MRI feature-based discrimination model for prediction of MGMT promoter methylation status in glioma
Objective To explore the potential value of expert-identified CT and MRI imaging features in predicting the MGMT promoter methylation status in glioma. Methods A retrospective analysis was conducted in 188 patients in The First Medical Center of Chinese PLA General Hospital from January 2019 to Dec...
Saved in:
| Main Authors: | , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Tianjin Huanhu Hospital
2025-07-01
|
| Series: | Chinese Journal of Contemporary Neurology and Neurosurgery |
| Subjects: | |
| Online Access: | http://www.cjcnn.org/index.php/cjcnn/article/view/3061 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | Objective To explore the potential value of expert-identified CT and MRI imaging features in predicting the MGMT promoter methylation status in glioma. Methods A retrospective analysis was conducted in 188 patients in The First Medical Center of Chinese PLA General Hospital from January 2019 to December 2020 with pathologically confirmed glioma. Imaging features were extracted, including calcification, clear lesion margins, peritumoral edema, T2WI/T2-FLAIR mismatch, cortical involvement, subventricular zone involvement, insular involvement, homogeneous signal on T2WI, and enhanced lesions. Pyrosequencing was used to detect the MGMT promoter methylation status. Univariate and multivariate Logistic regression analyses were used to find the imaging feature factors that affect the MGMT promoter methylation status. Then, by plotting the receiver operating characteristic (ROC) curve, verify the predictive efficacy of the imaging features. For the prediction task, further train and test 4 machine learning (ML) models, namely Logistic regression (LR), support vector machine (SVM), random forest (RF), and gradient boosting (GB). Results Logistic regression analysis showed that homogeneous signal on T2WI (OR = 2.843, 95%CI: 1.055-7.658; P = 0.039) and enhanced lesions (OR = 0.146, 95%CI: 0.069-0.308; P = 0.000) were imaging feature factors affecting the MGMT promoter methylation status. The comprehensive parameters combining both had higher prediction ability compared with homogeneous signal on T2WI (Z = 3.961, P = 0.000) and enhanced lesions (Z = 2.233, P = 0.026). The prediction accuracies rates of LR, SVM, RF and GB models were 0.84, 0.76, 0.68 and 0.76, respectively. However, there were no statistically significant differences in prediction efficacy when comparing the models pairwise (P > 0.05, for all). Conclusions Imaging features based on preoperative CT and MRI show promise for non-invasive prediction of MGMT promoter methylation status in glioma. |
|---|---|
| ISSN: | 1672-6731 |