Fetuin‐A and BMD in Older Persons: The Health Aging and Body Composition (Health ABC) Study
Fetuin‐A is a hepatic secretory protein that promotes bone mineralization in vitro. Whether fetuin‐A levels are associated with BMD in humans is unknown. The Health Aging and Body Composition study enrolled 3075 well‐functioning black and white persons 70–79 yr of age and measured BMD. This cross‐se...
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Veröffentlicht in: | Journal of bone and mineral research 2009-03, Vol.24 (3), p.514-521 |
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description | Fetuin‐A is a hepatic secretory protein that promotes bone mineralization in vitro. Whether fetuin‐A levels are associated with BMD in humans is unknown. The Health Aging and Body Composition study enrolled 3075 well‐functioning black and white persons 70–79 yr of age and measured BMD. This cross‐sectional study measured serum fetuin‐A using ELISA among a random sample of 508 participants within sex and race strata. Multivariate linear regression analysis evaluated the associations of fetuin‐A with BMD. Among women (n = 257), higher fetuin‐A levels were significantly associated with higher total hip (p = 0.02), lumbar spine (p = 0.03), and whole body BMD (p = 0.01) in models adjusted for age, race, diabetes, alcohol and tobacco use, physical activity, body mass index, C‐reactive protein levels, calcium supplement, and estrogen use. For example, each SD (0.38 g/liter) higher level of fetuin‐A was associated with 0.016 g/cm2 higher total hip areal BMD. The association was of similar magnitude and direction for femoral neck BMD but did not reach statistical significance (p = 0.11). In contrast, among men (n = 251), fetuin‐A had no significant associations with total hip (p = 0.79), lumbar spine (p = 0.35), whole body (p = 0.46), or femoral neck BMD (p = 0.54) in multivariable models. We conclude that higher fetuin‐A levels are independently associated with higher BMD among well‐functioning community‐dwelling older women but not older men. Future studies should evaluate whether fetuin‐A may refine fracture risk assessment in older women. |
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Whether fetuin‐A levels are associated with BMD in humans is unknown. The Health Aging and Body Composition study enrolled 3075 well‐functioning black and white persons 70–79 yr of age and measured BMD. This cross‐sectional study measured serum fetuin‐A using ELISA among a random sample of 508 participants within sex and race strata. Multivariate linear regression analysis evaluated the associations of fetuin‐A with BMD. Among women (n = 257), higher fetuin‐A levels were significantly associated with higher total hip (p = 0.02), lumbar spine (p = 0.03), and whole body BMD (p = 0.01) in models adjusted for age, race, diabetes, alcohol and tobacco use, physical activity, body mass index, C‐reactive protein levels, calcium supplement, and estrogen use. For example, each SD (0.38 g/liter) higher level of fetuin‐A was associated with 0.016 g/cm2 higher total hip areal BMD. The association was of similar magnitude and direction for femoral neck BMD but did not reach statistical significance (p = 0.11). In contrast, among men (n = 251), fetuin‐A had no significant associations with total hip (p = 0.79), lumbar spine (p = 0.35), whole body (p = 0.46), or femoral neck BMD (p = 0.54) in multivariable models. We conclude that higher fetuin‐A levels are independently associated with higher BMD among well‐functioning community‐dwelling older women but not older men. Future studies should evaluate whether fetuin‐A may refine fracture risk assessment in older women.</description><identifier>ISSN: 0884-0431</identifier><identifier>EISSN: 1523-4681</identifier><identifier>DOI: 10.1359/jbmr.081017</identifier><identifier>PMID: 19016589</identifier><identifier>CODEN: JBMREJ</identifier><language>eng</language><publisher>Washington, DC: John Wiley and Sons and The American Society for Bone and Mineral Research (ASBMR)</publisher><subject>Aged ; Aging - metabolism ; alpha-2-HS-Glycoprotein ; Biological and medical sciences ; Blood Proteins - metabolism ; BMD ; Body Composition ; Bone Density ; Demography ; elderly ; Female ; fetuin‐A ; Fundamental and applied biological sciences. 