内科学
医学
基因型
载脂蛋白E
血脂异常
内分泌学
阻塞性睡眠呼吸暂停
脂蛋白
载脂蛋白B
胃肠病学
胆固醇
肥胖
遗传学
生物
基因
疾病
作者
Jelena Vekic,Pavol Joppa,Viera Habalova,Radovan Tisko,Aleksandra Zeljkovic,Pavol Pobeha,Tamara Gojković,Vesna Spasojević-Kalimanovska,Zuzana Strbova,Zuzana Kuklisova,Eva Slabá,Manfredi Rizzo,Ruzena Tkacova,Jelena Vekic,Pavol Joppa,Viera Habalova,Radovan Tisko,Aleksandra Zeljkovic,Pavol Pobeha,Vesna Spasojević-Kalimanovska
出处
期刊:Angiology
[SAGE Publishing]
日期:2016-03-04
卷期号:67 (10): 937-944
被引量:6
标识
DOI:10.1177/0003319716636512
摘要
Obstructive sleep apnea (OSA) is associated with dyslipidemia and increased cardiovascular risk. We assessed the effects of apolipoprotein E ( APOE) genotype on low-density lipoprotein (LDL) and high-density lipoprotein (HDL) particle size and lipid subclasses (separated by gradient gel electrophoresis) in patients with OSA. Stable patients (n = 181) prospectively recruited underwent full polysomnography. Both LDL particle size and LDL I proportion were reduced from ∊3∊3 homozygotes to ∊2 carriers and to ∊4 carriers (analysis of variance: P = .024; P = .040, respectively); carriers of the ∊4 allele of the APOE genotype had significantly lower LDL particle size and LDL I proportion compared to ∊3∊3 homozygotes ( P < .05 for both comparisons). Insulin resistance increased from patients with no OSA to those with mild–moderate and to those with severe OSA ( P < .001). In multivariate analysis, LDL size was independently predicted by APOE genotype, male gender, and the presence of metabolic syndrome (MetS; P = .001, P = .020, P = .027, respectively). The HDL particle size was not affected by APOE genotype. Our data demonstrate that both the ∊4 APOE genotype and MetS are independently related to smaller LDL size in patients with OSA.
科研通智能强力驱动
Strongly Powered by AbleSci AI