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Right Heart Dysfunction and Pulmonary Hypertension Evaluation in Airway Disease Using Cardiac Magnetic Resonance (RiPAIR)

29 stycznia 2020 zaktualizowane przez: University of Leicester

Poor function of the right side of the heart and rise in pressure of the blood vessels leading to the lungs are two main heart-related factors that are associated with worsening of airway disease. A relatively new method which uses magnetic field to create images of the heart called cardiac magnetic resonance (CMR) imaging shows immense promise in detailed and accurate assessment of the heart in patients with airway diseases. This project aims to assess the heart in patients with asthma and chronic obstructive pulmonary disease (COPD) as well as healthy participants using CMR to help us determine features on CMR that are different is patients with asthma and COPD compared to healthy participants. This may help with early identification of patients who are at risk of episodes of acute worsening of airway disease, called exacerbation, and potentially halt the progression of the heart dysfunction with currently available or new treatments.

Study involves one visit at Glenfiled Hospital, Leicester, lasting approximately 4 hours. The visit will include following assessments: clinical history, health status, physical examination, electrocardiogram (ECG), blood tests, lung function testing, echocardiogram and CMR. Part of the study will involve a participant questionnaire in which the participants will rate their CMR experience. The results will potentially change the way CMR is undertaken. A sub-set of the participants will also be invited back to do a one off focus group discussing the CMR experience further.

Przegląd badań

Status

Zakończony

Szczegółowy opis

Background and Importance:

Chronic respiratory diseases, which include asthma, COPD and pulmonary hypertension (PH), were responsible for 4.2 million deaths globally in 2008. COPD and asthma affect more than 500 million people worldwide and present an enormous health and economic burden.

Exacerbations of airway disease contribute to disease progression and represent a substantial proportion of acute hospital admissions. Early identification of patients at risk of such events is therefore important. There is unclear distinction between the two airway diseases, particularly in their severe form with evidence of heterogeneity. Right ventricular dysfunction(RVD) and PH secondary to lung disease and/or hypoxia are now recognised as important elements of chronic airway disease pathogenesis and play an important role in the development of frequent comorbidities. There are now data suggesting that pulmonary artery dilatation in COPD patients is associated with increased risk of exacerbations. This indicates that cardiovascular factors in addition to airway inflammation may be associated with exacerbations in airway diseases. Development of RVD and PH in COPD patients are also associated with poor exercise tolerance.RVD can be seen before the development of PH and cor pulmonale in COPD. This underpins the importance of early diagnosis as this may improve overall survival and quality of life.

Clinical diagnosis of PH in chronic airway diseases is often difficult, particularly in the mild form due to similarity in clinical presentation. Other methods for diagnosis of RVD and PH are echocardiography and right heart catheterisation(RHC). The echocardiographic measurements have been shown to lack sensitivity and specificity on patients with COPD and the RHC is an invasive test, with risk of complications. Cardiac magnetic resonance (CMR) imaging provides an excellent alternative for diagnosis of RVD and PH. CMR is a non-invasive test, free from ionizing radiation and the CMR morphometric indices have dramatically lower inter-observer and intra-observer variability and test-retest reproducibility compared to echocardiography. There is a paucity of information on the value of CMR in Group 3 PH. It is also unclear whether PH plays a role in severe asthma patients who have airway inflammation and airflow limitation comparable to COPD patients.

Study Participants:

The investigators plan to recruit a total of 86 participants for this study. Adult asthma and COPD subjects with airflow limitation (FEV1% predicted < 80%) will be recruited for this study. Healthy participants with no past history of cardiovascular or respiratory disease will also be recruited. The investigators plan to recruit 33 participants (n=13 with FEV1% predicted < 50%, n=20 with FEV1% predicted ≥ 50% and < 80%) in each group with airway disease (COPD and asthma) and 20 healthy participants.

