Resting-State vs. Task-Based Functional Magnetic Resonance Imaging in Neurosurgical Planning: A Narrative Review of Clinical Applications
Abstract
1. Introduction
2. Clinical Importance of Functional Localization in Neurosurgery
3. Tb-fMRI in Neurosurgical Planning
4. Limitations and Failure Modes of Task-Based fMRI in Neurosurgical Candidates
4.1. Aphasia and Language Deficits: Unreliable or Absent Activations and False Negatives
4.2. Cognitive Impairment, Fatigue, Anxiety, and Pain: Performance Variability, Noncompliance, and Motion
4.3. Motor Impairment and Paresis: Inability to Execute Paradigms and Compromised Mapping
4.4. Pediatric and Other Non-Cooperative Patients: Developmental Limits and Sedation Constraints
4.5. Tumor Physiology and Neurovascular Confounds: Attenuated and Displaced BOLD Responses
4.6. Practical Implication: tb-fMRI Fails Most Often in the Patients Who Need Accurate Mapping the Most
4.7. List of Key Failure Modes and Surgical Consequences
- Cognitive impairment or reduced ability to cooperate: inconsistent task performance and head motion can produce limited or non-diagnostic tb-fMRI maps, increasing reliance on anatomical landmarks and invasive mapping. In such cases, complementary techniques like rs-fMRI or additional neurophysiological testing may be considered [50,54].
- Tumor physiology, including altered hemodynamics: neurovascular changes can attenuate or distort task-evoked BOLD responses, leading to false negative findings or spatially shifted activations that may misinform resection planning. Calibration with CVR measures, such as breath-hold mapping, and awareness of non-neural vascular or anatomical influences on BOLD magnitude can help interpret these maps [52,60].
5. Resting-State fMRI for Presurgical Mapping
- Preprocessing with motion correction, distortion correction, and a denoising strategy such as ICA-based cleaning with FIX [71].
6. Clinical Evidence and Validation
6.1. Motor Network Mapping
6.1.1. Concordance with tb-fMRI Localization
6.1.2. Concordance with DCS/DES
6.1.3. Test–Retest Reliability Themes
6.2. Language Network Mapping
6.2.1. Distributed Anatomy and Variability
6.2.2. Evidence for Lateralization Concordance
6.2.3. Practical Interpretation: Adjunctive, Not Definitive
6.3. Tumor Patients: Perilesional Issues
6.3.1. Mechanisms and Manifestations of Distortion
6.3.2. Rs-fMRI Resilience and Limits
6.3.3. Mitigation Strategies
6.4. Patients in Whom rs-fMRI Adds the Most Value
6.4.1. Clinical Groups with Few Alternatives
6.4.2. Coverage and Feasibility
6.5. Synthesis and Practical Recommendations
7. Integration into Practice
7.1. Purpose and Overview
7.2. Preoperative Workflow: When to Obtain tb-fMRI, When to Add rs-fMRI, and When rs-fMRI May Be Primary
7.3. Practical Preoperative Acquisition and Fusion Steps
7.4. Neuronavigation Integration and Practical Utility for Approach Planning
7.5. Multimodal Strategy: Combining fMRI with Diffusion Tensor Imaging/Tractography and Intraoperative Mapping
7.6. Brain Shift, Intraoperative Updating, and the Continued Role of Direct Mapping
7.7. Final Note and Recommendations
8. Controversies and Barriers to Routine Adoption
8.1. Motion and Physiological Noise
8.2. Preprocessing Variability and Clinical Consequences
8.3. Specificity Limits: Connectivity Is Not Causality
8.4. Inter-Center Variability and the Need for Validated Clinical Pipelines
8.5. Clinical Positioning and Practical Recommendations
9. Future Directions
10. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
Abbreviations
| BOLD | blood-oxygen-level-dependent |
| CT | computed tomography |
| CVR | cerebrovascular reactivity |
| DCS | direct cortical stimulation |
| DES | direct electrical stimulation |
| DICOM | Digital Imaging and Communications in Medicine |
| DMN | default mode network |
| DTI | diffusion tensor imaging |
| EOR | extent of resection |
| FIX | FMRIB’s ICA-based X-noiseifier |
| FLAIR | fluid-attenuated inversion recovery |
| fMRI | functional magnetic resonance imaging |
| GLM | general linear model |
| ICA | independent component analysis |
| MRI | magnetic resonance imaging |
| nTMS | navigated transcranial magnetic stimulation |
| NVU | neurovascular uncoupling |
| QC | quality control |
| RSN | resting-state network |
| SMN | sensorimotor network |
| rs-fMRI | resting-state functional magnetic resonance imaging |
| tb-fMRI | task-based functional magnetic resonance imaging |
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| Failure Mode | Mechanism | Typical tb-fMRI Map Appearance | Practical Mitigation | Risk if Unrecognized |
|---|---|---|---|---|
