在患有严重喘的患者中评估阿迪波金状况和勒素受体基因多态性
Saule Maimysheva1, Lyudmila Karazhanova1, Andrey Orekhov1
1Department of Internal Medicine, Semey Medical University, Semey 071400, Kazakhstan.
莱普和阿迪波内克水平,以及一种特定的莱普受体基因变异,可以预测严重的喘. 叶黄素受体基因的A/A基因型与患上失控喘的风险更高有关.
科学领域:
- 肺部病理学 肺部病理学
- 遗传学 是一个遗传学.
- 代谢综合征是代谢综合征的一种.
背景情况:
- 在发达国家,严重的喘影响3-10%的患者.
- 勒普丁和阿迪波内克丁等阿迪波金在炎症和新陈代谢中起作用.
- 勒受体基因 (LEPR) 多态性正在被研究,以确定它们与喘严重程度的关联.
研究的目的:
- 调查莱普和阿迪波内克的预后作用.
- 为了检查丁受体基因多态性的关联 Gln223Arg.
- 要将这些因素与难以控制和严重的喘相关联.
主要方法:
- 研究包括200名住院的喘患者.
- 测量了腺素,素,它们的比例,以及促炎性细胞因子 (IL-6,IL-8,TNF-alpha).
- 通过实时PCR评估呼吸功能 (FEV1,FVC) 和基因型的LEPR Gln223Arg多态性.
主要成果:
- 没有控制的喘患者显示了代谢综合征的高患病率 (74.3%).
- 阿迪波涅克/莱普丁比率与埃索诺菲尔和细胞因子相反相关,与FEV1/FVC直接相关.
- 莱普尔Gln223Arg的同卵性A/A等位基因与失控喘风险增加有关 (p=0.007).
结论:
- 莱普受体多态性,特别是A/A基因型,可能表明患有严重,难以控制的喘的可能性更高.
- 阿迪波金水平和LEPR基因型是喘严重程度的潜在生物标志物.
- 进一步的研究可以探索与喘中瘦素信号传递相关的治疗点.
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