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Assessment the effect of vitamin D supplementation on plasma vitamin D levels, inflammation, and oxidative stress biomarkers based on vitamin D receptor genetic variation in breast cancer survivors: a protocol for clinical trial
Both human genes and environmental exposures, due to complex interplay, play important role in the cancer etiology. Vitamin D is associated with a reduced risk of incidence and mortality of several human cancers. This study will aim to investigate the possible effects of individual polymorphisms in...
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Published in: | Journal of health, population and nutrition population and nutrition, 2021-11, Vol.40 (1), p.46-46, Article 46 |
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creator | Kazemian, Elham Akbari, Mohammad Esmaeil Moradi, Nariman Gharibzadeh, Safoora Amouzegar, Atieh Rozek, Laura S Mondul, Alison M Khademolmele, Maryam Zarins, Katie R Ghodoosi, Nasim Shateri, Zahra Fallah, Soudabeh Davoodi, Sayed Hossein |
description | Both human genes and environmental exposures, due to complex interplay, play important role in the cancer etiology. Vitamin D is associated with a reduced risk of incidence and mortality of several human cancers. This study will aim to investigate the possible effects of individual polymorphisms in vitamin D receptor (VDR) as well as effects of VDR haplotypes on response to vitamin D supplementation in breast cancer survivors.
This is an interventional study in which the effects of vitamin D supplementation on plasma vitamin D levels, inflammatory and antioxidant biomarkers and factors associated with cell proliferation, differentiation, damage, and apoptosis will be investigated stratified by variations in VDR genotype. The present study will be conducted on breast cancer survivors referred to the Shohadaye Tajrish hospital and its associated clinics. One hundred ninety-eight breast cancer survivors will receive 4000 IU of vitamin D3 daily for 12 weeks. VDR Fok1, ApaI, TaqI, BsmI, and Cdx-2 genotype will be determined at the end of the study and responses to vitamin D supplements (inflammatory, antioxidant, cell proliferation, differentiation, damage, and apoptosis biomarkers) will be compared between the three subgroups of each VDR polymorphism as well as different VDR haplotype categories.
Genetic variation is a fundamental factor influencing individuals' divergent responses to diet, nutritional status, metabolic response, and diet-related health disorders. Furthermore, studies of gene and environment interactions will provide a precise and accurate assessments of individuals' dietary requirements by considering both the genetic and environmental aspects simultaneously. The results of the current study, to some extent, will highlight the discrepancies existing in the findings of different studies regarding vitamin D, VDR, and cancer by considering both the genetic and environmental aspects simultaneously. If responses to vitamin D supplementation could be modified by VDR SNPs, determining the distribution of VDR polymorphisms in both breast cancer survivors and healthy populations will provide a new insight into the vitamin D requirements of individuals to prevent cancer and its related mortality based on their genotypes. Trial registration This trial has been registered on Iranian Registry of Clinical Trials (IRCT) under the identification code: IRCT2017091736244N1, registration date: 2017-11-10, http://www.irct.ir/trial/27153. |
doi_str_mv | 10.1186/s41043-021-00272-9 |
format | article |
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This is an interventional study in which the effects of vitamin D supplementation on plasma vitamin D levels, inflammatory and antioxidant biomarkers and factors associated with cell proliferation, differentiation, damage, and apoptosis will be investigated stratified by variations in VDR genotype. The present study will be conducted on breast cancer survivors referred to the Shohadaye Tajrish hospital and its associated clinics. One hundred ninety-eight breast cancer survivors will receive 4000 IU of vitamin D3 daily for 12 weeks. VDR Fok1, ApaI, TaqI, BsmI, and Cdx-2 genotype will be determined at the end of the study and responses to vitamin D supplements (inflammatory, antioxidant, cell proliferation, differentiation, damage, and apoptosis biomarkers) will be compared between the three subgroups of each VDR polymorphism as well as different VDR haplotype categories.
