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Observational Study
. 2022 Jan 1;107(1):e281-e292.
doi: 10.1210/clinem/dgab574.

Determinants and Outcomes Associated With Urinary Calcium Excretion in Chronic Kidney Disease

Affiliations
Observational Study

Determinants and Outcomes Associated With Urinary Calcium Excretion in Chronic Kidney Disease

Jing Liu et al. J Clin Endocrinol Metab. .

Abstract

Context: Abnormalities in calcium metabolism are common in chronic kidney disease (CKD). Diminished urinary calcium excretion may promote vascular calcification and increased urinary calcium excretion may lead to nephrolithiasis and nephrocalcinosis, conditions associated with CKD.

Objective: To study predictors of urinary calcium excretion and its association with adverse clinical outcomes in CKD.

Design, setting and patients: This study assessed 3768 nondialysis participants in the Chronic Renal Insufficiency Cohort study from April 2003 to September 2008. Participants were followed up to October 2018.

Exposure: Clinically plausible predictors of urinary calcium excretion and 24-h urinary calcium excretion at baseline.

Main outcome measures: Urinary calcium excretion; incident end stage kidney disease (ESKD), CKD progression [50% estimated glomerular filtration rate (eGFR) decline or incident ESKD], all-cause mortality, and atherosclerotic cardiovascular disease events.

Results: eGFR was positive correlated with 24-h urinary calcium excretion. The variables most strongly associated with 24-h urinary calcium excretion in males and females were 24-h urinary sodium (β = 0.19 and 0.28, respectively), serum parathyroid hormone (β = -0.22 and -0.20, respectively), loop diuretics (β = 0.36 and 0.26, respectively), thiazide diuretics (β = -0.49 and -0.53, respectively), and self-identified black race (β = -0.23 and -0.27, respectively). Lower urinary calcium excretion was associated with greater risks of adverse outcomes, but these associations were greatly attenuated or nullified after adjustment for baseline eGFR.

Conclusion: Urinary calcium excretion is markedly lower in individuals with CKD compared to the general population. Determinants of urinary calcium excretion differed between sexes and levels of CKD. Associations between urinary calcium excretion and adverse clinical events were substantially confounded by eGFR.

Keywords: all-cause mortality; cardiovascular events; chronic kidney disease; determinants; renal outcomes; urinary calcium excretion.

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Figures

Figure 1.
Figure 1.
Correlation between 24-h urinary calcium excretion and estimated glomerular filtration rate (eGFR). (A) 24-h urinary calcium excretion distributions across different chronic kidney disease stages. (B) Correlations between eGFR and natural log of 24-h urinary calcium excretion in males and females, respectively.
Figure 2.
Figure 2.
Features of calcification measurements across chronic kidney disease (CKD) stages and quintiles of 24-h urinary calcium excretion. (A) Percentage of mitral annulus calcification (MAC) and ankle brachial index (ABI) <0.9 across CKD stages. (B) Percentage of MAC and ABI <0.9 across quintiles of 24-h urinary calcium excretion.

References

    1. Peacock M. Calcium metabolism in health and disease. Clin J Am Soc Nephrol. 2010;5(suppl 1):S23-S30. - PubMed
    1. Bonny O, Rubin A, Huang CL, Frawley WH, Pak CY, Moe OW. Mechanism of urinary calcium regulation by urinary magnesium and pH. J Am Soc Nephrol. 2008;19(8):1530-1537. - PMC - PubMed
    1. GBD Chronic Kidney Disease Collaboration. Global, regional, and national burden of chronic kidney disease, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2020;395(10225):709-733. - PMC - PubMed
    1. Spiegel DM, Brady K. Calcium balance in normal individuals and in patients with chronic kidney disease on low- and high-calcium diets. Kidney Int. 2012;81(11):1116-1122. - PMC - PubMed
    1. Godron A, Harambat J, Boccio V, et al. . Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutations. Clin J Am Soc Nephrol. 2012;7(5):801-809. - PMC - PubMed

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