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Circulatory shocks (CS) are life-threatening, acute organ dysfunction. Advances in critical care medicine have decreased early hospital mortality, increasing the number of surviving patients. Regrettably, these survivors are at increased risk of new infections but also of cardiovascular disease.
The investigators hypothesize that CS with multi-organ dysfunction is associated with premature senescence of endothelial cells and immune cells and promotes endothelial thrombogenicity and immunosenescence leading to cardiovascular disease and secondary infections.
The aim of this work is therefore to evaluate the contribution of endothelial and leucocytes senescence to the occurrence of secondary events (infectious and cardiovascular) in patients with a CS. It will provide a better understanding of the pathogenesis of cardiovascular and immune diseases following a CS, likely to guide new management strategies to prevent their occurrence.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with circulatory shock | 500 patients with circulatory shock hospitalize in ICU will be prospectively included to assess the effect of this pathology on the senescence phenotype |
| |
| Healthy volunteers | 20 healthy volunteers will be included to assess the effect of no pathology on the senescence phenotype. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Biological samples will be done to evaluate the endothelial and leukocyte senescence. | Biological | Noninvasive, reproducible, and sensitive methods to measure cardiac function, endothelial function, and arterial stiffness will be assess. |
| Measure | Description | Time Frame |
|---|---|---|
| The main criterion will be the acquisition of a senescent phenotype concerning leukocytes and endothelial cells. | Biological samples will be done to evaluate the endothelial and leukocyte senescence. | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of cardiovascular events and secondary infection in hospitalized patients in intensive care unit for circulatory shock states | 5 years |
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Inclusion criteria:
Exclusion criteria:
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All patients admitted in the intensive care unit of the "Nouvel Hôpital Civil de Strasbourg" for a circulatory shock will be included.
Healthy volunteer will be included in our Clinical Investigation Center of the "Hôpitaux Universitaires de Strasbourg"
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Morgane CLERC | Contact | 03 88 11 68 55 | +33 | morgane.clerc@chru-strasbourg.fr |
| Madoé JULIANS | Contact | 03 88 11 61 86 | +33 | madoe.julians@chru-strasbourg.fr |
| Name | Affiliation | Role |
|---|---|---|
| Ferhat MEZIANI | Hôpitaux Universitaires de Strasbourg | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hôpitaux Universitaires de Strasbourg - Service de Réanimation médicale du NHC | Recruiting | Strasbourg | 67091 | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 38461810 | Derived | Chomel L, Vogt M, Demiselle J, Le Borgne P, Tschirhart M, Morandeau V, Merdji H, Miguet L, Helms J, Meziani F, Mauvieux L. TLRs1-10 Protein Expression in Circulating Human White Blood Cells during Bacterial and COVID-19 Infections. J Innate Immun. 2024;16(1):216-225. doi: 10.1159/000536593. Epub 2024 Mar 8. |
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| ID | Term |
|---|---|
| D012769 | Shock |
| D002318 | Cardiovascular Diseases |
| D007239 | Infections |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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Only whole blood will be collected