Effects of soy isoflavone supplements on bone turnover markers in menopausal women: Systematic review and meta-analysis of randomized controlled trials
Abstract Introduction Effects of soy isoflavone supplements on bone turnover markers remain unclear. This up-to-date systematic review and meta-analysis of randomized controlled trials (RCTs) was performed primarily to more completely and precisely clarify the effects on urinary deoxypyridinoline (D...
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description | Abstract Introduction Effects of soy isoflavone supplements on bone turnover markers remain unclear. This up-to-date systematic review and meta-analysis of randomized controlled trials (RCTs) was performed primarily to more completely and precisely clarify the effects on urinary deoxypyridinoline (DPD) and serum bone alkaline phosphatase (BAP) and secondarily to evaluate the effects on other bone turnover markers, compared with placebo in menopausal women. Methods PubMed, CENTRAL, ICHUSHI, and CNKI were searched in June 2009 for relevant studies of RCTs. Data on study design, participants, interventions, and outcomes were extracted and methodological quality of each included trial was assessed. Results From 3740 identified relevant articles, 10 (887 participants), 10 (1210 participants), and 8 (380 participants) RCTs were selected for meta-analysis of effects on DPD, BAP, and serum osteocalcin (OC), respectively, using Review Manager 5.0.22. Daily ingestion of an average 56 mg soy isoflavones (aglycone equivalents) for 10 weeks to 12 months significantly decreased DPD by 14.1% (95% CI: − 26.8% to − 1.5%; P = 0.03) compared to baseline (heterogeneity: P < 0.00001; I2 = 93%; random effects model). The overall effect of soy isoflavones on DPD compared with placebo was a significant decrease of − 18.0% (95% CI: − 28.4% to − 7.7%, P = 0.0007; heterogeneity: P = 0.0001; I2 = 73%; random effects model). Subgroup analyses and meta-regressions revealed that isoflavone dose and intervention duration did not significantly relate to the variable effects on DPD. Daily supplementation of about 84 mg and 73 mg of soy isoflavones for up to 12 months insignificantly increased BAP by 8.0% (95% CI: − 4.2% to 20.2%, P = 0.20; heterogeneity: P < 0.00001; I2 = 98%) and OC by 10.3% (95% CI: − 3.1% to 23.7%, P = 0.13; heterogeneity: P = 0.002; I2 = 69%) compared with placebo (random effects model), respectively. Conclusions Soy isoflavone supplements moderately decreased the bone resorption marker DPD, but did not affect bone formation markers BAP and OC in menopausal women. The effects varied between studies, and further studies are needed to address factors relating to the observed effects of soy isoflavones on DPD and to verify effects on other bone turnover markers. |
doi_str_mv | 10.1016/j.bone.2010.05.001 |
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This up-to-date systematic review and meta-analysis of randomized controlled trials (RCTs) was performed primarily to more completely and precisely clarify the effects on urinary deoxypyridinoline (DPD) and serum bone alkaline phosphatase (BAP) and secondarily to evaluate the effects on other bone turnover markers, compared with placebo in menopausal women. Methods PubMed, CENTRAL, ICHUSHI, and CNKI were searched in June 2009 for relevant studies of RCTs. Data on study design, participants, interventions, and outcomes were extracted and methodological quality of each included trial was assessed. Results From 3740 identified relevant articles, 10 (887 participants), 10 (1210 participants), and 8 (380 participants) RCTs were selected for meta-analysis of effects on DPD, BAP, and serum osteocalcin (OC), respectively, using Review Manager 5.0.22. Daily ingestion of an average 56 mg soy isoflavones (aglycone equivalents) for 10 weeks to 12 months significantly decreased DPD by 14.1% (95% CI: − 26.8% to − 1.5%; P = 0.03) compared to baseline (heterogeneity: P < 0.00001; I2 = 93%; random effects model). The overall effect of soy isoflavones on DPD compared with placebo was a significant decrease of − 18.0% (95% CI: − 28.4% to − 7.7%, P = 0.0007; heterogeneity: P = 0.0001; I2 = 73%; random effects model). Subgroup analyses and meta-regressions revealed that