The UK Interstitial Lung Disease Long-COVID19 study (UKILD-Long COVID): understanding the burden of Interstitial Lung Disease in Long COVID.

  • Funded by UK Research and Innovation (UKRI)
  • Total publications:14 publications

Grant number: MR/W006111/1

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2021
    2023
  • Known Financial Commitments (USD)

    $2,713,174.61
  • Funder

    UK Research and Innovation (UKRI)
  • Principal Investigator

    Professor Gisli Jenkins
  • Research Location

    United Kingdom
  • Lead Research Institution

    Imperial College London
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Pathogen morphology, shedding & natural history

  • Special Interest Tags

    N/A

  • Study Type

    Clinical

  • Clinical Trial Details

    Not applicable

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

The COVID-19 pandemic has caused significant worldwide mortality and morbidity with >1 million people infected and >170,000 people hospitalised in the UK. Current estimates suggest 10-20% of non-hospitalised patients and 40-60% of hospitalised patients have long term symptoms, including breathlessness and fatigue, so-called "Long COVID". Emerging radiological and physiological features suggest Interstitial Lung diseases (ILD) including organising pneumonia and pulmonary fibrosis occur in up to 20% of hospitalised patients, although the precise burden and natural history of Long COVID related ILD (LCILD) is not clear. Given the large number of patients with persisting breathlessness there is an urgent need to identify and prevent the development LCILD. To improve outcomes for survivors of COVID-19 we will a) determine the prevalence of ILD following COVID-19, stratified by severity of infection and treatment, b) describe the phenotypes, c) determine the natural history and d) identify pathomechanisms and biomarkers of LCILD. Patients with documented COVID-19 will be recruited and the proportion of patients with symptoms, signs and investigations consistent with ILD between 3 and 6 months will be documented. In patients where ILD is suspected clinically this will be confirmed by Computerised Tomography (CT) scanning and patients will be stratified by pre-existing ILD, hospitalisation status, and therapy received. A subgroup of patients with proven LCILD will be re-consented for 12-month follow-up and deep phenotyping including 129Xenon-MRI and bronchoalveolar lavage. These data will define the burden of LCILD and inform the design of clinical trials to assess potential therapies to modulate progression of LCILD.

Publicationslinked via Europe PMC

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The respiratory microbiome in patients with post-COVID-19 residual lung abnormalities resembles that of healthy individuals and is distinct from idiopathic pulmonary fibrosis.

Mapping the amplitude and phase of dissolved <sup>129</sup>Xe red blood cell signal oscillations with keyhole spectroscopic lung imaging.

Respiratory sequelae of COVID-19: pulmonary and extrapulmonary origins, and approaches to clinical care and rehabilitation.

Determinants of recovery from post-COVID-19 dyspnoea: analysis of UK prospective cohorts of hospitalised COVID-19 patients and community-based controls.

Effects of sleep disturbance on dyspnoea and impaired lung function following hospital admission due to COVID-19 in the UK: a prospective multicentre cohort study.

Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post-COVID-19 Study.

Longitudinal Lung Function Assessment of Patients Hospitalized With COVID-19 Using <sup>1</sup>H and <sup>129</sup>Xe Lung MRI.

Prevalence of physical frailty, including risk factors, up to 1 year after hospitalisation for COVID-19 in the UK: a multicentre, longitudinal cohort study.

SARS-CoV-2-specific nasal IgA wanes 9 months after hospitalisation with COVID-19 and is not induced by subsequent vaccination.