Volume 7, Issue 11, Pages 1151-1154 (November 2009)

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Chronic Diarrhea Due to Excessive Bile Acid Synthesis and Not Defective Ileal Transport: A New Syndrome of Defective Fibroblast Growth Factor 19 Release

published online 10 August 2009.

Article Outline

• References

• Copyright

Elsewhere in this issue Julian Walters and his colleagues report a major advance in our understanding of the pathogenesis of chronic diarrhea associated with idiopathic bile acid malabsorption.1 The story is a fascinating one and unites longstanding and very recent discoveries in physiology, biochemistry, and molecular biology.

Conjugated bile acids are absorbed from the terminal ileum by the combined action of an apical sodium-dependent transporter that takes bile acids into the cell and a basolateral transporter that takes bile acids out of the cell and into portal venous blood. The ileum was recognized as the preferential site of bile acid absorption by Tappeiner2 in 1878, and his observations were confirmed repeatedly. In 1960, Lack and Weiner3 used the everted gut sac technique to show that conjugated bile acids moved uphill, against a concentration gradient, in segments prepared from the distal ileum. Expression cloning was used by Paul Dawson and his colleagues to clone the apical sodium-dependent bile acid transporter in 1994.4 Seven years later, the heterodimeric basolateral transporter OSTα/OSTβ of the skate hepatocyte was cloned by Wang et al5 and Ballatori et al,6 and its essential role in the transport of bile acids across the basolateral membrane of the ileal enterocyte was established by Dawson et al.7

Bile acid biosynthesis from cholesterol is under negative feedback control. Interruption of the enterohepatic circulation by a biliary fistula8 or ileal dysfunction9, 10, 11, 12, 13 leads to a marked increase in bile acid biosynthesis. Pandak et al14 made the observation that such up-regulated bile acid synthesis could be down-regulated by bile acid infusion into the small intestine but not by intravenous infusion. This observation was confirmed and extended by a Japanese surgical group who showed that duodenal infusion down-regulated bile acid biosynthesis, whereas portal venous infusion did not.15 These experiments raised the intriguing possibility that an unknown intestinal factor was released by bile acids and was necessary for feedback inhibition of bile acid synthesis. Ten years later, this intestinal factor was discovered by Inagaki et al16 to be a protein, fibroblast growth factor (FGF) 19, an atypical FGF family member that functions as a hormone. FGF19 is synthesized in the ileal enterocytes in response to bile acids and released into the portal venous circulation. On reaching the liver, FGF19 signals through a cell surface receptor on hepatocytes to repress bile acid synthesis.

Increased bile acid biosynthesis in patients with bile acid malabsorption because of ileal dysfunction meant that more bile acids passed into the colon. A group of studies in animals and humans led by Sidney Phillips at the Mayo Clinic showed that colonic perfusion with dihydroxy bile salts induced colonic secretion,17, 18 and elevated concentrations of fecal bile acids were shown to be present in patients with ileal resection.9, 10, 11 The elevated concentrations were the result of greatly increased bile acid synthesis.9, 10, 11, 12, 13

It was quite straightforward to combine these findings and predict the sequence of events in patients undergoing ileal resection.19 Defective bile acid absorption led to increased hepatic synthesis. In this new steady state, increased bile acids passed into the colon and induced secretion, manifested clinically as diarrhea. If diarrhea were caused by bile acid–induced secretion in the colon, it should respond to a bile acid sequestrant. Indeed, cholestyramine was shown to be effective for the treatment of diarrhea in a small clinical study.20 Colesevelam, a more potent bile acid sequestrant, was developed a few years ago, and its off-label utility in diarrhea associated with bile acid malabsorption has been claimed in anecdotal reports.21 Colesevelam is available in tablet form and appears to be better tolerated than cholestyramine, which is marketed as a granular powder.

The diagnosis of bile acid malabsorption is not simple. One can measure fecal bile acids by gas chromatography22 or by an enzymatic method,23 but both methods are complex, and patients do not like to collect stool samples. Boyd, a Scottish biochemist, had the idea of synthesizing a taurocholate analogue tagged with a gamma emitting isotope. A 75selenium atom (a gamma particle emitter) was inserted into the side chain of the bile acid (between the 22nd and 23rd carbon atom), and this compound 75seleno-homocholyltaurine (SeHCAT) was shown to behave physiologically like taurocholate.24 In patients with bile acid malabsorption, the compound is lost from the body much more rapidly than in patients without bile acid malabsorption as quantified by whole body scanning with a gamma camera.25, 26, 27, 28 However, this valuable diagnostic radionuclide has never been available for clinical purposes in the United States.

A blood test for the detection of bile acid malabsorption would be more convenient. Gälman et al29 showed that an intermediate in bile acid synthesis named C4 (actually 7α-hydroxy-cholest-4-ene-3-one) spills over from the hepatocyte into plasma in direct proportion to the rate of bile acid synthesis. When bile acid synthesis was increased, plasma levels of C4 were markedly elevated.30, 31

In the meantime, the mechanistic details of the negative feedback regulation of bile acid biosynthesis in the hepatocyte were being clarified.32 An orphan member of the steroid hormone receptor family, named FXR, was discovered to be activated by bile acids and to play a central role in the regulation of bile acid homeostasis.33, 34, 35, 36 In the ileum, bile acid–mediated activation of FXR was shown to induce the synthesis and secretion of the protein hormone FGF19, which subsequently represses bile acid synthesis in hepatocytes by binding to a cell surface receptor composed of the FGF receptor 4, a tyrosine kinase, and β-klotho, a single pass transmembrane protein.37, 38, 39 Activation of the FGF receptor 4/β-klotho complex activates phosphorylation cascades that culminate in the transcriptional repression of the gene encoding cholesterol 7α-hydroxylase, the rate-limiting enzyme in bile acid synthesis.16, 40, 41 In mice, elimination of FXR, FGF15 (the mouse ortholog of FGF19), FGF receptor 4, or β-klotho increases cholesterol 7α-hydroxylase expression and bile acid synthesis,16, 42, 43, 44, 45 highlighting the importance of each of these proteins in the feedback regulatory pathway. This pathway of feedback inhibition of bile acid synthesis is illustrated in Figure 1.

