A new machine learning software can be used to analyze entries in electronic health records (EHRs) to find symptoms in common between people who have been diagnosed with long COVID and to define subtypes of the condition.
The research, which is described in a new paper in eBioMedicine, also identified strong correlations between different long COVID subtypes and pre-existing conditions such as diabetes and hypertension.
According to Reese, a computer research scientist in Berkeley Lab’s Biosciences Area, this research will help improve our understanding of how and why some individuals develop long COVID symptoms and may enable more effective treatments by helping clinicians develop tailored therapies for each group. For example, the best treatment for patients experiencing nausea and abdominal pain might be quite different from a treatment for those suffering from persistent cough and other lung symptoms.
The team developed and validated their software using a database of EHR information from 6,469 patients diagnosed with long COVID after confirmed COVID-19 infections. “Basically, we found long COVID features in the EHR data for each long COVID patient, and then assessed patient-patient similarity using semantic similarity, which essentially allows ‘fuzzy matching’ between features – for example, ‘cough’ is not the same as ‘shortness of breath,’ but they are similar since they both involve lung problems,” Reese said. “We compare all symptoms for the pair of the patients in this way, and get a score of how similar the two long COVID patients are. We can then perform unsupervised machine learning on these scores to find different subtypes of long COVID.”
They applied machine learning to these patient-patient similarity scores to cluster patients into groups, which were then characterized by analyzing relationships between symptoms and pre-existing diseases and other demographic features, such as age, gender, or race.
Reese and his colleagues note that the tool will be convenient for researchers because the machine learning approach at its core self-adapts for different EHR systems, allowing researchers to gather data from a wide variety of medical establishments.
This research builds on previous work to develop the Human Phenotype Ontology, an open-access database and research tool that provides a standardized vocabulary of symptoms and features found in all human diseases.