RESUMEN
BACKGROUND: Observational studies have suggested that low blood pressure and blood pressure variability may partially explain adverse neurological outcome after endovascular therapy with general anaesthesia (GA) for acute ischaemic stroke. The aim of this study was to further examine whether blood pressure related parameters during endovascular therapy are associated with neurological outcome. METHODS: The GOLIATH trial randomised 128 patients to either GA or conscious sedation for endovascular therapy in acute ischaemic stroke. The primary outcome was 90 day modified Rankin Score. The haemodynamic protocol aimed at keeping the systolic blood pressure >140 mm Hg and mean blood pressure >70 mm Hg during the procedure. Blood pressure related parameters of interest included 20% reduction in mean blood pressure; mean blood pressure <70 mm Hg, <80 mm Hg, and <90 mm Hg, respectively; time with systolic blood pressure <140 mm Hg; procedural minimum and maximum mean and systolic blood pressure; mean blood pressure at the time of groin puncture; postreperfusion mean blood pressure; blood pressure variability; and use of vasopressors. Sensitivity analyses were performed in the subgroup of reperfused patients. RESULTS: Procedural average mean and systolic blood pressures were higher in the conscious sedation group (P<0.001). The number of patients with mean blood pressure <70-90 mm Hg and systolic blood pressure <140 mm Hg, blood pressure variability, and use of vasopressors were all higher in the GA group (P<0.001). There was no statistically significant association between any of the examined blood pressure related parameters and the modified Rankin Score in the overall patient population, and in the subgroup of patients with full reperfusion. CONCLUSION: We found no statistically significant association between blood pressure related parameters during endovascular therapy and neurological outcome. CLINICAL TRIAL REGISTRATION: NCT 02317237.
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Presión Sanguínea/fisiología , Isquemia Encefálica/cirugía , Procedimientos Endovasculares/métodos , Cuidados Intraoperatorios/métodos , Accidente Cerebrovascular/cirugía , Anciano , Anciano de 80 o más Años , Anestesia General/métodos , Isquemia Encefálica/fisiopatología , Isquemia Encefálica/rehabilitación , Revascularización Cerebral/métodos , Revascularización Cerebral/rehabilitación , Sedación Consciente/métodos , Evaluación de la Discapacidad , Procedimientos Endovasculares/rehabilitación , Femenino , Humanos , Masculino , Persona de Mediana Edad , Monitoreo Intraoperatorio/métodos , Recuperación de la Función , Método Simple Ciego , Accidente Cerebrovascular/fisiopatología , Resultado del TratamientoRESUMEN
OBJECTIVES: Endothelial dysfunction and inflammation have been demonstrated to be markers of cardiovascular risk. We investigated the effects of HIV infection per se and the antiretroviral treatment prescribed on the levels of risk factors of cardiovascular disease. METHODS: This was a prospective study of 20 treatment-naïve, nonsmoking, HIV-positive patients examined before and after 3 months of treatment with a protease inhibitor (PI)-containing regimen followed by 3 months of treatment with nonnucleoside reverse transcriptase inhibitor (NNRTI)-containing therapy. Parameters of inflammation, endothelial function and coagulation were examined. The results were compared with those for an age- and gender-matched, nonsmoking, healthy control group. RESULTS: Compared with controls, treatment-naïve HIV-infected patients exhibited endothelial dysfunction [flow-mediated dilation (FMD) 108 vs. 111% for HIV-infected vs. control groups, respectively; P < 0.05] and activation [von Willebrand factor 2.0 vs. 0.9 U/l; soluble intercellular adhesion molecule (sICAM) 313 vs. 211 ng/L, respectively; P < 0.01]. Inflammation [C-reactive protein (CRP) 24 vs. 8.6 nmol/L; fibrinogen 9.4 vs. 8.6 µmol/L, respectively; P < 0.05] and coagulation/fibrinolysis (D-dimers 0.55 vs. 0.23 µg/mL, respectively; P < 0.01) were increased. Initiating therapy resulted in normalization of FMD and a significant decrease in endothelial activation and CRP. CONCLUSION: Endothelial dysfunction together with increased inflammation and coagulation were more prevalent in untreated HIV-infected patients compared with controls. These cardiovascular risk factors improved with treatment, although not all parameters normalized after 6 months.
