Evidence map›Paper›PMID 36011350›Full record

ArticleGenes2022

Prognostic Analysis of the IDH1 G105G (rs11554137) SNP in IDH-Wildtype Glioblastoma.

Ayoub Saaid, Matteo Monticelli, Alessia Andrea Ricci, Giulia Orlando, Cristina Botta, Pietro Zeppa, Andrea Bianconi, Simona Osella-Abate, Francesco Bruno, Alessia Pellerino and 5 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 24 citations in OpenAlex.

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  9. Association ofInternational journal of molecular sciences · 2025
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  19. Genes · 2023
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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

15 authors at 3 institutions in 1 country.

Ayoub SaaidNeurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.
Matteo MonticelliNeurosurgery Unit, Department of Neuroscience and Rehabilitation, University of Ferrara, 44100 Ferrara, Italy.ORCID 0000-0002-3738-5106
Alessia Andrea RicciPathology Unit, Department of Medical Sciences, University of Turin, 10126 Turin, Italy.
Giulia OrlandoPathology Unit, Department of Oncology, University of Turin, 10126 Turin, Italy.
Cristina BottaPathology Unit, Department of Medical Sciences, University of Turin, 10126 Turin, Italy.ORCID 0000-0003-1320-7484
Pietro ZeppaNeurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.ORCID 0000-0002-8649-3621
Andrea BianconiNeurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.ORCID 0000-0002-1014-0731
Simona Osella-AbatePathology Unit, Department of Medical Sciences, University of Turin, 10126 Turin, Italy.ORCID 0000-0002-9886-7694
Francesco BrunoNeuro-Oncology Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.
Alessia PellerinoNeuro-Oncology Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.ORCID 0000-0003-3243-0059
Roberta RudàNeuro-Oncology Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.
Paola CassoniPathology Unit, Department of Medical Sciences, University of Turin, 10126 Turin, Italy.ORCID 0000-0003-1977-7410
Diego GarbossaNeurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.ORCID 0000-0002-2692-7133
Fabio CofanoNeurosurgery Unit, Department of Neuroscience "Rita Levi Montalcini", University of Turin, 10126 Turin, Italy.
Luca BerteroPathology Unit, Department of Medical Sciences, University of Turin, 10126 Turin, Italy.ORCID 0000-0001-9887-7668
University of Turin · ITNeuroscience Institute · ITUniversity of Ferrara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The G105G SNP (rs11554137) in the IDH1 gene is observed in about 10-15% of patients with a diffuse glioma. Data regarding its impact on gliomas are poor and partially conflicting, possibly due to the evolving classification of CNS tumors. The aim of this study was to investigate the G105G SNP prognostic significance in a homogenous cohort of IDH-wildtype glioblastomas, in agreement with the 2021 WHO classification. The study analyzed 211 patients by collecting several clinico-pathological and molecular characteristics, including the age, lesion localization, number of involved lobes, type of surgical treatment, disease outcome and MGMT promoter methylation status. PFS and DSS curves were plotted according to the Kaplan-Meier method and statistical analyses were performed using parametric and non-parametric tests. A total of 32 patients out of 211 (15.2%) were found to be G105G SNP carriers. No significant impact of the IDH1 G105G SNP on patients' outcomes was observed in terms of PFS and DSS, while MGMT promoter methylation and gross total resection resulted as key prognostic factors in our cohort as expected. No prognostic impact of the IDH1 G105G SNP was detected in this strict cohort of IDH-wildtype glioblastomas. Analysis of larger cohorts is warranted to address the sample size limitations.

Indexed as

Brain NeoplasmsGlioblastomaGliomaPolymorphism, Single NucleotideHumansIsocitrate DehydrogenaseMutationPrognosisIDH1 protein, humanIsocitrate DehydrogenaseglioblastomaIDH1prognosisrs11554137SNP

Identifiers

PMID36011350
PMCPMC9408597
OpenAlexW4291464459

What OpenQuestion holds

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Registered trials

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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.