Adipose tissue quantity and composition contribute to adipokine concentrations in the subclavian vein and the inferior mesenteric vein
BACKGROUND: Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived adipokines, which are released in the portal circulation may influence liver metabolism. OBJECTIVES: (1) To estimate the contribution of VAT a...
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| Vydáno v: | International Journal of Obesity Ročník 36; číslo 8; s. 1078 - 1085 |
|---|---|
| Hlavní autoři: | , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
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London
Nature Publishing Group UK
01.08.2012
Nature Publishing Group |
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| ISSN: | 0307-0565, 1476-5497, 1476-5497 |
| On-line přístup: | Získat plný text |
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| Abstract | BACKGROUND:
Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived adipokines, which are released in the portal circulation may influence liver metabolism.
OBJECTIVES:
(1) To estimate the contribution of VAT and subcutaneous adipose tissue (SAT) on adipokine levels by measuring differences in adipokine concentrations between the portal draining inferior mesenteric vein and the subclavian vein. (2) To determine the relation of both VAT and SAT quantity and composition to mesenteric and systemic concentrations of adipokines.
DESIGN:
Cross-sectional cohort study.
SUBJECTS:
A total of 32 patients undergoing abdominal aortic surgery.
MEASUREMENTS:
A panel of 18 adipokines was measured in perioperatively obtained blood samples from the subclavian vein and the inferior mesenteric vein. Adipocyte size, macrophage infiltration and capillary density were measured in subcutaneous and mesenteric adipose tissue biopsies; SAT and VAT areas were measured on computed tomography images.
RESULTS:
Serum interferon-γ-inducible protein 10 (IP-10) and hepatocyte growth factor (HGF) concentrations were significantly higher in the inferior mesenteric vein vs the subclavian vein. SAT area (β –18; 95% confidence interval (CI) −35 to −2), subcutaneous adipocyte size (β –488; 95% CI −938 to −38) and SAT macrophages quantity (β –1439; 95% CI −2387 to −491) were negatively associated with adiponectin levels in the systemic circulation. SAT area was related to systemic concentrations of leptin. Mesenteric adiponectin concentrations were related to VAT area (β –20; 95% CI −35 to −5) and visceral adipocyte size (β −1076; 95% CI −1624 to −527). VAT area, adipocyte size and capillary density were related to systemic adiponectin concentrations.
CONCLUSION:
SAT and VAT quantities as well as morphologic characteristics of both adipose tissue depots are related to systemic and mesenteric adipokine concentrations. There were no differences in adipokine concentrations between the mesenteric and subclavian vein, except for higher IP-10 and HGF concentrations in the inferior mesenteric vein, indicating a possible contribution of VAT to IP-10 and HGF levels. |
|---|---|
| AbstractList | BACKGROUND: Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived adipokines, which are released in the portal circulation may influence liver metabolism. OBJECTIVES: (1) To estimate the contribution of VAT and subcutaneous adipose tissue (SAT) on adipokine levels by measuring differences in adipokine concentrations between the portal draining inferior mesenteric vein and the subclavian vein. (2) To determine the relation of both VAT and SAT quantity and composition to mesenteric and systemic concentrations of adipokines. DESIGN: Cross-sectional cohort study. SUBJECTS: A total of 32 patients undergoing abdominal aortic surgery. MEASUREMENTS: A panel of 18 adipokines was measured in perioperatively obtained blood samples from the subclavian vein and the inferior mesenteric vein. Adipocyte size, macrophage infiltration and capillary density were measured in subcutaneous and mesenteric