Camelo André Luiz Melo, de Oliveira André Matos, Zamora-Obando Hans Rolando, Dias Aline Cristina, de Assis Lopes Thaís, Oliveira Regina Vincenzi, Farah João Pedro Simon, Franco Maggi Tavares Marina, Tavares Maggi, Antunes Alberto Azoubel, Valéria Ana, Simionato Colnaghi
Laboratory of Analysis of Biomolecules Tiselius, Department of Analytical Chemistry, Institute of Chemistry, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, Brazil.
Division of Urology, School of Medicine, University of São Paulo, São Paulo, São Paulo, Brazil.
Metabolomics. 2025 Jun 19;21(4):83. doi: 10.1007/s11306-025-02290-8.
Population aging is increasing rapidly, representing a global trend that has launched many discussions regarding older adult's quality of life. Benign prostatic hyperplasia (BPH) is a commonly found condition among older men, affecting the lower urinary tract and quality of life. BPH diagnosis typically involves clinical evaluations which cannot accurately identify patients who will develop a clinically significant disease in the future. Metabolomics emerges as a promising approach to understand the metabolic pathways associated with BPH, offering potential aid in early diagnosis.
To investigate the metabolic profile of BPH patients compared with a control group for diagnosing BPH at different stages.
A total of 62 individuals were selected and divided into two groups: 32 BPH (prostate volume > 40 mL) and 30 healthy individuals (prostate volume ≤ 40 mL and normal voiding patterns). Plasma samples were analyzed by LC-HRMS. Data were processed using unsupervised and supervised techniques. Self-organizing maps were further used to aid in the identification of potential biomarkers.
Self-organizing maps revealed three distinct groups which expanded upon the existing groups indicated by the medical team. Discriminant analysis models showed good predictive ability and accuracy, providing a classification perspective of patients and expanding diagnostic possibilities for different health states. Integration of chemical data with clinical variables revealed meaningful correlations. Our results also suggest the presence of discriminatory metabolites related to inflammation and oxidation processes, clarifying the metabolic basis of BPH.
Self-organizing maps proved their effectiveness in classifying groups of samples from BPH patients, revealing potential biomarkers that went undetected by conventional data analysis methods. This approach underscores metabolomics as a relevant tool in identifying hidden patterns and supporting the development of more robust diagnostic and prognostic models.
人口老龄化正在迅速加剧,这是一个全球趋势,引发了许多关于老年人生活质量的讨论。良性前列腺增生(BPH)是老年男性中常见的疾病,会影响下尿路和生活质量。BPH的诊断通常涉及临床评估,但无法准确识别未来会发展为具有临床意义疾病的患者。代谢组学作为一种有前景的方法出现,用于了解与BPH相关的代谢途径,为早期诊断提供潜在帮助。
比较BPH患者与对照组的代谢谱,以诊断不同阶段的BPH。
共选取62人,分为两组:32例BPH患者(前列腺体积>40 mL)和30例健康个体(前列腺体积≤40 mL且排尿模式正常)。血浆样本通过液相色谱-高分辨质谱(LC-HRMS)进行分析。数据使用无监督和有监督技术进行处理。自组织映射进一步用于辅助识别潜在生物标志物。
自组织映射揭示了三个不同的组,扩展了医疗团队指出的现有组。判别分析模型显示出良好的预测能力和准确性,提供了患者的分类视角,并扩大了不同健康状态的诊断可能性。化学数据与临床变量的整合揭示了有意义的相关性。我们的结果还表明存在与炎症和氧化过程相关的鉴别性代谢物,阐明了BPH的代谢基础。
自组织映射证明了其在对BPH患者样本组进行分类方面的有效性,揭示了传统数据分析方法未检测到的潜在生物标志物。这种方法强调了代谢组学作为识别隐藏模式和支持开发更强大的诊断和预后模型的相关工具。