isoflavone dose and intervention duration did not significantly relate to the variable effects on DPD. Daily supplementation of about 84 mg and 73 mg of soy isoflavones for up to 12 months insignificantly increased BAP by 8.0% (95% CI: − 4.2% to 20.2%, P = 0.20; heterogeneity: P < 0.00001; I2 = 98%) and OC by 10.3% (95% CI: − 3.1% to 23.7%, P = 0.13; heterogeneity: P = 0.002; I2 = 69%) compared with placebo (random effects model), respectively. Conclusions Soy isoflavone supplements moderately decreased the bone resorption marker DPD, but did not affect bone formation markers BAP and OC in menopausal women. The effects varied between studies, and further studies are needed to address factors relating to the observed effects of soy isoflavones on DPD and to verify effects on other bone turnover markers.</description><identifier>ISSN: 8756-3282</identifier><identifier>EISSN: 1873-2763</identifier><identifier>DOI: 10.1016/j.bone.2010.05.001</identifier><identifier>PMID: 20452475</identifier><language>eng</language><publisher>Amsterdam: Elsevier</publisher><subject>Aged ; Alkaline Phosphatase - blood ; Amino Acids - urine ; Biological and medical sciences ; Biomarkers - blood ; Bone Remodeling - drug effects ; Collagen Type I - blood ; Dietary Supplements ; Female ; Fundamental and applied biological sciences. Psychology ; Glycine max - chemistry ; Humans ; Isoflavones - pharmacology ; Menopause - blood ; Menopause - drug effects ; Menopause - urine ; Middle Aged ; Orthopedics ; Osteocalcin - blood ; Peptide Fragments - blood ; Peptides - blood ; Procollagen - blood ; Randomized Controlled Trials as Topic ; Skeleton and joints ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Vertebrates: osteoarticular system, musculoskeletal system</subject><ispartof>Bone (New York, N.Y.), 2010-08, Vol.47 (2), p.413-423</ispartof><rights>Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright 2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-9284030ce17ac6f2f5dd3e064e8af39b8507f980c9569aa395070893762f194d3</citedby><cites>FETCH-LOGICAL-c419t-9284030ce17ac6f2f5dd3e064e8af39b8507f980c9569aa395070893762f194d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23111238$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20452475$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Taku, Kyoko</creatorcontrib><creatorcontrib>Melby, Melissa K</creatorcontrib><creatorcontrib>Kurzer, Mindy S</creatorcontrib><creatorcontrib>Mizuno, Shoichi</creatorcontrib><creatorcontrib>Watanabe, Shaw</creatorcontrib><creatorcontrib>Ishimi, Yoshiko</creatorcontrib><title>Effects of soy isoflavone supplements on bone turnover markers in menopausal women: Systematic review and meta-analysis of randomized controlled trials</title><title>Bone (New York, N.Y.)</title><addtitle>Bone</addtitle><description>Abstract Introduction Effects of soy isoflavone supplements on bone turnover markers remain unclear. This up-to-date systematic review and meta-analysis of randomized controlled trials (RCTs) was performed primarily to more completely and precisely clarify the effects on urinary deoxypyridinoline (DPD) and serum bone alkaline phosphatase (BAP) and secondarily to evaluate the effects on other bone turnover markers, compared with placebo in menopausal women. Methods PubMed, CENTRAL, ICHUSHI, and CNKI were searched in June 2009 for relevant studies of RCTs. Data on study design, participants, interventions, and outcomes were extracted and methodological quality of each included trial was assessed. Results From 3740 identified relevant articles, 10 (887 participants), 10 (1210 participants), and 8 (380 participants) RCTs were selected for meta-analysis of effects on DPD, BAP, and serum osteocalcin (OC), respectively, using Review Manager 5.0.22. Daily ingestion of an average 56 mg soy isoflavones (aglycone equivalents) for 10 weeks to 12 months significantly decreased DPD by 14.1% (95% CI: − 26.8% to − 1.5%; P = 0.03) compared to baseline (heterogeneity: P < 0.00001; I2 = 93%; random effects model). The overall effect of soy isoflavones on DPD compared with placebo was a significant decrease of − 18.0% (95% CI: − 28.4% to − 7.7%, P = 0.0007; heterogeneity: P = 0.0001; I2 = 73%; random effects model). Subgroup analyses and meta-regressions