Evidence map›Paper›PMID 29844459›Full record

ArticleScientific reports2018

The effect of N-acetyl-l-cysteine (NAC) on liver toxicity and clinical outcome after hematopoietic stem cell transplantation.

Ibrahim El-Serafi, Mats Remberger, Ahmed El-Serafi, Fadwa Benkessou, Wenyi Zheng, Eva Martell, Per Ljungman, Jonas Mattsson, Moustapha Hassan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

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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

9 authors at 3 institutions in 2 countries.

Ibrahim El-SerafiECM, KFC, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Mats RembergerCenter for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Stockholm, Sweden.
Ahmed El-SerafiECM, KFC, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Fadwa BenkessouECM, KFC, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Wenyi ZhengECM, KFC, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Eva MartellCenter for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Stockholm, Sweden.
Per LjungmanCenter for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Stockholm, Sweden.
Jonas MattssonCenter for Allogeneic Stem Cell Transplantation, Karolinska University Hospital, Stockholm, Sweden.
Moustapha HassanECM, KFC, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden. moustapha.hassan@ki.se.
Karolinska Institutet · SEKarolinska University Hospital · SELinköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Busulphan (Bu) is a myeloablative drug used for conditioning prior to hematopoietic stem cell transplantation. Bu is predominantly metabolized through glutathione conjugation, a reaction that consumes the hepatic glutathione. N-acetyl-l-cysteine (NAC) is a glutathione precursor used in the treatment of acetaminophen hepatotoxicity. NAC does not interfere with the busulphan myeloablative effect. We investigated the effect of NAC concomitant treatment during busulphan conditioning on the liver enzymes as well as the clinical outcome. Prophylactic NAC treatment was given to 54 patients upon the start of busulphan conditioning. These patients were compared with 54 historical matched controls who did not receive NAC treatment. In patients treated with NAC, aspartate transaminase (AST), alanine transaminase (ALT) and alkaline phosphatase (ALP) were significantly (P < 0.05) decreased after conditioning compared to their start values. Within the NAC-group, liver enzymes were normalized in those patients (30%) who had significantly high start values. No significant decrease in enzyme levels was observed in the control group. Furthermore, NAC affected neither Bu kinetics nor clinical outcome (sinusoidal obstruction syndrome incidence, graft-versus-host disease and/or graft failure). IN

conclusionNAC is a potential prophylactic treatment for hepatotoxicity during busulphan conditioning. NAC therapy did not alter busulphan kinetics or affect clinical outcome.

Indexed as

Hematopoietic Stem Cell TransplantationAcetylcysteineAntineoplastic Agents, AlkylatingBilirubinBusulfanHumansLiverLiver Function TestsTransplantation ConditioningTreatment OutcomeAcetylcysteineAntineoplastic Agents, AlkylatingBilirubinBusulfan

Identifiers

PMID29844459
PMCPMC5974141
OpenAlexW2806868511

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.