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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">The metabolic syndrome &#40;MetS&#41; is a constellation of metabolic risk factors closely linked to insulin resistance&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> At present&#44; various definitions for MetS are used&#46; According to the criteria described by of the Adults Treatment Panel III recently revised by the American Heart Association&#47;National Heart&#44; Lung&#44; and Blood Institute &#40;rATP III-MetS&#41;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> the MetS is defined as an alteration in three or more of the following features&#58; abdominal obesity &#40;waist circumference &#62;102<span class="elsevierStyleHsp" style=""></span>cm in men&#59; &#62;88<span class="elsevierStyleHsp" style=""></span>cm in women&#41;&#44; elevated blood pressure &#40;&#62;130<span class="elsevierStyleHsp" style=""></span>mmHg systolic or &#62;85<span class="elsevierStyleHsp" style=""></span>mmHg diastolic&#44; and&#47;or use of antihypertensive agents&#41;&#44; hypertriglyceridemia &#40;&#62;150<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41;&#44; low levels of serum HDLc &#40;&#60;40<span class="elsevierStyleHsp" style=""></span>mg&#47;dL in men&#44; &#60;50<span class="elsevierStyleHsp" style=""></span>mg&#47;dL in women&#41;&#44; and high fasting glucose &#40;&#62;100<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; and&#47;or use of glucose-lowering agents&#41;&#46; Using International Diabetes Federation &#40;IDF&#41; criteria&#44;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> MetS was diagnosed in patients who had a waist circumference &#62;94<span class="elsevierStyleHsp" style=""></span>cm in men and &#62;80<span class="elsevierStyleHsp" style=""></span>cm in women&#44; plus two or more of the following&#58; elevated blood pressure&#44; hypertriglyceridemia&#44; low HDLc levels&#44; and high fasting glucose&#44; each defined by the same criteria used for the rATP III definition&#46; Diabetes mellitus was defined as fasting plasma glucose &#62;126<span class="elsevierStyleHsp" style=""></span>mg&#47;dL or use of glucose-lowering agents&#46; MetS is a very common clinical condition in Western countries&#58; in the last decade&#44; the prevalence of MetS has increased in the United States<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> and elsewhere&#46; In people &#62;20 years old it is 24&#37; and it rises to &#62;40&#37; in patients &#8805;60 years of age&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> Several studies evaluated the presence of the Mets in different populations&#46; However&#44; the use of different diagnostic criteria for the Mets is&#44; at least in part&#44; the reasons for differences in prevalence rate&#44; hindering meaningful comparisons between populations&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a> In a study by Trevisan et al&#46;&#44; in patients aged 50 years or above&#44; women showed a higher prevalence than men&#44;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> although the prevalence of the Mets was not influenced by age&#46; The pathogenesis of the syndrome has multiple origins&#44; but obesity and sedentary lifestyle coupled with diet and still largely unknown genetic factors clearly interact and may determine the syndrome&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> The combination of risk factors comprising the Mets interacts synergistically causing or accelerating the progression of atherosclerosis&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Several clinical studies recognized MetS as a cause responsible for the endothelial dysfunction&#44; which represents the first &#8220;step&#8221; in atherothrombotic disease and&#44; in addition&#44; observed an association between increased carotid intima-media thickness &#40;IMT&#41; and MetS&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10&#44;11</span></a> Therefore&#44; patients with Mets have a higher risk of developing cardiovascular morbidity and mortality than subjects without the syndrome &#40;12&#46;0&#37; versus 2&#46;2&#37;&#41;&#58; a two- to three-fold increased risk of coronary heart disease &#40;CHD&#41; and stroke and cardiovascular mortality has been reported in literature&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;6&#44;8&#44;12</span></a> A prospective study published by Novo et al&#46; showed that in the subgroup of patients with MetS&#44; the prevalence of subclinical atherosclerosis&#44; defined as increased IMT &#40;common carotid IMT<span class="elsevierStyleHsp" style=""></span>&#62;<span class="elsevierStyleHsp" style=""></span>0&#46;90<span class="elsevierStyleHsp" style=""></span>mm&#41; with or without atherosclerotic plaque&#44; was significantly higher than in participants without MetS and defined this Syndrome as a CV risk factor&#58; participants with MetS had a significantly higher prevalence of vascular