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      Novel Risk Factors for Premature Peripheral Arterial Occlusive Disease in Non-Diabetic Patients: A Case-Control Study

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          Abstract

          Background

          This study aimed to determine the prevalence of genetic and environmental vascular risk factors in non diabetic patients with premature peripheral arterial disease, either peripheral arterial occlusive disease or thromboangiitis obliterans, the two main entities of peripheral arterial disease, and to established whether some of them are specifically associated with one or another of the premature peripheral arterial disease subgroups.

          Methods and Results

          This study included 113 non diabetic patients with premature peripheral arterial disease (diagnosis <45-year old) presenting either a peripheral arterial occlusive disease (N = 64) or a thromboangiitis obliterans (N = 49), and 241 controls matched for age and gender. Both patient groups demonstrated common traits including cigarette smoking, low physical activity, decreased levels of HDL-cholesterol, apolipoprotein A–I, pyridoxal 5′-phosphate (active form of B6 vitamin) and zinc. Premature peripheral arterial occlusive disease was characterized by the presence of a family history of peripheral arterial and carotid artery diseases (OR 2.3 and 5.8 respectively, 95% CI), high lipoprotein (a) levels above 300 mg/L (OR 2.3, 95% CI), the presence of the factor V Leiden (OR 5.1, 95% CI) and the glycoprotein Ia 807T,837T,873A allele (OR 2.3, 95% CI). In thromboangiitis obliterans group, more patients were regular consumers of cannabis (OR 3.5, 95% CI) and higher levels in plasma copper has been shown (OR 6.5, 95% CI).

          Conclusions

          According to our results from a non exhaustive list of study parameters, we might hypothesize for 1) a genetic basis for premature peripheral arterial occlusive disease development and 2) the prevalence of environmental factors in the development of thromboangiitis obliterans (tobacco and cannabis). Moreover, for the first time, we demonstrated that the 807T/837T/873A allele of platelet glycoprotein Ia may confer an additional risk for development of peripheral atherosclerosis in premature peripheral arterial occlusive disease.

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          Most cited references30

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          Mortality over a period of 10 years in patients with peripheral arterial disease.

          Previous investigators have observed a doubling of the mortality rate among patients with intermittent claudication, and we have reported a fourfold increase in the overall mortality rate among subjects with large-vessel peripheral arterial disease, as diagnosed by noninvasive testing. In this study, we investigated the association of large-vessel peripheral arterial disease with rates of mortality from all cardiovascular diseases and from coronary heart disease. We examined 565 men and women (average age, 66 years) for the presence of large-vessel peripheral arterial disease by means of two noninvasive techniques--measurement of segmental blood pressure and determination of flow velocity by Doppler ultrasound. We identified 67 subjects with the disease (11.9 percent), whom we followed prospectively for 10 years. Twenty-one of the 34 men (61.8 percent) and 11 of the 33 women (33.3 percent) with large-vessel peripheral arterial disease died during follow-up, as compared with 31 of the 183 men (16.9 percent) and 26 of the 225 women (11.6 percent) without evidence of peripheral arterial disease. After multivariate adjustment for age, sex, and other risk factors for cardiovascular disease, the relative risk of dying among subjects with large-vessel peripheral arterial disease as compared with those with no evidence of such disease was 3.1 (95 percent confidence interval, 1.9 to 4.9) for deaths from all causes, 5.9 (95 percent confidence interval, 3.0 to 11.4) for all deaths from cardiovascular disease, and 6.6 (95 percent confidence interval, 2.9 to 14.9) for deaths from coronary heart disease. The relative risk of death from causes other than cardiovascular disease was not significantly increased among the subjects with large-vessel peripheral arterial disease. After the exclusion of subjects who had a history of cardiovascular disease at base line, the relative risks among those with large-vessel peripheral arterial disease remained significantly elevated. Additional analyses revealed a 15-fold increase in rates of mortality due to cardiovascular disease and coronary heart disease among subjects with large-vessel peripheral arterial disease that was both severe and symptomatic. Patients with large-vessel peripheral arterial disease have a high risk of death from cardiovascular causes.
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            Cigarette smoking and serum lipid and lipoprotein concentrations: an analysis of published data.