Genetic variation is a fundamental factor influencing individuals' divergent responses to diet, nutritional status, metabolic response, and diet-related health disorders. Furthermore, studies of gene and environment interactions will provide a precise and accurate assessments of individuals' dietary requirements by considering both the genetic and environmental aspects simultaneously. The results of the current study, to some extent, will highlight the discrepancies existing in the findings of different studies regarding vitamin D, VDR, and cancer by considering both the genetic and environmental aspects simultaneously. If responses to vitamin D supplementation could be modified by VDR SNPs, determining the distribution of VDR polymorphisms in both breast cancer survivors and healthy populations will provide a new insight into the vitamin D requirements of individuals to prevent cancer and its related mortality based on their genotypes. Trial registration This trial has been registered on Iranian Registry of Clinical Trials (IRCT) under the identification code: IRCT2017091736244N1, registration date: 2017-11-10, http://www.irct.ir/trial/27153.</description><identifier>ISSN: 2072-1315</identifier><identifier>ISSN: 1606-0997</identifier><identifier>EISSN: 2072-1315</identifier><identifier>DOI: 10.1186/s41043-021-00272-9</identifier><identifier>PMID: 34727991</identifier><language>eng</language><publisher>Bangladesh: BioMed Central Ltd</publisher><subject>Alfacalcidol ; Antioxidants ; Apoptosis ; Biological markers ; Biomarkers ; Breast cancer ; Breast cancer survivors ; Breast Neoplasms - genetics ; Calcifediol ; Calciferol ; Cancer ; Cancer Survivors ; Cancer therapies ; Cell differentiation ; Cell growth ; Cell proliferation ; Chemotherapy ; Clinical research ; Clinical trials ; Damage ; Diet ; Dietary Supplements ; Differentiation ; Discrepancies ; Environmental aspects ; Etiology ; Female ; Food science ; Gene polymorphism ; Genes ; Genetic aspects ; Genetic diversity ; Genetic polymorphisms ; Genetic research ; Genotype ; Genotypes ; Haplotypes ; Humans ; Inflammation ; Insight ; Iran ; Medical research ; Metabolic response ; Metabolism ; Mortality ; Nutrition ; Nutritional status ; Oncology, Experimental ; Oxidative stress ; Oxidative Stress - drug effects ; Plasma ; Polymorphism ; Polymorphism, Single Nucleotide ; Prevention ; Receptors ; Receptors, Calcitriol - genetics ; Receptors, Calcitriol - metabolism ; Requirements ; Risk management ; Risk reduction ; Single-nucleotide polymorphism ; Subgroups ; Surgery ; Survival ; Survivor ; Tumors ; Vitamin D ; Vitamin D - administration & dosage ; Vitamin D receptor ; Vitamin D receptors ; Vitamin D, Simultaneously ; Vitamin D3 ; Womens health</subject><ispartof>Journal of health, population and nutrition, 2021-11, Vol.40 (1), p.46-46, Article 46</ispartof><rights>2021. The Author(s).</rights><rights>COPYRIGHT 2021 BioMed Central Ltd.</rights><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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Vitamin D is associated with a reduced risk of incidence and mortality of several human cancers. This study will aim to investigate the possible effects of individual polymorphisms in vitamin D receptor (VDR) as well as effects of VDR haplotypes on response to vitamin D supplementation in breast cancer survivors.
This is an interventional study in which the effects of vitamin D supplementation on plasma vitamin D levels, inflammatory and antioxidant biomarkers and factors associated with cell proliferation, differentiation, damage, and apoptosis will be investigated stratified by variations in VDR genotype. The present study will be conducted on breast cancer survivors referred to the Shohadaye Tajrish hospital and its associated clinics. One hundred ninety-eight breast cancer survivors will receive 4000 IU of vitamin D3 daily for 12 weeks. VDR Fok1, ApaI, TaqI, BsmI, and Cdx-2 genotype will be determined at the end of the study and responses to vitamin D supplements (inflammatory, antioxidant, cell proliferation, differentiation, damage, and apoptosis biomarkers) will be compared between the three subgroups of each VDR polymorphism as well as different VDR haplotype categories.
