Loading…
Cancer and Cardiovascular Risk in Women With Hypertensive Disorders of Pregnancy Carrying a Common IGF1R Variant
To evaluate the impact of insulin-like growth factor 1 receptor variant rs2016347 on the risk for breast and nonbreast cancers and cardiovascular disease in women with a history of hypertensive disorders of pregnancy (HDP). This retrospective cohort study included all parous women in the UK Biobank...
Saved in:
Published in: | Mayo Clinic proceedings 2020-12, Vol.95 (12), p.2684-2696 |
---|---|
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-c436t-5a90fc72b4077a5c6d096d9463871fa257116097c4b6341297750463f2b076953 |
---|---|
cites | cdi_FETCH-LOGICAL-c436t-5a90fc72b4077a5c6d096d9463871fa257116097c4b6341297750463f2b076953 |
container_end_page | 2696 |
container_issue | 12 |
container_start_page | 2684 |
container_title | Mayo Clinic proceedings |
container_volume | 95 |
creator | Powell, Mark J. Dufault, Suzanne M. Gunderson, Erica P. Benz, Christopher C. |
description | To evaluate the impact of insulin-like growth factor 1 receptor variant rs2016347 on the risk for breast and nonbreast cancers and cardiovascular disease in women with a history of hypertensive disorders of pregnancy (HDP).
This retrospective cohort study included all parous women in the UK Biobank with prior rs2016347 genotyping (N=204,155), with enrollment taking place from March 2006 to July 2010. History of HDP was self-reported, and outcomes included breast and all nonbreast cancers, hospital diagnoses of hypertension and cardiovascular disease, and direct blood pressure measurements.
Women with previous HDP had a higher risk for future hypertension and cardiovascular diagnoses, increased blood pressures, and lower risk for breast cancer compared with women without HDP, consistent with prior studies. Hazard ratios for all nonbreast cancers were unchanged. However, when taking genotype into account, HDP-positive women carrying at least 1 thymine (T) allele of rs2016347 had a lower risk for nonbreast cancer (hazard ratio, 0.59; 95% CI, 0.37 to 0.92; P=.02) and lower systolic blood pressure (−2.08±0.98 mm Hg; P=.03) compared with women with the guanine/guanine (GG) genotype with positive evidence of interaction (HDP:T allele) for both outcomes; P=.04 and P=.03, respectively.
Women who experience HDP and carry a T allele of rs2016347 have 41% lower risk for developing nonbreast cancer and a lower systolic blood pressure of 2.08 mm Hg when compared with those with the GG genotype, suggesting a possible role of the insulin-like growth factor 1 axis for both cardiovascular and cancer risk in women with HDP. |
doi_str_mv | 10.1016/j.mayocp.2020.03.037 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2459348463</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0025619620306522</els_id><sourcerecordid>2467352498</sourcerecordid><originalsourceid>FETCH-LOGICAL-c436t-5a90fc72b4077a5c6d096d9463871fa257116097c4b6341297750463f2b076953</originalsourceid><addsrcrecordid>eNp9kcuKFDEYhYMoTjv6BiIBN26q_XPvbAQpnQsMKIOXZUinUmParqRMqhrq7U3T4yxmIfwki3znJORD6DWBNQEi3-_Wg12SG9cUKKyB1VFP0IpoThshuHyKVgBUNJJoeYZelLIDAKU1f47OGCNyQ4ReobG10fmMbexwa3MX0sEWN-9txreh_MYh4p9p8HUN0y98tYw-Tz6WcPD4Uygpdz4XnHr8Nfu7WKuWY0teQrzDFrdpGFLE15cX5Bb_sDnYOL1Ez3q7L_7V_X6Ovl98_tZeNTdfLq_bjzeN40xOjbAaeqfoloNSVjjZgZad5pJtFOktFYoQCVo5vpWME6qVElBPe7oFJbVg5-jdqXfM6c_sy2SGUJzf7230aS6GcqEZ39RIRd8-QndpzrG-rlJSMUG53lSKnyiXUynZ92bMYbB5MQTM0YjZmZMRczRigNVRNfbmvnzeDr57CP1TUIEPJ8DX3zgEn01xwVcpXcjeTaZL4f83_AXXk5v7</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2467352498</pqid></control><display><type>article</type><title>Cancer and Cardiovascular Risk in Women With Hypertensive Disorders of Pregnancy Carrying a Common IGF1R Variant</title><source>ScienceDirect®</source><creator>Powell, Mark J. ; Dufault, Suzanne M. ; Gunderson, Erica P. ; Benz, Christopher C.</creator><creatorcontrib>Powell, Mark J. ; Dufault, Suzanne M. ; Gunderson, Erica P. ; Benz, Christopher C.</creatorcontrib><description>To evaluate the impact of insulin-like growth factor 1 receptor variant rs2016347 on the risk for breast and nonbreast cancers and cardiovascular disease in women with a history of hypertensive disorders of pregnancy (HDP).
