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  • 标题:Obstructive sleep apnea and effects of continuous positive airway pressure on triglyceride-rich lipoprotein metabolism
  • 作者:Luciano F. Drager ; Thauany M. Tavoni ; Vanessa M. Silva
  • 期刊名称:JLR Papers In Press
  • 印刷版ISSN:0022-2275
  • 电子版ISSN:1539-7262
  • 出版年度:2018
  • 卷号:59
  • 期号:6
  • 页码:1027-1033
  • DOI:10.1194/jlr.M083436
  • 语种:English
  • 出版社:American Society for Biochemistry and Molecular Biology
  • 摘要:This study aimed to explore lipoprotein metabolism in obstructive sleep apnea (OSA) and the effects of continuous positive airway pressure (CPAP). We studied 15 men with severe OSA [apnea-hypopnea index (AHI) ≥30 events/hour] and 12 age-, BMI-, and waist circumference-matched volunteers without OSA (AHI <5 events/hour). Carotid intima-media thickness (CIMT) was determined by a blind examiner. After 12 h fasting, a triglyceride-rich chylomicron-like emulsion, labeled with [14C]cholesteryl oleate and [3H]triolein, was injected intravenously followed by blood sample collection at preestablished times. Fractional clearance rate (FCR) of the radiolabeled lipids was estimated by compartmental analysis of radioisotope decay curves. Compared with controls, patients with OSA showed a significant delay in both cholesteryl ester FCR (0.0126 ± 0.0187 vs. 0.0015 ± 0.0025 min−1; P = 0.0313) and triglycerides FCR (0.0334 ± 0.0390 vs. 0.0051 ± 0.0074 min−1; P = 0.0001). CIMT was higher in the OSA group: 620 ± 17 vs. 725 ± 29 µm; P = 0.004. Cholesteryl ester FCRs were inversely related to total sleep time <90% ( r = −0.463; P = 0.029) and CIMT ( r = −0.601; P = 0.022). The triglyceride FCR was inversely correlated with AHI ( r = −0.537; P = 0.04). In a subgroup of patients treated with CPAP for 3 months (n = 7), triglyceride FCR increased 5-fold ( P = 0.025), but the cholesteryl ester FCR was unchanged. In conclusion, severe OSA decreased lipolysis of triglyceride-rich lipoproteins and delayed removal of remnants. CPAP treatment may be effective to restore the lipolysis rates.
  • 关键词:chylomicrons ; chylomicron remnants ; lipid and lipoprotein metabolism ; lipoprotein kinetics ; postprandial lipidemia ; cardiovascular diseases ; clinical studies
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