adipose tissue biopsies; SAT and VAT areas were measured on computed tomography images. RESULTS: Serum interferon-γ-inducible protein 10 (IP-10) and hepatocyte growth factor (HGF) concentrations were significantly higher in the inferior mesenteric vein vs the subclavian vein. SAT area (β -18;95% confidence interval (CI) -35 to -2), subcutaneous adipocyte size (β -488;95% CI -938 to -38) and SAT macrophages quantity (β -1439;95% CI -2387 to -491) were negatively associated with adiponectin levels in the systemic circulation. SAT area was related to systemic concentrations of leptin. Mesenteric adiponectin concentrations were related to VAT area (β -20;95% CI -35 to -5) and visceral adipocyte size (β -1076;95% CI -1624 to -527). VAT area, adipocyte size and capillary density were related to systemic adiponectin concentrations. CONCLUSION: SAT and VAT quantities as well as morphologic characteristics of both adipose tissue depots are related to systemic and mesenteric adipokine concentrations. There were no differences in adipokine concentrations between the mesenteric and subclavian vein, except for higher IP-10 and HGF concentrations in the inferior mesenteric vein, indicating a possible contribution of VAT to IP-10 and HGF levels. International Journal of Obesity (2012) 36, 1078-1085; doi:10.1038/ijo.2011.214; published online 8 November 2011 Keywords: adipose tissue; adipokines; inflammation BACKGROUND: Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived adipokines, which are released in the portal circulation may influence liver metabolism. OBJECTIVES: (1) To estimate the contribution of VAT and subcutaneous adipose tissue (SAT) on adipokine levels by measuring differences in adipokine concentrations between the portal draining inferior mesenteric vein and the subclavian vein. (2) To determine the relation of both VAT and SAT quantity and composition to mesenteric and systemic concentrations of adipokines. DESIGN: Cross-sectional cohort study. SUBJECTS: A total of 32 patients undergoing abdominal aortic surgery. MEASUREMENTS: A panel of 18 adipokines was measured in perioperatively obtained blood samples from the subclavian vein and the inferior mesenteric vein. Adipocyte size, macrophage infiltration and capillary density were measured in subcutaneous and mesenteric adipose tissue biopsies; SAT and VAT areas were measured on computed tomography images. RESULTS: Serum interferon-γ-inducible protein 10 (IP-10) and hepatocyte growth factor (HGF) concentrations were significantly higher in the inferior mesenteric vein vs the subclavian vein. SAT area (β –18; 95% confidence interval (CI) −35 to −2), subcutaneous adipocyte size (β –488; 95% CI −938 to −38) and SAT macrophages quantity (β –1439; 95% CI −2387 to −491) were negatively associated with adiponectin levels in the systemic circulation. SAT area was related to systemic concentrations of leptin. Mesenteric adiponectin concentrations were related to VAT area (β –20; 95% CI −35 to −5) and visceral adipocyte size (β −1076; 95% CI −1624 to −527). VAT area, adipocyte size and capillary density were related to systemic adiponectin concentrations. CONCLUSION: SAT and VAT quantities as well as morphologic characteristics of both adipose tissue depots are related to systemic and mesenteric adipokine concentrations. There were no differences in adipokine concentrations between the mesenteric and subclavian vein, except for higher IP-10 and HGF concentrations in the inferior mesenteric vein, indicating a possible contribution of VAT to IP-10 and HGF levels. BACKGROUND: Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived adipokines, which are released in the portal circulation may influence liver metabolism. OBJECTIVES: (1) To estimate the contribution of VAT and subcutaneous adipose tissue (SAT) on adipokine levels by measuring differences in adipokine concentrations between the portal draining inferior mesenteric vein and the subclavian vein. (2) To