This retrospective cohort study included all parous women in the UK Biobank with prior rs2016347 genotyping (N=204,155), with enrollment taking place from March 2006 to July 2010. History of HDP was self-reported, and outcomes included breast and all nonbreast cancers, hospital diagnoses of hypertension and cardiovascular disease, and direct blood pressure measurements.
Women with previous HDP had a higher risk for future hypertension and cardiovascular diagnoses, increased blood pressures, and lower risk for breast cancer compared with women without HDP, consistent with prior studies. Hazard ratios for all nonbreast cancers were unchanged. However, when taking genotype into account, HDP-positive women carrying at least 1 thymine (T) allele of rs2016347 had a lower risk for nonbreast cancer (hazard ratio, 0.59; 95% CI, 0.37 to 0.92; P=.02) and lower systolic blood pressure (−2.08±0.98 mm Hg; P=.03) compared with women with the guanine/guanine (GG) genotype with positive evidence of interaction (HDP:T allele) for both outcomes; P=.04 and P=.03, respectively.
Women who experience HDP and carry a T allele of rs2016347 have 41% lower risk for developing nonbreast cancer and a lower systolic blood pressure of 2.08 mm Hg when compared with those with the GG genotype, suggesting a possible role of the insulin-like growth factor 1 axis for both cardiovascular and cancer risk in women with HDP.</description><identifier>ISSN: 0025-6196</identifier><identifier>EISSN: 1942-5546</identifier><identifier>DOI: 10.1016/j.mayocp.2020.03.037</identifier><identifier>PMID: 33168159</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Adult ; Age ; Alleles ; Biobanks ; Blood pressure ; Blood Pressure Determination - statistics & numerical data ; Breast cancer ; Cardiovascular disease ; Cardiovascular diseases ; Cohort Studies ; Female ; Genotype & phenotype ; Genotypes ; Genotyping ; Guanine ; Haplotypes ; Heart Disease Risk Factors ; Humans ; Hypertension ; Hypertension, Pregnancy-Induced - diagnosis ; Hypertension, Pregnancy-Induced - epidemiology ; Hypertension, Pregnancy-Induced - genetics ; Insulin ; Insulin-like growth factors ; Mortality ; Neoplasms - diagnosis ; Neoplasms - epidemiology ; Neoplasms - genetics ; Polymorphism, Single Nucleotide ; Population ; Preeclampsia ; Pregnancy ; Pregnancy Complications, Cardiovascular - diagnosis ; Pregnancy Complications, Cardiovascular - epidemiology ; Pregnancy Complications, Cardiovascular - genetics ; Receptor, IGF Type 1 - genetics ; Retrospective Studies ; Risk Assessment - methods ; Thymine ; United Kingdom - epidemiology ; Womens health</subject><ispartof>Mayo Clinic proceedings, 2020-12, Vol.95 (12), p.2684-2696</ispartof><rights>2020 Mayo Foundation for Medical Education and Research</rights><rights>Copyright © 2020 Mayo Foundation for Medical Education and Research. Published by Elsevier Inc. All rights reserved.</rights><rights>Copyright Mayo Foundation for Medical Education and Research Dec 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-5a90fc72b4077a5c6d096d9463871fa257116097c4b6341297750463f2b076953</citedby><cites>FETCH-LOGICAL-c436t-5a90fc72b4077a5c6d096d9463871fa257116097c4b6341297750463f2b076953</cites><orcidid>0000-0001-9945-5360 ; 0000-0002-6316-6548</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0025619620306522$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>315,786,790,3568,27957,27958,45815</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33168159$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Powell, Mark J.</creatorcontrib><creatorcontrib>Dufault, Suzanne M.</creatorcontrib><creatorcontrib>Gunderson, Erica P.</creatorcontrib><creatorcontrib>Benz, Christopher C.</creatorcontrib><title>Cancer and Cardiovascular Risk in Women With Hypertensive Disorders of Pregnancy Carrying a Common IGF1R Variant</title><title>Mayo Clinic proceedings</title><addtitle>Mayo Clin Proc</addtitle><description>To evaluate the impact of insulin-like growth factor 1 receptor variant rs2016347 on the risk for breast and nonbreast cancers and cardiovascular disease in women with a history of hypertensive disorders of pregnancy (HDP).
