Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach
Simple Summary Health-related quality of life (HRQOL) is associated with cancer prognosis as well as with age, sex, race, and lifestyle factors, including diet and physical activity. To investigate the hypothesis that HRQOL has genetic underpinnings in patients with cancer, we performed a genome-wid...
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Veröffentlicht in: | Cancers 2021-02, Vol.13 (4), p.716, Article 716 |
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description | Simple Summary
Health-related quality of life (HRQOL) is associated with cancer prognosis as well as with age, sex, race, and lifestyle factors, including diet and physical activity. To investigate the hypothesis that HRQOL has genetic underpinnings in patients with cancer, we performed a genome-wide association study to evaluate genetic variants (single nucleotide polymorphisms, SNPs) associated with mental and physical QOL as measured by the PROMIS assessment tool in breast cancer survivors participating in a longitudinal cohort study, the Mayo Clinic Breast Disease Registry (MCBDR). Age and financial concerns were associated with worse physical and mental health, and previous receipt of chemotherapy was associated with worse mental health. SNPs in SCN10A, LMX1B, SGCD, PARP12, and SEMA5A were associated with physical and mental QOL, but none at the genome-wide significance thresholds of p < 5 x 10(-8).
Health-related quality of life (HRQOL) is an important prognostic patient-reported outcome in oncology. Because prior studies suggest that HRQOL is, in part, heritable, we performed a GWAS to elucidate genetic factors associated with HRQOL in breast cancer survivors. Physical and mental HRQOL were measured via paper surveys that included the PROMIS-10 physical and mental health domain scales in 1442 breast cancer survivors participating in the Mayo Clinic Breast Disease Registry (MCBDR). In multivariable regression analyses, age and financial concerns were significantly associated with global physical health (age: p = 1.6 x 10(-23); financial concerns: p = 4.8 x 10(-40)) and mental health (age: p = 3.5 x 10(-7); financial concerns: p = 2.0 x 10(-69)). Chemotherapy was associated with worse global mental health (p = 0.01). In the GWAS, none of the SNPs reached the genome-wide association significance threshold of 5 x 10(-8) for associations with either global physical or global mental health, however, a cluster of SNPs in SCN10A, particularly rs112718371, appeared to be linked to worse global physical health (p = 5.21 x 10(-8)). Additionally, SNPs in LMX1B, SGCD, PARP12 and SEMA5A were also moderately associated with worse physical and mental health (p < 10(-6)). These biologically plausible candidate SNPs warrant further study as possible predictors of HRQOL. |
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Health-related quality of life (HRQOL) is associated with cancer prognosis as well as with age, sex, race, and lifestyle factors, including diet and physical activity. To investigate the hypothesis that HRQOL has genetic underpinnings in patients with cancer, we performed a genome-wide association study to evaluate genetic variants (single nucleotide polymorphisms, SNPs) associated with mental and physical QOL as measured by the PROMIS assessment tool in breast cancer survivors participating in a longitudinal cohort study, the Mayo Clinic Breast Disease Registry (MCBDR). Age and financial concerns were associated with worse physical and mental health, and previous receipt of chemotherapy was associated with worse mental health. SNPs in SCN10A, LMX1B, SGCD, PARP12, and SEMA5A were associated with physical and mental QOL, but none at the genome-wide significance thresholds of p < 5 x 10(-8).
