ArticleMagnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine2026
Diagnostic Potential of Macromolecular Proton Fraction Mapping Combined with Quantitative Susceptibility Mapping as a Subcortical Biomarker for Parkinson's Disease.
Article in Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Comment on "Diagnostic Potential of Macromolecular Proton Fraction Mapping Combined with Quantitative Susceptibility Mapping as a Subcortical Biomarker for Parkinson's Disease" by Fujiwara et al.Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine · 2026Article
- Macromolecular Proton Fraction Reveals Divergent White Matter Myelination in Bipolar Disorder and Unipolar Recurrent Depression.Bioengineering (Basel, Switzerland) · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeThis study aimed to evaluate the diagnostic potential of macromolecular proton fraction (MPF) mapping combined with magnetic susceptibility measurements as subcortical biomarkers in Parkinson's disease (PD).
methodsTwenty patients with PD and 9 age-matched healthy controls underwent 3.0T magnetic resonance imaging, including MPF mapping and quantitative susceptibility mapping (QSM). MPF and magnetic susceptibility values of the 16 subcortical nuclei were measured in both the PD group and healthy control group, and these values were compared between the 2 groups. Diagnostic performance of MPF and magnetic susceptibility in the subcortical nuclei was individually evaluated using receiver operating characteristic (ROC) analysis. A logistic regression model was developed for the diagnosis of PD using a combination of MPF and magnetic susceptibility values.
resultsQuantitative analyses revealed significantly reduced MPF values (false discovery rate-corrected P < 0.05) in 7 subcortical nuclei in the PD group, namely the hypothalamus, parabrachial pigmented nucleus, red nucleus, substantia nigra pars reticulata, substantia nigra pars compacta, ventral pallidum, and ventral tegmental area. Additionally, magnetic susceptibility was significantly elevated (false discovery rate-corrected P < 0.05) in the parabrachial pigmented nucleus and substantia nigra pars compacta. ROC curve analysis demonstrated strong diagnostic performance, with the ventral pallidum showing the highest MPF-based diagnostic accuracy (area under the curve [AUC] = 0.82) and the substantia nigra pars compacta showing the highest QSM-based accuracy (AUC = 0.88). The logistic regression model combining MPF and magnetic susceptibility showed the best performance (AUC = 0.93).
conclusionMPF mapping, particularly when combined with magnetic susceptibility measurements, may serve as a quantitative diagnostic biomarker for PD, and the observed widespread alterations across multiple subcortical nuclei provide new insights into the pathology of PD beyond the classic nigrostriatal pathway.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.