Literature DB >> 35046690

Non-Invasive Risk Stratification in NAFLD/NASH Patients for Screening EGD.

John Romano1, Thaer Abdelfattah2, Paul P Manka3, Michael Fuchs2,4, Wing-Kin Syn1,5,6.   

Abstract

Entities:  

Year:  2022        PMID: 35046690      PMCID: PMC8759994          DOI: 10.2147/CEG.S339850

Source DB:  PubMed          Journal:  Clin Exp Gastroenterol        ISSN: 1178-7023


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Portal hypertension is a major complication of cirrhosis, as it predisposes patients to manifestations of hepatic decompensation, including the development of esophageal variceal bleeding, hepatic encephalopathy, and ascites.1 Esophageal varices are present in approximately 50% of patients with cirrhosis. The mortality during a variceal bleeding event is high, with estimates ranging from 15% to 20%, being largely dependent upon whether patients have received the standard of care with endoscopic band ligation, vasoactive drugs, and antibiotics.2 The hepatic venous pressure gradient (HVPG) is considered the gold standard in ascertaining the presence of portal hypertension (PH). Clinically significant portal hypertension (CSPH), which is associated with the development of the aforementioned manifestations of decompensation, has been defined as an HVPG greater than or equal to 10 mmHg. After a diagnosis of cirrhosis, current guidelines recommend screening for esophageal varices with esophagogastroduodenoscopy (EGD). This procedure is carried out to identify patients who are at risk for variceal hemorrhage and would benefit from starting prophylactic therapy with beta blockade.3,4 This procedure carries risks, which include any type of respiratory or cardiac suppression from anesthesia, infection, bleeding, and perforation. In addition, a significant majority of patients with varices who are indeed at high risk for bleeding do not have any symptoms from the varices themselves, making EGD a non-ideal screening test.5 Previous studies suggest that non-invasive blood-based markers are useful to identify patients with liver damage (fibrosis or cirrhosis) and may identify those who will develop complications such as liver cancer.6 Examples of these markers include the Fibrosis-4 Index (FIB-4), which is a non-invasive estimate of liver scarring in HCV and HBV patients; the NAFLD (Non-Alcoholic Fatty Liver Disease) Fibrosis Score (NFS), which is used to estimate the amount of scarring in the liver based on several laboratory tests; the BARD score, based upon BMI, AST/ALT ratio, and the presence or absence of diabetes; and the AST to Platelet Ratio Index (APRI). We evaluated whether these non-invasive markers and/or any other clinical parameters may be used to identify patients with liver cirrhosis who are likely to have large esophageal varices, and therefore would benefit most from screening EGD. We retrospectively evaluated a cohort of non-alcoholic fatty liver disease (NAFLD)/non-alcoholic steatohepatitis (NASH) patients at two tertiary care Veterans Affairs (VA) Hospitals between January 1st 2017 and February 15th 2021. A total of 1476 patients was initially investigated; however, 1221 patients were excluded owing to stage 1 or 2 fibrosis on fibroscan or liver biopsy. Patients who had advanced liver fibrosis or cirrhosis on the basis of elastography measurements and/or liver biopsies were further evaluated. Endoscopic records for these patients were reviewed for the presence and size of esophageal varices. Variables that were collected included race, sex, BMI, age, liver enzymes (including AST/ALT), platelet count, albumin, uric acid levels, and the presence or absence of comorbidities, including diabetes, to calculate the BARD score, FIB-4, APRI, and NFS. We also evaluated the utility of the BAVENO VI expanded criteria (patients with liver stiffness <20 kPa and platelet count >150,000/µL are at low risk of having varices that require treatment and, therefore, do not require screening EGD) in this cohort.7 Forty-four patients met the inclusion criterion, which is defined as stage 3 or 4 fibrosis or cirrhosis on the basis of elastography and/or liver biopsies. These patients were divided into two groups. Group A: 26 subjects with small esophageal varices or no varices (mean age: 59.3 years; male: 24, female: 2; African American: 2, Asian: 3, White: 19); group B: 18 subjects with large esophageal varices (mean age: 65.4 years; male: 16, female: 2; African American: 1, Asian: 2, White: 15). Patients in group B had significantly higher non-invasive scores than those in group A: FIB-4 (1.87 vs 3.28; p<0.001), APRI (0.39 vs 1.08; p<0.001), NFS (0.58 vs 1.82; p<0.01), and BARD (2 vs 3; p<0.05). FIB-4 provided the overall highest AUROC of 0.82 (specificity: 77%; NPV: 74%) for the presence of large varices. While APRI showed an AUROC of 0.812 (specificity: 100%; NPV: 70%), NFS had an AUROC of 0.777 (specificity: 54%; NPV: 88%), and BARD presented an AUROC of 0.696 (specificity: 65%; NPV: 73%). In addition, BAVENO VI expanded criteria were able to significantly distinguish between groups A and B by chi-squared analysis (p=0.0139) and Fisher's exact test (p=0.0292). We also found significant differences between groups A and B with regard to the presence of splenomegaly (p=0.046) and uric acid levels (p=0.027). Non-invasive tests are increasingly being used to stratify the risks of patients with chronic liver disease. As these tests have excellent negative predictive value, they are generally used to identify those who are unlikely to have significant or advanced liver disease, and therefore do not require invasive evaluation such as a liver biopsy. This study extends their utility and suggests that the FIB-4 and APRI may be able to accurately identify individuals likely to have large esophageal varices and who would therefore benefit most from screening EGD. The extended BAVENO VI guidelines further recommend that patients with liver stiffness <15 kPa and platelet count >150,000/µL can safely avoid endoscopic screening for varices owing to a very low probability of their having large varices that require treatment.7 Petta et al retrospectively investigated a large cohort and showed that 58% of EGDs could be spared using the extended BAVENO VI criteria, while missing only 0.9% of varices that would need treatment.8 Our data build upon this information. Additional parameters that should be investigated to assess for the presence or absence of varices include splenomegaly and uric acid levels, as there was a significant difference between groups A and B for both of these factors. Findings from a 2021 study suggest that there is a relationship between splenomegaly and NAFLD/NASH.9 Spleen stiffness on elastography is also a developing non-invasive indicator for the presence or absence of esophageal varices and should be studied further. Overall, this VA study is clinically significant because it may allow providers to better identify individuals with advanced liver disease who are most at risk for variceal bleed and who need a screening EGD. Conversely, those with low non-invasive scores, FIB-4 <1.45 or APRI <0.5, or who do not meet BAVENO VI criteria, may be able to avoid unnecessary EGDs. Further prospective studies with larger cohorts will be needed to validate these findings.
  9 in total

