Li Yihan, Wang Haoyu, Wang Han, Ren Yansong, Sun Fanfan, Xue Mei, Liang Haoyue, Zhou Yuan
State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China; Tianjin Institutes of Health Science, Tianjin 301600, China.
School of Medical Technology, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China.
Spectrochim Acta A Mol Biomol Spectrosc. 2026 Jan 15;345:126770. doi: 10.1016/j.saa.2025.126770. Epub 2025 Aug 5.
In recent years, Raman spectroscopy analysis of hematological diseases is increasingly applied in research, but its application in serum analysis of myeloid neoplastic diseases represented by myeloproliferative neoplasms (MPN), myelodysplastic/myeloproliferative neoplasms (MDS/MPN), and acute myeloid leukemia (AML) has not been fully tested. To establish an oversimplified non-invasive serum test approach for MPN, MDS/MPN and AML, we systematically examined peripheral blood serum samples from 8 patients diagnosed with MPN, 4 patients with MDS/MPN, 3 patients with AML, and 9 control participants. A laser Raman spectroscopy was utilized together with orthogonal partial least squares discriminant analysis (OPLS-DA). Next, a differentiation model for MPN, MDS/MPN, AML, and the control was constructed. Compared with the healthy participants, the serum spectral data of patients with myeloid tumors were specific, and the intensities of Raman peaks representing nucleic acids (786, 1579 cm), proteins (643, 759, 1031, 1260, 1603, 1616 cm), lipids (1437, 1443, 1446 cm), and β-carotene (957 cm) were significantly decreased, while the intensity of the Raman peak representing collagen (1345 cm) was significantly increased. Metabolic serum marker analysis revealed consistent patterns across MPN, MDS/MPN, and AML patients: adenosine deaminase (ADA) levels were significantly elevated, while both total protein and low-density lipoprotein concentrations showed marked reductions compared to controls. This provides spectroscopic evidence that will guide early differentiation of massive serum test data of patients with MPN, MDS/MPN and AML, and simultaneously uncovers crucial details for rapid and rudimentary differentiating them. This exploratory study show that the Raman spectroscopy analysis is an innovative non-invasive clinical instrument for the detection of MPN, MDS/MPN and AML.
近年来,拉曼光谱分析在血液系统疾病研究中的应用日益广泛,但其在以骨髓增殖性肿瘤(MPN)、骨髓增生异常/骨髓增殖性肿瘤(MDS/MPN)和急性髓系白血病(AML)为代表的髓系肿瘤性疾病血清分析中的应用尚未得到充分验证。为建立一种针对MPN、MDS/MPN和AML的过于简化的非侵入性血清检测方法,我们系统地检测了8例MPN确诊患者、4例MDS/MPN患者、3例AML患者和9名对照参与者的外周血血清样本。使用激光拉曼光谱结合正交偏最小二乘法判别分析(OPLS-DA)。接下来,构建了MPN、MDS/MPN、AML和对照的鉴别模型。与健康参与者相比,髓系肿瘤患者的血清光谱数据具有特异性,代表核酸(786、1579 cm)、蛋白质(643、759、1031、1260、1603、1616 cm)、脂质(1437、1443、1446 cm)和β-胡萝卜素(957 cm)的拉曼峰强度显著降低,而代表胶原蛋白(1345 cm)的拉曼峰强度显著增加。代谢血清标志物分析显示MPN、MDS/MPN和AML患者呈现一致模式:腺苷脱氨酶(ADA)水平显著升高,而总蛋白和低密度脂蛋白浓度与对照组相比均显著降低。这提供了光谱学证据,将指导MPN、MDS/MPN和AML患者大量血清检测数据的早期鉴别,同时揭示快速初步鉴别它们的关键细节。这项探索性研究表明,拉曼光谱分析是一种用于检测MPN、MDS/MPN和AML的创新性非侵入性临床仪器。