The Value of Cerebral Blood Volume Derived from Dynamic Susceptibility Contrast Perfusion MRI in Predicting IDH Mutation Status of Brain Gliomas—A Systematic Review and Meta-Analysis
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Martínez Barbero, José Pablo; Pérez García, Francisco Javier; Jiménez Gutierrez, Paula María; García Cerezo, Marta; López Cornejo, David; Olivares Granados, Gonzalo; Benítez, José Manuel; Láinez Ramos-Bossini, Antonio JesúsEditorial
MDPI
Materia
Glioma Brain Magnetic resonance imaging
Date
2025-04-01Referencia bibliográfica
Martínez Barbero, J.P.; Pérez García, F.J.; Jiménez Gutiérrez, P.M.; García Cerezo, M.; López Cornejo, D.; Olivares Granados, G.; Benítez, J.M.; Láinez Ramos-Bossini, A.J. The Value of Cerebral Blood Volume Derived from Dynamic Susceptibility Contrast Perfusion MRI in Predicting IDH Mutation Status of Brain Gliomas—A Systematic Review and Meta-Analysis. Diagnostics 2025, 15, 896. [https://doi.org/10.3390/diagnostics15070896]
Sponsorship
Grant number PID2020-118224RB-I00 and grant number PID2023-151336OB-I00, both funded by MICIU/AIE/10.13039/501100011033; FEDER, EUAbstract
Background: Dynamic susceptibility contrast perfusion MRI (DSC-MRI) is a
promising non-invasive examination to predict histological and molecular characteristics
of brain gliomas. However, the diagnostic accuracy of relative cerebral blood volume
(rCBV) is heterogeneously reported in the literature. This systematic review and metaanalysis
aims to assess the diagnostic accuracy of mean rCBV derived from DSC-MRI
in differentiating Isocitrate Dehydrogenase (IDH)-mutant from IDH-wildtype gliomas.
Methods: A comprehensive literature search was conducted in PubMed,Web of Science,
and EMBASE up to January 2025, following PRISMA guidelines. Eligible studies reported
mean CBV values in treatment-naïve gliomas with histologically confirmed IDH status.
Pooled estimates of standardized mean differences (SMDs), diagnostic odds ratios (DOR),
and area under the receiver-operating characteristic curve (AUC) were computed using
a random-effects model. Heterogeneity was assessed via I2 statistic. Meta-regression
analyses were also performed. Results: An analysis of 18 studies (n = 1733) showed
that mean rCBV is significantly lower in IDH-mutant gliomas (SMD = −0.86; p < 0.0001).
The pooled AUC was 0.80 (95% CI, 0.75–0.90), with moderate sensitivity and specificity.
Meta-regression revealed no significant influence of DSC-MRI acquisition parameters,
although a flip angle showed a trend toward significance (p = 0.055). Conclusions: Mean
rCBV is a reliable imaging biomarker for IDH mutation status in gliomas, demonstrating
good diagnostic performance. However, heterogeneity in acquisition parameters and
post-processing methods limits generalizability of results. Future research should focus on
standardizing DSC-MRI protocols.