Completed Bones, Joints & Muscles Diabetes, Hormones & Metabolism

The role of size, shape and structure of bones and joints, in explaining common musculoskeletal diseases

In plain English

AI plain-English summary

A single DXA scan—a type of bone density X-ray—can now reveal the precise 3D shape of a person’s hip or knee joint, not just its mineral content, and researchers plan to analyse 100,000 such scans from UK Biobank participants. Osteoarthritis, vertebral fractures, and scoliosis are common, painful conditions that are poorly understood at the level of bone and joint geometry. Current risk prediction is crude, relying mainly on age and body mass index. This project aims to fill that gap by systematically linking variations in bone shape, fat mass, and muscle strength to disease onset and progression. If successful, the work could produce new algorithms that predict an individual’s risk of osteoarthritis or spinal fracture years before symptoms appear. It may also identify genetic pathways that control joint shape, pointing to novel drug targets. The Mendelian randomisation analyses will clarify whether factors such as muscle weakness actually *cause* fractures or are merely associated with them—a distinction that determines whether modifying those factors would prevent disease. The research is fundamentally epidemiological and genetic; it will not directly produce a new treatment or device, but it will provide the mechanistic understanding needed to design future prevention strategies and clinical trials.

View original technical description
Combining our expertise in epidemiological, genetic and causal pathway analysis, with that in statistical shape modelling (SSM), our collaboration aims to develop new approaches for the prediction, prevention and treatment of common musculoskeletal diseases, by improving understanding of the role of size, shape and structure of bones and joints in their pathogenesis. For example, we aim to establish the roles of hip and knee shape in prevalent and incident osteoarthritis (OA), and fat mass and muscle strength in vertebral fractures and scoliosis, as well as pursuing hypothesis-free approaches. Seven endophenotypes will be generated from the unique dual energy X-ray absorptiometry (DXA) resource of the UKBiobank Imaging Enhancement Study; following automation of existing algorithms, scans from 100,000 individuals to be examined (work package (WP)1). Cross sectional and longitudinal relationships between these endophenotypes and hypothesized risk factors and disease outcomes will subsequently be analysed, providing a basis for new disease prediction algorithms (WP2). Genome wide association studies (GWAS; WP3) and functional annotation (WP4) will identify novel genetic mechanisms and putative drug targets. Mendelian Randomisation studies (WP5), exploiting GWAS results from WP3, will establish whether relationships identified in WP2 reflect causal associations, suggesting new approaches for disease prevention through risk factor modification.

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Researchers

Jonathan Tobias (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Quantitative 3-dimensional assessment of multi-tissue pathology in knee osteoarthritis
Use of Mendelian randomisation to examine the role of abnormal hip shape in the development of hip osteoarthritis
Identifying New Disease Genes & Mechanisms for Musculoskeletal Disorders in 100K Genomes Project using Bioinformatics, Phenotyping & Machine Learning
Genome-wide association analysis of extensive osteoarthritis-related phenotypes in the arcOGEN study
Characterisation of osteoarthritis phenotype in a unique multi-centre cohort of individuals with extremely high bone mass

Original classification

Collaborative Award in Science

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