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Fármacos Anti-VIH/uso terapéutico , Enfermedades Cardiovasculares/tratamiento farmacológico , Endotelio Vascular/efectos de los fármacos , Infecciones por VIH/tratamiento farmacológico , Inhibidores de la Transcriptasa Inversa/uso terapéutico , Adulto , Terapia Antirretroviral Altamente Activa , Biomarcadores/sangre , Coagulación Sanguínea/efectos de los fármacos , Enfermedades Cardiovasculares/sangre , Enfermedades Cardiovasculares/fisiopatología , Endotelio Vascular/fisiopatología , Femenino , Infecciones por VIH/sangre , Infecciones por VIH/fisiopatología , Infecciones por VIH/virología , Inhibidores de la Proteasa del VIH/uso terapéutico , Humanos , Inflamación/sangre , Inflamación/fisiopatología , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Factores de Riesgo , Carga ViralRESUMEN
Mutations in the gene for desmoplakin (DSP) may cause arrhythmogenic right ventricular cardiomyopathy (ARVC) and Carvajal syndrome (CS). Desmoplakin is part of all desmosomes, which are abundantly expressed in both myocardial and epidermal tissue and serve as intercellular mechanical junctions. This study aimed to investigate protein expression in myocardial and epidermal tissue of ARVC and CS patients carrying DSP mutations in order to elucidate potential molecular disease mechanisms. Genetic investigations identified three ARVC patients carrying different heterozygous DSP mutations in addition to a homozygous DSP mutation in a CS patient. The protein expression of DSP in mutation carriers was evaluated in biopsies from myocardial and epidermal tissue by immunohistochemistry. Keratinocyte cultures were established from skin biopsies of mutation carriers and characterized by reverse transcriptase polymerase chain reaction, western blotting, and protein mass spectrometry. The results showed that the mutation carriers had abnormal DSP expression in both myocardial and epidermal tissue. The investigations revealed that the disease mechanisms varied accordingly to the specific types of DSP mutation identified and included haploinsufficiency, dominant-negative effects, or a combination hereof. Furthermore, the results suggest that the keratinocytes cultured from patients are a valuable and easily accessible resource to elucidate the effects of desmosomal gene mutations in humans.
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Displasia Ventricular Derecha Arritmogénica/genética , Cardiomiopatías/genética , Desmoplaquinas/genética , Expresión Génica , Enfermedades del Cabello/genética , Queratodermia Palmoplantar/genética , Mutación , Miocardio/metabolismo , Adulto , Displasia Ventricular Derecha Arritmogénica/metabolismo , Displasia Ventricular Derecha Arritmogénica/patología , Cardiomiopatías/metabolismo , Cardiomiopatías/patología , Cardiomiopatía Dilatada , Niño , Desmoplaquinas/metabolismo , Epidermis/metabolismo , Epidermis/patología , Femenino , Enfermedades del Cabello/metabolismo , Enfermedades del Cabello/patología , Haploinsuficiencia , Heterocigoto , Homocigoto , Humanos , Queratinocitos/metabolismo , Queratinocitos/patología , Queratodermia Palmoplantar/metabolismo , Queratodermia Palmoplantar/patología , Persona de Mediana Edad , Miocardio/patología , Linaje , Cultivo Primario de Células , Isoformas de Proteínas/genética , Isoformas de Proteínas/metabolismoRESUMEN