Genetic variation is a fundamental factor influencing individuals' divergent responses to diet, nutritional status, metabolic response, and diet-related health disorders. Furthermore, studies of gene and environment interactions will provide a precise and accurate assessments of individuals' dietary requirements by considering both the genetic and environmental aspects simultaneously. The results of the current study, to some extent, will highlight the discrepancies existing in the findings of different studies regarding vitamin D, VDR, and cancer by considering both the genetic and environmental aspects simultaneously. If responses to vitamin D supplementation could be modified by VDR SNPs, determining the distribution of VDR polymorphisms in both breast cancer survivors and healthy populations will provide a new insight into the vitamin D requirements of individuals to prevent cancer and its related mortality based on their genotypes. Trial registration This trial has been registered on Iranian Registry of Clinical Trials (IRCT) under the identification code: IRCT2017091736244N1, registration date: 2017-11-10, http://www.irct.ir/trial/27153.</description><subject>Alfacalcidol</subject><subject>Antioxidants</subject><subject>Apoptosis</subject><subject>Biological markers</subject><subject>Biomarkers</subject><subject>Breast cancer</subject><subject>Breast cancer survivors</subject><subject>Breast Neoplasms - genetics</subject><subject>Calcifediol</subject><subject>Calciferol</subject><subject>Cancer</subject><subject>Cancer Survivors</subject><subject>Cancer therapies</subject><subject>Cell differentiation</subject><subject>Cell growth</subject><subject>Cell proliferation</subject><subject>Chemotherapy</subject><subject>Clinical research</subject><subject>Clinical trials</subject><subject>Damage</subject><subject>Diet</subject><subject>Dietary Supplements</subject><subject>Differentiation</subject><subject>Discrepancies</subject><subject>Environmental aspects</subject><subject>Etiology</subject><subject>Female</subject><subject>Food science</subject><subject>Gene polymorphism</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic diversity</subject><subject>Genetic polymorphisms</subject><subject>Genetic research</subject><subject>Genotype</subject><subject>Genotypes</subject><subject>Haplotypes</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Insight</subject><subject>Iran</subject><subject>Medical research</subject><subject>Metabolic response</subject><subject>Metabolism</subject><subject>Mortality</subject><subject>Nutrition</subject><subject>Nutritional status</subject><subject>Oncology, Experimental</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Plasma</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Prevention</subject><subject>Receptors</subject><subject>Receptors, Calcitriol - genetics</subject><subject>Receptors, Calcitriol - metabolism</subject><subject>Requirements</subject><subject>Risk management</subject><subject>Risk reduction</subject><subject>Single-nucleotide polymorphism</subject><subject>Subgroups</subject><subject>Surgery</subject><subject>Survival</subject><subject>Survivor</subject><subject>Tumors</subject><subject>Vitamin D</subject><subject>Vitamin D - administration & dosage</subject><subject>Vitamin D receptor</subject><subject>Vitamin D receptors</subject><subject>Vitamin D, Simultaneously</subject><subject>Vitamin D3</subject><subject>Womens