Metabolic Syndrome: epidemiology and more extensive phenotypic description. Cross-sectional data from the Bruneck Study
OBJECTIVES: The present study aimed at evaluating the prevalence of the Metabolic Syndrome and at identifying its additional clinical features. RESEARCH DESIGN AND METHODS: Within a prospective population-based survey examining 888 subjects aged 40–79 y, subjects were identified fulfilling the WHO a...
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Published in | International Journal of Obesity Vol. 27; no. 10; pp. 1283 - 1289 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.10.2003
Nature Publishing Nature Publishing Group |
Subjects | |
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Abstract | OBJECTIVES:
The present study aimed at evaluating the prevalence of the Metabolic Syndrome and at identifying its additional clinical features.
RESEARCH DESIGN AND METHODS:
Within a prospective population-based survey examining 888 subjects aged 40–79 y, subjects were identified fulfilling the WHO and the National Cholesterol Education Program-Adult Treatment Panel III (NCEP-ATPIII) criteria for diagnosing the Metabolic Syndrome. In these subjects and in the rest of the sample (controls), several metabolic and nonmetabolic biochemical parameters were compared.
RESULTS:
The prevalence of the Metabolic Syndrome by WHO criteria was 34.1% (95% CI 31.0–37.2) and by NCEP-ATPIII criteria 17.8% (15.5–20.3). The prevalence was significantly higher in older subjects and in those less physically active. Subjects with the Metabolic Syndrome either by WHO or by NCEP-ATPIII criteria showed higher levels of oxidized low-density lipoprotein, apolipoprotein B, urate, leptin, fibrinogen, leukocytes, erythrocyte sedimentation rate, GOT, gamma-GT and soluble endothelial adhesion molecules (E-selectin, vascular adhesion molecule-1 and intercellular adhesion molecule-1) and lower apolipoprotein A concentrations. Insulin resistance, as assessed by the Homeostasis Model Assessment, increased with the increase in the number of traits composing the syndrome found within the single individual. Subjects with insulin resistance had more pronounced abnormalities in several parameters, including the additional features of the syndrome (eg fibrinogen and soluble adhesion molecules).
CONCLUSIONS:
The Metabolic Syndrome occurs very frequently in the general population aged 40–79 y, and is associated with several additional metabolic and nonmetabolic abnormalities that likely contribute to an increased cardiovascular risk. Insulin resistance seems to play a major role in classic and additional abnormalities featuring the Metabolic Syndrome. |
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AbstractList | OBJECTIVES: The present study aimed at evaluating the prevalence of the Metabolic Syndrome and at identifying its additional clinical features. RESEARCH DESIGN AND METHODS: Within a prospective population-based survey examining 888 subjects aged 40-79 y, subjects were identified fulfilling the WHO and the National Cholesterol Education Program-Adult Treatment Panel III (NCEP-ATPIII) criteria for diagnosing the Metabolic Syndrome. In these subjects and in the rest of the sample (controls), several metabolic and nonmetabolic biochemical parameters were compared. RESULTS: The prevalence of the Metabolic Syndrome by WHO criteria was 34.1% (95% CI 31.0-37.2) and by NCEP-ATPIII criteria 17.8% (15.5-20.3). The prevalence was significantly higher in older subjects and in those less physically active. Subjects with the Metabolic Syndrome either by WHO or by NCEP-ATPIII criteria showed higher levels of oxidized low-density lipoprotein, apolipoprotein B, urate, leptin, fibrinogen, leukocytes, erythrocyte sedimentation rate, GOT, gamma-GT and soluble endothelial adhesion molecules (E-selectin, vascular adhesion molecule-1 and intercellular adhesion molecule-1) and lower apolipoprotein A concentrations. Insulin resistance, as assessed by the Homeostasis Model Assessment, increased with the increase in the number of traits composing the syndrome found within the single individual. Subjects with insulin resistance had more pronounced abnormalities in several parameters, including the additional features of the syndrome (eg fibrinogen and soluble adhesion molecules). CONCLUSIONS: The Metabolic Syndrome occurs very frequently in the general population aged 40-79 y, and is associated with several additional metabolic and nonmetabolic abnormalities that likely contribute to an increased cardiovascular risk. Insulin resistance seems to play a major role in classic and additional abnormalities featuring the Metabolic Syndrome. OBJECTIVES: The present study aimed at evaluating the prevalence of the Metabolic Syndrome and at identifying its additional clinical features. RESEARCH DESIGN