School of Mathematics, South China University of Technology, Guangzhou, Guangdong Province, China.
School of Mathematics and Big Data, Foshan University, Foshan, China.
PeerJ. 2023 Jul 24;11:e15695. doi: 10.7717/peerj.15695. eCollection 2023.
The progression of complex diseases sometimes undergoes a drastic critical transition, at which the biological system abruptly shifts from a relatively healthy state (before-transition stage) to a disease state (after-transition stage). Searching for such a critical transition or critical state is crucial to provide timely and effective scientific treatment to patients. However, in most conditions where only a small sample size of clinical data is available, resulting in failure when detecting the critical states of complex diseases, particularly only single-sample data.
In this study, different from traditional methods that require multiple samples at each time, a model-free computational method, single-sample Markov flow entropy (sMFE), provides a solution to the identification problem of critical states/pre-disease states of complex diseases, solely based on a single-sample. Our proposed method was employed to characterize the dynamic changes of complex diseases from the perspective of network entropy.
The proposed approach was verified by unmistakably identifying the critical state just before the occurrence of disease deterioration for four tumor datasets from The Cancer Genome Atlas (TCGA) database. In addition, two new prognostic biomarkers, optimistic sMFE (O-sMFE) and pessimistic sMFE (P-sMFE) biomarkers, were identified by our method and enable the prognosis evaluation of tumors.
The proposed method has shown its capability to accurately detect pre-disease states of four cancers and provide two novel prognostic biomarkers, O-sMFE and P-sMFE biomarkers, to facilitate the personalized prognosis of patients. This is a remarkable achievement that could have a major impact on the diagnosis and treatment of complex diseases.
复杂疾病的进展有时会经历急剧的关键转变,在此期间,生物系统会突然从相对健康的状态(转变前阶段)转变为疾病状态(转变后阶段)。寻找这样的关键转变或关键状态对于为患者提供及时有效的科学治疗至关重要。然而,在大多数情况下,只有少量的临床数据可用,导致无法检测到复杂疾病的关键状态,特别是只有单一样本数据的情况。
在这项研究中,与传统方法不同,传统方法需要在每个时间点使用多个样本,一种无模型计算方法,即单样本马尔可夫流熵(sMFE),为识别复杂疾病的关键状态/疾病前状态提供了一种解决方案,仅基于单个样本。我们提出的方法用于从网络熵的角度描述复杂疾病的动态变化。
该方法通过明确识别来自癌症基因组图谱(TCGA)数据库的四个肿瘤数据集在疾病恶化发生前的关键状态得到了验证。此外,我们的方法还识别出了两个新的预后生物标志物,乐观的 sMFE(O-sMFE)和悲观的 sMFE(P-sMFE)生物标志物,可用于肿瘤的预后评估。
该方法已显示出能够准确检测四种癌症的疾病前状态并提供两个新的预后生物标志物 O-sMFE 和 P-sMFE 生物标志物的能力,以促进患者的个性化预后。这是一项重大成就,可能对复杂疾病的诊断和治疗产生重大影响。