . Activation of Nrf2 by dimethyl fumarate improves vascular calcification. Vascul Pharmacol. 2014; 63(1):29-36. DOI: 10.1016/j.vph.2014.06.007. View

2.
Husain K, Ferder L, Mizobuchi M, Finch J, Slatopolsky E . Combination therapy with paricalcitol and enalapril ameliorates cardiac oxidative injury in uremic rats. Am J Nephrol. 2008; 29(5):465-72. DOI: 10.1159/000178251. View

3.
Kooman J, Kotanko P, Schols A, Shiels P, Stenvinkel P . Chronic kidney disease and premature ageing. Nat Rev Nephrol. 2014; 10(12):732-42. DOI: 10.1038/nrneph.2014.185. View

4.
Arefin S, Buchanan S, Hobson S, Steinmetz J, Alsalhi S, Shiels P . Nrf2 in early vascular ageing: Calcification, senescence and therapy. Clin Chim Acta. 2020; 505:108-118. DOI: 10.1016/j.cca.2020.02.026. View

5.
Singh S, Grabner A, Yanucil C, Schramm K, Czaya B, Krick S . Fibroblast growth factor 23 directly targets hepatocytes to promote inflammation in chronic kidney disease. Kidney Int. 2016; 90(5):985-996. PMC: 5065745. DOI: 10.1016/j.kint.2016.05.019. View