After the Fontan procedure, patients face an increased risk for thromboembolic events (TE). The etiology for this increased thrombogenecity is incompletely understood. This study aimed to determine the prevalence of TE in Danish Fontan patients and to bring new insights into the etiology of TE. Using a population-based design, we retrospectively identified all TEs in 210 Fontan patients. Whole blood assays (thromboelastography, thromboelastography functional fibrinogen and Multiplate) reflecting global hemostasis, clot strength and platelet aggregation were analyzed prospectively in 112 patients and plasma was analyzed in 76 patients for biomarkers reflecting endothelial-, glycocalyx-, platelet-, and fibrinolysis function (histone-complexed DNA fragments, Protein C, soluble CD40 ligand, soluble thrombomodulin, syndecan-1, tissue-type plasminogen activator). The results were compared in groups stratified according to age, antithrombotic therapy, TE, and glycocalyx degradation (syndecan-1 < or ≥ median). Correlation between biomarkers and demographic-, anatomical-, clinical- and biochemical parameters was investigated. The prevalence of TE was 8.1 % after a mean follow-up of 8.4 years. None of the stratified groups demonstrated evidence of hypercoagulability in the whole blood assays and no unexpected significant differences were found between the groups. All biomarkers, except protein C, correlated with one another and after stratification of glycocalyx degradation only syndecan-1 levels ≥ median correlated with other biomarkers. The prevalence of TEs was 8.1 % after mean follow-up of 8.4 years. Overall, the hemostatic profile appeared normal, however, in a subset of patients, evidence of some endothelial activation/damage including glycocalyx degradation and fibrinolysis was found, identifying a potentially more thrombogenic group.
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Procedimiento de Fontan/efectos adversos , Vigilancia de la Población , Complicaciones Posoperatorias , Tromboembolia/epidemiología , Adolescente , Biomarcadores/sangre , Coagulación Sanguínea , Estudios Transversales , Dinamarca/epidemiología , Impedancia Eléctrica , Femenino , Estudios de Seguimiento , Cardiopatías Congénitas/cirugía , Humanos , Masculino , Agregación Plaquetaria , Prevalencia , Pronóstico , Estudios Retrospectivos , Factores de Riesgo , Tasa de Supervivencia/tendencias , Tromboelastografía , Tromboembolia/sangre , Tromboembolia/etiología , Factores de TiempoRESUMEN
The force-frequency relationship (FFR) reflects alterations in intracellular calcium cycling during changing heart rate (HR). Tachycardia-induced heart failure is associated with depletion of intracellular calcium. We hypothesized (1) that the relative resistance to tachycardia-induced heart failure seen in neonatal pigs is related to differences in calcium cycling, resulting in different FFR responses and (2) that pretreatment with digoxin to increase intracellular calcium would modifies these changes. LV +dP/dt was measured during incremental right atrial pacing in 16 neonatal and 14 adult pigs. FFR was measured as the change in +dP/dt as HR was increased. Animals were randomized to control or intravenous bolus digoxin (n = 8 neonate pigs in the 0.05 mg/kg group and n = 7 adult pigs in the 0.025 mg/kg group) and paced for 90 min at 25 bpm greater than the rate of peak +dP/dt. Repeat FFR was then obtained. The postpacing FFR in neonatal control pigs shifted rightward, with peak force occurring 30 bpm greater than baseline (P < 0.03). There was no vertical shift; thus, force at 150 bpm decreased (P < 0.03) and force at 300 beats/min increased (P < 0.08). In adult control pigs, FFR shifted downward (P < 0.01), with decreased force generation at all HRs. In both neonates and adult pigs, digoxin increased +dP/dt at all HRs; however, in neonate pigs digoxin decreased the contractile reserve by abrogation of the rightward shift of FFR. An adaptive response to tachycardia in the neonate pig leads to improved force generation at greater HRs. Conversely, the response of the mature pig heart is maladaptive with decreased force generation. Pretreatment with digoxin modifies these responses.
