Evidence map›Paper›PMID 28740837›Full record

ArticleAutopsy & case reports

Histological remission of autoimmune hepatitis after the addition of allopurinol and azathioprine dose reduction.

Ana Luiza Vilar Guedes, Adriana Ribas Andrade, Vinicius Santos Nunes, Fabiana Roberto Lima, Evandro Sobroza de Mello, Suzane Kioko Ono, Débora Raquel Benedita Terrabuio, Eduardo Luiz Rachid Cançado

Open access · diamondAbstract read
In one paragraph

Article in Autopsy & case reports. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 49% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Ana Luiza Vilar GuedesUniversity of São Paulo, School of Medicine, Department of Gastroenterology. São Paulo, SP, Brazil.
Adriana Ribas AndradeUniversity of São Paulo, School of Medicine, Department of Gastroenterology. São Paulo, SP, Brazil.
Vinicius Santos NunesUniversity of São Paulo, School of Medicine, Department of Gastroenterology. São Paulo, SP, Brazil.
Fabiana Roberto LimaUniversity of São Paulo, School of Medicine, Department of Pathology. São Paulo, SP, Brazil.
Evandro Sobroza de MelloUniversity of São Paulo, School of Medicine, Department of Pathology. São Paulo, SP, Brazil.
Suzane Kioko OnoUniversity of São Paulo, School of Medicine, Department of Gastroenterology. São Paulo, SP, Brazil.
Débora Raquel Benedita TerrabuioUniversity of São Paulo, School of Medicine, Department of Gastroenterology. São Paulo, SP, Brazil.
Eduardo Luiz Rachid CançadoUniversity of São Paulo, School of Medicine, Department of Gastroenterology. São Paulo, SP, Brazil.
Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The standard therapy for some autoimmune diseases consists of a combination of corticosteroids and thiopurines. In non-responders to thiopurine drugs, the measurement of the metabolites of azathioprine, 6-thioguanine, and 6-methylmercaptopurine, can be a useful tool. The measurement has been used during the treatment of inflammatory bowel diseases and, less commonly, in autoimmune hepatitis. Many patients preferentially metabolize thiopurines to 6-methylmercaptopurine (6-MMP), which is potentially hepatotoxic, instead of 6-thioguanine, the active immunosuppressive metabolite. The addition of allopurinol shifts the metabolism of thiopurine towards 6-thioguanine, improving the immunosuppressive effect. We present the case of a 51-year-old female with autoimmune hepatitis who had a biochemical response after azathioprine and prednisone treatment without histological remission, and who preferentially shunted to 6-MMP. After the addition of allopurinol, the patient's 6-thioguanine levels increased, and she reached histological remission with a reduction of 67% of the original dose of azathioprine. The patient did not develop clinical manifestations as a consequence of her increased immunosuppressive state. We also review the relevant literature related to this issue. In conclusion, the addition of allopurinol to thiopurine seems to be an option for those patients who do not reach histological remission and who have a skewed thiopurine metabolite profile.

Indexed as

AllopurinolAzathioprineAzathioprine MetabolismHepatitis, Autoimmune

Identifiers

PMID28740837
PMCPMC5507567
OpenAlexW2726880625

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.