BDNF (rs6265)、VDR (rs2228570)和NMDA (rs4880213)基因型联合对自身免疫性甲状腺炎和甲状腺功能减退患者认知障碍发展的复杂影响

I. Kamyshna, L. Pavlovych, I. Pankiv, V. Pankiv, V. Maslyanko, N. Bytsko, A. Kamyshnyi
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引用次数: 1

摘要

背景。大量研究表明,甲状腺疾病会影响认知功能。与内分泌和神经系统病理相关的基因多态性具有民族和人群特异性,这决定了需要在某一地区对其进行研究。本研究的目的是研究BDNF (rs6265)、VDR (rs2228570)和NMDA (rs4880213)基因多态性对乌克兰西部地区人群自身免疫性甲状腺炎和甲状腺功能减退患者认知功能障碍的联合影响,并预测认知障碍的发生。材料和方法。该研究共涉及153名自身免疫性甲状腺炎和甲状腺功能减退患者。使用TaqMan探针和TaqMan基因分型Master Mix(4371355)对VDR (rs2228570)、BDNF (rs6265)和NMDA (rs4880213)基因多态性在CFX96™实时荧光定量PCR检测系统(Bio-Rad Laboratories, Inc., USA)上进行基因分型。按照试剂盒说明书(Applied Biosystems, USA)进行TaqMan基因分型的聚合酶链反应。我们通过简易精神状态检查来检测认知功能的下降。结果。携带CC/AG/CC基因型的组合显著降低发生认知障碍的风险(优势比(OR) = 0.1410;95%置信区间(CI) 0.0181 ~ 1.0965;p = 0.0416)。同时,携带CT/AG/CT基因型组合的患者发生认知障碍的风险增加5倍以上(OR = 5.1915;95% ci 1.2471-21.6107;p = 0.0214)和CT/AG/TT基因型组合- 10倍(OR = 10.1224;95% ci 1.1037-92.8401;p = 0.0281)。CT/AA/CT基因型组合携带者发生认知障碍的风险增加6.4倍(OR = 6.4062;95% ci 1.2019-34.1471;p = 0.0253)。结论。在自身免疫性甲状腺炎和甲状腺功能减退患者中,携带CC/AG/CC基因型组合BDNF (rs6265)、VDR (rs2228570)和NMDA (rs4880213)基因的患者发生认知障碍的风险降低,而携带CT/AG/CT、CT/AG/TT和CT/AA/CT的患者发生认知障碍的风险增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The complex influence of the combination of the BDNF (rs6265), VDR (rs2228570), and NMDA (rs4880213) genotypes on the development of cognitive disorders in patients with autoimmune thyroiditis and hypothyroidism
Background. Numerous studies have demonstrated that thyroid conditions can affect cognitive function. Gene polymorphisms associated with pathology of the endocrine and nervous system have ethnic and population specificity, which determines the need to study them in a certain region. The purpose of the study was to investigate the combined impact of the BDNF (rs6265), VDR (rs2228570), and NMDA (rs4880213) gene polymorphisms on cognitive impairment in patients with autoimmune thyroiditis and hypothyroidism among the population of Western regions of Ukraine, and to predict the onset of cognitive disorders. Materials and methods. The study involved a total of 153 patients with autoimmune thyroiditis and hypothyroidism. Genotyping of the VDR (rs2228570), BDNF (rs6265), and NMDA (rs4880213) gene polymorphism using TaqMan probes and TaqMan Genotyping Master Mix (4371355) was performed on CFX96™ Real-Time PCR Detection System (Bio-Rad Laboratories, Inc., USA). Polymerase chain reaction for TaqMan genotyping was carried out according to the kit instructions (Applied Biosystems, USA). We detect a decline in cognitive function using the Mini-Mental State Examination. Results. Carrying a combination of CC/AG/CC genotypes significantly reduces the risk of developing cognitive impairment (odds ratio (OR) = 0.1410; 95% confidence interval (CI) 0.0181–1.0965; p = 0.0416). At the same time, carrying a combination of CT/AG/CT genotypes increases the risk of cognitive impairment by more than 5 times (OR = 5.1915; 95% CI 1.2471–21.6107; p = 0.0214) and a combination of CT/AG/TT genotypes — by 10 times (OR = 10.1224; 95% CI 1.1037–92.8401; p = 0.0281). Carriers of the CT/AA/CT genotype combination have a 6.4-fold increased risk of cognitive impairment (OR = 6.4062; 95% CI 1.2019–34.1471; p = 0.0253). Conclusions. Among patients with autoimmune thyroiditis and hypothyroidism, carriers of the CC/AG/CC genotype combination of the BDNF (rs6265), VDR (rs2228570) and NMDA (rs4880213) genes have a reduced risk of developing cognitive disorders, while carriers of the CT/AG/CT, CT/AG/TT and CT/AA/CT have an increased risk of cognitive impairment.
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