# Longitudinal functional lung imaging in children with Post-COVID-19 syndrome

**Authors:** Calvin Kraus, Lina Tan, Maximilian Hinsen, Sandy Schmidt, Emmanuel Nedoschill, Felix Wachter, Henriette Mandelbaum, Alexandra L. Wagner, Isabelle Schöffl, Annika Weigelt, Manfred Rauh, Joachim Woelfle, Michael Uder, Regina Trollmann, Jens Vogel-Claussen, Adrian P. Regensburger, Rafael Heiss, Ferdinand Knieling, Roman Raming

PMC · DOI: 10.1186/s40348-025-00216-x · 2026-01-31

## TL;DR

This study investigates whether lung defects cause persistent symptoms in children after recovering from COVID-19.

## Contribution

The study introduces longitudinal functional lung imaging to assess Post-COVID-19 syndrome in children.

## Key findings

- Vaccinated children had lower baseline ventilation compared to those with PCS.
- Ventilation and perfusion matching improved over time in both recovered and PCS groups.
- Clinical symptoms decreased over six months, but no significant lung defects were found.

## Abstract

Respiratory distress and COVID-19-related symptoms persist as Post-COVID-19 syndrome (PCS) in a proportion of children and adolescents.

We aimed to determine whether ventilation or perfusion defects constitute a possible cause for PCS.

Mean ventilation was lower at baseline in vaccinated than in PCS (p=0.04) and V/Qmatchnon-defected increased from baseline to follow-up in vaccinated (p=0.03). In post-hoc comparison with historic data, V/Qmatchnon-defected improved in recovered (historic: 63.5±18.7%; baseline: 88.8±9.0%, p<0.0001; follow-up: 88.1±10.6%; p=0.0002) and PCS (historic: 57.3±19.5%; baseline: 86.1±7.6%, p<0.0001; follow-up: 86.6±7.7%, p=0.0110). Symptom load in PCS decreased from infection and baseline time points to 6-month follow-up. Laboratory assessments showed no differences.

Despite persisting clinical symptoms, PREFUL MRI demonstrates no significant difference between cohorts, not supporting the hypothesis of persisting defects of the lung as causative.

The online version contains supplementary material available at 10.1186/s40348-025-00216-x.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** USO1 (USO1 vesicle transport factor) [NCBI Gene 8615] {aka P115, TAP, VDP}, COX1 (cytochrome c oxidase subunit I) [NCBI Gene 4512] {aka COI, MTCO1}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** loss of scent (MESH:D016388), gastrointestinal symptoms (MESH:D012817), deaths (MESH:D003643), cognitive dysfunction (MESH:D003072), defects of the lung (MESH:D008171), asthma (MESH:D001249), tinnitus (MESH:D014012), PCC (MESH:D000094024), vomiting (MESH:D014839), cough (MESH:D003371), PREFUL (MESH:D000210), chest pain (MESH:D002637), pneumonia (MESH:D011014), hematoma (MESH:D006406), Diarrhea (MESH:D003967), chronic obstructive pulmonary disease (MESH:D029424), dyspnea (MESH:D004417), Ventilation Defects (MESH:D053717), respiratory disease (MESH:D012140), inflammation (MESH:D007249), pulmonary dysfunction (MESH:D011660), airway dysfunction (MESH:D000402), lung injuries (MESH:D055370), sight and sleeping disorder (MESH:D012893), abdominal pain (MESH:D015746), paresthesia (MESH:D010292), seizure (MESH:D012640), ME/CFS (MESH:D015673), fatigue (MESH:D005221), short stature (MESH:D006130), Respiratory distress (MESH:D012128), sore throat (MESH:D010612), long-term sequelae of the infection (MESH:D000088562), nausea (MESH:D009325), hyperventilation syndrome (MESH:D006985), aphasia (MESH:D001037), PEM (MESH:D000092202), V/Q defects (MESH:D011778), allergies (MESH:D004342), cold (MESH:D000067390), Cystic Fibrosis (MESH:D003550), lung impairment (MESH:D009422), COVID (MESH:D000086382), phantosmia (MESH:D000857), depression (MESH:D003866), allergic rhinitis (MESH:D065631), loss of taste (MESH:D000370), Infection (MESH:D007239), neurological symptoms (MESH:D009461), fever (MESH:D005334), idiopathic pulmonary fibrosis (MESH:D054990), headache (MESH:D006261), Perfusion defects (MESH:D000013), panic disorders (MESH:D016584), strabismus (MESH:D013285), cramping fingers (MESH:D009120)
- **Chemicals:** xenon (MESH:D014978), 129Xe (-)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12858673/full.md

---
Source: https://tomesphere.com/paper/PMC12858673