Loading…
Inheritance of Susceptibility to Malignant Blood Disorders
Malignant blood disorders depend on heritable susceptibility genes and occur in familial aggregations. We suggest a model of transgenerational segregation of the susceptibility genes based on the study of malignant blood disorders in Norwegian and Danish families with unrelated parents, and in the i...
Saved in:
Published in: | Scientific reports 2019-02, Vol.9 (1), p.2444-2444, Article 2444 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c498t-7b962ac9a7465733a1f202344ec631442c5f52eb9a3e9a5af2d68cf29eda11fc3 |
---|---|
cites | cdi_FETCH-LOGICAL-c498t-7b962ac9a7465733a1f202344ec631442c5f52eb9a3e9a5af2d68cf29eda11fc3 |
container_end_page | 2444 |
container_issue | 1 |
container_start_page | 2444 |
container_title | Scientific reports |
container_volume | 9 |
creator | Jønsson, Viggo Awan, Haneef Jones, Neil D. Johannesen, Tom B. Steig, Bjarni á Andosdottir, Gudrid Tjønnfjord, Geir E. |
description | Malignant blood disorders depend on heritable susceptibility genes and occur in familial aggregations. We suggest a model of transgenerational segregation of the susceptibility genes based on the study of malignant blood disorders in Norwegian and Danish families with unrelated parents, and in the inbred Faroese population with related parents. This model, consisting of parental genomic imprinting and mother-son microchimerism, can explain the male predominance in most of the diseases, the predominance of affected parent-offspring when parents are not related, and the different modes of segregation in males and females. The model displays a specific pattern in the distribution of affected relatives for each diagnosis, viz. a characteristic distribution in the pedigrees of family members with malignant blood disorder related to the proband. Three such patterns, each reflecting a specific transgenerational passage, were identified: (1) alterations in the number of affected relatives in paternal lines alone, e.g. in patterns for probands with multiple myeloma; (2) alterations in the number of affected relatives in both paternal and maternal lines for probands with chronic lymphocytic leukemia; and (3) no alterations in the numbers of male and female affected relatives in the parental lines, e.g. for probands with some types of malignant lymphoma. |
doi_str_mv | 10.1038/s41598-019-38879-y |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6385281</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2184516530</sourcerecordid><originalsourceid>FETCH-LOGICAL-c498t-7b962ac9a7465733a1f202344ec631442c5f52eb9a3e9a5af2d68cf29eda11fc3</originalsourceid><addsrcrecordid>eNp9kU9vGyEQxVHVKI6SfIEckpV66WUTGGAXeqjU5r-UqIe2Z4RZ1iZagwtsJX_7kDh20xzCBaT5zXvDPISOCD4lmIqzxAiXosZE1lSIVtarD2gPMOM1UICPr94TdJjSAy6Hg2RE7qIJxa0EBnIPfbn1cxtd1t7YKvTVzzEZu8xu6gaXV1UO1b0e3Mxrn6vvQwhddeFSiJ2N6QDt9HpI9vDl3ke_ry5_nd_Udz-ub8-_3dWGSZHrdiob0EbqljW8pVSTHjBQxqxpKGEMDO852KnU1ErNdQ9dI0wP0naakN7QffR1rbscpwvbGetz1INaRrfQcaWCdur_indzNQt_VUMFB0GKwMlawESXsvPKh6gVwaWqWk5bWYjPLxYx_Bltymrhyh6GQXsbxqSACM4b2goo6Kc36EMYoy8LeKIYJw2nuFCwsQwpRdtvxyVYPeWn1vmpkp96zk-tStPx649uWzZpFYCugVRKfmbjP-93ZB8BkwilJA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2184516530</pqid></control><display><type>article</type><title>Inheritance of Susceptibility to Malignant Blood Disorders</title><source>NORA - Norwegian Open Research Archives</source><source>Publicly Available Content Database</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Jønsson, Viggo ; Awan, Haneef ; Jones, Neil D. ; Johannesen, Tom B. ; Steig, Bjarni á ; Andosdottir, Gudrid ; Tjønnfjord, Geir E.</creator><creatorcontrib>Jønsson, Viggo ; Awan, Haneef ; Jones, Neil D. ; Johannesen, Tom B. ; Steig, Bjarni á ; Andosdottir, Gudrid ; Tjønnfjord, Geir E.</creatorcontrib><description>Malignant blood disorders depend on heritable susceptibility genes and occur in familial aggregations. We suggest a model of transgenerational segregation of the susceptibility genes based on the study of malignant blood disorders in Norwegian and Danish families with unrelated parents, and in the inbred Faroese population with related parents. This model, consisting of parental genomic imprinting and mother-son microchimerism, can explain the male predominance in most of the diseases, the predominance of affected parent-offspring when parents are not related, and the different modes of segregation in males and females. The model displays a specific pattern in the distribution of affected relatives for each diagnosis, viz. a characteristic distribution in the pedigrees of family members with malignant blood disorder related to the proband. Three such patterns, each reflecting a specific transgenerational passage, were identified: (1) alterations in the number of affected relatives in paternal lines alone, e.g. in patterns for probands with multiple myeloma; (2) alterations in the number of affected relatives in both paternal and maternal lines for probands with chronic lymphocytic leukemia; and (3) no alterations in the numbers of male and female affected relatives in the parental lines, e.g. for probands with some types of malignant lymphoma.