The metabolic syndrome defined by modified International Diabetes Federation criteria and mortality: A 9-year follow-up of the aged in Finland
Abstract Aim The aim of this study was to investigate the relationship between the metabolic syndrome (MetS) and mortality in the aged population. Methods In this prospective population-based study with a 9-year follow-up, the participants were all residents of the municipality of Lieto, Finland, ag...
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description | Abstract Aim The aim of this study was to investigate the relationship between the metabolic syndrome (MetS) and mortality in the aged population. Methods In this prospective population-based study with a 9-year follow-up, the participants were all residents of the municipality of Lieto, Finland, aged 64 and over in 1998–99 ( n = 1529). Altogether, 1260 (82%) were included in the study. Cox proportional-hazard models were used to estimate hazard ratios (HRs) for all-cause, cardiovascular (CVD), coronary heart disease (CHD) and cerebrovascular (CV) mortality as predicted by MetS (defined by modified International Diabetes Federation criteria). Results At baseline, 17% of the men and 21% of the women had MetS. During the 9-year follow-up, 422 deaths occurred. After multivariable adjustment, no significant differences were found between subjects with and without MetS for all-cause, CVD, CHD or CV mortality in all study participants or by gender. On evaluating MetS components separately, elevated blood pressure was found to predict lower all-cause mortality in all participants [HR: 0.65; 95% confidence interval (CI): 0.47–0.89], and lower CHD mortality in men (HR: 0.42; 95% CI: 0.18–0.97). In women, high triglyceride levels predicted lower all-cause mortality (HR: 0.67; 95% CI: 0.47–0.95), whereas low HDL cholesterol predicted higher all-cause (HR: 1.61; 95% CI: 1.15–2.24) and CV (HR: 2.44; 95% CI: 1.05–5.67) mortality. Conclusion These findings suggest that MetS does not predict mortality later in life and, of the separate components of MetS, only low HDL cholesterol is predictive of mortality in women. Also, even markedly higher blood pressure values than those included in the criteria for MetS fail to predict mortality in this age group. |
doi_str_mv | 10.1016/j.diabet.2010.05.002 |
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Methods In this prospective population-based study with a 9-year follow-up, the participants were all residents of the municipality of Lieto, Finland, aged 64 and over in 1998–99 ( n = 1529). Altogether, 1260 (82%) were included in the study. Cox proportional-hazard models were used to estimate hazard ratios (HRs) for all-cause, cardiovascular (CVD), coronary heart disease (CHD) and cerebrovascular (CV) mortality as predicted by MetS (defined by modified International Diabetes Federation criteria). Results At baseline, 17% of the men and 21% of the women had MetS. During the 9-year follow-up, 422 deaths occurred. After multivariable adjustment, no significant differences were found between subjects with and without MetS for all-cause, CVD, CHD or CV mortality in all study participants or by gender. On evaluating MetS components separately, elevated blood pressure was found to predict lower all-cause mortality in all participants [HR: 0.65; 95% confidence interval (CI): 0.47–0.89], and lower CHD mortality in men (HR: 0.42; 95% CI: 0.18–0.97). In women, high triglyceride levels predicted lower all-cause mortality (HR: 0.67; 95% CI: 0.47–0.95), whereas low HDL cholesterol predicted higher all-cause (HR: 1.61; 95% CI: 1.15–2.24) and CV (HR: 2.44; 95% CI: 1.05–5.67) mortality. Conclusion These findings suggest that MetS does not predict mortality later in life and, of the separate components of MetS, only low HDL cholesterol is predictive of mortality in women. Also, even markedly higher blood pressure values than those included in the criteria for MetS fail to predict mortality in this age group.