Vitamin D in endometriosis: A causative or confounding factor?
Abstract Objective The aim of this paper is to review the evidence from studies that evaluated the relationship between vitamin D and endometriosis. Design Comprehensive review. Materials and Methods Systematic literature search in Medline for relevant publications from 1946 until June 2013. Results...
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description | Abstract Objective The aim of this paper is to review the evidence from studies that evaluated the relationship between vitamin D and endometriosis. Design Comprehensive review. Materials and Methods Systematic literature search in Medline for relevant publications from 1946 until June 2013. Results Endometriosis risk may be influenced by dietary vitamin D intake and plasma hydroxyvitamin D concentration. Vitamin D receptor and vitamin D metabolizing enzymes, 24-hydroxylase and 1-α hydroxylase, are found in the normal cycling endometrium and also in the eutopic and ectopic endometrium of women with endometriosis. The endometrium is a target of 1, 25 dihydroxyvitamin D actions through regulation of specific genes and via immunomodulation. The endometrium in endometriosis expresses dysregulation of some vitamin D enzymes and receptors. If vitamin D and its metabolites are implicated in endometriosis-associated infertility, it is likely through interference with HOXA10 gene expression. The Gc2 phenotype of vitamin D binding protein is prevalent in women with endometriosis and may be implicated in its pathogenesis. In a mouse model, Elocalcitol, a VDR-agonist was shown to reduce the development of endometriotic lesions and recurrence. Conclusion A biological plausibility for a role of vitamin D, as an immunomodulator and anti-inflammatory agent, in the pathogenesis and treatment of endometriosis is suggested in this article, but is difficult to illustrate due to sparse evidence from human studies limited primarily to case–control studies. A significant knowledge gap precludes the establishment of a clear cause–effect relationship. The intriguing leads presented herein need to be investigated further with placebo-controlled supplementation trials. |
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Design Comprehensive review. Materials and Methods Systematic literature search in Medline for relevant publications from 1946 until June 2013. Results Endometriosis risk may be influenced by dietary vitamin D intake and plasma hydroxyvitamin D concentration. Vitamin D receptor and vitamin D metabolizing enzymes, 24-hydroxylase and 1-α hydroxylase, are found in the normal cycling endometrium and also in the eutopic and ectopic endometrium of women with endometriosis. The endometrium is a target of 1, 25 dihydroxyvitamin D actions through regulation of specific genes and via immunomodulation. The endometrium in endometriosis expresses dysregulation of some vitamin D enzymes and receptors. If vitamin D and its metabolites are implicated in endometriosis-associated infertility, it is likely through interference with HOXA10 gene expression. The Gc2 phenotype of vitamin D binding protein is prevalent in women with endometriosis and may be implicated in its pathogenesis. In a mouse model, Elocalcitol, a VDR-agonist was shown to reduce the development of endometriotic lesions and recurrence. Conclusion A biological plausibility for a role of vitamin D, as an immunomodulator and anti-inflammatory agent, in the pathogenesis and treatment of endometriosis is suggested in this article, but is difficult to illustrate due to sparse evidence from human studies limited primarily to case–control studies. A significant knowledge gap precludes the establishment of a clear cause–effect relationship. The intriguing leads presented herein need to be investigated further with placebo-controlled supplementation trials.</description><identifier>ISSN: 0026-0495</identifier><identifier>EISSN: 1532-8600</identifier><identifier>DOI: 10.1016/j.metabol.2013.09.012</identifier><identifier>PMID: 24135500</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Antineoplastic Agents - pharmacology ; Autoimmunity ; Biological and medical sciences ; Calcitriol - analogs & derivatives ; Calcitriol - blood ; Calcitriol - pharmacology ; Chronic Pain - etiology ; Dietary Supplements ; Dysmenorrhea - drug therapy ; Dysmenorrhea - etiology ; Elocalcitol ; Endocrinology & Metabolism ; Endometriosis - complications ; Endometriosis - immunology ; Endometriosis - metabolism ; Endometrium ; Endometrium - metabolism ; Endometrium - pathology ; Feeding. Feeding behavior ; Female ; Female genital diseases ; Fundamental and applied biological sciences. Psychology ; Gynecology. Andrology. Obstetrics ; Homeodomain Proteins - genetics ; HOXA 10 gene ; Humans ; Immunologic Factors - pharmacology ; Infertility, Female - etiology ; Infertility, Female - prevention & control ; Medical sciences ; Mice ; Non tumoral diseases ; Osteopontin - genetics ; Receptors, Calcitriol - metabolism ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Vitamin D - administration & dosage ; Vitamin D - immunology ; Vitamin D - metabolism ; Vitamin D binding protein</subject><ispartof>Metabolism, clinical and experimental, 2014, Vol.63 (1), p.32-41</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>2013.