health</subject><issn>2072-1315</issn><issn>1606-0997</issn><issn>2072-1315</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>7QJ</sourceid><sourceid>ALSLI</sourceid><sourceid>HEHIP</sourceid><sourceid>M2R</sourceid><sourceid>M2S</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptk9tu1DAQhiMEoqXwAlwgS0gIpG7xIQeHC6SqnCpVQuJwbTnOZNfFiYPtROV9eRAm3dLuIpRImdjf_09m4smyp4yeMCbL1zFnNBcrytmKUl7xVX0vO-QUAyZYcX8nPsgexXiJUE0lf5gdiLziVV2zw-z3aYwQYw9DImkDBLoOTCK-I7NNurcDeUfiNI4OFkQn6weC9-h07PUO42AGF4-JHTqn-_4aPCZ6aIm_si2-zkBiCpiKNNb3OvyAgKGO0C5-d0YBDIzJB7KGAZI1ZNbBbvPifhNAx0SMHgwE_LAw29mH-IZoMgafvPGOdCg2zg7WaEcSit3j7EGnXYQnN8-j7PuH99_OPq0uPn88Pzu9WJmSy7Rqci4aA7LQsqi0KEFUTJpC87otGpOzUrRUFAVrdUPzImd1ldOOc8NbUXctZeIoO9_6tl5fqjFYrPOX8tqq6wUf1koHrMmBqqSgBdPoJIpccF7XsmlpwxtTAhcA6PV26zVOTQ-twe4H7fZM93cGu1FrPytZlKwuJRq8vDEI_ucEManeRgPO6QH8FBUvakG55DJH9Pk_6KWfwoCtWqia0rzk_I5aaywAf7THvGYxVaelZHgWc754nfyHwquF3ho_QGdxfU_wak-ATIKrtNZTjOr865d99sUOuwHt0iZ6Ny3HI-6DfAua4GMM0N02jlG1DI_aDo_C4VHXw6NqFD3bbfmt5O-0iD9dIxb1</recordid><startdate>20211102</startdate><enddate>20211102</enddate><creator>Kazemian, Elham</creator><creator>Akbari, Mohammad Esmaeil</creator><creator>Moradi, Nariman</creator><creator>Gharibzadeh, Safoora</creator><creator>Amouzegar, Atieh</creator><creator>Rozek, Laura S</creator><creator>Mondul, Alison M</creator><creator>Khademolmele, Maryam</creator><creator>Zarins, Katie R</creator><creator>Ghodoosi, Nasim</creator><creator>Shateri, Zahra</creator><creator>Fallah, Soudabeh</creator><creator>Davoodi, Sayed Hossein</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>ISR</scope><scope>0-V</scope><scope>3V.</scope><scope>7QJ</scope><scope>7QL</scope><scope>7RQ</scope><scope>7RV</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>88J</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HEHIP</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2R</scope><scope>M2S</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20211102</creationdate><title>Assessment the effect of vitamin D supplementation on plasma vitamin D levels, inflammation, and oxidative stress biomarkers based on vitamin D receptor genetic variation in breast cancer survivors: a protocol for clinical trial</title><author>Kazemian, Elham ; Akbari, Mohammad Esmaeil ; Moradi, Nariman ; Gharibzadeh, Safoora ; Amouzegar, Atieh ; Rozek, Laura S ; Mondul, Alison M ; Khademolmele, Maryam ; Zarins, Katie R ; Ghodoosi, Nasim ; Shateri, Zahra ; Fallah, Soudabeh ; Davoodi, Sayed Hossein</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c628t-b423bce85a857a36e3718c5a29d5bc4163d03551dab045419740f22c2d39fd013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alfacalcidol</topic><topic>Antioxidants</topic><topic>Apoptosis</topic><topic>Biological markers</topic><topic>Biomarkers</topic><topic>Breast cancer</topic><topic>Breast cancer survivors</topic><topic>Breast Neoplasms - genetics</topic><topic>Calcifediol</topic><topic>Calciferol</topic><topic>Cancer</topic><topic>Cancer Survivors</topic><topic>Cancer therapies</topic><topic>Cell differentiation</topic><topic>Cell growth</topic><topic>Cell proliferation</topic><topic>Chemotherapy</topic><topic>Clinical research</topic><topic>Clinical trials</topic><topic>Damage</topic><topic>Diet</topic><topic>Dietary Supplements</topic><topic>Differentiation</topic><topic>Discrepancies</topic><topic>Environmental aspects</topic><topic>Etiology</topic><topic>Female</topic><topic>Food science</topic><topic>Gene polymorphism</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic diversity</topic><topic>Genetic polymorphisms</topic><topic>Genetic research</topic><topic>Genotype</topic><topic>Genotypes</topic><topic>Haplotypes</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Insight</topic><topic>Iran</topic><topic>Medical research</topic><topic>Metabolic response</topic><topic>Metabolism</topic><topic>Mortality</topic><topic>Nutrition</topic><topic>Nutritional