|
|
|
|
|
by n-e-w
915 days ago
|
|
I try not to immediately call BS on these types of studies…but in this case there are some concerns. “The data sets were randomly divided into training (85%) and test (15%) sets. We used 10-fold cross-validation to obtain generalized results of model performance. Data splitting was performed at the participant level and stratified based on the outcome variables. Because the data classes were imbalanced for symptom severity (ADOS-2 and SRS-2), we performed a random undersampling of the data at the participant level before conducting data splitting. Moreover, we examined different split ratios (80:20 and 90:10) to assess the robustness and consistency of the predictive performances across diverse splitting proportions.” * undersampling is problematic here and probably introduced some bias. These imbalanced class problems are just plain hard. Claiming one hundred percent on an imbalanced class problem should probably cause some concern.
* data split at the participant level has to be done really careful or you’ll over fit
* multiple comparisons bias by testing multiple split ratios on the same test data. Same with the 10-fold cross Val.
* not sure if they validated results on any external test data
* outcome variable stratification also has to be done really carefully or it will introduce bias; seems particularly sensitive in this case
* using severity of symptoms as class labels is problematic. These have to really have been diagnosed the same way / consistently to be meaningful. I also note a long time history in collection of these images (15 years iirc). Hard to believe such a diverse set of images (collection, equipment etc) led to perfect results. ML issues aside, super interested in the basic medical concept. I wasn’t aware retinal abnormalities could be indicative of issues like ASD. |
|
> The photography sessions for patients with ASD took place in a space dedicated to their needs, distinct from a general ophthalmology examination room. This space was designed to be warm and welcoming, thus creating a familiar environment for patients. Retinal photographs of typically developing (TD) individuals were obtained in a general ophthalmology examination room. Each eye required an average of 10–30 s for photography, although some cases involved longer periods to help the patient calm down, sometimes exceeding 5–10 min. All images were captured in a dark room to optimize their quality. Retinal photographs of both patients with ASD and TD were obtained using non-mydriatic fundus cameras, including EIDON (iCare), Nonmyd 7 (Kowa), TRC-NW8 (Topcon), and Visucam NM/FA (Carl Zeiss Meditec).
So two questions:
1. Are we positive that the difference in rooms does not effect these images?
2. If we are in a dark room, and ASD patients are in it for 5-10 minutes longer, are we sure this doesn't effect the retina?
3. Were all cameras used for both ASD and TD images?
Want to make sure the AI is being trained to detect autism, and wasn't accidentally trained to identify camera models, length-in-dark-room or room-welcomingness.
Hopefully not, but I assume you have to be so careful with these sort of things when the model is entirely black-box and you can't actually validate what it's actually doing inside.