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-019-38879-y</identifier><identifier>PMID: 30792429</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>38/39 ; 38/44 ; 631/67/68/2486 ; 692/4028/67 ; Blood ; Blood diseases ; Chimerism ; Chronic lymphocytic leukemia ; Genomic imprinting ; Health risk assessment ; Humanities and Social Sciences ; Imprinting ; Inbreeding ; Leukemia ; Lymphatic leukemia ; Lymphoma ; multidisciplinary ; Multiple myeloma ; Offspring ; Science ; Science (multidisciplinary)</subject><ispartof>Scientific reports, 2019-02, Vol.9 (1), p.2444-2444, Article 2444</ispartof><rights>The Author(s) 2019</rights><rights>This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>info:eu-repo/semantics/openAccess</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c498t-7b962ac9a7465733a1f202344ec631442c5f52eb9a3e9a5af2d68cf29eda11fc3</citedby><cites>FETCH-LOGICAL-c498t-7b962ac9a7465733a1f202344ec631442c5f52eb9a3e9a5af2d68cf29eda11fc3</cites><orcidid>0000-0003-1576-871X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2184516530/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2184516530?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,26567,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30792429$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jønsson, Viggo</creatorcontrib><creatorcontrib>Awan, Haneef</creatorcontrib><creatorcontrib>Jones, Neil D.</creatorcontrib><creatorcontrib>Johannesen, Tom B.</creatorcontrib><creatorcontrib>Steig, Bjarni á</creatorcontrib><creatorcontrib>Andosdottir, Gudrid</creatorcontrib><creatorcontrib>Tjønnfjord, Geir E.</creatorcontrib><title>Inheritance of Susceptibility to Malignant Blood Disorders</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Malignant blood disorders depend on heritable susceptibility genes and occur in familial aggregations. We suggest a model of transgenerational segregation of the susceptibility genes based on the study of malignant blood disorders in Norwegian and Danish families with unrelated parents, and in the inbred Faroese population with related parents. This model, consisting of parental genomic imprinting and mother-son microchimerism, can explain the male predominance in most of the diseases, the predominance of affected parent-offspring when parents are not related, and the different modes of segregation in males and females. The model displays a specific pattern in the distribution of affected relatives for each diagnosis, viz. a characteristic distribution in the pedigrees of family members with malignant blood disorder related to the proband. Three such patterns, each reflecting a specific transgenerational passage, were identified: (1) alterations in the number of affected relatives in paternal lines alone, e.g. in patterns for probands with multiple myeloma; (2) alterations in the number of affected relatives in both paternal and maternal lines for probands with chronic lymphocytic leukemia; and (3) no alterations in the numbers of male and female affected relatives in the parental lines, e.g. for probands with some types of malignant lymphoma.</description><subject>38/39</subject><subject>38/44</subject><subject>631/67/68/2486</subject><subject>692/4028/67</subject><subject>Blood</subject><subject>Blood diseases</subject><subject>Chimerism</subject><subject>Chronic lymphocytic leukemia</subject><subject>Genomic imprinting</subject><subject>Health risk assessment</subject><subject>Humanities and Social Sciences</subject><subject>Imprinting</subject><subject>Inbreeding</subject><subject>Leukemia</subject><subject>Lymphatic leukemia</subject><subject>Lymphoma</subject><subject>multidisciplinary</subject><subject>Multiple myeloma</subject><subject>Offspring</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>3HK</sourceid><recordid>eNp9kU9vGyEQxVHVKI6SfIEckpV66WUTGGAXeqjU5r-UqIe2Z4RZ1iZagwtsJX_7kDh20xzCBaT5zXvDPISOCD4lmIqzxAiXosZE1lSIVtarD2gPMOM1UICPr94TdJjSAy6Hg2RE7qIJxa0EBnIPfbn1cxtd1t7YKvTVzzEZu8xu6gaXV1UO1b0e3Mxrn6vvQwhddeFSiJ2N6QDt9HpI9vDl3ke_ry5_nd_Udz-ub8-_3dWGSZHrdiob0EbqljW8pVSTHjBQxqxpKGEMDO852KnU1ErNdQ9dI0wP0naakN7QffR1rbscpwvbGetz1INaRrfQcaWCdur_indzNQt_VUMFB0GKwMlawESXsvPKh6gVwaWqWk5bWYjPLxYx_Bltymrhyh6GQXsbxqSACM4b2goo6Kc36EMYoy8LeKIYJw2nuFCwsQwpRdtvxyVYPeWn1vmpkp96zk-tStPx649uWzZpFYCugVRKfmbjP-93ZB8BkwilJA</recordid><startdate>20190221</startdate><enddate>20190221</enddate><creator>Jønsson, Viggo</creator><creator>Awan, Haneef</creator><creator>Jones, Neil D.</creator><creator>Johannesen, Tom B.</creator><creator>Steig, Bjarni á</creator><creator>Andosdottir, Gudrid</creator><creator>Tjønnfjord, Geir E.