Persistent symptoms and clinical findings in adults with post-acute sequelae of COVID-19/post-COVID-19 syndrome in the second year after acute infection: A population-based, nested case-control study.

Publication date: Jan 01, 2025

Self-reported health problems following severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are common and often include relatively non-specific complaints such as fatigue, exertional dyspnoea, concentration or memory disturbance and sleep problems. The long-term prognosis of such post-acute sequelae of COVID-19/post-COVID-19 syndrome (PCS) is unknown, and data finding and correlating organ dysfunction and pathology with self-reported symptoms in patients with non-recovery from PCS is scarce. We wanted to describe clinical characteristics and diagnostic findings among patients with PCS persisting for >1 year and assessed risk factors for PCS persistence versus improvement. This nested population-based case-control study included subjects with PCS aged 18-65 years with (n = 982) and age- and sex-matched control subjects without PCS (n = 576) according to an earlier population-based questionnaire study (6-12 months after acute infection, phase 1) consenting to provide follow-up information and to undergo comprehensive outpatient assessment, including neurocognitive, cardiopulmonary exercise, and laboratory testing in four university health centres in southwestern Germany (phase 2, another 8. 5 months [median, range 3-14 months] after phase 1). The mean age of the participants was 48 years, and 65% were female. At phase 2, 67. 6% of the patients with PCS at phase 1 developed persistent PCS, whereas 78. 5% of the recovered participants remained free of health problems related to PCS. Improvement among patients with earlier PCS was associated with mild acute index infection, previous full-time employment, educational status, and no specialist consultation and not attending a rehabilitation programme. The development of new symptoms related to PCS among participants initially recovered was associated with an intercurrent secondary SARS-CoV-2 infection and educational status. Patients with persistent PCS were less frequently never smokers (61. 2% versus 75. 7%), more often obese (30. 2% versus 12. 4%) with higher mean values for body mass index (BMI) and body fat, and had lower educational status (university entrance qualification 38. 7% versus 61. 5%) than participants with continued recovery. Fatigue/exhaustion, neurocognitive disturbance, chest symptoms/breathlessness and anxiety/depression/sleep problems remained the predominant symptom clusters. Exercise intolerance with post-exertional malaise (PEM) for >14 h and symptoms compatible with myalgic encephalomyelitis/chronic fatigue syndrome were reported by 35. 6% and 11. 6% of participants with persistent PCS patients, respectively. In analyses adjusted for sex-age class combinations, study centre and university entrance qualification, significant differences between participants with persistent PCS versus those with continued recovery were observed for performance in three different neurocognitive tests, scores for perceived stress, subjective cognitive disturbances, dysautonomia, depression and anxiety, sleep quality, fatigue and quality of life. In persistent PCS, handgrip strength (40. 2 [95% confidence interval (CI) [39. 4, 41. 1]] versus 42. 5 [95% CI [41. 5, 43. 6]] kg), maximal oxygen consumption (27. 9 [95% CI [27. 3, 28. 4]] versus 31. 0 [95% CI [30. 3, 31. 6]] ml/min/kg body weight) and ventilatory efficiency (minute ventilation/carbon dioxide production slope, 28. 8 [95% CI [28. 3, 29. 2]] versus 27. 1 [95% CI [26. 6, 27. 7]]) were significantly reduced relative to the control group of participants with continued recovery after adjustment for sex-age class combinations, study centre, education, BMI, smoking status and use of beta blocking agents. There were no differences in measures of systolic and diastolic cardiac function at rest, in the level of N-terminal brain natriuretic peptide blood levels or other laboratory measurements (including complement activity, markers of Epstein-Barr virus [EBV] reactivation, inflammatory and coagulation markers, serum levels of cortisol, adrenocorticotropic hormone and dehydroepiandrosterone sulfate). Screening for viral persistence (PCR in stool samples and SARS-CoV-2 spike antigen levels in plasma) in a subgroup of the patients with persistent PCS was negative. Sensitivity analyses (pre-existing illness/comorbidity, obesity, medical care of the index acute infection) revealed similar findings. Patients with persistent PCS and PEM reported more pain symptoms and had worse results in almost all tests. A limitation was that we had no objective information on exercise capacity and cognition before acute infection. In addition, we did not include patients unable to attend the outpatient clinic for whatever reason including severe illness, immobility or social deprivation or exclusion. In this study, we observed that the majority of working age patients with PCS did not recover in the second year of their illness. Patterns of reported symptoms remained essentially similar, non-specific and dominated by fatigue, exercise intolerance and cognitive complaints. Despite objective signs of cognitive deficits and reduced exercise capacity, there was no major pathology in laboratory investigations, and our findings do not support viral persistence, EBV reactivation, adrenal insufficiency or increased complement turnover as pathophysiologically relevant for persistent PCS. A history of PEM was associated with more severe symptoms and more objective signs of disease and might help stratify cases for disease severity.

