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RECRUITINGINTERVENTIONAL

Long-term Alterations of Host-microbiome Interactions and Cardiovascular and Respiratory Diseases Progression After Pneumonia

Long-term Alterations of Host-microbiome Interactions and Cardiovascular and Respiratory Diseases Progression After Pneumonia - the HOMI-LUNG Project - Hospital-Acquired-Pneumonia

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The HOMI-LUNG - HAP study is part of the HOMI-LUNG project, funded by the Horizon Europe program. The "HOMI-LUNG" project is an international, interdisciplinary project that aims to better understand the causal links between respiratory tract infections (i.e. pneumonia) and the progression of cardiovascular disease. More specifically, the project aims to quantify the burden of cardiovascular disease after pneumonia and assess patients\' acceptability of long-term health alterations, as well as to define pneumonia endotypes with distinct pathobiological mechanisms associated with exacerbation of cardiovascular disease.

Who May Be Eligible (Plain English)

Who May Qualify: Group A (patients with acute cardiac disease) - Male or female - Age ≥ 40years old - Hospitalized for acute coronary syndrome for less than 7 days. - willing to sign a consent form from the patient - Person insured under a health insurance scheme Group B (patients with chronic cardiovascular disease) - Male or female, - Age ≥ 40 years old - Undergoing coronary artery by-pass surgery - Hospitalized in intensive care unit for \> 12 hours - willing to sign a consent form from the patient - Person insured under a health insurance scheme Group C (patients at risk of CVRD without chronic cardiovascular disease) - Male or female, - Age ≥ 40 years old - Familial high levels of cholesterol or triglycerides - With no personal history of CVRD, with a recent negative cardiac exercise test (last test inferior to 12 months) - Follow-up for lipid abnormalities at high risk of CVRD events - willing to sign a consent form from the patient - Person insured under a health insurance scheme Group D (patients with HAP) - Male or female - Age ≥ 40years old - With one or more risk factors for CVD among: smoking, abnormal lipidic levels, high blood pressure, obesity, diabetes mellitus, chronic kidney disease - Cured from mechanically ventilated HAP during the current hospitalization - willing to sign a consent form from the patient or relatives - Person insured under a health insurance scheme Who Should NOT Join This Trial: - o Groups A, B, C and D - Age \>80 years old - Immunosuppression pre-existing to the index hospitalisation, defined as lymphopenia \< 500 elements/mm3, haematologic cancer, aplasia, chemotherapy/radiotherapy for cancer within 3 months prior to the inclusion, or anti-graft rejection drug. - Pregnant women, breastfeeding women. - Adults under guardianship or trusteeship. - Low probability of survival at day 28. o Groups A, B, C - Community-acquired pneumonia or Hospital-acquired pneumonia within the last year. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: Group A (patients with acute cardiac disease) * Male or female * Age ≥ 40years old * Hospitalized for acute coronary syndrome for less than 7 days. * Informed consent from the patient * Person insured under a health insurance scheme Group B (patients with chronic cardiovascular disease) * Male or female, * Age ≥ 40 years old * Undergoing coronary artery by-pass surgery * Hospitalized in intensive care unit for \> 12 hours * Informed consent from the patient * Person insured under a health insurance scheme Group C (patients at risk of CVRD without chronic cardiovascular disease) * Male or female, * Age ≥ 40 years old * Familial high levels of cholesterol or triglycerides * With no personal history of CVRD, with a recent negative cardiac exercise test (last test inferior to 12 months) * Follow-up for lipid abnormalities at high risk of CVRD events * Informed consent from the patient * Person insured under a health insurance scheme Group D (patients with HAP) * Male or female * Age ≥ 40years old * With one or more risk factors for CVD among: smoking, abnormal lipidic levels, high blood pressure, obesity, diabetes mellitus, chronic kidney disease * Cured from mechanically ventilated HAP during the current hospitalization * Informed consent from the patient or relatives * Person insured under a health insurance scheme Exclusion Criteria: * o Groups A, B, C and D * Age \>80 years old * Immunosuppression pre-existing to the index hospitalisation, defined as lymphopenia \< 500 elements/mm3, haematologic cancer, aplasia, chemotherapy/radiotherapy for cancer within 3 months prior to the inclusion, or anti-graft rejection drug. * Pregnant women, breastfeeding women. * Adults under guardianship or trusteeship. * Low probability of survival at day 28. o Groups A, B, C * Community-acquired pneumonia or Hospital-acquired pneumonia within the last year.

Treatments Being Tested

OTHER

Blood samples

Four blood samples will be taken outside standard care for groups A, B, C and D: at inclusion, M6, M18 and M30 (only at inclusion for group C).

OTHER

Oropharyngeal swabs

An oropharyngeal swab will be taken to analyze patients\' upper airway microbiome at inclusion, M6, M18 and M30.

OTHER

Calcium score (CT scan)

A calcium score will be taken at 30 months, to assess individual cardiovascular risk.

OTHER

ECG

Performed at inclusion, M6, M18 and M30

OTHER

Cardiopulmonary exercise test, spirometry, plethysmography, pulmonary absorption of carbon monoxide in a single inspiration, and 6-minute walk test

Cardiopulmonary exercise test, spirometry, plethysmography, pulmonary absorption of carbon monoxide in a single inspiration, and 6-minute walk test: These tests will be performed consecutively for 2 hours at inclusion (6-minute walk test only), at M6 and at M30. These tests will be performed to assess respiratory and cardiac function.

Locations (5)

Angers University Hospital
Angers, France
Nantes University Hospital
Nantes, France
Rennes University Hospital
Rennes, France
Rouen University Hospital
Rouen, France
Toulouse University Hospital
Toulouse, France