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Animales Recién Nacidos , Frecuencia Cardíaca/fisiología , Contracción Miocárdica/fisiología , Taquicardia/fisiopatología , Factores de Edad , Animales , Canales de Calcio/efectos de los fármacos , Canales de Calcio/fisiología , Estimulación Cardíaca Artificial , Cardiotónicos/farmacología , Citoplasma/efectos de los fármacos , Citoplasma/metabolismo , Citosol/efectos de los fármacos , Citosol/metabolismo , Digoxina/farmacología , Electrocardiografía/efectos de los fármacos , Insuficiencia Cardíaca/fisiopatología , Frecuencia Cardíaca/efectos de los fármacos , Modelos Teóricos , Contracción Miocárdica/efectos de los fármacos , Retículo Sarcoplasmático/efectos de los fármacos , Retículo Sarcoplasmático/fisiología , Porcinos , Función Ventricular Izquierda/efectos de los fármacos , Función Ventricular Izquierda/fisiologíaRESUMEN
Familial hypercholesterolemia is associated with premature atherosclerosis. Since endothelial dysfunction is an early event in atherogenesis, we used a noninvasive method to assess endothelial function in the systemic arteries of 30 children aged 7-17 yr (median 11) with familial hypercholesterolemia (2 homozygotes, 28 heterozygotes, total cholesterol 240-696 mg/dl) and 30 healthy age- and sex-matched controls. Using high resolution ultrasound, the diameter of the superficial femoral artery was measured at rest, in response to reactive hyperemia (with increased flow causing endothelium-dependent dilation), and after sublingual glyceryltrinitrate (causing endothelium-independent vasodilation). Flow-mediated dilation was present in the controls (7.5 +/- 0.7%) but was impaired or absent in the hypercholesterolemic children (1.2 +/- 0.4%, P < 0.0001). Total cholesterol was inversely correlated with flow-mediated dilation (r = -0.61, P < 0.0001). In the hypercholesterolemic children, flow-mediated dilation was inversely related to the lipoprotein(a) level (r = -0.61, P = 0.027) but not to other lipid fractions. Glyceryltrinitrate-induced dilation was present in all subjects but was lower in the hypercholesterolemia group (10.0 +/- 0.6% vs 12.4 +/- 0.8%, P = 0.023). Thus, impaired endothelium-dependent dilation is present in children with familial hypercholesterolemia as young as 7 yr of age and the degree of impairment is related to the lipoprotein(a) level.
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Endotelio Vascular/fisiopatología , Arteria Femoral/fisiopatología , Hiperlipoproteinemia Tipo II/fisiopatología , Lipoproteína(a)/sangre , Vasodilatación , Adolescente , Factores de Edad , Niño , Preescolar , Colesterol/sangre , Endotelio Vascular/diagnóstico por imagen , Endotelio Vascular/fisiología , Femenino , Arteria Femoral/diagnóstico por imagen , Arteria Femoral/fisiología , Humanos , Hiperlipoproteinemia Tipo II/sangre , Hiperlipoproteinemia Tipo II/diagnóstico por imagen , Lipoproteínas HDL/sangre , Lipoproteínas LDL/sangre , Masculino , Análisis Multivariante , Nitroglicerina , Valores de Referencia , Análisis de Regresión , Factores Sexuales , Triglicéridos/sangre , Ultrasonografía , Vasodilatación/efectos de los fármacosRESUMEN
BACKGROUND: Fetal tachycardia often leads to cardiac failure, which in experimental settings can be prevented by direct fetal glucose-insulin administration. In this study, we hypothesize that similar effects can be obtained indirectly by inducing maternal hyperglycemia. METHODS AND RESULTS: Systolic and diastolic indices (dP/dt(max) and tau) of left ventricular function were measured by use of high-fidelity catheters during 180 minutes of aggressive atrial pacing ( approximately 300 bpm) in 12 preterm porcine fetuses. In 6 fetuses, maternal hyperglycemia (15 mmol/L) was induced for the last 120 minutes of pacing. The remaining fetuses served as controls. Glucose, insulin, and free fatty acid levels were determined, as was fetal myocardial glycogen content. Maternal glucose infusion led to significant fetal hyperglycemia and hyperinsulinemia but did not change the inherently low fetal levels of free fatty acids. There were no differences between groups with regard to dP/dt(max) (1025+/-226 and 1037+/-207 mm Hg, P=NS) and tau (20.6+/-2.0 and 21.4+/-1.6 ms, P=NS) at baseline (100%). During the 180 minutes of pacing, systolic function (dP/dt(max)) and diastolic function (tau) deteriorated more in the control group than in the hyperglycemic group (P<0.001 for both). At 180 minutes, dP/dt(max) was 62+/-18% of baseline in controls and 85+/-11% in hyperglycemic fetuses (P=0.03), and tau was 117+/-12% and 98+/-4%, respectively (P=0.004). CONCLUSIONS: Induced maternal hyperglycemia improves fetal cardiac function during fetal tachycardia and suggests a possible additional therapeutic option to improve the function of the failing fetal heart before or during antiarrhythmic therapy. The findings may be relevant in fetal heart failure in general.
