This is a prospective observational cohort study that will aim to recruit 60 participants who have had COVID-19, were admitted to hospital, required intensive care, and/or developed AKI during their hospital stay. Potential participants will be approached either by telephone by a member of the research team or via clinics (nephrology, post-ICU follow up clinics).
After the participants have read and understand the Participant Information Sheet, and had sufficient time (at least 24 hours) to consider their participation in this study, the investigators will ask them to sign a consent form, which shows their willingness to take part. The investigators will then collect information from their medical records about their hospital admission with COVID-19, including their age, ethnicity, medical conditions, length of hospital stay, tablets or any other treatments they received, as well as details of their stay in the ICU. The investigators will also arrange their first study visit which should be 3-6 months after they had been discharged from the hospital. During this first study day, the investigators will: * Measure weight and height and take blood pressure. * Take blood and urine samples. * Ask participants to complete three questionnaires about their health, symptoms of fatigue and quality of life (SF-36, EQ-5D-5L and Fatigue Questionnaires). * Measure the accumulation of toxins in the skin using a safe, quick (less than five minutes) and painless technique called skin autofluorescence. This involves placing the forearm on a piece of equipment that shines a light on the skin and measures the amount of light that is reflected back. * Conduct an MRI scan of the kidneys, muscles, abdomen and heart. The MRI scan will take 60-70 minutes in total. The investigators will ask participants not to eat or drink anything two hours before the MRI scan. After this visit, the investigators will ask participants to come back for two more study visits, which will be arranged at 12 and 24 months after their hospital discharge. These visits will consist of the same procedures and measurements done in the first study visit.
Study Type
OBSERVATIONAL
Enrollment
15
This study does not involve any intervention or new treatment. We will conduct MRI scans of the kidneys, muscles, abdomen and heart at baseline, 12 and 24 months after hospital discharge. The MRI scan will take 60-70 minutes in total.
University Hospitals of Derby and Burton NHS Foundation Trust
Derby, Derbyshire, United Kingdom
MRI assessment of global organ structure at 12 months.
Global organ structure will be assessed through structural T1- and T2-weighted MRI scans which will provide information about automated segmentation and volume assessment of whole kidney (and both cortex and medulla) as well as other abdominal organs (including liver and spleen). Global organ structure will also be assessed through longitudinal (T1) and transverse (T2) relaxation time mapping. T1 and T2 increase with tissue inflammation, oedema and fibrosis. A respiratory-triggered inversion recovery (IR) spin-echo echo-planar scheme will be used for abdominal T1 mapping and a Gradient and spin echo (T2-GraSE) scheme for abdominal T2 mapping.
Time frame: 12 months
MRI assessment of thrombi (R2*) at 12 months.
R2\* data will be acquired using a multi-echo fast field echo (mFFE) scheme to assess thrombi. Conventionally R2\* mapping is used as a measure of oxygenation, but R2\*is likely to be altered by other factors in COVID-19, including oedema and small vessel thrombotic processes.
Time frame: 12 months
MRI assessment of organ perfusion (Arterial spin labelling [ASL]) at 12 months.
Mean transit time and perfusion depicting changes in microvascular blood flow and large vessel flow/thrombosis will be determined using a FAIR labelling scheme with a multi-slice spin-echo echo-planar imaging readout and multiple labelling delay times.
Time frame: 12 months
MRI assessment of global organ structure.
Global organ structure will be assessed through structural T1- and T2-weighted MRI scans which will provide information about automated segmentation and volume assessment of whole kidney (and both cortex and medulla) as well as other abdominal organs (including liver and spleen). Global organ structure will also be assessed through longitudinal (T1) and transverse (T2) relaxation time mapping. T1 and T2 increase with tissue inflammation, oedema and fibrosis. A respiratory-triggered inversion recovery (IR) spin-echo echo-planar scheme will be used for abdominal T1 mapping and a Gradient and spin echo (T2-GraSE) scheme for abdominal T2 mapping.
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Time frame: 3-6 and 24 months
MRI assessment of thrombi (R2*).
R2\* data will be acquired using a multi-echo fast field echo (mFFE) scheme to assess thrombi. Conventionally R2\* mapping is used as a measure of oxygenation, but R2\*is likely to be altered by other factors in COVID-19, including oedema and small vessel thrombotic processes.
Time frame: 3-6 and 24 months
MRI assessment of organ perfusion (ASL)
Mean transit time and perfusion depicting changes in microvascular blood flow and large vessel flow/thrombosis will be determined using a FAIR labelling scheme with a multi-slice spin-echo echo-planar imaging readout and multiple labelling delay times.
Time frame: 3-6 and 24 months
Correlations between MRI measures with estimated glomerular filtration rate.
Correlations between MRI measures (Cortical T1, ASL-perfusion, T2, R2\*) with estimated glomerular filtration rate (ml/min/1.73m2).
Time frame: 3-6, 12 and 24 months
Correlations between MRI measures with urine albumin and protein creatinine ratios.
