Bone turnover and mineral metabolism in adult patients with hypophosphatasia treated with asfotase alfa
Autor: | Lothar Seefried, Anna Petryk, F Genest, D Rak |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Adult medicine.medical_specialty Bone turnover Endocrinology Diabetes and Metabolism Recombinant Fusion Proteins Parathyroid hormone Hypophosphatasia 030209 endocrinology & metabolism Bone remodeling 03 medical and health sciences 0302 clinical medicine N-terminal telopeptide Internal medicine medicine Bone mineral density Humans ddc:610 Child Bone mineral Minerals biology business.industry medicine.disease Alkaline Phosphatase Endocrinology Asfotase alfa Enzyme replacement therapy Immunoglobulin G Osteocalcin biology.protein Alkaline phosphatase Original Article 030101 anatomy & morphology Bone Remodeling business |
Zdroj: | Osteoporosis International |
ISSN: | 1433-2965 0937-941X |
Popis: | Summary There is limited understanding of how asfotase alfa affects mineral metabolism and bone turnover in adults with pediatric-onset hypophosphatasia. This study showed that adults with hypophosphatasia treated with asfotase alfa experienced significant changes in biochemical markers of bone and mineral metabolism, possibly reflecting enhanced bone remodeling of previously osteomalacic bone. Introduction Hypophosphatasia (HPP), due to a tissue nonspecific alkaline phosphatase (TNSALP) deficiency, can cause impaired bone mineralization and turnover. Although HPP may be treated with asfotase alfa, an enzyme replacement therapy, limited data are available on how treatment with asfotase alfa affects mineral metabolism and bone turnover in adults with HPP. Methods ALP substrates, bone turnover and mineral metabolism markers, and bone mineral density (BMD) data from EmPATHY, a single-center, observational study of adults (≥ 18 years) with pediatric-onset HPP treated with asfotase alfa (NCT03418389), were collected during routine clinical care and analyzed from baseline through 24 months of treatment. Results Data from 21 patients showed significantly increased ALP activity and reduced urine phosphoethanolamine (PEA)/creatinine (Cr) ratios after baseline through 24 months of asfotase alfa treatment. There were significant transient increases in parathyroid hormone 1-84 (PTH), osteocalcin, and procollagen type 1 N-propeptide (P1NP) levels at 3 and 6 months and in tartrate-resistant acid phosphatase 5b (TRAP5b) levels at 3 months, with a significant decrease in N-terminal telopeptide of type 1 collagen (NTX) levels at 24 months. Lumbar spine BMD T scores continuously increased during treatment. Conclusion Significant changes in bone turnover and mineral metabolism markers after asfotase alfa treatment suggest that treatment-mediated mineralization may enable remodeling and bone turnover on previously unmineralized surfaces. Urine PEA/Cr ratios may be a useful parameter in monitoring treatment during routine care. Supplementary Information The online version contains supplementary material available at 10.1007/s00198-021-06025-y. |
Databáze: | OpenAIRE |
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