AND METHODS: Within a prospective population-based survey examining 888 subjects aged 40–79 y, subjects were identified fulfilling the WHO and the National Cholesterol Education Program-Adult Treatment Panel III (NCEP-ATPIII) criteria for diagnosing the Metabolic Syndrome. In these subjects and in the rest of the sample (controls), several metabolic and nonmetabolic biochemical parameters were compared. RESULTS: The prevalence of the Metabolic Syndrome by WHO criteria was 34.1% (95% CI 31.0–37.2) and by NCEP-ATPIII criteria 17.8% (15.5–20.3). The prevalence was significantly higher in older subjects and in those less physically active. Subjects with the Metabolic Syndrome either by WHO or by NCEP-ATPIII criteria showed higher levels of oxidized low-density lipoprotein, apolipoprotein B, urate, leptin, fibrinogen, leukocytes, erythrocyte sedimentation rate, GOT, gamma-GT and soluble endothelial adhesion molecules (E-selectin, vascular adhesion molecule-1 and intercellular adhesion molecule-1) and lower apolipoprotein A concentrations. Insulin resistance, as assessed by the Homeostasis Model Assessment, increased with the increase in the number of traits composing the syndrome found within the single individual. Subjects with insulin resistance had more pronounced abnormalities in several parameters, including the additional features of the syndrome (eg fibrinogen and soluble adhesion molecules). CONCLUSIONS: The Metabolic Syndrome occurs very frequently in the general population aged 40–79 y, and is associated with several additional metabolic and nonmetabolic abnormalities that likely contribute to an increased cardiovascular risk. Insulin resistance seems to play a major role in classic and additional abnormalities featuring the Metabolic Syndrome. The present study aimed at evaluating the prevalence of the Metabolic Syndrome and at identifying its additional clinical features. Within a prospective population-based survey examining 888 subjects aged 40-79 y, subjects were identified fulfilling the WHO and the National Cholesterol Education Program-Adult Treatment Panel III (NCEP-ATPIII) criteria for diagnosing the Metabolic Syndrome. In these subjects and in the rest of the sample (controls), several metabolic and nonmetabolic biochemical parameters were compared. The prevalence of the Metabolic Syndrome by WHO criteria was 34.1% (95% CI 31.0-37.2) and by NCEP-ATPIII criteria 17.8% (15.5-20.3). The prevalence was significantly higher in older subjects and in those less physically active. Subjects with the Metabolic Syndrome either by WHO or by NCEP-ATPIII criteria showed higher levels of oxidized low-density lipoprotein, apolipoprotein B, urate, leptin, fibrinogen, leukocytes, erythrocyte sedimentation rate, GOT, gamma-GT and soluble endothelial adhesion molecules (E-selectin, vascular adhesion molecule-1 and intercellular adhesion molecule-1) and lower apolipoprotein A concentrations. Insulin resistance, as assessed by the Homeostasis Model Assessment, increased with the increase in the number of traits composing the syndrome found within the single individual. Subjects with insulin resistance had more pronounced abnormalities in several parameters, including the additional features of the syndrome (eg fibrinogen and soluble adhesion molecules). The Metabolic Syndrome occurs very frequently in the general population aged 40-79 y, and is associated with several additional metabolic and nonmetabolic abnormalities that likely contribute to an increased cardiovascular risk. Insulin resistance seems to play a major role in classic and additional abnormalities featuring the Metabolic Syndrome. OBJECTIVES:: The present study aimed at evaluating the prevalence of the Metabolic Syndrome and at identifying its additional clinical features. RESEARCH DESIGN AND METHODS:: Within a prospective population-based survey examining 888 subjects aged 40-79 y, subjects were identified fulfilling the WHO and the National Cholesterol Education Program-Adult Treatment Panel III (NCEP-ATPIII) criteria for diagnosing the Metabolic Syndrome. In these subjects and in the rest of the sample (controls), several metabolic and nonmetabolic biochemical parameters were compared. RESULTS:: The prevalence of the Metabolic Syndrome by WHO criteria was 34.1% (95% CI 31.0-37.2) and by NCEP-ATPIII criteria 17.8% (15.5-20.3). The prevalence was significantly higher in older subjects and in those less physically active. Subjects with the Metabolic Syndrome either by WHO or by NCEP-ATPIII criteria showed higher levels of oxidized low-density lipoprotein, apolipoprotein B, urate, leptin, fibrinogen, leukocytes, erythrocyte sedimentation rate, GOT, gamma-GT and soluble endothelial adhesion molecules (E-selectin, vascular adhesion molecule-1 and intercellular adhesion molecule-1) and lower apolipoprotein