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Figure 1. Pathway by which the enterohepatic circulation of bile acids down-regulates bile acid biosynthesis. Bile acids traversing the ileal enterocyte activate FXR, the nuclear receptor for bile acids (shown as a heterodimer with RXR, the retinoid X receptor). FXR activation promotes the synthesis of FGF19, a protein that exits the ileal enterocyte by an unknown mechanism and travels to the liver in portal venous blood. FGF19 interacts with the dimeric receptor FGFR4/β-klotho present on the basolateral surface of the hepatocyte. The activated receptor initiates a phosphorylation cascade that culminates in the transcriptional repression of the gene encoding cholesterol 7α-hydroxylase, the rate-limiting enzyme in bile acid biosynthesis.32 In patients with ileal dysfunction causing defective ileal transport of bile acids, the concentration of bile acids in the ileal enterocyte is low, and FGF19 formation and release are decreased, leading to increased hepatic bile acid biosynthesis that in turn causes diarrhea. In patients with idiopathic bile acid malabsorption, ileal bile acid transport is unimpaired. FGF19 release from the ileal enterocyte is impaired for unknown reasons, leading to increased hepatic bile acid biosynthesis that in turn causes diarrhea.

The late Hess Thaysen,46 working in Denmark, identified a group of patients who had bile acid malabsorption and diarrhea responsive to cholestyramine, yet they had no detectable ileal pathology. The defect has been termed primary bile acid malabsorption or idiopathic bile acid malabsorption. Merrick and colleagues showed that bile acid malabsorption was common in patients diagnosed as having irritable bowel syndrome, diarrhea predominant.47, 48 This observation was confirmed by Bardhan and his colleagues working in Rotherham, United Kingdom49 as well as in Italy50 and Sweden.51 It was logical to assume that such patients would have a defect in the gene encoding the ileal apical bile acid transporter. However, in a careful study by Montagnani et al,52 no defects in the gene encoding the apical sodium-dependent bile acid transporter (SLC10a2) were identified. Moreover, independent studies by van Tilburg et al53 and Bajor et al54 showed that conjugated bile acid transport by human ileal biopsy samples was not defective, but either normal or increased. Patients were also shown to have an enlarged bile acid pool55 and to be overweight.56

In this issue of Clinical Gastroenterology and Hepatology, Julian Walters and his colleagues1 present evidence for a new and fascinating explanation for the altered bile acid metabolism that is present in such patients. They describe a group of patients with chronic diarrhea responsive to cholestyramine who have bile acid malabsorption based on SeHCAT non-retention and increased plasma levels of C4. Their exciting discovery was that these patients had low plasma levels of FGF19. A low plasma level of FGF19 should in turn lead to defective negative feedback of bile acid biosynthesis and increased bile acid biosynthesis. In this new steady state, ileal transport should be saturated, and increased bile acids pass into the colon, inducing secretion that in turn is manifest clinically as diarrhea. This pathophysiologic defect can explain why van Tilburg et al53 and Bajor et al54 found unimpaired bile acid transport in their ileal biopsy samples and also explains why the bile acid pool is enlarged.55 It is not known why plasma levels of FGF19 are abnormally low, and this will surely be investigated. The pathophysiologic defect is also shown in Figure 1.

At last, we have a satisfying explanation for at least some cases of idiopathic bile acid malabsorption. Such patients should have increased bile acid biosynthesis and increased bile acid secretion. As noted above, the bile acid pool (measured by isotope dilution) is enlarged.55 Presumably, ileal transport is at its maximum, although some animal and human studies suggest that the ileal bile acid transport system should down-regulate when exposed to an increased flux of bile acids.57

The observation by the Walters group is the culmination of 50 years of research on the enterohepatic circulation of bile acids. For the physician, an explanation is now available for a subset of patients with chronic diarrhea. The diagnosis of bile acid malabsorption can be made by finding an increased plasma level of C4. However, a simple therapeutic trial of a bile acid sequestrant such as colesevelam or cholestyramine should generally be sufficient to establish the diagnosis and, if the patient responds, indicate successful therapy, providing symptomatic relief.

References

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⁎ Department of Medicine, University of California, San Diego, California

‡ Department of Pharmacology, University of Texas, Southwestern Medical Center, Dallas, Texas

∥ Department of Molecular Biology, University of Texas, Southwestern Medical Center, Dallas, Texas

§ Howard Hughes Medical Institute, University of Texas, Southwestern Medical Center, Dallas, Texas

Conflicts of interest The authors disclose the following: All of the authors have served as ad hoc consultants to Daiichi Sankyo Inc, who market colesevelam for the treatment of type 2 diabetes in the United States.

Funding This work was supported by National Institutes of Health grant DK067158 and the Welch Foundation (D.J.M. and S.A.K.) and the Howard Hughes Medical Institute (D.J.M.).

PII: S1542-3565(09)00745-9

doi:10.1016/j.cgh.2009.07.026

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