determine the relation of both VAT and SAT quantity and composition to mesenteric and systemic concentrations of adipokines.DESIGN:Cross-sectional cohort study.SUBJECTS:A total of 32 patients undergoing abdominal aortic surgery.MEASUREMENTS:A panel of 18 adipokines was measured in perioperatively obtained blood samples from the subclavian vein and the inferior mesenteric vein. Adipocyte size, macrophage infiltration and capillary density were measured in subcutaneous and mesenteric adipose tissue biopsies; SAT and VAT areas were measured on computed tomography images. RESULTS: Serum interferon- gamma -inducible protein 10 (IP-10) and hepatocyte growth factor (HGF) concentrations were significantly higher in the inferior mesenteric vein vs the subclavian vein. SAT area ( beta -18; 95% confidence interval (CI) -35 to -2), subcutaneous adipocyte size ( beta -488; 95% CI -938 to -38) and SAT macrophages quantity ( beta -1439; 95% CI -2387 to -491) were negatively associated with adiponectin levels in the systemic circulation. SAT area was related to systemic concentrations of leptin. Mesenteric adiponectin concentrations were related to VAT area ( beta -20; 95% CI -35 to -5) and visceral adipocyte size ( beta -1076; 95% CI -1624 to -527). VAT area, adipocyte size and capillary density were related to systemic adiponectin concentrations. CONCLUSION: SAT and VAT quantities as well as morphologic characteristics of both adipose tissue depots are related to systemic and mesenteric adipokine concentrations. There were no differences in adipokine concentrations between the mesenteric and subclavian vein, except for higher IP-10 and HGF concentrations in the inferior mesenteric vein, indicating a possible contribution of VAT to IP-10 and HGF levels. Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived adipokines, which are released in the portal circulation may influence liver metabolism. (1) To estimate the contribution of VAT and subcutaneous adipose tissue (SAT) on adipokine levels by measuring differences in adipokine concentrations between the portal draining inferior mesenteric vein and the subclavian vein. (2) To determine the relation of both VAT and SAT quantity and composition to mesenteric and systemic concentrations of adipokines. Cross-sectional cohort study. A total of 32 patients undergoing abdominal aortic surgery. A panel of 18 adipokines was measured in perioperatively obtained blood samples from the subclavian vein and the inferior mesenteric vein. Adipocyte size, macrophage infiltration and capillary density were measured in subcutaneous and mesenteric adipose tissue biopsies; SAT and VAT areas were measured on computed tomography images. Serum interferon-γ-inducible protein 10 (IP-10) and hepatocyte growth factor (HGF) concentrations were significantly higher in the inferior mesenteric vein vs the subclavian vein. SAT area ([beta] -18; 95% confidence interval (CI) -35 to -2), subcutaneous adipocyte size ([beta] -488; 95% CI -938 to -38) and SAT macrophages quantity ([beta] -1439; 95% CI -2387 to -491) were negatively associated with adiponectin levels in the systemic circulation. SAT area was related to systemic concentrations of leptin. Mesenteric adiponectin concentrations were related to VAT area ([beta] -20; 95% CI -35 to -5) and visceral adipocyte size ([beta] -1076; 95% CI -1624 to -527). VAT area, adipocyte size and capillary density were related to systemic adiponectin concentrations. SAT and VAT quantities as well as morphologic characteristics of both adipose tissue depots are related to systemic and mesenteric adipokine concentrations. There were no differences in adipokine concentrations between the mesenteric and subclavian vein, except for higher IP-10 and HGF concentrations in the inferior mesenteric vein, indicating a possible contribution of VAT to IP-10 and HGF levels. Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived adipokines, which are released in the portal circulation may influence liver metabolism.BACKGROUNDAdipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived adipokines, which are released in the portal circulation may influence liver metabolism.(1) To estimate the contribution of VAT and subcutaneous adipose tissue (SAT) on adipokine levels by measuring differences in adipokine concentrations between the portal draining inferior mesenteric vein and the subclavian vein. (2) To determine the relation of both VAT and SAT quantity and composition to mesenteric and systemic concentrations of adipokines.OBJECTIVES(1) To estimate the contribution of VAT and subcutaneous adipose tissue (SAT) on adipokine levels by measuring differences in adipokine concentrations between the portal draining inferior mesenteric vein and the subclavian vein. (2) To determine the relation of both VAT and SAT quantity and composition to mesenteric and systemic concentrations of adipokines.Cross-sectional cohort study.DESIGNCross-sectional cohort study.A total of 32 patients undergoing abdominal aortic surgery.SUBJECTSA total of 32 patients undergoing abdominal aortic surgery.A panel of 18 adipokines was measured in perioperatively obtained blood samples from the subclavian vein and the inferior mesenteric vein. Adipocyte size, macrophage infiltration and capillary density were measured in subcutaneous and mesenteric adipose tissue biopsies; SAT and VAT areas were measured on computed tomography images.MEASUREMENTSA panel of 18 adipokines was measured in perioperatively obtained blood samples from the subclavian vein and the inferior mesenteric vein. Adipocyte size, macrophage infiltration and capillary density were measured in subcutaneous and mesenteric adipose tissue biopsies; SAT and VAT areas were measured on computed tomography images.Serum interferon-γ-inducible protein 10 (IP-10) and hepatocyte growth factor (HGF) concentrations were significantly higher in the inferior mesenteric vein vs the subclavian vein. SAT area (β -18; 95% confidence interval (CI) -35 to -2), subcutaneous adipocyte size (β -488; 95% CI -938 to -38) and SAT macrophages quantity (β -1439; 95% CI -2387 to -491) were negatively associated with adiponectin levels in the systemic circulation. SAT area was related to systemic concentrations of leptin. Mesenteric adiponectin concentrations were related to VAT area (β -20; 95% CI -35 to -5) and visceral adipocyte size (β -1076; 95% CI -1624 to -527). VAT area, adipocyte size and capillary density were related to systemic adiponectin concentrations.RESULTSSerum interferon-γ-inducible protein 10 (IP-10) and hepatocyte growth factor (HGF) concentrations were significantly higher in the inferior mesenteric vein vs the subclavian vein. SAT area (β -18; 95% confidence interval (CI) -35 to -2), subcutaneous adipocyte size (β -488; 95% CI -938 to -38) and SAT macrophages quantity (β -1439; 95% CI -2387 to -491) were negatively associated with adiponectin levels in the systemic circulation. SAT area was related to systemic concentrations of leptin. Mesenteric adiponectin concentrations were related to VAT area (β -20; 95% CI -35 to -5) and visceral adipocyte size (β -1076; 95% CI -1624 to -527). VAT area, adipocyte size and capillary density were related to systemic adiponectin concentrations.SAT and VAT quantities as well as morphologic characteristics of both adipose tissue depots are related to systemic and mesenteric adipokine concentrations. There were no differences in adipokine concentrations between the mesenteric and subclavian vein, except for higher IP-10 and HGF concentrations in the inferior mesenteric vein, indicating a possible contribution of VAT to IP-10 and HGF levels.CONCLUSIONSAT and VAT quantities as well as morphologic characteristics of both adipose tissue depots are related to systemic and mesenteric adipokine concentrations. There were no differences in adipokine concentrations between the mesenteric and subclavian vein, except for higher IP-10 