Optimizing thiopurine therapy in autoimmune hepatitis: A multi-center study on monitoring metabolite profiles and co-therapy with allopurinol

Author:

Weltzsch Jan Philipp12,Bartel Claudius F.1,Waldmann Moritz3,Renné Thomas3,Schulze Stephanie1,Terziroli Beretta-Piccoli Benedetta456,Papp Maria7,Ye Oo28,Ronca 8,Sebode Marcial12,Lohse Ansgar W.12,Schramm Christoph12910,Hartl Johannes12

Affiliation:

1. I. Department of Medicine, University Medical Centre Hamburg-Eppendorf (UKE), Hamburg, Germany

2. European Reference Network on Hepatological Diseases (ERN RARE-LIVER) Hamburg, Germany

3. Institute for Clinical Chemistry and Laboratory Medicine, University Medical Centre Hamburg-Eppendorf (UKE), Hamburg, Germany

4. Epatocentro Ticino, Lugano, Switzerland

5. Faculty of Biochemical Sciences, Università della Svizzera Italiana, Lugano, Switzerland

6. Mowat Labs, Faculty of Life Sciences & Medicine, King’s College London, King’s College Hospital, London, UK

7. University of Debrecen, Faculty of Medicine, Institute of Medicine, Department of Gastroenterology, Debrecen, Hungary

8. Liver Transplant Unit, Centre for Rare Disease, Birmingham & Centre for Liver and Gastro Research, Institute of Immunology and Immunotherapy, Queen Elizabeth Hospital, University Hospital of Birmingham, University of Birmingham, Birmingham, UK

9. Hamburg Centre for Translational Immunology (HCTI), University Medical Centre Hamburg-Eppendorf, Hamburg, Germany

10. Martin Zeitz Centre for Rare Diseases, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany

Abstract

Background & aims: In autoimmune hepatitis (AIH), achieving complete biochemical remission (CBR) with current weight-based thiopurine dosing is challenging. We investigated whether patients could be stratified regarding CBR according to a target range of thiopurine metabolites. Moreover, we explored the effects of azathioprine dosage increases and co-therapy of allopurinol with low-dose thiopurines on metabolite profiles and treatment response. Approach & results: The relation between metabolites and treatment response was assessed in 337 individuals from four European centers. In a global, cross-sectional analysis, active metabolites 6-thioguanin nucleotides (6TGN) were similar in those with and without CBR. However, analyzing patients with sequential measurements over 4 years (N=146) revealed higher average 6TGN levels in those with stable CBR (260 pmol/0.2 ml) compared to those failing to maintain CBR (181 pmol/0.2 ml;p=0.0014) or never achieving CBR (153 pmol/0.2 ml;p<0.0001), with an optimal 6TGN-cutoff of ≥223 pmol/0.2 ml (sensitivity: 76%, specificity: 78%). Only 42% exhibited 6TGN ≥223 pmol/0.2 ml following weight-based dosing, as doses weakly correlated with 6TGN but with 6-methylmercaptopurine (6MMP), a metabolite associated with toxicity. Azathioprine dose increases led to preferential 6MMP formation (+127% vs. 6TGN +34%;p<0.0001). Conversely, adding allopurinol to thiopurines in difficult-to-treat patients (N=36) raised 6TGN (168→321 pmol/0.2 ml;p<0.0001) and lowered 6MMP (2125→184 pmol/0.2 ml;p<0.0001), resulting in improved transaminases in all patients and long-term CBR in 75%. Conclusions: Maintaining CBR in AIH was associated with 6TGN ≥223 pmol/0.2 ml. For patients who fail to achieve CBR and therapeutic 6TGN levels despite thiopurine dose increase due to preferential 6MMP formation, co-medication of allopurinol alongside low-dose thiopurines represents an efficient alternative.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Fellows’ Corner;Hepatology;2024-08-19

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