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1.
Eur J Vasc Endovasc Surg ; 58(6): 805-812, 2019 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-31653610

RESUMO

OBJECTIVES: The metabolic syndrome (MetS) is a cluster of risk factors for cardiovascular disease. The effect of MetS on clinical outcome in patients with cerebrovascular disease remains largely unknown because conflicting results have been published. This study aimed to determine the influence of MetS on the occurrence of restenosis after carotid endarterectomy (CEA). METHODS: All patients who underwent CEA between June 2003 and December 2014 in two tertiary academic referral centres in The Netherlands were included. MetS was defined if three or more of the following criteria were present: hypertension, obesity, high fasting serum blood glucose, high serum triglycerides, or low serum high density lipoprotein cholesterol. The primary outcome measure was the occurrence of ipsilateral restenosis after index surgery. The secondary outcome measure was (all cause) mortality during follow up. For the primary analysis, missing data were multiply imputed using multivariable imputation by chained equations. A Cox proportional hazards model was used to perform an adjusted analysis on the multiply imputed data sets. RESULTS: A total of 1668 CEA procedures (in 1577 patients) were performed. The presence or absence of MetS could not be determined in 263 patients because of missing data. There was no significant difference in freedom from restenosis in the MetS group vs. the no-MetS group (hazard ratio [HR], 1.10; 95% confidence interval [CI] 0.98-1.23; p = .10) or in all cause mortality (HR 1.20; 95% CI 0.94-1.54; p = .14). CONCLUSION: This study shows that MetS does not predict restenosis after CEA. Also, the presence of MetS did not influence patient survival negatively.


Assuntos
Estenose das Carótidas/cirurgia , Endarterectomia das Carótidas/efeitos adversos , Síndrome Metabólica/epidemiologia , Idoso , Estenose das Carótidas/epidemiologia , Comorbidade , Endarterectomia das Carótidas/instrumentação , Feminino , Seguimentos , Humanos , Estimativa de Kaplan-Meier , Masculino , Síndrome Metabólica/complicações , Pessoa de Meia-Idade , Países Baixos/epidemiologia , Estudos Prospectivos , Recidiva , Medição de Risco , Fatores de Risco , Stents , Fatores de Tempo , Resultado do Tratamento
2.
Mol Imaging Biol ; 18(2): 283-91, 2016 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-26377769

RESUMO

PURPOSE: In this study, the potential of matrix metalloproteinase (MMP) sense for detection of atherosclerotic plaque instability was explored. Secondly, expression of MMPs by macrophage subtypes and smooth muscle cells (SMCs) was investigated. PROCEDURES: Twenty-three consecutive plaques removed during carotid endarterectomy were incubated in MMPSense™ 680 and imaged with IVIS® Spectrum. mRNA levels of MMPs, macrophage markers, and SMCs were determined in plaque specimens, and in in vitro differentiated M1 and M2 macrophages. RESULTS: There was a significant difference between autofluorescence signals and MMPSense signals, both on the intraluminal and extraluminal sides of plaques. MMP-9 and CD68 messenger RNA (mRNA) expression was higher in hot spots, whereas MMP-2 and αSMA expression was higher in cold spots. In vitro M2 macrophages had higher mRNA expression of MMP-1, MMP-9, MMP-12, and TIMP-1 compared to M1 macrophages. CONCLUSION: MMP-9 is most dominantly MMP present in atherosclerotic plaques and is produced by M2 rather than M1 macrophages.


Assuntos
Estenose das Carótidas/enzimologia , Macrófagos/enzimologia , Metaloproteinase 2 da Matriz/metabolismo , Metaloproteinase 9 da Matriz/metabolismo , Miócitos de Músculo Liso/enzimologia , Placa Aterosclerótica/enzimologia , Idoso , Idoso de 80 Anos ou mais , Estenose das Carótidas/patologia , Demografia , Ensaio de Imunoadsorção Enzimática , Feminino , Fluorescência , Regulação Enzimológica da Expressão Gênica , Humanos , Macrófagos/patologia , Masculino , Metaloproteinase 2 da Matriz/genética , Metaloproteinase 9 da Matriz/genética , Pessoa de Meia-Idade , Miócitos de Músculo Liso/patologia , Placa Aterosclerótica/patologia , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Fatores de Risco
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