A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia
The absence of comparable epidemiological data challenges the correct estimation of the prevalence of congenital hearing loss (HL) around the world. Sign language (SL) is known as the main type of communication of deaf people. We suggest that the distribution of SL can be interpreted as an indirect...
Gespeichert in:
Veröffentlicht in: | PloS one 2020-11, Vol.15 (11), p.e0242219-e0242219 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e0242219 |
---|---|
container_issue | 11 |
container_start_page | e0242219 |
container_title | PloS one |
container_volume | 15 |
creator | Romanov, Georgii P Pshennikova, Vera G Lashin, Sergey A Solovyev, Aisen V Teryutin, Fedor M Cherdonova, Aleksandra M Borisova, Tuyara V Sazonov, Nikolay N Khusnutdinova, Elza K Posukh, Olga L Fedorova, Sardana A Barashkov, Nikolay A |
description | The absence of comparable epidemiological data challenges the correct estimation of the prevalence of congenital hearing loss (HL) around the world. Sign language (SL) is known as the main type of communication of deaf people. We suggest that the distribution of SL can be interpreted as an indirect indicator of the prevalence of congenital HL. Since a significant part of congenital HL is due to genetic causes, an assessment of the distribution of SL users can reveal regions with an extensive accumulation of hereditary HL. For the first time, we analyzed the data on the distribution of SL users that became available for the total population of Russia by the 2010 census. Seventy-three out of 85 federal regions of Russia were ranked into three groups by the 25th and 75th percentiles of the proportion of SL users: 14 regions-"low proportion"; 48 regions-"average proportion"; and 11 regions-"high proportion". We consider that the observed uneven prevalence of SL users can reflect underlying hereditary forms of congenital HL accumulated in certain populations by specific genetic background and population structure. At least, the data from this study indicate that the highest proportions of SL users detected in some Siberian regions are consistent with the reported accumulation of specific hereditary HL forms in indigenous Yakut, Tuvinian and Altaian populations. |
doi_str_mv | 10.1371/journal.pone.0242219 |
format | Article |
fullrecord | <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_2465724661</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A643313546</galeid><doaj_id>oai_doaj_org_article_1fad53822f4a4f9f985e33c6a373c125</doaj_id><sourcerecordid>A643313546</sourcerecordid><originalsourceid>FETCH-LOGICAL-c692t-269061e55d519d41e8945f9b2219fb9fcbccae9519c232fb70f401cdd3299af33</originalsourceid><addsrcrecordid>eNqNk21rFDEQxxdRbK1-A9GAIPrizs3D7l58IRzFh0KhUB_ehmx2speyl5xJttoP43d19notPekLWciGyW8mmf_MFMVzWs4pb-i7izBGr4f5JniYl0wwRuWD4pBKzmY1K_nDO_uD4klKF2VZ8UVdPy4OOGcVZ6I6LP4siYdfRG82MWizIjkQSNmtdXa-J3kFZBPhUg_gDZBgyQoidC7reIVbHSdoCCm9J0tPND7nKrk0cZNn51KOrh2zC36yJdd7Mmjfj7oHMiaIibQ6QUfw3IBPYyKdzpo4T87HlJx-WjyyekjwbPc_Kr5_-vjt-Mvs9OzzyfHydGZqyfKM1bKsKVRVV1HZCQoLKSor20kS20prWmM0SDw0jDPbNqUVJTVdx5mU2nJ-VLy8jrvBZNRO2aSYqKsGl5oicXJNdEFfqE1EheKVCtqprSHEXumYnRlAUas7FJoxK7Sw0spFBZybWvOGG4rCHxUfdreN7Ro6zDxHPewF3T_xbqX6cKmapuSLRmCAN7sAMfwcsV5q7ZKBAbWFMG7fXZeCigVD9NU_6P3Z7ageK62ctwHvNVNQtawF55RXokZqfg-FXwdrZ7ANrUP7nsPbPQdkMvzOvcbiqpOv5__Pnv3YZ1_fYbEPh7xKYdg2WtoHxTVoIjZpBHsrMi3VNEU3aqhpitRuitDtxd0C3TrdjA3_C48KGPQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2465724661</pqid></control><display><type>article</type><title>A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Public Library of Science (PLoS)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Romanov, Georgii P ; Pshennikova, Vera G ; Lashin, Sergey A ; Solovyev, Aisen V ; Teryutin, Fedor M ; Cherdonova, Aleksandra M ; Borisova, Tuyara V ; Sazonov, Nikolay N ; Khusnutdinova, Elza K ; Posukh, Olga L ; Fedorova, Sardana A ; Barashkov, Nikolay A</creator><contributor>Azaiez, Hela</contributor><creatorcontrib>Romanov, Georgii P ; Pshennikova, Vera G ; Lashin, Sergey A ; Solovyev, Aisen V ; Teryutin, Fedor M ; Cherdonova, Aleksandra M ; Borisova, Tuyara V ; Sazonov, Nikolay N ; Khusnutdinova, Elza K ; Posukh, Olga L ; Fedorova, Sardana A ; Barashkov, Nikolay A ; Azaiez, Hela</creatorcontrib><description>The absence of comparable epidemiological data challenges the correct estimation of the prevalence of congenital hearing loss (HL) around the world. Sign language (SL) is known as the main type of communication of deaf people. We suggest