2010
DOI: 10.2147/ceg.s7556
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Hepatic manifestations of celiac disease

Abstract: Different hepatic and biliary tract disorders may occur with celiac disease. Some have been hypothesized to share genetic or immunopathogenetic factors, such as primary biliary cirrhosis, primary sclerosing cholangitis, and autoimmune hepatitis. Other hepatic changes in celiac disease may occur with malnutrition resulting from impaired nutrient absorption, including hepatic steatosis. In addition, celiac disease may be associated with rare hepatic complications, such as hepatic T-cell lymphoma.

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Cited by 25 publications
(13 citation statements)
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“…As expected, the patients frequently show an alteration in serum lipid levels, that is, low serum total and high-density lipoprotein cholesterol as a consequence of lipid malabsorption and decreased intake [38]. The autoimmune insult seems to involve many organs besides the gut, such as the adipose tissue and the clinical manifestations vary among different populations [39,40]. It can also be associated with other autoimmune diseases such as T1DM [6,7].…”
Section: Discussionmentioning
confidence: 60%
“…As expected, the patients frequently show an alteration in serum lipid levels, that is, low serum total and high-density lipoprotein cholesterol as a consequence of lipid malabsorption and decreased intake [38]. The autoimmune insult seems to involve many organs besides the gut, such as the adipose tissue and the clinical manifestations vary among different populations [39,40]. It can also be associated with other autoimmune diseases such as T1DM [6,7].…”
Section: Discussionmentioning
confidence: 60%
“…Cryptogenic hypertransaminasaemia (celiac hepatitis), a common extraintestinal presentation of CD, is closely related to gluten intake. Additionally, CD can simply coexist as a coincidental finding with several liver diseases, such as non-alcoholic fatty liver disease (NAFLD) (and its subgroup termed non-alcoholic steatohepatitis (NASH)), chronic viral hepatitis B or C, alcoholic liver disease, hemochromatosis, Wilson’s disease, and other hereditary hepatic diseases [ 3 , 44 , 49 , 50 , 51 ]. Swedish epidemiological studies have revealed that patients with CD have an increased risk of both prior and subsequent liver disease, four-times and six-times, respectively [ 52 ], and an eight-times increased risk of mortality from liver cirrhosis [ 53 ]; however, no increased risk of liver transplantation was found (HR, 1.07; 95% CI, 0.12–9.62; p = 0.954) [ 52 ].…”
Section: Celiac Disease and Liver Disorders In The Clinical Contexmentioning
confidence: 99%
“…Many organs or systems such as cardiac, neurological, bone, skin, liver, and endocrin may be involved in the course of CD (13)(14)(15)(16)(17)(18)(19). Although it is an intestinal autoimmune disease, as the diagnostic age of CD getting older, the disease presents itself with complaints that not directed to gastrointestinal tract.…”
Section: Discussionmentioning
confidence: 99%