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Coronary vasomotor control in obesity and morbid obesity: contrasting flow responses with endocannabinoids, leptin, and inflammation
This study sought to investigate abnormalities in coronary circulatory function in 2 different disease entities of obese (OB) and morbidly obese (MOB) individuals and to evaluate whether these would differ in severity with different profiles of endocannabinoids, leptin, and C-reactive protein (CRP)...
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Published in: | JACC. Cardiovascular imaging 2012-08, Vol.5 (8), p.805-815 |
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creator | Quercioli, Alessandra Pataky, Zoltan Montecucco, Fabrizio Carballo, Sebastian Thomas, Aurélien Staub, Christian Di Marzo, Vincenzo Vincenti, Gabriella Ambrosio, Giuseppe Ratib, Osman Golay, Alain Mach, François Harsch, Elisabetta Schindler, Thomas H |
description | This study sought to investigate abnormalities in coronary circulatory function in 2 different disease entities of obese (OB) and morbidly obese (MOB) individuals and to evaluate whether these would differ in severity with different profiles of endocannabinoids, leptin, and C-reactive protein (CRP) plasma levels.
There is increasing evidence that altered plasma levels of endocannabinoids, leptin, and CRP may affect coronary circulatory function in OB and MOB.
Myocardial blood flow (MBF) responses to cold pressor test from rest and during pharmacologically induced hyperemia were measured with N-13 ammonia positron emission tomography/computed tomography. Study participants (n = 111) were divided into 4 groups based on their body mass index (BMI) (kg/m(2)): 1) control group (BMI: 20 to 24.9, n = 30); 2) overweight group (BMI: 25 to 29.9, n = 31), 3) OB group (BMI: 30 to 39.9, n = 25); and 4) MOB group (BMI ≥40, n = 25).
The cold pressor test-induced change in endothelium-related MBF response (ΔMBF) progressively declined in overweight and OB groups when compared with the control group [median: 0.19 (interquartile range [IQR] 0.08, 0.27) and 0.11 (0.03, 0.17) vs. 0.27 (0.23, 0.38) ml/g/min; p ≤ 0.01, respectively], whereas it did not differ significantly between OB and MOB groups [median: 0.11 (IQR: 0.03, 0.17) and 0.09 (-0.01, 0.19) ml/g/min; p = 0.93]. Compared with control subjects, hyperemic MBF subjects comparably declined in the overweight, OB, and MOB groups [median: 2.40 (IQR 1.92, 2.63) vs. 1.94 (1.65, 2.30), 2.05 (1.67, 2.38), and 2.14 (1.78, 2.76) ml/g/min; p ≤ 0.05, respectively]. In OB individuals, ΔMBF was inversely correlated with increase in endocannabinoid anandamide (r = -0.45, p = 0.044), but not with leptin (r = -0.02, p = 0.946) or with CRP (r = -0.33, p = 0.168). Conversely, there was a significant and positive correlation among ΔMBF and elevated leptin (r = 0.43, p = 0.031) and CRP (r = 0.55, p = 0.006), respectively, in MOB individuals that was not observed for endocannabinoid anandamide (r = 0.07, p = 0.740).
Contrasting associations of altered coronary endothelial function with increases in endocannabinoid anandamide, leptin, and CRP plasma levels identify and characterize OB and MOB as different disease entities affecting coronary circulatory function. |
doi_str_mv | 10.1016/j.jcmg.2012.01.020 |
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There is increasing evidence that altered plasma levels of endocannabinoids, leptin, and CRP may affect coronary circulatory function in OB and MOB.
Myocardial blood flow (MBF) responses to cold pressor test from rest and during pharmacologically induced hyperemia were measured with N-13 ammonia positron emission tomography/computed tomography. Study participants (n = 111) were divided into 4 groups based on their body mass index (BMI) (kg/m(2)): 1) control group (BMI: 20 to 24.9, n = 30); 2) overweight group (BMI: 25 to 29.9, n = 31), 3) OB group (BMI: 30 to 39.9, n = 25); and 4) MOB group (BMI ≥40, n = 25).