</description><identifier>ISSN: 1262-3636</identifier><identifier>EISSN: 1878-1780</identifier><identifier>DOI: 10.1016/j.diabet.2010.05.002</identifier><identifier>PMID: 20708423</identifier><language>eng</language><publisher>Paris: Elsevier Masson SAS</publisher><subject>Aged ; Aged, 80 and over ; Biological and medical sciences ; Body Mass Index ; Cardiovascular Diseases - mortality ; Cerebrovascular Disorders - mortality ; Coronary Disease - mortality ; Diabetes. Impaired glucose tolerance ; Elderly ; Endocrine pancreas. Apud cells (diseases) ; Endocrinology & Metabolism ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Female ; Finland ; Finlande ; Humans ; Internal Medicine ; Longitudinal Studies ; Male ; Medical sciences ; Metabolic diseases ; Metabolic syndrome ; Metabolic Syndrome - diagnosis ; Metabolic Syndrome - epidemiology ; Metabolic Syndrome - mortality ; Metabolic Syndrome - physiopathology ; Middle Aged ; Miscellaneous ; Mortality ; Mortalité ; Other metabolic disorders ; Personnes âgées ; Population-based study ; Practice Guidelines as Topic ; Prevalence ; Prognosis ; Proportional Hazards Models ; Risk Factors ; Societies, Medical ; Syndrome métabolique ; Valeur pronostique ; Étude en population</subject><ispartof>Diabetes & metabolism, 2010-12, Vol.36 (6), p.437-442</ispartof><rights>Elsevier Masson SAS</rights><rights>2010 Elsevier Masson SAS</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier Masson SAS. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-832f460ed0ced4be0a04a48d0a61cb4d1789fb790e3919ba2a85d558f7fd6f2c3</citedby><cites>FETCH-LOGICAL-c376t-832f460ed0ced4be0a04a48d0a61cb4d1789fb790e3919ba2a85d558f7fd6f2c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.diabet.2010.05.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23650819$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20708423$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Salminen, M</creatorcontrib><creatorcontrib>Kuoppamäki, M</creatorcontrib><creatorcontrib>Vahlberg, T</creatorcontrib><creatorcontrib>Räihä, I</creatorcontrib><creatorcontrib>Irjala, K</creatorcontrib><creatorcontrib>Kivelä, S.L</creatorcontrib><title>The metabolic syndrome defined by modified International Diabetes Federation criteria and mortality: A 9-year follow-up of the aged in Finland</title><title>Diabetes & metabolism</title><addtitle>Diabetes Metab</addtitle><description>Abstract Aim The aim of this study was to investigate the relationship between the metabolic syndrome (MetS) and mortality in the aged population. Methods In this prospective population-based study with a 9-year follow-up, the participants were all residents of the municipality of Lieto, Finland, aged 64 and over in 1998–99 ( n = 1529). Altogether, 1260 (82%) were included in the study. Cox proportional-hazard models were used to estimate hazard ratios (HRs) for all-cause, cardiovascular (CVD), coronary heart disease (CHD) and cerebrovascular (CV) mortality as predicted by MetS (defined by modified International Diabetes Federation criteria). Results At baseline, 17% of the men and 21% of the women had MetS. During the 9-year follow-up, 422 deaths occurred. After multivariable adjustment, no significant differences were found between subjects with and without MetS for all-cause, CVD, CHD or CV mortality in all study participants or by gender. On evaluating MetS components separately, elevated blood pressure was found to predict lower all-cause mortality in all participants [HR: 0.65; 95% confidence interval (CI): 0.47–0.89], and lower CHD mortality in men (HR: 0.42; 95% CI: 0.18–0.97). In women, high triglyceride levels predicted lower all-cause mortality (HR: 0.67; 95% CI: 0.47–0.95), whereas low HDL cholesterol predicted higher all-cause (HR: 1.61; 95% CI: 1.15–2.24) and CV (HR: 2.44; 95% CI: 1.05–5.67) mortality. Conclusion These findings suggest that MetS does not predict mortality later in life and, of the separate components of MetS, only low HDL cholesterol is predictive of mortality in women. Also, even markedly higher blood pressure values than those included in the criteria for MetS fail to predict mortality in this age group.