A clinical scoring system for predicting nonalcoholic steatohepatitis in morbidly obese patients

Hepatology ◽  
2008 ◽  
Vol 47 (6) ◽  
pp. 1916-1923 ◽  
Author(s):  
Guilherme M. Campos ◽  
Kiran Bambha ◽  
Eric Vittinghoff ◽  
Charlotte Rabl ◽  
Andrew M. Posselt ◽  
...  
2019 ◽  
Vol 2019 ◽  
pp. 1-7 ◽  
Author(s):  
Patrick H. Alizai ◽  
Isabella Lurje ◽  
Andreas Kroh ◽  
Sophia Schmitz ◽  
Tom Luedde ◽  
...  

Background. More than half of the obese patients develop nonalcoholic fatty liver disease (NAFLD), which may further progress to nonalcoholic steatohepatitis (NASH) and cirrhosis. The aim of this study was to assess alterations in liver function in obese patients with a noninvasive liver function test. Methods. In a prospective cohort study 102 morbidly obese patients undergoing bariatric surgery were evaluated for their liver function. Liver function capacity was determined by the LiMAx® test (enzymatic capacity of cytochrome P450 1A2). Liver biopsy specimens were obtained intraoperatively and classified according to the NAFLD Activity Score (NAS). NASH clinical score was additionally calculated from laboratory and clinical parameters. Results. Median liver function capacity was 286 (IQR=141) μg/kg/h. 27% of patients were histologically categorized as definite NASH, 39% as borderline, and 34% as not NASH. A significant correlation was observed between liver function capacity and NAS (r=−0.492; p<0.001). The sensitivity and specificity of the LiMAx® test to distinguish between definite NASH and not NASH were 85.2% and 82.9% (AUROC 0.859), respectively. According to the NASH clinical scoring system, 14% were classified as low risk, 31% as intermediate, 26% as high, and 29% as very high risk. Liver function capacity is also significantly correlated with the NASH clinical scoring system (r=−0.411; p<0.001). Conclusions. Obese patients show a diminished liver function capacity, especially those suffering from type 2 diabetes. The liver function capacity correlates with histological and clinical scoring systems. The LiMAx® test may be a valuable tool for noninvasive screening for NASH in obese patients.


2010 ◽  
Vol 20 (6) ◽  
pp. 685-691 ◽  
Author(s):  
Alex Ulitsky ◽  
Ashwin N. Ananthakrishnan ◽  
Richard Komorowski ◽  
James Wallace ◽  
Sri Naveen Surapaneni ◽  
...  

2008 ◽  
Vol 134 (4) ◽  
pp. A-780
Author(s):  
Kamran Qureshi ◽  
Michelle S. Johnson ◽  
Ronald H. Clements ◽  
Gary A. Abrams ◽  
Aimee L. Landar

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Sophia Marie-Therese Schmitz ◽  
Andreas Kroh ◽  
Tom Florian Ulmer ◽  
Julia Andruszkow ◽  
Tom Luedde ◽  
...  

Abstract Background Non-alcoholic fatty liver disease (NAFLD) is a frequent condition in obese patients and regularly progresses to non-alcoholic steatohepatitis (NASH) and subsequent cirrhosis. Histologic evaluation is the gold standard for grading and staging, but invasive biopsies are associated with obvious risks. The aim of this study was to evaluate different non-invasive tools for screening of NAFLD and fibrosis in obese patients. Methods In a prospective cohort study liver specimens of 141 patients were taken during bariatric surgery. Serological parameters and clinical data were collected and the following scores calculated: NASH clinical scoring system (NCS), aspartate aminotransferase to platelet ratio index (APRI), FIB-4 as well as NAFLD fibrosis score (NFS). Liver function capacity was measured preoperatively by LiMAx test (enzymatic capacity of cytochrome P450 1A2). Intraoperative liver biopsies were classified using NAFLD activity score (NAS) and steatosis, activity and fibrosis (SAF) score. Results APRI was able to differentiate between not NASH and definite NASH with a sensitivity of 74% and specificity of 67% (AUROC 0.76). LiMAx and NCS also showed significant differences between not NASH and definite NASH. No significant differences were found for NFS and Fib-4. APRI had a high sensitivity (83%) and specificity (76%) in distinguishing fibrosis from no fibrosis (AUROC = 0.81). NCS and Fib-4 also revealed high AUROCs (0.85 and 0.67), whereas LiMAx and NFS did not show statistically significant differences between fibrosis stages. Out of the patients with borderline NASH in the histologic NAS score, 48% were classified as NASH by SAF score. Conclusions APRI allows screening of NAFLD as well as fibrosis in obese patients. This score is easy to calculate and affordable, while conveniently only using routine clinical parameters. Using the NAS histologic scoring system bears the risk of underdiagnosing NASH in comparison to SAF score.