The cold pressor test-induced change in endothelium-related MBF response (ΔMBF) progressively declined in overweight and OB groups when compared with the control group [median: 0.19 (interquartile range [IQR] 0.08, 0.27) and 0.11 (0.03, 0.17) vs. 0.27 (0.23, 0.38) ml/g/min; p ≤ 0.01, respectively], whereas it did not differ significantly between OB and MOB groups [median: 0.11 (IQR: 0.03, 0.17) and 0.09 (-0.01, 0.19) ml/g/min; p = 0.93]. Compared with control subjects, hyperemic MBF subjects comparably declined in the overweight, OB, and MOB groups [median: 2.40 (IQR 1.92, 2.63) vs. 1.94 (1.65, 2.30), 2.05 (1.67, 2.38), and 2.14 (1.78, 2.76) ml/g/min; p ≤ 0.05, respectively]. In OB individuals, ΔMBF was inversely correlated with increase in endocannabinoid anandamide (r = -0.45, p = 0.044), but not with leptin (r = -0.02, p = 0.946) or with CRP (r = -0.33, p = 0.168). Conversely, there was a significant and positive correlation among ΔMBF and elevated leptin (r = 0.43, p = 0.031) and CRP (r = 0.55, p = 0.006), respectively, in MOB individuals that was not observed for endocannabinoid anandamide (r = 0.07, p = 0.740).
Contrasting associations of altered coronary endothelial function with increases in endocannabinoid anandamide, leptin, and CRP plasma levels identify and characterize OB and MOB as different disease entities affecting coronary circulatory function.</description><identifier>EISSN: 1876-7591</identifier><identifier>DOI: 10.1016/j.jcmg.2012.01.020</identifier><identifier>PMID: 22897994</identifier><language>eng</language><publisher>United States</publisher><subject>Adipokines - blood ; Adult ; Body Mass Index ; C-Reactive Protein - analysis ; Cardiovascular System - physiopathology ; Coronary Circulation - drug effects ; Coronary Circulation - physiology ; Endocannabinoids - blood ; Endothelium, Vascular - physiology ; Female ; Humans ; Leptin - blood ; Middle Aged ; Multimodal Imaging ; Muscle, Smooth, Vascular - physiology ; Obesity - blood ; Obesity - physiopathology ; Obesity, Morbid - blood ; Obesity, Morbid - physiopathology ; Positron-Emission Tomography ; Regional Blood Flow - drug effects ; Tomography, X-Ray Computed ; Vasodilation - physiology</subject><ispartof>JACC. Cardiovascular imaging, 2012-08, Vol.5 (8), p.805-815</ispartof><rights>Copyright © 2012 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22897994$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Quercioli, Alessandra</creatorcontrib><creatorcontrib>Pataky, Zoltan</creatorcontrib><creatorcontrib>Montecucco, Fabrizio</creatorcontrib><creatorcontrib>Carballo, Sebastian</creatorcontrib><creatorcontrib>Thomas, Aurélien</creatorcontrib><creatorcontrib>Staub, Christian</creatorcontrib><creatorcontrib>Di Marzo, Vincenzo</creatorcontrib><creatorcontrib>Vincenti, Gabriella</creatorcontrib><creatorcontrib>Ambrosio, Giuseppe</creatorcontrib><creatorcontrib>Ratib, Osman</creatorcontrib><creatorcontrib>Golay, Alain</creatorcontrib><creatorcontrib>Mach, François</creatorcontrib><creatorcontrib>Harsch, Elisabetta</creatorcontrib><creatorcontrib>Schindler, Thomas H</creatorcontrib><title>Coronary vasomotor control in obesity and morbid obesity: contrasting flow responses with endocannabinoids, leptin, and inflammation</title><title>JACC. Cardiovascular imaging</title><addtitle>JACC Cardiovasc Imaging</addtitle><description>This study sought to investigate abnormalities in coronary circulatory function in 2 different disease entities of obese (OB) and morbidly obese (MOB) individuals and to evaluate whether these would differ in severity with different profiles of endocannabinoids, leptin, and C-reactive protein (CRP) plasma levels.
