Benchmarking the AI-based diagnostic potential of plasma proteomics for neurodegenerative disease in 17,170 people
An, L.; Binette, A. P.; Hristovska, I.; Vilkaite, G.; Xiao, Y.; Smets, B.; Saloner, R.; Tasaki, S.; Xu, Y.; Krish, V.; Imam, F.; Janelidze, S.; van Westen, D.; the Global Neurodegeneration Proteomics Consortium (GNPC), ; Stomrud, E.; Whelan, C. D.; Palmqvist, S.; Ossenkoppele, R.; Mattsson-Carlgren, N.; Hansson, O.; Vogel, J. W.
Show abstract
Co-pathology is a common feature of neurodegenerative diseases that complicates diagnosis, treatment and clinical management. However, sensitive, specific and scalable biomarkers for in vivo pathological diagnosis are not available for most neurodegenerative neuropathologies. Here, we present ProtAIDe-Dx, a deep joint-learning model trained on 17,187 patients and controls (Age=70.3{+/-}11.5, 53.2% of Female) that uses plasma proteomics to provide simultaneous probabilistic diagnosis across six conditions associated with dementia in aging. ProtAIDe-Dx achieves cross-validated balanced classification accuracy of 70%-95% and AUCs > 78% across all conditions. The models diagnostic probabilities highlighted subgroups of patients with co-pathologies, and were associated with pathology-specific biomarkers in an external memory clinic sample, even among cognitively unimpaired people. Model interpretation revealed a suite of protein networks marking shared and specific biological processes across diseases, and identified novel and previously described proteins discriminating each diagnosis. ProtAIDe-Dx significantly improved biomarker-based differential diagnosis in a memory clinic sample, pinpointing proteins leading to diagnostic decisions at an individual level. Together, this work highlights the promise of plasma proteomics to improve patient-level diagnostic work-up with a single blood draw.
Matching journals
The top 6 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Molecular estimation of neurodegeneration pseudotime in older brains 97%
- Cell-type-specific Alzheimer’s disease polygenic risk scores are associated with distinct disease processes in Alzheimer’s disease 96%
- Novel brain-penetrant inhibitor of G9a methylase blocks Alzheimer’s disease proteopathology for precision medication 96%
Similar papers in this journal
- Synapse protein signatures in cerebrospinal fluid and plasma predict cognitive maintenance versus decline in Alzheimers disease 97%
- Amyloid and Tau PET positive cognitively unimpaired individuals: Destined to decline? 95%
- Proteomic aging clock predicts mortality and risk of common age-related diseases in diverse populations 94%
Similar papers in this journal
Similar papers in this journal
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.