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J Pediatr Gastroenterol Nutr. 2019 May 6. doi: 10.1097/MPG.0000000000002353. [Epub ahead of print]

Altered Bile Transporter Expression and Cholesterol Metabolism in Children with Cholesterol and Pigment Gallstones.

Author information

1
Section of pediatric surgery, Pediatric Liver and Gut Research Group, Children's Hospital, University of Helsinki, Finland.
2
Department of Internal Medicine at Helsinki University Hospital, Pediatric Liver and Gut Research Group, University of Helsinki, Finland.
3
Clinic of Gastroenterology, Abdominal Centre at Helsinki University Hospital, Pediatric Liver and Gut Research Group University of Helsinki, Finland.

Abstract

OBJECTIVES.:

We elucidated pathophysiology of pediatric gallstone disease by assessing liver expression of bile transporters in relation to bile acids and surrogates of cholesterol absorption and synthesis in serum and gallstones.

METHODS.:

RNA expression of canalicular bile transporters in liver biopsies from 32 pediatric gallstone patients and from six liver donors (controls) was measured by qRT-PCR. Concentrations of cholesterol and precursors, plant sterols and bile acids in gallstones, and in serum of the patients and 82 healthy children were measured. Primary outcomes were the difference in RNA expressions and serum sterol profiles between patients and controls.

RESULTS.:

Cholesterol stones (CS; n = 15) contained cholesterol >42% and pigment stones (PS; n = 17) <9% of weight. CS-patients had markedly lower serum plant sterols (absorption) and higher cholesterol precursors (synthesis) than PS-patients or healthy controls. CS contained several times more cholesterol precursors and less plant sterols relative to cholesterol than PS, which were enriched by primary bile acids (12-5.2 fold, p<0.001). Liver RNA expression of ABCG5/G8 was similarly increased 2.5-1.8 fold (p < 0.002) in CS and PS-patients, while PS-patients had higher ABCB11 expression (p < 0.05). In PS bile acid concentration correlated with gallstone plant sterols (R = 0.83, p < 0.0001), and ABCG5 expression with ACBC11 expression (R2 = 0.27, p = 0.03).

CONCLUSIONS:

In CS, upregulation of ABCG5/G8 expression associates with low absorption and high gallstone content of cholesterol. In PS, activation of bile acid transport by ACBC11 interconnects with hepatic upregulation of ABCG5/G8 enriching PS with bile acids and plant sterols.

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