Evidence map›Paper›PMID 34702870›Full record

Trial reportScientific reports2021

Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genes.

Jayant Mahadevan, Ajai Kumar Pathak, Alekhya Vemula, Ravi Kumar Nadella, Biju Viswanath, Sanjeev Jain, Accelerator Program for Discovery in Brain disorders using Stem cells (ADBS) Consortium, Meera Purushottam, Mayukh Mondal

Abstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
  4. Article
  5. 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.

Jayant Mahadevan *Department of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, India.
Ajai Kumar Pathak *Institute of Genomics, University of Tartu, Tartu, Estonia.
Alekhya VemulaDepartment of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, India.
Ravi Kumar NadellaDepartment of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, India.
Biju ViswanathDepartment of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, India.
Sanjeev JainDepartment of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, India.
Accelerator Program for Discovery in Brain disorders using Stem cells (ADBS) Consortium
Meera PurushottamDepartment of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, India. meera.purushottam@gmail.com.
Mayukh MondalInstitute of Genomics, University of Tartu, Tartu, Estonia. mayukh.mondal@ut.ee.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evolutionary trends may underlie some aspects of the risk for common, non-communicable disorders, including psychiatric disease. We analyzed whole exome sequencing data from 80 unique individuals from India coming from families with two or more individuals with severe mental illness. We used Population Branch Statistics (PBS) to identify variants and genes under positive selection and identified 74 genes as candidates for positive selection. Of these, 20 were previously associated with Schizophrenia, Alzheimer's disease and cognitive abilities in genome wide association studies. We then checked whether any of these 74 genes were involved in common biological pathways or related to specific cellular or molecular functions. We found that immune related pathways and functions related to innate immunity such as antigen binding were over-represented. We also evaluated for the presence of Neanderthal introgressed segments in these genes and found Neanderthal introgression in a single gene out of the 74 candidate genes. However, the introgression pattern indicates the region is unlikely to be the source for selection. Our findings hint at how selection pressures in individuals from families with a history of severe mental illness may diverge from the general population. Further, it also provides insights into the genetic architecture of severe mental illness, such as schizophrenia and its link to immune factors.

Indexed as

BrainExome SequencingMental DisordersAnimalsFemaleHumansImmunity, InnateMaleNeanderthals

Identifiers

PMID34702870
PMCPMC8548332

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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.