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. 2023 Jun 17;28(8):483-488.
doi: 10.1093/pch/pxad031. eCollection 2023 Dec.

Aetiologies of low alkaline phosphatase in a Canadian Paediatric Tertiary Care Centre

Affiliations

Aetiologies of low alkaline phosphatase in a Canadian Paediatric Tertiary Care Centre

Anne Marie Sbrocchi et al. Paediatr Child Health. .

Abstract

Objectives: Increasingly, laboratories flag low serum alkaline phosphatase (sALP) that are age-and sex-specific in paediatrics. The aim of this study was to report clinical manifestations of paediatric patients with age-and sex-specific low sALP, thereby increasing awareness of its potential aetiologies.

Methods: This retrospective Canadian tertiary care paediatric hospital study assessed all sALP of ambulatory patients aged less than 18 years from 2015 to 2017. The hospital used a Beckman Coulter AU assay to measure sALP and compared values to the Canadian age-and sex-specific reference intervals from CALIPER. All children who had at least one subnormal age-and sex-specific sALP were evaluated. A review of medical charts of included patients was performed and demographic characteristics, medical history and diagnosis were collected, and categorized under groups of medical disorders.

Results: Of 11,874 included patients, 1,001 patients (9.2%) had low sALP. Of those, 48% (485/1,001) had transient low sALP activity and 9.6% (96/1,001) had persistently low sALP. Prolonged immobilization and inflammatory bowel disease represented the main aetiologies for persistently low sALP. Interestingly, 13.5% (13/96) of patients with persistently low sALP had no apparent aetiology.

Conclusions: Our results report aetiologies of low sALP in a Canadian paediatric population using age-and sex-specific Canadian reference ranges. This study highlights that healthcare providers should be aware that a low sALP may have clinical significance and should be repeated if warranted based on further clinical assessment.

Keywords: Alkaline phosphatase; Children; Laboratories; Paediatrics.

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Conflict of interest statement

MB and TF report that they are employee of AZ—Alexion Rare Disease. The authors have no other disclosures.

Figures

Figure 1.
Figure 1.
Flow chart of patients analyzed in the study

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