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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Main Authors: Esmée Botman, Melissa S. A. M. Bevers, Caroline E. Wyers, Bert van Rietbergen, Bernd P. Teunissen, Pieter G. Raijmakers, Jan Coen Netelenbos, Joop P. van den Bergh, Elisabeth M. W. Eekhoff
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Cell and Developmental Biology
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Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2021.627784/full
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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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spelling 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