Evidence map›Paper›PMID 42339267›Full record

ArticleOxford open immunology2026

Algorithm dependence of patient phenotypes in Long COVID: a patient-led, multi-method clustering of 6031 patients using 162 self-reported symptoms.

Tessa D Green, Chris McWilliams, Leonardo de Figueiredo, Letícia Soares, Beth Pollack, Alison K Cohen, Tan Zhi-Xuan, Tess Falor, Hannah E Davis

Abstract read
In one paragraph

Article in Oxford open immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Tessa D GreenPatient-Led Research Collaborative, Calabasas, CA, 91302, United States.ORCID https://orcid.org/0000-0002-6075-2058
Chris McWilliamsPatient-Led Research Collaborative, Calabasas, CA, 91302, United States.ORCID https://orcid.org/0000-0003-3816-5217
Leonardo de FigueiredoPatient-Led Research Collaborative, Calabasas, CA, 91302, United States.
Letícia SoaresPatient-Led Research Collaborative, Calabasas, CA, 91302, United States.ORCID https://orcid.org/0000-0002-6933-8048
Beth PollackPatient-Led Research Collaborative, Calabasas, CA, 91302, United States.ORCID https://orcid.org/0009-0008-9268-1275
Alison K CohenPatient-Led Research Collaborative, Calabasas, CA, 91302, United States.ORCID https://orcid.org/0000-0001-9848-934X
Tan Zhi-XuanDepartment of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA, 02139, United States.ORCID https://orcid.org/0000-0002-1549-8492
Tess FalorPatient-Led Research Collaborative, Calabasas, CA, 91302, United States.ORCID https://orcid.org/0000-0003-0111-3114
Hannah E DavisPatient-Led Research Collaborative, Calabasas, CA, 91302, United States.ORCID https://orcid.org/0000-0002-1245-2034

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Long COVID, characterized by symptoms that remain or emerge in the months after acute COVID-19 infection, is a multisystemic condition with highly variable patient presentations. Phenotyping studies have reported divergent symptom clusters, increasingly used to design trials and interpret biomarker data. However, robustness of these clusters across analytic methods remains uncertain. Methods: We analyzed data from 6 031 adults with ≥ 90 days of illness from a patient-led international survey. Participants reported presence/absence of 162 symptoms, post-exertional malaise severity and demographics. We applied three unsupervised machine learning approaches to the same symptom matrix, evaluating the resulting clusterings for concordance, robustness to subsampling, and relationship to symptom burden, post-exertional malaise severity, age and gender. Results: Each method produced clinically plausible symptom clusters, but concordance across methods was low. All three approaches identified a high-symptom-burden group enriched for post-exertional malaise severity, and lower-symptom-burden groups with older mean age and a lower proportion of women. Symptom count consistently correlated with higher post-exertional malaise severity and a greater proportion of women. Manifold analysis revealed that the overall symptom space was largely continuous, lacking clear cluster boundaries. Conclusions: The strong dependence of patient clusters on algorithm choice suggests that single-method Long COVID phenotyping may produce incomplete or unstable subgroup definitions. Clustering methods may impose artificial boundaries on a smoothly varying symptom landscape, especially in studies capturing fewer symptoms. Phenotyping efforts should assess clustering robustness and avoid overinterpreting single-method results. Our multi-method analysis highlights the importance of considering the full breadth of patient symptoms when evaluating treatments.

Identifiers

PMID42339267
PMCPMC13284999

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.