医学
磷酸肌酸
鉴别诊断
体内磁共振波谱
生物标志物
内科学
逻辑回归
前瞻性队列研究
磁共振成像
病理
帕金森病
糖尿病
神经影像学
胃肠病学
置信区间
中脑
疾病
肿瘤科
内分泌学
中枢神经系统疾病
病例对照研究
试验预测值
心脏病学
疾病严重程度
优势比
成像生物标志物
高能磷酸盐
诊断准确性
作者
Qiurong Yu,Youmin Zhang,Peng Huang,Yan Li,Peng Liu,Zhijia Jin,Xiaohai Wang,Baoyi Zhang,Jinyuan Weng,Peng Wu,Ewart Mark Haacke,Evita Wiegers,Jannie P. Wijnen,Dennis W. J. Klomp,Sven Haller,S. Chen,F. H. Yan,Na He
出处
期刊:Radiology
[Radiological Society of North America]
日期:2026-04-01
卷期号:319 (1): e251533-e251533
标识
DOI:10.1148/radiol.251533
摘要
Background Whether phosphorus 31 (31P) MR spectroscopy outperforms or complements conventional hydrogen 1 (1H) MRI biomarkers in the differential diagnosis of early-stage Parkinson disease (PD) remains unclear. Purpose To evaluate 31P MR spectroscopy and its integration with conventional 1H MRI for discriminating early-stage PD from mimics. Materials and Methods This prospective study consecutively enrolled participants with early-stage PD, participants with PD mimics, and controls (November 2023 to October 2024). Participants underwent 31P MR spectroscopy for inorganic phosphate (Pi), phosphocreatine (PCr), and adenosine triphosphate (ATP); quantitative susceptibility mapping for iron; and neuromelanin-sensitive MRI. Intergroup imaging differences were assessed using multivariable general linear models, and partial correlations with clinical scores were analyzed. A penalized logistic regression classifier evaluated discrimination performance of energy metabolites, alone and combined with iron and/or neuromelanin. Results Seventy-two participants with early-stage PD (mean age, 60.1 years ± 6.8 [SD]; 44 male participants), 34 with PD mimics (mean age, 62.1 years ± 7.9; 18 male participants), and 46 controls (mean age, 56.3 years ± 9.6; 33 female controls) were included. Early-stage PD showed a decreased Pi/PCr ratio (mean, 0.47 [95% CI: 0.44, 0.50] vs 0.57 [95% CI: 0.52, 0.63]) and an increased total ATP/Pi ratio (mean, 4.89 [95% CI: 4.57, 5.24] vs 4.06 [95% CI: 3.50, 4.68]) in the left midbrain compared with participants with PD mimics (both Bonferroni-corrected P < .05). The Pi/PCr ratio correlated with nonmotor symptom scores (r = 0.42; 95% CI: 0.12, 0.69; P = .008) and autonomic symptom scores (r = 0.60; 95% CI: 0.34, 0.80; P < .001) in PD. Energy metabolites outperformed both iron (area under the receiver operating characteristic curve [AUC], 0.90 vs 0.50; P < .001) and neuromelanin (AUC, 0.90 vs 0.64; P = .04) in differentiating PD from mimics. There was no evidence that combining iron and/or neuromelanin improved AUC over energy metabolites alone (0.90 vs 0.90 with the addition of iron [P > .99] vs 0.91 with the addition of neuromelanin [P = .70] vs 0.93 with the addition of both [P = .42]). Conclusion 31P MR spectroscopy revealed disrupted midbrain energy homeostasis in early-stage PD and effectively helped differentiate it from mimics. © RSNA, 2026 Supplemental material is available for this article.
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