Evidence map›Paper›PMID 41258276›Full record

ArticleBMC global and public health2025

Multi-systemic risk of post-acute sequelae associated with SARS-CoV-2 reinfection.

Jue Tao Lim, Liang En Wee, Janice Yu Jin Tan, Luis J Ponce, Calvin J Chiew, Benjamin Ong, David Chien Boon Lye, Kelvin Bryan Tan

Abstract read
In one paragraph

Article in BMC global and public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Jue Tao Lim *National Centre for Infectious Diseases, Singapore, Singapore. juetao.lim@ntu.edu.sg.
Liang En Wee *National Centre for Infectious Diseases, Singapore, Singapore. ian.wee.l.e@singhealth.com.sg.
Janice Yu Jin Tan *National Centre for Infectious Diseases, Singapore, Singapore.
Luis J PonceLee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.
Calvin J ChiewNational Centre for Infectious Diseases, Singapore, Singapore.
Benjamin OngMinistry of Health, Singapore, Singapore.
David Chien Boon LyeNational Centre for Infectious Diseases, Singapore, Singapore.
Kelvin Bryan TanNational Centre for Infectious Diseases, Singapore, Singapore.

Funding

Ministry of Education - Singapore Start-up grantNational Medical Research Council Clinical Scientist New Investigator Grant
6 · The paper itself

Abstract

backgroundIncreased risk of post-acute sequelae was found to occur in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2 reinfections). However, it is unclear whether these increases in post-acute risk are found in milder Omicron reinfections, or persist in a highly boosted population.

methodsWe utilised national COVID-19 databases and healthcare-claims records of Singapore to construct SARS-CoV-2 infected and uninfected cohorts over periods of Delta, Omicron BA.1/2, BA.4/5 and XBB predominance (1 July 2021-28 February 2023). The 300-day risk and excess burdens of pre-specified new-incident diagnoses across cardiovascular, neuropsychiatric, endocrine, auto-immune, renal, respiratory and gastrointestinal domains was compared across SARS-CoV-2 re-infected individuals (N = 57,222), SARS-CoV-2-infected individuals without documented re-infection (N = 1,239,119), and population-based un-infected controls (N = 3,409,170). Risk trajectories between groups were compared to examine whether differences in risk of post-acute sequelae persisted over follow-up time.

resultsThere was an estimated 21% (hazards ratios (HR) = 1.21; 95% Confidence interval (CI) [1.15-1.28]) increase in risk of any post-acute sequelae, and increased post-acute risk of cardiovascular (HR = 1.20; 95% CI [1.09-1.32]), gastrointestinal (HR 1.26; 95% CI [1.16-1.38]), neurological (HR 1.32; 95% CI [1.23-1.42]), endocrine (HR 1.26; 95% CI [1.18-1.35]), respiratory (HR 1.63; 95% CI [1.44-1.83]) and renal (HR 1.28; 95% CI [1.12-1.47]) sequelae associated with SARS-CoV-2 reinfections. Associated risks of post-acute sequelae were greater in reinfections compared to first infections. Excess burdens per 1000 of any post-acute sequelae were also higher in reinfected individuals, and reinfected individuals also had higher outcome probabilities of post-acute sequelae over follow-up time. Risks of post-acute sequelae persisted in fully vaccinated and boosted individuals.

conclusionsReinfection with SARS-CoV-2 is associated with increased risk of post-acute sequelae. Reducing burden of post-acute complications due to SARS-CoV-2 necessitates strategies for preventing reinfection, such as updated vaccines with better effectiveness against infection.

Indexed as

COVID-19DeltaMulti-organ sequelaeOmicronReinfectionSARS-CoV-2

Identifiers

PMID41258276
PMCPMC12632001

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.