Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/33920
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dc.contributor.authorBotman, Esmee-
dc.contributor.authorBevers, Melissa S. A. M.-
dc.contributor.authorWyers, Caroline E.-
dc.contributor.authorvan Rietbergen, Bert-
dc.contributor.authorTeunissen, Bernd P.-
dc.contributor.authorRaijmakers, Pieter G.-
dc.contributor.authorNetelenbos, Jan Coen-
dc.contributor.authorVAN DEN BERGH, Joop-
dc.contributor.authorEekhoff, Elisabeth M. W.-
dc.date.accessioned2021-04-14T15:30:54Z-
dc.date.available2021-04-14T15:30:54Z-
dc.date.issued2021-
dc.date.submitted2021-04-14T07:41:53Z-
dc.identifier.citationFrontiers in Cell and Developmental Biology, 9 (Art N° 627784)-
dc.identifier.issn2296-634X-
dc.identifier.urihttp://hdl.handle.net/1942/33920-
dc.description.abstractIt 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.-
dc.description.sponsorshipWe thank the two fibrodysplasia ossificans progressiva patients for their participation. We also thank Dr. S. K. Boyd for providing the normative dataset.-
dc.language.isoen-
dc.publisherFRONTIERS MEDIA SA-
dc.rights2021 Botman, Bevers, Wyers, van Rietbergen, Teunissen, Raijmakers, Netelenbos, van den Bergh and Eekhoff. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.-
dc.subject.otherfibrodysplasia ossificans progressiva-
dc.subject.otherheterotopic ossification-
dc.subject.otherhigh-resolution peripheral quantitative computed tomography-
dc.subject.otherbone strength-
dc.subject.otherbone microarchitecture-
dc.titleMicroarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case Series-
dc.typeJournal Contribution-
dc.identifier.volume9-
local.format.pages10-
local.bibliographicCitation.jcatA1-
dc.description.notesEekhoff, EMW (corresponding author), Vrije Univ Amsterdam, Amsterdam Movement Sci, Amsterdam Bone Ctr, Dept Internal Med,Sect Endocrinol,Amsterdam UMC, Amsterdam, Netherlands.-
dc.description.notesemw.eekhoff@amsterdamumc.nl-
dc.description.otherEekhoff, EMW (corresponding author); Vrije Univ Amsterdam, Amsterdam Movement Sci, Amsterdam Bone Ctr, Dept Internal Med,Sect Endocrinol,Amsterdam UMC, Amsterdam, Netherlands. emw.eekhoff@amsterdamumc.nl-
local.publisher.placeAVENUE DU TRIBUNAL FEDERAL 34, LAUSANNE, CH-1015, SWITZERLAND-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.artnr627784-
dc.identifier.doi10.3389/fcell.2021.627784-
dc.identifier.pmid33777936-
dc.identifier.isiWOS:000632423300001-
local.provider.typewosris-
local.uhasselt.uhpubyes-
local.description.affiliation[Botman, Esmee; Netelenbos, Jan Coen; Eekhoff, Elisabeth M. W.] Vrije Univ Amsterdam, Amsterdam Movement Sci, Amsterdam Bone Ctr, Dept Internal Med,Sect Endocrinol,Amsterdam UMC, Amsterdam, Netherlands.-
local.description.affiliation[Bevers, Melissa S. A. M.; Wyers, Caroline E.; van den Bergh, Joop P.] VieCuri Med Ctr, Dept Internal Med, Venlo, Netherlands.-
local.description.affiliation[Bevers, Melissa S. A. M.; Wyers, Caroline E.; van den Bergh, Joop P.] Maastricht Univ, Med Ctr, NUTRIM Sch Nutr & Translat Res Metab, Maastricht, Netherlands.-
local.description.affiliation[Bevers, Melissa S. A. M.; van Rietbergen, Bert] Eindhoven Univ Technol, Dept Biomed Engn, Orthoped Biomech, Eindhoven, Netherlands.-
local.description.affiliation[Wyers, Caroline E.; van den Bergh, Joop P.] Maastricht Univ, Med Ctr, Subdiv Rheumatol, Dept Internal Med, Maastricht, Netherlands.-
local.description.affiliation[van Rietbergen, Bert] Maastricht Univ, Med Ctr, Dept Orthoped Surg, Maastricht, Netherlands.-
local.description.affiliation[Teunissen, Bernd P.; Raijmakers, Pieter G.] Vrije Univ Amsterdam, Dept Radiol & Nucl Med, Amsterdam UMC, Amsterdam, Netherlands.-
local.description.affiliation[van den Bergh, Joop P.] Hasselt Univ, Dept Med & Life Sci, Hasselt, Belgium.-
local.uhasselt.internationalyes-
item.validationecoom 2022-
item.contributorBotman, Esmee-
item.contributorBevers, Melissa S. A. M.-
item.contributorWyers, Caroline E.-
item.contributorvan Rietbergen, Bert-
item.contributorTeunissen, Bernd P.-
item.contributorRaijmakers, Pieter G.-
item.contributorNetelenbos, Jan Coen-
item.contributorVAN DEN BERGH, Joop-
item.contributorEekhoff, Elisabeth M. W.-
item.accessRightsOpen Access-
item.fullcitationBotman, Esmee; Bevers, Melissa S. A. M.; Wyers, Caroline E.; van Rietbergen, Bert; Teunissen, Bernd P.; Raijmakers, Pieter G.; Netelenbos, Jan Coen; VAN DEN BERGH, Joop & Eekhoff, Elisabeth M. W. (2021) Microarchitecture of Heterotopic Ossification in Fibrodysplasia Ossificans Progressiva: An HR-pQCT Case Series. In: Frontiers in Cell and Developmental Biology, 9 (Art N° 627784).-
item.fulltextWith Fulltext-
crisitem.journal.issn2296-634X-
crisitem.journal.eissn2296-634X-
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