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Glucemia , Gasto Cardíaco Bajo/prevención & control , Enfermedades Fetales/prevención & control , Intercambio Materno-Fetal , Taquicardia/complicaciones , Animales , Glucemia/análisis , Gasto Cardíaco Bajo/etiología , Gasto Cardíaco Bajo/fisiopatología , Femenino , Enfermedades Fetales/metabolismo , Enfermedades Fetales/fisiopatología , Feto/fisiopatología , Embarazo , Porcinos , Función Ventricular IzquierdaRESUMEN
In insulin-dependent diabetic patients, nephropathy is a predictor of mortality and coronary heart disease. Impaired cardiac vagal function is an important factor in the pathophysiology of sudden cardiac death in coronary heart disease. Autonomic neuropathy in diabetes in particular involves vagal function. Bedside tests and 24-h measurements of cardiac parasympathetic activity were compared in 37 insulin-dependent diabetic patients, and the relationship between 24-h vagal activity and degree of nephropathy was investigated. Nephropathy was classified according to urinary albumin excretion as normoalbuminuria, incipient, and overt nephropathy. Mean age (approximately 30 yr) was not different among groups. The 24-h measurements of parasympathetic activity appeared more sensitive than bedside tests, as 33% of patients without cardiac autonomic neuropathy in bedside tests had 24-h vagal activity values below the 95% confidence limits of 14 healthy control subjects. Patients with incipient or overt nephropathy had significantly lower mean values for vagal activity during both wake and sleep time than healthy control subjects. Increasing degree of nephropathy was associated significantly with increasing attenuation of 24-h vagal activity (P less than 0.001). The covariation of degree of neuropathy and nephropathy may suggest common pathogenetic mechanisms. The reduced 24-h vagal activity, even in the early stages of nephropathy, could be an important risk factor for cardiac death in insulin-dependent diabetic patients.
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Ritmo Circadiano , Diabetes Mellitus Tipo 1/fisiopatología , Nefropatías Diabéticas/fisiopatología , Corazón/inervación , Sistema Nervioso Parasimpático/fisiopatología , Nervio Vago/fisiopatología , Adulto , Albuminuria , Presión Sanguínea , Electrocardiografía Ambulatoria , Ejercicio Físico , Femenino , Tasa de Filtración Glomerular , Humanos , Masculino , Valores de Referencia , Sueño , Fumar/fisiopatología , VigiliaRESUMEN
OBJECTIVES: We sought to assess the prevalence of atherosclerotic lesions in the human brachial artery. BACKGROUND: Many investigators have recently studied endothelial and vascular function in the brachial circulation in humans to further their understanding of coronary artery disease and early atherogenesis. However, the prevalence of brachial atherosclerosis and its relation to coronary disease have never been documented. METHODS: Arterial segments from the brachial, common carotid and left anterior descending coronary arteries were obtained during autopsy in 52 consecutively examined subjects (35 men, 17 women; 21 to 79 years old, mean [+/-SD] age 51 +/- 16) and studied by light microscopy using standard histologic techniques. Severity of the atherosclerotic lesions was categorized as fatty streaks (grade 1), fibrous plaques (grade 2) and advanced lesions (grade 3). RESULTS: Atherosclerotic lesions of any grade were found in the brachial artery in 39 (75%) subjects, common carotid artery in 51 (98%) and left anterior descending coronary artery in 52 (100%), and the prevalence and severity of disease increased with age in all three arteries. The grade of lesion severity in the brachial and coronary arteries was significantly correlated (r = 0.41, p = 0.003), as was severity in the brachial and carotid arteries (r = 0.53, p = 0.0001) and the carotid and coronary arteries (r = 0.69, p = 0.0001). The correlation between the brachial artery and the left anterior descending coronary artery was highly significant in subjects < or = 50 years old (r = 0.54, p = 0.002), but not in those > or = 50 years old (r = 0.37, p = NS). CONCLUSIONS: Atherosclerosis is common in the human brachial artery and is significantly correlated with both coronary and carotid disease. These results suggest that the brachial circulation may serve as a reasonable "surrogate" for studying atherosclerosis, particularly in younger adults.