revealed that isoflavone dose and intervention duration did not significantly relate to the variable effects on DPD. Daily supplementation of about 84 mg and 73 mg of soy isoflavones for up to 12 months insignificantly increased BAP by 8.0% (95% CI: − 4.2% to 20.2%, P = 0.20; heterogeneity: P < 0.00001; I2 = 98%) and OC by 10.3% (95% CI: − 3.1% to 23.7%, P = 0.13; heterogeneity: P = 0.002; I2 = 69%) compared with placebo (random effects model), respectively. Conclusions Soy isoflavone supplements moderately decreased the bone resorption marker DPD, but did not affect bone formation markers BAP and OC in menopausal women. The effects varied between studies, and further studies are needed to address factors relating to the observed effects of soy isoflavones on DPD and to verify effects on other bone turnover markers.</description><subject>Aged</subject><subject>Alkaline Phosphatase - blood</subject><subject>Amino Acids - urine</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Bone Remodeling - drug effects</subject><subject>Collagen Type I - blood</subject><subject>Dietary Supplements</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glycine max - chemistry</subject><subject>Humans</subject><subject>Isoflavones - pharmacology</subject><subject>Menopause - blood</subject><subject>Menopause - drug effects</subject><subject>Menopause - urine</subject><subject>Middle Aged</subject><subject>Orthopedics</subject><subject>Osteocalcin - blood</subject><subject>Peptide Fragments - blood</subject><subject>Peptides - blood</subject><subject>Procollagen - blood</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Skeleton and joints</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Vertebrates: osteoarticular system, musculoskeletal system</subject><issn>8756-3282</issn><issn>1873-2763</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkU1v1DAQhiMEotvCH-CAfEGcsvgjiW0OSKhqAakSh8LZ8jpjyVsnXuxkq_BH-LtM2AVO4xk_86H3rapXjG4ZZd27_XaXRthyigXabillT6oNU1LUXHbiabVRsu1qwRW_qC5L2VNKhZbseXXBadPyRrab6teN9-CmQpInJS0klOSjPeJcUubDIcIA4_o7knUXmeY8piNkMtj8ALmQMBIk0sHOxUbymDB5T-6XMsFgp-BIhmOAR2LHHrnJ1na0cSnhz76M1TSEn9ATl8YppxjxOeVgY3lRPfMY4OU5XlXfb2--XX-u775--nL98a52DdNTrblqqKAOmLSu89y3fS-Adg0o64XeqZZKrxV1uu20tUJjTpUWsuOe6aYXV9Xb09xDTj9mKJMZQnEQox0hzcUoKVvFVUeR5CfS5VRKBm8OOaAMi2HUrH6YvVk1MqsfhrYG_cCm1-fx826A_l_LXwMQeHMGbHE2etTEhfKfE4wxLhRyH04coBgoaTYuhjFgywMsUPYJjUGdDDOFG2ruV-tX5xlewdpOit9SmayD</recordid><startdate>20100801</startdate><enddate>20100801</enddate><creator>Taku, Kyoko</creator><creator>Melby, Melissa K</creator><creator>Kurzer, Mindy S</creator><creator>Mizuno, Shoichi</creator><creator>Watanabe, Shaw</creator><creator>Ishimi, Yoshiko</creator><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>7QP</scope></search><sort><creationdate>20100801</creationdate><title>Effects of soy isoflavone supplements on bone turnover markers in menopausal women: Systematic review and meta-analysis of randomized controlled trials</title><author>Taku, Kyoko ; Melby, Melissa K ; Kurzer, Mindy S ; Mizuno, Shoichi ; Watanabe, Shaw ; Ishimi, Yoshiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-9284030ce17ac6f2f5dd3e064e8af39b8507f980c9569aa395070893762f194d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Aged</topic><topic>Alkaline Phosphatase - blood</topic><topic>Amino Acids - urine</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Bone Remodeling - drug effects</topic><topic>Collagen Type I - blood</topic><topic>Dietary Supplements</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glycine max - chemistry</topic><topic>Humans</topic><topic>Isoflavones - pharmacology</topic><topic>Menopause - blood</topic><topic>Menopause - drug effects</topic><topic>Menopause - urine</topic><topic>Middle Aged</topic><topic>Orthopedics</topic><topic>Osteocalcin - blood</topic><topic>Peptide Fragments - blood</topic><topic>Peptides - blood</topic><topic>Procollagen - blood</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Skeleton and joints</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Vertebrates: osteoarticular system, musculoskeletal system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Taku, Kyoko</creatorcontrib><creatorcontrib>Melby, Melissa K</creatorcontrib><creatorcontrib>Kurzer, Mindy