status</topic><topic>Oncology, Experimental</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Plasma</topic><topic>Polymorphism</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Prevention</topic><topic>Receptors</topic><topic>Receptors, Calcitriol - genetics</topic><topic>Receptors, Calcitriol - metabolism</topic><topic>Requirements</topic><topic>Risk management</topic><topic>Risk reduction</topic><topic>Single-nucleotide polymorphism</topic><topic>Subgroups</topic><topic>Surgery</topic><topic>Survival</topic><topic>Survivor</topic><topic>Tumors</topic><topic>Vitamin D</topic><topic>Vitamin D - administration & dosage</topic><topic>Vitamin D receptor</topic><topic>Vitamin D receptors</topic><topic>Vitamin D, Simultaneously</topic><topic>Vitamin D3</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kazemian, Elham</creatorcontrib><creatorcontrib>Akbari, Mohammad Esmaeil</creatorcontrib><creatorcontrib>Moradi, Nariman</creatorcontrib><creatorcontrib>Gharibzadeh, Safoora</creatorcontrib><creatorcontrib>Amouzegar, Atieh</creatorcontrib><creatorcontrib>Rozek, Laura S</creatorcontrib><creatorcontrib>Mondul, Alison M</creatorcontrib><creatorcontrib>Khademolmele, Maryam</creatorcontrib><creatorcontrib>Zarins, Katie R</creatorcontrib><creatorcontrib>Ghodoosi, Nasim</creatorcontrib><creatorcontrib>Shateri, Zahra</creatorcontrib><creatorcontrib>Fallah, Soudabeh</creatorcontrib><creatorcontrib>Davoodi, Sayed 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>Gale In Context: Science</collection><collection>ProQuest Social Sciences Premium Collection【Remote access available】</collection><collection>ProQuest Central (Corporate)</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Career & Technical Education Database</collection><collection>ProQuest Nursing and Allied Health Source</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>Social Science Database (Alumni Edition)</collection><collection>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>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Social Science Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Sociology Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>Social Science Database</collection><collection>Sociology Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest - 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>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of health, population and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kazemian, Elham</au><au>Akbari, Mohammad Esmaeil</au><au>Moradi, Nariman</au><au>Gharibzadeh, Safoora</au><au>Amouzegar, Atieh</au><au>Rozek, Laura S</au><au>Mondul, Alison M</au><au>Khademolmele, Maryam</au><au>Zarins, Katie R</au><au>Ghodoosi, Nasim</au><au>Shateri, Zahra</au><au>Fallah, Soudabeh</au><au>Davoodi, Sayed Hossein</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessment the effect of vitamin D supplementation on plasma vitamin D levels, inflammation, and oxidative stress biomarkers based on vitamin D receptor genetic variation in breast cancer survivors: a protocol for clinical trial</atitle><jtitle>Journal of health, population and nutrition</jtitle><addtitle>J Health Popul Nutr</addtitle><date>2021-11-02</date><risdate>2021</risdate><volume>40</volume><issue>1</issue><spage>46</spage><epage>46</epage><pages>46-46</pages><artnum>46</artnum><issn>2072-1315</issn><issn>1606-0997</issn><eissn>2072-1315</eissn><abstract>Both human genes and environmental exposures, due to complex interplay, play important role in the cancer etiology. Vitamin D is associated with a reduced risk of incidence and mortality of several human cancers. This study will aim to investigate the possible effects of individual polymorphisms in vitamin D receptor (VDR) as well as effects of VDR haplotypes on response to vitamin D supplementation in breast cancer survivors.
