ID | 58565 |
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Author |
Akiyama, Tomoyuki
Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kaken ID
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Kubota, Takuo
Department of Pediatrics, Osaka University Graduate School of Medicine
Ozono, Keiichi
Department of Pediatrics, Osaka University Graduate School of Medicine
Michigami, Toshimi
Department of Bone and Mineral Research, Osaka Women's and Children's Hospital
Kobayashi, Daisuke
Department of Food and Chemical Toxicology, School of Pharmaceutical Sciences, Health Sciences University of Hokkaido
Takeyari, Shinji
Department of Pediatrics, Osaka University Graduate School of Medicine
Sugiyama, Yuichiro
Department of Pediatrics, Nagoya University Graduate School of Medicine
Noda, Masahiro
Department of Pediatrics, Showa General Hospital
Harada, Daisuke
Department of Pediatrics, Osaka Hospital, Japan Community Healthcare Organization
Namba, Noriyuki
Department of Pediatrics, Osaka Hospital, Japan Community Healthcare Organization
Suzuki, Atsushi
Department of Neonatology and Pediatrics, Nagoya City University Graduate School of Medical Sciences
Utoyama, Maiko
Department of Pediatrics, Faculty of Medicine, University of Miyazaki
Kitanaka, Sachiko
Department of Pediatrics, Graduate School of Medicine, University of Tokyo
Uematsu, Mitsugu
Department of Pediatrics, Tohoku University Graduate School of Medicine
Mitani, Yusuke
Department of Pediatrics, Kanazawa University Hospital
Matsunami, Kunihiro
Department of Pediatrics, Gifu Prefectural General Medical Center
Takishima, Shigeru
Department of Pediatrics, Soka Municipal Hospital
Ogawa, Erika
Department of Pediatrics and Child Health, Nihon University School of Medicine
Kobayashi, Katsuhiro
Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
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Abstract | Objective
To investigate the utility of serum pyridoxal 5′-phosphate (PLP), pyridoxal (PL), and 4-pyridoxic acid (PA) as a diagnostic marker of hypophosphatasia (HPP) and an indicator of the effect of, and patient compliance with, enzyme replacement therapy (ERT), we measured PLP, PL, and PA concentrations in serum samples from HPP patients with and without ERT.
Methods
Blood samples were collected from HPP patients and serum was frozen as soon as possible (mostly within one hour). PLP, PL, and PA concentrations were analyzed using high-performance liquid chromatography with fluorescence detection after pre-column derivatization by semicarbazide. We investigated which metabolites are associated with clinical phenotypes and how these metabolites change with ERT.
Results
Serum samples from 20 HPP patients were analyzed. The PLP-to-PL ratio and PLP concentration were elevated in all HPP patients. They correlated negatively with serum alkaline phosphatase (ALP) activity and showed higher values in more severe phenotypes (perinatal severe and infantile HPP) compared with other phenotypes. PL concentration was reduced only in perinatal severe HPP. ERT reduced the PLP-to-PL ratio to mildly reduced or low-normal levels and the PLP concentration was reduced to normal or mildly elevated levels. Urine phosphoethanolamine (PEA) concentration did not return to normal levels with ERT in most patients.
Conclusions
The serum PLP-to-PL ratio is a better indicator of the effect of ERT for HPP than serum PLP and urine PEA concentrations, and a PLP-to-PL ratio of <4.0 is a good indicator of the effect of, and patient compliance with, ERT.
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Keywords | Asfotase alfa
Liquid chromatography
Vitamin B6
Diagnostic marker
Therapeutic monitoring
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Published Date | 2018-07-17
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Publication Title |
Molecular Genetics and Metabolism
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Volume | volume125
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Issue | issue1-2
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Publisher | Elsevier
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Start Page | 174
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End Page | 180
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ISSN | 10967192
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NCID | AA11158931
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Content Type |
Journal Article
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language |
English
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OAI-PMH Set |
岡山大学
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File Version | author
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PubMed ID | |
DOI | |
Web of Science KeyUT | |
Related Url | isVersionOf https://doi.org/10.1016/j.ymgme.2018.07.006
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Funder Name |
Ministry of Education, Culture, Sports, Science and Technology
Japan Agency for Medical Research and Development
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助成番号 | JP15K09622
17ek0109135h0003
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