Study of circulating hepcidin in association with iron excess, metabolic syndrome, and BMP-6 expression in granulosa cells in women with polycystic ovary syndrome
Objective To identify the role of hepcidin in polycystic ovary syndrome (PCOS) patients. Design Cross-sectional case-control study. Setting Academic medical center. Patient(s) Sixty-seven PCOS patients and 94 healthy parous women volunteered for the study. Intervention(s) None. Main Outcome Measure(...
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container_title | Fertility and sterility |
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creator | Kim, Ji Won, M.D., Ph.D Kang, Kyung Min, M.Sc Yoon, Tae Ki, M.D., Ph.D Shim, Sung Han, Ph.D Lee, Woo Sik, M.D., Ph.D |
description | Objective To identify the role of hepcidin in polycystic ovary syndrome (PCOS) patients. Design Cross-sectional case-control study. Setting Academic medical center. Patient(s) Sixty-seven PCOS patients and 94 healthy parous women volunteered for the study. Intervention(s) None. Main Outcome Measure(s) Serum levels of hepcidin, hormone and lipid profiles, parameters of iron and glucose metabolism, high-sensitivity C-reactive protein (hs-CRP), and bone morphogenetic protein 6 ( BMP-6 ) mRNA expressions in the granulosa cells (GCs). Result(s) PCOS patients showed increased serum iron concentration and higher circulating hepcidin levels compared with control subjects, even with only lean subjects. Circulating hepcidin correlated with iron parameters, androgen index, hs-CRP, and fasting glucose and insulin levels, and with iron and ferritin levels after multiple regression analysis. We analyzed BMP-6 mRNA expression in the 89 GCs from nine PCOS patients and five non-PCOS women with the use of quantitative real-time polymerase chain reaction, and no correlations existed between iron parameters, including circulating hepcidin, and BMP-6 expression in the GCs from PCOS women. Conclusion(s) PCOS patients had iron excess and higher hepcidin levels, which are associated with metabolic derangements. Circulating hepcidin is appropriately increased relative to the iron burden even in PCOS women, suggesting that iron excess in PCOS women does not result from a defect in the production of hepcidin. But there were no correlations between iron parameters and the expression of the BMP-6 in GCs from PCOS patients. |
doi_str_mv | 10.1016/j.fertnstert.2014.04.031 |
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Design Cross-sectional case-control study. Setting Academic medical center. Patient(s) Sixty-seven PCOS patients and 94 healthy parous women volunteered for the study. Intervention(s) None. Main Outcome Measure(s) Serum levels of hepcidin, hormone and lipid profiles, parameters of iron and glucose metabolism, high-sensitivity C-reactive protein (hs-CRP), and bone morphogenetic protein 6 ( BMP-6 ) mRNA expressions in the granulosa cells (GCs). Result(s) PCOS patients showed increased serum iron concentration and higher circulating hepcidin levels compared with control subjects, even with only lean subjects. Circulating hepcidin correlated with iron parameters, androgen index, hs-CRP, and fasting glucose and insulin levels, and with iron and ferritin levels after multiple regression analysis. We analyzed BMP-6 mRNA expression in the 89 GCs from nine PCOS patients and five non-PCOS women with the use of quantitative real-time polymerase chain reaction, and no correlations existed between iron parameters, including circulating hepcidin, and BMP-6 expression in the GCs from PCOS women. Conclusion(s) PCOS patients had iron excess and higher hepcidin levels, which are associated with metabolic derangements. Circulating hepcidin is appropriately increased relative to the iron burden even in PCOS women, suggesting that iron excess in PCOS women does not result from a defect in the production of hepcidin. But there were no correlations between iron parameters and the expression of the BMP-6 in GCs from PCOS patients.</description><identifier>ISSN: 0015-0282</identifier><identifier>EISSN: 1556-5653</identifier><identifier>DOI: 10.1016/j.fertnstert.2014.04.031</identifier><identifier>PMID: 24875397</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Biomarkers - blood ; BMP-6 ; Bone Morphogenetic Protein 6 - genetics ; Bone Morphogenetic Protein 6 - metabolism ; Case-Control Studies ; Cross-Sectional Studies ; Female ; Granulosa Cells - metabolism ; hepcidin ; Hepcidins - blood ; Humans ; Internal Medicine ; Iron - blood ; iron excess ; metabolic syndrome ; Metabolic Syndrome - blood ; Metabolic Syndrome - diagnosis ; Obstetrics and Gynecology ; Polycystic ovary syndrome ; Polycystic Ovary Syndrome - blood ; Polycystic Ovary Syndrome - diagnosis ; Polycystic Ovary Syndrome - genetics ; Real-Time Polymerase Chain Reaction ; RNA, Messenger - analysis ; Up-Regulation</subject><ispartof>Fertility and sterility, 2014-08, Vol.102 (2), p.548-554.e2</ispartof><rights>American Society for Reproductive Medicine</rights><rights>2014 American Society for Reproductive Medicine</rights><rights>Copyright © 2014 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c549t-85e7fea4e7766db879714aba8f91bf8477e3314747ab3069bd582fa535ee71e03</citedby><cites>FETCH-LOGICAL-c549t-85e7fea4e7766db879714aba8f91bf8477e3314747ab3069bd582fa535ee71e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0015028214003914$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24875397$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Ji Won, M.D., Ph.D</creatorcontrib><creatorcontrib>Kang, Kyung Min, M.Sc</creatorcontrib><creatorcontrib>Yoon, Tae Ki, M.D., Ph.D</creatorcontrib><creatorcontrib>Shim, Sung Han, Ph.D</creatorcontrib><creatorcontrib>Lee, Woo Sik, M.D., Ph.D</creatorcontrib><title>Study of circulating hepcidin in association with iron excess, metabolic syndrome, and BMP-6 expression in granulosa cells in women with polycystic ovary syndrome</title><title>Fertility and sterility</title><addtitle>Fertil Steril</addtitle><description>Objective To identify the role of hepcidin in polycystic ovary syndrome (PCOS) patients. Design Cross-sectional case-control study. Setting Academic medical center. Patient(s) Sixty-seven PCOS patients and 94 healthy parous women volunteered for the study. Intervention(s) None. Main Outcome Measure(s) Serum levels of hepcidin, hormone and lipid profiles, parameters of iron and glucose metabolism, high-sensitivity C-reactive protein (hs-CRP), and bone morphogenetic protein 6 ( BMP-6 ) mRNA expressions in the granulosa cells (GCs). Result(s) PCOS patients showed increased serum iron concentration and higher circulating hepcidin levels compared with control subjects, even with only lean subjects. Circulating hepcidin correlated with iron parameters, androgen index, hs-CRP, and fasting glucose and insulin levels, and with iron and ferritin levels after multiple regression analysis. We analyzed BMP-6 mRNA expression in the 89 GCs from nine PCOS patients and five non-PCOS women with the use of quantitative real-time polymerase chain reaction, and no correlations existed between iron parameters, including circulating hepcidin, and BMP-6 expression in the GCs from PCOS women. Conclusion(s) PCOS patients had iron excess and higher hepcidin levels, which are associated with metabolic derangements. Circulating hepcidin is appropriately increased relative to the iron burden even in PCOS women, suggesting that iron excess in PCOS women does not result from a defect in the production of hepcidin. But there were no correlations between iron parameters and the expression of the BMP-6 in GCs from PCOS patients.</description><subject>Adult</subject><subject>Biomarkers - blood</subject><subject>BMP-6</subject><subject>Bone Morphogenetic Protein 6 - genetics</subject><subject>Bone Morphogenetic Protein 6 - metabolism</subject><subject>Case-Control Studies</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>Granulosa Cells - metabolism</subject><subject>hepcidin</subject><subject>Hepcidins - blood</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Iron - blood</subject><subject>iron excess</subject><subject>metabolic syndrome</subject><subject>Metabolic Syndrome - blood</subject><subject>Metabolic Syndrome - diagnosis</subject><subject>Obstetrics and Gynecology</subject><subject>Polycystic ovary syndrome</subject><subject>Polycystic Ovary Syndrome - blood</subject><subject>Polycystic Ovary Syndrome - diagnosis</subject><subject>Polycystic Ovary Syndrome - genetics</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>RNA, Messenger - analysis</subject><subject>Up-Regulation</subject><issn>0015-0282</issn><issn>1556-5653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUk1v1DAQtRCILoW_gHzk0Cx2bMfJBYlW5UMqAqlwthxn0nrJ2sGTtOTv8EtxtEuROCGNbGv03pvxvCGEcrbljFevd9se0hRwyue2ZFxuWQ7BH5ENV6oqVKXEY7JhjKuClXV5Qp4h7hhjFdflU3JSylor0egN-XU9zd1CY0-dT24e7OTDDb2F0fnOB5rDIkbncz4Geu-nW-pTfsFPB4hndA-TbePgHcUldCnu4Yza0NHzT1-KKqPGlGErNSvdJBvmIaKlDoYB19R9JhxlxzgsbsEpS8U7m5YHwefkSW8HhBfH-5R8e3f59eJDcfX5_ceLt1eFU7KZilqB7sFK0LqqurbWjebStrbuG972tdQahOBSS21bwaqm7VRd9lYJBaA5MHFKXh10xxR_zICT2XtcO7UB4owmT5azUknJM7Q-QF2KiAl6Mya_z00bzszqkNmZvw6Z1SHDcoiV-vJYZW730D0Q_1iSAecHAOS_3nlIBp2H4KDzCdxkuuj_p8qbf0Tc4IN3dvgOC-AuzinkWRpusDTMXK-bsi4Kl4yJhkvxG_LUwCs</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Kim, Ji Won, M.D., Ph.D</creator><creator>Kang, Kyung Min, M.Sc</creator><creator>Yoon, Tae Ki, M.D., Ph.D</creator><creator>Shim, Sung Han, Ph.D</creator><creator>Lee, Woo Sik, M.D., Ph.D</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>20140801</creationdate><title>Study of circulating hepcidin in association with iron excess, metabolic syndrome, and BMP-6 expression in granulosa cells in women with polycystic ovary syndrome</title><author>Kim, Ji Won, M.D., Ph.D ; Kang, Kyung Min, M.Sc ; Yoon, Tae Ki, M.D., Ph.D ; Shim, Sung Han, Ph.D ; Lee, Woo Sik, M.D., Ph.