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白细胞介素-6 基因与阻塞性睡眠呼吸暂停关系的研究。

Study of the relationship between the interleukin-6 gene and obstructive sleep apnea.

机构信息

Division of Allergy, Pulmonary and Critical Care, Vanderbilt University Medical Center, Nashville, Tenessee, USA.

出版信息

Clin Transl Sci. 2010 Dec;3(6):337-9. doi: 10.1111/j.1752-8062.2010.00236.x.

Abstract

Because obstructive sleep apnea (OSA) is associated with increased levels of inflammatory cytokines, we examined the relationship between OSA and polymorphisms for interleukin‐6 (). Six single nucleotide polymorphisms (SNPs) within were genotyped in 259 African Americans from the Cleveland Family Study with replication conducted in the Cardiovascular Health Study (= 124). OSA was dichotomized into apnea hypopnea index (AHI) > 15, or on treatment versus absent: AHI < 5. Logistic regression was conducted, adjusting for age and sex in models with and without body mass index (BMI). SNP –6021 was associated with a decreased risk of OSA after adjusting for BMI (Odds Ratio for T allele 0.24, 95%CI [0.09–0.67], = 0.006, = 0.07) under an additive model. This same allele was associated with increased BMI. The results from the replication sample were consistent in direction though not statistically significant (= 0.23). The SNPs were studied in European‐ Americans, although, the minor allele frequency in –6021 was too low (4%) for meaningful comparisons. A synonymous SNP within the coding region was protective of OSA in African Americans; with qualitatively similar findings observed in another cohort. This suggests that variants in may influence the risk of OSA in a pathway that is not explained by obesity. Clin Trans Sci 2010; Volume 3: 337–339

摘要

由于阻塞性睡眠呼吸暂停(OSA)与炎症细胞因子水平升高有关,我们研究了 OSA 与白细胞介素-6()的多态性之间的关系。在克利夫兰家族研究中的 259 名非裔美国人中,对 内的 6 个单核苷酸多态性(SNP)进行了基因分型,并在心血管健康研究中进行了复制(= 124)。将 OSA 分为呼吸暂停低通气指数(AHI)>15 或治疗与无:AHI <5。在有和没有体重指数(BMI)的模型中,通过逻辑回归进行调整,调整年龄和性别。在调整 BMI 后,SNP-6021 与 OSA 的风险降低相关(T 等位基因的优势比为 0.24,95%CI [0.09-0.67],= 0.006,= 0.07),呈加性模型。同一等位基因与 BMI 增加相关。复制样本的结果在方向上一致,但没有统计学意义(= 0.23)。尽管在-6021 中,次要等位基因的频率太低(4%),无法进行有意义的比较,但这些 SNP 仍在欧洲裔美国人中进行了研究。在另一个队列中观察到了 编码区域内同义 SNP 对 OSA 的保护作用。这表明 中的变体可能以肥胖无法解释的途径影响 OSA 的风险。临床转化科学 2010;第 3 卷:337-339

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