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ID 58565
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Akiyama, Tomoyuki Department of Child Neurology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences Kaken ID researchmap
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
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.
Keywords
Asfotase alfa
Liquid chromatography
Vitamin B6
Diagnostic marker
Therapeutic monitoring
Published Date
2018-07-17
Publication Title
Molecular Genetics and Metabolism
Volume
volume125
Issue
issue1-2
Publisher
Elsevier
Start Page
174
End Page
180
ISSN
10967192
NCID
AA11158931
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
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author
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Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.1016/j.ymgme.2018.07.006
Funder Name
Ministry of Education, Culture, Sports, Science and Technology
Japan Agency for Medical Research and Development
助成番号
JP15K09622
17ek0109135h0003