A genome-wide scan for pleiotropy between bone mineral density and nonbone phenotypes

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INTRODUCTIONrnOsteoporosis is the most common metabolic bone disorder globally, causing low trauma fractures that lead to significant morbidity and mortality. Especially in high-income countries, osteoporotic fractures lead to a substantial loss of healthy life-years in older adults.1 Osteoporosis is characterized by impaired bone quality and/or reduced bone mass, resulting from an imbalance between bone formation and resorption. Noninvasive diagnosis of osteoporosis currently relies heavily on measurement of bοne mineral density (BMD) by dual energy X-ray absorptio-metry (DXA), which is the most widely used predictor of osteoporotic fractures.
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INTRODUCTIONrnIn adult bone, bone remodeling maintains structural integrity via the clearance and repair of damaged bone and regulates mineral homeostasis.1–2
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