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-ef5b197d521ee1db6f0350ba89b9647298425520b9e37e26dbd43b9ee89acf8f3</citedby><cites>FETCH-LOGICAL-c450t-ef5b197d521ee1db6f0350ba89b9647298425520b9e37e26dbd43b9ee89acf8f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.metabol.2013.09.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28348275$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24135500$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sayegh, Lamia</creatorcontrib><creatorcontrib>Fuleihan, Ghada El-Hajj</creatorcontrib><creatorcontrib>Nassar, Anwar H</creatorcontrib><title>Vitamin D in endometriosis: A causative or confounding factor?</title><title>Metabolism, clinical and experimental</title><addtitle>Metabolism</addtitle><description>Abstract Objective The aim of this paper is to review the evidence from studies that evaluated the relationship between vitamin D and endometriosis. Design Comprehensive review. Materials and Methods Systematic literature search in Medline for relevant publications from 1946 until June 2013. Results Endometriosis risk may be influenced by dietary vitamin D intake and plasma hydroxyvitamin D concentration. Vitamin D receptor and vitamin D metabolizing enzymes, 24-hydroxylase and 1-α hydroxylase, are found in the normal cycling endometrium and also in the eutopic and ectopic endometrium of women with endometriosis. The endometrium is a target of 1, 25 dihydroxyvitamin D actions through regulation of specific genes and via immunomodulation. The endometrium in endometriosis expresses dysregulation of some vitamin D enzymes and receptors. If vitamin D and its metabolites are implicated in endometriosis-associated infertility, it is likely through interference with HOXA10 gene expression. The Gc2 phenotype of vitamin D binding protein is prevalent in women with endometriosis and may be implicated in its pathogenesis. In a mouse model, Elocalcitol, a VDR-agonist was shown to reduce the development of endometriotic lesions and recurrence. Conclusion A biological plausibility for a role of vitamin D, as an immunomodulator and anti-inflammatory agent, in the pathogenesis and treatment of endometriosis is suggested in this article, but is difficult to illustrate due to sparse evidence from human studies limited primarily to case–control studies. A significant knowledge gap precludes the establishment of a clear cause–effect relationship. The intriguing leads presented herein need to be investigated further with placebo-controlled supplementation trials.</description><subject>Animals</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Autoimmunity</subject><subject>Biological and medical sciences</subject><subject>Calcitriol - analogs & derivatives</subject><subject>Calcitriol - blood</subject><subject>Calcitriol - pharmacology</subject><subject>Chronic Pain - etiology</subject><subject>Dietary Supplements</subject><subject>Dysmenorrhea - drug therapy</subject><subject>Dysmenorrhea - etiology</subject><subject>Elocalcitol</subject><subject>Endocrinology & Metabolism</subject><subject>Endometriosis - complications</subject><subject>Endometriosis - immunology</subject><subject>Endometriosis - metabolism</subject><subject>Endometrium</subject><subject>Endometrium - metabolism</subject><subject>Endometrium - pathology</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Homeodomain Proteins - genetics</subject><subject>HOXA 10 gene</subject><subject>Humans</subject><subject>Immunologic Factors - pharmacology</subject><subject>Infertility, Female - etiology</subject><subject>Infertility, Female - prevention & control</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Non tumoral diseases</subject><subject>Osteopontin - genetics</subject><subject>Receptors, Calcitriol - metabolism</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Vitamin D - administration & dosage</subject><subject>Vitamin D - immunology</subject><subject>Vitamin D - metabolism</subject><subject>Vitamin D binding protein</subject><issn>0026-0495</issn><issn>1532-8600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi1ERZfCTwDlgtRLwtiOHZtDq6pQqFSphwJXy3EmyEtiFzup1H-PV7sFiQsXf0jPvDN6hpA3FBoKVL7fNjMuto9Tw4DyBnQDlD0jGyo4q5UEeE42AEzW0GpxTF7mvAWArlPyBTlmLeVCAGzI2Xe_2NmH6mNVDgxDLLHJx-zzh-qicnbNdvEPWMVUuRjGuIbBhx_VaN0S0_krcjTaKePrw31Cvl19-nr5pb65_Xx9eXFTu1bAUuMoeqq7QTCKSIdejsAF9FbpXsu2Y1q1TAgGvUbeIZNDP7S8fFBp60Y18hNyus-9T_HXinkxs88Op8kGjGs2tJUdSNUqVVCxR12KOScczX3ys02PhoLZqTNbc1BnduoMaFPUlbq3hxZrP-Pwp-rJVQHeHQCbnZ3GZIPz-S-neKtYJwp3vuewCHnwmEx2HoPDwSd0ixmi_-8oZ_8kuMkHX5r-xEfM27imUGwbajIzYO52e96tmfLy0lLw38hAotw</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Sayegh, Lamia</creator><creator>Fuleihan, Ghada El-Hajj</creator><creator>Nassar, Anwar H</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>2014</creationdate><title>Vitamin D in endometriosis: A causative or confounding factor?