Risk of multiple myeloma and other malignancies among first‐ and second‐degree relatives of patients with multiple myeloma: A population‐based study

Objectives We conducted a population‐based study to assess the risk for multiple myeloma (MM) and other cancers in first‐ and second‐degree relatives of MM patients, and to investigate whether evidence of anticipation is present in familial MM. Methods We retrieved 24 845 first‐degree relatives and...

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Veröffentlicht in:European journal of haematology 2022-06, Vol.108 (6), p.486-492
Hauptverfasser: Langseth, Øystein O., Myklebust, Tor Å., Johannesen, Tom B., Hjertner, Øyvind, Waage, Anders
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container_end_page 492
container_issue 6
container_start_page 486
container_title European journal of haematology
container_volume 108
creator Langseth, Øystein O.
Myklebust, Tor Å.
Johannesen, Tom B.
Hjertner, Øyvind
Waage, Anders
description Objectives We conducted a population‐based study to assess the risk for multiple myeloma (MM) and other cancers in first‐ and second‐degree relatives of MM patients, and to investigate whether evidence of anticipation is present in familial MM. Methods We retrieved 24 845 first‐degree relatives and 41 008 second‐degree relatives of 7847 MM patients, and 86 984 first‐degree relatives, and 138 660 second‐degree relatives of 26 511 matched controls. A Cox model was used to assess the risk for MM and other cancers in relatives of MM patients. Anticipation was assessed by a Cox model, where all parents and offspring of MM patients were included in the risk set. Results In second‐degree relatives of MM patients, no overall significant association with an MM diagnosis was observed (HR 1.99; 95%CI:0.86–4.57). In parents and offspring of MM patients, we found no significant difference in the ages at onset of MM (HR 1.28;95% CI:0.50–3.28). In affected parent‐offspring pairs, we observed no statistically significant difference in overall survival between the generations (HR 0.74; 95%CI:0.20–2.69). Conclusions Overall, second‐degree relatives of MM patients were not associated with an increased risk for MM. Our study supports that genetic anticipation is not present in familial MM.
doi_str_mv 10.1111/ejh.13757
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Methods We retrieved 24 845 first‐degree relatives and 41 008 second‐degree relatives of 7847 MM patients, and 86 984 first‐degree relatives, and 138 660 second‐degree relatives of 26 511 matched controls. A Cox model was used to assess the risk for MM and other cancers in relatives of MM patients. Anticipation was assessed by a Cox model, where all parents and offspring of MM patients were included in the risk set. Results In second‐degree relatives of MM patients, no overall significant association with an MM diagnosis was observed (HR 1.99; 95%CI:0.86–4.57). In parents and offspring of MM patients, we found no significant difference in the ages at onset of MM (HR 1.28;95% CI:0.50–3.28). In affected parent‐offspring pairs, we observed no statistically significant difference in overall survival between the generations (HR 0.74; 95%CI:0.20–2.69). Conclusions Overall, second‐degree relatives of MM patients were not associated with an increased risk for MM. Our study supports that genetic anticipation is not present in familial MM.</description><identifier>ISSN: 0902-4441</identifier><identifier>EISSN: 1600-0609</identifier><identifier>DOI: 10.1111/ejh.13757</identifier><identifier>PMID: 35184337</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>hematologic neoplasms ; Multiple myeloma ; Original ; Population studies ; Population-based studies ; population‐based study ; relatives. anticipation ; Statistical analysis</subject><ispartof>European journal of haematology, 2022-06, Vol.108 (6), p.486-492</ispartof><rights>2022 The Authors. published by John Wiley &amp; Sons Ltd.</rights><rights>2022 The Authors. European Journal of Haematology published by John Wiley &amp; Sons Ltd.</rights><rights>2022. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). 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Methods We retrieved 24 845 first‐degree relatives and 41 008 second‐degree relatives of 7847 MM patients, and 86 984 first‐degree relatives, and 138 660 second‐degree relatives of 26 511 matched controls. A Cox model was used to assess the risk for MM and other cancers in relatives of MM patients. Anticipation was assessed by a Cox model, where all parents and offspring of MM patients were included in the risk set. Results In second‐degree relatives of MM patients, no overall significant association with an MM diagnosis was observed (HR 1.99; 95%CI:0.86–4.57). In parents and offspring of MM patients, we found no significant difference in the ages at onset of MM (HR 1.28;95% CI:0.50–3.28). In affected parent‐offspring pairs, we observed no statistically significant difference in overall survival between the generations (HR 0.74; 95%CI:0.20–2.69). Conclusions Overall, second‐degree relatives of MM patients were not associated with an increased risk for MM. Our study supports that genetic anticipation is not present in familial MM.