Microarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case Series
It is challenging to study heterotopic ossification (HO) in patients with fibrodysplasia ossificans progressiva (FOP) due to the contraindication of invasive techniques (i.e., bone biopsies), which can trigger flare-ups. The aim of this case study was to assess mature HO at the microarchitectural le...
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Frontiers Media S.A.
2021-03-01
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Online Access: | https://www.frontiersin.org/articles/10.3389/fcell.2021.627784/full |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Esmée Botman Melissa S. A. M. Bevers Melissa S. A. M. Bevers Melissa S. A. M. Bevers Caroline E. Wyers Caroline E. Wyers Caroline E. Wyers Bert van Rietbergen Bert van Rietbergen Bernd P. Teunissen Pieter G. Raijmakers Jan Coen Netelenbos Joop P. van den Bergh Joop P. van den Bergh Joop P. van den Bergh Joop P. van den Bergh Elisabeth M. W. Eekhoff |
spellingShingle |
Esmée Botman Melissa S. A. M. Bevers Melissa S. A. M. Bevers Melissa S. A. M. Bevers Caroline E. Wyers Caroline E. Wyers Caroline E. Wyers Bert van Rietbergen Bert van Rietbergen Bernd P. Teunissen Pieter G. Raijmakers Jan Coen Netelenbos Joop P. van den Bergh Joop P. van den Bergh Joop P. van den Bergh Joop P. van den Bergh Elisabeth M. W. Eekhoff Microarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case Series Frontiers in Cell and Developmental Biology fibrodysplasia ossificans progressiva heterotopic ossification high-resolution peripheral quantitative computed tomography bone strength bone microarchitecture |
author_facet |
Esmée Botman Melissa S. A. M. Bevers Melissa S. A. M. Bevers Melissa S. A. M. Bevers Caroline E. Wyers Caroline E. Wyers Caroline E. Wyers Bert van Rietbergen Bert van Rietbergen Bernd P. Teunissen Pieter G. Raijmakers Jan Coen Netelenbos Joop P. van den Bergh Joop P. van den Bergh Joop P. van den Bergh Joop P. van den Bergh Elisabeth M. W. Eekhoff |
author_sort |
Esmée Botman |
title |
Microarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case Series |
title_short |
Microarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case Series |
title_full |
Microarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case Series |
title_fullStr |
Microarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case Series |
title_full_unstemmed |
Microarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case Series |
title_sort |
microarchitecture of heterotopic ossification in fibrodysplasia ossificans progressiva: an hr-pqct case series |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cell and Developmental Biology |
issn |
2296-634X |
publishDate |
2021-03-01 |
description |
It is challenging to study heterotopic ossification (HO) in patients with fibrodysplasia ossificans progressiva (FOP) due to the contraindication of invasive techniques (i.e., bone biopsies), which can trigger flare-ups. The aim of this case study was to assess mature HO at the microarchitectural level non-invasively with high-resolution peripheral quantitative computed tomography (HR-pQCT). Depending on the patient’s mobility, HR-pQCT scans were acquired of peripherally located HO and standard distal radius and tibia regions in two FOP patients, a 33-year-old woman and a 23-year-old man, with the classical mutation (p.R206H). HO was located around the halluces, the ankles, and in the Achilles tendon. Standard HR-pQCT analyses were performed of the distal radius, tibia, and HO to quantify bone mineral density (BMD) and bone microarchitecture. Micro-finite element analysis was used to estimate failure load (FL). The outcomes were compared between HO and neighboring skeletal bone and with an age- and gender-matched normative dataset from literature. The bone parameters of the radius were within the interquartile range (IQR) of normative data. In contrast, in the tibiae of both patients, total and trabecular BMD were below the IQR, as were trabecular bone volume fraction, number, and thickness, cortical thickness, and FL. Trabecular separation and heterogeneity were above the IQR. Isolated HO in the Achilles tendon had a lower total, trabecular, and cortical BMD, trabecular bone volume fraction, and cortical thickness than the normative tibia data. Trabecular microarchitecture was within the IQR, and FL was approximately 10% higher than that of the neighboring tibia after accounting for areal differences. Other scanned HO could only be qualitatively assessed, which revealed coalescence with the neighboring skeletal bone, development of a neo-cortex, and partial replacement of the original skeletal cortex with trabeculae. To conclude, isolated HO seemed microarchitecturally more comparable to reference tibia data than the peripheral skeleton of the FOP patients. HO and skeleton also appear to be able to become one entity when contiguous. |
topic |
fibrodysplasia ossificans progressiva heterotopic ossification high-resolution peripheral quantitative computed tomography bone strength bone microarchitecture |