2020 ◽  
Vol 9 (4) ◽  
pp. 933 ◽  
Author(s):  
Michael Doulberis ◽  
Simone Srivastava ◽  
Stergios A Polyzos ◽  
Jannis Kountouras ◽  
Apostolis Papaefthymiou ◽  
...  

Nonalcoholic fatty liver disease (NAFLD) emerges as an important global burden and Helicobacter pylori infection (Hp-I) has been suggested as a risk factor of NAFLD, although controversy exists. This retrospective study aimed to investigate a potential impact of active Hp-I on NAFLD severity in morbidly obese patients, subjected to bariatric surgery and gastric biopsy for documentation of Hp-I. Of 64 eligible participants, 15 (23.4%) were diagnosed with active Hp-I, showing higher rates of nonalcoholic steatohepatitis (NASH) than those without Hp-I (86.7% vs. 26.5%, respectively; p < 0.001). Concerning histological lesions, steatosis grade (p = 0.027), ballooning (p < 0.001), lobular inflammation (p = 0.003), and fibrosis stage (p < 0.001) were also more severe in Hp-I positive patients. Likewise, liver function tests, insulin resistance, dyslipidemia, and arterial hypertension were significantly higher in Hp-I positive patients. Hp-I was independently positively associated with NASH (beta = 3.27; p = 0.002), severe NASH (beta = 2.37; p = 0.018), and the presence of fibrosis (beta = 3.86; p = 0.001) in a binary regression model, after adjustment for potential confounders. In conclusion, active Hp-Ι was independently associated with NASH and fibrosis, findings offering potential clinical implication.


Hepatology ◽  
2012 ◽  
Vol 56 (5) ◽  
pp. 1751-1759 ◽  
Author(s):  
Pierre Bedossa ◽  
Christine Poitou ◽  
Nicolas Veyrie ◽  
Jean-Luc Bouillot ◽  
Arnaud Basdevant ◽  
...  

2015 ◽  
Vol 15 (7) ◽  
Author(s):  
Morteza Ghoghaei ◽  
Foad Taghdiri ◽  
Elias Khajeh ◽  
Farid Azmoudeh Ardalan ◽  
Mojtaba Sedaghat ◽  
...  

2014 ◽  
Vol 80 (6) ◽  
pp. 595-599 ◽  
Author(s):  
Jeffrey L. Reha ◽  
Sukhyung Lee ◽  
Luke J. Hofmann

Nonalcoholic steatohepatitis (NASH) is a silent liver disease that can lead to inflammation and subsequent scaring. If left untreated, cirrhosis may ensue. Morbidly obese patients are at an increased risk of NASH. We report the prevalence and predictors of NASH in patients undergoing morbid obesity surgery. A retrospective review was conducted on morbidly obese patients undergoing weight reduction surgery from September 2005 through December 2008. A liver biopsy was performed at the time of surgery. Patients who had a history of hepatitis infection or previous alcohol dependency were excluded. Prevalence of NASH was studied. Predictors of NASH among clinical and biochemical variables were analyzed using multivariate regression analysis. One hundred thirteen patients were analyzed (84% female; mean age, 42.6 ± 11.4 years; mean body mass index, 45.1 ± 5.7 kg/m2). Sixty-one patients had systemic hypertension (54%) and 35 patients had diabetes (31%). The prevalence of NASH in this study population was 35 per cent (40 of 113). An additional 59 patients (52%) had simple steatosis without NASH. Only 14 patients had normal liver histology. On multivariate analysis, only elevated aspartate aminotransferase (AST) (greater than 41 IU/L) was the independent predictor for NASH (odds ratio, 5.85; confidence interval, 1.06 to 32.41). Patient age, body mass index, hypertension, diabetes, hypercholesterolemia, and abnormal alanine aminotransferase did not predict NASH. NASH is a common finding in obese population. Abnormal AST was the only predictive factor for NASH.


2015 ◽  
Vol 149 (2) ◽  
pp. 379-388 ◽  
Author(s):  
Guillaume Lassailly ◽  
Robert Caiazzo ◽  
David Buob ◽  
Marie Pigeyre ◽  
Hélène Verkindt ◽  
...  

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