1.  Revising consensus in portal hypertension: report of the Baveno V consensus workshop on methodology of diagnosis and therapy in portal hypertension.

Authors:  Roberto de Franchis
Journal:  J Hepatol       Date:  2010-06-27       Impact factor: 25.083

Review 2.  Natural history and prognostic indicators of survival in cirrhosis: a systematic review of 118 studies.

Authors:  Gennaro D'Amico; Guadalupe Garcia-Tsao; Luigi Pagliaro
Journal:  J Hepatol       Date:  2005-11-09       Impact factor: 25.083

3.  Expanding consensus in portal hypertension: Report of the Baveno VI Consensus Workshop: Stratifying risk and individualizing care for portal hypertension.

Authors:  Roberto de Franchis
Journal:  J Hepatol       Date:  2015-06-03       Impact factor: 25.083

4.  Portal hypertensive bleeding in cirrhosis: Risk stratification, diagnosis, and management: 2016 practice guidance by the American Association for the study of liver diseases.

Authors:  Guadalupe Garcia-Tsao; Juan G Abraldes; Annalisa Berzigotti; Jaime Bosch
Journal:  Hepatology       Date:  2016-12-01       Impact factor: 17.425

5.  Expanding the Baveno VI criteria for the screening of varices in patients with compensated advanced chronic liver disease.

Authors:  Salvador Augustin; Mònica Pons; James B Maurice; Christophe Bureau; Horia Stefanescu; Michel Ney; Hélène Blasco; Bogdan Procopet; Emmanuel Tsochatzis; Rachel H Westbrook; Jaime Bosch; Annalisa Berzigotti; Juan G Abraldes; Joan Genescà
Journal:  Hepatology       Date:  2017-10-30       Impact factor: 17.425

6.  Non-invasive prediction of esophageal varices by stiffness and platelet in non-alcoholic fatty liver disease cirrhosis.

Authors:  Salvatore Petta; Giada Sebastiani; Elisabetta Bugianesi; Mauro Viganò; Vincent Wai-Sun Wong; Annalisa Berzigotti; Anna Ludovica Fracanzani; Quentin M Anstee; Fabio Marra; Marco Barbara; Vincenza Calvaruso; Calogero Cammà; Vito Di Marco; Antonio Craxì; Victor de Ledinghen
Journal:  J Hepatol       Date:  2018-05-24       Impact factor: 25.083

7.  Effectiveness of combined pharmacologic and ligation therapy in high-risk patients with acute esophageal variceal bleeding.

Authors:  Salvador Augustin; José Altamirano; Antonio González; Joan Dot; Monder Abu-Suboh; Josep Ramón Armengol; Fernando Azpiroz; Rafael Esteban; Jaime Guardia; Joan Genescà
Journal:  Am J Gastroenterol       Date:  2011-05-31       Impact factor: 10.864

8.  Role of Spleen Stiffness Measurement by 2D-Shear Wave Elastography in Ruling Out the Presence of High-Risk Varices in Cirrhotic Patients.

Authors:  Dimitrios S Karagiannakis; Theodoros Voulgaris; Evgenia Koureta; Elissavet Chloupi; George V Papatheodoridis; John Vlachogiannakos
Journal:  Dig Dis Sci       Date:  2019-04-15       Impact factor: 3.199

Review 9.  Liver-spleen axis in nonalcoholic fatty liver disease.

Authors:  Giovanni Tarantino; Vincenzo Citro; Clara Balsano
Journal:  Expert Rev Gastroenterol Hepatol       Date:  2021-04-20       Impact factor: 3.869

  9 in total

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