Health-related quality of life (HRQOL) is an important prognostic patient-reported outcome in oncology. Because prior studies suggest that HRQOL is, in part, heritable, we performed a GWAS to elucidate genetic factors associated with HRQOL in breast cancer survivors. Physical and mental HRQOL were measured via paper surveys that included the PROMIS-10 physical and mental health domain scales in 1442 breast cancer survivors participating in the Mayo Clinic Breast Disease Registry (MCBDR). In multivariable regression analyses, age and financial concerns were significantly associated with global physical health (age: p = 1.6 x 10(-23); financial concerns: p = 4.8 x 10(-40)) and mental health (age: p = 3.5 x 10(-7); financial concerns: p = 2.0 x 10(-69)). Chemotherapy was associated with worse global mental health (p = 0.01). In the GWAS, none of the SNPs reached the genome-wide association significance threshold of 5 x 10(-8) for associations with either global physical or global mental health, however, a cluster of SNPs in SCN10A, particularly rs112718371, appeared to be linked to worse global physical health (p = 5.21 x 10(-8)). Additionally, SNPs in LMX1B, SGCD, PARP12 and SEMA5A were also moderately associated with worse physical and mental health (p < 10(-6)). These biologically plausible candidate SNPs warrant further study as possible predictors of HRQOL.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers13040716</identifier><identifier>PMID: 33578652</identifier><language>eng</language><publisher>BASEL: Mdpi</publisher><subject>Age ; Breast cancer ; Cancer therapies ; Chemotherapy ; Chromosomes ; Disease ; Expected values ; Genes ; Genetic diversity ; Genetic factors ; Genomes ; Inflammation ; Life Sciences & Biomedicine ; Lung cancer ; Medical diagnosis ; Mental health ; Metabolism ; Oncology ; Pain ; Quality of life ; Science & Technology ; Single-nucleotide polymorphism</subject><ispartof>Cancers, 2021-02, Vol.13 (4), p.716, Article 716</ispartof><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>2</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000623348300001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c487t-6f48848f89c261bf49972e3cb9811f65f032487139d877c7abd8f5c45a77a9a63</citedby><cites>FETCH-LOGICAL-c487t-6f48848f89c261bf49972e3cb9811f65f032487139d877c7abd8f5c45a77a9a63</cites><orcidid>0000-0003-4516-8088 ; 0000-0002-2234-7430</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/PMC7916362/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916362/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,39263,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33578652$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Adjei, Araba A.</creatorcontrib><creatorcontrib>Lopez, Camden L.</creatorcontrib><creatorcontrib>Schaid, Daniel J.</creatorcontrib><creatorcontrib>Sloan, Jeff A.</creatorcontrib><creatorcontrib>Le-Rademacher, Jennifer G.</creatorcontrib><creatorcontrib>Loprinzi, Charles L.</creatorcontrib><creatorcontrib>Norman, Aaron D.</creatorcontrib><creatorcontrib>Olson, Janet E.</creatorcontrib><creatorcontrib>Couch, Fergus J.</creatorcontrib><creatorcontrib>Beutler, Andreas S.</creatorcontrib><creatorcontrib>Vachon, Celine M.</creatorcontrib><creatorcontrib>Ruddy, Kathryn J.</creatorcontrib><title>Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach</title><title>Cancers</title><addtitle>CANCERS</addtitle><addtitle>Cancers (Basel)</addtitle><description>Simple Summary
Health-related quality of life (HRQOL) is associated with cancer prognosis as well as with age, sex, race, and lifestyle factors, including diet and physical activity. To investigate the hypothesis that HRQOL has genetic underpinnings in patients with cancer, we performed a genome-wide association study to evaluate genetic variants (single nucleotide polymorphisms, SNPs) associated with mental and physical QOL as measured by the PROMIS assessment tool in breast cancer survivors participating in a longitudinal cohort study, the Mayo Clinic Breast Disease Registry (MCBDR). Age and financial concerns were associated with worse physical and mental health, and previous receipt of chemotherapy was associated with worse mental health. SNPs in SCN10A, LMX1B, SGCD, PARP12, and SEMA5A were associated with physical and mental QOL, but none at the genome-wide significance thresholds of p < 5 x 10(-8).
