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Related Concept Videos

Bone Remodeling01:40

Bone Remodeling

Bone remodeling is a continuous and balanced process of bone resorption by osteoclasts and bone formation by osteoblasts. In adults, it helps maintain bone mass and calcium homeostasis. While mechanical stress can stimulate turnover as part of the normal maintenance and reparative process, several hormones also regulate bone remodeling.
Osteoclasts in Bone Remodeling01:31

Osteoclasts in Bone Remodeling

Osteoclasts are cells responsible for bone resorption and remodeling. They originate from hematopoietic progenitor cells present in the bone marrow. Numerous progenitor cells fuse to form multinucleated cells, each with 10-20 nuclei. A single osteoclast has a diameter of 150 to 200 µM. These cells have ruffled borders that break down the underlying bone tissue and release minerals such as calcium into the blood in bone resorption. Osteoclasts cling to bones with their ruffled edges during bone...
Bone Remodeling and Repair01:31

Bone Remodeling and Repair

Osteoclasts are cells responsible for bone resorption and remodeling. They originate from hematopoietic progenitor cells present in the bone marrow. Numerous progenitor cells fuse to form multinucleated cells, each with 10-20 nuclei. A single osteoclast has a diameter of 150 to 200 µM. These cells have ruffled borders that break down the underlying bone tissue and release minerals such as calcium into the blood in bone resorption. Osteoclasts cling to bones with their ruffled edges during bone...
Genetic Variation01:25

Genetic Variation

Genetic variation is the diversity in DNA sequences found among individuals of the same species. This diversity is crucial for a species' survival because it helps organisms adapt to environmental changes. Genetic variation begins with fertilization, where an egg and sperm cell merge. Each of these cells carries 23 chromosomes, up to 46 in the fertilized egg. Chromosomes are long DNA strands that contain genes, the basic units of heredity.
Genes exist in different versions called alleles, which...
X-linked Traits01:19

X-linked Traits

In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
X-linked Traits01:19

X-linked Traits

In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.

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Related Experiment Video

Updated: May 8, 2026

Midface Hypoplasia and Cranial Base Morphology in Syndromic Craniosynostosis: A Comparative Analysis Study Using a Predictive Regression Model
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Midface Hypoplasia and Cranial Base Morphology in Syndromic Craniosynostosis: A Comparative Analysis Study Using a Predictive Regression Model

Published on: November 4, 2025

Intracortical bone remodeling variation shows strong genetic effects.

L M Havill1, M R Allen, J A K Harris

  • 1Department of Genetics, Texas Biomedical Research Institute, San Antonio, TX, 78227, USA, Lorena@TxBiomedGenetics.org.

Calcified Tissue International
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PubMed
Summary

Genes significantly influence bone

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Area of Science:

  • Bone biology
  • Genetics
  • Biomechanics

Background:

  • Intracortical microstructure is crucial for bone's mechanical integrity and fracture resistance.
  • Genetic factors influencing bone remodeling may impact fracture risk.
  • Understanding the genetic basis of intracortical variation is key to assessing fracture susceptibility.

Purpose of the Study:

  • To quantify the heritability of intracortical microstructural traits in a baboon model.
  • To determine the extent to which population-level variation in bone microstructure is genetically determined.
  • To link genetic influences on microstructure to potential mechanisms underlying fracture risk.

Main Methods:

  • Analysis of intracortical microstructural properties (osteon number, area, density, etc.) in baboon femurs (n=101).
  • Utilized a variance decomposition approach to estimate the contribution of additive genetic effects (heritability).
  • Accounted for significant effects of age and sex on microstructural traits.

Main Results:

  • Age and sex explained 9-21% of the variation in intracortical properties.
  • Significant heritability was found for osteon area (h²=0.79), percent osteonal bone (h²=0.82), and wall thickness (h²=0.61) after accounting for age and sex.
  • Additive genetic effects accounted for 61-82% of residual variation, representing 48-75% of total phenotypic variance.

Conclusions:

  • Population-level variation in intracortical bone microstructure is substantially influenced by genetic factors.
  • Genetic control over microstructural traits provides a mechanism linking genetic variation to bone fracture risk.
  • These findings highlight the importance of genetic predisposition in bone mechanical properties and skeletal health.