            To examine the association between cigarette smoking in adults and serum lipid and lipoprotein concentrations the results of 54 published studies were analysed. Overall, smokers had significantly higher serum concentrations of cholesterol (3.0%), triglycerides (9.1%), very low density lipoprotein cholesterol (10.4%), and low density lipoprotein cholesterol (1.7%) and lower serum concentrations of high density lipoprotein cholesterol (-5.7%) and apolipoprotein AI (-4.2%) compared with nonsmokers. Among non-smokers and light, moderate, and heavy smokers a significant dose response effect was present for cholesterol (0, 1.8, 4.3, and 4.5% respectively), triglycerides (0, 10.7, 11.5, and 18.0%), very low density lipoprotein cholesterol (0, 7.2, 44.4, and 39.0%), low density lipoprotein cholesterol (0, -1.1, 1.4, and 11.0%), high density lipoprotein cholesterol (0, -4.6, -6.3, and -8.9%), and apolipoprotein AI (0, -3.7 and -5.7% in non-smokers and light and heavy smokers). These dose response effects may provide new evidence for a causal relation between exposure to cigarette smoke and changes in serum lipid and lipoprotein concentrations whether as a direct result of physiological changes or of dietary changes induced by smoking. Adequate prospective data to estimate the excess risk of coronary artery disease existed only for cholesterol concentration. When that information was combined with data from the present study, and given that smokers as a group face an average overall excess risk of coronary artery disease of 70%, it was estimated that the observed increased serum cholesterol concentration in smokers may account for at least 9% of that excess risk. Furthermore, the dose response effect of smoking on serum cholesterol concentration suggests a gradient of increased absolute risk of coronary artery disease between light and heavy smokers.
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              Critical issues in peripheral arterial disease detection and management: a call to action.

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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2013
                22 March 2013
                : 8
                : 3
                : e37882
                Affiliations
                [1 ]Service de Biochimie, CHU Bordeaux, Bordeaux, France
                [2 ]Equipe de Recherche Universitaire « Facteurs de risque vasculaires », Université Bordeaux, Bordeaux, France
                [3 ]Usines FORD, Blanquefort, France
                [4 ]Service d'Hématologie, CHU Bordeaux, Bordeaux, France
                [5 ]CNRS-CHU Bordeaux, Bordeaux, France
                [6 ]Service de Chirurgie Vasculaire, de Médecine Interne et de Chirurgie Générale, CHU de Besançon, Besançon, France
                [7 ]Service de Médecine Interne et Pneumologie, CHU de Brest, Brest, France
                [8 ]Service de Chirurgie Thoracique et Cardiovasculaire et Angiologique, CHU de Limoges, Limoges, France
                [9 ]Service de Médecine Vasculaire, CHU de Toulouse, Toulouse, France
                [10 ]Service de Médecine Vasculaire, Hôpital Européen Georges Pompidou, Paris, France
                [11 ]Service de Médecine Vasculaire et Médecine Interne, CHU Bordeaux, Bordeaux, France
                Goethe University, Germany
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: AMB AB RLT GF AN SC VG MCV FB GC LB PL JPC ABR JE MD AMD SM BC VV CC JC. Performed the experiments: AMB RLT GF SC VG MCV FB GC LB PL JPC ABR JE SM BC VV CC JC. Analyzed the data: AMB AB RLT GF AN SC VG MCV FB GC LB PL JPC ABR JE MD AMD SM BC VV CC JC. Contributed reagents/materials/analysis tools: AMB AB GF AN SC VG MCV MD AMD SM BC VV JC. Wrote the paper: AMB AB RLT GF AN SC VG MCV FB GC LB PL JPC ABR JE MD AMD SM BC VV CC JC.

                Article
                PONE-D-11-25334
                10.1371/journal.pone.0037882
                3606168
                23533563
                19c0d140-3388-496c-89d5-362c58357f9e
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 18 December 2011
                : 26 April 2012
                Page count
                Pages: 10
                Funding
                This study was supported by grants from the “Fondation de France” ( http://www.fondationdefrance.org/) and the “Institut d'AthéroThrombose” ( http://www.atherothrombose.org/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Biochemistry
                Blood Chemistry
                Lipids
                Genomics
                Genomic Medicine
                Genetic Testing
                Population Biology
                Epidemiology
                Medicine
                Cardiovascular
                Peripheral Vascular Diseases
                Clinical Research Design
                Case-Control Studies
                Epidemiology
                Diagnostic Medicine

                Uncategorized
                Uncategorized

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