Health-related quality of life (HRQOL) is an important prognostic patient-reported outcome in oncology. Because prior studies suggest that HRQOL is, in part, heritable, we performed a GWAS to elucidate genetic factors associated with HRQOL in breast cancer survivors. Physical and mental HRQOL were measured via paper surveys that included the PROMIS-10 physical and mental health domain scales in 1442 breast cancer survivors participating in the Mayo Clinic Breast Disease Registry (MCBDR). In multivariable regression analyses, age and financial concerns were significantly associated with global physical health (age: p = 1.6 x 10(-23); financial concerns: p = 4.8 x 10(-40)) and mental health (age: p = 3.5 x 10(-7); financial concerns: p = 2.0 x 10(-69)). Chemotherapy was associated with worse global mental health (p = 0.01). In the GWAS, none of the SNPs reached the genome-wide association significance threshold of 5 x 10(-8) for associations with either global physical or global mental health, however, a cluster of SNPs in SCN10A, particularly rs112718371, appeared to be linked to worse global physical health (p = 5.21 x 10(-8)). Additionally, SNPs in LMX1B, SGCD, PARP12 and SEMA5A were also moderately associated with worse physical and mental health (p < 10(-6)). These biologically plausible candidate SNPs warrant further study as possible predictors of HRQOL.</description><subject>Age</subject><subject>Breast cancer</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Chromosomes</subject><subject>Disease</subject><subject>Expected values</subject><subject>Genes</subject><subject>Genetic diversity</subject><subject>Genetic factors</subject><subject>Genomes</subject><subject>Inflammation</subject><subject>Life Sciences & Biomedicine</subject><subject>Lung cancer</subject><subject>Medical diagnosis</subject><subject>Mental health</subject><subject>Metabolism</subject><subject>Oncology</subject><subject>Pain</subject><subject>Quality of life</subject><subject>Science & Technology</subject><subject>Single-nucleotide polymorphism</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkc1rFDEYh4MottSevUnAS0XGJpNMPjwIy6JdYaG0fh08DJnMGzdldrImGWX_e7PdutSezCWBPO8v-fEg9JySN4xpcm7NaCEmyggnkopH6Lgmsq6E0PzxvfMROk3phpTFGJVCPkVHjDVSiaY-Rt8vYITsLf5qojfZhzFhM_Z4AWbIq-oaBpOhx1eTGXze4uDw0jvAZ4vrq8vlq7d4hktAWEP1zfeAP-Wp3-LZZhODsatn6IkzQ4LTu_0Effnw_vN8US0vLz7OZ8vKciVzJRxXiiuntK0F7RzXWtbAbKcVpU40jrC6gJTpXklppel65RrLGyOl0UawE_Run7uZujX0FsYczdBuol-buG2D8e2_N6NftT_Cr1ZqKpioS8DZXUAMPydIuV37ZGEYzAhhSm15XteNEmSHvnyA3oQpjqXeLcWpIlQV6nxP2RhSiuAOn6Gk3blrH7grEy_udzjwf00VQO2B39AFl6yHEnDAitzSg3HFdp7p3Odbl_MwjbmMvv7_UfYH1ZC01Q</recordid><startdate>20210210</startdate><enddate>20210210</enddate><creator>Adjei, Araba A.</creator><creator>Lopez, Camden L.</creator><creator>Schaid, Daniel J.</creator><creator>Sloan, Jeff A.</creator><creator>Le-Rademacher, Jennifer G.</creator><creator>Loprinzi, Charles L.</creator><creator>Norman, Aaron D.</creator><creator>Olson, Janet E.</creator><creator>Couch, Fergus J.</creator><creator>Beutler, Andreas S.</creator><creator>Vachon, Celine M.</creator><creator>Ruddy, Kathryn J.</creator><general>Mdpi</general><general>MDPI AG</general><general>MDPI</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</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>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4516-8088</orcidid><orcidid>https://orcid.org/0000-0002-2234-7430</orcidid></search><sort><creationdate>20210210</creationdate><title>Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach</title><author>Adjei, Araba A. ; Lopez, Camden L. ; Schaid, Daniel J. ; Sloan, Jeff A. ; Le-Rademacher, Jennifer G. ; Loprinzi, Charles L. ; Norman, Aaron D. ; Olson, Janet E. ; Couch, Fergus J. ; Beutler, Andreas S. ; Vachon, Celine M. ; Ruddy, Kathryn J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-6f48848f89c261bf49972e3cb9811f65f032487139d877c7abd8f5c45a77a9a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Age</topic><topic>Breast cancer</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Chromosomes</topic><topic>Disease</topic><topic>Expected values</topic><topic>Genes</topic><topic>Genetic diversity</topic><topic>Genetic factors</topic><topic>Genomes</topic><topic>Inflammation</topic><topic>Life Sciences & Biomedicine</topic><topic>Lung cancer</topic><topic>Medical diagnosis</topic><topic>Mental health</topic><topic>Metabolism</topic><topic>Oncology</topic><topic>Pain</topic><topic>Quality of life</topic><topic>Science & Technology</topic><topic>Single-nucleotide polymorphism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Adjei, Araba A.