Study Assessments:

Participants will undergo the following assessments on the day of their visit:

  1. Clinical History Clinical history will be recorded as done routinely in clinics, which will include date of birth, gender, disease duration, age of onset, other medical conditions, smoking history, occupational history, severe exacerbations in last one year (requiring use of steroid tablets or emergency hospital visit) and treatment.
  2. Health status and disease control questionnaires (Only for Airway Disease Participants) Participants will be asked to complete routine health status and disease control questionnaires.
  3. Focused physical examination Participant's height and weight will be measured. Pulse oximetry will also be performed. Pulse oximetry is a non-invasive method to measure the oxygen level in the blood by placing a sensor device on a person's body, usually fingertip or earlobe.
  4. Electrocardiogram (ECG) An ECG will be performed on all participants.
  5. Blood test Blood will be obtained for the following: (1) assessment of a protein secreted by the heart chambers in response to excessive stretching of the heart muscles, (2) full blood count [FBC] (3) urea and electrolytes [U&E] and (4) storage of plasma extracted from the blood for biomarker (characteristic biological properties or molecules detected in blood that indicate normal or diseased processes in the body) analysis at a future date to complement similar ethically approved research at University of Leicester / University Hospitals of Leicester or other United Kingdom or international academic partners. The plasma will be stored anonymously at -80°C indefinitely at the NIHR Leicester Respiratory Biomedical Research Unit.
  6. Spirometry Lung function of all the participants will be assessed using spirometry (breathing test).
  7. Echocardiogram A focussed test will be performed to measure the pressure with the pulmonary artery
  8. Cardiac magnetic resonance (CMR) imaging

    After identification of the position of the heart using localisers the following sequences will be obtained:

    (i) Cine Imaging: Biventricular volume, function and mass. Interventricular septum and left ventricle eccentricity index will be calculated. Pulmonary artery(PA) stiffness and pulsatility will be assessed by measuring the relative area change of the pulmonary trunk during the cardiac cycle.

    (ii) Phase-contrast magnetic resonance imaging(MRI) Cardiac output and flow profile will be determined. (iii) Magnetic Resonance Angiography(MRA) Contrast-enhanced MRA will be acquired to assess the pulmonary vascular tree to accurately quantify dimensions and assess angiogram pattern of the pulmonary vascular tree.

    (iv) Late Gadolinium Enhancement(LGE) T1-weighted inversion recovery gradient echo images will be acquired approximately 15-20 minutes after intravenous injection of gadolinium based contrast agent. Degree of LGE at the insertion points of the interventricular septum will be assessed.

    (v) Myocardial T1 mapping T1-mapping sequence based on Modified Look-Locker Inversion-recovery(MOLLI) technique will be used for assessment of myocardial fibrosis.

  9. CMR survey A questionnaire will be given to the participants after the CMR scan to find out about their experience during the examination.

Typ studiów

Obserwacyjny

Zapisy (Rzeczywisty)

86

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Leicestershire
      • Leicester, Leicestershire, Zjednoczone Królestwo, LE3 9QP
        • Glenfield Hospital

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat i starsze (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Tak

Płeć kwalifikująca się do nauki

Wszystko

Metoda próbkowania

Próbka bez prawdopodobieństwa

Badana populacja

The investigators plan to recruit a total of 86 participants for this study. Adult asthma and chronicobstructive airway disease (COPD) patients with airflow limitation (FEV1% predicted < 80%) will be recruited for this study. Healthy participants with no past history of cardiovascular or respiratory disease will also be recruited. The investigators plan to recruit 33 participants (n=13 with FEV1% predicted < 50%, n=20 with FEV1% predicted ≥ 50% and < 80%) in each group with airway disease (COPD and asthma) and 20 healthy participants.

