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Association of sick building syndrome with neuropathy target esterase (NTE) activity in Japanese
Authors:Yasunari Matsuzaka  Tomoichi Ohkubo  Yukie Y. Kikuti  Akiko Mizutani  Michio Tsuda  Yoshiko Aoyama  Kazuhiko Kakuta  Akira Oka  Hidetoshi Inoko  Kou Sakabe  Satoshi Ishikawa  Jerzy K. Kulski  Minoru Kimura
Affiliation:1. Department of Molecular Life Science, Division of Basic Medical Science and Molecular Medicine, Tokai University School of Medicine, , Bohseidai, Isehara, Kanagawa, Japan;2. Teaching and Research Support Center, Tokai University School of Medicine, , Bohseidai, Isehara, Kanagawa, Japan;3. Aoyama Internal Medicine Children's Hospital, , Gumma, Japan;4. Kakuta Children & Allergy Clinic, , Miyagi, Japan;5. Department of Public Health and Molecular Toxicology, Kitasato University School of Pharmaceutical Sciences, , Tokyo, Japan;6. Division of Environmental Medical Center, Kitasato Institute Hospital, , Tokyo, Japan;7. Centre for Forensic Science, University of Western Australia, , Nedlands 6009, Western Australia, Australia
Abstract:Sick building syndrome (SBS) is a set of several clinically recognizable symptoms reported by occupants of a building without a clear cause. Neuropathy target esterase (NTE) is a membrane bound serine esterase and its reaction with organophosphates (OPs) can lead to OP‐induced delayed neuropathy (OPIDN) and nerve axon degeneration. The aim of our study was to determine whether there was a difference in NTE activity in the peripheral blood mononuclear cells (PBMCs) of Japanese patients with SBS and healthy controls and whether PNPLA6 (alias NTE) gene polymorphisms were associated with SBS. We found that the enzymatic activity of NTE was significantly higher (P < 0.0005) in SBS patients compared with controls. Moreover, population with an AA genotype of a single nucleotide polymorphism (SNP), rs480208, in intron 21 of the PNPLA6 gene strongly reduced the activity of NTE. Fifty‐eight SNP markers within the PNPLA6 gene were tested for association in a case–control study of 188 affected individuals and 401 age‐matched controls. Only one SNP, rs480208, was statistically different in genotype distribution (P = 0.005) and allele frequency (P = 0.006) between the cases and controls (uncorrected for testing multiple SNP sites), but these were not significant by multiple corrections. The findings of the association between the enzymatic activity of NTE and SBS in Japanese show for the first time that NTE activity might be involved with SBS. © 2013 Wiley Periodicals, Inc. Environ Toxicol 29: 1217–1226, 2014.
Keywords:sick building syndrome  NTE  microsatellite  SNPs  PNPLA6
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