There is increasing evidence that altered plasma levels of endocannabinoids, leptin, and CRP may affect coronary circulatory function in OB and MOB.
Myocardial blood flow (MBF) responses to cold pressor test from rest and during pharmacologically induced hyperemia were measured with N-13 ammonia positron emission tomography/computed tomography. Study participants (n = 111) were divided into 4 groups based on their body mass index (BMI) (kg/m(2)): 1) control group (BMI: 20 to 24.9, n = 30); 2) overweight group (BMI: 25 to 29.9, n = 31), 3) OB group (BMI: 30 to 39.9, n = 25); and 4) MOB group (BMI ≥40, n = 25).
The cold pressor test-induced change in endothelium-related MBF response (ΔMBF) progressively declined in overweight and OB groups when compared with the control group [median: 0.19 (interquartile range [IQR] 0.08, 0.27) and 0.11 (0.03, 0.17) vs. 0.27 (0.23, 0.38) ml/g/min; p ≤ 0.01, respectively], whereas it did not differ significantly between OB and MOB groups [median: 0.11 (IQR: 0.03, 0.17) and 0.09 (-0.01, 0.19) ml/g/min; p = 0.93]. Compared with control subjects, hyperemic MBF subjects comparably declined in the overweight, OB, and MOB groups [median: 2.40 (IQR 1.92, 2.63) vs. 1.94 (1.65, 2.30), 2.05 (1.67, 2.38), and 2.14 (1.78, 2.76) ml/g/min; p ≤ 0.05, respectively]. In OB individuals, ΔMBF was inversely correlated with increase in endocannabinoid anandamide (r = -0.45, p = 0.044), but not with leptin (r = -0.02, p = 0.946) or with CRP (r = -0.33, p = 0.168). Conversely, there was a significant and positive correlation among ΔMBF and elevated leptin (r = 0.43, p = 0.031) and CRP (r = 0.55, p = 0.006), respectively, in MOB individuals that was not observed for endocannabinoid anandamide (r = 0.07, p = 0.740).
Contrasting associations of altered coronary endothelial function with increases in endocannabinoid anandamide, leptin, and CRP plasma levels identify and characterize OB and MOB as different disease entities affecting coronary circulatory function.</description><subject>Adipokines - blood</subject><subject>Adult</subject><subject>Body Mass Index</subject><subject>C-Reactive Protein - analysis</subject><subject>Cardiovascular System - physiopathology</subject><subject>Coronary Circulation - drug effects</subject><subject>Coronary Circulation - physiology</subject><subject>Endocannabinoids - blood</subject><subject>Endothelium, Vascular - physiology</subject><subject>Female</subject><subject>Humans</subject><subject>Leptin - blood</subject><subject>Middle Aged</subject><subject>Multimodal Imaging</subject><subject>Muscle, Smooth, Vascular - physiology</subject><subject>Obesity - blood</subject><subject>Obesity - physiopathology</subject><subject>Obesity, Morbid - blood</subject><subject>Obesity, Morbid - physiopathology</subject><subject>Positron-Emission Tomography</subject><subject>Regional Blood Flow - drug effects</subject><subject>Tomography, X-Ray Computed</subject><subject>Vasodilation - physiology</subject><issn>1876-7591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNo1kDtPwzAUhS0kREvhDzAgjwxN8COJazZU8ZIqscAcXSdOcRXbwXapuvPDiWg7naujT590D0I3lOSU0Op-k28au84ZoSwnNCeMnKEpXYgqE6WkE3QZ44aQilSFuEATxhZSSFlM0e_SB-8g7PEPRG998gE33qXge2wc9kpHk_YYXIutD8q0p-rhgEFMxq1x1_sdDjoO3kUd8c6kL6xd6xtwDpRx3rRxjns9jPT832Zc14O1kIx3V-i8gz7q62PO0Ofz08fyNVu9v7wtH1fZwChNWSG5hI4zIEA5F11JuGCiaYEWpRzfBMILqQinoKBslS6F0kXBKSsV13y8Zuju4B2C_97qmGprYqP7Hpz221jTUUDlomLViN4e0a2yuq2HYOy4Un1ajv8BcyFyDA</recordid><startdate>20120801</startdate><enddate>20120801</enddate><creator>Quercioli, Alessandra</creator><creator>Pataky, Zoltan</creator><creator>Montecucco, Fabrizio</creator><creator>Carballo, Sebastian</creator><creator>Thomas, Aurélien</creator><creator>Staub, Christian</creator><creator>Di