Non-invasive Biomarkers of Liver Inflammation and Cell Death in Response to Alcohol Detoxification
IntroductionAlcohol-related liver disease (ALD) represents the most common liver disease worldwide, however, the underlying molecular mechanisms are still poorly understood. Namely centrilobular inflammation and programmed cell death are characteristic to ALD and it remains to be elucidated why they...
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doaj-c9ea4844e86a43aa9d4912d7386681102021-07-07T06:03:40ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2021-07-011210.3389/fphys.2021.678118678118Non-invasive Biomarkers of Liver Inflammation and Cell Death in Response to Alcohol DetoxificationManuela G. Neuman0Johannes Mueller1Sebastian Mueller2Sebastian Mueller3In Vitro Drug Safety and Biotechnology, Department of Pharmacology and Toxicology, Temerity Faculty of Medicine, University of Toronto, Toronto, ON, CanadaCenter for Alcohol Research, University of Heidelberg, Heidelberg, GermanyCenter for Alcohol Research, University of Heidelberg, Heidelberg, GermanyDepartment of Internal Medicine, Salem Medical Center, Heidelberg, GermanyIntroductionAlcohol-related liver disease (ALD) represents the most common liver disease worldwide, however, the underlying molecular mechanisms are still poorly understood. Namely centrilobular inflammation and programmed cell death are characteristic to ALD and it remains to be elucidated why they persist despite the absence of alcohol.AimsTo study the effects of alcohol withdrawal in a cohort of heavy drinkers and the role of cirrhosis by using non-invasive biomarkers such as cytokines, apoptotic and angiogenic markers.MethodsCaspase 3-cleaved M30, M65, cytokines (IL-6, IL-8), tumor necrosis factor alpha (TNF-α), transforming growth factor (TGF-β) and vascular endothelial growth factor (VEGF) were measured in 114 heavy drinkers. The role of alcohol detoxification was investigated in 45 patients. The liver histology was available in 23 patients. Fibrosis stage and steatosis were assessed by measuring liver stiffness (LS) and controlled attenuation parameter (CAP) in all patients using transient elastography (FibroScan, Echosens, Paris). Mean observation interval between the measurements was 5.7 ± 1.4 days (mean + –SD).ResultsPatients consumed a mean of 204 ± 148 g/day alcohol with a heavy drinking duration of 15.3 ± 11.0 years. Mean LS was 20.7 ± 24.4 kPa and mean CAP was 303 ± 51 dB/m. Fibrosis distribution was F0–38.1%, F1-2–31%, F3–7.1 and F4–23.9%. Apoptotic markers M30 and M65 were almost five times above normal. In contrast, TNF- α a, IL-8 and VEGF were only slightly elevated. Patients with manifest liver cirrhosis (F4) had significantly higher levels of M30, M65, IL-6 and IL-8. Histology features such as hepatocyte ballooning, Mallory-Denk bodies, inflammation and fibrosis were all significantly associated with elevated LS, and serum levels of TNF-alpha, M30 and M65 but not with CAP and other cytokines. During alcohol detoxification, LS, transaminases, TGF- β, IL-6, IL-8 and VEGF decreased significantly. In contrast, no significant changes were observed for M30, M65 and TNF- α and M30 even increased during detoxification in non-cirrhotic patients. Profibrogenic cytokine TGF-beta and pro-angiogenic cytokine VEGF showed a delayed decrease in patients with manifest cirrhosis.ConclusionPatients with alcohol-related cirrhosis have a pronounced apoptotic activity and a distinct inflammatory response that only partly improves after 1 week of alcohol detoxification. Alcohol withdrawal may represent an important approach to better dissect the underlying mechanisms in the setting of alcohol metabolism.https://www.frontiersin.org/articles/10.3389/fphys.2021.678118/fullcytokinesliver stiffnessalcoholic liver diseaseapoptosisinflammation/hepatitis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Manuela G. Neuman Johannes Mueller Sebastian Mueller Sebastian Mueller |
spellingShingle |
