Cardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, WA, United States.
Cardiovascular Health Research Unit, Department of Epidemiology, University of Washington, Seattle, WA, United States.
EBioMedicine. 2019 Mar;41:44-49. doi: 10.1016/j.ebiom.2018.12.046. Epub 2018 Dec 26.
Animal studies suggest sphingolipids as an early marker of impaired glucose metabolism; however, research in humans is limited. We evaluated whether individual sphingolipid species were associated with fasting plasma glucose and incident impaired fasting glucose in a longitudinal cohort study.
We measured 15 sphingolipid species from blood samples collected in 2001-2003 from 2145 participants without prevalent diabetes in the Strong Heart Family Study. Fasting plasma glucose was measured in blood samples collected at baseline and follow-up (mean 5.5 years after baseline).
The average age of study participants was 38 years; 41% were men. Ceramide, sphingomyelin, and glucosylceramide species levels were higher in older participants; lactosyl-ceramide levels were higher in participants with lower BMIs. In adjusted analyses, greater concentrations of most ceramide species and lower lactosyl-ceramide with palmitic acid (LC-16) were associated with higher glucose levels at baseline. We did not observe associations of sphingomyelin species or glucosyl-ceramide species with glucose levels. Associations of sphingolipid levels with fasting glucose levels at follow-up were similar but had greater uncertainty than associations with baseline glucose. Although no statistically significant associations of sphingolipids with incident impaired fasting glucose were present, results were similar to glucose analyses.
We identified several ceramide species associated with higher fasting glucose levels and one sphingolipid, LC-16, that was associated with lower fasting glucose levels. These findings compliment previous research, which linked these sphingolipids with fasting insulin levels, and suggest that higher levels of these ceramides and lower LC-16 may be an early marker of impaired glucose metabolism. FUND: US National Institutes Health.
动物研究表明神经酰胺作为葡萄糖代谢受损的早期标志物;然而,人类的研究有限。我们评估了在一项纵向队列研究中,个体神经酰胺种类是否与空腹血糖和新发空腹血糖受损相关。
我们从 2145 名无糖尿病的 Strong Heart 家族研究参与者于 2001-2003 年采集的血液样本中测量了 15 种神经酰胺种类。空腹血糖在基线和随访时(基线后平均 5.5 年)的血液样本中测量。
研究参与者的平均年龄为 38 岁;41%为男性。在年龄较大的参与者中,神经酰胺、神经鞘磷脂和葡萄糖神经酰胺种类的水平较高;在 BMI 较低的参与者中,乳糖神经酰胺水平较高。在调整后的分析中,大多数神经酰胺种类的浓度较高,棕榈酸乳糖神经酰胺(LC-16)较低,与基线时的高血糖水平相关。我们没有观察到神经鞘磷脂种类或葡萄糖神经酰胺种类与血糖水平之间的关联。与空腹血糖水平的随访关联与基线葡萄糖的关联相似,但不确定性更大。尽管神经鞘磷脂与新发空腹血糖受损之间没有统计学显著关联,但结果与血糖分析相似。
我们确定了几种与空腹血糖水平升高相关的神经酰胺种类,以及一种与空腹血糖水平降低相关的神经鞘磷脂,LC-16。这些发现补充了先前的研究,该研究将这些神经鞘磷脂与空腹胰岛素水平联系起来,并表明这些神经酰胺水平较高和 LC-16 水平较低可能是葡萄糖代谢受损的早期标志物。
美国国立卫生研究院。