journal article·2025Open access

Multimodal Convolutional Mixer for Mild Cognitive Impairment Detection

Ovidijus Grigas, Robertas Damaševičius, Rytis Maskeliūnas

Computers, Materials & Continua· Volume 84· Issue 1

Abstract

Brain imaging is important in detecting Mild Cognitive Impairment (MCI) and related dementias. Magnetic Resonance Imaging (MRI) provides structural insights, while Positron Emission Tomography (PET) evaluates metabolic activity, aiding in the identification of dementia-related pathologies. This study integrates multiple data modalities—T1-weighted MRI, Pittsburgh Compound B (PiB) PET scans, cognitive assessments such as Mini-Mental State Examination (MMSE), Clinical Dementia Rating (CDR) and Functional Activities Questionnaire (FAQ), blood pressure parameters, and demographic data—to improve MCI detection. The proposed improved Convolutional Mixer architecture, incorporating B-cos modules, multi-head self-attention, and a custom classifier, achieves a classification accuracy of 96.3% on the Mayo Clinic Study of Aging (MCSA) dataset (sagittal plane), outperforming state-of-the-art models by 5%–20%. On the full dataset, the model maintains a high accuracy of 94.9%, with sensitivity and specificity reaching 89.1% and 98.3%, respectively. Extensive evaluations across different imaging planes confirm that the sagittal plane offers the highest diagnostic performance, followed by axial and coronal planes. Feature visualization highlights contributions from central brain structures and lateral ventricles in differentiating MCI from cognitively normal subjects. These results demonstrate that the proposed multimodal deep learning approach improves accuracy and interpretability in MCI detection.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Brain Tumor Detection and Classification · Health, Environment, Cognitive Aging

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (61)

