Metabolomics facilitates differential diagnosis in common inherited retinal degenerations by exploring their profiles of serum metabolites.
Wei-Chieh WangChu-Hsuan HuangHsin-Hsiang ChungPei-Lung ChenFung-Rong HuChang-Hao YangChung-May YangChao-Wen LinCheng-Chih HsuTa-Ching ChenPublished in: Nature communications (2024)
The diagnosis of inherited retinal degeneration (IRD) is challenging owing to its phenotypic and genotypic complexity. Clinical information is important before a genetic diagnosis is made. Metabolomics studies the entire picture of bioproducts, which are determined using genetic codes and biological reactions. We demonstrated that the common diagnoses of IRD, including retinitis pigmentosa (RP), cone-rod dystrophy (CRD), Stargardt disease (STGD), and Bietti's crystalline dystrophy (BCD), could be differentiated based on their metabolite heatmaps. Hundreds of metabolites were identified in the volcano plot compared with that of the control group in every IRD except BCD, considered as potential diagnosing markers. The phenotypes of CRD and STGD overlapped but could be differentiated by their metabolomic features with the assistance of a machine learning model with 100% accuracy. Moreover, EYS-, USH2A-associated, and other RP, sharing considerable similar characteristics in clinical findings, could also be diagnosed using the machine learning model with 85.7% accuracy. Further study would be needed to validate the results in an external dataset. By incorporating mass spectrometry and machine learning, a metabolomics-based diagnostic workflow for the clinical and molecular diagnoses of IRD was proposed in our study.
Keyphrases
- machine learning
- mass spectrometry
- artificial intelligence
- optical coherence tomography
- big data
- liquid chromatography
- healthcare
- early onset
- deep learning
- gene expression
- copy number
- social media
- high performance liquid chromatography
- risk assessment
- capillary electrophoresis
- electronic health record
- climate change