Contemporary kidney transplantation has a limited impact on bone microarchitecture.

2D, two-dimensional 3D, three-dimensional BALP, bone-specific alkaline phosphatase BMD, bone mineral density Bone density Bone histomorphometry CKD, chronic kidney disease Chronic kidney disease – mineral and bone disorder DXA, dual-energy x-ray absorptiometry HRpQCT, high-resolution peripheral quantitative computed tomography Kidney transplantation Osteoporosis PINP, intact pro-collagen type I N-terminal pro-peptide PTH, parathyroid hormone TMV, Turnover, mineralization, and volume TRAP5b, tartrate resistant acid phosphatase type 5b X-Ray Microtomography eGFR, estimated glomerular filtration rate μCT, micro computed tomography

Journal

Bone reports
ISSN: 2352-1872
Titre abrégé: Bone Rep
Pays: United States
ID NLM: 101646176

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 19 01 2022
accepted: 03 02 2022
entrez: 24 2 2022
pubmed: 25 2 2022
medline: 25 2 2022
Statut: epublish

Résumé

Bone microarchitecture is an important component of bone quality and disturbances may reduce bone strength and resistance to trauma. Kidney transplant recipients have an excess risk of fractures, and bone loss affecting both trabecular and cortical bone compartments have been demonstrated after kidney transplantation. The primary aim of this study was to investigate the impact of kidney transplantation on trabecular and cortical bone microarchitecture, assessed by histomorphometry and micro computed tomography (μCT). Iliac crest bone biopsies, analyzed by bone histomorphometry and μCT, were performed at time of kidney transplantation and 12 months post-transplantation in an unselected cohort of 30 patients. Biochemical markers of mineral metabolism and bone turnover were measured at both time-points. At 12 months post-transplantation, bone turnover was low in 5 (17%) and normal in 25 (83%) patients. By histomorphometry, bone remodeling normalized, with decreases in eroded perimeters (4.0 to 2.1%,

Identifiants

pubmed: 35198658
doi: 10.1016/j.bonr.2022.101172
pii: S2352-1872(22)00007-9
pmc: PMC8851083
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101172

Informations de copyright

© 2022 The Authors. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

PE reports personal fees from Amgen and Vifor-FMC. Remaining authors have no conflicts of interest to declare.

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Auteurs

Catarina Meng (C)

Department of Microbiology, Immunology and Transplantation, Nephrology and Renal Transplantation Research Group, KU Leuven, Leuven, Belgium.
Faculty of Medicine, University of Porto, Porto, Portugal.

Hanne Skou Jørgensen (HS)

Department of Microbiology, Immunology and Transplantation, Nephrology and Renal Transplantation Research Group, KU Leuven, Leuven, Belgium.
Department of Kidney Diseases, Aarhus University Hospital, Aarhus, Denmark.

Lieve Verlinden (L)

Department of Chronic Diseases and Metabolism, Laboratory of Clinical and Experiment Endocrinology, KU Leuven, Leuven, Belgium.

Nathalie Bravenboer (N)

Department of Clinical Chemistry, Amsterdam University Medical Center, Vrije Universiteit, Amsterdam Movement Sciences, Amsterdam, the Netherlands.

Henriette de Loor (H)

Department of Microbiology, Immunology and Transplantation, Nephrology and Renal Transplantation Research Group, KU Leuven, Leuven, Belgium.

Patrick C D'Haese (PC)

Laboratory of Pathophysiology, University of Antwerp, Wilrijk, Belgium.

Geert Carmeliet (G)

Department of Chronic Diseases and Metabolism, Laboratory of Clinical and Experiment Endocrinology, KU Leuven, Leuven, Belgium.

Pieter Evenepoel (P)

Department of Microbiology, Immunology and Transplantation, Nephrology and Renal Transplantation Research Group, KU Leuven, Leuven, Belgium.
Department of Nephrology and Renal Transplantation, University Hospitals Leuven, Leuven, Belgium.

Classifications MeSH