Adipose tissue mass and location affect circulating adiponectin levels

Aims/hypothesis Plasma levels of adiponectin are inversely associated with body mass. We hypothesised that adipose tissue distribution and body composition influences adiponectin levels. Methods We assessed plasma adiponectin concentrations and dual-energy X-ray absorptiometry (DEXA) measurements of...

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Veröffentlicht in:Diabetologia 2011-10, Vol.54 (10), p.2515-2524
Hauptverfasser: Turer, A. T., Khera, A., Ayers, C. R., Turer, C. B., Grundy, S. M., Vega, G. L., Scherer, P. E.
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container_title Diabetologia
container_volume 54
creator Turer, A. T.
Khera, A.
Ayers, C. R.
Turer, C. B.
Grundy, S. M.
Vega, G. L.
Scherer, P. E.
description Aims/hypothesis Plasma levels of adiponectin are inversely associated with body mass. We hypothesised that adipose tissue distribution and body composition influences adiponectin levels. Methods We assessed plasma adiponectin concentrations and dual-energy X-ray absorptiometry (DEXA) measurements of body composition among 2,820 participants from the Dallas Heart Study. Results Among both women and men, adiponectin levels were higher in whites than in either Hispanics or African-Americans (for women: median 9.99 μg/ml [25th,75th percentile 7.11, 13.77] vs 7.56 μg/ml [5.05, 9.98] vs 6.39 μg/ml [4.37, 9.41], respectively, p  
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T. ; Khera, A. ; Ayers, C. R. ; Turer, C. B. ; Grundy, S. M. ; Vega, G. L. ; Scherer, P. E.</creator><creatorcontrib>Turer, A. T. ; Khera, A. ; Ayers, C. R. ; Turer, C. B. ; Grundy, S. M. ; Vega, G. L. ; Scherer, P. E.</creatorcontrib><description><![CDATA[Aims/hypothesis Plasma levels of adiponectin are inversely associated with body mass. We hypothesised that adipose tissue distribution and body composition influences adiponectin levels. Methods We assessed plasma adiponectin concentrations and dual-energy X-ray absorptiometry (DEXA) measurements of body composition among 2,820 participants from the Dallas Heart Study. Results Among both women and men, adiponectin levels were higher in whites than in either Hispanics or African-Americans (for women: median 9.99 μg/ml [25th,75th percentile 7.11, 13.77] vs 7.56 μg/ml [5.05, 9.98] vs 6.39 μg/ml [4.37, 9.41], respectively, p  < 0.0001; for men: 6.43 μg/ml [4.66, 9.19] vs 5.55 μg/ml [3.64, 7.50] vs 5.03 μg/ml [3.39, 7.28], p  < 0.0001). In univariate analysis, each individual component of body mass was inversely associated with adiponectin. After multivariate analysis, adiponectin levels were found to be positively associated with lower extremity fat, whether expressed in absolute mass (for women: β  = 0.055, p  < 0.0001; for men: β  = 0.061, p  < 0.0001), or as a relative proportion (for women: β  = 0.035, p  < 0.0001; for men: β  = 0.034, p  < 0.0001). This association was consistent across ethnicities. Conversely, adiponectin was negatively correlated with truncal fat, both in absolute (for women: β  = −0.039, p  < 0.0001; for men: β  = −0.044, p  < 0.0001) and relative terms (for women: β  = −0.027, p  < 0.0001; for men β  = −0.033, p  < 0.0001). At the extreme of body mass, higher degrees of lower extremity and truncal adiposity were associated with higher levels of adiponectin. Conclusions/interpretation These data suggest that the location of adipose depots differentially influences circulating adiponectin concentrations—a finding observed across ethnicity and sex. Gross measures of body mass alone do not adequately account for adiponectin levels. This supports a role of adiponectin as a mediator of the positive effects of lower extremity adiposity on improvements in insulin sensitivity.]]></description><identifier>ISSN: 0012-186X</identifier><identifier>EISSN: 1432-0428</identifier><identifier>DOI: 10.1007/s00125-011-2252-z</identifier><identifier>PMID: 21779869</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Absorptiometry, Photon ; Adiponectin - blood ; Adipose Tissue - metabolism ; Adiposity - physiology ; Adult ; African Americans ; Biological and medical sciences ; Body composition ; Body Composition - physiology ; Body fat ; Body Mass Index ; Body Weight - physiology ; Diabetes ; Diabetes. Impaired glucose tolerance ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Ethnicity ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Female ; Human Physiology ; Humans ; Insulin ; Internal Medicine ; Male ; Medical sciences ; Medicine ; Medicine &amp; Public Health ; Metabolic Diseases ; Middle Aged ; Minority &amp; ethnic groups ; Multivariate Analysis ; Obesity ; Obesity - blood ; Obesity - metabolism ; Pediatrics ; Women ; Young Adult</subject><ispartof>Diabetologia, 2011-10, Vol.54 (10), p.2515-2524</ispartof><rights>Springer-Verlag 2011</rights><rights>2015 INIST-CNRS</rights><rights>Springer-Verlag 2011 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c564t-299cc43e2fab2f0faf4aad59387bb17f306dc181c1680550bf2bd6538c3b43f53</citedby><cites>FETCH-LOGICAL-c564t-299cc43e2fab2f0faf4aad59387bb17f306dc181c1680550bf2bd6538c3b43f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00125-011-2252-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00125-011-2252-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,315,782,786,887,27931,27932,41495,42564,51326</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=24516161$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21779869$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Turer, A. T.