Adipokines and cardiometabolic function: How are they interlinked?
Adipokines contribute directly to the coexistence of insulin resistance and endothelial dysfunction. Most studies focus on a single adipokine. We therefore investigated the independent relationships of leptin, adiponectin, tumor necrosis factor-α, resistin and visfatin, as well as the gut hormone gh...
Gespeichert in:
Veröffentlicht in: | Regulatory peptides 2010-09, Vol.164 (2), p.133-138 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 138 |
---|---|
container_issue | 2 |
container_start_page | 133 |
container_title | Regulatory peptides |
container_volume | 164 |
creator | Schutte, Aletta Elisabeth Huisman, Hugo Willem Schutte, Rudolph van Rooyen, Johannes Marthinus Malan, Leoné Fourie, Catharina Maria Theresia Malan, Nicolaas Theodore |
description | Adipokines contribute directly to the coexistence of insulin resistance and endothelial dysfunction. Most studies focus on a single adipokine. We therefore investigated the independent relationships of leptin, adiponectin, tumor necrosis factor-α, resistin and visfatin, as well as the gut hormone ghrelin with blood pressure and insulin resistance. Secondly we evaluated the interrelationships of adipokines and ghrelin in concert with various cardiometabolic markers.
Caucasian women (
N
=
115) with varying levels of obesity (aged 31.3
±
9.18 years) were included. Significant correlations of leptin, adiponectin, ghrelin and visfatin with mean arterial pressure (
p
<
0.05) disappeared after adjustment for age, body mass index and waist circumference. But significant correlations with insulin resistance (HOMA) (for leptin, adiponectin and ghrelin) remained significant after adjustments. Factor analyses yielded five factors, but two main clusters, namely a metabolic syndrome cluster (including leptin, adiponectin and ghrelin) and a vascular atherosclerotic cluster (including tumor necrosis factor-α, visfatin and resistin).
Factor analyses identified patterns which indicate specific roles of the various adipokines. Leptin, adiponectin and ghrelin were more closely related to insulin resistance and central obesity as core components of the metabolic syndrome. Visfatin, tumor necrosis factor-α and resistin seem to direct their effects onto the vascular system possibly by means of mechanisms such as inflammation, vasoconstriction and coagulation. |
doi_str_mv | 10.1016/j.regpep.2010.06.008 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_749011561</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0167011510001527</els_id><sourcerecordid>749011561</sourcerecordid><originalsourceid>FETCH-LOGICAL-c391t-d33c66711a7d4a866d9b0feceb0155d4f512c3da665cd99926e1b31d17cac47e3</originalsourceid><addsrcrecordid>eNp9kE1P3DAQhi1EVRbaf4CqXBCnbD1xYic9FAGCUgmpl_ZsOeMJeMnaqZ2l4t_j1S7traeRRs87Hw9jp8CXwEF-Xi0jPUw0LSueW1wuOW8P2AJaJUqQrTxki4ypkgM0R-w4pRXn0Cgl3rOjiktoaiEX7OrSuik8OU-pMN4WaKJ1YU2z6cPosBg2HmcX_JfiLvwpTKRifqSXwvmZ4uj8E9mLD-zdYMZEH_f1hP26vfl5fVfe__j2_fryvkTRwVxaIVBKBWCUrU0rpe16PhBSn89qbD00UKGwRsoGbdd1lSToBVhQaLBWJE7Y-W7uFMPvDaVZr11CGkfjKWySVnW3_VVCJusdiTGkFGnQU3RrE180cL2Vp1d6J09v5WkudZaXY5_2Czb9muzf0JutDJztAZPQjEM0Hl36x4mqblvgmfu64yjreHYUdUJHHsm6SDhrG9z_L3kF3eKOzQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>749011561</pqid></control><display><type>article</type><title>Adipokines and cardiometabolic function: How are they interlinked?</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Schutte, Aletta Elisabeth ; Huisman, Hugo Willem ; Schutte, Rudolph ; van Rooyen, Johannes Marthinus ; Malan, Leoné ; Fourie, Catharina Maria Theresia ; Malan, Nicolaas Theodore</creator><creatorcontrib>Schutte, Aletta Elisabeth ; Huisman, Hugo Willem ; Schutte, Rudolph ; van Rooyen, Johannes Marthinus ; Malan, Leoné ; Fourie, Catharina Maria Theresia ; Malan, Nicolaas Theodore</creatorcontrib><description>Adipokines contribute directly to the coexistence of insulin resistance and endothelial dysfunction. Most studies focus on a single adipokine. We therefore investigated the independent relationships of leptin, adiponectin, tumor necrosis factor-α, resistin and visfatin, as well as the gut hormone ghrelin with blood pressure and insulin resistance. Secondly we evaluated the interrelationships of adipokines and ghrelin in concert with various cardiometabolic markers.
