Association of MTHFR 677C>T Polymorphism with Susceptibility to Ovarian and Cervical Cancers: A Systematic Review and Meta-Analysis

Background: Previous studies have evaluated the impact of MTHFR 677C>T polymorphism on susceptibility to ovarian and cervical cancers in women, but the conclusions are still controversial. To get a more precise evaluation of the association between MTHFR 677C>T polymorphism and risk of ovarian...

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Veröffentlicht in:Asian Pacific Journal of Cancer Prevention 2019-09, Vol.20 (9), p.2569-2577
Hauptverfasser: Karimi-Zarchi, Mojgan, Moghimi, Mansour, Abbasi, Hajar, Hadadan, Amaneh, Salimi, Erfaneh, Morovati-Sharifabad, Majid, Akbarian-Bafghi, Mohammad Javad, Zare-Shehneh, Masoud, Mosavi-Jarrahi, Alireza, Neamatzadeh, Hossein
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container_end_page 2577
container_issue 9
container_start_page 2569
container_title Asian Pacific Journal of Cancer Prevention
container_volume 20
creator Karimi-Zarchi, Mojgan
Moghimi, Mansour
Abbasi, Hajar
Hadadan, Amaneh
Salimi, Erfaneh
Morovati-Sharifabad, Majid
Akbarian-Bafghi, Mohammad Javad
Zare-Shehneh, Masoud
Mosavi-Jarrahi, Alireza
Neamatzadeh, Hossein
description Background: Previous studies have evaluated the impact of MTHFR 677C>T polymorphism on susceptibility to ovarian and cervical cancers in women, but the conclusions are still controversial. To get a more precise evaluation of the association between MTHFR 677C>T polymorphism and risk of ovarian and cervical cancers, we performed a meta-analysis of the association of all eligible studies. Methods: A comprehensive search performed in PubMed, Google Scholar, CNKI, and Web of Science databases to identify the relevant studies up to October 15, 2018. The strength of the association was estimated by odds ratios (OR) with 95% confidence interval (CI). Results: A total of 27 case-control studies including eleven studies with 4990 cases 7730 controls on ovarian cancer and 16 studies with 4990 cases and 7730 controls on cervical cancer were selected. Pooled data revealed that the MTHFR 677C>T polymorphism not significantly associated with an increased risk of ovarian and cervical cancers under all five genetic models. However, stratified analysis by ethnicity showed that the MTHFR 677C>T polymorphism was significantly associated with risk of ovarian cancer in Asians. No publication bias was found in the current meta-analysis. Conclusions: The results of this meta-analysis proposes that the MTHFR 677C>T polymorphism may not play a role in development of ovarian and cervical cancers in overall population. Further well-designed studies are necessary to clarify the precise role of the MTHFR 677C>T polymorphism on ovarian and cervical cancers risk.
