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几丁质酶基因多态性和突变限制了结节病中几丁质酶表达的测定。

Chitotriosidase gene polymorphisms and mutations limit the determination of chitotriosidase expression in sarcoidosis.

机构信息

Division of Clinical Physiology, Department of Cardiology, Faculty of Medicine, 22 Móricz Zsigmond str., H-4032 Debrecen, Hungary; University of Debrecen, Kálmán Laki Doctoral School of Biomedical and Clinical Sciences, Hungary.

University of Debrecen, Kálmán Laki Doctoral School of Biomedical and Clinical Sciences, Hungary; Department of Cardiology, Faculty of Medicine, University of Debrecen, 22 Móricz Zsigmond str., H-4032 Debrecen, Hungary.

出版信息

Clin Chim Acta. 2021 Feb;513:50-56. doi: 10.1016/j.cca.2020.11.025. Epub 2020 Dec 8.

Abstract

Serum chitotriosidase (CTO) activity was proposed as a biomarker in sarcoidosis being potentially useful in diagnostics. Nevertheless, a common duplication polymorphism (c.1049_1072dup24, Dup24) of the CTO gene influences CTO activity and thereby compromises its use in sarcoidosis. Here we aimed to substitute CTO activity with CTO concentration to prevent the confounding effect of Dup24. CTO activity, concentration and genetic backgrounds were determined in 80 histopathology proven sarcoidosis patients and 133 healthy individuals. CTO activities were lower in healthy individuals and sarcoidosis patients heterozygous for Dup24 mutation (472 ± 367 mU/L, n = 49; 2300 ± 2105 mU/L, n = 29) than in homozygous wild types (838 ± 856 mU/L, n = 81; 5125 ± 4802 mU/L, n = 48; p < 0.001, respectively). Sera of Dup24 homozygous individuals had no CTO activity. CTO concentrations were also lower in healthy individuals and sarcoidosis patients heterozygous for Dup24 mutation (7.2 ± 1.9 µg/L, n = 11; 63.16 ± 56.5 µg/L, n = 29) than in homozygous wild types (18.9 ± 13.0 µg/L, n = 36; 157.1 ± 132.4 µg/L, n = 47, p < 0.001, respectively) suggestive for an interaction between Dup24 mutation and CTO concentration determinations. We also identified a healthy Hungarian male subject without CTO activity carrying a rare mutation (c.(965_993)del), which mutation has been considered unique for Cypriot population to date. Taken together, CTO concentration determination does not add to the CTO activity measurement when CTO is used as a biomarker in sarcoidosis. Therefore, genotyping of CTO gene should be involved in the interpretation of laboratory findings.

摘要

血清几丁质酶(CTO)活性被提议作为结节病的生物标志物,在诊断中可能有用。然而,CTO 基因的常见重复多态性(c.1049_1072dup24,Dup24)会影响 CTO 活性,从而影响其在结节病中的应用。在这里,我们旨在用 CTO 浓度替代 CTO 活性,以防止 Dup24 的混杂影响。在 80 例组织病理学证实的结节病患者和 133 名健康个体中,测定了 CTO 活性、浓度和遗传背景。Dup24 突变杂合子(472 ± 367 mU/L,n = 49;2300 ± 2105 mU/L,n = 29)的健康个体和结节病患者的 CTO 活性低于野生型纯合子(838 ± 856 mU/L,n = 81;5125 ± 4802 mU/L,n = 48;p < 0.001)。Dup24 纯合子个体的血清中没有 CTO 活性。Dup24 突变杂合子(7.2 ± 1.9 µg/L,n = 11;63.16 ± 56.5 µg/L,n = 29)的健康个体和结节病患者的 CTO 浓度也低于野生型纯合子(18.9 ± 13.0 µg/L,n = 36;157.1 ± 132.4 µg/L,n = 47,p < 0.001),提示 Dup24 突变和 CTO 浓度测定之间存在相互作用。我们还发现了一名没有 CTO 活性的匈牙利男性健康个体,携带一种罕见的突变(c.(965_993)del),迄今为止,这种突变被认为是塞浦路斯人所独有的。综上所述,当 CTO 作为结节病的生物标志物时,CTO 浓度的测定并不能增加 CTO 活性的测定。因此,在解释实验室结果时,应该对 CTO 基因进行基因分型。

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