This is an interventional study in which the effects of vitamin D supplementation on plasma vitamin D levels, inflammatory and antioxidant biomarkers and factors associated with cell proliferation, differentiation, damage, and apoptosis will be investigated stratified by variations in VDR genotype. The present study will be conducted on breast cancer survivors referred to the Shohadaye Tajrish hospital and its associated clinics. One hundred ninety-eight breast cancer survivors will receive 4000 IU of vitamin D3 daily for 12 weeks. VDR Fok1, ApaI, TaqI, BsmI, and Cdx-2 genotype will be determined at the end of the study and responses to vitamin D supplements (inflammatory, antioxidant, cell proliferation, differentiation, damage, and apoptosis biomarkers) will be compared between the three subgroups of each VDR polymorphism as well as different VDR haplotype categories.
Genetic variation is a fundamental factor influencing individuals' divergent responses to diet, nutritional status, metabolic response, and diet-related health disorders. Furthermore, studies of gene and environment interactions will provide a precise and accurate assessments of individuals' dietary requirements by considering both the genetic and environmental aspects simultaneously. The results of the current study, to some extent, will highlight the discrepancies existing in the findings of different studies regarding vitamin D, VDR, and cancer by considering both the genetic and environmental aspects simultaneously. If responses to vitamin D supplementation could be modified by VDR SNPs, determining the distribution of VDR polymorphisms in both breast cancer survivors and healthy populations will provide a new insight into the vitamin D requirements of individuals to prevent cancer and its related mortality based on their genotypes. Trial registration This trial has been registered on Iranian Registry of Clinical Trials (IRCT) under the identification code: IRCT2017091736244N1, registration date: 2017-11-10, http://www.irct.ir/trial/27153.</abstract><cop>Bangladesh</cop><pub>BioMed Central Ltd</pub><pmid>34727991</pmid><doi>10.1186/s41043-021-00272-9</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2072-1315 |
ispartof | Journal of health, population and nutrition, 2021-11, Vol.40 (1), p.46-46, Article 46 |
issn | 2072-1315 1606-0997 2072-1315 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_783051aab0354322998bd0b2bc6e23ee |
source | Applied Social Sciences Index & Abstracts (ASSIA); PubMed Central(OpenAccess); Social Science Premium Collection (Proquest) (PQ_SDU_P3); Sociology Collection; ProQuest - Publicly Available Content Database |
subjects | Alfacalcidol Antioxidants Apoptosis Biological markers Biomarkers Breast cancer Breast cancer survivors Breast Neoplasms - genetics Calcifediol Calciferol Cancer Cancer Survivors Cancer therapies Cell differentiation Cell growth Cell proliferation Chemotherapy Clinical research Clinical trials Damage Diet Dietary Supplements Differentiation Discrepancies Environmental aspects Etiology Female Food science Gene polymorphism Genes Genetic aspects Genetic diversity Genetic polymorphisms Genetic research Genotype Genotypes Haplotypes Humans Inflammation Insight Iran Medical research Metabolic response Metabolism Mortality Nutrition Nutritional status Oncology, Experimental Oxidative stress Oxidative Stress - drug effects Plasma Polymorphism Polymorphism, Single Nucleotide Prevention Receptors Receptors, Calcitriol - genetics Receptors, Calcitriol - metabolism Requirements Risk management Risk reduction Single-nucleotide polymorphism Subgroups Surgery Survival Survivor Tumors Vitamin D Vitamin D - administration & dosage Vitamin D receptor Vitamin D receptors Vitamin D, Simultaneously Vitamin D3 Womens health |
title | Assessment the effect of vitamin D supplementation on plasma vitamin D levels, inflammation, and oxidative stress biomarkers based on vitamin D receptor genetic variation in breast cancer survivors: a protocol for clinical trial |
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