that the distribution of SL can be interpreted as an indirect indicator of the prevalence of congenital HL. Since a significant part of congenital HL is due to genetic causes, an assessment of the distribution of SL users can reveal regions with an extensive accumulation of hereditary HL. For the first time, we analyzed the data on the distribution of SL users that became available for the total population of Russia by the 2010 census. Seventy-three out of 85 federal regions of Russia were ranked into three groups by the 25th and 75th percentiles of the proportion of SL users: 14 regions-"low proportion"; 48 regions-"average proportion"; and 11 regions-"high proportion". We consider that the observed uneven prevalence of SL users can reflect underlying hereditary forms of congenital HL accumulated in certain populations by specific genetic background and population structure. At least, the data from this study indicate that the highest proportions of SL users detected in some Siberian regions are consistent with the reported accumulation of specific hereditary HL forms in indigenous Yakut, Tuvinian and Altaian populations.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0242219</identifier><identifier>PMID: 33253245</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Accumulation ; Biology and Life Sciences ; Cellular biology ; Census ; Census of Population ; Censuses ; Congenital diseases ; Deafness ; Deafness - congenital ; Deafness - epidemiology ; Epidemiology ; Genetic disorders ; Genetics ; Hearing ; Hearing loss ; Humans ; Industrialized nations ; Laboratories ; Language ; Medical screening ; Medicine and Health Sciences ; Methods ; Molecular biology ; People and Places ; Population genetics ; Population structure ; Populations ; Prevalence ; Prevalence studies (Epidemiology) ; Research and Analysis Methods ; Russia - epidemiology ; Sign Language ; Social Sciences ; Statistics ; User statistics</subject><ispartof>PloS one, 2020-11, Vol.15 (11), p.e0242219-e0242219</ispartof><rights>COPYRIGHT 2020 Public Library of Science</rights><rights>2020 Romanov et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 Romanov et al 2020 Romanov et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-269061e55d519d41e8945f9b2219fb9fcbccae9519c232fb70f401cdd3299af33</citedby><cites>FETCH-LOGICAL-c692t-269061e55d519d41e8945f9b2219fb9fcbccae9519c232fb70f401cdd3299af33</cites><orcidid>0000-0002-6984-7934 ; 0000-0003-3138-381X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703874/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703874/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2926,23864,27922,27923,53789,53791,79370,79371</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33253245$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Azaiez, Hela</contributor><creatorcontrib>Romanov, Georgii P</creatorcontrib><creatorcontrib>Pshennikova, Vera G</creatorcontrib><creatorcontrib>Lashin, Sergey A</creatorcontrib><creatorcontrib>Solovyev, Aisen V</creatorcontrib><creatorcontrib>Teryutin, Fedor M</creatorcontrib><creatorcontrib>Cherdonova, Aleksandra M</creatorcontrib><creatorcontrib>Borisova, Tuyara V</creatorcontrib><creatorcontrib>Sazonov, Nikolay N</creatorcontrib><creatorcontrib>Khusnutdinova, Elza K</creatorcontrib><creatorcontrib>Posukh, Olga L</creatorcontrib><creatorcontrib>Fedorova, Sardana A</creatorcontrib><creatorcontrib>Barashkov, Nikolay A</creatorcontrib><title>A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The absence of comparable epidemiological data challenges the correct estimation of the prevalence of congenital hearing loss (HL) around the world. Sign language (SL) is known as the main type of communication of deaf people. We suggest that the distribution of SL can be interpreted as an indirect indicator of the prevalence of congenital HL. Since a significant part of congenital HL is due to genetic causes, an assessment of the distribution of SL users can reveal regions with an extensive accumulation of hereditary HL. For the first time, we analyzed the data on the distribution of SL users that became available for the total population of Russia by the 2010 census. Seventy-three out of 85 federal regions of Russia were ranked into three groups by the 25th and 75th percentiles of the proportion of SL users: 14 regions-"low proportion"; 48 regions-"average proportion"; and 11 regions-"high proportion". We consider that the observed uneven prevalence of SL users can reflect underlying hereditary forms of congenital HL accumulated in certain populations by specific genetic background and population structure. At least, the data from this study indicate that the highest proportions of SL users detected in some Siberian regions are consistent with the reported accumulation of specific hereditary HL forms in indigenous Yakut, Tuvinian and Altaian populations.