Powrózek Tomasz, Mlak Radosław, Brzozowska Anna, Mazurek Marcin, Gołębiowski Paweł, Małecka-Massalska Teresa
Department of Human Physiology, Medical University of Lublin, Radziwiłłowska 11, 20-080 Lublin, Poland.
Department of Oncology, Medical University of Lublin, Jaczewskiego 7, 20-090 Lublin, Poland.
Cancers (Basel). 2018 Aug 30;10(9):294. doi: 10.3390/cancers10090294.
Investigation of novel cachexia-related markers is one of the major challenges in contemporary oncology. Among studied markers, the miRNA seems to be promising due to its possibility to regulate genes responsible for induction of inflammatory response, muscle atrophy and fat tissue wasting. The aim of the study was to investigate the role of blood-circulating miRNA-130a in prediction of cancer cachexia in 70 head and neck cancer patients (HNC) subjected to radiotherapy. Moreover, diagnostic accuracy of SGA (Subjective Global Assessment) scoring and miRNA-130a level was evaluated in various cachexia models.
miRNA-130a level negatively correlated with plasma TNF-α concentration ( = -0.560; < 0.001). Patients with low miRNA expression had over 3-fold higher risk of body mass index (BMI) decrease below 18.5 after the termination of therapy; over 6-fold higher risk of losing over 5% of body weight and higher risk of >10% weight reduction odds ratio (OR) = 14.18 compared to other cases. ROC analysis performed for miRNA-130a allowed to distinguish cachectic patients (body weight loss >5%) from moderately or mildly malnourished ones with optimal sensitivity of 79.4% and specificity of 80.8% area under the curve (AUC) = 0.865). miRNA significantly improved nutritional assessment conducted using SGA, achieving the following values: sensitivity 88.6%, specificity 94.3%, positive predictive value (PPV) 93.9%, negative predictive value (NPV).89.2%.
miRNA-130a demonstrates potential clinical utility in prediction of cachexia prior to the therapy in HNC patients. Simultaneous use of both tools-SGA and miRNA-significantly improved the accuracy in the diagnosis of cachexia.
研究新型恶病质相关标志物是当代肿瘤学的主要挑战之一。在已研究的标志物中,微小RNA(miRNA)似乎很有前景,因为它有可能调节负责诱导炎症反应、肌肉萎缩和脂肪组织消耗的基因。本研究的目的是调查循环血液中的miRNA-130a在70例接受放疗的头颈癌患者(HNC)中预测癌症恶病质的作用。此外,还评估了主观全面评定法(SGA)评分和miRNA-130a水平在各种恶病质模型中的诊断准确性。
miRNA-130a水平与血浆肿瘤坏死因子-α(TNF-α)浓度呈负相关(r = -0.560;P < 0.001)。miRNA表达低的患者在治疗结束后体重指数(BMI)降至18.5以下的风险高出3倍多;体重减轻超过5%的风险高出6倍多,体重减轻超过10%的风险更高(优势比[OR] = 14.18)。对miRNA-130a进行的ROC分析能够区分恶病质患者(体重减轻>5%)与中度或轻度营养不良患者,最佳灵敏度为79.4%,特异性为80.8%,曲线下面积(AUC) = 0.865)。miRNA显著改善了使用SGA进行的营养评估,达到以下数值:灵敏度88.6%,特异性94.3%,阳性预测值(PPV)93.9%,阴性预测值(NPV)89.2%。
miRNA-130a在预测HNC患者治疗前的恶病质方面显示出潜在的临床应用价值。同时使用SGA和miRNA这两种工具可显著提高恶病质诊断的准确性。