Literature DB >> 27109752

Activity and polymorphisms of butyrylcholinesterase in a Polish population.

Jacek Jasiecki1, Joanna Jońca2, Monika Żuk2, Anna Szczoczarz2, Anna Janaszak-Jasiecka2, Krzysztof Lewandowski2, Krzysztof Waleron2, Bartosz Wasąg2.   

Abstract

Butyrylcholinesterase (BChE) activity assay and inhibitor phenotyping can help to identify individuals at risk of prolonged paralysis following the administration of neuromuscular blocking agents, like succinylcholine, pesticides and nerve agents. In this study, the activity of BChE and its sensitivity to inhibition by dibucaine and fluoride was evaluated in 1200 Polish healthy individuals. In addition, molecular analysis of all exons, exon-intron boundaries and the 3'UTR sequence of the BCHE gene was performed in a group of 72 subjects with abnormal BChE activity (<2000 U/L and >5745 U/L) or with DN (Dibucaine Number) or FN (Fluoride-Number) values outside the reference range (DN < 78 and FN < lower than wild type). In a studied group, BChE activity range was similar to those observed in other populations. BChE activity screening allowed to detect UA and UF phenotypes in 26 (2.2%) and 15 (1.2%) individuals, respectively. Observed UA or UF phenotypes were confirmed by direct sequencing and heterozygous c.293A > G or c.1253G > T substitutions were identified in all cases. Nine out of 18 (50%) individuals with BChE activity below 2000 U/L had a mutation in 5'UTR (32G/A), intron 2 (c.1518-121T/C) or exon 4 (c.1699G/A; the K variant mutation). Majority of the individuals with BChE activity ≥6000 U/L were wild type. To summarize, the range of BChE activity in a Polish population is similar to those observed in other countries. We conclude that the BChE phenotyping assay is a reliable method for identification of individuals with the UA and UF genotypes. Copyright Â
© 2016 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  BCHE gene variants; BChE; BChE activity assay; Butyrylcholinesterase; Polymorphisms; Pseudocholinesterase

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Substances:

Year:  2016        PMID: 27109752     DOI: 10.1016/j.cbi.2016.04.030

Source DB:  PubMed          Journal:  Chem Biol Interact        ISSN: 0009-2797            Impact factor:   5.192


  5 in total

1.  Genetic Testing for BCHE Variants Identifies Patients at Risk of Prolonged Neuromuscular Blockade in Response to Succinylcholine.

Authors:  Guang-Dan Zhu; Eric Dawson; Angela Huskey; Ronald J Gordon; Andria L Del Tredici
Journal:  Pharmgenomics Pers Med       Date:  2020-09-30

2.  Synergy between the alteration in the N-terminal region of butyrylcholinesterase K variant and apolipoprotein E4 in late-onset Alzheimer's disease.

Authors:  Jacek Jasiecki; Anna Limon-Sztencel; Monika Żuk; Magdalena Chmara; Dominik Cysewski; Janusz Limon; Bartosz Wasąg
Journal:  Sci Rep       Date:  2019-03-26       Impact factor: 4.379

3.  Butyrylcholinesterase Protein Ends in the Pathogenesis of Alzheimer's Disease-Could BCHE Genotyping Be Helpful in Alzheimer's Therapy?

Authors:  Jacek Jasiecki; Bartosz Wasąg
Journal:  Biomolecules       Date:  2019-10-09

Review 4.  The Role of Butyrylcholinesterase and Iron in the Regulation of Cholinergic Network and Cognitive Dysfunction in Alzheimer's Disease Pathogenesis.

Authors:  Jacek Jasiecki; Monika Targońska; Bartosz Wasąg
Journal:  Int J Mol Sci       Date:  2021-02-18       Impact factor: 5.923

5.  Genetic polymorphism analysis of patients with primary hyperhidrosis.

Authors:  Bryce C Simes; Joshua P Moore; Terry C Brown; Tyler J Rushforth; Angela L Bookout; Chante L Richardson
Journal:  Clin Cosmet Investig Dermatol       Date:  2018-10-11
  5 in total

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