Show source-provided references
1. Mild cognitive impairment10.1016/S0140-6736(06)68542-5 ↗
2. Computerized cognitive training for memory functions in mild cognitive impairment or dementia: a systematic review and meta-analysis10.1038/s41746-023-00987-5 ↗
3. Longitudinal CSF isoprostane and MRI atrophy in the progression to AD10.1007/s00415-007-0610-z ↗
4. Dual attention aware octave convolution network for early-stage alzheimer’s disease detection10.5755/j01.itc.53.1.34536 ↗
5. Optimizing parkinson’s disease diagnosis with multimodal data fusion techniques10.5755/j01.itc.53.1.34718 ↗
6. Hypothetical model of dynamic biomarkers of the Alzheimer’s pathological cascade10.1016/S1474-4422(09)70299-6 ↗
7. Brain imaging of mild cognitive impairment and Alzheimer’s disease
8. Multimodal measurement approach to identify individuals with mild cognitive impairment: study protocol for a cross-sectional trial10.1136/bmjopen-2020-046879 ↗
9. Multimodal 3D deep learning for early diagnosis of alzheimer’s disease10.1109/ACCESS.2024.3381862 ↗
10. Pyramid-attentive GAN for multimodal brain image complementation in Alzheimer’s disease classification10.1016/j.bspc.2023.105652 ↗
11. Clinical impact of 11C-Pittsburgh compound-B positron emission tomography in addition to magnetic resonance imaging and single-photon emission computed tomography on diagnosis of mild cognitive impairment to Alzheimer’s disease10.1097/MD.0000000000023969 ↗
12. Artificial intelligence in medicine: current trends and future possibilities10.3399/bjgp18X695213 ↗
13. Improving alzheimer’s disease diagnosis with multi-modal PET embedding features by a 3D multi-task MLP-mixer neural network10.1109/JBHI.2023.3280823 ↗
14. Deep networks for behavioral variant frontotemporal dementia identification from multiple acquisition sources10.1016/j.compbiomed.2022.105937 ↗
15. Multibranch CNN with MLP-mixer-based feature exploration for high-performance disease diagnosis10.1109/TNNLS.2023.3250490 ↗
16. Trockman A, Kolter JZ. Patches are all you need? arXiv:2201.09792. 2022.
17. Artificial intelligence in medicine10.1016/j.metabol.2017.01.011 ↗
18. Causability and explainability of artificial intelligence in medicine10.1002/widm.1312 ↗
19. Deep learning-based classification of healthy aging controls, mild cognitive impairment and Alzheimer’s disease using fusion of MRI-PET imaging10.1016/j.bspc.2022.104312 ↗
20. A Gaussian-based model for early detection of mild cognitive impairment using multimodal neuroimaging10.1016/j.jneumeth.2019.108544 ↗
21. Mild cognitive impairment classification using combined structural and diffusion imaging biomarkers10.1088/1361-6560/ac0e77 ↗
22. Identifying early mild cognitive impairment by multi-modality MRI-based deep learning10.3389/fnagi.2020.00206 ↗
23. Multimodal predictive classification of Alzheimer’s disease based on attention-combined fusion network: integrated neuroimaging modalities and medical examination data10.1049/ipr2.12841 ↗
24. Multimodal fusion-based deep learning network for effective diagnosis of alzheimer’s disease10.1109/MMUL.2022.3156471 ↗
25. Pareto optimized adaptive learning with transposed convolution for image fusion alzheimer’s disease classification10.3390/brainsci13071045 ↗
26. Multimodal neuroimaging fusion for alzheimer’s disease: an image colorization approach with mobile vision transformer10.1002/ima.23158 ↗
27. Positive effect of super-resolved structural magnetic resonance imaging for mild cognitive impairment detection10.3390/brainsci14040381 ↗
28. Optimized convolutional fusion for multimodal neuroimaging in alzheimer’s disease diagnosis: enhancing data integration and feature extraction10.3390/jpm13101496 ↗
29. Alzheimer’s disease stage recognition from MRI and PET imaging data using Pareto-optimal quantum dynamic optimization10.1016/j.heliyon.2024.e34402 ↗
30. Brain structural and functional changes in cognitive impairment due to alzheimer’s disease10.3389/fpsyg.2022.886619 ↗
31. Hypertension and the risk of mild cognitive impairment10.1001/archneur.64.12.1734 ↗
32. Effect of intensive blood pressure control on subtypes of mild cognitive impairment and risk of progression from SPRINT study10.1111/jgs.17583 ↗
33. Ways toward an early diagnosis in Alzheimer’s disease: the Alzheimer’s Disease Neuroimaging Initiative (ADNI)10.1016/j.jalz.2005.06.003 ↗
34. Mayo Clinic. Alzheimer’s Disease Research Center. [cited 2024 Dec 8]. Available from: https://www.mayo.edu/research/centers-programs/alzheimers-disease-research-center/research-activities/mayo-clinic-study-aging/overview.
35. LaMontagne PJ, Benzinger TL, Morris JC, Keefe S, Hornbeck R, Xiong C, et al. OASIS-3: longitudinal neuroimaging, clinical, and cognitive dataset for normal aging and alzheimer disease. 2019. doi:10.1101/2019.12.13.19014902.10.1101/2019.12.13.19014902 ↗
36. Advances in functional and structural MR image analysis and implementation as FSL10.1016/j.neuroimage.2004.07.051 ↗
37. Andrew Hoopes ZK Alexander Zsikla. Freesurfer: Neuroimaging Analysis and Visualization Suite. [cited 2024 Dec 8]. Available from: https://github.com/freesurfer/freesurfer.
38. SynthStrip: skull-stripping for any brain image10.1016/j.neuroimage.2022.119474 ↗
39. Cortical surface-based analysis reduces bias and variance in kinetic modeling of brain PET data10.1016/j.neuroimage.2013.12.021 ↗
40. Different partial volume correction methods lead to different conclusions: an 18F-FDG-PET study of aging10.1016/j.neuroimage.2016.02.042 ↗
41. Partial-volume effect correction in positron emission tomography brain scan image using super-resolution image reconstruction10.1259/bjr.20140119 ↗
42. Yildirim N. Deep image fusion: multi-sensor image (infrared and visible) Fusion using deep learning framework, Principal Component Analysis, Discrete Wavelet Transform—github.com. [cited 2024 Dec 27]. Available from: https://github.com/nuriyeyldrm/deep_image_fusion.
43. Hendrycks D, Gimpel K. Gaussian error linear units (GELUs). arXiv:1606.08415. 2016.
44. B-Cos alignment for inherently interpretable CNNs and vision transformers10.1109/TPAMI.2024.3355155 ↗
45. Xception: deep learning with depthwise separable convolutions
46. Dosovitskiy A, Beyer L, Kolesnikov A, Weissenborn D, Zhai XH, Unterthiner T, et al. An image is worth 16 × 16 words: transformers for image recognition at scale. arXiv:2010.11929. 2020.
47. Slide-transformer: hierarchical vision transformer with local self-attention
48. Leem S, Seo H. Attention guided CAM: visual explanations of vision transformer guided by self-attention. arXiv:2402.04563. 2024.10.1609/aaai.v38i4.28077 ↗
49. Grad-CAM: visual explanations from deep networks via gradient-based localization10.1007/s11263-019-01228-7 ↗
50. Lundberg S, Lee SI. A unified approach to interpreting model predictions. arXiv:1705.07874. 2017.
51. Vaswani A, Shazeer N, Parmar N, Uszkoreit J, Jones L, Gomez AN, et al. Attention is all you need. arXiv:1706.03762. 2017.
52. He K, Zhang X, Ren S, Sun J. Deep residual learning for image recognition. arXiv:1512.03385. 2015.10.1109/CVPR.2016.90 ↗
53. Huang G, Liu Z, van der Maaten L, Weinberger KQ. Densely connected convolutional networks. arXiv:1608.06993. 2016.10.1109/CVPR.2017.243 ↗
54. Qin D, Leichner C, Delakis M, Fornoni M, Luo S, Yang F, et al. MobileNetV4: universal models for the mobile ecosystem. arXiv:2404.10518. 2024.10.1007/978-3-031-73661-2_5 ↗
55. Magnetic resonance imaging white matter hyperintensities and brain volume in the prediction of mild cognitive impairment and dementia10.1001/archneurol.2007.23 ↗
56. Brain structure and function related to cognitive reserve variables in normal aging, mild cognitive impairment and Alzheimer’s disease10.1016/j.neurobiolaging.2007.10.008 ↗
57. MRI markers for mild cognitive impairment: comparisons between white matter integrity and gray matter volume measurements10.1371/journal.pone.0066367 ↗
58. Volume, density, and thickness brain abnormalities in mild cognitive impairment: an ALE meta-analysis controlling for age and education10.1007/s11682-022-00659-0 ↗
59. Mapping the genetic architecture of cortical morphology through neuroimaging: progress and perspectives10.1038/s41398-022-02193-5 ↗
60. Tolstikhin I, Houlsby N, Kolesnikov A, Beyer L, Zhai XH, Unterthiner T, et al. MLP-Mixer: an all-MLP architecture for vision. arXiv:2105.01601. 2021.
61. Multi-Scale MLP-Mixer for image classification10.1016/j.knosys.2022.109792 ↗