Published November 2024 | Version Supplemental material
Journal Article Open

Magnitude and timescales of Ca isotope variability in human urine: implications for bone mass balance monitoring

Abstract

Calcium (Ca) isotopes in blood/urine are emerging biomarkers of bone mineral balance (BMB) in the human body. While multiple studies have investigated Ca isotopes in patients suffering from diseases affecting BMB, comparatively little effort has been devoted to understanding the homeostasis of Ca isotopes in healthy individuals. Here, we report on a longitudinal study of the urine Ca isotope composition (δ44/42CaUrine) from 22 healthy participants (age 19–60) over timescales ranging from days to months. Data from a single participant collected over a 30-day period show that morning urine is an excellent proxy for 24-h pooled urine fractions. Data from all participants reveal large inter-individual variability in δ44/42CaUrine (up to 2.2‰), which is partly due to anthropometric differences, as shown by a correlation between the participants’ body mass index (BMI) and δ44/42CaUrine values. In contrast, intra-individual data reveal encouraging stability (within ∼±0.2–0.3‰) over timescales >160 days, indicating that self-referencing approaches for BMB monitoring hold greater promise than cross-sectional ones. Our data confirm that intra-individual δ44/42CaUrine variations are mainly a function of Ca reabsorption in the kidney, but also reveal the impact of other (and at times equally important) drivers, such as diet, alcohol consumption, physical exercise, or fasting. We also find that a magnetic resonance imaging contrast agent (gadolinium) can lead to artifacts during Ca isotope analysis. Based on our results, a series of practical considerations for the use of Ca isotopes in urine as tracers of BMB are presented.

Copyright and License

© The Author(s) 2024. Published by Oxford University Press.

Acknowledgement

We thank Clara Blättler for generously providing an aliquot of SRM 915b. We thank two anonymous reviewers for constructive reviews that helped improve the manuscript, and editor Maria Montes-Bayon for prompt and careful editorial handling.

Funding

This work was supported by an Investigator award from the Heritage Medical Research Institute (to F.L.H.T.), as well as start-up funds provided by Caltech.

Data Availability

The data underlying this article are available in the article and in its online supplementary material. Additional data related to this paper may be requested from the authors.

Supplemental Material

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Additional details

Identifiers

Funding

Heritage Medical Research Institute
California Institute of Technology

Dates

Submitted
2024-07-28
Accepted
2024-10-30
Available
2024-11-05
Published
Available
2024-11-19
Corrected and typeset