Evidence map›Paper›PMID 38444575›Full record

ArticleJIMD reports2024

Non-Hodgkin lymphoma in a kidney transplanted patient with methylmalonic acidemia: Metabolic susceptibility and the role of immunosuppression.

Alberto B Burlina, Alessandro P Burlina, Renzo Mignani, Chiara Cazzorla, Daniela Gueraldi, Andrea Puma, Christian Loro, Matthias R Baumgartner, Vincenza Gragnaniello

Open access · goldAbstract readCase Reports
In one paragraph

Article in JIMD reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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.

Alberto B BurlinaDivision of Inherited Metabolic Diseases, Department of Women's and Children's Health University Hospital of Padua Padua Italy.
Alessandro P BurlinaNeurology Unit St Bassiano Hospital Bassano del Grappa Italy.
Renzo MignaniNephrology and Dialysis Department Infermi Hospital Rimini Italy.
Chiara CazzorlaDivision of Inherited Metabolic Diseases, Department of Women's and Children's Health University Hospital of Padua Padua Italy.
Daniela GueraldiDivision of Inherited Metabolic Diseases, Department of Women's and Children's Health University Hospital of Padua Padua Italy.
Andrea PumaDivision of Inherited Metabolic Diseases, Department of Women's and Children's Health University Hospital of Padua Padua Italy.
Christian LoroDivision of Inherited Metabolic Diseases, Department of Women's and Children's Health University Hospital of Padua Padua Italy.
Matthias R BaumgartnerDivision of Metabolism and Children's Research Center University Children's Hospital Zurich, University of Zurich Zurich Switzerland.
Vincenza GragnanielloDivision of Inherited Metabolic Diseases, Department of Women's and Children's Health University Hospital of Padua Padua Italy.
University of Padua · ITOspedale Infermi di Rimini · ITUniversity Children's Hospital Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methylmalonic acidemia cblB type (MMA cblB) is an autosomal recessive inborn error of amino acid metabolism that results in impaired synthesis of adenosylcobalamin, a cofactor of methylmalonyl-CoA mutase. It presents with episodes of coma, vomiting, hypotonia, metabolic acidosis, and hyperammonemia. End-stage kidney disease is a long-term complication. Treatments include vitamin B12 supplementation, L-carnitine, and a low-protein diet. Liver, kidney, or combined liver-kidney transplantations are promising options, but they are not without complications. We report a patient suffering from MMA cblB who developed end-stage kidney disease at 18 years of age. Kidney transplantation allowed him to recover normal kidney function and good metabolic control. Unfortunately, after two decades, he developed non-Hodgkin lymphoma and severe chemotherapy toxicity which led to his death. The risk of lymphoproliferative diseases is known to increase after solid organ transplantation. However, in MMA, factors including mitochondrial dysfunction and oncometabolites, may further increase the risk of malignancy and drug toxicity. Our report highlights the importance of considering the increased risk of cancer in long-term follow-up of MMA cblB patients, especially after solid organ transplantation. Moreover, when chemotherapy is needed, the increased risk of toxicity and metabolic decompensation should be considered and monitored.

Indexed as

chemotherapy toxicityimmunosuppressionkidney transplantationmethylmalonic acidemiamitochondrial dysfunctionpost‐transplant lymphoproliferative disorders

Identifiers

PMID38444575
PMCPMC10910225
OpenAlexW4390746474

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.