doi_str_mv 10.31557/APJCP.2019.20.9.2569
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To get a more precise evaluation of the association between MTHFR 677C&gt;T polymorphism and risk of ovarian and cervical cancers, we performed a meta-analysis of the association of all eligible studies. Methods: A comprehensive search performed in PubMed, Google Scholar, CNKI, and Web of Science databases to identify the relevant studies up to October 15, 2018. The strength of the association was estimated by odds ratios (OR) with 95% confidence interval (CI). Results: A total of 27 case-control studies including eleven studies with 4990 cases 7730 controls on ovarian cancer and 16 studies with 4990 cases and 7730 controls on cervical cancer were selected. Pooled data revealed that the MTHFR 677C&gt;T polymorphism not significantly associated with an increased risk of ovarian and cervical cancers under all five genetic models. However, stratified analysis by ethnicity showed that the MTHFR 677C&gt;T polymorphism was significantly associated with risk of ovarian cancer in Asians. No publication bias was found in the current meta-analysis. Conclusions: The results of this meta-analysis proposes that the MTHFR 677C&gt;T polymorphism may not play a role in development of ovarian and cervical cancers in overall population. 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To get a more precise evaluation of the association between MTHFR 677C&gt;T polymorphism and risk of ovarian and cervical cancers, we performed a meta-analysis of the association of all eligible studies. Methods: A comprehensive search performed in PubMed, Google Scholar, CNKI, and Web of Science databases to identify the relevant studies up to October 15, 2018. The strength of the association was estimated by odds ratios (OR) with 95% confidence interval (CI). Results: A total of 27 case-control studies including eleven studies with 4990 cases 7730 controls on ovarian cancer and 16 studies with 4990 cases and 7730 controls on cervical cancer were selected. Pooled data revealed that the MTHFR 677C&gt;T polymorphism not significantly associated with an increased risk of ovarian and cervical cancers under all five genetic models. However, stratified analysis by ethnicity showed that the MTHFR 677C&gt;T polymorphism was significantly associated with risk of ovarian cancer in Asians. No publication bias was found in the current meta-analysis. Conclusions: The results of this meta-analysis proposes that the MTHFR 677C&gt;T polymorphism may not play a role in development of ovarian and cervical cancers in overall population. Further well-designed studies are necessary to clarify the precise role of the MTHFR 677C&gt;T polymorphism on ovarian and cervical cancers risk.</description><subject>Case-Control Studies</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Methylenetetrahydrofolate Reductase (NADPH2) - genetics</subject><subject>Ovarian Neoplasms - etiology</subject><subject>Ovarian Neoplasms - pathology</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Prognosis</subject><subject>Review</subject><subject>Risk Factors</subject><subject>Uterine Cervical Neoplasms - etiology</subject><subject>Uterine Cervical Neoplasms - pathology</subject><issn>2476-762X</issn><issn>1513-7368</issn><issn>2476-762X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV1LwzAUhoMofkx_gpI_0JmmadJ4IZTiJxsbOsG7kKWJi7TNSLpJr_3j1k1l3rznQPI-5-IB4DxGwyROU3aZTx-L6RCjmPcx7COlfA8cY8JoxCh-3d_Zj8BJCO8IkTRj6SE4-iaQhLBj8JmH4JSVrXUNdAaOZ_e3T5AyVlzP4NRVXe38cmFDDT9su4DPq6D0srVzW9m2g62Dk7X0VjZQNiUstF9bJStYyEZpH65gDp-70Oq65yv4pNdWf2x-jnUro7yRVRdsOAUHRlZBn_3MAXi5vZkV99FocvdQ5KNIJZjyKJWIY14iqhjXChtCEMGGqjgjWca5inmGTRljlnHDUIkImzOUUGPmpSqTVCcDcL3lLlfzWpdKN62XlVh6W0vfCSet-P_S2IV4c2tBOaMZQT0g3QKUdyF4bf66MRIbK2JjRXxb6UP00Vvpexe7h_9avxqSL6FeiwM</recordid><startdate>20190901</startdate><enddate>20190901</enddate><creator>Karimi-Zarchi, Mojgan</creator><creator>Moghimi, Mansour</creator><creator>Abbasi, Hajar</creator><creator>Hadadan, Amaneh</creator><creator>Salimi, Erfaneh</creator><creator>Morovati-Sharifabad, Majid</creator><creator>Akbarian-Bafghi, Mohammad