Evidence map›Paper›PMID 35205123›Full record

ArticleBiology2022

Agent-Based Modeling of Autosomal Recessive Deafness 1A (DFNB1A) Prevalence with Regard to Intensity of Selection Pressure in Isolated Human Population.

Georgii P Romanov, Anna A Smirnova, Vladimir I Zamyatin, Aleksey M Mukhin, Fedor V Kazantsev, Vera G Pshennikova, Fedor M Teryutin, Aisen V Solovyev, Sardana A Fedorova, Olga L Posukh and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 54% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. TheGenes · 2023
    Article
  3. 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

12 authors at 3 institutions in 1 country.

Georgii P RomanovLaboratory of Molecular Biology, M. K. Ammosov North-Eastern Federal University, Kulakovskogo 46, 677010 Yakutsk, Russia.ORCID 0000-0002-2936-5818
Anna A SmirnovaSector for Computer Analysis and Modeling of Biological Systems, Federal Research Center Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Lavrentyeva 10, 630090 Novosibirsk, Russia.
Vladimir I ZamyatinSector for Computer Analysis and Modeling of Biological Systems, Federal Research Center Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Lavrentyeva 10, 630090 Novosibirsk, Russia.
Aleksey M MukhinSector for Computer Analysis and Modeling of Biological Systems, Federal Research Center Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Lavrentyeva 10, 630090 Novosibirsk, Russia.ORCID 0000-0002-1102-0934
Fedor V KazantsevSector for Computer Analysis and Modeling of Biological Systems, Federal Research Center Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Lavrentyeva 10, 630090 Novosibirsk, Russia.ORCID 0000-0002-5711-7539
Vera G PshennikovaLaboratory of Molecular Genetics, Yakut Science Centre of Complex Medical Problems, Yaroslavskogo 6/3, 677000 Yakutsk, Russia.
Fedor M TeryutinLaboratory of Molecular Biology, M. K. Ammosov North-Eastern Federal University, Kulakovskogo 46, 677010 Yakutsk, Russia.
Aisen V SolovyevLaboratory of Molecular Biology, M. K. Ammosov North-Eastern Federal University, Kulakovskogo 46, 677010 Yakutsk, Russia.
Sardana A FedorovaLaboratory of Molecular Biology, M. K. Ammosov North-Eastern Federal University, Kulakovskogo 46, 677010 Yakutsk, Russia.ORCID 0000-0002-6952-3868
Olga L PosukhNovosibirsk State University, Pirogova 1, 630090 Novosibirsk, Russia.ORCID 0000-0003-1352-3591
Sergey A LashinSector for Computer Analysis and Modeling of Biological Systems, Federal Research Center Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Lavrentyeva 10, 630090 Novosibirsk, Russia.ORCID 0000-0003-3138-381X
Nikolay A BarashkovLaboratory of Molecular Biology, M. K. Ammosov North-Eastern Federal University, Kulakovskogo 46, 677010 Yakutsk, Russia.ORCID 0000-0002-6984-7934
North-Eastern Federal University · RUInstitute of Cytology and Genetics · RUNovosibirsk State University · RU

Funding

Ministry of Science and High Education of the Russian Federation FSRG-2020-0016Project of the YSC CMP "Study of the genetic structure and burden of hereditary pathology in the populations of the Republic of Sakha (Yakutia)" noRFBR 18-05-60035_ArctikaRFBR 20-015-00328_ARussian State Budget program 0259-2021-0014.
6 · The paper itself

Abstract

An increase in the prevalence of autosomal recessive deafness 1A (DFNB1A) in populations of European descent was shown to be promoted by assortative marriages among deaf people. Assortative marriages became possible with the widespread introduction of sign language, resulting in increased genetic fitness of deaf individuals and, thereby, relaxing selection against deafness. However, the effect of this phenomenon was not previously studied in populations with different genetic structures. We developed an agent-based computer model for the analysis of the spread of DFNB1A. Using this model, we tested the impact of different intensities of selection pressure against deafness in an isolated human population over 400 years. Modeling of the "purifying" selection pressure on deafness ("No deaf mating" scenario) resulted in a decrease in the proportion of deaf individuals and the pathogenic allele frequency. Modeling of the "relaxed" selection ("Assortative mating" scenario) resulted in an increase in the proportion of deaf individuals in the first four generations, which then quickly plateaued with a subsequent decline and a decrease in the pathogenic allele frequency. The results of neutral selection pressure modeling ("Random mating" scenario) showed no significant changes in the proportion of deaf individuals or the pathogenic allele frequency after 400 years.

Indexed as

agent-based computer modelingassortative matinggenetic fitnessGJB2hereditary deafnessisolated populationsign language

Identifiers

PMID35205123
PMCPMC8869167
OpenAlexW4210926144

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.