Summary
The paper studies the problem of mental disorder diagnosis using multimodal MRI data. Specifically, it proposes a framework called CINP (Contrastive Image-Network Pre-training), which applies contrastive learning between 3D T1-weighted (T1w) MRI and functional connectivity networks (FCNs) derived from fMRI. CINP aims to create a joint latent space integrating functional and structural information, enhancing diagnostic capabilities. During pre-training, the framework incorporates masked image modeling and network-image matching losses to improve modality alignment and representation quality. Moreover, the CINP contains a network prompting, enables the use of 3D T1w MRI from suspected patients and FCNs from confirmed cases to differentiate mental disorders. Extensive results on public datasets shows CINP has good performance.
Strengths
1. The paper addresses a significant problem in mental disorder diagnosis by leveraging both structural and functional MRI data, a topic relevant and valuable to the ICLR communities.
2. The figures and descriptions in the paper are well-organized and clear, which aids in understanding the proposed approach and the CINP framework.
3. The writing in the paper is clear, making the methodology and results easy to follow.
Weaknesses
1. The paper's technical contributions appear limited, as it mainly combines existing methods like contrastive learning and masked autoencoders (MAE) without significant innovation in methodology. The CINP framework may be seen as a straightforward integration of known techniques rather than a novel approach.
2. There is still room for performance improvement. The performance of CINP on the ABIDE dataset is noticeably lower than that of the baselines, as indicated in Table 2. This suggests that the framework may not be fully optimized or may have limitations, and further improvements are needed to make it competitive across all datasets.
3. The assumption that sMRI and fMRI features can be effectively aligned using contrastive learning lacks theoretical or empirical support from a neuroimaging or neuroscience perspective. This forced alignment may overlook important modality-specific differences, making the approach less effective for capturing unique structural-functional relationships in brain data. (See my questions below.)
Questions
My main concern is with the rationale behind using contrastive loss in CINP to model sMRI and fMRI representations. Based on my knowledge, there is a clear distinction between neuroimaging and image-text domains. In the image-text domain, it makes sense to maximize the differences between different categories while minimizing the differences within the same category. For instance, aligning a cat’s textual description with its image, while creating a contrast with dog-related text and images, is logical. However, in neuroimaging studies, why should we align sMRI and fMRI feature representations in this way? And why should we increase inter-subject differences?
I also note that a healthy cohort was used for CINP’s pre-training. The differences within a healthy population do not fall into distinct categorical boundaries, so it is unclear what meaningful patterns are learned by maximizing inter-subject representation differences. Brain imaging features of healthy individuals are generally quite similar in terms of overall structure and function. By maximizing these differences within healthy individuals, the model may pick up biologically insignificant or irrelevant details, diverting its focus from core features. Such differences are more likely to be noise than meaningful information. In contrastive learning, distinct category boundaries are typically required to generate positive and negative samples, but healthy individuals do not naturally fall into clear categories, making the construction of inter-subject contrasts somewhat artificial.
Additionally, enforcing a “strict alignment” between sMRI and fMRI features may lack generalizability. For mental disorders, patients do not always exhibit abnormalities in both sMRI and fMRI simultaneously. For example, a patient might have a normal gray matter thickness in the prefrontal cortex as shown by sMRI, yet fMRI may reveal weakened functional connectivity between the prefrontal cortex and other regions (such as the parietal lobe or hippocampus). In such cases, a “strict alignment“ seems less appropriate. Similarly, even among healthy individuals, while there may be some correlation between gray matter thickness and functional connectivity, it is not necessarily consistent. Forcing alignment within a healthy cohort may lead the model to mistakenly assume a strong correlation between structural and functional features, thereby overlooking the natural variability and dynamic nature of functional connectivity.
I look forward to seeing the authors' response and would consider raising my score if they can adequately address my concerns.