Sun Lubing, Wu Yaping, Sun Tao, Li Panlong, Liang Junting, Yu Xuan, Yang Junpeng, Meng Nan, Wang Meiyun, Chen Chuanliang
Department of Radiology, Zhengzhou University People's Hospital and Henan Provincial People's Hospital, Zhengzhou, China.
Clinical Bioinformatics Experimental Center, Zhengzhou University People's Hospital and Henan Provincial People's Hospital, Zhengzhou, China.
Eur J Nucl Med Mol Imaging. 2025 May;52(6):2145-2156. doi: 10.1007/s00259-025-07081-w. Epub 2025 Jan 20.
The intricate interplay between organs can give rise to a multitude of physiological conditions. Disruptions such as inflammation or tissue damage can precipitate the development of chronic diseases such as tumors or diabetes mellitus (DM). While both lung cancer and DM are the consequences of disruptions in homeostasis, the relationship between them is intricate. This study sought to investigate the potential influence of DM on lung cancer by employing total-body dynamic PET imaging.
The present study proposes a framework for metabolic network analysis using total-body dynamic PET imaging of 20 lung cancer patients with DM (DM group) and 20 lung cancer patients without DM (Non-DM group), with the residuals of a third-order polynomial fit serving as an indicator of Pearson correlation.
The framework successfully captured the deviation of the DM group from the Non-DM group at both the edge and organ levels. At the edge level, there was a significant difference in the lesion- left ventricle (LV) between the DM and Non-DM groups (P < 0.05). Furthermore, we discovered a positive correlation between the absolute value of Z-score (ZCC) of lesion - LV and the duration of DM (R = 0.680, P < 0.001). At the organ level, there was a significant difference in the kidney, brain, and abdominal fat between the DM and Non-DM groups (P < 0.05).
This study demonstrated the feasibility of constructing metabolic networks to uncover complex alterations in lung cancer patients with DM. The findings contribute to understanding the systemic effects of DM on lung cancer metabolism and highlight the importance of personalized metabolic network analysis to comprehend the implications of concurrent diseases.
器官之间复杂的相互作用可引发多种生理状况。诸如炎症或组织损伤等干扰因素可促使肿瘤或糖尿病(DM)等慢性疾病的发展。虽然肺癌和糖尿病都是体内稳态破坏的后果,但它们之间的关系错综复杂。本研究旨在通过全身动态PET成像来探究糖尿病对肺癌的潜在影响。
本研究提出了一个代谢网络分析框架,对20例合并糖尿病的肺癌患者(糖尿病组)和20例无糖尿病的肺癌患者(非糖尿病组)进行全身动态PET成像,以三阶多项式拟合的残差作为Pearson相关性的指标。
该框架成功捕捉到了糖尿病组与非糖尿病组在边缘和器官水平上的差异。在边缘水平上,糖尿病组和非糖尿病组之间病变 - 左心室(LV)存在显著差异(P < 0.05)。此外,我们发现病变 - LV的Z评分绝对值(ZCC)与糖尿病病程之间存在正相关(R = 0.680,P < 0.001)。在器官水平上,糖尿病组和非糖尿病组之间的肾脏、大脑和腹部脂肪存在显著差异(P < 0.05)。
本研究证明了构建代谢网络以揭示合并糖尿病的肺癌患者复杂变化的可行性。这些发现有助于理解糖尿病对肺癌代谢的全身影响,并强调个性化代谢网络分析对于理解并发疾病影响的重要性。