</creatorcontrib><creatorcontrib>Lopez, Camden L.</creatorcontrib><creatorcontrib>Schaid, Daniel J.</creatorcontrib><creatorcontrib>Sloan, Jeff A.</creatorcontrib><creatorcontrib>Le-Rademacher, Jennifer G.</creatorcontrib><creatorcontrib>Loprinzi, Charles L.</creatorcontrib><creatorcontrib>Norman, Aaron D.</creatorcontrib><creatorcontrib>Olson, Janet E.</creatorcontrib><creatorcontrib>Couch, Fergus J.</creatorcontrib><creatorcontrib>Beutler, Andreas S.</creatorcontrib><creatorcontrib>Vachon, Celine M.</creatorcontrib><creatorcontrib>Ruddy, Kathryn J.</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</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 China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Adjei, Araba A.</au><au>Lopez, Camden L.</au><au>Schaid, Daniel J.</au><au>Sloan, Jeff A.</au><au>Le-Rademacher, Jennifer G.</au><au>Loprinzi, Charles L.</au><au>Norman, Aaron D.</au><au>Olson, Janet E.</au><au>Couch, Fergus J.</au><au>Beutler, Andreas S.</au><au>Vachon, Celine M.</au><au>Ruddy, Kathryn J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach</atitle><jtitle>Cancers</jtitle><stitle>CANCERS</stitle><addtitle>Cancers (Basel)</addtitle><date>2021-02-10</date><risdate>2021</risdate><volume>13</volume><issue>4</issue><spage>716</spage><pages>716-</pages><artnum>716</artnum><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Simple Summary
Health-related quality of life (HRQOL) is associated with cancer prognosis as well as with age, sex, race, and lifestyle factors, including diet and physical activity. To investigate the hypothesis that HRQOL has genetic underpinnings in patients with cancer, we performed a genome-wide association study to evaluate genetic variants (single nucleotide polymorphisms, SNPs) associated with mental and physical QOL as measured by the PROMIS assessment tool in breast cancer survivors participating in a longitudinal cohort study, the Mayo Clinic Breast Disease Registry (MCBDR). Age and financial concerns were associated with worse physical and mental health, and previous receipt of chemotherapy was associated with worse mental health. SNPs in SCN10A, LMX1B, SGCD, PARP12, and SEMA5A were associated with physical and mental QOL, but none at the genome-wide significance thresholds of p < 5 x 10(-8).
Health-related quality of life (HRQOL) is an important prognostic patient-reported outcome in oncology. Because prior studies suggest that HRQOL is, in part, heritable, we performed a GWAS to elucidate genetic factors associated with HRQOL in breast cancer survivors. Physical and mental HRQOL were measured via paper surveys that included the PROMIS-10 physical and mental health domain scales in 1442 breast cancer survivors participating in the Mayo Clinic Breast Disease Registry (MCBDR). In multivariable regression analyses, age and financial concerns were significantly associated with global physical health (age: p = 1.6 x 10(-23); financial concerns: p = 4.8 x 10(-40)) and mental health (age: p = 3.5 x 10(-7); financial concerns: p = 2.0 x 10(-69)). Chemotherapy was associated with worse global mental health (p = 0.01). In the GWAS, none of the SNPs reached the genome-wide association significance threshold of 5 x 10(-8) for associations with either global physical or global mental health, however, a cluster of SNPs in SCN10A, particularly rs112718371, appeared to be linked to worse global physical health (p = 5.21 x 10(-8)). Additionally, SNPs in LMX1B, SGCD, PARP12 and SEMA5A were also moderately associated with worse physical and mental health (p < 10(-6)). These biologically plausible candidate SNPs warrant further study as possible predictors of HRQOL.</abstract><cop>BASEL</cop><pub>Mdpi</pub><pmid>33578652</pmid><doi>10.3390/cancers13040716</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-4516-8088</orcidid><orcidid>https://orcid.org/0000-0002-2234-7430</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Age Breast cancer Cancer therapies Chemotherapy Chromosomes Disease Expected values Genes Genetic diversity Genetic factors Genomes Inflammation Life Sciences & Biomedicine Lung cancer Medical diagnosis Mental health Metabolism Oncology Pain Quality of life Science & Technology Single-nucleotide polymorphism |
title | Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach |
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