S</creatorcontrib><creatorcontrib>Mizuno, Shoichi</creatorcontrib><creatorcontrib>Watanabe, Shaw</creatorcontrib><creatorcontrib>Ishimi, Yoshiko</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>Calcium & Calcified Tissue Abstracts</collection><jtitle>Bone (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Taku, Kyoko</au><au>Melby, Melissa K</au><au>Kurzer, Mindy S</au><au>Mizuno, Shoichi</au><au>Watanabe, Shaw</au><au>Ishimi, Yoshiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of soy isoflavone supplements on bone turnover markers in menopausal women: Systematic review and meta-analysis of randomized controlled trials</atitle><jtitle>Bone (New York, N.Y.)</jtitle><addtitle>Bone</addtitle><date>2010-08-01</date><risdate>2010</risdate><volume>47</volume><issue>2</issue><spage>413</spage><epage>423</epage><pages>413-423</pages><issn>8756-3282</issn><eissn>1873-2763</eissn><abstract>Abstract Introduction Effects of soy isoflavone supplements on bone turnover markers remain unclear. This up-to-date systematic review and meta-analysis of randomized controlled trials (RCTs) was performed primarily to more completely and precisely clarify the effects on urinary deoxypyridinoline (DPD) and serum bone alkaline phosphatase (BAP) and secondarily to evaluate the effects on other bone turnover markers, compared with placebo in menopausal women. Methods PubMed, CENTRAL, ICHUSHI, and CNKI were searched in June 2009 for relevant studies of RCTs. Data on study design, participants, interventions, and outcomes were extracted and methodological quality of each included trial was assessed. Results From 3740 identified relevant articles, 10 (887 participants), 10 (1210 participants), and 8 (380 participants) RCTs were selected for meta-analysis of effects on DPD, BAP, and serum osteocalcin (OC), respectively, using Review Manager 5.0.22. Daily ingestion of an average 56 mg soy isoflavones (aglycone equivalents) for 10 weeks to 12 months significantly decreased DPD by 14.1% (95% CI: − 26.8% to − 1.5%; P = 0.03) compared to baseline (heterogeneity: P < 0.00001; I2 = 93%; random effects model). The overall effect of soy isoflavones on DPD compared with placebo was a significant decrease of − 18.0% (95% CI: − 28.4% to − 7.7%, P = 0.0007; heterogeneity: P = 0.0001; I2 = 73%; random effects model). Subgroup analyses and meta-regressions revealed that isoflavone dose and intervention duration did not significantly relate to the variable effects on DPD. Daily supplementation of about 84 mg and 73 mg of soy isoflavones for up to 12 months insignificantly increased BAP by 8.0% (95% CI: − 4.2% to 20.2%, P = 0.20; heterogeneity: P < 0.00001; I2 = 98%) and OC by 10.3% (95% CI: − 3.1% to 23.7%, P = 0.13; heterogeneity: P = 0.002; I2 = 69%) compared with placebo (random effects model), respectively. Conclusions Soy isoflavone supplements moderately decreased the bone resorption marker DPD, but did not affect bone formation markers BAP and OC in menopausal women. The effects varied between studies, and further studies are needed to address factors relating to the observed effects of soy isoflavones on DPD and to verify effects on other bone turnover markers.</abstract><cop>Amsterdam</cop><pub>Elsevier</pub><pmid>20452475</pmid><doi>10.1016/j.bone.2010.05.001</doi><tpages>11</tpages></addata></record> |
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subjects | Aged Alkaline Phosphatase - blood Amino Acids - urine Biological and medical sciences Biomarkers - blood Bone Remodeling - drug effects Collagen Type I - blood Dietary Supplements Female Fundamental and applied biological sciences. Psychology Glycine max - chemistry Humans Isoflavones - pharmacology Menopause - blood Menopause - drug effects Menopause - urine Middle Aged Orthopedics Osteocalcin - blood Peptide Fragments - blood Peptides - blood Procollagen - blood Randomized Controlled Trials as Topic Skeleton and joints Vertebrates: anatomy and physiology, studies on body, several organs or systems Vertebrates: osteoarticular system, musculoskeletal system |
title | Effects of soy isoflavone supplements on bone turnover markers in menopausal women: Systematic review and meta-analysis of randomized controlled trials |
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