A multi-stack registration technique to improve measurement accuracy and precision across longitudinal HR-pQCT scans.

Bone microarchitecture Bone remodelling High resolution peripheral quantitative computed tomography Image registration Precision

Journal

Bone
ISSN: 1873-2763
Titre abrégé: Bone
Pays: United States
ID NLM: 8504048

Informations de publication

Date de publication:
11 2023
Historique:
received: 15 05 2023
revised: 14 08 2023
accepted: 01 09 2023
medline: 19 9 2023
pubmed: 5 9 2023
entrez: 4 9 2023
Statut: ppublish

Résumé

Recent applications of high-resolution peripheral quantitative computed tomography (HR-pQCT) have demonstrated that changes in local bone remodelling can be quantified in vivo using longitudinal three-dimensional image registration. However, certain emerging applications, such as fracture healing and joint analysis, require larger multi-stack scan regions that can result in stack shift image artifacts. These artifacts can be detrimental to the accurate alignment of the bone structure across multiple timepoints. The purpose of this study was to establish a multi-stack registration protocol for evaluating longitudinal HR-pQCT images and to assess the accuracy and precision error in comparison with measures obtained using previously established three-dimensional longitudinal registration. Three same day multi-stack HR-pQCT scans of the radius (2 stacks in length) and tibia (3 stacks in length) were obtained from 39 healthy individuals who participated in a previous reproducibility study. A fully automated multi-stack registration algorithm was developed to re-align stacks within a scan by leveraging slight offsets between longitudinal scans. Stack shift severity before and after registration was quantified using a newly proposed stack-shift severity score. The false discovery rate for bone remodelling events and precision error of bone morphology and micro-finite element analysis parameters were compared between longitudinally registered scans with and without the addition of multi-stack registration. Most scans (82 %) improved in stack alignment or maintained the lowest stack shift severity score when multi-stack registration was implemented. The false discovery rate of bone remodelling events significantly decreased after multi-stack registration, resulting in median false detection of bone formation and resorption fractions between 3.2 to 7.5 % at the radius and 3.4 to 5.3 % at the tibia. Further, precision error was significantly reduced or remained unchanged in all standard bone morphology and micro-finite element analysis parameters, except for total and trabecular cross-sectional areas. Multi-stack registration is an effective strategy for accurately aligning multi-stack HR-pQCT scans without modification of the image acquisition protocol. The algorithm presented here is a viable approach for performing accurate morphological analysis on multi-stack HR-pQCT scans, particularly for advanced application investigating local bone remodelling in vivo.

Sections du résumé

BACKGROUND
Recent applications of high-resolution peripheral quantitative computed tomography (HR-pQCT) have demonstrated that changes in local bone remodelling can be quantified in vivo using longitudinal three-dimensional image registration. However, certain emerging applications, such as fracture healing and joint analysis, require larger multi-stack scan regions that can result in stack shift image artifacts. These artifacts can be detrimental to the accurate alignment of the bone structure across multiple timepoints. The purpose of this study was to establish a multi-stack registration protocol for evaluating longitudinal HR-pQCT images and to assess the accuracy and precision error in comparison with measures obtained using previously established three-dimensional longitudinal registration.
METHODS
Three same day multi-stack HR-pQCT scans of the radius (2 stacks in length) and tibia (3 stacks in length) were obtained from 39 healthy individuals who participated in a previous reproducibility study. A fully automated multi-stack registration algorithm was developed to re-align stacks within a scan by leveraging slight offsets between longitudinal scans. Stack shift severity before and after registration was quantified using a newly proposed stack-shift severity score. The false discovery rate for bone remodelling events and precision error of bone morphology and micro-finite element analysis parameters were compared between longitudinally registered scans with and without the addition of multi-stack registration.
RESULTS
Most scans (82 %) improved in stack alignment or maintained the lowest stack shift severity score when multi-stack registration was implemented. The false discovery rate of bone remodelling events significantly decreased after multi-stack registration, resulting in median false detection of bone formation and resorption fractions between 3.2 to 7.5 % at the radius and 3.4 to 5.3 % at the tibia. Further, precision error was significantly reduced or remained unchanged in all standard bone morphology and micro-finite element analysis parameters, except for total and trabecular cross-sectional areas.
CONCLUSION
Multi-stack registration is an effective strategy for accurately aligning multi-stack HR-pQCT scans without modification of the image acquisition protocol. The algorithm presented here is a viable approach for performing accurate morphological analysis on multi-stack HR-pQCT scans, particularly for advanced application investigating local bone remodelling in vivo.

Identifiants

pubmed: 37666441
pii: S8756-3282(23)00226-0
doi: 10.1016/j.bone.2023.116893
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

116893

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare they have no conflicts of interest.

Auteurs

Danielle E Whittier (DE)

Institute for Biomechanics, ETH Zurich, Zurich, Switzerland; Department of Osteoporosis, Inselspital, Bern University Hospital, University of Bern, Switzerland.

Matthias Walle (M)

Institute for Biomechanics, ETH Zurich, Zurich, Switzerland.

Denis Schenk (D)

ARTORG Center for Biomedical Engineering Research, University of Bern, Bern, Switzerland.

Penny R Atkins (PR)

Institute for Biomechanics, ETH Zurich, Zurich, Switzerland; Department of Osteoporosis, Inselspital, Bern University Hospital, University of Bern, Switzerland; Scientific Computing and Imaging Institute, University of Utah, Salt Lake City, United States.

Caitlyn J Collins (CJ)

Institute for Biomechanics, ETH Zurich, Zurich, Switzerland; Department of Biomedical Engineering and Mechanics, Virginia Tech, Blacksburg, United States.

Philippe Zysset (P)

ARTORG Center for Biomedical Engineering Research, University of Bern, Bern, Switzerland.

Kurt Lippuner (K)

Department of Osteoporosis, Inselspital, Bern University Hospital, University of Bern, Switzerland.

Ralph Müller (R)

Institute for Biomechanics, ETH Zurich, Zurich, Switzerland. Electronic address: ram@ethz.ch.

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