Opis

Inclusion Criteria:

Airway Disease (Asthma and COPD)

  1. Participant is willing and able to give informed consent for participation in the study.
  2. Male or Female, aged 18 years or above.
  3. Participants diagnosed with Asthma or COPD with airflow limitation (FEV1% predicted < 80%) with no exacerbations for at least 4 weeks prior to study entry.
  4. Participant has no clinical contraindication for CMR scan.
  5. Able (in the Investigators opinion) and willing to comply with all study requirements.
  6. Willing to allow his or her General Practitioner and consultant, if appropriate, to be notified of participation in the study.

Healthy Volunteers

  1. Participant is willing and able to give informed consent for participation in the study.
  2. Male or Female, aged 18 years or above.
  3. Healthy participant in good health with no past history of cardiovascular or respiratory disease.
  4. Participant has no clinical contraindication for CMR scan.
  5. Able (in the Investigators opinion) and willing to comply with all study requirements.
  6. Willing to allow his or her General Practitioner and consultant, if appropriate, to be notified of participation in the study.

Exclusion Criteria:

Airway Disease (Asthma and COPD)

The participant may not enter the study if ANY of the following apply:

  1. Female participants who are pregnant, lactating or planning pregnancy during the course of the study.
  2. Severe renal impairment eGFR < 30 ml/min.
  3. Contraindication for undergoing CMR scan including permanent pacemaker and surgical procedure within last 6 weeks.
  4. Unable to understand / read English
  5. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study.

Healthy Volunteers

The participant may not enter the study if ANY of the following apply:

  1. Female participants who are pregnant, lactating or planning pregnancy during the course of the study.
  2. Severe renal impairment eGFR < 30 ml/min.
  3. Contraindication for undergoing CMR scan including permanent pacemaker and surgical procedure within last 6 weeks.
  4. Unable to understand / read English
  5. Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

Kohorty i interwencje

Grupa / Kohorta
Adult asthma

Adult asthma subjects with airflow limitation (FEV1% predicted < 80%) will be recruited for this study.

Participants will undergo following study assessments:

  1. Clinical History
  2. Health status and disease control questionnaires
  3. Focused physical examination
  4. Electrocardiogram (ECG)
  5. Blood test
  6. Spirometry
  7. Echocardiogram
  8. Cardiac magnetic resonance (CMR) imaging
  9. CMR survey
Adult COPD

Adult COPD subjects with airflow limitation (FEV1% predicted < 80%) will be recruited for this study.

Participants will undergo following study assessments:

  1. Clinical History
  2. Health status and disease control questionnaires
  3. Focused physical examination
  4. Electrocardiogram (ECG)
  5. Blood test
  6. Spirometry
  7. Echocardiogram
  8. Cardiac magnetic resonance (CMR) imaging
  9. CMR survey
Healthy participants

Healthy participants with no past history of cardiovascular or respiratory disease.

Participants will undergo following study assessments:

  1. Clinical History
  2. Focused physical examination
  3. Electrocardiogram (ECG)
  4. Blood test
  5. Spirometry
  6. Echocardiogram
  7. Cardiac magnetic resonance (CMR) imaging
  8. CMR survey

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Ramy czasowe
Right ventricle End Diastolic volume assessed by cardiac magnetic resonance
Ramy czasowe: On the day of Cardiac Magnetic Resonance
On the day of Cardiac Magnetic Resonance

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Główny śledczy: Sumit Gupta, PhD, FRCR, University of Leicester / University Hospitals of Leicester NHS Trust

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

2 lipca 2016

Zakończenie podstawowe (Rzeczywisty)

29 listopada 2017

Ukończenie studiów (Rzeczywisty)

29 listopada 2017

Daty rejestracji na studia

Pierwszy przesłany

2 sierpnia 2016

Pierwszy przesłany, który spełnia kryteria kontroli jakości

9 sierpnia 2016

Pierwszy wysłany (Oszacować)

12 sierpnia 2016

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

30 stycznia 2020

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

29 stycznia 2020

Ostatnia weryfikacja

1 stycznia 2020

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • 0519
  • 171377 (Inny identyfikator: Integrated Research Application System)

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

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