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Concepts Keywords
Coronavirus Adolescent
Dehydroepiandrosterone Adult
Outpatient Aged
Pcr Case-Control Studies
COVID-19
Fatigue
Female
Germany
Humans
Male
Middle Aged
Post-Acute COVID-19 Syndrome
Risk Factors
SARS-CoV-2
Young Adult

Semantics

Type Source Name
disease MESH post-acute sequelae of COVID-19
disease MESH COVID-19
disease MESH syndrome
disease IDO acute infection
disease MESH infection
disease MESH educational status
pathway REACTOME SARS-CoV-2 Infection
disease MESH breathlessness
disease MESH anxiety
disease MESH depression
disease MESH myalgic encephalomyelitis
disease MESH dysautonomia
disease MESH sleep quality
disease IDO quality
drug DRUGBANK Oxygen
drug DRUGBANK Carbon dioxide
disease IDO production
disease IDO blood
drug DRUGBANK Hydrocortisone
drug DRUGBANK Corticotropin
drug DRUGBANK Prasterone sulfate
disease MESH comorbidity
disease MESH obesity
disease MESH adrenal insufficiency
disease IDO history
disease MESH sequelae
disease MESH Mody
disease IDO process
pathway REACTOME Reproduction
disease IDO immunodeficiency
disease MESH Infectious Diseases
drug DRUGBANK Coenzyme M
drug DRUGBANK Trestolone
disease IDO symptom
drug DRUGBANK Prasterone
disease MESH Sleepiness
disease MESH Anxiety Disorder
disease MESH Insomnia
disease MESH encephalopathy
drug DRUGBANK Nesiritide
disease MESH morbidity
disease MESH cognitive dysfunction
disease MESH lifestyle factors
drug DRUGBANK Etoperidone
disease MESH ramp
pathway REACTOME Release
disease MESH sleep disorder
disease MESH taste disorders
disease IDO infection prevalence
disease MESH confusion
disease MESH chest pain
disease MESH marital status
disease MESH Diabetes mellitus
disease MESH joint pain
disease MESH excessive daytime sleepiness
disease MESH dementia
disease MESH psychotic disorders
disease MESH epilepsy
disease MESH seizures
disease MESH psychiatric disorders
disease IDO site
pathway KEGG Viral replication
disease IDO replication
disease IDO protein
disease MESH hyperventilation
drug DRUGBANK Gold
disease IDO country
pathway REACTOME Metabolism
disease MESH neuroinflammatory disorders
drug DRUGBANK L-Alanine
disease MESH cardiovascular diseases
disease MESH respiratory diseases
disease MESH sensory disorders
disease MESH cancer
disease MESH metabolic diseases
drug DRUGBANK (S)-Des-Me-Ampa
disease MESH hypoxia
disease MESH inflammation
drug DRUGBANK Methylergometrine
disease MESH Influenza
disease MESH Symptom burden
disease MESH severe acute respiratory syndrome
disease MESH orthostatic intolerance
drug DRUGBANK Acetylcholine
disease MESH thromboinflammation
disease MESH Allergy
drug DRUGBANK Dimercaprol
disease MESH metabolic syndrome
disease MESH small fiber neuropathy

Original Article

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