Manuela G. Neuman Johannes Mueller Sebastian Mueller Sebastian Mueller Non-invasive Biomarkers of Liver Inflammation and Cell Death in Response to Alcohol Detoxification Frontiers in Physiology cytokines liver stiffness alcoholic liver disease apoptosis inflammation/hepatitis |
author_facet |
Manuela G. Neuman Johannes Mueller Sebastian Mueller Sebastian Mueller |
author_sort |
Manuela G. Neuman |
title |
Non-invasive Biomarkers of Liver Inflammation and Cell Death in Response to Alcohol Detoxification |
title_short |
Non-invasive Biomarkers of Liver Inflammation and Cell Death in Response to Alcohol Detoxification |
title_full |
Non-invasive Biomarkers of Liver Inflammation and Cell Death in Response to Alcohol Detoxification |
title_fullStr |
Non-invasive Biomarkers of Liver Inflammation and Cell Death in Response to Alcohol Detoxification |
title_full_unstemmed |
Non-invasive Biomarkers of Liver Inflammation and Cell Death in Response to Alcohol Detoxification |
title_sort |
non-invasive biomarkers of liver inflammation and cell death in response to alcohol detoxification |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Physiology |
issn |
1664-042X |
publishDate |
2021-07-01 |
description |
IntroductionAlcohol-related liver disease (ALD) represents the most common liver disease worldwide, however, the underlying molecular mechanisms are still poorly understood. Namely centrilobular inflammation and programmed cell death are characteristic to ALD and it remains to be elucidated why they persist despite the absence of alcohol.AimsTo study the effects of alcohol withdrawal in a cohort of heavy drinkers and the role of cirrhosis by using non-invasive biomarkers such as cytokines, apoptotic and angiogenic markers.MethodsCaspase 3-cleaved M30, M65, cytokines (IL-6, IL-8), tumor necrosis factor alpha (TNF-α), transforming growth factor (TGF-β) and vascular endothelial growth factor (VEGF) were measured in 114 heavy drinkers. The role of alcohol detoxification was investigated in 45 patients. The liver histology was available in 23 patients. Fibrosis stage and steatosis were assessed by measuring liver stiffness (LS) and controlled attenuation parameter (CAP) in all patients using transient elastography (FibroScan, Echosens, Paris). Mean observation interval between the measurements was 5.7 ± 1.4 days (mean + –SD).ResultsPatients consumed a mean of 204 ± 148 g/day alcohol with a heavy drinking duration of 15.3 ± 11.0 years. Mean LS was 20.7 ± 24.4 kPa and mean CAP was 303 ± 51 dB/m. Fibrosis distribution was F0–38.1%, F1-2–31%, F3–7.1 and F4–23.9%. Apoptotic markers M30 and M65 were almost five times above normal. In contrast, TNF- α a, IL-8 and VEGF were only slightly elevated. Patients with manifest liver cirrhosis (F4) had significantly higher levels of M30, M65, IL-6 and IL-8. Histology features such as hepatocyte ballooning, Mallory-Denk bodies, inflammation and fibrosis were all significantly associated with elevated LS, and serum levels of TNF-alpha, M30 and M65 but not with CAP and other cytokines. During alcohol detoxification, LS, transaminases, TGF- β, IL-6, IL-8 and VEGF decreased significantly. In contrast, no significant changes were observed for M30, M65 and TNF- α and M30 even increased during detoxification in non-cirrhotic patients. Profibrogenic cytokine TGF-beta and pro-angiogenic cytokine VEGF showed a delayed decrease in patients with manifest cirrhosis.ConclusionPatients with alcohol-related cirrhosis have a pronounced apoptotic activity and a distinct inflammatory response that only partly improves after 1 week of alcohol detoxification. Alcohol withdrawal may represent an important approach to better dissect the underlying mechanisms in the setting of alcohol metabolism. |
topic |
cytokines liver stiffness alcoholic liver disease apoptosis inflammation/hepatitis |
url |
https://www.frontiersin.org/articles/10.3389/fphys.2021.678118/full |
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