3.Activated stellate cells express the TRAIL receptor-2/death receptor-5 and undergo TRAIL-mediated apoptosis.
Geum Youn GWAK ; Jung Hwan YOON
The Korean Journal of Hepatology 2003;9(2):145-146
No abstract available.
Adult
;
*Fatty Liver/diagnosis/etiology/pathology
;
Humans
;
Male
4.Hepatocyte apoptosis fragment product cytokeratin-18 M30 level and non-alcoholic steatohepatitis risk diagnosis: an international registry study.
Huai ZHANG ; Rafael S RIOS ; Jerome BOURSIER ; Rodolphe ANTY ; Wah-Kheong CHAN ; Jacob GEORGE ; Yusuf YILMAZ ; Vincent Wai-Sun WONG ; Jiangao FAN ; Jean-François DUFOUR ; George PAPATHEODORIDIS ; Li CHEN ; Jörn M SCHATTENBERG ; Junping SHI ; Liang XU ; Grace Lai-Hung WONG ; Naomi F LANGE ; Margarita PAPATHEODORIDI ; Yuqiang MI ; Yujie ZHOU ; Christopher D BYRNE ; Giovanni TARGHER ; Gong FENG ; Minghua ZHENG
Chinese Medical Journal 2023;136(3):341-350
BACKGROUND:
Liver biopsy for the diagnosis of non-alcoholic steatohepatitis (NASH) is limited by its inherent invasiveness and possible sampling errors. Some studies have shown that cytokeratin-18 (CK-18) concentrations may be useful in diagnosing NASH, but results across studies have been inconsistent. We aimed to identify the utility of CK-18 M30 concentrations as an alternative to liver biopsy for non-invasive identification of NASH.
METHODS:
Individual data were collected from 14 registry centers on patients with biopsy-proven non-alcoholic fatty liver disease (NAFLD), and in all patients, circulating CK-18 M30 levels were measured. Individuals with a NAFLD activity score (NAS) ≥5 with a score of ≥1 for each of steatosis, ballooning, and lobular inflammation were diagnosed as having definite NASH; individuals with a NAS ≤2 and no fibrosis were diagnosed as having non-alcoholic fatty liver (NAFL).
RESULTS:
A total of 2571 participants were screened, and 1008 (153 with NAFL and 855 with NASH) were finally enrolled. Median CK-18 M30 levels were higher in patients with NASH than in those with NAFL (mean difference 177 U/L; standardized mean difference [SMD]: 0.87 [0.69-1.04]). There was an interaction between CK-18 M30 levels and serum alanine aminotransferase, body mass index (BMI), and hypertension ( P < 0.001, P = 0.026 and P = 0.049, respectively). CK-18 M30 levels were positively associated with histological NAS in most centers. The area under the receiver operating characteristics (AUROC) for NASH was 0.750 (95% confidence intervals: 0.714-0.787), and CK-18 M30 at Youden's index maximum was 275.7 U/L. Both sensitivity (55% [52%-59%]) and positive predictive value (59%) were not ideal.
CONCLUSION
This large multicenter registry study shows that CK-18 M30 measurement in isolation is of limited value for non-invasively diagnosing NASH.
Humans
;
Non-alcoholic Fatty Liver Disease/diagnosis*
;
Keratin-18
;
Biomarkers
;
Biopsy
;
Hepatocytes/pathology*
;
Apoptosis
;
Liver/pathology*
5.Pathology of nonalcoholic steatohepatitis.
The Korean Journal of Hepatology 2009;15(2):122-130
Nonalcoholic steatohepatitis (NASH), one of the NAFLDs (nonalcoholic fatty liver diseases), is regarded as a hepatic manifestation of metabolic syndrome. NASH can progress to cirrhosis, and possibly to hepatic malignancy. Currently, liver biopsy is the only reliable method of assessing the presence or absence of NASH and the stage of fibrosis. The finding of steatosis with evidence of hepatocyte injury such as inflammation, ballooning, degeneration, and/or fibrosis, is generally essential for making a diagnosis of NASH. However, its diagnostic criteria have not yet been established. The pathologic findings of NASH and related diseases, and the grading system currently in use are reviewed herein.
Biopsy, Fine-Needle
;
Fatty Liver/diagnosis/*pathology
;
Fibrosis/pathology
;
Humans
;
Severity of Illness Index
6.Pathological and clinical analysis of nonalcoholic steatohepatitis.
Hong-ying PAN ; Rong-xia YE ; Jun-ping SHI ; Xiao-feng GUO
Chinese Journal of Hepatology 2003;11(6):384-384
Adolescent
;
Adult
;
Child
;
Diagnosis, Differential
;
Fatty Liver
;
diagnosis
;
pathology
;
Female
;
Hepatitis
;
diagnosis
;
pathology
;
Hepatitis, Alcoholic
;
diagnosis
;
Humans
;
Male
;
Middle Aged
7.Nonalcoholic fatty liver disease in the elderly.
