Emory Nell Hodgson School of Nursing, Atlanta, GA, USA.
Emory Department of Psychology, Atlanta, GA, USA.
Sleep Breath. 2023 Dec;27(6):2139-2153. doi: 10.1007/s11325-023-02828-x. Epub 2023 May 6.
US adults who report experiencing insufficient sleep are more likely to suffer from metabolic disorders such as hyperlipidemia, diabetes, and obesity than those with sufficient sleep. Less is understood about the underlying molecular mechanisms connecting these phenomena. A systematic, qualitative review of metabolomics studies exploring metabolic changes in response to sleep insufficiency, sleep deprivation, or circadian disruption was conducted in accordance with PRISMA guidelines.
An electronic literature review in the PubMed database was performed considering publications through May 2021 and screening and eligibility criteria were applied to articles retrieved. The following keywords were used: "metabolomics" and "sleep disorders" or "sleep deprivation" or "sleep disturbance" or "circadian rhythm." After screening and addition of studies included from reference lists of retrieved studies, 16 records were identified for review.
Consistent changes in metabolites were observed across studies between individuals experiencing sleep deprivation compared to non-sleep deprived controls. Significant increases in phosphatidylcholines, acylcarnitines, sphingolipids, and other lipids were consistent across studies. Increased levels of amino acids such as tryptophan and phenylalanine were also noted. However, studies were limited to small samples of young, healthy, mostly male participants conducted in short inpatient sessions, limiting generalizability.
Changes in lipid and amino acid metabolites accompanying sleep deprivation and/or circadian rhythms may indicate cellular membrane and protein breakdown underlying the connection between sleep disturbance, hyperlipidemia, and other metabolic disorders. Larger epidemiological studies examining changes in the human metabolome in response to chronic insufficient sleep would help elucidate this relationship.
相较于睡眠充足的成年人,报告睡眠不足的美国成年人更有可能患有代谢紊乱,如高血脂、糖尿病和肥胖症。对于将这些现象联系起来的潜在分子机制,人们的了解较少。根据 PRISMA 指南,对探索睡眠不足、睡眠剥夺或昼夜节律紊乱对代谢变化的影响的代谢组学研究进行了系统的、定性的综述。
在 PubMed 数据库中进行电子文献检索,检索时间截至 2021 年 5 月,并对检索到的文章应用筛选和纳入标准。使用了以下关键词:“代谢组学”和“睡眠障碍”或“睡眠剥夺”或“睡眠紊乱”或“昼夜节律”。经过筛选和纳入从检索到的研究的参考文献列表中添加的研究,确定了 16 份记录进行综述。
与非睡眠剥夺对照组相比,睡眠剥夺个体之间的研究观察到代谢物的一致变化。跨研究观察到磷脂酰胆碱、酰基肉碱、鞘脂和其他脂质显著增加。还注意到色氨酸和苯丙氨酸等氨基酸水平升高。然而,这些研究仅限于在短期住院期间进行的、样本量小的、健康的、大多数为男性的参与者,限制了其普遍性。
伴随睡眠剥夺和/或昼夜节律变化的脂质和氨基酸代谢物的变化可能表明细胞膜和蛋白质分解是睡眠障碍、高血脂和其他代谢紊乱之间联系的基础。更大规模的流行病学研究检查人类代谢组对慢性睡眠不足的反应变化,将有助于阐明这种关系。