</creatorcontrib><creatorcontrib>Khera, A.</creatorcontrib><creatorcontrib>Ayers, C. R.</creatorcontrib><creatorcontrib>Turer, C. B.</creatorcontrib><creatorcontrib>Grundy, S. M.</creatorcontrib><creatorcontrib>Vega, G. L.</creatorcontrib><creatorcontrib>Scherer, P. E.</creatorcontrib><title>Adipose tissue mass and location affect circulating adiponectin levels</title><title>Diabetologia</title><addtitle>Diabetologia</addtitle><addtitle>Diabetologia</addtitle><description><![CDATA[Aims/hypothesis Plasma levels of adiponectin are inversely associated with body mass. We hypothesised that adipose tissue distribution and body composition influences adiponectin levels. Methods We assessed plasma adiponectin concentrations and dual-energy X-ray absorptiometry (DEXA) measurements of body composition among 2,820 participants from the Dallas Heart Study. Results Among both women and men, adiponectin levels were higher in whites than in either Hispanics or African-Americans (for women: median 9.99 μg/ml [25th,75th percentile 7.11, 13.77] vs 7.56 μg/ml [5.05, 9.98] vs 6.39 μg/ml [4.37, 9.41], respectively, p  < 0.0001; for men: 6.43 μg/ml [4.66, 9.19] vs 5.55 μg/ml [3.64, 7.50] vs 5.03 μg/ml [3.39, 7.28], p  < 0.0001). In univariate analysis, each individual component of body mass was inversely associated with adiponectin. After multivariate analysis, adiponectin levels were found to be positively associated with lower extremity fat, whether expressed in absolute mass (for women: β  = 0.055, p  < 0.0001; for men: β  = 0.061, p  < 0.0001), or as a relative proportion (for women: β  = 0.035, p  < 0.0001; for men: β  = 0.034, p  < 0.0001). This association was consistent across ethnicities. Conversely, adiponectin was negatively correlated with truncal fat, both in absolute (for women: β  = −0.039, p  < 0.0001; for men: β  = −0.044, p  < 0.0001) and relative terms (for women: β  = −0.027, p  < 0.0001; for men β  = −0.033, p  < 0.0001). At the extreme of body mass, higher degrees of lower extremity and truncal adiposity were associated with higher levels of adiponectin. Conclusions/interpretation These data suggest that the location of adipose depots differentially influences circulating adiponectin concentrations—a finding observed across ethnicity and sex. Gross measures of body mass alone do not adequately account for adiponectin levels. This supports a role of adiponectin as a mediator of the positive effects of lower extremity adiposity on improvements in insulin sensitivity.]]></description><subject>Absorptiometry, Photon</subject><subject>Adiponectin - blood</subject><subject>Adipose Tissue - metabolism</subject><subject>Adiposity - physiology</subject><subject>Adult</subject><subject>African Americans</subject><subject>Biological and medical sciences</subject><subject>Body composition</subject><subject>Body Composition - physiology</subject><subject>Body fat</subject><subject>Body Mass Index</subject><subject>Body Weight - physiology</subject><subject>Diabetes</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Ethnicity</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>Human Physiology</subject><subject>Humans</subject><subject>Insulin</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Metabolic Diseases</subject><subject>Middle Aged</subject><subject>Minority &amp; ethnic groups</subject><subject>Multivariate Analysis</subject><subject>Obesity</subject><subject>Obesity - blood</subject><subject>Obesity - metabolism</subject><subject>Pediatrics</subject><subject>Women</subject><subject>Young Adult</subject><issn>0012-186X</issn><issn>1432-0428</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kV1LHDEUhkNpqavtD-hNGQrSq9F8ziQ3gkj9AKE3FnoXMplkG8kma86MoL_eLLvVVpBcBM77vOeDF6EvBB8RjPtjwJhQ0WJCWkoFbR_foQXhjLaYU_keLTZyS2T3ew_tA9xijJng3Ue0R0nfK9mpBTo_HcM6g2umADC7ZmUAGpPGJmZrppBTY7x3dmpsKHaOtZSWjdl4Uq2G1ER37yJ8Qh-8ieA-7_4D9Ov8x83ZZXv98-Lq7PS6taLjU0uVspYzR70ZqMfeeG7MKBST_TCQ3jPcjZZIYkknsRB48HQYO8GkZQNnXrADdLLtu56HlRutS1MxUa9LWJnyoLMJ-n8lhT96me81xworKmuD77sGJd_NDia9CmBdjCa5PIOWUjKmJOOV_PaKvM1zSfW6CvWKS9WTCpEtZEsGKM4_r0Kw3mSktxnpmpHeZKQfq-frvzc8O_6GUoHDHWDAmuiLSTbAC8cF6eqrHN1yUKW0dOVlw7enPwEb8Ksl</recordid><startdate>20111001</startdate><enddate>20111001</enddate><creator>Turer, A. 