ArticleInternational journal of endocrinology2026
Associations of Dietary and Circulating Choline and Glycine With Bone Mineral Density: UK Biobank Analyses With Mendelian Randomization.
Article in International journal of endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Associations of Dietary and Circulating Choline and Glycine With Bone Mineral Density: UK Biobank Analyses With Mendelian Randomization.International journal of endocrinology · 2026Article
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Authors and funding
7 authors.
Funding
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Abstract
Background: Osteoporosis, characterized by reduced bone mass and compromised bone microarchitecture, significantly impacts public health, particularly among the elderly population. Although choline and its related metabolites are believed to influence bone health, their exact role and the effects of these metabolites on bone mineral density (BMD) remain unclear. Methods: We analyzed data from 18,769 UK Biobank (UKB) participants, excluding those with missing data or specific health conditions. All observational associations were assessed cross-sectionally at baseline. Choline intake was assessed using a self-administered 24-h dietary assessment, while circulating choline and related metabolites were quantified by nuclear magnetic resonance spectroscopy. BMD was measured using ultrasound densitometry. Linear regression models were used to assess the associations, adjusting for various covariates. Results: Overall, circulating choline levels demonstrated a borderline significant association with BMD ( Conclusions: Choline and glycine metabolism may play a role in bone metabolism, with choline showing particular effects in men and individuals with impaired renal function. Further research is necessary to better understand the underlying mechanisms and implications of these associations for osteoporosis risk in different populations.
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