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Prevalence and indicators of portal hypertension in patients with nonalcoholic fatty liver disease.

Publication ,  Journal Article
Mendes, FD; Suzuki, A; Sanderson, SO; Lindor, KD; Angulo, P
Published in: Clin Gastroenterol Hepatol
September 2012

BACKGROUND & AIMS: Little is known about the prevalence and severity of portal hypertension in patients with nonalcoholic fatty liver disease (NAFLD). We investigated the prevalence and noninvasive predictors of portal hypertension in patients with NAFLD. METHODS: Signs of portal hypertension, including esophageal varices, splenomegaly, portosystemic encephalopathy, and ascites, were investigated in 354 patients with NAFLD. RESULTS: One hundred patients had portal hypertension at the time of NAFLD diagnosis (28.2%), 88 of these patients had septal fibrosis or cirrhosis (88%). Fibrosis stage correlated with presence (r = 0.41, P < .0001) and number of findings (r = 0.48, P = .006) of portal hypertension. Of the 204 patients with no or mild fibrosis (stages, 0-2), 12 patients had portal hypertension (6%); they had a significantly higher grade of steatosis, based on biopsy analysis, compared with the 192 patients without portal hypertension (94%). Thrombocytopenia, hyperbilirubinemia, cirrhosis, and obesity were associated independently with portal hypertension. Esophageal varices were found in 57 of the 128 patients undergoing endoscopic screening (44.5%) and were associated independently with thrombocytopenia, type 2 diabetes, and splenomegaly. CONCLUSIONS: Signs of portal hypertension were present in 25% of patients at the time of diagnosis of NAFLD; most had advanced fibrosis or cirrhosis. Portal hypertension can occur in a small proportion of patients with mild or no fibrosis and is associated with the extent of steatosis. Features of advanced liver disease and insulin resistance might identify patients with NAFLD and portal hypertension, and those expected to derive the most benefit from endoscopic screening for esophageal varices.

Duke Scholars

Published In

Clin Gastroenterol Hepatol

DOI

EISSN

1542-7714

Publication Date

September 2012

Volume

10

Issue

9

Start / End Page

1028 / 33.e2

Location

United States

Related Subject Headings

  • Splenomegaly
  • Prevalence
  • Non-alcoholic Fatty Liver Disease
  • Middle Aged
  • Male
  • Hypertension, Portal
  • Humans
  • Hepatic Encephalopathy
  • Gastroenterology & Hepatology
  • Female
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Mendes, F. D., Suzuki, A., Sanderson, S. O., Lindor, K. D., & Angulo, P. (2012). Prevalence and indicators of portal hypertension in patients with nonalcoholic fatty liver disease. Clin Gastroenterol Hepatol, 10(9), 1028-33.e2. https://doi.org/10.1016/j.cgh.2012.05.008
Mendes, Flavia D., Ayako Suzuki, Schuyler O. Sanderson, Keith D. Lindor, and Paul Angulo. “Prevalence and indicators of portal hypertension in patients with nonalcoholic fatty liver disease.Clin Gastroenterol Hepatol 10, no. 9 (September 2012): 1028-33.e2. https://doi.org/10.1016/j.cgh.2012.05.008.
Mendes FD, Suzuki A, Sanderson SO, Lindor KD, Angulo P. Prevalence and indicators of portal hypertension in patients with nonalcoholic fatty liver disease. Clin Gastroenterol Hepatol. 2012 Sep;10(9):1028-33.e2.
Mendes, Flavia D., et al. “Prevalence and indicators of portal hypertension in patients with nonalcoholic fatty liver disease.Clin Gastroenterol Hepatol, vol. 10, no. 9, Sept. 2012, pp. 1028-33.e2. Pubmed, doi:10.1016/j.cgh.2012.05.008.
Mendes FD, Suzuki A, Sanderson SO, Lindor KD, Angulo P. Prevalence and indicators of portal hypertension in patients with nonalcoholic fatty liver disease. Clin Gastroenterol Hepatol. 2012 Sep;10(9):1028–33.e2.
Journal cover image

Published In

Clin Gastroenterol Hepatol

DOI

EISSN

1542-7714

Publication Date

September 2012

Volume

10

Issue

9

Start / End Page

1028 / 33.e2

Location

United States

Related Subject Headings

  • Splenomegaly
  • Prevalence
  • Non-alcoholic Fatty Liver Disease
  • Middle Aged
  • Male
  • Hypertension, Portal
  • Humans
  • Hepatic Encephalopathy
  • Gastroenterology & Hepatology
  • Female