A concentrations. Insulin resistance, as assessed by the Homeostasis Model Assessment, increased with the increase in the number of traits composing the syndrome found within the single individual. Subjects with insulin resistance had more pronounced abnormalities in several parameters, including the additional features of the syndrome (eg fibrinogen and soluble adhesion molecules). CONCLUSIONS:: The Metabolic Syndrome occurs very frequently in the general population aged 40-79 y, and is associated with several additional metabolic and nonmetabolic abnormalities that likely contribute to an increased cardiovascular risk. Insulin resistance seems to play a major role in classic and additional abnormalities featuring the Metabolic Syndrome.International Journal of Obesity (2003) 27, 1283-1289. doi:10.1038/sj.ijo.0802381 |
Audience | Academic |
Author | Muggeo, M Bonora, E Willeit, J Kiechl, S Egger, G Oberhollenzer, F Bonadonna, R C |
Author_xml | – sequence: 1 givenname: E surname: Bonora fullname: Bonora, E email: enzobonora@virgilio.it organization: Division of Endocrinology and Metabolic Diseases, University of Verona Medical School – sequence: 2 givenname: S surname: Kiechl fullname: Kiechl, S organization: Department of Neurology, University of Innsbruck Medical School – sequence: 3 givenname: J surname: Willeit fullname: Willeit, J organization: Department of Neurology, University of Innsbruck Medical School – sequence: 4 givenname: F surname: Oberhollenzer fullname: Oberhollenzer, F organization: Department of Internal Medicine, City Hospital of Bruneck – sequence: 5 givenname: G surname: Egger fullname: Egger, G organization: Department of Internal Medicine, City Hospital of Bruneck – sequence: 6 givenname: R C surname: Bonadonna fullname: Bonadonna, R C organization: Division of Endocrinology and Metabolic Diseases, University of Verona Medical School – sequence: 7 givenname: M surname: Muggeo fullname: Muggeo, M organization: Division of Endocrinology and Metabolic Diseases, University of Verona Medical School |
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Keywords | insulin resistance Metabolic Syndrome cardiovascular risk Endocrinopathy Human Obesity Nutrition disorder Metabolic diseases Cardiovascular disease Coronary heart disease Epidemiology Target tissue resistance Phenotype X Syndrome Nutritional status |
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PublicationPlace_xml | – name: London – name: Basingstoke – name: England – name: Hampshire |
PublicationTitle | International Journal of Obesity |
PublicationTitleAbbrev | Int J Obes |
PublicationTitleAlternate | Int J Obes Relat Metab Disord |
PublicationYear | 2003 |
Publisher | Nature Publishing Group UK Nature Publishing Nature Publishing Group |
Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing – name: Nature Publishing Group |
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The present study aimed at evaluating the prevalence of the Metabolic Syndrome and at identifying its additional clinical features.
RESEARCH DESIGN... The present study aimed at evaluating the prevalence of the Metabolic Syndrome and at identifying its additional clinical features. Within a prospective... OBJECTIVES:: The present study aimed at evaluating the prevalence of the Metabolic Syndrome and at identifying its additional clinical features. RESEARCH... OBJECTIVES: The present study aimed at evaluating the prevalence of the Metabolic Syndrome and at identifying its additional clinical features. RESEARCH DESIGN... |
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SubjectTerms | Adhesion Adult Age Distribution Aged apolipoprotein B Apolipoproteins Biological and medical sciences Body mass index Cardiology. Vascular system Cardiovascular diseases cholesterol Complications and side effects Coronary heart disease Cross-Sectional Studies Diagnosis education Epidemiology erythrocyte sedimentation rate Exercise Female fibrinogen Health Promotion and Disease Prevention Health risks Heart homeostasis Humans Insulin resistance Insulin Resistance - physiology Internal Medicine Italy Italy - epidemiology leptin leukocytes low density lipoprotein Male Medical sciences Medicine Medicine & Public Health Metabolic Diseases Metabolic disorders Metabolic syndrome Metabolic Syndrome - epidemiology Metabolic Syndrome - metabolism Metabolic syndrome X metabolism Middle Aged Miscellaneous Obesity Other metabolic disorders Phenotype Physical Exertion physiology Prevalence Prospective Studies Public Health Research design risk Risk Factors Sex Distribution Smoking Socioeconomic factors surveys World Health Organization |
Title | Metabolic Syndrome: epidemiology and more extensive phenotypic description. Cross-sectional data from the Bruneck Study |
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