This retrospective cohort study included all parous women in the UK Biobank with prior rs2016347 genotyping (N=204,155), with enrollment taking place from March 2006 to July 2010. History of HDP was self-reported, and outcomes included breast and all nonbreast cancers, hospital diagnoses of hypertension and cardiovascular disease, and direct blood pressure measurements.
Women with previous HDP had a higher risk for future hypertension and cardiovascular diagnoses, increased blood pressures, and lower risk for breast cancer compared with women without HDP, consistent with prior studies. Hazard ratios for all nonbreast cancers were unchanged. However, when taking genotype into account, HDP-positive women carrying at least 1 thymine (T) allele of rs2016347 had a lower risk for nonbreast cancer (hazard ratio, 0.59; 95% CI, 0.37 to 0.92; P=.02) and lower systolic blood pressure (−2.08±0.98 mm Hg; P=.03) compared with women with the guanine/guanine (GG) genotype with positive evidence of interaction (HDP:T allele) for both outcomes; P=.04 and P=.03, respectively.
Women who experience HDP and carry a T allele of rs2016347 have 41% lower risk for developing nonbreast cancer and a lower systolic blood pressure of 2.08 mm Hg when compared with those with the GG genotype, suggesting a possible role of the insulin-like growth factor 1 axis for both cardiovascular and cancer risk in women with HDP.</description><subject>Adult</subject><subject>Age</subject><subject>Alleles</subject><subject>Biobanks</subject><subject>Blood pressure</subject><subject>Blood Pressure Determination - statistics & numerical data</subject><subject>Breast cancer</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular diseases</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Genotype & phenotype</subject><subject>Genotypes</subject><subject>Genotyping</subject><subject>Guanine</subject><subject>Haplotypes</subject><subject>Heart Disease Risk Factors</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Hypertension, Pregnancy-Induced - diagnosis</subject><subject>Hypertension, Pregnancy-Induced - epidemiology</subject><subject>Hypertension, Pregnancy-Induced - genetics</subject><subject>Insulin</subject><subject>Insulin-like growth factors</subject><subject>Mortality</subject><subject>Neoplasms - diagnosis</subject><subject>Neoplasms - epidemiology</subject><subject>Neoplasms - genetics</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Population</subject><subject>Preeclampsia</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Cardiovascular - diagnosis</subject><subject>Pregnancy Complications, Cardiovascular - epidemiology</subject><subject>Pregnancy Complications, Cardiovascular - genetics</subject><subject>Receptor, IGF Type 1 - genetics</subject><subject>Retrospective Studies</subject><subject>Risk Assessment - methods</subject><subject>Thymine</subject><subject>United Kingdom - epidemiology</subject><subject>Womens health</subject><issn>0025-6196</issn><issn>1942-5546</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kcuKFDEYhYMoTjv6BiIBN26q_XPvbAQpnQsMKIOXZUinUmParqRMqhrq7U3T4yxmIfwki3znJORD6DWBNQEi3-_Wg12SG9cUKKyB1VFP0IpoThshuHyKVgBUNJJoeYZelLIDAKU1f47OGCNyQ4ReobG10fmMbexwa3MX0sEWN-9txreh_MYh4p9p8HUN0y98tYw-Tz6WcPD4Uygpdz4XnHr8Nfu7WKuWY0teQrzDFrdpGFLE15cX5Bb_sDnYOL1Ez3q7L_7V_X6Ovl98_tZeNTdfLq_bjzeN40xOjbAaeqfoloNSVjjZgZad5pJtFOktFYoQCVo5vpWME6qVElBPe7oFJbVg5-jdqXfM6c_sy2SGUJzf7230aS6GcqEZ39RIRd8-QndpzrG-rlJSMUG53lSKnyiXUynZ92bMYbB5MQTM0YjZmZMRczRigNVRNfbmvnzeDr57CP1TUIEPJ8DX3zgEn01xwVcpXcjeTaZL4f83_AXXk5v7</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Powell, Mark J.</creator><creator>Dufault, Suzanne M.</creator><creator>Gunderson, Erica P.</creator><creator>Benz, Christopher C.