Hepatocyte microvesicle levels improve prediction of mortality in patients with cirrhosis. Issue 4 (21st May 2018)
- Record Type:
- Journal Article
- Title:
- Hepatocyte microvesicle levels improve prediction of mortality in patients with cirrhosis. Issue 4 (21st May 2018)
- Main Title:
- Hepatocyte microvesicle levels improve prediction of mortality in patients with cirrhosis
- Authors:
- Payancé, Audrey
Silva‐Junior, Gilberto
Bissonnette, Julien
Tanguy, Marion
Pasquet, Blandine
Levi, Cristina
Roux, Olivier
Nekachtali, Ouardia
Baiges, Anna
Hernández‐Gea, Virginia
Laouénan, Cédric
Lebrec, Didier
Albuquerque, Miguel
Paradis, Valérie
Moreau, Richard
Valla, Dominique
Durand, François
Boulanger, Chantal M.
Garcia‐Pagan, Juan‐Carlos
Rautou, Pierre‐Emmanuel - Abstract:
- Abstract : Microvesicles (MVs) are extracellular vesicles released by cells following activation or apoptosis. Some MV subpopulations augment with cirrhosis severity and contribute to portal hypertension. This study aimed at determining if plasma MV levels can estimate the presence of hepatic venous pressure gradient (HVPG) ≥10 mm Hg and predict mortality in patients with advanced chronic liver disease. All patients with severe fibrosis or cirrhosis undergoing liver catheterization between 2013 and 2015 at two centers were prospectively included. We measured circulating levels of annexin V +, platelet, leukocyte, endothelial, and hepatocyte MVs. The test cohort included 139 patients. Hepatocyte MV levels were 4.0‐fold and 2.2‐fold higher in patients with Child‐Pugh C than in those with Child‐Pugh A or B liver disease, respectively. Levels of other MV subpopulations were not influenced by liver disease severity. Hepatocyte MV levels correlated with HVPG but could not identify patients with HVPG ≥10 mm Hg. Hepatocyte MV level >65 U/L predicted 6‐month mortality independently of Child‐Pugh score and of Model for End‐Stage Liver Disease (MELD). Patients with hepatocyte MV levels >65 U/L and MELD >15 had a higher 6‐month mortality than other patients (23% versus 3%; P = 0.001). These findings were confirmed in a validation cohort including 103 patients. Conclusion : Circulating MV levels cannot identify patients with HVPG ≥10 mm Hg; by contrast, hepatocyte MV levels stronglyAbstract : Microvesicles (MVs) are extracellular vesicles released by cells following activation or apoptosis. Some MV subpopulations augment with cirrhosis severity and contribute to portal hypertension. This study aimed at determining if plasma MV levels can estimate the presence of hepatic venous pressure gradient (HVPG) ≥10 mm Hg and predict mortality in patients with advanced chronic liver disease. All patients with severe fibrosis or cirrhosis undergoing liver catheterization between 2013 and 2015 at two centers were prospectively included. We measured circulating levels of annexin V +, platelet, leukocyte, endothelial, and hepatocyte MVs. The test cohort included 139 patients. Hepatocyte MV levels were 4.0‐fold and 2.2‐fold higher in patients with Child‐Pugh C than in those with Child‐Pugh A or B liver disease, respectively. Levels of other MV subpopulations were not influenced by liver disease severity. Hepatocyte MV levels correlated with HVPG but could not identify patients with HVPG ≥10 mm Hg. Hepatocyte MV level >65 U/L predicted 6‐month mortality independently of Child‐Pugh score and of Model for End‐Stage Liver Disease (MELD). Patients with hepatocyte MV levels >65 U/L and MELD >15 had a higher 6‐month mortality than other patients (23% versus 3%; P = 0.001). These findings were confirmed in a validation cohort including 103 patients. Conclusion : Circulating MV levels cannot identify patients with HVPG ≥10 mm Hg; by contrast, hepatocyte MV levels strongly improve prediction of 6‐month mortality in patients with advanced chronic liver disease; therapies associated with decreased levels of circulating hepatocyte MV might be attractive strategies in patients with severe cirrhosis. (Hepatology 2018). … (more)
- Is Part Of:
- Hepatology. Volume 68:Issue 4(2018)
- Journal:
- Hepatology
- Issue:
- Volume 68:Issue 4(2018)
- Issue Display:
- Volume 68, Issue 4 (2018)
- Year:
- 2018
- Volume:
- 68
- Issue:
- 4
- Issue Sort Value:
- 2018-0068-0004-0000
- Page Start:
- 1508
- Page End:
- 1518
- Publication Date:
- 2018-05-21
- Subjects:
- Heart -- Diseases -- Nursing -- Periodicals
Lungs -- Diseases -- Nursing -- Periodicals
Intensive care nursing -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1527-3350 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/hep.29903 ↗
- Languages:
- English
- ISSNs:
- 0270-9139
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.836000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11939.xml