Correlations between MRI measures (Cortical T1, ASL-perfusion, T2, R2\*) with urine albumin creatinine ratio (mg/mmol) and urine protein creatinine ratio (mg/mmol).
Time frame: 3-6, 12 and 24 months
Correlations between MRI measures with mental component score.
Correlations between MRI measures (Cortical T1, ASL-perfusion, T2, R2\*) with the mental component score. A score between 0 and 100 is calculated from the 36-Item Short-Form Health Survey; the higher the score, the better the quality of life mental domain.
Time frame: 3-6, 12 and 24 months
Correlations between MRI measures with physical component score.
Correlations between MRI measures (Cortical T1, ASL-perfusion, T2, R2\*) with the physical component score. A score between 0 and 100 is calculated from the 36-Item Short-Form Health Survey; the higher the score, the better the quality of life physical domain.
Time frame: 3-6, 12 and 24 months
Correlations between MRI measures with health state score.
Correlations between MRI measures (Cortical T1, ASL-perfusion, T2, R2\*) with the health state score calculated from the European Quality of Life 5-Dimensions questionnaire. The health state score ranges from -0.285 (for the worst health state) to 1 (for the best health state).
Time frame: 3-6, 12 and 24 months
Correlations between MRI measures with visual analogue score.
Correlations between MRI measures (Cortical T1, ASL-perfusion, T2, R2\*) with the visual analogue score from the European Quality of Life 5-Dimensions questionnaire. The visual analogue score uses a thermometer-like scale numbered from 0 to 100; the higher the score, the better the health state.
Time frame: 3-6, 12 and 24 months
Correlations between MRI measures with fatigue severity.
Correlations between MRI measures (Cortical T1, ASL-perfusion, T2, R2\*) with the fatigue score from the Fatigue Severity Scale, a 9-item questionnaire scored on a 7-point scale (minimum score=9; maximum score=63); the higher the score, the greater the fatigue severity.
Time frame: 3-6, 12 and 24 months
Correlations between MRI measures with fatigue score.
Correlations between MRI measures (Cortical T1, ASL-perfusion, T2, R2\*) with the fatigue score from the Visual Analogue Fatigue Scale, which uses an horizontal line scale numbered from 0 to 10; the higher the score, the higher the fatigue.
Time frame: 3-6, 12 and 24 months
Correlations with MRI measures with skin autofluorescence levels.
Correlations between MRI measures (Cortical T1, ASL-perfusion, T2, R2\*) with skin autofluorescence levels (arbitrary units) measured with the validated Autofluorescence Reader Standard Unit (SU) version 2.4.3 (AGE Reader SU, DiagnOptics Technologies BV, Aarhusweg 4-9, Groningen, The Netherlands).
Time frame: 3-6, 12 and 24 months
Mean change in mental component score.
Mean change in mental component score. A score between 0 and 100 is calculated from the 36-Item Short-Form Health Survey; the higher the score, the better the quality of life mental domain.
Time frame: 3-6, 12 and 24 months
Mean change in physical component score.
Mean change in physical component score. A score between 0 and 100 is calculated from the 36-Item Short-Form Health Survey; the higher the score, the better the quality of life physical domain.
Time frame: 3-6, 12 and 24 months
Mean change in health state score.
Mean change in health state score calculated from the European Quality of Life 5-Dimensions questionnaire. The health state score ranges from -0.285 (for the worst health state) to 1 (for the best health state).
Time frame: 3-6, 12 and 24 months
Mean change in visual analogue score.
Mean change in visual analogue score from the European Quality of Life 5-Dimensions questionnaire. The visual analogue score uses a thermometer-like scale numbered from 0 to 100; the higher the score, the better the health state.
Time frame: 3-6, 12 and 24 months
Mean change in fatigue severity scale.
Mean change in fatigue score as assessed by the Fatigue Severity Scale, a 9-item questionnaire scored on a 7-point scale (minimum score=9; maximum score=63); the higher the score, the greater the fatigue severity.
Time frame: 3-6, 12 and 24 months
Mean change in fatigue score.
Mean change in fatigue score as assessed by the Visual Analogue Fatigue Scale, which uses an horizontal line scale numbered from 0 to 10; the higher the score, the higher the fatigue.
Time frame: 3-6, 12 and 24 months
Mean change in skin autofluorescence levels.
Mean change in skin autofluorescence levels (arbitrary units) measured with the AGE Reader.
Time frame: 3-6, 12 and 24 months
Incidence of kidney disease progression.
Assessment of kidney disease progression defined as decrease in estimated glomerular filtration rate (eGFR) of ≥25% associated with a decline in eGFR stage.
Time frame: 3-6, 12 and 24 months
Incidence of cardiovascular events.
Recording of the number of participants who developed any cardiovascular events.
Time frame: 3-6, 12 and 24 months
Correlations between MRI measures with all-cause mortality.
Correlations between MRI measures (Cortical T1, ASL-perfusion, T2, R2\*) with all-cause mortality using multi-variable Cox proportional hazards models.
Time frame: 12 and 24 months