</title><author>Sayegh, Lamia ; Fuleihan, Ghada El-Hajj ; Nassar, Anwar H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-ef5b197d521ee1db6f0350ba89b9647298425520b9e37e26dbd43b9ee89acf8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Autoimmunity</topic><topic>Biological and medical sciences</topic><topic>Calcitriol - analogs & derivatives</topic><topic>Calcitriol - blood</topic><topic>Calcitriol - pharmacology</topic><topic>Chronic Pain - etiology</topic><topic>Dietary Supplements</topic><topic>Dysmenorrhea - drug therapy</topic><topic>Dysmenorrhea - etiology</topic><topic>Elocalcitol</topic><topic>Endocrinology & Metabolism</topic><topic>Endometriosis - complications</topic><topic>Endometriosis - immunology</topic><topic>Endometriosis - metabolism</topic><topic>Endometrium</topic><topic>Endometrium - metabolism</topic><topic>Endometrium - pathology</topic><topic>Feeding. Feeding behavior</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Homeodomain Proteins - genetics</topic><topic>HOXA 10 gene</topic><topic>Humans</topic><topic>Immunologic Factors - pharmacology</topic><topic>Infertility, Female - etiology</topic><topic>Infertility, Female - prevention & control</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Non tumoral diseases</topic><topic>Osteopontin - genetics</topic><topic>Receptors, Calcitriol - metabolism</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Vitamin D - administration & dosage</topic><topic>Vitamin D - immunology</topic><topic>Vitamin D - metabolism</topic><topic>Vitamin D binding protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sayegh, Lamia</creatorcontrib><creatorcontrib>Fuleihan, Ghada El-Hajj</creatorcontrib><creatorcontrib>Nassar, Anwar H</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Metabolism, clinical and experimental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sayegh, Lamia</au><au>Fuleihan, Ghada El-Hajj</au><au>Nassar, Anwar H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vitamin D in endometriosis: A causative or confounding factor?</atitle><jtitle>Metabolism, clinical and experimental</jtitle><addtitle>Metabolism</addtitle><date>2014</date><risdate>2014</risdate><volume>63</volume><issue>1</issue><spage>32</spage><epage>41</epage><pages>32-41</pages><issn>0026-0495</issn><eissn>1532-8600</eissn><abstract>Abstract Objective The aim of this paper is to review the evidence from studies that evaluated the relationship between vitamin D and endometriosis. Design Comprehensive review. Materials and Methods Systematic literature search in Medline for relevant publications from 1946 until June 2013. Results Endometriosis risk may be influenced by dietary vitamin D intake and plasma hydroxyvitamin D concentration. Vitamin D receptor and vitamin D metabolizing enzymes, 24-hydroxylase and 1-α hydroxylase, are found in the normal cycling endometrium and also in the eutopic and ectopic endometrium of women with endometriosis. The endometrium is a target of 1, 25 dihydroxyvitamin D actions through regulation of specific genes and via immunomodulation. The endometrium in endometriosis expresses dysregulation of some vitamin D enzymes and receptors. If vitamin D and its metabolites are implicated in endometriosis-associated infertility, it is likely through interference with HOXA10 gene expression. The Gc2 phenotype of vitamin D binding protein is prevalent in women with endometriosis and may be implicated in its pathogenesis. In a mouse model, Elocalcitol, a VDR-agonist was shown to reduce the development of endometriotic lesions and recurrence. Conclusion A biological plausibility for a role of vitamin D, as an immunomodulator and anti-inflammatory agent, in the pathogenesis and treatment of endometriosis is suggested in this article, but is difficult to illustrate due to sparse evidence from human studies limited primarily to case–control studies. A significant knowledge gap precludes the establishment of a clear cause–effect relationship. The intriguing leads presented herein need to be investigated further with placebo-controlled supplementation trials.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>24135500</pmid><doi>10.1016/j.metabol.2013.09.012</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Antineoplastic Agents - pharmacology Autoimmunity Biological and medical sciences Calcitriol - analogs & derivatives Calcitriol - blood Calcitriol - pharmacology Chronic Pain - etiology Dietary Supplements Dysmenorrhea - drug therapy Dysmenorrhea - etiology Elocalcitol Endocrinology & Metabolism Endometriosis - complications Endometriosis - immunology Endometriosis - metabolism Endometrium Endometrium - metabolism Endometrium - pathology Feeding. Feeding behavior Female Female genital diseases Fundamental and applied biological sciences. Psychology Gynecology. Andrology. Obstetrics Homeodomain Proteins - genetics HOXA 10 gene Humans Immunologic Factors - pharmacology Infertility, Female - etiology Infertility, Female - prevention & control Medical sciences Mice Non tumoral diseases Osteopontin - genetics Receptors, Calcitriol - metabolism Vertebrates: anatomy and physiology, studies on body, several organs or systems Vitamin D - administration & dosage Vitamin D - immunology Vitamin D - metabolism Vitamin D binding protein |
title | Vitamin D in endometriosis: A causative or confounding factor? |
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