Suzuki Yosuke, Koyama Teruhide, Negami Jun, Toyama Daiki, Oda Ayako, Tanaka Ryota, Iwao Motoshi, Tatsuta Ryosuke, Ando Tadasuke, Shin Toshitaka, Itoh Hiroki, Ohno Keiko
Department of Medication Use Analysis and Clinical Research, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588, Japan.
Department of Epidemiology for Community Health and Medicine, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto 602-8566, Japan.
ACS Omega. 2025 Jun 5;10(23):24214-24223. doi: 10.1021/acsomega.4c11248. eCollection 2025 Jun 17.
Mid-regional proadrenomedullin (MR-proADM) has been suggested to be a powerful biomarker for the onset, progression, and mortality of various diseases. To achieve sensitive quantification of MR-proADM without cross-reactivity, we established micro-liquid chromatography coupled to the quadrupole time-of-flight mass spectrometry (μLC-QTOF/MS) method using IonKey technology. 100 μL of plasma sample was pretreated by protein precipitation followed by solid-phase extraction. Using the established μLC-QTOF/MS method, plasma MR-proADM concentrations were measured in 198 individuals of the Japanese general population, 13 patients with chronic kidney disease (CKD) stage G3b-G4 (nondialysis), and 12 patients with CKD stage G5 (dialysis). The novel assay fulfilled the requirements of the US Food and Drug Administration guidance for bioanalytical method validation, with a lower limit of quantification of 0.05 ng/mL. Recovery rates from human plasma and matrix effects were 89.6-114.2% and 95.3-111.7%, respectively. Median plasma MR-proADM concentrations were 0.48, 1.16, and 2.75 ng/mL in general population, CKD stage G3b-G4, and CKD stage G5, respectively ( < 0.0001). All measured concentrations were within the calibration range (0.05-100 ng/mL). The robust Passing-Bablok regression plot between MR-proADM concentrations measured by μLC-QTOF/MS and by immunoluminometric assay showed systemic and proportional bias between methods. The values measured by the μLC-QTOF/MS method tended to be lower than those by immunoluminometric assay. An ultrasensitive and selective method using μLC-QTOF/MS for measuring plasma MR-proADM was established. The novel method can be used in the general population and patients and may have better specificity for MR-proADM than the immunoluminometric assay; thus, it may improve the performance of MR-proADM as a biomarker for predicting the prognosis of patients with various diseases.
中段肾上腺髓质素原(MR-proADM)已被认为是各种疾病发生、进展和死亡率的有力生物标志物。为了实现对MR-proADM的灵敏定量且无交叉反应,我们采用离子键技术建立了微液相色谱-四极杆飞行时间质谱联用(μLC-QTOF/MS)方法。100 μL血浆样本先经蛋白沉淀预处理,然后进行固相萃取。使用已建立的μLC-QTOF/MS方法,对198名日本普通人群、13例慢性肾脏病(CKD)G3b-G4期(非透析)患者和12例CKD G5期(透析)患者的血浆MR-proADM浓度进行了测定。该新检测方法符合美国食品药品监督管理局生物分析方法验证指南的要求,定量下限为0.05 ng/mL。人血浆的回收率和基质效应分别为89.6 - 114.2%和95.3 - 111.7%。普通人群、CKD G3b-G4期和CKD G5期的血浆MR-proADM中位数浓度分别为0.48、1.16和2.75 ng/mL(<0.0001)。所有测量浓度均在校准范围内(0.05 - 100 ng/mL)。μLC-QTOF/MS法和免疫发光分析法测定的MR-proADM浓度之间的稳健Passing-Bablok回归图显示,两种方法之间存在系统性和比例性偏差。μLC-QTOF/MS法测得的值往往低于免疫发光分析法测得的值。建立了一种使用μLC-QTOF/MS测量血浆MR-proADM的超灵敏和选择性方法。该新方法可用于普通人群和患者,并且可能比免疫发光分析法对MR-proADM具有更好的特异性;因此,它可能会提高MR-proADM作为预测各种疾病患者预后生物标志物的性能。