scholarly journals Cryptogenic cirrhosis and posttransplantation nonalcoholic fatty liver disease

2001 ◽  
Vol 7 (9) ◽  
pp. 797-801 ◽  
Author(s):  
J Ong
2001 ◽  
Vol 7 (4) ◽  
pp. 363-373 ◽  
Author(s):  
Melissa J. Contos ◽  
Wendy Cales ◽  
Richard K. Sterling ◽  
Velimir A. Luketic ◽  
Mitchell L. Shiffman ◽  
...  

Author(s):  
Jinping Lai ◽  
Hanlin L. Wang ◽  
Xuchen Zhang ◽  
Huamin Wang ◽  
Xiuli Liu

Context.— Nonalcoholic fatty liver disease (NAFLD) encompasses steatosis and steatohepatitis. The cause may be multifactorial, and diagnosis requires correlation with clinical information and laboratory results. Objective.— To provide an overview of the status of histology diagnosis of steatosis, steatohepatitis, and associated conditions. Data Sources.— A literature search was performed using the PubMed search engine. The terms ‘‘steatosis,'' ‘‘steatohepatitis,'' ‘‘nonalcoholic fatty liver disease (NAFLD),'' ‘‘nonalcoholic steatohepatitis (NASH),'' “alcoholic steatohepatitis (ASH),” ‘‘type 2 diabetes (T2DM),'' “cryptogenic cirrhosis,” “drug-induced liver injury (DILI),” “immune checkpoint inhibitor therapy,” and “COVID-19 and liver” were used. Conclusions.— Nonalcoholic fatty liver disease has become the most common chronic liver disease in the United States. NASH is the progressive form of nonalcoholic fatty liver disease. The hallmarks of steatohepatitis are steatosis, ballooned hepatocytes, and lobular inflammation. NASH and alcoholic steatohepatitis share similar histologic features, but some subtle differences may help their distinction. NASH is commonly seen in patients with metabolic dysfunction but can also be caused by other etiologies. Examples are medications including newly developed immune checkpoint inhibitors and viral infections such as coronavirus disease 2019 (COVID-19). NASH is also a common cause of cryptogenic cirrhosis but can be reversed. The results from recent clinical trials for NASH treatment are promising in reducing the severity of steatosis, ballooning, and fibrosis.


2009 ◽  
Vol 16 (4) ◽  
pp. 431-439 ◽  
Author(s):  
Kanthi Yalamanchili ◽  
Sherif Saadeh ◽  
Göran B. Klintmalm ◽  
Linda W. Jennings ◽  
Gary L. Davis

2016 ◽  
Vol 150 (2) ◽  
pp. 93-99 ◽  
Author(s):  
Ido Laish ◽  
Batya Mannasse-Green ◽  
Ruth Hadary ◽  
Tal Biron-Shental ◽  
Fred M. Konikoff ◽  
...  

Nonalcoholic fatty liver disease (NAFLD) and cryptogenic cirrhosis (CC) are considered preneoplastic conditions that might progress to hepatocellular carcinoma. We evaluated parameters of telomere dysfunction in these patient groups to study the correlation between telomere length and the progression of NAFLD. We analyzed peripheral lymphocytes from 22 patients with NAFLD, 20 patients with CC, and 20 healthy, age-matched controls. Telomere length was analyzed using quantitative fluorescence in situ hybridization, and cellular senescence was evaluated by the percentage of cells with senescence-associated heterochromatin foci. The expression of telomerase reverse transcriptase (hTERT) mRNA was measured using polymerase chain reaction, and telomere capture (TC) was assessed with 2 Cytocell probes, 15qter and 13qter. Shorter telomere length and increased cellular senescence was demonstrated in patients with NAFLD, compared to the CC patients and healthy controls. While hTERT mRNA was significantly decreased, TC was increased in CC patients, compared to the NAFLD group and healthy individuals. Thus, there is a correlation between hTERT mRNA expression and telomere length in patients with NAFLD, which might be related to associated metabolic disorders and the risk of malignant transformation. Patients with CC, on the contrary, elongate their telomeres through the TC mechanism.


Sign in / Sign up

Export Citation Format

Share Document