Caucasian women (
N
=
115) with varying levels of obesity (aged 31.3
±
9.18 years) were included. Significant correlations of leptin, adiponectin, ghrelin and visfatin with mean arterial pressure (
p
<
0.05) disappeared after adjustment for age, body mass index and waist circumference. But significant correlations with insulin resistance (HOMA) (for leptin, adiponectin and ghrelin) remained significant after adjustments. Factor analyses yielded five factors, but two main clusters, namely a metabolic syndrome cluster (including leptin, adiponectin and ghrelin) and a vascular atherosclerotic cluster (including tumor necrosis factor-α, visfatin and resistin).
Factor analyses identified patterns which indicate specific roles of the various adipokines. Leptin, adiponectin and ghrelin were more closely related to insulin resistance and central obesity as core components of the metabolic syndrome. Visfatin, tumor necrosis factor-α and resistin seem to direct their effects onto the vascular system possibly by means of mechanisms such as inflammation, vasoconstriction and coagulation.</description><identifier>ISSN: 0167-0115</identifier><identifier>EISSN: 1873-1686</identifier><identifier>DOI: 10.1016/j.regpep.2010.06.008</identifier><identifier>PMID: 20615436</identifier><identifier>CODEN: REPPDY</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Adipokines - blood ; Adiponectin ; Adiponectin - blood ; Adult ; Biological and medical sciences ; Blood Pressure - physiology ; Body Mass Index ; Female ; Fundamental and applied biological sciences. Psychology ; Ghrelin ; Ghrelin - blood ; Humans ; Insulin Resistance - physiology ; Leptin ; Leptin - blood ; Medical sciences ; Metabolic diseases ; Middle Aged ; Nicotinamide Phosphoribosyltransferase - blood ; Obesity ; Obesity - blood ; Resistin ; Resistin - blood ; Tumor Necrosis Factor-alpha ; Tumor necrosis factor-α ; Vertebrates: endocrinology ; Visfatin ; Women ; Young Adult</subject><ispartof>Regulatory peptides, 2010-09, Vol.164 (2), p.133-138</ispartof><rights>2010 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright 2010 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-d33c66711a7d4a866d9b0feceb0155d4f512c3da665cd99926e1b31d17cac47e3</citedby><cites>FETCH-LOGICAL-c391t-d33c66711a7d4a866d9b0feceb0155d4f512c3da665cd99926e1b31d17cac47e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0167011510001527$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23248810$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20615436$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schutte, Aletta Elisabeth</creatorcontrib><creatorcontrib>Huisman, Hugo Willem</creatorcontrib><creatorcontrib>Schutte, Rudolph</creatorcontrib><creatorcontrib>van Rooyen, Johannes Marthinus</creatorcontrib><creatorcontrib>Malan, Leoné</creatorcontrib><creatorcontrib>Fourie, Catharina Maria Theresia</creatorcontrib><creatorcontrib>Malan, Nicolaas Theodore</creatorcontrib><title>Adipokines and cardiometabolic function: How are they interlinked?</title><title>Regulatory peptides</title><addtitle>Regul Pept</addtitle><description>Adipokines contribute directly to the coexistence of insulin resistance and endothelial dysfunction. Most studies focus on a single adipokine. We therefore investigated the independent relationships of leptin, adiponectin, tumor necrosis factor-α, resistin and visfatin, as well as the gut hormone ghrelin with blood pressure and insulin resistance. Secondly we evaluated the interrelationships of adipokines and ghrelin in concert with various cardiometabolic markers.
Caucasian women (
N
=
115) with varying levels of obesity (aged 31.3
±
9.18 years) were included. Significant correlations of leptin, adiponectin, ghrelin and visfatin with mean arterial pressure (
p
<
0.05) disappeared after adjustment for age, body mass index and waist circumference. But significant correlations with insulin resistance (HOMA) (for leptin, adiponectin and ghrelin) remained significant after adjustments. Factor analyses yielded five factors, but two main clusters, namely a metabolic syndrome cluster (including leptin, adiponectin and ghrelin) and a vascular atherosclerotic cluster (including tumor necrosis factor-α, visfatin and resistin).
