# Potential amelioration of liver function by low-dose tolvaptan in heart failure patients

**Authors:** Yasuaki Mino, Kohei Hoshikawa, Takafumi Naito, Shunta Akutsu, Yumi Imoto, Emi Nakatsugawa, Masao Saotome, Yuichiro Maekawa, Junichi Kawakami

PMC · DOI: 10.1016/j.toxrep.2025.102009 · Toxicology Reports · 2025-03-24

## TL;DR

Low-dose tolvaptan may improve liver function in heart failure patients, contrary to previous reports, with no evidence of liver injury.

## Contribution

The study shows that low-dose tolvaptan may ameliorate liver function in heart failure patients, challenging prior assumptions about its hepatotoxicity.

## Key findings

- Tolvaptan concentration was inversely correlated with liver injury markers like AST and ALT.
- Low-dose tolvaptan did not cause liver injury and was associated with improved liver function.
- Bilirubin levels were lower in patients with a specific OATP1B3 genetic variant.

## Abstract

This study aimed to evaluate the relationships between the pharmacokinetics of tolvaptan and its metabolites (DM-4103 and DM-4107) and liver injury in heart failure patients, using relevant laboratory test values and markers of hepatocyte injury and biliary cholestasis.

The plasma concentrations of tolvaptan, DM-4103, and DM-4107 were determined using LC-MS/MS in 51 Japanese heart failure patients. The relationships between the concentrations and the N-terminal fragment of pro-B-type natriuretic peptide (NT-proBNP), AST, and ALT were assessed. K18 and glutamate dehydrogenase as a marker of liver injury and CP-I and CP-III as indicators of OATP activity were also determined.

The median concentrations of tolvaptan, DM-4103, and DM-4107 were 16.2, 287, and 38.0 ng/mL, respectively. AST, ALT, and T-Bil were significantly decreased after tolvaptan administration. They were negatively correlated with tolvaptan concentration. AST was also negatively correlated with DM-4107 concentration. CP-III was positively correlated with DM-4103 concentration; however, CP-I was negatively correlated with DM-4103 concentration. K18 and glutamate dehydrogenase were not correlated with tolvaptan concentration.

Low-dose tolvaptan did not cause liver injury. Pharmacokinetics of tolvaptan may be associated with potential amelioration of liver function in heart failure patients.

•Tolvaptan concentration was inversely correlated with liver function markers.•Bilirubin was lower in patients with OATP1B3c.1683–5676 A>G.•Coproporphyrin was not correlated with tolvaptan pharmacokinetics.•Low-dose tolvaptan improved liver function, contrary to previous reports.•Specific mechanism underlying the improvement was not determined.

Tolvaptan concentration was inversely correlated with liver function markers.

Bilirubin was lower in patients with OATP1B3c.1683–5676 A>G.

Coproporphyrin was not correlated with tolvaptan pharmacokinetics.

Low-dose tolvaptan improved liver function, contrary to previous reports.

Specific mechanism underlying the improvement was not determined.

## Linked entities

- **Genes:** SLCO1B3 (solute carrier organic anion transporter family member 1B3) [NCBI Gene 28234]
- **Chemicals:** tolvaptan (PubChem CID 216237), DM-4103 (PubChem CID 71752623), DM-4107 (PubChem CID 71752622), ALT (PubChem CID 10219674), K18 (PubChem CID 615353), glutamate dehydrogenase (PubChem CID 168009864), CP-I (PubChem CID 68271)
- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** SLCO1A2 (solute carrier organic anion transporter family member 1A2) [NCBI Gene 6579] {aka OATP, OATP-A, OATP1A2, SLC21A3}, KRT18 (keratin 18) [NCBI Gene 3875] {aka CK-18, CYK18, K18}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** biliary cholestasis (MESH:D002779), hepatocyte injury (MESH:D014947), liver injury (MESH:D017093), heart failure (MESH:D006333)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11987637/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC11987637/full.md

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Source: https://tomesphere.com/paper/PMC11987637