Genetic Profiling of the Nitric Oxide Synthases’ System in a 55-Year-Old Woman with the Tension-Type Headache and Arterial Hypertension Phenotype: Case Report

P. V. Alyabyeva
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Abstract

The tension-type headache (TTH) and arterial hypertension (AH) phenotype is a common overlap syndrome in adult patients. A genetically determined disturbance of the nitric oxide (NO) synthesis system is actively considered as one of the important possible pathogenetic mechanisms for the development of this phenotype. Neuronal NO-synthase is expressed both in the brain, skeletal muscles, and in the vascular endothelium; therefore, single-nucleotide variants of the NOS1 gene, encoding this enzyme, are the most interesting, but insufficiently studied genetic biomarkers of the TTH and AH phenotype. The aim of the case report is to present the experience of using genetic profiling of the nitric oxide synthases’ system in a 55-year-old patient with treatment-resistant TTH and AH phenotype.
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一名55岁紧张性头痛和动脉高血压表型女性一氧化氮合酶系统的遗传谱分析:病例报告
紧张性头痛(TTH)和动脉高血压(AH)表型是成人患者常见的重叠综合征。一氧化氮(NO)合成系统的遗传干扰被积极认为是该表型发展的重要可能的发病机制之一。神经元no合酶在脑、骨骼肌和血管内皮中均有表达;因此,编码这种酶的NOS1基因的单核苷酸变异是最有趣的,但研究不足的TTH和AH表型的遗传生物标志物。本病例报告的目的是介绍一名55岁TTH和AH表型难治性患者使用一氧化氮合酶系统遗传谱分析的经验。
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