Abstract
Background: Numerous publications describe the clinical manifestations of post-acute sequelae of SARS-CoV-2 (PASC or “long COVID”), but they are difficult to integrate because of heterogeneous methods and the lack of a standard for denoting the many phenotypic manifestations. Patient-led studies are of particular importance for understanding the natural history of COVID-19, but integration is hampered because they often use different terms to describe the same symptom or condition. This significant disparity in patient versus clinical characterization motivated the proposed ontological approach to specifying manifestations, which will improve capture and integration of future long COVID studies. Methods: The Human Phenotype Ontology (HPO) is a widely used standard for exchange and analysis of phenotypic abnormalities in human disease but has not yet been applied to the analysis of COVID-19. Findings: We identified 303 articles published before April 29, 2021, curated 59 relevant manuscripts that described clinical manifestations in 81 cohorts three weeks or more following acute COVID-19, and mapped 287 unique clinical findings to HPO terms. We present layperson synonyms and definitions that can be used to link patient self-report questionnaires to standard medical terminology. Long COVID clinical manifestations are not assessed consistently across studies, and most manifestations have been reported with a wide range of synonyms by different authors. Across at least 10 cohorts, authors reported 31 unique clinical features corresponding to HPO terms; the most commonly reported feature was Fatigue (median 45.1%) and the least commonly reported was Nausea (median 3.9%), but the reported percentages varied widely between studies. Interpretation: Translating long COVID manifestations into computable HPO terms will improve analysis, data capture, and classification of long COVID patients. If researchers, clinicians, and patients share a common language, then studies can be compared/pooled more effectively. Furthermore, mapping lay terminology to HPO will help patients assist clinicians and researchers in creating phenotypic characterizations that are computationally accessible, thereby improving the stratification, diagnosis, and treatment of long COVID. Funding: U24TR002306; UL1TR001439; P30AG024832; GBMF4552; R01HG010067; UL1TR002535; K23HL128909; UL1TR002389; K99GM145411.
| Original language | English |
|---|---|
| Article number | 103722 |
| Journal | EBioMedicine |
| Volume | 74 |
| DOIs | |
| State | Published - Dec 2021 |
Bibliographical note
Publisher Copyright:© 2021 The Author(s)
Funding
RRD, TDB, JBB, CGC, WBH, JAM, AMP, ERP, HMR, JS, RAS, AES, JS, GS, MAH, PNR report funding from NIH. MAH and JAM are co-founders of Pryzm Health. This work was supported by NCATS U24 TR002306. Rachel R. Deer supported by UTMB CTSA UL1TR001439 and NIA P30AG024832; Halie M. Rando was supported by The Gordon and Betty Moore Foundation (GBMF 4552) and the National Human Genome Research Institute (R01 HG010067); Tellen D. Bennett supported by NIH UL1TR002535 03S2 and NIH UL1TR002535; James Brian Byrd supported by NIH grant K23HL128909; Christopher G. Chute supported by U24 TR002306. Julian Solway supported by UL1TR002389. Mallory A. Perry supported by K99GM145411.
| Funders | Funder number |
|---|---|
| National Institutes of Health (NIH) | K23HL128909, K99GM145411 |
| National Institutes of Health (NIH) | |
| National Institute on Aging | P30AG024832 |
| National Institute on Aging | |
| National Human Genome Research Institute | R01 HG010067 |
| National Human Genome Research Institute | |
| Gordon and Betty Moore Foundation | GBMF 4552 |
| Gordon and Betty Moore Foundation | |
| National Center for Advancing Translational Sciences (NCATS) | UL1TR002535 03S2, UL1TR002389, U24TR002306, UL1TR001439 |
| National Center for Advancing Translational Sciences (NCATS) | |
| AES Corporation | |
| University of Texas Medical Branch | |
| Russian Academy of Sciences |
Keywords
- COVID-19
- human phenotype ontology
- long COVID
- of post-acute sequelae of SARS-CoV-2
- phenotyping
ASJC Scopus subject areas
- General Medicine
- General Biochemistry, Genetics and Molecular Biology