Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Nat Med. 2023 Mar;29(3):710-718. doi: 10.1038/s41591-023-02223-9. Epub 2023 Feb 27.
Artificial sweeteners are widely used sugar substitutes, but little is known about their long-term effects on cardiometabolic disease risks. Here we examined the commonly used sugar substitute erythritol and atherothrombotic disease risk. In initial untargeted metabolomics studies in patients undergoing cardiac risk assessment (n = 1,157; discovery cohort, NCT00590200 ), circulating levels of multiple polyol sweeteners, especially erythritol, were associated with incident (3 year) risk for major adverse cardiovascular events (MACE; includes death or nonfatal myocardial infarction or stroke). Subsequent targeted metabolomics analyses in independent US (n = 2,149, NCT00590200 ) and European (n = 833, DRKS00020915 ) validation cohorts of stable patients undergoing elective cardiac evaluation confirmed this association (fourth versus first quartile adjusted hazard ratio (95% confidence interval), 1.80 (1.18-2.77) and 2.21 (1.20-4.07), respectively). At physiological levels, erythritol enhanced platelet reactivity in vitro and thrombosis formation in vivo. Finally, in a prospective pilot intervention study ( NCT04731363 ), erythritol ingestion in healthy volunteers (n = 8) induced marked and sustained (>2 d) increases in plasma erythritol levels well above thresholds associated with heightened platelet reactivity and thrombosis potential in in vitro and in vivo studies. Our findings reveal that erythritol is both associated with incident MACE risk and fosters enhanced thrombosis. Studies assessing the long-term safety of erythritol are warranted.
人工甜味剂被广泛用作糖的替代品,但人们对其对心血管疾病风险的长期影响知之甚少。在这里,我们研究了常用的糖替代品赤藓糖醇和动脉粥样硬化血栓形成疾病风险。在对接受心脏风险评估的患者进行的初步非靶向代谢组学研究(n=1157;发现队列,NCT00590200)中,多种多元醇甜味剂的循环水平,特别是赤藓糖醇,与主要不良心血管事件(MACE;包括死亡或非致死性心肌梗死或中风)的(3 年)发病风险相关。随后,在独立的美国(n=2149,NCT00590200)和欧洲(n=833,DRKS00020915)稳定患者的验证队列中进行的靶向代谢组学分析证实了这一关联(第四与第一四分位的调整后的危险比(95%置信区间),分别为 1.80(1.18-2.77)和 2.21(1.20-4.07))。在生理水平下,赤藓糖醇增强了体外血小板反应性和体内血栓形成。最后,在一项前瞻性的试验性干预研究(NCT04731363)中,在健康志愿者(n=8)中摄入赤藓糖醇会导致血浆赤藓糖醇水平显著且持续(>2d)升高,远高于体外和体内研究中与血小板反应性和血栓形成潜力升高相关的阈值。我们的研究结果表明,赤藓糖醇既与 MACE 风险的发生相关,又促进血栓形成。需要评估赤藓糖醇长期安全性的研究。