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Calcium state estimation by total calcium: the evidence to end the never-ending story

  • Jean-David Pekar , Guillaume Grzych EMAIL logo , Gatien Durand , Joël Haas , Arnaud Lionet , Thierry Brousseau , François Glowacki and Patrice Maboudou
Published/Copyright: September 2, 2019

Abstract

Background

Total blood calcium (TCa) is routinely used to diagnose and manage mineral and bone metabolism disorders. Numerous laboratories adjust TCa by albumin, though literature suggests there are some limits to this approach. Here we report a large retrospective study on agreement rate between ionized calcium (iCa) measurement and TCa or albumin-adjusted calcium measurements.

Methods

We retrospectively selected 5055 samples with simultaneous measurements of iCa, TCa, albumin and pH. We subgrouped our patients according to their estimated glomerular filtration rate (eGFR), albumin levels and pH. We analyzed each patient’s calcium state with iCa as reference to determine agreement rate with TCa and albumin-adjusted calcium using Payne, Clase, Jain and Ridefelt formulas.

Results

The Payne formula performed poorly in patients with abnormal albumin, eGFR or pH levels. In patients with low albumin levels or blood pH disorders, Payne-adjusted calcium may overestimate the calcium state in up to 80% of cases. Similarly, TCa has better agreement with iCa in the case of hypoalbuminemia, but performed similarly to the Payne formula in patients with physiological albumin levels. The global agreement rate for Clase, Jain and Ridefelt formulas suggests significant improvement compared to Payne calcium adjustment but no significant improvement compared to TCa.

Conclusions

Total and albumin-adjusted calcium measurement leads to a misclassification of calcium status. Moreover, accurate calcium state determination depends on blood pH levels, whose measurement requires the same pre-analytical restrictions as iCa measurement. We propose that iCa should instead become the reference method to determine the real calcium state.


Corresponding author: Dr. Guillaume Grzych, Centre de Biologie Pathologie, Laboratoire d’Hormonologie, Métabolisme-Nutrition, Oncologie, rue du Pr J. Leclercq, CHU Lille, F-59000 Lille, France; and Université de Lille, INSERM UMR-1011, Lille, France, Phone: +33(0)3.20.44.5454

  1. Author contributions: J.D.P., G.G., A.L., F.G. and P.M. designed the study; J.D.P. and G.D. collected the data; G.D. and G.G. analyzed the data; J.D.P. and G.G. drafted the paper; P.M., A.L., J.T.H., T.B. and F.G. revised the paper; all authors approved the final version of the manuscript. All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: None declared.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2019-06-08
Accepted: 2019-08-07
Published Online: 2019-09-02
Published in Print: 2020-01-28

© 2019 Walter de Gruyter GmbH, Berlin/Boston

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