url |
https://www.frontiersin.org/articles/10.3389/fcell.2021.627784/full |
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doaj-60f21234755f40b8b0ddaaedac4c16792021-03-11T05:16:57ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-03-01910.3389/fcell.2021.627784627784Microarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case SeriesEsmée Botman0Melissa S. A. M. Bevers1Melissa S. A. M. Bevers2Melissa S. A. M. Bevers3Caroline E. Wyers4Caroline E. Wyers5Caroline E. Wyers6Bert van Rietbergen7Bert van Rietbergen8Bernd P. Teunissen9Pieter G. Raijmakers10Jan Coen Netelenbos11Joop P. van den Bergh12Joop P. van den Bergh13Joop P. van den Bergh14Joop P. van den Bergh15Elisabeth M. W. Eekhoff16Department of Internal Medicine Section Endocrinology, Amsterdam Bone Center, Amsterdam Movement Sciences, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, NetherlandsDepartment of Internal Medicine, VieCuri Medical Center, Venlo, NetherlandsNUTRIM School for Nutrition and Translational Research in Metabolism, Maastricht University Medical Center, Maastricht, NetherlandsOrthopedic Biomechanics, Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, NetherlandsDepartment of Internal Medicine, VieCuri Medical Center, Venlo, NetherlandsNUTRIM School for Nutrition and Translational Research in Metabolism, Maastricht University Medical Center, Maastricht, NetherlandsDepartment of Internal Medicine, Subdivision Rheumatology, Maastricht University Medical Center, Maastricht, NetherlandsOrthopedic Biomechanics, Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, NetherlandsDepartment of Orthopedic Surgery, Maastricht University Medical Center, Maastricht, NetherlandsDepartment of Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, NetherlandsDepartment of Radiology and Nuclear Medicine, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, NetherlandsDepartment of Internal Medicine Section Endocrinology, Amsterdam Bone Center, Amsterdam Movement Sciences, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, NetherlandsDepartment of Internal Medicine, VieCuri Medical Center, Venlo, NetherlandsNUTRIM School for Nutrition and Translational Research in Metabolism, Maastricht University Medical Center, Maastricht, NetherlandsDepartment of Internal Medicine, Subdivision Rheumatology, Maastricht University Medical Center, Maastricht, NetherlandsDepartment of Medicine and Life Sciences, Hasselt University, Hasselt, BelgiumDepartment of Internal Medicine Section Endocrinology, Amsterdam Bone Center, Amsterdam Movement Sciences, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, NetherlandsIt is challenging to study heterotopic ossification (HO) in patients with fibrodysplasia ossificans progressiva (FOP) due to the contraindication of invasive techniques (i.e., bone biopsies), which can trigger flare-ups. The aim of this case study was to assess mature HO at the microarchitectural level non-invasively with high-resolution peripheral quantitative computed tomography (HR-pQCT). Depending on the patient’s mobility, HR-pQCT scans were acquired of peripherally located HO and standard distal radius and tibia regions in two FOP patients, a 33-year-old woman and a 23-year-old man, with the classical mutation (p.R206H). HO was located around the halluces, the ankles, and in the Achilles tendon. Standard HR-pQCT analyses were performed of the distal radius, tibia, and HO to quantify bone mineral density (BMD) and bone microarchitecture. Micro-finite element analysis was used to estimate failure load (FL). The outcomes were compared between HO and neighboring skeletal bone and with an age- and gender-matched normative dataset from literature. The bone parameters of the radius were within the interquartile range (IQR) of normative data. In contrast, in the tibiae of both patients, total and trabecular BMD were below the IQR, as were trabecular bone volume fraction, number, and thickness, cortical thickness, and FL. Trabecular separation and heterogeneity were above the IQR. Isolated HO in the Achilles tendon had a lower total, trabecular, and cortical BMD, trabecular bone volume fraction, and cortical thickness than the normative tibia data. Trabecular microarchitecture was within the IQR, and FL was approximately 10% higher than that of the neighboring tibia after accounting for areal differences. Other scanned HO could only be qualitatively assessed, which revealed coalescence with the neighboring skeletal bone, development of a neo-cortex, and partial replacement of the original skeletal cortex with trabeculae. To conclude, isolated HO seemed microarchitecturally more comparable to reference tibia data than the peripheral skeleton of the FOP patients. HO and skeleton also appear to be able to become one entity when contiguous.https://www.frontiersin.org/articles/10.3389/fcell.2021.627784/fullfibrodysplasia ossificans progressivaheterotopic ossificationhigh-resolution peripheral quantitative computed tomographybone strengthbone microarchitecture |