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Whether fetuin‐A levels are associated with BMD in humans is unknown. The Health Aging and Body Composition study enrolled 3075 well‐functioning black and white persons 70–79 yr of age and measured BMD. This cross‐sectional study measured serum fetuin‐A using ELISA among a random sample of 508 participants within sex and race strata. Multivariate linear regression analysis evaluated the associations of fetuin‐A with BMD. Among women (n = 257), higher fetuin‐A levels were significantly associated with higher total hip (p = 0.02), lumbar spine (p = 0.03), and whole body BMD (p = 0.01) in models adjusted for age, race, diabetes, alcohol and tobacco use, physical activity, body mass index, C‐reactive protein levels, calcium supplement, and estrogen use. For example, each SD (0.38 g/liter) higher level of fetuin‐A was associated with 0.016 g/cm2 higher total hip areal BMD. The association was of similar magnitude and direction for femoral neck BMD but did not reach statistical significance (p = 0.11). In contrast, among men (n = 251), fetuin‐A had no significant associations with total hip (p = 0.79), lumbar spine (p = 0.35), whole body (p = 0.46), or femoral neck BMD (p = 0.54) in multivariable models. We conclude that higher fetuin‐A levels are independently associated with higher BMD among well‐functioning community‐dwelling older women but not older men. Future studies should evaluate whether fetuin‐A may refine fracture risk assessment in older women.</description><subject>Aged</subject><subject>Aging - metabolism</subject><subject>alpha-2-HS-Glycoprotein</subject><subject>Biological and medical sciences</subject><subject>Blood Proteins - metabolism</subject><subject>BMD</subject><subject>Body Composition</subject><subject>Bone Density</subject><subject>Demography</subject><subject>elderly</subject><subject>Female</subject><subject>fetuin‐A</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Health</subject><subject>Humans</subject><subject>Male</subject><subject>Original</subject><subject>Sex Characteristics</subject><subject>Skeleton and joints</subject><subject>Vertebrates: osteoarticular system, musculoskeletal system</subject><issn>0884-0431</issn><issn>1523-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0UFv0zAYBmALgVg3OHFHvoCGUMZnO3ZsDkhtYQy0aQjGEVlO4rSeErvYCag3fgK_kV9CqpQBF5As-eBHr_35RegBgRPCuHp2XXbxBCQBUtxCM8Ipy3IhyW00AynzDHJGDtBhStcAILgQd9EBUUAEl2qGPp3afnD-x7fvc2x8jRcXL7Hz-LKtbcTvbEzBp-f4am3xmTVtv8bzlfOriYZ6i5eh24Tkehc8Pv5FFssn-EM_1Nt76E5j2mTv7_cj9PH01dXyLDu_fP1mOT_PqlxKnvGykZCbQqoyV6WtOAdqAOqKlqIsOEimSlNAAU3JDBhVN4RLGAUbV20kO0IvptzNUHa2rqzvo2n1JrrOxK0Oxum_T7xb61X4oqngilM6BjzeB8TwebCp151LlW1b420YkhZCKSkV-y-kwKSi-Q4-nWAVQ0rRNjevIaB3veldb3rqbdQP_xzgt90XNYJHe2BSZdomGl-5dOMooSBITkZXTO6ra-32X3fqt4uL91yMX50DI5z9BKkWsHk</recordid><startdate>200903</startdate><enddate>200903</enddate><creator>Ix, Joachim H</creator><creator>Wassel, Christina L</creator><creator>Bauer, Douglas C</creator><creator>Toroian, Damon</creator><creator>Tylavsky, Frances A</creator><creator>Cauley, Jane A</creator><creator>Harris, Tamara B</creator><creator>Price, Paul A</creator><creator>Cummings, Steven R</creator><creator>Shlipak, Michael G</creator><general>John Wiley and Sons and The American Society for Bone and Mineral Research (ASBMR)</general><general>Wiley</general><general>Amer Soc Bone & Mineral Res</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><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>200903</creationdate><title>Fetuin‐A and BMD in Older Persons: The Health Aging and Body Composition (Health ABC) Study</title><author>Ix, Joachim H ; Wassel, Christina L ; Bauer, Douglas C ; Toroian, Damon ; Tylavsky, Frances A ; Cauley, Jane A ; Harris, Tamara B ; Price, Paul A ; Cummings, Steven R ; Shlipak, Michael G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4885-5bf804a789b49bec5502a00dc2b6b750839ba7070fb3a0a9df1580a003003da83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aged</topic><topic>Aging - metabolism</topic><topic>alpha-2-HS-Glycoprotein</topic><topic>Biological and medical sciences</topic><topic>Blood