</description><subject>Accumulation</subject><subject>Biology and Life Sciences</subject><subject>Cellular biology</subject><subject>Census</subject><subject>Census of Population</subject><subject>Censuses</subject><subject>Congenital diseases</subject><subject>Deafness</subject><subject>Deafness - congenital</subject><subject>Deafness - epidemiology</subject><subject>Epidemiology</subject><subject>Genetic disorders</subject><subject>Genetics</subject><subject>Hearing</subject><subject>Hearing loss</subject><subject>Humans</subject><subject>Industrialized nations</subject><subject>Laboratories</subject><subject>Language</subject><subject>Medical screening</subject><subject>Medicine and Health Sciences</subject><subject>Methods</subject><subject>Molecular biology</subject><subject>People and Places</subject><subject>Population genetics</subject><subject>Population structure</subject><subject>Populations</subject><subject>Prevalence</subject><subject>Prevalence studies (Epidemiology)</subject><subject>Research and Analysis Methods</subject><subject>Russia - epidemiology</subject><subject>Sign Language</subject><subject>Social Sciences</subject><subject>Statistics</subject><subject>User statistics</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk21rFDEQxxdRbK1-A9GAIPrizs3D7l58IRzFh0KhUB_ehmx2speyl5xJttoP43d19notPekLWciGyW8mmf_MFMVzWs4pb-i7izBGr4f5JniYl0wwRuWD4pBKzmY1K_nDO_uD4klKF2VZ8UVdPy4OOGcVZ6I6LP4siYdfRG82MWizIjkQSNmtdXa-J3kFZBPhUg_gDZBgyQoidC7reIVbHSdoCCm9J0tPND7nKrk0cZNn51KOrh2zC36yJdd7Mmjfj7oHMiaIibQ6QUfw3IBPYyKdzpo4T87HlJx-WjyyekjwbPc_Kr5_-vjt-Mvs9OzzyfHydGZqyfKM1bKsKVRVV1HZCQoLKSor20kS20prWmM0SDw0jDPbNqUVJTVdx5mU2nJ-VLy8jrvBZNRO2aSYqKsGl5oicXJNdEFfqE1EheKVCtqprSHEXumYnRlAUas7FJoxK7Sw0spFBZybWvOGG4rCHxUfdreN7Ro6zDxHPewF3T_xbqX6cKmapuSLRmCAN7sAMfwcsV5q7ZKBAbWFMG7fXZeCigVD9NU_6P3Z7ageK62ctwHvNVNQtawF55RXokZqfg-FXwdrZ7ANrUP7nsPbPQdkMvzOvcbiqpOv5__Pnv3YZ1_fYbEPh7xKYdg2WtoHxTVoIjZpBHsrMi3VNEU3aqhpitRuitDtxd0C3TrdjA3_C48KGPQ</recordid><startdate>20201130</startdate><enddate>20201130</enddate><creator>Romanov, Georgii P</creator><creator>Pshennikova, Vera G</creator><creator>Lashin, Sergey A</creator><creator>Solovyev, Aisen V</creator><creator>Teryutin, Fedor M</creator><creator>Cherdonova, Aleksandra M</creator><creator>Borisova, Tuyara V</creator><creator>Sazonov, Nikolay N</creator><creator>Khusnutdinova, Elza K</creator><creator>Posukh, Olga L</creator><creator>Fedorova, Sardana A</creator><creator>Barashkov, Nikolay A</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6984-7934</orcidid><orcidid>https://orcid.org/0000-0003-3138-381X</orcidid></search><sort><creationdate>20201130</creationdate><title>A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia</title><author>Romanov, Georgii P ; Pshennikova, Vera G ; Lashin, Sergey A ; Solovyev, Aisen V ; Teryutin, Fedor M ; Cherdonova, Aleksandra M ; Borisova, Tuyara V ; Sazonov, Nikolay N ; Khusnutdinova, Elza K ; Posukh, Olga L ; Fedorova, Sardana A ; Barashkov, Nikolay A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-269061e55d519d41e8945f9b2219fb9fcbccae9519c232fb70f401cdd3299af33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Accumulation</topic><topic>Biology and Life Sciences</topic><topic>Cellular biology</topic><topic>Census</topic><topic>Census of Population</topic><topic>Censuses</topic><topic>Congenital diseases</topic><topic>Deafness</topic><topic>Deafness - congenital</topic><topic>Deafness - epidemiology</topic><topic>Epidemiology</topic><topic>Genetic disorders</topic><topic>Genetics</topic><topic>Hearing</topic><topic>Hearing loss</topic><topic>Humans</topic><topic>Industrialized nations</topic><topic>Laboratories</topic><topic>Language</topic><topic>Medical screening</topic><topic>Medicine and Health Sciences</topic><topic>Methods</topic><topic>Molecular biology</topic><topic>People and Places</topic><topic>Population genetics</topic><topic>Population structure</topic><topic>Populations</topic><topic>Prevalence</topic><topic>Prevalence studies (Epidemiology)</topic><topic>Research and Analysis Methods</topic><topic>Russia - epidemiology</topic><topic>Sign Language</topic><topic>Social Sciences</topic><topic>Statistics</topic><topic>User