Factor analyses identified patterns which indicate specific roles of the various adipokines. Leptin, adiponectin and ghrelin were more closely related to insulin resistance and central obesity as core components of the metabolic syndrome. Visfatin, tumor necrosis factor-α and resistin seem to direct their effects onto the vascular system possibly by means of mechanisms such as inflammation, vasoconstriction and coagulation.</description><subject>Adipokines - blood</subject><subject>Adiponectin</subject><subject>Adiponectin - blood</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - physiology</subject><subject>Body Mass Index</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ghrelin</subject><subject>Ghrelin - blood</subject><subject>Humans</subject><subject>Insulin Resistance - physiology</subject><subject>Leptin</subject><subject>Leptin - blood</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Middle Aged</subject><subject>Nicotinamide Phosphoribosyltransferase - blood</subject><subject>Obesity</subject><subject>Obesity - blood</subject><subject>Resistin</subject><subject>Resistin - blood</subject><subject>Tumor Necrosis Factor-alpha</subject><subject>Tumor necrosis factor-α</subject><subject>Vertebrates: endocrinology</subject><subject>Visfatin</subject><subject>Women</subject><subject>Young Adult</subject><issn>0167-0115</issn><issn>1873-1686</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1P3DAQhi1EVRbaf4CqXBCnbD1xYic9FAGCUgmpl_ZsOeMJeMnaqZ2l4t_j1S7traeRRs87Hw9jp8CXwEF-Xi0jPUw0LSueW1wuOW8P2AJaJUqQrTxki4ypkgM0R-w4pRXn0Cgl3rOjiktoaiEX7OrSuik8OU-pMN4WaKJ1YU2z6cPosBg2HmcX_JfiLvwpTKRifqSXwvmZ4uj8E9mLD-zdYMZEH_f1hP26vfl5fVfe__j2_fryvkTRwVxaIVBKBWCUrU0rpe16PhBSn89qbD00UKGwRsoGbdd1lSToBVhQaLBWJE7Y-W7uFMPvDaVZr11CGkfjKWySVnW3_VVCJusdiTGkFGnQU3RrE180cL2Vp1d6J09v5WkudZaXY5_2Czb9muzf0JutDJztAZPQjEM0Hl36x4mqblvgmfu64yjreHYUdUJHHsm6SDhrG9z_L3kF3eKOzQ</recordid><startdate>20100924</startdate><enddate>20100924</enddate><creator>Schutte, Aletta Elisabeth</creator><creator>Huisman, Hugo Willem</creator><creator>Schutte, Rudolph</creator><creator>van Rooyen, Johannes Marthinus</creator><creator>Malan, Leoné</creator><creator>Fourie, Catharina Maria Theresia</creator><creator>Malan, Nicolaas Theodore</creator><general>Elsevier B.V</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>20100924</creationdate><title>Adipokines and cardiometabolic function: How are they interlinked?</title><author>Schutte, Aletta Elisabeth ; Huisman, Hugo Willem ; Schutte, Rudolph ; van Rooyen, Johannes Marthinus ; Malan, Leoné ; Fourie, Catharina Maria Theresia ; Malan, Nicolaas Theodore</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-d33c66711a7d4a866d9b0feceb0155d4f512c3da665cd99926e1b31d17cac47e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adipokines - blood</topic><topic>Adiponectin</topic><topic>Adiponectin - blood</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - physiology</topic><topic>Body Mass Index</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ghrelin</topic><topic>Ghrelin - blood</topic><topic>Humans</topic><topic>Insulin Resistance - physiology</topic><topic>Leptin</topic><topic>Leptin - blood</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Middle Aged</topic><topic>Nicotinamide Phosphoribosyltransferase - blood</topic><topic>Obesity</topic><topic>Obesity - blood</topic><topic>Resistin</topic><topic>Resistin - blood</topic><topic>Tumor Necrosis Factor-alpha</topic><topic>Tumor necrosis factor-α</topic><topic>Vertebrates: endocrinology</topic><topic>Visfatin</topic><topic>Women</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schutte, Aletta Elisabeth</creatorcontrib><creatorcontrib>Huisman, Hugo Willem</creatorcontrib><creatorcontrib>Schutte, Rudolph</creatorcontrib><creatorcontrib>van Rooyen, Johannes Marthinus</creatorcontrib><creatorcontrib>Malan, Leoné</creatorcontrib><creatorcontrib>Fourie, Catharina Maria Theresia</creatorcontrib><creatorcontrib>Malan, Nicolaas Theodore</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>Regulatory peptides</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schutte, Aletta Elisabeth</au><au>Huisman, Hugo Willem</au><au>Schutte, Rudolph</au><au>van Rooyen, Johannes Marthinus</au><au>Malan, Leoné</au><au>Fourie, Catharina Maria Theresia</au><au>Malan, Nicolaas Theodore</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adipokines and cardiometabolic function: How are they interlinked?