Dijon, France.
Reims, France.
Aliment Pharmacol Ther. 2020 Nov;52(9):1503-1515. doi: 10.1111/apt.16022. Epub 2020 Aug 11.
Disturbances in fatty acid (FA) metabolism have been reported in cirrhosis, but the role of FAs in the development of hepatocellular carcinoma (HCC) is still unclear. Biomarkers are a promising means to explore the associations between exogenous intake or endogenous production of FAs and cancer risk.
To estimate the relationship between fatty acid content in erythrocyte membranes and HCC risk in cirrhotic patients METHODS: The "CiRCE" case-control study recruited cirrhotic patients from six French hospitals between 2008 and 2012. Cases were cirrhotic patients with HCC (n = 349); controls were cirrhotic patients without HCC at inclusion (n = 550). FA composition of phospholipids in erythrocyte membranes was determined by high performance gas chromatography. Odds ratios for HCC risk according to FA concentrations were estimated with multivariable logistic regression.
HCC patients were older and more often men (P < 0.001). In both groups, saturated FAs represented more than 39% of all FAs in erythrocyte membranes, mono-unsaturated FAs around 14%, and polyunsaturated FAs around 46%. High levels of C15:0 + C17:0, C20:1 n-9, C18:2 n-6 and C20:2 n-6 were associated with higher risk of HCC. The levels of C18:0 and C20:4 n-6 were lower in HCC cases than in controls.
The FA composition of erythrocyte membranes differed according to the presence of HCC with higher levels of saturated FAs, linoleic and eicosadienoic acids, and lower levels of stearic and arachidonic acids. These alterations may reflect particular dietary patterns and/or altered FA metabolism. Further investigations are warranted.
已有研究报道,肝硬化患者的脂肪酸(FA)代谢出现紊乱,但 FA 在肝细胞癌(HCC)发展中的作用仍不清楚。生物标志物是探索外源性摄入或内源性产生的 FA 与癌症风险之间关联的一种很有前途的方法。
评估红细胞膜中 FA 含量与肝硬化患者 HCC 风险之间的关系。
“CiRCE”病例对照研究于 2008 年至 2012 年在法国六家医院招募了肝硬化患者。病例为合并 HCC 的肝硬化患者(n=349);对照组为入组时无 HCC 的肝硬化患者(n=550)。采用高效气相色谱法测定红细胞膜中磷脂的 FA 组成。采用多变量逻辑回归估计 FA 浓度与 HCC 风险的比值比。
HCC 患者年龄较大且更多为男性(P<0.001)。在两组中,红细胞膜中饱和 FA 均超过所有 FA 的 39%,单不饱和 FA 约为 14%,多不饱和 FA 约为 46%。C15:0+C17:0、C20:1 n-9、C18:2 n-6 和 C20:2 n-6 水平较高与 HCC 风险增加相关。与对照组相比,HCC 病例中 C18:0 和 C20:4 n-6 的水平较低。
根据是否存在 HCC,红细胞膜中 FA 组成存在差异,表现为饱和 FA、亚油酸和二十碳二烯酸水平升高,硬脂酸和花生四烯酸水平降低。这些改变可能反映了特定的饮食模式和/或 FA 代谢改变。需要进一步研究。