statistics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Romanov, Georgii P</creatorcontrib><creatorcontrib>Pshennikova, Vera G</creatorcontrib><creatorcontrib>Lashin, Sergey A</creatorcontrib><creatorcontrib>Solovyev, Aisen V</creatorcontrib><creatorcontrib>Teryutin, Fedor M</creatorcontrib><creatorcontrib>Cherdonova, Aleksandra M</creatorcontrib><creatorcontrib>Borisova, Tuyara V</creatorcontrib><creatorcontrib>Sazonov, Nikolay N</creatorcontrib><creatorcontrib>Khusnutdinova, Elza K</creatorcontrib><creatorcontrib>Posukh, Olga L</creatorcontrib><creatorcontrib>Fedorova, Sardana A</creatorcontrib><creatorcontrib>Barashkov, Nikolay A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Romanov, Georgii P</au><au>Pshennikova, Vera G</au><au>Lashin, Sergey A</au><au>Solovyev, Aisen V</au><au>Teryutin, Fedor M</au><au>Cherdonova, Aleksandra M</au><au>Borisova, Tuyara V</au><au>Sazonov, Nikolay N</au><au>Khusnutdinova, Elza K</au><au>Posukh, Olga L</au><au>Fedorova, Sardana A</au><au>Barashkov, Nikolay A</au><au>Azaiez, Hela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2020-11-30</date><risdate>2020</risdate><volume>15</volume><issue>11</issue><spage>e0242219</spage><epage>e0242219</epage><pages>e0242219-e0242219</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The absence of comparable epidemiological data challenges the correct estimation of the prevalence of congenital hearing loss (HL) around the world. Sign language (SL) is known as the main type of communication of deaf people. We suggest that the distribution of SL can be interpreted as an indirect indicator of the prevalence of congenital HL. Since a significant part of congenital HL is due to genetic causes, an assessment of the distribution of SL users can reveal regions with an extensive accumulation of hereditary HL. For the first time, we analyzed the data on the distribution of SL users that became available for the total population of Russia by the 2010 census. Seventy-three out of 85 federal regions of Russia were ranked into three groups by the 25th and 75th percentiles of the proportion of SL users: 14 regions-"low proportion"; 48 regions-"average proportion"; and 11 regions-"high proportion". We consider that the observed uneven prevalence of SL users can reflect underlying hereditary forms of congenital HL accumulated in certain populations by specific genetic background and population structure. At least, the data from this study indicate that the highest proportions of SL users detected in some Siberian regions are consistent with the reported accumulation of specific hereditary HL forms in indigenous Yakut, Tuvinian and Altaian populations.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>33253245</pmid><doi>10.1371/journal.pone.0242219</doi><tpages>e0242219</tpages><orcidid>https://orcid.org/0000-0002-6984-7934</orcidid><orcidid>https://orcid.org/0000-0003-3138-381X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2020-11, Vol.15 (11), p.e0242219-e0242219 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2465724661 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science (PLoS); EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Accumulation Biology and Life Sciences Cellular biology Census Census of Population Censuses Congenital diseases Deafness Deafness - congenital Deafness - epidemiology Epidemiology Genetic disorders Genetics Hearing Hearing loss Humans Industrialized nations Laboratories Language Medical screening Medicine and Health Sciences Methods Molecular biology People and Places Population genetics Population structure Populations Prevalence Prevalence studies (Epidemiology) Research and Analysis Methods Russia - epidemiology Sign Language Social Sciences Statistics User statistics |
title | A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T20%3A35%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20new%20approach%20to%20estimating%20the%20prevalence%20of%20hereditary%20hearing%20loss:%20An%20analysis%20of%20the%20distribution%20of%20sign%20language%20users%20based%20on%20census%20data%20in%20Russia&rft.jtitle=PloS%20one&rft.au=Romanov,%20Georgii%20P&rft.date=2020-11-30&rft.volume=15&rft.issue=11&rft.spage=e0242219&rft.epage=e0242219&rft.pages=e0242219-e0242219&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0242219&rft_dat=%3Cgale_plos_%3EA643313546%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2465724661&rft_id=info:pmid/33253245&rft_galeid=A643313546&rft_doaj_id=oai_doaj_org_article_1fad53822f4a4f9f985e33c6a373c125&rfr_iscdi=true |