and HGF concentrations in the inferior mesenteric vein, indicating a possible contribution of VAT to IP-10 and HGF levels. SUBJECTS: A total of 32 patients undergoing abdominal aortic surgery. International Journal of Obesity (2012) 36, 1078-1085; doi:10.1038/ijo.2011.214; published online 8 November 2011 Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived adipokines, which are released in the portal circulation may influence liver metabolism. (1) To estimate the contribution of VAT and subcutaneous adipose tissue (SAT) on adipokine levels by measuring differences in adipokine concentrations between the portal draining inferior mesenteric vein and the subclavian vein. (2) To determine the relation of both VAT and SAT quantity and composition to mesenteric and systemic concentrations of adipokines. Cross-sectional cohort study. A total of 32 patients undergoing abdominal aortic surgery. A panel of 18 adipokines was measured in perioperatively obtained blood samples from the subclavian vein and the inferior mesenteric vein. Adipocyte size, macrophage infiltration and capillary density were measured in subcutaneous and mesenteric adipose tissue biopsies; SAT and VAT areas were measured on computed tomography images. Serum interferon-γ-inducible protein 10 (IP-10) and hepatocyte growth factor (HGF) concentrations were significantly higher in the inferior mesenteric vein vs the subclavian vein. SAT area (β -18; 95% confidence interval (CI) -35 to -2), subcutaneous adipocyte size (β -488; 95% CI -938 to -38) and SAT macrophages quantity (β -1439; 95% CI -2387 to -491) were negatively associated with adiponectin levels in the systemic circulation. SAT area was related to systemic concentrations of leptin. Mesenteric adiponectin concentrations were related to VAT area (β -20; 95% CI -35 to -5) and visceral adipocyte size (β -1076; 95% CI -1624 to -527). VAT area, adipocyte size and capillary density were related to systemic adiponectin concentrations. SAT and VAT quantities as well as morphologic characteristics of both adipose tissue depots are related to systemic and mesenteric adipokine concentrations. There were no differences in adipokine concentrations between the mesenteric and subclavian vein, except for higher IP-10 and HGF concentrations in the inferior mesenteric vein, indicating a possible contribution of VAT to IP-10 and HGF levels. |
| Audience | Academic |
| Author | Faber, D R Monajemi, H Visseren, F L J Moll, F L van der Waal, C Vink, A Schipper, H S Kalkhoven, E Hajer, G R |
| Author_xml | – sequence: 1 givenname: D R surname: Faber fullname: Faber, D R organization: Department of Vascular Medicine, University Medical Center Utrecht – sequence: 2 givenname: F L surname: Moll fullname: Moll, F L organization: Department of Vascular Surgery, University Medical Center Utrecht – sequence: 3 givenname: A surname: Vink fullname: Vink, A organization: Department of Pathology, University Medical Center Utrecht – sequence: 4 givenname: C surname: van der Waal fullname: van der Waal, C organization: Department of Vascular Surgery, Gelderse Vallei Hospital – sequence: 5 givenname: E surname: Kalkhoven fullname: Kalkhoven, E organization: Department of Endocrine and Metabolic Diseases, University Medical Center Utrecht – sequence: 6 givenname: H S surname: Schipper fullname: Schipper, H S organization: Department of Endocrine and Metabolic Diseases, University Medical Center Utrecht – sequence: 7 givenname: G R surname: Hajer fullname: Hajer, G R organization: Department of Vascular Medicine, University Medical Center Utrecht – sequence: 8 givenname: H surname: Monajemi fullname: Monajemi, H organization: Department of Vascular Medicine, University Medical Center Utrecht – sequence: 9 givenname: F L J surname: Visseren fullname: Visseren, F L J email: F.L.J.Visseren@umcutrecht.nl organization: Department of Vascular Medicine, University Medical Center Utrecht |
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| Issue | 8 |
