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Abstract Details

Diagnostic Accuracy of Neuromelanin Sensitive MRI in Parkinsonian Disorders: A Systematic Review and Meta-analysis
Movement Disorders
P1 - Poster Session 1 (8:00 AM-9:00 AM)
16-005

This meta-analysis aimed to evaluate diagnostic accuracy of Neuromelanin-sensitive MRI (NM-MRI) in distinguishing Parkinson’s disease (PD) and related syndromes from healthy controls.


PD remains difficult to diagnose, with misdiagnosis rates of up to 25% due to symptom overlap and the absence of validated biomarkers. NM-MRI enables in vivo assessment of neuromelanin in the substantia nigra and locus coeruleus, where signal loss reflects dopaminergic neurodegeneration. 
We searched PubMed, Embase, and Cochrane databases from inception to February 2025 for studies assessing the diagnostic accuracy of NM-MRI for patients with PD. Primary diagnostic accuracy measure was defined as the best-balanced sensitivity and specificity reported in each study. Subgroup analyses were conducted to evaluate diagnostic accuracy of NM-MRI in specific target regions, such as substantia nigra and locus coeruleus, according to each imaging parameter such as volume and signal intensity metrics. All statistical analyses were performed using R software, version 4.5.1.

28 studies comprising 2,268 patients were included. NM-MRI showed high diagnostic accuracy for differentiating PD from healthy controls, with pooled sensitivity and specificity of 88.0% and 84.4%, respectively. Subgroup analyses indicated that volumetric and areal assessments of the substantia nigra were highly accurate, with an area under the curve (AUC) of 0.869 and 0.857, respectively. Signal intensity performed less effectively, with an AUC of 0.848. Subjective approaches yielded the highest sensitivity (90.8%). 


NM-MRI demonstrates high overall diagnostic accuracy in differentiating PD from healthy controls, with pooled sensitivity of 88% and specificity of 84%. Among evaluated parameters, volumetric and areal analyses of the substantia nigra proved robust, while subjective approaches yielded the highest sensitivity but with limited reproducibility.


Authors/Disclosures
ELISA C. FERREIRA, MD
PRESENTER
Dr. FERREIRA has nothing to disclose.
Cláudia Figueredo Nascimento Salomão Santos Miss Figueredo Nascimento Salomão Santos has nothing to disclose.
Iago M. Hezel Mr. Hezel has nothing to disclose.
Filipe R. Barra, PhD Dr. Barra has nothing to disclose.
Maria Clara Merighi Miss Merighi has nothing to disclose.
GUSTAVO R. SCHUSTER, MD Dr. SCHUSTER has nothing to disclose.
Rodrigo d. Schevz, Sr., Medical Student Dr. Schevz has nothing to disclose.
Bernard G. Campos, MD Dr. Campos has nothing to disclose.