| Inconsistent task performance | Patient lacks comprehension | Sparse or diffuse activation | Pre-scan task training, simplified paradigms, behavioral monitoring during scanning, repeated acquisitions if needed | Mislocalization leading to language deficits |
| Patient motion artifacts | Restlessness or inability to remain still | Blurred signals, false positives | Mock scanning when feasible, head stabilization, shorter or repeated runs, framewise displacement assessment, motion correction plus censoring/scrubbing criteria, reacquisition when QC is inadequate | Resection of functional areas |
| Incomplete motor task execution | Weak contraction or fatigue | Reduced or asymmetric activation | Passive motor paradigms, alternative motor tasks, behavioral or EMG monitoring when available, repeated runs, nTMS or intraoperative stimulation for confirmation | Postoperative motor deficits |
| Pediatric cooperation issues | Attention span limitations | Artifacts and poor signal | Age-appropriate tasks, mock scanner preparation, sleep/sedation-compatible rs-fMRI when task paradigms are not feasible, multimodal confirmation | Under-representation of functional areas |
| Tumor-related hemodynamic failure | Localized hemodynamic changes | Distorted activation patterns | CVR or breath-hold mapping, perfusion imaging, careful assessment of perilesional signal dropout, tractography, nTMS, and intraoperative stimulation as confirmatory methods | Resection of functional cortex |
| Clinical Question | Evidence Is Strongest for | Main Practical Implication | Main Limitation |
|---|---|---|---|
| Cooperative adult with motor or language lesion near eloquent cortex | tb-fMRI, especially when task performance is reliable | Use tb-fMRI as first-line noninvasive mapping and integrate with tractography and neuronavigation | Task performance, thresholding, susceptibility artifacts, and NVU can reduce reliability |
| Sensorimotor mapping when task performance is limited | rs-fMRI sensorimotor network mapping | Add rs-fMRI, especially when voluntary movement is unreliable or impossible | Motion, preprocessing choices, and perilesional BOLD confounds still require QC |
| Language mapping | Multimodal interpretation of tb-fMRI, rs-fMRI, and intraoperative mapping | Use rs-fMRI as hypothesis-generating and supportive information, not as a standalone determinant of essential language sites | Language networks are distributed and more variable than sensorimotor networks |
| Suspected neurovascular uncoupling | CVR/perfusion-informed multimodal interpretation | Interpret absent or attenuated BOLD activation cautiously and consider CVR, perfusion imaging, tractography, nTMS, and intraoperative stimulation | Neither tb-fMRI nor rs-fMRI can fully exclude function in areas with abnormal hemodynamics |
| Non-cooperative, aphasic, pediatric, sedated, or cognitively impaired patients | rs-fMRI as task-free noninvasive mapping | rs-fMRI may serve as the primary noninvasive mapping approach when tb-fMRI is infeasible | Results should still be confirmed or contextualized with other modalities when clinically necessary |
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Rakowski, M.; Koc, N.A.; Dębska, A.; Szmyd, B.; Zawadzka, A.; Zaczkowski, K.; Podstawka, M.; Wilmańska, D.; Dobek, A.; Stefańczyk, L.; et al. Resting-State vs. Task-Based Functional Magnetic Resonance Imaging in Neurosurgical Planning: A Narrative Review of Clinical Applications. Biomedicines 2026, 14, 1449. https://doi.org/10.3390/biomedicines14071449
Rakowski M, Koc NA, Dębska A, Szmyd B, Zawadzka A, Zaczkowski K, Podstawka M, Wilmańska D, Dobek A, Stefańczyk L, et al. Resting-State vs. Task-Based Functional Magnetic Resonance Imaging in Neurosurgical Planning: A Narrative Review of Clinical Applications. Biomedicines. 2026; 14(7):1449. https://doi.org/10.3390/biomedicines14071449
Chicago/Turabian StyleRakowski, Maurycy, Natalia Anna Koc, Anna Dębska, Bartosz Szmyd, Agata Zawadzka, Karol Zaczkowski, Małgorzata Podstawka, Dagmara Wilmańska, Adam Dobek, Ludomir Stefańczyk, and et al. 2026. "Resting-State vs. Task-Based Functional Magnetic Resonance Imaging in Neurosurgical Planning: A Narrative Review of Clinical Applications" Biomedicines 14, no. 7: 1449. https://doi.org/10.3390/biomedicines14071449
APA StyleRakowski, M., Koc, N. A., Dębska, A., Szmyd, B., Zawadzka, A., Zaczkowski, K., Podstawka, M., Wilmańska, D., Dobek, A., Stefańczyk, L., Jaskólski, D. J., & Wiśniewski, K. (2026). Resting-State vs. Task-Based Functional Magnetic Resonance Imaging in Neurosurgical Planning: A Narrative Review of Clinical Applications. Biomedicines, 14(7), 1449. https://doi.org/10.3390/biomedicines14071449