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>3HK</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1576-871X</orcidid></search><sort><creationdate>20190221</creationdate><title>Inheritance of Susceptibility to Malignant Blood Disorders</title><author>Jønsson, Viggo ; Awan, Haneef ; Jones, Neil D. ; Johannesen, Tom B. ; Steig, Bjarni á ; Andosdottir, Gudrid ; Tjønnfjord, Geir E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c498t-7b962ac9a7465733a1f202344ec631442c5f52eb9a3e9a5af2d68cf29eda11fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>38/39</topic><topic>38/44</topic><topic>631/67/68/2486</topic><topic>692/4028/67</topic><topic>Blood</topic><topic>Blood diseases</topic><topic>Chimerism</topic><topic>Chronic lymphocytic leukemia</topic><topic>Genomic imprinting</topic><topic>Health risk assessment</topic><topic>Humanities and Social Sciences</topic><topic>Imprinting</topic><topic>Inbreeding</topic><topic>Leukemia</topic><topic>Lymphatic leukemia</topic><topic>Lymphoma</topic><topic>multidisciplinary</topic><topic>Multiple myeloma</topic><topic>Offspring</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jønsson, Viggo</creatorcontrib><creatorcontrib>Awan, Haneef</creatorcontrib><creatorcontrib>Jones, Neil D.</creatorcontrib><creatorcontrib>Johannesen, Tom B.</creatorcontrib><creatorcontrib>Steig, Bjarni á</creatorcontrib><creatorcontrib>Andosdottir, Gudrid</creatorcontrib><creatorcontrib>Tjønnfjord, Geir E.</creatorcontrib><collection>SpringerOpen</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech 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>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>NORA - Norwegian Open Research Archives</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jønsson, Viggo</au><au>Awan, Haneef</au><au>Jones, Neil D.</au><au>Johannesen, Tom B.</au><au>Steig, Bjarni á</au><au>Andosdottir, Gudrid</au><au>Tjønnfjord, Geir E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inheritance of Susceptibility to Malignant Blood Disorders</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2019-02-21</date><risdate>2019</risdate><volume>9</volume><issue>1</issue><spage>2444</spage><epage>2444</epage><pages>2444-2444</pages><artnum>2444</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Malignant blood disorders depend on heritable susceptibility genes and occur in familial aggregations. We suggest a model of transgenerational segregation of the susceptibility genes based on the study of malignant blood disorders in Norwegian and Danish families with unrelated parents, and in the inbred Faroese population with related parents. This model, consisting of parental genomic imprinting and mother-son microchimerism, can explain the male predominance in most of the diseases, the predominance of affected parent-offspring when parents are not related, and the different modes of segregation in males and females. The model displays a specific pattern in the distribution of affected relatives for each diagnosis, viz. a characteristic distribution in the pedigrees of family members with malignant blood disorder related to the proband. Three such patterns, each reflecting a specific transgenerational passage, were identified: (1) alterations in the number of affected relatives in paternal lines alone, e.g. in patterns for probands with multiple myeloma; (2) alterations in the number of affected relatives in both paternal and maternal lines for probands with chronic lymphocytic leukemia; and (3) no alterations in the numbers of male and female affected relatives in the parental lines, e.g. for probands with some types of malignant lymphoma.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30792429</pmid><doi>10.1038/s41598-019-38879-y</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-1576-871X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2045-2322 |
ispartof | Scientific reports, 2019-02, Vol.9 (1), p.2444-2444, Article 2444 |
issn | 2045-2322 2045-2322 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6385281 |
source | NORA - Norwegian Open Research Archives; Publicly Available Content Database; PubMed Central; Free Full-Text Journals in Chemistry; Springer Nature - nature.com Journals - Fully Open Access |
subjects | 38/39 38/44 631/67/68/2486 692/4028/67 Blood Blood diseases Chimerism Chronic lymphocytic leukemia Genomic imprinting Health risk assessment Humanities and Social Sciences Imprinting Inbreeding Leukemia Lymphatic leukemia Lymphoma multidisciplinary Multiple myeloma Offspring Science Science (multidisciplinary) |
title | Inheritance of Susceptibility to Malignant Blood Disorders |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T18%3A26%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Inheritance%20of%20Susceptibility%20to%20Malignant%20Blood%20Disorders&rft.jtitle=Scientific%20reports&rft.au=J%C3%B8nsson,%20Viggo&rft.date=2019-02-21&rft.volume=9&rft.issue=1&rft.spage=2444&rft.epage=2444&rft.pages=2444-2444&rft.artnum=2444&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/s41598-019-38879-y&rft_dat=%3Cproquest_pubme%3E2184516530%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c498t-7b962ac9a7465733a1f202344ec631442c5f52eb9a3e9a5af2d68cf29eda11fc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2184516530&rft_id=info:pmid/30792429&rfr_iscdi=true |