患有非炎症性疾病的老年门诊患者体内循环一氧化氮与白细胞介素-17之间的相互作用。

International journal of molecular epidemiology and genetics Pub Date : 2018-06-15 eCollection Date: 2018-01-01
Gleiciane G Avelar, Wilcelly Machado-Silva, Adriane D Henriques, Jeeser A Almeida, Aparecido P Ferreira, Ciro J Brito, Lucy Gomes, Clayton F Moraes, Otávio T Nóbrega
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引用次数: 0

摘要

生物系统中一氧化氮(NOx)的可用性与有利或不利的结果有关。从这个意义上说,一些研究提供的证据表明,一氧化氮产生的不平衡可能是血管疾病病理生理学的基础。我们的研究调查了无重大炎症的老年患者的临床、生化和炎症变量与循环中氮氧化物总水平之间可能存在的关联。我们对 168 名符合初级保健资格的老年病门诊患者的临床(人口统计学、生活方式、人体测量、血压特征)和生化特征(血脂、血糖和荷尔蒙谱)进行了评估。此外,还测量了 10 种炎症介质和氮氧化物的循环水平。相关性测试根据血清氮氧化物对分类或连续性特征进行了分析,结果发现氮氧化物与任何临床或实验室数据之间均无关联,但血浆氮氧化物浓度与免疫介质 IL17a 的水平之间存在负相关(r = -0.236;P = 0.004)。循环氮氧化物和 IL17 之间存在相关性的证据已见诸于文献,其中大部分来自炎症条件下进行的研究。我们的假设是,这种负相关可归因于一种内源性平衡系统,即由血管内皮构成性产生的 NOx 产生 IL17。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Interplay between circulating nitric oxide and interleukin-17 in elderly outpatients with non-inflammatory conditions.

Interplay between circulating nitric oxide and interleukin-17 in elderly outpatients with non-inflammatory conditions.

Nitric oxide (NOx) availability in biological systems is associated with either favorable or unfavorable outcomes. In this sense, several studies bring about evidence that unbalanced NOx production may be underlying to the pathophysiology of vascular disorders. Our study investigated the possible association of clinical, biochemical and inflammatory variables with total circulating levels of NOx in elderly patients devoid of major inflammatory conditions. Clinical (demographics, lifestyle, anthropometry, pressoric traits) and biochemical characteristics (lipemic, glycemic and hormonal profiles) were assessed from 168 geriatrics outpatients eligible for primary care for age-related disorders. Furthermore, circulating levels of 10 inflammatory mediators and of NOx were measured. Correlation tests analyzed categorical or continuous traits according to serum NOx and found no association between NOx and any of the clinical or laboratory data but a negative correlation between plasma NOx concentrations and levels of the immune mediator IL17a (r = -0.236; P = 0.004). Evidence for a correlation between circulating NOx and IL17 is already present in the literature, mostly from studies conducted under inflammatory conditions. Our hypothesis is that such negative correlation can be attributed to an endogenous homeostatic system that IL17 production by the constitutively produced NOx from the vascular endothelium.

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