disease in a 20- year follow-up &#40;49&#37;&#41; than participants without MetS &#40;29&#37;&#41; &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;01&#41;&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">9&#44;13</span></a> Conversely&#44; little is known about the predictive role of MetS in peripheral arterial disease &#40;PAD&#41;&#44; which affecting about 27 million people in Europe and the United States&#46; Brevetti et al&#46; found that more than 50&#37; of PAD patients met the criteria for rATP III-MetS&#46; Nevertheless&#44; the results show that IDF-MEtS&#44; but not rATPIII-MetS&#44; is an independent predictor of cardiovascular events&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">14</span></a> In a study by Gorter et al&#46; has emerged that the metabolic syndrome&#44; according to the ATP III criteria&#44; is highly prevalent in patients with a recent diagnose of a clinical manifestation of atherosclerosis &#40;46&#37;&#41;&#44; especially in PAD patients &#40;58&#37;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> A more recent study revealed that patients with occlusive or aneurysmatic PAD have a high prevalence of metabolic syndrome and that in both groups of patients the presence of metabolic syndrome was independently associated with an increased risk for the occurrence of CV events during long-term follow-up but no with an incremental risk for CV mortality&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> The Mets is a common comorbidity in claudicants and must be actively searched because the early diagnosis and treatment of MetS may influence PAD progression&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">17</span></a> There are few studies in literature which evaluated the association between MetS and PAD&#46; These studies demonstrated that the prevalence of MetS is higher in patients with PAD but their limits were that the patients often exhibited clinical manifestations of arteriosclerosis in other vascular territories&#46;<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">14&#8211;17</span></a> In this regard the objective of the <span class="elsevierStyleItalic">study presented in this issue of Rev Clin Esp b</span>y Estirado et al&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a> is to assess the prevalence of MetS in patients with PAD but without known atherosclerosis in other districts&#46; The authors demonstrated that the prevalence of MetS in PAD patients is high &#40;63&#37;&#41; and is independent of the evolution time of PAD&#46; According to our experience we are agree with Estirado et al&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a>&#59; we believe that PAD &#40;documented using ABI &#60;0&#46;9&#44; lower limb amputation due to chronic ischemia or prior revascularization in the lower limbs&#41;&#44; can be presented in MetS patients and that it is a validated marker of subclinical atherosclerosis and a predictor of CV events&#44; like an increased carotid IMT&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Considering the close association between MetS and GCVR &#40;global cardiovascular risk&#41;&#44; it is relevant to screen already high-risk patients for the MetS&#46; Instead of treating individual components of the metabolic syndrome&#44; treating the underlying pathophysiological disturbance &#40;for instance&#44; insulin resistance&#41; would ideally be the therapeutic option of first choice&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> It is also recommend preventing the development of MetS abnormalities &#40;for example with daily physical activity&#44; Mediterranean diet and early started pharmacological treatment of modifiable risk factors&#44; as suggested by many studies&#41;<a class="elsevierStyleCrossRefs" href="#bib0095"><span class="elsevierStyleSup">19&#44;20</span></a> and investigating the presence of subclinical atherosclerosis in all patients over 45 years&#44; by ultrasound test&#44; because in primary prevention&#44; the IMT measurement can give further information for a better stratification of GCVR&#46;<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">21</span></a></p></span>"
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Vol. 214. Núm. 8.
Páginas 455-456 (noviembre 2014)
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Vol. 214. Núm. 8.
Páginas 455-456 (noviembre 2014)
Editorial
Metabolic syndrome and peripheral arterial disease
Síndrome metabólico y enfermedad arterial periférica
Visitas
432
S. Novo
Autor para correspondencia
salvatore.novo@unipa.it

Corresponding author.
, C. Paleologo
Chair and Division of Cardiology, Department of Internal Medicine, Cardiovascular Disease and Nephro-Urological Disease, University Hospital “P. Giaccone” of Palermo, Palermo, Italy
Contenido relacionado
Rev Clin Esp. 2014;214:437-4410.1016/j.rce.2014.05.005
E. Estirado, C. Lahoz, F. Laguna, F. García-Iglesias, M.T. González-Alegre, J.M. Mostaza
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