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Published on: July 5, 2021
Abnormal bone turnover in individuals with low serum alkaline phosphatase
L López-Delgado1, L Riancho-Zarrabeitia2, M T García-Unzueta3
1Service of Internal Medicine, Hospital U.M. Valdecilla, University of Cantabria, IDIVAL, Av Valdecilla SN, 39008, Santander, Spain.
Individuals with low serum alkaline phosphatase (ALP) show reduced bone turnover, even without overt hypophosphatasia (HPP) symptoms or low bone density. This suggests caution when considering bone antiresorptive treatments for these patients.
Area of Science:
- Endocrinology
- Metabolic Bone Disease
- Biochemistry
Background:
- Hypophosphatasia (HPP) presents with a wide clinical spectrum, including mild adult forms discovered incidentally through low serum alkaline phosphatase (ALP).
- The skeletal implications of persistently low ALP in adults without overt HPP manifestations remain unclear, particularly regarding bone remodeling and mass.
Purpose of the Study:
- To investigate the skeletal phenotype in adults with persistently low serum ALP.
- To analyze bone mineral density (BMD), bone microarchitecture (trabecular bone score, TBS), and bone turnover markers (P1NP, ß-crosslaps).
Main Methods:
- Study included 42 adults with persistently low serum ALP.
- Evaluated bone mineral density (BMD), trabecular bone score (TBS), and serum markers of bone turnover (P1NP and ß-crosslaps).
- Compared findings with a control group.
Main Results:
- Individuals with low ALP exhibited significantly lower levels of P1NP and ß-crosslaps compared to controls, indicating reduced bone turnover.
- No significant differences were observed in BMD, bone mineral content, or TBS between the low ALP group and controls.
- These findings suggest a generalized reduction in bone remodeling in individuals with hypophosphatasemia.
Conclusions:
- Adults with persistently low serum ALP have reduced bone turnover, irrespective of overt HPP symptoms or normal BMD.
- The data support avoiding antiresorptive agents, such as bisphosphonates, in individuals with hypophosphatasemia due to altered bone remodeling.
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