Role and mechanism of IL - 17 and its gene polymorphisms in dyslipidemia caused by obstructive sleep apnea syndrome in children.

Jin Yang
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Abstract

The current research was carried out to explore the role and mechanism of IL - 17 and its gene polymorphisms in dyslipidemia caused by obstructive sleep apnea syndrome in children. For this aim, a total of 86 children with obstructive sleep apnea syndrome admitted to our hospital from January 2018 to January 2020 were selected as the study subjects, and the lipid-related indexes of the children were detected by a fully automatic biochemical analyzer, and they were divided into OSAHS group (54 cases), combined dyslipidemia group (32 cases), and another 40 healthy children who underwent physical examination in our hospital during the same period were selected as the healthy group. Levels of IL-7 and AHI, FEV1 / FVC were analyzed in each group, and levels of TC, TG, and LDL-C were compared to observe different sites of IL-17, namely IL-17A (rs3748067; The loci of IL-17F (rs763780, rs2397084) were genotyped in different groups to analyze the association between IL-17 and dyslipidemia in children with OSAHS. Results showed that higher IL-7 and AHI levels and lower FEV1 / FVC levels were found in the combined dyslipidemia and OSAHS groups compared with the healthy group, and higher IL-7 and AHI levels and lower FEV1 / FVC levels were found in the combined dyslipidemia group compared with the OSAHS group (P < 0.05); TC, TG and LDL-C level expression were higher in the combined dyslipidemia and OSAHS groups compared with the healthy group, and TC, TG and LDL-C level expression were higher in the combined dyslipidemia group compared with the OSAHS group (P < 0.05). IL-17 was positively correlated with TC, TG and LDL-C. It was concluded that in the development of OSAHS, IL-7 levels are significantly expressed, at the same time OSAHS children progress dyslipidemia, which has some correlation with IL-17, and IL-17 gene polymorphism, IL-17A (rs3748067); All were significantly expressed in the IL-17F (rs763780, rs2397084) locus.

IL - 17及其基因多态性在儿童阻塞性睡眠呼吸暂停综合征所致血脂异常中的作用、机制
本研究旨在探讨IL - 17及其基因多态性在儿童阻塞性睡眠呼吸暂停综合征所致血脂异常中的作用及机制。为此,选取2018年1月至2020年1月我院收治的阻塞性睡眠呼吸暂停综合征患儿86例为研究对象,采用全自动生化分析仪检测患儿脂质相关指标,分为OSAHS组(54例)、合并血脂异常组(32例)、选取同期在我院体检的健康儿童40名作为健康组。分析各组患者IL-7、AHI、FEV1 / FVC水平,比较TC、TG、LDL-C水平,观察IL-17的不同位点,即IL-17A (rs3748067;对不同组IL-17F位点rs763780、rs2397084进行基因分型,分析IL-17与OSAHS患儿血脂异常的关系。结果显示:血脂异常与OSAHS合并组与健康组比较,IL-7、AHI水平升高,FEV1 / FVC水平降低;血脂异常合并组与OSAHS合并组比较,IL-7、AHI水平升高,FEV1 / FVC水平降低(P < 0.05);血脂异常组和OSAHS联合组TC、TG、LDL-C水平表达高于健康组,且合并血脂异常组TC、TG、LDL-C水平表达高于OSAHS组(P < 0.05)。IL-17与TC、TG、LDL-C呈正相关。综上所述,在OSAHS的发展过程中,IL-7水平显著表达,同时OSAHS患儿进展为血脂异常,这与IL-17、IL-17基因多态性、IL-17A (rs3748067)有一定的相关性;IL-17F (rs763780, rs2397084)位点均显著表达。
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