Obesity and body fat classification in the metabolic syndrome: impact on cardiometabolic risk metabotype

Obesity is a key factor in the development of the metabolic syndrome (MetS), which is associated with increased cardiometabolic risk. We investigated whether obesity classification by BMI and body fat percentage (BF%) influences cardiometabolic profile and dietary responsiveness in 486 MetS subjects...

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Veröffentlicht in:Obesity (Silver Spring, Md.) Md.), 2013-01, Vol.21 (1), p.E154
Hauptverfasser: Phillips, Catherine M, Tierney, Audrey C, Perez-Martinez, Pablo, Defoort, Catherine, Blaak, Ellen E, Gjelstad, Ingrid M F, Lopez-Miranda, Jose, Kiec-Klimczak, Malgorzata, Malczewska-Malec, Malgorzata, Drevon, Christian A, Hall, Wendy, Lovegrove, Julie A, Karlstrom, Brita, Risérus, Ulf, Roche, Helen M
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container_end_page
container_issue 1
container_start_page E154
container_title Obesity (Silver Spring, Md.)
container_volume 21
creator Phillips, Catherine M
Tierney, Audrey C
Perez-Martinez, Pablo
Defoort, Catherine
Blaak, Ellen E
Gjelstad, Ingrid M F
Lopez-Miranda, Jose
Kiec-Klimczak, Malgorzata
Malczewska-Malec, Malgorzata
Drevon, Christian A
Hall, Wendy
Lovegrove, Julie A
Karlstrom, Brita
Risérus, Ulf
Roche, Helen M
description Obesity is a key factor in the development of the metabolic syndrome (MetS), which is associated with increased cardiometabolic risk. We investigated whether obesity classification by BMI and body fat percentage (BF%) influences cardiometabolic profile and dietary responsiveness in 486 MetS subjects (LIPGENE dietary intervention study). Anthropometric measures, markers of inflammation and glucose metabolism, lipid profiles, adhesion molecules, and hemostatic factors were determined at baseline and after 12 weeks of four dietary interventions (high saturated fat (SFA), high monounsaturated fat (MUFA), and two low fat high complex carbohydrate (LFHCC) diets, one supplemented with long chain n-3 polyunsaturated fatty acids (LC n-3 PUFAs)). About 39 and 87% of subjects classified as normal and overweight by BMI were obese according to their BF%. Individuals classified as obese by BMI (≥ 30 kg/m(2)) and BF% (≥ 25% (men) and ≥ 35% (women)) (OO, n = 284) had larger waist and hip measurements, higher BMI and were heavier (P < 0.001) than those classified as nonobese by BMI but obese by BF% (NOO, n = 92). OO individuals displayed a more proinflammatory (higher C reactive protein (CRP) and leptin), prothrombotic (higher plasminogen activator inhibitor-1 (PAI-1)), proatherogenic (higher leptin/adiponectin ratio) and more insulin resistant (higher HOMA-IR) metabolic profile relative to the NOO group (P < 0.001). Interestingly, tumor necrosis factor-α (TNF-α) concentrations were lower post-intervention in NOO individuals compared with OO subjects (P < 0.001). In conclusion, assessing BF% and BMI as part of a metabotype may help to identify individuals at greater cardiometabolic risk than BMI alone.
doi_str_mv 10.1002/oby.20263
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We investigated whether obesity classification by BMI and body fat percentage (BF%) influences cardiometabolic profile and dietary responsiveness in 486 MetS subjects (LIPGENE dietary intervention study). Anthropometric measures, markers of inflammation and glucose metabolism, lipid profiles, adhesion molecules, and hemostatic factors were determined at baseline and after 12 weeks of four dietary interventions (high saturated fat (SFA), high monounsaturated fat (MUFA), and two low fat high complex carbohydrate (LFHCC) diets, one supplemented with long chain n-3 polyunsaturated fatty acids (LC n-3 PUFAs)). About 39 and 87% of subjects classified as normal and overweight by BMI were obese according to their BF%. Individuals classified as obese by BMI (≥ 30 kg/m(2)) and BF% (≥ 25% (men) and ≥ 35% (women)) (OO, n = 284) had larger waist and hip measurements, higher BMI and were heavier (P &lt; 0.001) than those classified as nonobese by BMI but obese by BF% (NOO, n = 92). OO individuals displayed a more proinflammatory (higher C reactive protein (CRP) and leptin), prothrombotic (higher plasminogen activator inhibitor-1 (PAI-1)), proatherogenic (higher leptin/adiponectin ratio) and more insulin resistant (higher HOMA-IR) metabolic profile relative to the NOO group (P &lt; 0.001). Interestingly, tumor necrosis factor-α (TNF-α) concentrations were lower post-intervention in NOO individuals compared with OO subjects (P &lt; 0.001). 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OO individuals displayed a more proinflammatory (higher C reactive protein (CRP) and leptin), prothrombotic (higher plasminogen activator inhibitor-1 (PAI-1)), proatherogenic (higher leptin/adiponectin ratio) and more insulin resistant (higher HOMA-IR) metabolic profile relative to the NOO group (P &lt; 0.001). Interestingly, tumor necrosis factor-α (TNF-α) concentrations were lower post-intervention in NOO individuals compared with OO subjects (P &lt; 0.001). In conclusion, assessing BF% and BMI as part of a metabotype may help to identify individuals at greater cardiometabolic risk than BMI alone.</abstract><cop>United States</cop><pmid>23505198</pmid><doi>10.1002/oby.20263</doi></addata></record>
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source MEDLINE; Wiley Online Library Free Content; Wiley Online Library All Journals
subjects Adiponectin - blood
Adipose Tissue
Body Composition
Body Mass Index
C-Reactive Protein - metabolism
Cardiovascular Diseases - blood
Cardiovascular Diseases - etiology
Diet Therapy
Female
Humans
Insulin Resistance
Leptin - blood
Male
Metabolic Syndrome - blood
Metabolic Syndrome - complications
Middle Aged
Obesity - blood
Obesity - complications
Obesity - diagnosis
Overweight
Plasminogen Activator Inhibitor 1 - blood
Reference Values
Risk Factors
Tumor Necrosis Factor-alpha - blood
title Obesity and body fat classification in the metabolic syndrome: impact on cardiometabolic risk metabotype
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