| Keywords | adipose tissue inflammation adipokines Obesity Composition Adipose tissue Nutrition Nutrition disorder Subclaviar vein Metabolic diseases Inflammation Adipokine Concentration Inferior mesenteric vein Nutritional status |
| Language | English |
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| PublicationPlace | London |
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| PublicationTitle | International Journal of Obesity |
| PublicationTitleAbbrev | Int J Obes |
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| PublicationYear | 2012 |
| Publisher | Nature Publishing Group UK Nature Publishing Group |
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Adipose tissue dysfunction in obesity, diabetes, and vascular diseases publication-title: Eur Heart J doi: 10.1093/eurheartj/ehn387 – volume: 291 start-page: E843 year: 2006 ident: BFijo2011214_CR34 publication-title: Am J Physiol Endocrinol Metab doi: 10.1152/ajpendo.00174.2006 – volume: 145 start-page: 2273 year: 2004 ident: BFijo2011214_CR4 publication-title: Endocrinology doi: 10.1210/en.2003-1336 – volume: 20 start-page: 1932 year: 2000 ident: BFijo2011214_CR35 publication-title: Arterioscler Thromb Vasc Biol doi: 10.1161/01.ATV.20.8.1932 – volume: 212 start-page: 274 year: 2010 ident: BFijo2011214_CR16 publication-title: Atherosclerosis doi: 10.1016/j.atherosclerosis.2010.04.029 – volume: 116 start-page: 1234 year: 2007 ident: BFijo2011214_CR17 publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.107.710509 – volume: 116 start-page: 39 year: 2007 ident: BFijo2011214_CR12 publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.106.675355 – volume: 281 start-page: E1110 year: 2001 ident: BFijo2011214_CR37 publication-title: Am J Physiol Endocrinol Metab doi: 10.1152/ajpendo.2001.281.5.E1110 – volume: 56 start-page: 1320 year: 2010 ident: BFijo2011214_CR14 publication-title: Clin Chem doi: 10.1373/clinchem.2010.146118 – volume: 164 start-page: 79 year: 2002 ident: BFijo2011214_CR30 publication-title: Atherosclerosis doi: 10.1016/S0021-9150(02)00062-X – volume: 34 start-page: 781 year: 2010 ident: BFijo2011214_CR15 publication-title: Int J Obes (Lond) doi: 10.1038/ijo.2009.279 – volume: 177 start-page: 1809 year: 1993 ident: BFijo2011214_CR27 publication-title: J Exp Med doi: 10.1084/jem.177.6.1809 – volume: 24 start-page: 1139 year: 2000 ident: BFijo2011214_CR21 publication-title: Int J Obes Relat Metab Disord doi: 10.1038/sj.ijo.0801385 – volume: 31 start-page: 403 year: 2007 ident: BFijo2011214_CR29 publication-title: Int J Obes (Lond) doi: 10.1038/sj.ijo.0803432 – volume: 59 start-page: 105 year: 2010 ident: BFijo2011214_CR7 publication-title: Diabetes doi: 10.2337/db09-0942 – volume: 15 start-page: 1933 year: 2007 ident: BFijo2011214_CR39 publication-title: Obesity (Silver Spring) doi: 10.1038/oby.2007.231 – volume: 56 start-page: 1010 year: 2007 ident: BFijo2011214_CR5 publication-title: Diabetes doi: 10.2337/db06-1656 – volume: 278 start-page: E941 year: 2000 ident: BFijo2011214_CR38 publication-title: Am J Physiol Endocrinol Metab doi: 10.1152/ajpendo.2000.278.5.E941 – volume: 33 start-page: 2013 year: 2010 ident: BFijo2011214_CR32 publication-title: Diabetes Care doi: 10.2337/dc10-0710 – volume: 8 start-page: 41 issue: Suppl 1 year: 2007 ident: BFijo2011214_CR1 publication-title: Obes Rev doi: 10.1111/j.1467-789X.2007.00316.x – volume: 285 start-page: E527 year: 2003 ident: BFijo2011214_CR25 publication-title: Am J Physiol Endocrinol Metab doi: 10.1152/ajpendo.00110.2003 – volume: 366 start-page: 1640 year: 2005 ident: BFijo2011214_CR2 publication-title: Lancet doi: 10.1016/S0140-6736(05)67663-5 – volume: 16 start-page: 1983 year: 2008 ident: BFijo2011214_CR40 publication-title: Obesity (Silver Spring) doi: 10.1038/oby.2008.326 – volume: 29 start-page: 2959 year: 2008 ident: BFijo2011214_CR22 publication-title: Eur Heart J doi: 10.1093/eurheartj/ehn387 – volume: 28 start-page: 1039 year: 