Abstract
Low activity of serum alkaline phosphatase (ALP) is a hallmark of hypophosphatasia (HPP), but low readings of ALP are not always recognized in clinical routine. Understanding the clinical presentations associated with low ALP may contribute to a timelier diagnosis of HPP. Data from paediatric patients with low ALP, excluding patients in intensive care and with oncological/haematological disorders, were analysed. Most recent ALP values, previous diagnoses, medication and relevant symptoms were extracted from patient records at nine specialised centres and analysed descriptively. A relationship between body height and ALP values was scrutinised by linear regression. Of 370 children, 15 (4.1%) had a diagnosis of HPP. In the subgroup without a diagnosis of HPP, 241 (67.9%) out of 355 patients had one or more medical conditions known to be associated with low serum ALP. Of those, hypothyroidism, malnutrition and steroid administration were most frequent. Characteristic symptoms, particularly, short stature, muscle weakness and delay of motor development were more frequent and ALP values were lower in patients with documented HPP diagnosis compared to patients without diagnosis of HPP (Ø z-scores:-2.52) (interquartile range [IQR]=0.20) vs.-1.96 (IQR=0.87). A weak positive linear relationship between z-scores of ALP and body height was identified (p<0.001). This analysis of paediatric patient records elucidates a wide range of disorders associated with low ALP activity. In case of additional specific symptoms, HPP should always be considered as a differential diagnosis.
Highlights
Alkaline phosphatase (ALP) is a membrane-bound ubiquitous phosphomonoesterase that catalyses the hydrolysis of phosphate monoesters [1,2,3]
Four isoenzymes of ALP are encoded by separate genes with three tissue-specific – intestinal, placental and germ-cell – isoforms and the ubiquitously expressed tissue-non-specific alkaline phosphatase (TNSALP) [1, 4]
Twelve medical conditions associated with low ALP activity other than HPP were identified, whereby only 15 out of the 370 records included in the analysis had a documented diagnosis of HPP
Summary
Alkaline phosphatase (ALP) is a membrane-bound ubiquitous phosphomonoesterase that catalyses the hydrolysis of phosphate monoesters [1,2,3]. Four isoenzymes of ALP are encoded by separate genes with three tissue-specific – intestinal, placental and germ-cell – isoforms and the ubiquitously expressed tissue-non-specific alkaline phosphatase (TNSALP) [1, 4]. TNSALP is most abundant in the bone, liver, kidney and deciduous teeth and accounts for about 95% of the total ALP activity in the serum [1, 5]. Unlike elevated serum levels of ALP being an established marker of multiple pathologic conditions, low serum ALP activity is less frequently encountered in clinical practice and is not always recognised. Low ALP readings may be overlooked and potentially lead to a diagnostic delay in patients with hypophosphatasia (HPP), adding to the burden of the disease [11,12,13]
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