Evidence map›Paper›PMID 41639746›Full record

ArticleBMC global and public health2026

Characterization of post-acute multi-organ sequelae following SARS-CoV-2 Infection in the Delta and Omicron Eras in a highly boosted population.

Peihong Guo, Jue Tao Lim, Liang En Wee, An Ting Tay, Yichen Zhai, Calvin J Chiew, Benjamin Ong, David Chien Boon Lye, Kelvin Bryan Tan

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Article in BMC global and public health, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Peihong GuoNational Centre for Infectious Diseases, Singapore, Singapore.
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.
An Ting TayNational Centre for Infectious Diseases, Singapore, Singapore.
Yichen ZhaiLee 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

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMulti-organ post-acute sequelae of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection (PASC) is extensively documented. Recent studies in predominantly Caucasian populations suggest that the evolution of SARS-CoV-2 variants can influence risk (as measured by hazard ratios) and rates (as measured by incidence rate ratios) of PASC, and they also highlight the protective effects of COVID-19 vaccination. However, it is unclear whether risks or rates of PASC have changed over different Omicron subvariants in an Asian population with high uptake of COVID-19 vaccine booster doses.

methodsWe constructed a national cohort of individuals infected with SARS-CoV-2 and estimated the 31-300-day risks and rates of pre-specified new-incident diagnoses across the cardiovascular, neuropsychiatric, auto-immune, renal, and gastrointestinal domains between 1,427,985 and 3,284,081 unique individuals who tested positive or negative for SARS-CoV-2 infection respectively, across Delta, Omicron BA.1/2, BA.4/5, and XBB predominance. We compared risks/rates of new-incident diagnoses between test positives and test negatives in each era.

resultsCompared to test-negatives, asides from increased risk of renal outcomes in BA.1/2 (aHR, 1.17; 95% CI, 1.09-1.26), there were no increased risks of composite diagnoses in other organ systems across all 4 variants of concern. In terms of individual outcomes, there were increased risks or rates of diagnosis of individual neuropsychiatric outcomes, such as memory problems, Alzheimer's disease across all eras, and loss of smell or taste only in Delta. There were also increased risks of diagnosis of individual renal outcomes, such as end stage renal failure in BA.1/2 (aHR, 1.52; 95% CI, 1.27-1.81). In COVID-19 survivors who were hospitalised, risks and rates of cardiovascular, neuropsychiatric, and renal diagnoses in the post-acute period were increased in most eras. COVID-19 vaccinations reduced the risks of composite diagnoses.

conclusionsThe risks/rates of pre-specified new-incident multi-organ PASC were modest over all studied COVID-19 eras. The risk was further attenuated with booster vaccination during the Omicron BA.4/5 and XBB periods compared with the Omicron BA.1/2 period.

Indexed as

Alzheimer’s diseaseBooster uptakeLong COVID-19Multi-organ sequelaeSevere acute respiratory syndrome coronavirus 2

Identifiers

PMID41639746
PMCPMC12874983

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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 OpenQuestion graph.