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Ontogenetic Patterning of Human Subchondral Bone Microarchitecture in the Proximal Tibia
SIMPLE SUMMARY: The objective of this study is to explain the subchondral trabecular and the cortical ontogenetic changes that occur in the proximal tibia in both the medial and lateral condylar regions due to differential loadings associated with changing knee joint kinetics and body mass. The diff...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9312028/ https://www.ncbi.nlm.nih.gov/pubmed/36101383 http://dx.doi.org/10.3390/biology11071002 |
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author | Goliath, Jesse R. Gosman, James H. Stout, Sam D. Ryan, Timothy M. |
author_facet | Goliath, Jesse R. Gosman, James H. Stout, Sam D. Ryan, Timothy M. |
author_sort | Goliath, Jesse R. |
collection | PubMed |
description | SIMPLE SUMMARY: The objective of this study is to explain the subchondral trabecular and the cortical ontogenetic changes that occur in the proximal tibia in both the medial and lateral condylar regions due to differential loadings associated with changing knee joint kinetics and body mass. The differential response of subchondral bone to changing mechanical loads during growth and development serves as a powerful tool to evaluate the significance of mechanical loading on subchondral bone morphology and joint development, and can offer insight into adult morphological variation for joint health. ABSTRACT: High-resolution computed tomography images were acquired for 31 proximal human tibiae, age 8 to 37.5 years, from Norris Farms #36 cemetery site (A.D. 1300). Morphometric analysis of subchondral cortical and trabecular bone architecture was performed between and within the tibial condyles. Kruskal–Wallis and Wilcoxon signed-rank tests were used to examine the association between region, age, body mass, and each morphometric parameter. The findings indicate that age-related changes in mechanical loading have varied effects on subchondral bone morphology. With age, trabecular microstructure increased in bone volume fraction (p = 0.033) and degree of anisotropy (p = 0.012), and decreased in connectivity density (p = 0.001). In the subchondral cortical plate, there was an increase in thickness (p < 0.001). When comparing condylar regions, only degree of anisotropy differed (p = 0.004) between the medial and lateral condyles. Trabeculae in the medial condyle were more anisotropic than in the lateral region. This research represents an innovative approach to quantifying both cortical and trabecular subchondral bone microarchitecture in archaeological remains. |
format | Online Article Text |
id | pubmed-9312028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93120282022-07-26 Ontogenetic Patterning of Human Subchondral Bone Microarchitecture in the Proximal Tibia Goliath, Jesse R. Gosman, James H. Stout, Sam D. Ryan, Timothy M. Biology (Basel) Article SIMPLE SUMMARY: The objective of this study is to explain the subchondral trabecular and the cortical ontogenetic changes that occur in the proximal tibia in both the medial and lateral condylar regions due to differential loadings associated with changing knee joint kinetics and body mass. The differential response of subchondral bone to changing mechanical loads during growth and development serves as a powerful tool to evaluate the significance of mechanical loading on subchondral bone morphology and joint development, and can offer insight into adult morphological variation for joint health. ABSTRACT: High-resolution computed tomography images were acquired for 31 proximal human tibiae, age 8 to 37.5 years, from Norris Farms #36 cemetery site (A.D. 1300). Morphometric analysis of subchondral cortical and trabecular bone architecture was performed between and within the tibial condyles. Kruskal–Wallis and Wilcoxon signed-rank tests were used to examine the association between region, age, body mass, and each morphometric parameter. The findings indicate that age-related changes in mechanical loading have varied effects on subchondral bone morphology. With age, trabecular microstructure increased in bone volume fraction (p = 0.033) and degree of anisotropy (p = 0.012), and decreased in connectivity density (p = 0.001). In the subchondral cortical plate, there was an increase in thickness (p < 0.001). When comparing condylar regions, only degree of anisotropy differed (p = 0.004) between the medial and lateral condyles. Trabeculae in the medial condyle were more anisotropic than in the lateral region. This research represents an innovative approach to quantifying both cortical and trabecular subchondral bone microarchitecture in archaeological remains. MDPI 2022-07-01 /pmc/articles/PMC9312028/ /pubmed/36101383 http://dx.doi.org/10.3390/biology11071002 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Goliath, Jesse R. Gosman, James H. Stout, Sam D. Ryan, Timothy M. Ontogenetic Patterning of Human Subchondral Bone Microarchitecture in the Proximal Tibia |
title | Ontogenetic Patterning of Human Subchondral Bone Microarchitecture in the Proximal Tibia |
title_full | Ontogenetic Patterning of Human Subchondral Bone Microarchitecture in the Proximal Tibia |
title_fullStr | Ontogenetic Patterning of Human Subchondral Bone Microarchitecture in the Proximal Tibia |
title_full_unstemmed | Ontogenetic Patterning of Human Subchondral Bone Microarchitecture in the Proximal Tibia |
title_short | Ontogenetic Patterning of Human Subchondral Bone Microarchitecture in the Proximal Tibia |
title_sort | ontogenetic patterning of human subchondral bone microarchitecture in the proximal tibia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9312028/ https://www.ncbi.nlm.nih.gov/pubmed/36101383 http://dx.doi.org/10.3390/biology11071002 |
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