Alcohol withdrawal alleviates adipose tissue inflammation in patients with alcoholic liver disease

作者:Voican Cosmin S; Njike Nakseu Micheline; Boujedidi Hedia; Barri Ova Nadege; Bouchet Delbos Laurence; Agostini Helene; Maitre Sophie; Prevot Sophie; Cassard Doulcier Anne Marie; Naveau Sylvie; Perlemuter Gabriel*
来源:Liver International, 2015, 35(3): 967-978.
DOI:10.1111/liv.12575

摘要

Background & AimsPatients with alcoholic liver disease (ALD) display inflammation of the subcutaneous adipose tissue (SAT) which correlates with liver lesions. We examined macrophage markers and polarization in the SAT of alcoholic patients and adipokine expression according to liver inflammation; we studied the consequences of alcohol withdrawal. Patients and methodsForty-seven patients with ALD were prospectively included. SAT and blood samples were collected at inclusion and after 1week of alcohol withdrawal. Pro-inflammatory cytokines/chemokines, inflammasome components and products, adipokine expression levels, macrophage markers and polarization in liver and SAT samples were assessed by RT-PCR arrays. ResultsmRNA expression level of chemokines (IL8, semaphorin 7A) correlated with hepatic steatosis in both liver and SAT. Liver expression of inflammasome components (IL1, IL18, caspase-1) and SAT IL6 and CCL2 correlated with liver damage. In patients with mild ALD, 1week of alcohol withdrawal was sufficient to decrease expression level of total macrophage markers in the adipose tissue, to orient adipose tissue macrophages (ATM) towards an anti-inflammatory M2 phenotype and to decrease the mRNA expression of cytokines/chemokines (IL18, CCL2, osteopontin, semaphorin 7A). In patients with severe ALD, 1week of abstinence was also associated with an increase in CCL18 expression. ConclusionsIn alcoholic patients, upregulation of chemotactic factors in the liver and SAT is an early event that begins as early as the steatosis stage. The inflammasome pathway is upregulated in the liver of patients with ALD. One week of alcohol withdrawal alleviates macrophage infiltration in SAT and orients ATM towards a M2 anti-inflammatory phenotype; this implicates alcohol in adipose tissue inflammation (ClinicalTrials.gov NCT00388323).

  • 出版日期2015-3