</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</scope><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>3V.</scope><scope>4U-</scope><scope>7RV</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9945-5360</orcidid><orcidid>https://orcid.org/0000-0002-6316-6548</orcidid></search><sort><creationdate>202012</creationdate><title>Cancer and Cardiovascular Risk in Women With Hypertensive Disorders of Pregnancy Carrying a Common IGF1R Variant</title><author>Powell, Mark J. ; Dufault, Suzanne M. ; Gunderson, Erica P. ; Benz, Christopher C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-5a90fc72b4077a5c6d096d9463871fa257116097c4b6341297750463f2b076953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Age</topic><topic>Alleles</topic><topic>Biobanks</topic><topic>Blood pressure</topic><topic>Blood Pressure Determination - statistics & numerical data</topic><topic>Breast cancer</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular diseases</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Genotype & phenotype</topic><topic>Genotypes</topic><topic>Genotyping</topic><topic>Guanine</topic><topic>Haplotypes</topic><topic>Heart Disease Risk Factors</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Hypertension, Pregnancy-Induced - diagnosis</topic><topic>Hypertension, Pregnancy-Induced - epidemiology</topic><topic>Hypertension, Pregnancy-Induced - genetics</topic><topic>Insulin</topic><topic>Insulin-like growth factors</topic><topic>Mortality</topic><topic>Neoplasms - diagnosis</topic><topic>Neoplasms - epidemiology</topic><topic>Neoplasms - genetics</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Population</topic><topic>Preeclampsia</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Cardiovascular - diagnosis</topic><topic>Pregnancy Complications, Cardiovascular - epidemiology</topic><topic>Pregnancy Complications, Cardiovascular - genetics</topic><topic>Receptor, IGF Type 1 - genetics</topic><topic>Retrospective Studies</topic><topic>Risk Assessment - methods</topic><topic>Thymine</topic><topic>United Kingdom - epidemiology</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Powell, Mark J.</creatorcontrib><creatorcontrib>Dufault, Suzanne M.</creatorcontrib><creatorcontrib>Gunderson, Erica P.</creatorcontrib><creatorcontrib>Benz, Christopher C.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>University Readers</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Public Health Database</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>eLibrary</collection><collection>AUTh Library subscriptions: ProQuest Central</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>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database (ProQuest)</collection><collection>Nursing & Allied Health Premium</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>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Mayo Clinic proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Powell, Mark J.</au><au>Dufault, Suzanne M.</au><au>Gunderson, Erica P.</au><au>Benz, Christopher C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cancer and Cardiovascular Risk in Women With Hypertensive Disorders of Pregnancy Carrying a Common IGF1R Variant</atitle><jtitle>Mayo Clinic proceedings</jtitle><addtitle>Mayo Clin Proc</addtitle><date>2020-12</date><risdate>2020</risdate><volume>95</volume><issue>12</issue><spage>2684</spage><epage>2696</epage><pages>2684-2696</pages><issn>0025-6196</issn><eissn>1942-5546</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><abstract>To evaluate the impact of insulin-like growth factor 1 receptor variant rs2016347 on the risk for breast and nonbreast cancers and cardiovascular disease in women with a history of hypertensive disorders of pregnancy (HDP).
