# Informing Osteoporosis GWAS Using Networks

> **NIH NIH R01** · UNIVERSITY OF VIRGINIA · 2020 · $583,619

## Abstract

Project Summary: Osteoporosis is a complex disease characterized by low bone mineral density (BMD),
bone fragility, and an increased risk of fracture. Genome-wide association studies (GWASs) for BMD have
identified over 1100 associations. This “treasure trove” of novel genetic information has the potential to
revolutionize our understanding of bone biology and the treatment of bone diseases; however, few of the
causal genes underlying associations have been identified. The long-term goal of my lab is to reduce this
knowledge gap using innovative analytical and experimental strategies. A number of approaches exist to
identify genes responsible for GWAS associations. However, most rely on population-based “-omics” data,
which are scarce for human bone, to connect variants to molecular alterations. Furthermore, most approaches
do not provide information on how causal genes impact “systems-level” function. To address these limitations,
we recently used co-expression networks generated from mouse bone transcriptomic datasets to inform BMD
GWAS. The idea is simple – genes that play a central role in the regulation of a complex trait are often
functionally-related and functionally-related genes are often co-expressed. We demonstrated that by identifying
modules of co-expressed genes in bone tissue that were enriched for genes implicated by GWAS, we were
able to predict target genes and infer how they impact BMD. We have shown experimentally that several
genes (MARK3, PPP6R3, etc.) identified using this approach are true regulators of BMD. However, to date our
analyses have been based only on enrichment of genes implicated by GWAS in undirected networks
generated from heterogenous bulk bone transcriptomic datasets of limited cellular diversity. Here, we address
these limitations using an innovative analytical approach incorporating Bayesian networks and key driver
analysis (KDA) and apply this strategy to transcriptomic data from primary bone cell cultures and osteoblast
subtypes defined by single cell RNA-seq (scRNA-seq). We hypothesize that our approach of integrating GWAS
with directed networks representing all major bone cell types will identify novel genes with direct and central
roles in regulating BMD and elucidate how such genes impact network architecture. We will test this
hypothesis through three specific aims. In Aim 1, we will discover novel BMD GWAS target genes through the
integration of bone and bone cell networks and GWAS data. In Aim 2, we will discover novel BMD GWAS
target genes through the integration of osteoblast cell-type specific networks and GWAS data. In Aim 3, we will
define the impact of novel BMD GWAS target genes on BMD and bone network homeostasis. Our innovative
approach for informing GWAS will identify causal BMD genes and lead to the discovery of putative therapeutic
targets for the prevention and treatment of bone fragility.

## Key facts

- **NIH application ID:** 10070744
- **Project number:** 1R01AR077992-01
- **Recipient organization:** UNIVERSITY OF VIRGINIA
- **Principal Investigator:** Charles R Farber
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $583,619
- **Award type:** 1
- **Project period:** 2020-07-15 → 2025-04-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10070744

## Citation

> US National Institutes of Health, RePORTER application 10070744, Informing Osteoporosis GWAS Using Networks (1R01AR077992-01). Retrieved via AI Analytics 2026-05-22 from https://api.ai-analytics.org/grant/nih/10070744. Licensed CC0.

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