# Decline of Persistent Jaundice in a Patient With Autoimmune Hepatitis and Vanishing Bile Duct Syndrome Treated With Elobixibat for Constipation

**Authors:** Tân Trần Thị, Norihiro Imai, Yosuke Inukai, Takashi Honda, Hiroki Kawashima

PMC · DOI: 10.7759/cureus.80021 · Cureus · 2025-03-04

## TL;DR

A patient with autoimmune hepatitis and bile duct issues showed improved jaundice after being treated with elobixibat for constipation.

## Contribution

The novel finding is that elobixibat, used for constipation, may also help treat severe cholestasis in autoimmune liver disease.

## Key findings

- Standard therapies failed to resolve the patient's jaundice.
- Elobixibat treatment led to a marked improvement in jaundice.
- Elobixibat may be a valuable adjunctive therapy for severe cholestasis.

## Abstract

We present the case of a 49-year-old woman with autoimmune hepatitis and persistent jaundice. On admission, pathology and laboratory results supported the diagnosis of autoimmune hepatitis-primary biliary cholangitis (AIH-PBC) overlap syndrome with vanishing bile duct syndrome (VBDS). Standard treatment, including methylprednisolone pulse therapy, prednisolone, azathioprine, bezafibrate, and ursodeoxycholic acid, failed to resolve jaundice. In addition to jaundice, the patient also had constipation and regularly used magnesium oxide and sennoside. Notably, the addition of elobixibat, initially prescribed for constipation, resulted in a marked improvement in jaundice. This case highlights the diagnostic and therapeutic challenges of AIH-PBC overlap syndrome with VBDS, particularly in cases of refractory jaundice. The observed efficacy of elobixibat suggests that it may be a valuable adjunctive therapy for severe cholestasis. Further research is warranted to clarify its therapeutic potential and underlying mechanisms in similar cases.

## Linked entities

- **Chemicals:** elobixibat (PubChem CID 9939892), methylprednisolone (PubChem CID 6741), prednisolone (PubChem CID 5755), azathioprine (PubChem CID 2265), bezafibrate (PubChem CID 39042), ursodeoxycholic acid (PubChem CID 31401), magnesium oxide (PubChem CID 14792), sennoside (PubChem CID 656822)
- **Diseases:** autoimmune hepatitis (MONDO:0016264), primary biliary cholangitis (MONDO:0005388)

## Full-text entities

- **Diseases:** Persistent Jaundice (MESH:D007565), overlap (MESH:C536030), Autoimmune Hepatitis (MESH:D019693), cholestasis (MESH:D002779), AIH-PBC (MESH:D008105), VBDS (MESH:D001649), Constipation (MESH:D003248)
- **Chemicals:** magnesium oxide (MESH:D008277), sennoside (MESH:D000081226), ursodeoxycholic acid (MESH:D014580), methylprednisolone (MESH:D008775), bezafibrate (MESH:D001629), prednisolone (MESH:D011239), azathioprine (MESH:D001379), Elobixibat (MESH:C581303)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11967287/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC11967287/full.md

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Source: https://tomesphere.com/paper/PMC11967287