Marzo, Vincenzo</creator><creator>Vincenti, Gabriella</creator><creator>Ambrosio, Giuseppe</creator><creator>Ratib, Osman</creator><creator>Golay, Alain</creator><creator>Mach, François</creator><creator>Harsch, Elisabetta</creator><creator>Schindler, Thomas H</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20120801</creationdate><title>Coronary vasomotor control in obesity and morbid obesity: contrasting flow responses with endocannabinoids, leptin, and inflammation</title><author>Quercioli, Alessandra ; Pataky, Zoltan ; Montecucco, Fabrizio ; Carballo, Sebastian ; Thomas, Aurélien ; Staub, Christian ; Di Marzo, Vincenzo ; Vincenti, Gabriella ; Ambrosio, Giuseppe ; Ratib, Osman ; Golay, Alain ; Mach, François ; Harsch, Elisabetta ; Schindler, Thomas H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p211t-4939af32a0a1337f503727cda1459759a0349b031aba5dbe57be443125b3e3443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adipokines - blood</topic><topic>Adult</topic><topic>Body Mass Index</topic><topic>C-Reactive Protein - analysis</topic><topic>Cardiovascular System - physiopathology</topic><topic>Coronary Circulation - drug effects</topic><topic>Coronary Circulation - physiology</topic><topic>Endocannabinoids - blood</topic><topic>Endothelium, Vascular - physiology</topic><topic>Female</topic><topic>Humans</topic><topic>Leptin - blood</topic><topic>Middle Aged</topic><topic>Multimodal Imaging</topic><topic>Muscle, Smooth, Vascular - physiology</topic><topic>Obesity - blood</topic><topic>Obesity - physiopathology</topic><topic>Obesity, Morbid - blood</topic><topic>Obesity, Morbid - physiopathology</topic><topic>Positron-Emission Tomography</topic><topic>Regional Blood Flow - drug effects</topic><topic>Tomography, X-Ray Computed</topic><topic>Vasodilation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quercioli, Alessandra</creatorcontrib><creatorcontrib>Pataky, Zoltan</creatorcontrib><creatorcontrib>Montecucco, Fabrizio</creatorcontrib><creatorcontrib>Carballo, Sebastian</creatorcontrib><creatorcontrib>Thomas, Aurélien</creatorcontrib><creatorcontrib>Staub, Christian</creatorcontrib><creatorcontrib>Di Marzo, Vincenzo</creatorcontrib><creatorcontrib>Vincenti, Gabriella</creatorcontrib><creatorcontrib>Ambrosio, Giuseppe</creatorcontrib><creatorcontrib>Ratib, Osman</creatorcontrib><creatorcontrib>Golay, Alain</creatorcontrib><creatorcontrib>Mach, François</creatorcontrib><creatorcontrib>Harsch, Elisabetta</creatorcontrib><creatorcontrib>Schindler, Thomas H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>JACC. Cardiovascular imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quercioli, Alessandra</au><au>Pataky, Zoltan</au><au>Montecucco, Fabrizio</au><au>Carballo, Sebastian</au><au>Thomas, Aurélien</au><au>Staub, Christian</au><au>Di Marzo, Vincenzo</au><au>Vincenti, Gabriella</au><au>Ambrosio, Giuseppe</au><au>Ratib, Osman</au><au>Golay, Alain</au><au>Mach, François</au><au>Harsch, Elisabetta</au><au>Schindler, Thomas H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coronary vasomotor control in obesity and morbid obesity: contrasting flow responses with endocannabinoids, leptin, and inflammation</atitle><jtitle>JACC. Cardiovascular imaging</jtitle><addtitle>JACC Cardiovasc Imaging</addtitle><date>2012-08-01</date><risdate>2012</risdate><volume>5</volume><issue>8</issue><spage>805</spage><epage>815</epage><pages>805-815</pages><eissn>1876-7591</eissn><abstract>This study sought to investigate abnormalities in coronary circulatory function in 2 different disease entities of obese (OB) and morbidly obese (MOB) individuals and to evaluate whether these would differ in severity with different profiles of endocannabinoids, leptin, and C-reactive protein (CRP) plasma levels.