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Body Mass Index</subject><subject>Cardiovascular Diseases - mortality</subject><subject>Cerebrovascular Disorders - mortality</subject><subject>Coronary Disease - mortality</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Elderly</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinology & Metabolism</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>Finland</subject><subject>Finlande</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Metabolic syndrome</subject><subject>Metabolic Syndrome - diagnosis</subject><subject>Metabolic Syndrome - epidemiology</subject><subject>Metabolic Syndrome - mortality</subject><subject>Metabolic Syndrome - physiopathology</subject><subject>Middle Aged</subject><subject>Miscellaneous</subject><subject>Mortality</subject><subject>Mortalité</subject><subject>Other metabolic disorders</subject><subject>Personnes âgées</subject><subject>Population-based study</subject><subject>Practice Guidelines as Topic</subject><subject>Prevalence</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Risk Factors</subject><subject>Societies, Medical</subject><subject>Syndrome métabolique</subject><subject>Valeur pronostique</subject><subject>Étude en population</subject><issn>1262-3636</issn><issn>1878-1780</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksuKFDEUhgtRnHH0DUSyEVfVnqRuKRfCMNo6MODCcR1SyYmmTSVtklLqJXxm09OtghtXOYTvP7f_VNVTChsKtH-522grJ8wbBuULug0Au1edUz7wmg4c7peY9axu-qY_qx6ltAOgbGz4w-qMwQC8Zc159fP2C5IZs5yCs4qk1esYZiQajfWoybSSOWhrbImvfcboZbbBS0fe3FXHRLaoMd79EhVtQawk0uuii1k6m9dX5JKM9YoyEhOcCz_qZU-CIbmUlp9LYuvJ1npXRI-rB0a6hE9O70X1afv29up9ffPh3fXV5U2tmqHPNW-YaXtADQp1OyFIaGXLNcieqqnVZf7RTMMI2Ix0nCSTvNNdx81gdG-Yai6qF8e8-xi-LZiymG1S6EoPGJYkOKPdyHk7FLI9kiqGlCIasY92lnEVFMTBCLETRyPEwQgBnShGFNmzU4FlmlH_Ef3efAGenwCZlHQmSq9s-ss1fQecjoV7feSwrOO7xSiSsujL3DaiykIH-79O_k2gnPW21PyKK6ZdWIqnLgkqEhMgPh6O5nAzFMq9tKxtfgFXiL63</recordid><startdate>20101201</startdate><enddate>20101201</enddate><creator>Salminen, M</creator><creator>Kuoppamäki, M</creator><creator>Vahlberg, T</creator><creator>Räihä, I</creator><creator>Irjala, K</creator><creator>Kivelä, S.L</creator><general>Elsevier Masson SAS</general><general>Masson</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>20101201</creationdate><title>The metabolic syndrome defined by modified International Diabetes Federation criteria and mortality: A 9-year follow-up of the aged in Finland</title><author>Salminen, M ; Kuoppamäki, M ; Vahlberg, T ; Räihä, I ; Irjala, K ; Kivelä, S.L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-832f460ed0ced4be0a04a48d0a61cb4d1789fb790e3919ba2a85d558f7fd6f2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Body Mass Index</topic><topic>Cardiovascular Diseases - mortality</topic><topic>Cerebrovascular Disorders - mortality</topic><topic>Coronary Disease - mortality</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Elderly</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinology & Metabolism</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>Finland</topic><topic>Finlande</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Metabolic syndrome</topic><topic>Metabolic Syndrome - diagnosis</topic><topic>Metabolic Syndrome - epidemiology</topic><topic>Metabolic Syndrome - mortality</topic><topic>Metabolic Syndrome - physiopathology</topic><topic>Middle Aged</topic><topic>Miscellaneous</topic><topic>Mortality</topic><topic>Mortalité</topic><topic>Other metabolic disorders</topic><topic>Personnes âgées</topic><topic>Population-based study</topic><topic>Practice Guidelines as Topic</topic><topic>Prevalence</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Risk Factors</topic><topic>Societies, Medical</topic><topic>Syndrome métabolique</topic><topic>Valeur pronostique</topic><topic>Étude en