Proteins - metabolism</topic><topic>BMD</topic><topic>Body Composition</topic><topic>Bone Density</topic><topic>Demography</topic><topic>elderly</topic><topic>Female</topic><topic>fetuin‐A</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Health</topic><topic>Humans</topic><topic>Male</topic><topic>Original</topic><topic>Sex Characteristics</topic><topic>Skeleton and joints</topic><topic>Vertebrates: osteoarticular system, musculoskeletal system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ix, Joachim H</creatorcontrib><creatorcontrib>Wassel, Christina L</creatorcontrib><creatorcontrib>Bauer, Douglas C</creatorcontrib><creatorcontrib>Toroian, Damon</creatorcontrib><creatorcontrib>Tylavsky, Frances A</creatorcontrib><creatorcontrib>Cauley, Jane A</creatorcontrib><creatorcontrib>Harris, Tamara B</creatorcontrib><creatorcontrib>Price, Paul A</creatorcontrib><creatorcontrib>Cummings, Steven R</creatorcontrib><creatorcontrib>Shlipak, Michael G</creatorcontrib><creatorcontrib>Health ABC Study</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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of bone and mineral research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ix, Joachim H</au><au>Wassel, Christina L</au><au>Bauer, Douglas C</au><au>Toroian, Damon</au><au>Tylavsky, Frances A</au><au>Cauley, Jane A</au><au>Harris, Tamara B</au><au>Price, Paul A</au><au>Cummings, Steven R</au><au>Shlipak, Michael G</au><aucorp>Health ABC Study</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fetuin‐A and BMD in Older Persons: The Health Aging and Body Composition (Health ABC) Study</atitle><jtitle>Journal of bone and mineral research</jtitle><addtitle>J Bone Miner Res</addtitle><date>2009-03</date><risdate>2009</risdate><volume>24</volume><issue>3</issue><spage>514</spage><epage>521</epage><pages>514-521</pages><issn>0884-0431</issn><eissn>1523-4681</eissn><coden>JBMREJ</coden><abstract>Fetuin‐A is a hepatic secretory protein that promotes bone mineralization in vitro. Whether fetuin‐A levels are associated with BMD in humans is unknown. The Health Aging and Body Composition study enrolled 3075 well‐functioning black and white persons 70–79 yr of age and measured BMD. This cross‐sectional study measured serum fetuin‐A using ELISA among a random sample of 508 participants within sex and race strata. Multivariate linear regression analysis evaluated the associations of fetuin‐A with BMD. Among women (n = 257), higher fetuin‐A levels were significantly associated with higher total hip (p = 0.02), lumbar spine (p = 0.03), and whole body BMD (p = 0.01) in models adjusted for age, race, diabetes, alcohol and tobacco use, physical activity, body mass index, C‐reactive protein levels, calcium supplement, and estrogen use. For example, each SD (0.38 g/liter) higher level of fetuin‐A was associated with 0.016 g/cm2 higher total hip areal BMD. The association was of similar magnitude and direction for femoral neck BMD but did not reach statistical significance (p = 0.11). In contrast, among men (n = 251), fetuin‐A had no significant associations with total hip (p = 0.79), lumbar spine (p = 0.35), whole body (p = 0.46), or femoral neck BMD (p = 0.54) in multivariable models. We conclude that higher fetuin‐A levels are independently associated with higher BMD among well‐functioning community‐dwelling older women but not older men. Future studies should evaluate whether fetuin‐A may refine fracture risk assessment in older women.</abstract><cop>Washington, DC</cop><pub>John Wiley and Sons and The American Society for Bone and Mineral Research (ASBMR)</pub><pmid>19016589</pmid><doi>10.1359/jbmr.081017</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aging - metabolism alpha-2-HS-Glycoprotein Biological and medical sciences Blood Proteins - metabolism BMD Body Composition Bone Density Demography elderly Female fetuin‐A Fundamental and applied biological sciences. Psychology Health Humans Male Original Sex Characteristics Skeleton and joints Vertebrates: osteoarticular system, musculoskeletal system |
title | Fetuin‐A and BMD in Older Persons: The Health Aging and Body Composition (Health ABC) Study |
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