Evidence map›Paper›PMID 40680300›Full record

SynthesisJMIR public health and surveillance2025

Symptom Trajectories and Clinical Subtypes in Post-COVID-19 Condition: Systematic Review and Clustering Analysis.

Mingzhi Hu, Tian Song, Zhaoyuan Gong, Qianzi Che, Jing Guo, Lin Chen, Haili Zhang, Huizhen Li, Ning Liang, Guozhen Zhao and 3 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in JMIR public health and surveillance, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Cognitive impairment in long-COVID: frequency, trajectories and risk factors in a cohort study from Italy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  6. Article
  7. Article
  8. Article
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

13 authors.

Mingzhi Hu *Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0009-0006-0534-9422
Tian Song *Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0000-0003-4215-6591
Zhaoyuan Gong *Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0009-0002-6880-4673
Qianzi CheInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0000-0002-8688-6628
Jing GuoInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0000-0002-4781-8200
Lin ChenInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0009-0008-6243-6594
Haili ZhangInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0000-0002-6103-5456
Huizhen LiInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0000-0003-1123-8914
Ning LiangInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0000-0003-0260-2331
Guozhen ZhaoInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0000-0001-5736-1323
Yanping WangInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0000-0002-4885-7746
Nannan ShiInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0000-0003-0278-1608
Bin LiuInstitute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, No 16, Nanxiao Street, Dongzhimen, Dongcheng District, Beijing, 100700, China, 86 18515189525.ORCID 0000-0003-1162-5930

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Post-COVID-19 condition presents complex symptomatology involving multifaceted interactions, which has resulted in a current lack of comprehensive understanding of its disease trajectory. This knowledge gap significantly compromises the efficiency of symptom management and adversely affects patients' quality of life. Objective: This study aims to comprehensively characterize the temporal evolution of post-COVID-19 condition by identifying core symptom clusters and clinical phenotypes, thereby enhancing understanding of the disease trajectory. Methods: The PubMed, Web of Science, and Embase databases were searched from December 1, 2019, to March 1, 2024. Observational studies related to the prevalence of symptoms in post-COVID-19 condition had been included. We conducted a meta-analysis to synthesize symptom prevalence across different follow-up intervals following PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines and used a network to explore interrelationships and co-occurrence patterns among symptoms, enabling the identification of core symptoms and changes over time. Clustering analysis was used to classify included studies into distinct clinical subtypes. Results: This study analyzed 155 sets of macrolevel data from 108 clinical studies, encompassing 63,771 patients. Fatigue was the most prevalent symptom across all 4 follow-up points (52%, 48%, 46%, and 54%). Dyspnea peaked at the third and sixth follow-ups (36% and 31%) and then declined steadily (28% and 22%). Subgroup analysis revealed that Africa reported the fewest symptoms overall, yet showed high early incidences of fatigue (68%, 95% CI 50%-85%) and dyspnea (56%, 95% CI 15%-98%). The Americas placed greater emphasis on symptom evolution within the first postinfection year, with notably higher prevalence of anxiety (60%, 95% CI 54%-66%) and depression (36%, 95% CI 16%-55%). Asia and Europe documented the most comprehensive symptom profiles, with Asia reporting lower early dyspnea rates (29%, 95% CI 18%-40%) and Europe exhibiting more complex multisystem involvement during long-term follow-up. Network analysis showed that core post-COVID-19 symptoms evolved from early respiratory-neurological manifestations to chronic multisystem symptoms dominated by dizziness. Clustering analysis further indicated a progressive convergence of 2 initially distinct post-COVID-19 subtypes, with the acute inflammatory type becoming less prominent and gradually transitioning into a more chronic, persistent pattern. Conclusions: This study provides a comprehensive characterization of the dynamic evolution of post-COVID-19 condition symptoms and clinical subtypes, highlighting their multisystem involvement. The results reveal a progressive decline in respiratory symptoms over time, while neurological manifestations emerge as the most persistent and systemically impactful core symptoms. Our findings emphasize the need for region-specific surveillance and early warning systems informed by symptom progression patterns. By continuously monitoring the trajectories of symptom clusters, this approach offers valuable insights for identifying early warning signals and targeted intervention points in the management of postinfectious sequelae arising from future large-scale epidemics.

Indexed as

COVID-19Cluster AnalysisFatigueHumansPost-Acute COVID-19 SyndromePrevalencepost–COVID-19 conditionsubtypessymptomssystematic reviewtemporal dynamic

Identifiers

PMID40680300
PMCPMC12296217

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.