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首页> 外文期刊>Cancer causes and control: CCC >Metabolomics profiling of visceral and abdominal subcutaneous adipose tissue in colorectal cancer patients: results from the ColoCare study
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Metabolomics profiling of visceral and abdominal subcutaneous adipose tissue in colorectal cancer patients: results from the ColoCare study

机译:结肠直肠癌患者的内脏和腹部皮下脂肪组织的代谢组科分析:Colocare研究的结果

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Purpose Underlying mechanisms of the relationship between body fatness and colorectal cancer remain unclear. This study investigated associations of circulating metabolites with visceral (VFA), abdominal subcutaneous (SFA), and total fat area (TFA) in colorectal cancer patients. Methods Pre-surgery plasma samples from 212 patients (stage I-IV) from the ColoCare Study were used to perform targeted metabolomics. VFA, SFA, and TFA were quantified by computed tomography scans. Partial correlation and linear regression analyses of VFA, SFA, and TFA with metabolites were computed and corrected for multiple testing. Cox proportional hazards were used to assess 2-year survival. Results In patients with metastatic tumors, SFA and TFA were statistically significantly inversely associated with 16 glycerophospholipids (SFA: p(FDR) range 0.017-0.049; TFA: p(FDR) range 0.029-0.048), while VFA was not. Doubling of ten of the aforementioned glycerophospholipids was associated with increased risk of death in patients with metastatic tumors, but not in patients with non-metastatic tumors (p(het) range: 0.00044-0.049). Doubling of PC ae C34:0 was associated with ninefold increased risk of death in metastatic tumors (Hazard Ratio [HR], 9.05; 95% confidence interval [CI] 2.17-37.80); an inverse association was observed in non-metastatic tumors (HR 0.17; 95% CI 0.04-0.87; p(het) = 0.00044). Conclusion These data provide initial evidence that glycerophospholipids in metastatic colorectal cancer are uniquely associated with subcutaneous adiposity, and may impact overall survival.
机译:目的的脂肪和结直肠癌之间关系的基础机制仍然不清楚。本研究调查了循环代谢物与内脏(VFA),腹部皮下(SFA)和结肠直肠癌患者的总脂肪区域(TFA)的关联。方法采用来自Colocare研究的212名患者(第IV阶段IV)的前术前血浆样品进行靶向代谢组学。 VFA,SFA和TFA通过计算机断层扫描扫描量化。计算和校正VFA,SFA和TFA的局部相关和线性回归分析,并校正多次测试。 COX比例危害用于评估2年生存率。结果患有转移性肿瘤的患者,SFA和TFA与16种甘油磷脂(SFA:P(FDR)范围0.017-0.049; TFA:P(FDR)范围0.029-0.048),SFA和TFA统计学显着呈统计学上显着呈统计学上。上述10个上述甘油磷脂的加倍与转移性肿瘤患者的死亡风险增加有关,但不含非转移性肿瘤的患者(P(HET)范围:0.00044-0.049)。 PC AE C34的加倍C34:0与九倍增加了转移性肿瘤死亡风险(危险比[HR],9.05; 95%; 95%置信区间[CI] 2.17-37.80);在非转移性肿瘤中观察到逆关联(HR 0.17; 95%CI 0.04-0.87; P(HET)= 0.00044)。结论这些数据提供了初步证据,即转移性结肠直肠癌中的甘油磷脂是唯一与皮下肥胖相关的,并且可能会影响整体存活。

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