From the Mallinckrodt Institute of Radiology (G.K.N., V.M.M., J.E.I.), Department of Genetics (A.K.Y.Y., J.E.I.), Computational and Systems Biology Program (A.K.Y.Y.), and Division of Biostatistics (A.S.), Washington University School of Medicine, 660 S Euclid Ave, Campus Box 8131, St Louis, MO 63110.
Radiology. 2018 Jun;287(3):884-892. doi: 10.1148/radiol.2018171504. Epub 2018 Mar 20.
Purpose To determine if sex differences in abdominal visceral fat composition, measured by using computed tomography (CT), and tumor glucose metabolism, measured by gene expression, can help predict outcomes in patients with clear cell renal cell carcinoma (RCC). Materials and Methods This retrospective cohort study included 222 patients with clear cell RCC from The Cancer Imaging Atlas. By using CT, body fat was segmented into subcutaneous fat and visceral fat areas (VFAs) and normalized to total fat to obtain the relative VFA (rVFA) and relative subcutaneous fat area. Multivariate Cox proportional hazard regression models were performed to identify effects of rVFA on sex-specific survival. Expression profiles for 39 glycolytic genes in tumors from these patients were obtained from The Cancer Genome Atlas to determine sex differences in metabolism and compared with rVFA. Key mutations in clear cell RCC were analyzed for association with rVFA and tumor glycolytic profiles. Results Women with rVFA greater than 30.9% had an increased risk of death (hazard ratio, 3.66 [95% confidence interval: 1.64, 8.19]) for women vs 1.13 ([95% confidence interval: 0.58, 2.18] for men, P = .028). Glycolytic gene expression stratified both men and women, and the combination of low rVFA and low glycolysis identified 19 women with excellent overall survival (P < .001). SETD2 and BAP1 mutations were uniquely enriched in female tumors with high glycolysis (P = .036 and .001, respectively). No significant differences were identified in tumor mutations between patients with high and low rVFA. Conclusion Sex differences in visceral fat and tumor glucose metabolism may provide a new risk-stratification system for patients with clear cell RCC. RSNA, 2018 Online supplemental material is available for this article.
通过 CT 测量的腹部内脏脂肪成分和基因表达测量的肿瘤葡萄糖代谢,确定这些性别差异是否可以帮助预测透明细胞肾细胞癌(RCC)患者的结局。
本回顾性队列研究纳入了来自癌症影像学图谱的 222 例透明细胞 RCC 患者。通过 CT 测量,将体脂分为皮下脂肪和内脏脂肪区域(VFA),并与总脂肪归一化以获得相对 VFA(rVFA)和相对皮下脂肪面积。多变量 Cox 比例风险回归模型用于确定 rVFA 对性别特异性生存的影响。从癌症基因组图谱中获取这些患者肿瘤中 39 个糖酵解基因的表达谱,以确定代谢的性别差异,并与 rVFA 进行比较。分析透明细胞 RCC 的关键突变与 rVFA 和肿瘤糖酵解谱的关系。
rVFA 大于 30.9%的女性死亡风险增加(危险比,3.66[95%置信区间:1.64,8.19]),而男性为 1.13[95%置信区间:0.58,2.18],P =.028)。糖酵解基因表达在男性和女性中均分层,rVFA 低和糖酵解低的组合确定了 19 名女性具有极好的总生存(P <.001)。SETB2 和 BAP1 突变在女性高糖酵解肿瘤中特有富集(P =.036 和.001)。高 rVFA 和低 rVFA 患者的肿瘤突变之间未发现显著差异。
内脏脂肪和肿瘤葡萄糖代谢的性别差异可能为透明细胞 RCC 患者提供新的风险分层系统。
RSNA,2018 在线补充材料可在本文中获得。