</description><subject>hematologic neoplasms</subject><subject>Multiple myeloma</subject><subject>Original</subject><subject>Population studies</subject><subject>Population-based studies</subject><subject>population‐based study</subject><subject>relatives. anticipation</subject><subject>Statistical analysis</subject><issn>0902-4441</issn><issn>1600-0609</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNp1kc1qFTEYhoMo9lhdeAMScKOL0-ZvkhkXhVKqVQqC6DpkZr6ck2MmGZOZlrPzErru5Xklpj21-IMhkIQ835MvvAg9p-SAlnEIm_UB5apSD9CCSkKWRJLmIVqQhrClEILuoSc5bwghrKHqMdrjFa0F52qBrj-5_BVHi4fZT270gIct-DgYbEKP47SGhAfj3SqY0DnI2AwxrLB1KU8_vl_dUhm6GPpy6mGVAHACbyZ3UeDiHcsWwpTxpZvW_7zyBh_jMY7zTUEMRdGaDMU4zf32KXpkjc_w7G7dR1_enn4-OVuef3z3_uT4fNkJwdWybazseCtYa0hvrDGc2abvJWeMtJYpq2QvalA1qamAqhYVq2RlOy4NU7Lu-D462nnHuR2g70q3yXg9JjeYtNXROP3nTXBrvYoXuuGUKF4Xwas7QYrfZsiTHlzuwHsTIM5ZM8lpmVTSgr78C93EOYXyvULJAhLGq0K93lFdijknsPfNUKJvEtclcX2beGFf_N79Pfkr4gIc7oBL52H7f5M-_XC2U_4ECmi7xA</recordid><startdate>202206</startdate><enddate>202206</enddate><creator>Langseth, Øystein O.</creator><creator>Myklebust, Tor Å.</creator><creator>Johannesen, Tom B.</creator><creator>Hjertner, Øyvind</creator><creator>Waage, Anders</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0736-7086</orcidid></search><sort><creationdate>202206</creationdate><title>Risk of multiple myeloma and other malignancies among first‐ and second‐degree relatives of patients with multiple myeloma: A population‐based study</title><author>Langseth, Øystein O. ; Myklebust, Tor Å. ; Johannesen, Tom B. ; Hjertner, Øyvind ; Waage, Anders</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4437-b9f6c3b42ba0dafaa32f9dd63220bf27f76d48e780814e58452565fc36a2768c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>hematologic neoplasms</topic><topic>Multiple myeloma</topic><topic>Original</topic><topic>Population studies</topic><topic>Population-based studies</topic><topic>population‐based study</topic><topic>relatives. anticipation</topic><topic>Statistical analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Langseth, Øystein O.</creatorcontrib><creatorcontrib>Myklebust, Tor Å.</creatorcontrib><creatorcontrib>Johannesen, Tom B.</creatorcontrib><creatorcontrib>Hjertner, Øyvind</creatorcontrib><creatorcontrib>Waage, Anders</creatorcontrib><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Langseth, Øystein O.</au><au>Myklebust, Tor Å.</au><au>Johannesen, Tom B.</au><au>Hjertner, Øyvind</au><au>Waage, Anders</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk of multiple myeloma and other malignancies among first‐ and second‐degree relatives of patients with multiple myeloma: A population‐based study</atitle><jtitle>European journal of haematology</jtitle><addtitle>Eur J Haematol</addtitle><date>2022-06</date><risdate>2022</risdate><volume>108</volume><issue>6</issue><spage>486</spage><epage>492</epage><pages>486-492</pages><issn>0902-4441</issn><eissn>1600-0609</eissn><abstract>Objectives We conducted a population‐based study to assess the risk for multiple myeloma (MM) and other cancers in first‐ and second‐degree relatives of MM patients, and to investigate whether evidence of anticipation is present in familial MM. Methods We retrieved 24 845 first‐degree relatives and 41 008 second‐degree relatives of 7847 MM patients, and 86 984 first‐degree relatives, and 138 660 second‐degree relatives of 26 511 matched controls. A Cox model was used to assess the risk for MM and other cancers in relatives of MM patients. Anticipation was assessed by a Cox model, where all parents and offspring of MM patients were included in the risk set. Results In second‐degree relatives of MM patients, no overall significant association with an MM diagnosis was observed (HR 1.99; 95%CI:0.86–4.57). In parents and offspring of MM patients, we found no significant difference in the ages at onset of MM (HR 1.28;95% CI:0.50–3.28). In affected parent‐offspring pairs, we observed no statistically significant difference in overall survival between the generations (HR 0.74; 95%CI:0.20–2.69). Conclusions Overall, second‐degree relatives of MM patients were not associated with an increased risk for MM. 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subjects hematologic neoplasms
Multiple myeloma
Original
Population studies
Population-based studies
population‐based study
relatives. anticipation
Statistical analysis
title Risk of multiple myeloma and other malignancies among first‐ and second‐degree relatives of patients with multiple myeloma: A population‐based study
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