{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Lim JT"],"funding":["Ministry of Education - Singapore","National Medical Research Council"],"pagination":["103"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12632001"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["3(1)"],"pubmed_abstract":["<h4>Background</h4>Increased 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.<h4>Methods</h4>We 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.<h4>Results</h4>There 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.<h4>Conclusions</h4>Reinfection 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."],"journal":["BMC global and public health"],"pubmed_title":["Multi-systemic risk of post-acute sequelae associated with SARS-CoV-2 reinfection."],"pmcid":["PMC12632001"],"funding_grant_id":["Clinical Scientist New Investigator Grant","Start-up grant"],"pubmed_authors":["Lim JT","Wee LE","Tan JYJ","Ponce LJ","Ong B","Tan KB","Chiew CJ","Lye DCB"],"additional_accession":[]},"is_claimable":false,"name":"Multi-systemic risk of post-acute sequelae associated with SARS-CoV-2 reinfection.","description":"<h4>Background</h4>Increased 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.<h4>Methods</h4>We 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.<h4>Results</h4>There 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.<h4>Conclusions</h4>Reinfection 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.","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Nov","modification":"2026-06-05T17:24:40.671Z","creation":"2026-05-19T03:11:43.171Z"},"accession":"S-EPMC12632001","cross_references":{"pubmed":["41258276"],"doi":["10.1186/s44263-025-00222-1"]}}