This retrospective cohort study included all parous women in the UK Biobank with prior rs2016347 genotyping (N=204,155), with enrollment taking place from March 2006 to July 2010. History of HDP was self-reported, and outcomes included breast and all nonbreast cancers, hospital diagnoses of hypertension and cardiovascular disease, and direct blood pressure measurements.
Women with previous HDP had a higher risk for future hypertension and cardiovascular diagnoses, increased blood pressures, and lower risk for breast cancer compared with women without HDP, consistent with prior studies. Hazard ratios for all nonbreast cancers were unchanged. However, when taking genotype into account, HDP-positive women carrying at least 1 thymine (T) allele of rs2016347 had a lower risk for nonbreast cancer (hazard ratio, 0.59; 95% CI, 0.37 to 0.92; P=.02) and lower systolic blood pressure (−2.08±0.98 mm Hg; P=.03) compared with women with the guanine/guanine (GG) genotype with positive evidence of interaction (HDP:T allele) for both outcomes; P=.04 and P=.03, respectively.
Women who experience HDP and carry a T allele of rs2016347 have 41% lower risk for developing nonbreast cancer and a lower systolic blood pressure of 2.08 mm Hg when compared with those with the GG genotype, suggesting a possible role of the insulin-like growth factor 1 axis for both cardiovascular and cancer risk in women with HDP.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>33168159</pmid><doi>10.1016/j.mayocp.2020.03.037</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-9945-5360</orcidid><orcidid>https://orcid.org/0000-0002-6316-6548</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0025-6196 |
ispartof | Mayo Clinic proceedings, 2020-12, Vol.95 (12), p.2684-2696 |
issn | 0025-6196 1942-5546 |
language | eng |
recordid | cdi_proquest_miscellaneous_2459348463 |
source | ScienceDirect® |
subjects | Adult Age Alleles Biobanks Blood pressure Blood Pressure Determination - statistics & numerical data Breast cancer Cardiovascular disease Cardiovascular diseases Cohort Studies Female Genotype & phenotype Genotypes Genotyping Guanine Haplotypes Heart Disease Risk Factors Humans Hypertension Hypertension, Pregnancy-Induced - diagnosis Hypertension, Pregnancy-Induced - epidemiology Hypertension, Pregnancy-Induced - genetics Insulin Insulin-like growth factors Mortality Neoplasms - diagnosis Neoplasms - epidemiology Neoplasms - genetics Polymorphism, Single Nucleotide Population Preeclampsia Pregnancy Pregnancy Complications, Cardiovascular - diagnosis Pregnancy Complications, Cardiovascular - epidemiology Pregnancy Complications, Cardiovascular - genetics Receptor, IGF Type 1 - genetics Retrospective Studies Risk Assessment - methods Thymine United Kingdom - epidemiology Womens health |
title | Cancer and Cardiovascular Risk in Women With Hypertensive Disorders of Pregnancy Carrying a Common IGF1R Variant |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-09-22T06%3A42%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cancer%20and%20Cardiovascular%20Risk%20in%20Women%20With%20Hypertensive%20Disorders%20of%20Pregnancy%20Carrying%20a%20Common%20IGF1R%20Variant&rft.jtitle=Mayo%20Clinic%20proceedings&rft.au=Powell,%20Mark%20J.&rft.date=2020-12&rft.volume=95&rft.issue=12&rft.spage=2684&rft.epage=2696&rft.pages=2684-2696&rft.issn=0025-6196&rft.eissn=1942-5546&rft_id=info:doi/10.1016/j.mayocp.2020.03.037&rft_dat=%3Cproquest_cross%3E2467352498%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c436t-5a90fc72b4077a5c6d096d9463871fa257116097c4b6341297750463f2b076953%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2467352498&rft_id=info:pmid/33168159&rfr_iscdi=true |