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c549t-85e7fea4e7766db879714aba8f91bf8477e3314747ab3069bd582fa535ee71e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Biomarkers - blood</topic><topic>BMP-6</topic><topic>Bone Morphogenetic Protein 6 - genetics</topic><topic>Bone Morphogenetic Protein 6 - metabolism</topic><topic>Case-Control Studies</topic><topic>Cross-Sectional Studies</topic><topic>Female</topic><topic>Granulosa Cells - metabolism</topic><topic>hepcidin</topic><topic>Hepcidins - blood</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Iron - blood</topic><topic>iron excess</topic><topic>metabolic syndrome</topic><topic>Metabolic Syndrome - blood</topic><topic>Metabolic Syndrome - diagnosis</topic><topic>Obstetrics and Gynecology</topic><topic>Polycystic ovary syndrome</topic><topic>Polycystic Ovary Syndrome - blood</topic><topic>Polycystic Ovary Syndrome - diagnosis</topic><topic>Polycystic Ovary Syndrome - genetics</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>RNA, Messenger - analysis</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Ji Won, M.D., Ph.D</creatorcontrib><creatorcontrib>Kang, Kyung Min, M.Sc</creatorcontrib><creatorcontrib>Yoon, Tae Ki, M.D., Ph.D</creatorcontrib><creatorcontrib>Shim, Sung Han, Ph.D</creatorcontrib><creatorcontrib>Lee, Woo Sik, M.D., Ph.D</creatorcontrib><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>Fertility and sterility</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Ji Won, M.D., Ph.D</au><au>Kang, Kyung Min, M.Sc</au><au>Yoon, Tae Ki, M.D., Ph.D</au><au>Shim, Sung Han, Ph.D</au><au>Lee, Woo Sik, M.D., Ph.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study of circulating hepcidin in association with iron excess, metabolic syndrome, and BMP-6 expression in granulosa cells in women with polycystic ovary syndrome</atitle><jtitle>Fertility and sterility</jtitle><addtitle>Fertil Steril</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>102</volume><issue>2</issue><spage>548</spage><epage>554.e2</epage><pages>548-554.e2</pages><issn>0015-0282</issn><eissn>1556-5653</eissn><abstract>Objective To identify the role of hepcidin in polycystic ovary syndrome (PCOS) patients. Design Cross-sectional case-control study. Setting Academic medical center. Patient(s) Sixty-seven PCOS patients and 94 healthy parous women volunteered for the study. Intervention(s) None. Main Outcome Measure(s) Serum levels of hepcidin, hormone and lipid profiles, parameters of iron and glucose metabolism, high-sensitivity C-reactive protein (hs-CRP), and bone morphogenetic protein 6 ( BMP-6 ) mRNA expressions in the granulosa cells (GCs). Result(s) PCOS patients showed increased serum iron concentration and higher circulating hepcidin levels compared with control subjects, even with only lean subjects. Circulating hepcidin correlated with iron parameters, androgen index, hs-CRP, and fasting glucose and insulin levels, and with iron and ferritin levels after multiple regression analysis. We analyzed BMP-6 mRNA expression in the 89 GCs from nine PCOS patients and five non-PCOS women with the use of quantitative real-time polymerase chain reaction, and no correlations existed between iron parameters, including circulating hepcidin, and BMP-6 expression in the GCs from PCOS women. Conclusion(s) PCOS patients had iron excess and higher hepcidin levels, which are associated with metabolic derangements. Circulating hepcidin is appropriately increased relative to the iron burden even in PCOS women, suggesting that iron excess in PCOS women does not result from a defect in the production of hepcidin. But there were no correlations between iron parameters and the expression of the BMP-6 in GCs from PCOS patients.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24875397</pmid><doi>10.1016/j.fertnstert.2014.04.031</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biomarkers - blood BMP-6 Bone Morphogenetic Protein 6 - genetics Bone Morphogenetic Protein 6 - metabolism Case-Control Studies Cross-Sectional Studies Female Granulosa Cells - metabolism hepcidin Hepcidins - blood Humans Internal Medicine Iron - blood iron excess metabolic syndrome Metabolic Syndrome - blood Metabolic Syndrome - diagnosis Obstetrics and Gynecology Polycystic ovary syndrome Polycystic Ovary Syndrome - blood Polycystic Ovary Syndrome - diagnosis Polycystic Ovary Syndrome - genetics Real-Time Polymerase Chain Reaction RNA, Messenger - analysis Up-Regulation |
title | Study of circulating hepcidin in association with iron excess, metabolic syndrome, and BMP-6 expression in granulosa cells in women with polycystic ovary syndrome |
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