population</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salminen, M</creatorcontrib><creatorcontrib>Kuoppamäki, M</creatorcontrib><creatorcontrib>Vahlberg, T</creatorcontrib><creatorcontrib>Räihä, I</creatorcontrib><creatorcontrib>Irjala, K</creatorcontrib><creatorcontrib>Kivelä, S.L</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>Diabetes & metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salminen, M</au><au>Kuoppamäki, M</au><au>Vahlberg, T</au><au>Räihä, I</au><au>Irjala, K</au><au>Kivelä, S.L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The metabolic syndrome defined by modified International Diabetes Federation criteria and mortality: A 9-year follow-up of the aged in Finland</atitle><jtitle>Diabetes & metabolism</jtitle><addtitle>Diabetes Metab</addtitle><date>2010-12-01</date><risdate>2010</risdate><volume>36</volume><issue>6</issue><spage>437</spage><epage>442</epage><pages>437-442</pages><issn>1262-3636</issn><eissn>1878-1780</eissn><abstract>Abstract Aim The aim of this study was to investigate the relationship between the metabolic syndrome (MetS) and mortality in the aged population. Methods In this prospective population-based study with a 9-year follow-up, the participants were all residents of the municipality of Lieto, Finland, aged 64 and over in 1998–99 ( n = 1529). Altogether, 1260 (82%) were included in the study. Cox proportional-hazard models were used to estimate hazard ratios (HRs) for all-cause, cardiovascular (CVD), coronary heart disease (CHD) and cerebrovascular (CV) mortality as predicted by MetS (defined by modified International Diabetes Federation criteria). Results At baseline, 17% of the men and 21% of the women had MetS. During the 9-year follow-up, 422 deaths occurred. After multivariable adjustment, no significant differences were found between subjects with and without MetS for all-cause, CVD, CHD or CV mortality in all study participants or by gender. On evaluating MetS components separately, elevated blood pressure was found to predict lower all-cause mortality in all participants [HR: 0.65; 95% confidence interval (CI): 0.47–0.89], and lower CHD mortality in men (HR: 0.42; 95% CI: 0.18–0.97). In women, high triglyceride levels predicted lower all-cause mortality (HR: 0.67; 95% CI: 0.47–0.95), whereas low HDL cholesterol predicted higher all-cause (HR: 1.61; 95% CI: 1.15–2.24) and CV (HR: 2.44; 95% CI: 1.05–5.67) mortality. Conclusion These findings suggest that MetS does not predict mortality later in life and, of the separate components of MetS, only low HDL cholesterol is predictive of mortality in women. Also, even markedly higher blood pressure values than those included in the criteria for MetS fail to predict mortality in this age group.</abstract><cop>Paris</cop><pub>Elsevier Masson SAS</pub><pmid>20708423</pmid><doi>10.1016/j.diabet.2010.05.002</doi><tpages>6</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Biological and medical sciences Body Mass Index Cardiovascular Diseases - mortality Cerebrovascular Disorders - mortality Coronary Disease - mortality Diabetes. Impaired glucose tolerance Elderly Endocrine pancreas. Apud cells (diseases) Endocrinology & Metabolism Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Female Finland Finlande Humans Internal Medicine Longitudinal Studies Male Medical sciences Metabolic diseases Metabolic syndrome Metabolic Syndrome - diagnosis Metabolic Syndrome - epidemiology Metabolic Syndrome - mortality Metabolic Syndrome - physiopathology Middle Aged Miscellaneous Mortality Mortalité Other metabolic disorders Personnes âgées Population-based study Practice Guidelines as Topic Prevalence Prognosis Proportional Hazards Models Risk Factors Societies, Medical Syndrome métabolique Valeur pronostique Étude en population |
title | The metabolic syndrome defined by modified International Diabetes Federation criteria and mortality: A 9-year follow-up of the aged in Finland |
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