There is increasing evidence that altered plasma levels of endocannabinoids, leptin, and CRP may affect coronary circulatory function in OB and MOB.
Myocardial blood flow (MBF) responses to cold pressor test from rest and during pharmacologically induced hyperemia were measured with N-13 ammonia positron emission tomography/computed tomography. Study participants (n = 111) were divided into 4 groups based on their body mass index (BMI) (kg/m(2)): 1) control group (BMI: 20 to 24.9, n = 30); 2) overweight group (BMI: 25 to 29.9, n = 31), 3) OB group (BMI: 30 to 39.9, n = 25); and 4) MOB group (BMI ≥40, n = 25).
The cold pressor test-induced change in endothelium-related MBF response (ΔMBF) progressively declined in overweight and OB groups when compared with the control group [median: 0.19 (interquartile range [IQR] 0.08, 0.27) and 0.11 (0.03, 0.17) vs. 0.27 (0.23, 0.38) ml/g/min; p ≤ 0.01, respectively], whereas it did not differ significantly between OB and MOB groups [median: 0.11 (IQR: 0.03, 0.17) and 0.09 (-0.01, 0.19) ml/g/min; p = 0.93]. Compared with control subjects, hyperemic MBF subjects comparably declined in the overweight, OB, and MOB groups [median: 2.40 (IQR 1.92, 2.63) vs. 1.94 (1.65, 2.30), 2.05 (1.67, 2.38), and 2.14 (1.78, 2.76) ml/g/min; p ≤ 0.05, respectively]. In OB individuals, ΔMBF was inversely correlated with increase in endocannabinoid anandamide (r = -0.45, p = 0.044), but not with leptin (r = -0.02, p = 0.946) or with CRP (r = -0.33, p = 0.168). Conversely, there was a significant and positive correlation among ΔMBF and elevated leptin (r = 0.43, p = 0.031) and CRP (r = 0.55, p = 0.006), respectively, in MOB individuals that was not observed for endocannabinoid anandamide (r = 0.07, p = 0.740).
Contrasting associations of altered coronary endothelial function with increases in endocannabinoid anandamide, leptin, and CRP plasma levels identify and characterize OB and MOB as different disease entities affecting coronary circulatory function.</abstract><cop>United States</cop><pmid>22897994</pmid><doi>10.1016/j.jcmg.2012.01.020</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adipokines - blood Adult Body Mass Index C-Reactive Protein - analysis Cardiovascular System - physiopathology Coronary Circulation - drug effects Coronary Circulation - physiology Endocannabinoids - blood Endothelium, Vascular - physiology Female Humans Leptin - blood Middle Aged Multimodal Imaging Muscle, Smooth, Vascular - physiology Obesity - blood Obesity - physiopathology Obesity, Morbid - blood Obesity, Morbid - physiopathology Positron-Emission Tomography Regional Blood Flow - drug effects Tomography, X-Ray Computed Vasodilation - physiology |
title | Coronary vasomotor control in obesity and morbid obesity: contrasting flow responses with endocannabinoids, leptin, and inflammation |
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