Chinese Journal of Hepatology 2016;24(2):92-95
Along with the aging process, the spectrum of liver disease changes greatly. Nonalcoholic fatty liver disease (NAFLD) in elderly people lead to low liver function and is also the major cause of extrahepatic diseases, such as cardiovascular disease and malignant tumor. This review provides an overview of the morphological structure and function of the liver in aged people, and discusses the characteristics of weakness, malnutrition and limited movement in the elderly, as well as the current status of multiple diseases and multiple drug use. Finally, this article puts forward some appropriate regimens for the diagnosis and treatment of NAFLD in elderly people to provide a reference for clinical practice.
Aged
;
Cardiovascular Diseases
;
Humans
;
Liver
;
pathology
;
Malnutrition
;
Neoplasms
;
Non-alcoholic Fatty Liver Disease
;
diagnosis
;
pathology
;
therapy
;
Risk Factors
8.Steatocholecystitis.
Kang Nyeong LEE ; Ho Soon CHOI
The Korean Journal of Gastroenterology 2010;55(6):347-349
No abstract available.
Aged
;
Cholecystitis/*diagnosis/radiography/ultrasonography
;
Endosonography
;
Fatty Liver/pathology
;
Female
;
Humans
;
Recurrence
;
Tomography, X-Ray Computed
9.Nonalcoholic steatohepatitis: a clinicopathological analysis of liver biopsy in 32 cases.
Jia-rong MENG ; Rui-dan ZHENG ; Ming-feng ZHANG ; Yi-he GUO ; Ming-zhu LIN ; Tai-jian DAI
Journal of Southern Medical University 2006;26(3):339-341
OBJECTIVETo investigate the clinicopathological features of nonalcoholic steatohepatitis (NASH) and elucidate its diagnosis and differential diagnosis.
METHODSLiver biopsy tissues and clinical data of 32 patients with NASH were collected and the clinicopathological findings by HE and Masson staining were evaluated for NASH grading.
RESULTSBallooning degeneration of the liver cells and fibrosis around hepatic sinusoid was scarce in mild NASH cases and increased in moderate to severe cases. Steatotic and inflammatory cells in the liver lobes decrease in liver cirrhosis related to seatohepatitis.
CONCLUSIONBallooning degeneration of the liver cells and fibrosis around the hepatic sinusoid have important value in differential diagnosis of mild from moderate to severe NASH, and correct histological grading benefits clinical intervention and prognostic evaluation of NASH.
Adult ; Biopsy, Needle ; Diagnosis, Differential ; Fatty Liver ; diagnosis ; pathology ; Female ; Humans ; Image Interpretation, Computer-Assisted ; Liver ; pathology ; Male ; Middle Aged ; Prognosis
10.Non-alcoholic fatty liver diseases: update on the challenge of diagnosis and treatment.
Hyunwoo OH ; Dae Won JUN ; Waqar K SAEED ; Mindie H NGUYEN
Clinical and Molecular Hepatology 2016;22(3):327-335
The prevalence of non-alcoholic fatty liver disease (NAFLD) is estimated to be 25-30% of the population, and is the most common cause of elevated liver enzymes in Korea. NAFLD is a "hot potato" for pharmaceutical companies. Many clinical trials are underway to develop a first-in-class drug to treat NAFLD. However, there are several challenging issues regarding the diagnosis of NAFLD. Currently, liver biopsy is the gold standard method for the diagnosis of NAFLD and steatohepatitis. Ideally, globally recognized standards for histological diagnosis and methods to optimize observer agreement on biopsy interpretation should be developed. Liver biopsy is the best method rather than a perfect one. Recently, multi-parametric magnetic resonance imagery can estimate the amount of intrahepatic fat successfully and is widely used in clinical trials. But no diagnostic method can discriminate between steatohepatitis and simple steatosis. The other unresolved issue in regard to NAFLD is the absence of satisfactory treatment options. Vitamin E and obeticholic acid have shown protective effects in randomized controlled trials, but this drug has not been approved for use in Korea. This study will provide a description of diagnostic methods and treatments that are currently recommended for NAFLD.
Biomarkers/analysis
;
Chenodeoxycholic Acid/analogs & derivatives/therapeutic use
;
Clinical Trials as Topic
;
Fatty Liver/diagnosis
;
Fibrosis
;
Humans
;
Liver/diagnostic imaging/pathology
;
Magnetic Resonance Imaging
;
Non-alcoholic Fatty Liver Disease/*diagnosis/drug therapy
;
Tomography, X-Ray Computed
;
Ultrasonography
;
Vitamin E/therapeutic use