2008 ident: BFijo2011214_CR13 publication-title: Arterioscler Thromb Vasc Biol doi: 10.1161/ATVBAHA.107.159228 – volume: 6 start-page: 343 year: 2008 ident: BFijo2011214_CR8 publication-title: Expert Rev Cardiovasc Ther doi: 10.1586/14779072.6.3.343 – volume: 58 start-page: 463 year: 1993 ident: BFijo2011214_CR36 publication-title: Am J Clin Nutr doi: 10.1093/ajcn/58.4.463 – volume: 47 start-page: 913 year: 1998 ident: BFijo2011214_CR18 publication-title: Diabetes doi: 10.2337/diabetes.47.6.913 – volume: 92 start-page: 1023 year: 2007 ident: BFijo2011214_CR24 publication-title: J Clin Endocrinol Metab doi: 10.1210/jc.2006-1055 – volume: 60 start-page: 1504 year: 2011 ident: BFijo2011214_CR10 publication-title: Diabetes doi: 10.2337/db10-1039 – volume: 100 start-page: 227 year: 2008 ident: BFijo2011214_CR26 publication-title: Br J Nutr doi: 10.1017/S0007114508971282 – volume: 168 start-page: 3195 year: 2002 ident: BFijo2011214_CR28 publication-title: J Immunol doi: 10.4049/jimmunol.168.7.3195 – volume: 10 start-page: 554 year: 2009 ident: BFijo2011214_CR3 publication-title: Obes Rev doi: 10.1111/j.1467-789X.2009.00593.x – volume: 5 start-page: e9997 year: 2010 ident: BFijo2011214_CR9 publication-title: PLoS One doi: 10.1371/journal.pone.0009997 – volume: 41 start-page: 1408 year: 2003 ident: BFijo2011214_CR33 publication-title: J Am Coll Cardiol doi: 10.1016/S0735-1097(03)00231-6 – volume: 26 start-page: 2387 year: 2005 ident: BFijo2011214_CR31 publication-title: Eur Heart J doi: 10.1093/eurheartj/ehi436 – volume: 112 start-page: 1796 year: 2003 ident: BFijo2011214_CR6 publication-title: J Clin Invest doi: 10.1172/JCI200319246 – volume: 123 start-page: 186 year: 2011 ident: BFijo2011214_CR11 publication-title: Circulation doi: 10.1161/CIRCULATIONAHA.110.970145 – volume: 62 start-page: 189 year: 2005 ident: BFijo2011214_CR20 publication-title: Clin Endocrinol (Oxf) doi: 10.1111/j.1365-2265.2005.02195.x – volume: 257 start-page: 79 year: 1999 ident: BFijo2011214_CR23 publication-title: Biochem Biophys Res Commun doi: 10.1006/bbrc.1999.0255 – volume: 395 start-page: 763 year: 1998 ident: BFijo2011214_CR19 publication-title: Nature doi: 10.1038/27376 |
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| Snippet | BACKGROUND:
Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived... Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived adipokines,... BACKGROUND: Adipose tissue dysfunction is associated with inflammation, type 2 diabetes mellitus and vascular diseases. Visceral adipose tissue (VAT)-derived... SUBJECTS: A total of 32 patients undergoing abdominal aortic surgery. International Journal of Obesity (2012) 36, 1078-1085; doi:10.1038/ijo.2011.214;... |
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| SubjectTerms | 631/250/256 631/443/592 631/45/127 692/699/2743 Abdomen Adipocytes Adipokines - metabolism Adipose tissue Adipose tissues Aged Biological and medical sciences Biopsy Blood Body fat Chemokine CXCL10 - blood Cohort Studies Computed tomography Cross-Sectional Studies Cytokines Diabetes Epidemiology Fatty acids Female Health Promotion and Disease Prevention Hepatocyte Growth Factor - blood Hormone replacement therapy Humans Infiltration Inflammation - metabolism Insulin resistance Internal Medicine Intra-Abdominal Fat - metabolism Intra-Abdominal Fat - pathology Liver Liver - metabolism Liver - pathology Male Medical sciences Medicine Medicine & Public Health Mesenteric Veins - metabolism Mesenteric Veins - pathology Metabolic Diseases Metabolic disorders Obesity original-article Physiological aspects Public Health Subclavian Vein - metabolism Subclavian Vein - pathology Subcutaneous Fat - metabolism Subcutaneous Fat - pathology Vascular diseases Vascular surgery Veins Veins & arteries |
| Title | Adipose tissue quantity and composition contribute to adipokine concentrations in the subclavian vein and the inferior mesenteric vein |
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