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L. ; Scherer, P. E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c564t-299cc43e2fab2f0faf4aad59387bb17f306dc181c1680550bf2bd6538c3b43f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Absorptiometry, Photon</topic><topic>Adiponectin - blood</topic><topic>Adipose Tissue - metabolism</topic><topic>Adiposity - physiology</topic><topic>Adult</topic><topic>African Americans</topic><topic>Biological and medical sciences</topic><topic>Body composition</topic><topic>Body Composition - physiology</topic><topic>Body fat</topic><topic>Body Mass Index</topic><topic>Body Weight - physiology</topic><topic>Diabetes</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Ethnicity</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>Human Physiology</topic><topic>Humans</topic><topic>Insulin</topic><topic>Internal Medicine</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Metabolic Diseases</topic><topic>Middle Aged</topic><topic>Minority &amp; ethnic groups</topic><topic>Multivariate Analysis</topic><topic>Obesity</topic><topic>Obesity - blood</topic><topic>Obesity - metabolism</topic><topic>Pediatrics</topic><topic>Women</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Turer, A. T.</creatorcontrib><creatorcontrib>Khera, A.</creatorcontrib><creatorcontrib>Ayers, C. R.</creatorcontrib><creatorcontrib>Turer, C. B.</creatorcontrib><creatorcontrib>Grundy, S. M.</creatorcontrib><creatorcontrib>Vega, G. L.</creatorcontrib><creatorcontrib>Scherer, P. 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T.</au><au>Khera, A.</au><au>Ayers, C. R.</au><au>Turer, C. B.</au><au>Grundy, S. M.</au><au>Vega, G. L.</au><au>Scherer, P. E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adipose tissue mass and location affect circulating adiponectin levels</atitle><jtitle>Diabetologia</jtitle><stitle>Diabetologia</stitle><addtitle>Diabetologia</addtitle><date>2011-10-01</date><risdate>2011</risdate><volume>54</volume><issue>10</issue><spage>2515</spage><epage>2524</epage><pages>2515-2524</pages><issn>0012-186X</issn><eissn>1432-0428</eissn><abstract><![CDATA[Aims/hypothesis Plasma levels of adiponectin are inversely associated with body mass. We hypothesised that adipose tissue distribution and body composition influences adiponectin levels. Methods We assessed plasma adiponectin concentrations and dual-energy X-ray absorptiometry (DEXA) measurements of body composition among 2,820 participants from the Dallas Heart Study. Results Among both women and men, adiponectin levels were higher in whites than in either Hispanics or African-Americans (for women: median 9.99 μg/ml [25th,75th percentile 7.11, 13.77] vs 7.56 μg/ml [5.05, 9.98] vs 6.39 μg/ml [4.37, 9.41], respectively, p  < 0.0001; for men: 6.43 μg/ml [4.66, 9.19] vs 5.55 μg/ml [3.64, 7.50] vs 5.03 μg/ml [3.39, 7.28], p  < 0.0001). In univariate analysis, each individual component of body mass was inversely associated with adiponectin. After multivariate analysis, adiponectin levels were found to be positively associated with lower extremity fat, whether expressed in absolute mass (for women: β  = 0.055, p  < 0.0001; for men: β  = 0.061, p  < 0.0001), or as a relative proportion (for women: β  = 0.035, p  < 0.0001; for men: β  = 0.034, p  < 0.0001). This association was consistent across ethnicities. Conversely, adiponectin was negatively correlated with truncal fat, both in absolute (for women: β  = −0.039, p  < 0.0001; for men: β  = −0.044, p  < 0.0001) and relative terms (for women: β  = −0.027, p  < 0.0001; for men β  = −0.033, p  < 0.0001). At the extreme of body mass, higher degrees of lower extremity and truncal adiposity were associated with higher levels of adiponectin. Conclusions/interpretation These data suggest that the location of adipose depots differentially influences circulating adiponectin concentrations—a finding observed across ethnicity and sex. Gross measures of body mass alone do not adequately account for adiponectin levels. This supports a role of adiponectin as a mediator of the positive effects of lower extremity adiposity on improvements in insulin sensitivity.]]></abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21779869</pmid><doi>10.1007/s00125-011-2252-z</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Absorptiometry, Photon
Adiponectin - blood
Adipose Tissue - metabolism
Adiposity - physiology
Adult
African Americans
Biological and medical sciences
Body composition
Body Composition - physiology
Body fat
Body Mass Index
Body Weight - physiology
Diabetes
Diabetes. Impaired glucose tolerance
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Ethnicity
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Female
Human Physiology
Humans
Insulin
Internal Medicine
Male
Medical sciences
Medicine
Medicine & Public Health
Metabolic Diseases
Middle Aged
Minority & ethnic groups
Multivariate Analysis
Obesity
Obesity - blood
Obesity - metabolism
Pediatrics
Women
Young Adult
title Adipose tissue mass and location affect circulating adiponectin levels
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