Celiac Disease and Elevated Liver Enzymes: A Review

被引:21
作者
Kim, Jaimy Villavicencio [1 ]
Wu, George Y. [2 ]
机构
[1] Univ Connecticut, Dept Med, Hlth Ctr, 263 Farmington Ave, Farmington, CT 06032 USA
[2] Univ Connecticut, Div Gastroenterol Hepatol, Hlth Ctr, Farmington, CT 06032 USA
关键词
Celiac disease; Gluten free diet; Celiac hepatitis; Autoimmune liver disease; PRIMARY BILIARY-CIRRHOSIS; GLUTEN-FREE DIET; INTESTINAL PERMEABILITY; PREVALENCE; ANTIBODIES; HYPERTRANSAMINASEMIA; TRANSGRESSIONS; ABNORMALITIES; COMPLICATIONS; GUT;
D O I
10.14218/JCTH.2020.00089
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aminotransferases are commonly found to be elevated in patients with celiac disease in association with two different types of liver dysfunction: cryptogenic liver disorders and autoimmune disorders. The purpose of this review is to discuss the mechanisms by which aminotransferases become elevated in celiac disease, clinical manifestations, and response to glutenfree diet. Many studies have shown that celiac patients with cryptogenic liver disease have normalization in aminotransferases, intestinal histologic improvement and serologic resolution after 6-12 months of strict gluten-free diet. In patients with an underlying autoimmune liver disease, simultaneous treatment for both conditions resulted in normalized elevated aminotransferases. The literature suggests that intestinal permeability may be at least one of the mechanisms by which liver damage occurs. Patients with celiac disease should have liver enzymes routinely checked and treated with a strict gluten-free diet if found to be abnormal. Lack of improvement in patients who have strictly adhered to gluten-free diet should prompt further workup for other causes of liver disease.
引用
收藏
页码:116 / 124
页数:9
相关论文
共 58 条
[31]  
LOGAN RFA, 1978, LANCET, V1, P230
[32]   Celiac disease-related hepatic injury: Insights into associated conditions and underlying pathomechanisms [J].
Marciano, Francesca ;
Savoia, Marcella ;
Vajro, Pietro .
DIGESTIVE AND LIVER DISEASE, 2016, 48 (02) :112-119
[33]   Infections and Risk of Celiac Disease in Childhood: A Prospective Nationwide Cohort Study [J].
Marild, Karl ;
Kahrs, Christian R. ;
Tapia, German ;
Stene, Lars C. ;
Stordal, Ketil .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2015, 110 (10) :1475-1484
[34]   Increased Intestinal Permeability and Tight Junction Alterations in Nonalcoholic Fatty Liver Disease [J].
Miele, Luca ;
Valenza, Venanzio ;
La Torre, Giuseppe ;
Montalto, Massimo ;
Cammarota, Giovanni ;
Ricci, Riccardo ;
Masciana, Roberta ;
Forgione, Alessandra ;
Gabrieli, Maria L. ;
Perotti, Germano ;
Vecchio, Fabio M. ;
Rapaccini, Gianlodovico ;
Gasbarrini, Giovanni ;
Day, Chris P. ;
Grieco, Antonio .
HEPATOLOGY, 2009, 49 (06) :1877-1887
[35]   The Liver in Celiac Disease Clinical Manifestations, Histologic Features, and Response to Gluten-Free Diet in 30 Patients [J].
Mounajjed, Taofic ;
Oxentenko, Amy ;
Shmidt, Eugenia ;
Smyrk, Thomas .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2011, 136 (01) :128-137
[36]   PBC and the gut: the villi atrophy, the plot thickens [J].
Neuberger, J .
GUT, 1999, 44 (05) :594-595
[37]   Prevalence and clinical importance of hypertransaminasaemia in coeliac disease [J].
Novacek, G ;
Miehsler, W ;
Wrba, F ;
Ferenci, P ;
Penner, E ;
Vogelsang, H .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1999, 11 (03) :283-288
[38]   How many duodenal biopsy specimens are required to make a diagnosis of celiac disease? [J].
Pais, Wilson P. ;
Duerksen, Donald R. ;
Pettigrew, Norman M. ;
Bernstein, Charles N. .
GASTROINTESTINAL ENDOSCOPY, 2008, 67 (07) :1082-1087
[39]   Hepatobiliary Disorders in Celiac Disease: An Update [J].
Prasad, Kaushal K. ;
Debi, Uma ;
Sinha, Saroj K. ;
Nain, Chander K. ;
Singh, Kartar .
INTERNATIONAL JOURNAL OF HEPATOLOGY, 2011, 2011
[40]   Increased risk of non-alcoholic fatty liver disease after diagnosis of celiac disease [J].
Reilly, Norelle R. ;
Lebwohl, Benjamin ;
Hultcrantz, Rolf ;
Green, Peter H. R. ;
Ludvigsson, Jonas F. .
JOURNAL OF HEPATOLOGY, 2015, 62 (06) :1405-1411