</atitle><jtitle>Regulatory peptides</jtitle><addtitle>Regul Pept</addtitle><date>2010-09-24</date><risdate>2010</risdate><volume>164</volume><issue>2</issue><spage>133</spage><epage>138</epage><pages>133-138</pages><issn>0167-0115</issn><eissn>1873-1686</eissn><coden>REPPDY</coden><abstract>Adipokines contribute directly to the coexistence of insulin resistance and endothelial dysfunction. Most studies focus on a single adipokine. We therefore investigated the independent relationships of leptin, adiponectin, tumor necrosis factor-α, resistin and visfatin, as well as the gut hormone ghrelin with blood pressure and insulin resistance. Secondly we evaluated the interrelationships of adipokines and ghrelin in concert with various cardiometabolic markers.
Caucasian women (
N
=
115) with varying levels of obesity (aged 31.3
±
9.18 years) were included. Significant correlations of leptin, adiponectin, ghrelin and visfatin with mean arterial pressure (
p
<
0.05) disappeared after adjustment for age, body mass index and waist circumference. But significant correlations with insulin resistance (HOMA) (for leptin, adiponectin and ghrelin) remained significant after adjustments. Factor analyses yielded five factors, but two main clusters, namely a metabolic syndrome cluster (including leptin, adiponectin and ghrelin) and a vascular atherosclerotic cluster (including tumor necrosis factor-α, visfatin and resistin).
Factor analyses identified patterns which indicate specific roles of the various adipokines. Leptin, adiponectin and ghrelin were more closely related to insulin resistance and central obesity as core components of the metabolic syndrome. Visfatin, tumor necrosis factor-α and resistin seem to direct their effects onto the vascular system possibly by means of mechanisms such as inflammation, vasoconstriction and coagulation.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>20615436</pmid><doi>10.1016/j.regpep.2010.06.008</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0167-0115 |
ispartof | Regulatory peptides, 2010-09, Vol.164 (2), p.133-138 |
issn | 0167-0115 1873-1686 |
language | eng |
recordid | cdi_proquest_miscellaneous_749011561 |
source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Adipokines - blood Adiponectin Adiponectin - blood Adult Biological and medical sciences Blood Pressure - physiology Body Mass Index Female Fundamental and applied biological sciences. Psychology Ghrelin Ghrelin - blood Humans Insulin Resistance - physiology Leptin Leptin - blood Medical sciences Metabolic diseases Middle Aged Nicotinamide Phosphoribosyltransferase - blood Obesity Obesity - blood Resistin Resistin - blood Tumor Necrosis Factor-alpha Tumor necrosis factor-α Vertebrates: endocrinology Visfatin Women Young Adult |
title | Adipokines and cardiometabolic function: How are they interlinked? |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T12%3A23%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Adipokines%20and%20cardiometabolic%20function:%20How%20are%20they%20interlinked?&rft.jtitle=Regulatory%20peptides&rft.au=Schutte,%20Aletta%20Elisabeth&rft.date=2010-09-24&rft.volume=164&rft.issue=2&rft.spage=133&rft.epage=138&rft.pages=133-138&rft.issn=0167-0115&rft.eissn=1873-1686&rft.coden=REPPDY&rft_id=info:doi/10.1016/j.regpep.2010.06.008&rft_dat=%3Cproquest_cross%3E749011561%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=749011561&rft_id=info:pmid/20615436&rft_els_id=S0167011510001527&rfr_iscdi=true |