Evidence map›Paper›PMID 40903457›Full record

ArticleTranslational psychiatry2025

Detecting suicide risk in bipolar disorder patients from lymphoblastoid cell lines genetic signatures.

Omveer Sharma, Ritu Nayak, Liron Mizrahi, Wote Amelo Rike, Ashwani Choudhary, Hagit Sadis, Yara Hussein, Idan Rosh, Utkarsh Tripathi, Aviram Shemen and 4 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Review
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

14 authors.

Omveer Sharma *Sagol Department of Neurobiology, University of Haifa, Haifa, Israel.
Ritu Nayak *Sagol Department of Neurobiology, University of Haifa, Haifa, Israel.
Liron MizrahiSagol Department of Neurobiology, University of Haifa, Haifa, Israel.
Wote Amelo RikeSagol Department of Neurobiology, University of Haifa, Haifa, Israel.
Ashwani ChoudharySagol Department of Neurobiology, University of Haifa, Haifa, Israel.ORCID http://orcid.org/0009-0009-1922-6732
Hagit SadisSagol Department of Neurobiology, University of Haifa, Haifa, Israel.
Yara HusseinSagol Department of Neurobiology, University of Haifa, Haifa, Israel.ORCID http://orcid.org/0000-0001-6173-8584
Idan RoshSagol Department of Neurobiology, University of Haifa, Haifa, Israel.
Utkarsh TripathiSagol Department of Neurobiology, University of Haifa, Haifa, Israel.ORCID http://orcid.org/0000-0001-9503-3793
Aviram ShemenSagol Department of Neurobiology, University of Haifa, Haifa, Israel.
Yam SternSagol Department of Neurobiology, University of Haifa, Haifa, Israel.
Alessio SquassinaDepartment of Biomedical Sciences, University of Cagliari, Cagliari, Italy. squassina@unica.it.ORCID http://orcid.org/0000-0001-7415-7607
Martin AldaDepartment of Psychiatry, Dalhousie University, Halifax, NS, Canada. malda@dal.ca.ORCID http://orcid.org/0000-0001-9544-3944
Shani SternSagol Department of Neurobiology, University of Haifa, Haifa, Israel. sstern@univ.haifa.ac.il.ORCID http://orcid.org/0000-0002-2644-7068

Funding

Dalhousie Medical Research Foundation (DMRF) 166098Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) 166098Israel Science Foundation (ISF) 3252/21
6 · The paper itself

Abstract

This research aimed to develop a machine learning algorithm to predict suicide risk in bipolar disorder (BD) patients using RNA sequencing analysis of lymphoblastoid cell lines (LCLs). By identifying differentially expressed genes (DEGs) between high and low risk patients and their enrichment in relevant pathways, we gained insights into the molecular mechanisms underlying suicide risk. LCL gene expression analysis revealed pathway enrichment related to primary immunodeficiency, ion channels, and cardiovascular defects. Notably, genes such as LCK, KCNN2, and GRIA1 emerged as pivotal, suggesting their potential roles as biomarkers. Machine learning algorithms trained on a subset of the patients and tested on others demonstrated high accuracy in distinguishing low and high risk of suicide in BD patients. Additionally, the study explored the genetic overlap between suicide-related genes and several psychiatric disorders. Our study enhances the understanding of the complex interplay between genetics and suicidal behaviour, providing a foundation for prevention strategies.

Indexed as

Bipolar DisorderGene Expression ProfilingMachine LearningSuicideAdolescentAdultBiomarkersCell LineChildFemaleHumansLymphocyte Specific Protein Tyrosine Kinase p56(lck)MaleReceptors, AMPARisk AssessmentSmall-Conductance Calcium-Activated Potassium ChannelsBiomarkersKCNN2 protein, humanLCK protein, humanLymphocyte Specific Protein Tyrosine Kinase p56(lck)Receptors, AMPASmall-Conductance Calcium-Activated Potassium Channels

Identifiers

PMID40903457
PMCPMC12408843

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.