Javad</creator><creator>Zare-Shehneh, Masoud</creator><creator>Mosavi-Jarrahi, Alireza</creator><creator>Neamatzadeh, Hossein</creator><general>West Asia Organization for Cancer Prevention</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>5PM</scope></search><sort><creationdate>20190901</creationdate><title>Association of MTHFR 677C&gt;T Polymorphism with Susceptibility to Ovarian and Cervical Cancers: A Systematic Review and Meta-Analysis</title><author>Karimi-Zarchi, Mojgan ; Moghimi, Mansour ; Abbasi, Hajar ; Hadadan, Amaneh ; Salimi, Erfaneh ; Morovati-Sharifabad, Majid ; Akbarian-Bafghi, Mohammad Javad ; Zare-Shehneh, Masoud ; Mosavi-Jarrahi, Alireza ; Neamatzadeh, Hossein</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3269-5a0929d06c79ec2f44042f6c1848899c1982fd12789f70d047b7036ffbdcd35e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Case-Control Studies</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Humans</topic><topic>Methylenetetrahydrofolate Reductase (NADPH2) - genetics</topic><topic>Ovarian Neoplasms - etiology</topic><topic>Ovarian Neoplasms - pathology</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Prognosis</topic><topic>Review</topic><topic>Risk Factors</topic><topic>Uterine Cervical Neoplasms - etiology</topic><topic>Uterine Cervical Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karimi-Zarchi, Mojgan</creatorcontrib><creatorcontrib>Moghimi, Mansour</creatorcontrib><creatorcontrib>Abbasi, Hajar</creatorcontrib><creatorcontrib>Hadadan, Amaneh</creatorcontrib><creatorcontrib>Salimi, Erfaneh</creatorcontrib><creatorcontrib>Morovati-Sharifabad, Majid</creatorcontrib><creatorcontrib>Akbarian-Bafghi, Mohammad Javad</creatorcontrib><creatorcontrib>Zare-Shehneh, Masoud</creatorcontrib><creatorcontrib>Mosavi-Jarrahi, Alireza</creatorcontrib><creatorcontrib>Neamatzadeh, Hossein</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Asian Pacific Journal of Cancer Prevention</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karimi-Zarchi, Mojgan</au><au>Moghimi, Mansour</au><au>Abbasi, Hajar</au><au>Hadadan, Amaneh</au><au>Salimi, Erfaneh</au><au>Morovati-Sharifabad, Majid</au><au>Akbarian-Bafghi, Mohammad Javad</au><au>Zare-Shehneh, Masoud</au><au>Mosavi-Jarrahi, Alireza</au><au>Neamatzadeh, Hossein</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of MTHFR 677C&gt;T Polymorphism with Susceptibility to Ovarian and Cervical Cancers: A Systematic Review and Meta-Analysis</atitle><jtitle>Asian Pacific Journal of Cancer Prevention</jtitle><addtitle>Asian Pac J Cancer Prev</addtitle><date>2019-09-01</date><risdate>2019</risdate><volume>20</volume><issue>9</issue><spage>2569</spage><epage>2577</epage><pages>2569-2577</pages><issn>2476-762X</issn><issn>1513-7368</issn><eissn>2476-762X</eissn><abstract>Background: Previous studies have evaluated the impact of MTHFR 677C&gt;T polymorphism on susceptibility to ovarian and cervical cancers in women, but the conclusions are still controversial. 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No publication bias was found in the current meta-analysis. Conclusions: The results of this meta-analysis proposes that the MTHFR 677C&gt;T polymorphism may not play a role in development of ovarian and cervical cancers in overall population. Further well-designed studies are necessary to clarify the precise role of the MTHFR 677C&gt;T polymorphism on ovarian and cervical cancers risk.</abstract><cop>Thailand</cop><pub>West Asia Organization for Cancer Prevention</pub><pmid>31554347</pmid><doi>10.31557/APJCP.2019.20.9.2569</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Case-Control Studies
Female
Genetic Predisposition to Disease
Humans
Methylenetetrahydrofolate Reductase (NADPH2) - genetics
Ovarian Neoplasms - etiology
Ovarian Neoplasms - pathology
Polymorphism, Single Nucleotide
Prognosis
Review
Risk Factors
Uterine Cervical Neoplasms - etiology
Uterine Cervical Neoplasms - pathology
title Association of MTHFR 677C>T Polymorphism with Susceptibility to Ovarian and Cervical Cancers: A Systematic Review and Meta-Analysis
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