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ORIGINAL ARTICLE

Metabolic syndrome and cardiometabolic risk: An update

, , , , &
Pages 7-16 | Received 14 Oct 2008, Published online: 08 Jul 2009

Figures & data

Figure 1. Prevalence of the metabolic syndrome in the PAMELA population, accordingly to the subjects' gender and age decades. Data from ref. Citation[23].

Figure 1. Prevalence of the metabolic syndrome in the PAMELA population, accordingly to the subjects' gender and age decades. Data from ref. Citation[23].

Figure 2. Prevalence of the various compounds of the metabolic syndrome in the PAMELA population. BP, Blood pressure; TG, Triglycerides; IFG, Impaired fasting glucose. ↑: Increase. Data from ref. Citation[23].

Figure 2. Prevalence of the various compounds of the metabolic syndrome in the PAMELA population. BP, Blood pressure; TG, Triglycerides; IFG, Impaired fasting glucose. ↑: Increase. Data from ref. Citation[23].

Figure 3. Kaplan‐Meier survival curves for cardiovascular death and all‐cause death in subjects without (MS–) and with (MS+) metabolic syndrome. p‐values refer to the statistical difference between the two curves. Modified from ref. Citation[23].

Figure 3. Kaplan‐Meier survival curves for cardiovascular death and all‐cause death in subjects without (MS–) and with (MS+) metabolic syndrome. p‐values refer to the statistical difference between the two curves. Modified from ref. Citation[23].

Table I. Intermediate (surrogate) endpoints of prognostic relevance in hypertension and in metabolic syndrome.

Figure 4. Prevalence (%) of left ventricular hypertrophy (LVH) in the subjects of the PAMELA study without (blue bars) and with (grey bars) metabolic syndrome in the whole population samples and in males and females, after exclusion of hypertensive patients or adjustment for 24‐h systolic blood pressure values and in different age decades. Asterisks (*p,0.05) refer to the statistical significance between groups. Data are shown as mean ± SEM. Modified from ref. Citation[23].

Figure 4. Prevalence (%) of left ventricular hypertrophy (LVH) in the subjects of the PAMELA study without (blue bars) and with (grey bars) metabolic syndrome in the whole population samples and in males and females, after exclusion of hypertensive patients or adjustment for 24‐h systolic blood pressure values and in different age decades. Asterisks (*p,0.05) refer to the statistical significance between groups. Data are shown as mean ± SEM. Modified from ref. Citation[23].

Figure 5. Left ventricular mass index (LVMI) and prevalence of left ventricular hypertrophy (LVH) in the subjects of the PAMELA study with metabolic syndrome examined in 1991–1992 and reassessed 10 years later. Data are shown as absolute (LVMI) or percentage (LVH) mean values. Data from ref. Citation[40].

Figure 5. Left ventricular mass index (LVMI) and prevalence of left ventricular hypertrophy (LVH) in the subjects of the PAMELA study with metabolic syndrome examined in 1991–1992 and reassessed 10 years later. Data are shown as absolute (LVMI) or percentage (LVH) mean values. Data from ref. Citation[40].

Figure 6. Values of muscle sympathetic nerve activity (MSNA) in obesity. Panel A, data in controls (C) and in obese (O) subjects; Panel B in visceral (CO) and peripheral (PO) overweight; Panel C, in the obese state (O+ HT); panel D, in the metabolic syndrome state (MS). Asterisks (*p<0.05, **p< 0.01) refer to the statistical significance between groups. Data from refs Citation[61–64].

Figure 6. Values of muscle sympathetic nerve activity (MSNA) in obesity. Panel A, data in controls (C) and in obese (O) subjects; Panel B in visceral (CO) and peripheral (PO) overweight; Panel C, in the obese state (O+ HT); panel D, in the metabolic syndrome state (MS). Asterisks (*p<0.05, **p< 0.01) refer to the statistical significance between groups. Data from refs Citation[61–64].

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