LUNAM University, Angers, France; Department of Respiratory Diseases, Angers University Hospital, Angers, France; INSERM U1063, Angers, France.
CERMES, CNRS UMR8211-INSERM U988-EHESS, Villejuif, France.
Chest. 2013 Jun;143(6):1584-1589. doi: 10.1378/chest.12-1652.
There is growing evidence from animal models that intermittent hypoxemia (IH) may induce dyslipidemia. Altered lipid metabolism may contribute to the increased cardiovascular risk observed in obstructive sleep apnea (OSA). In this multisite, cross-sectional study, we tested the hypothesis that there is an independent association between nocturnal IH and dyslipidemia in OSA.
Fasting serum lipid levels were measured in 2,081 patients (638 women) undergoing nocturnal recording for clinical suspicion of OSA. Multivariate regression analyses were performed to evaluate the independent associations between oxygen desaturation index (ODI) and lipid profile after adjustment for potential confounders, including components of the metabolic syndrome (MS) or the MS itself. Adjusted OR for metabolic dyslipidemia (triglycerides [TG] ≥ 150 mg/dL and high-density lipoprotein cholesterol [HDL-C] ≤ 50 mg/dL for women and ≤ 40 mg/dL for men) according to quartiles of ODI were determined by logistic regression.
Total cholesterol and low-density lipoprotein cholesterol were not associated with ODI. In contrast, nocturnal IH and OSA severity were associated with higher TG levels and lower HDL-C levels after adjustment for confounding factors. The association between ODI and TG and HDL-C levels was independent of the MS. Adjusted OR (95% CIs) for metabolic dyslipidemia were 1 (reference), 1.56 (1.24-1.96), 1.72 (1.29-2.29), and 1.93 (1.55-2.41) for ODI ≤ 7, > 7 to ≤ 18, > 18 to ≤ 38, and > 38, respectively (P < .0001 for linear trend).
Nocturnal IH is independently associated with metabolic dyslipidemia, which may predispose patients with OSA to a higher risk of cardiovascular disease.
越来越多的动物模型证据表明,间歇性低氧血症(IH)可能导致血脂异常。脂质代谢的改变可能导致阻塞性睡眠呼吸暂停(OSA)患者观察到的心血管风险增加。在这项多中心、横断面研究中,我们检验了这样一个假设,即夜间 IH 与 OSA 患者的血脂异常之间存在独立的关联。
对 2081 名(638 名女性)因临床怀疑 OSA 而接受夜间记录的患者进行空腹血清脂质水平检测。进行多元回归分析,以评估在调整潜在混杂因素(包括代谢综合征[MS]的组成部分或 MS 本身)后,氧饱和度下降指数(ODI)与脂质谱之间的独立关联。根据 ODI 的四分位数,通过逻辑回归确定代谢性血脂异常(甘油三酯[TG]≥150mg/dL,女性高密度脂蛋白胆固醇[HDL-C]≤50mg/dL,男性 HDL-C≤40mg/dL)的调整后 OR。
总胆固醇和低密度脂蛋白胆固醇与 ODI 无关。相反,夜间 IH 和 OSA 严重程度与 TG 水平升高和 HDL-C 水平降低相关,在调整混杂因素后也是如此。ODI 与 TG 和 HDL-C 水平之间的关联独立于 MS。代谢性血脂异常的调整后 OR(95%置信区间)分别为 1(参考)、1.56(1.24-1.96)、1.72(1.29-2.29)和 1.93(1.55-2.41),对于 ODI≤7、>7 至≤18、>18 至≤38 和 >38(P < 0.0001 线性趋势)。
夜间 IH 与代谢性血脂异常独立相关,这可能使 OSA 患者更容易发生心血管疾病风险。