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Arteriosclerosis , Arteria Braquial/patología , Adulto , Factores de Edad , Anciano , Arteriosclerosis/patología , Arteria Carótida Común/patología , Enfermedad de la Arteria Coronaria/patología , Femenino , Humanos , Masculino , Persona de Mediana EdadRESUMEN
OBJECTIVES: This study attempted to assess whether coronary risk factors are associated with endothelial dysfunction in the systemic arteries of asymptomatic men and women. BACKGROUND: Endothelial dysfunction is present in adults with established atherosclerosis. It is not known whether risk factors interact to produce endothelial dysfunction in clinically well subjects early in the natural history. METHODS: Using high resolution ultrasound, we measured arterial diameter at rest, after reactive hyperemia (with increased flow causing endothelium-dependent dilation) and after sublingual nitroglycerin (an endothelium-independent dilator). Arterial responses were studied noninvasively in 500 clinically well, nonhypertensive subjects (252 men, 248 women; mean [+/- SD] age 36 +/- 15 years, range 5 to 73), including 179 current and former smokers. The superficial femoral artery was studied in 46 subjects and the brachial artery in 454. RESULTS: Flow-mediated dilation ranged from -1% to +17%. All arteries dilated in response to administration of nitroglycerin (17 +/- 6%), suggesting an abnormality of endothelial function in subjects with impaired flow-mediated dilation. On univariate analysis, reduced flow-mediated dilation was significantly related to hypercholesterolemia, cigarette smoking, higher blood pressure, male gender, older age, family history of premature vascular disease and larger vessel size (p < 0.01). By multiple stepwise regression analysis, reduced flow-mediated dilation was independently associated with cigarette smoking, older age, male gender and larger vessel size (p < 0.005) but not with total cholesterol level, blood pressure or family history. A composite risk factor score was independently related to flow-mediated dilation (r = -0.30, p < 0.0001), suggesting risk factor interaction. CONCLUSIONS: Loss of endothelium-dependent dilation in the systemic arteries occurs in the preclinical phase of vascular disease and is associated with interaction of the same risk factors known to predispose to atherosclerosis and its complications in later life.
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Arterias/fisiología , Enfermedad Coronaria/fisiopatología , Endotelio Vascular/fisiología , Vasodilatación/fisiología , Adolescente , Adulto , Anciano , Análisis de Varianza , Arteria Braquial/fisiología , Niño , Preescolar , Femenino , Arteria Femoral/fisiología , Humanos , Modelos Lineales , Masculino , Persona de Mediana Edad , Factores de RiesgoRESUMEN
OBJECTIVES: This study assessed whether aging is associated with progressive endothelial dysfunction, whether the pattern of any age-related decline in vascular health is different in men and women and whether any gender difference is consistent with known changes in hormonal status. BACKGROUND: Coronary and cerebrovascular disease are much less common in young and middle-aged women compared with men, although the gender difference in death from atherosclerosis is less marked after the menopause. Endothelial dysfunction is an early event in atherogenesis and is important in dynamic plaque stenosis in later life. The effect of aging on endothelial function in men and women, however, is not well known. METHODS: We used high resolution ultrasound to study endothelium-dependent and endothelium-independent vascular responses. Brachial artery physiology was investigated in 238 subjects (103 men, 135 women; mean [+/- SD] age 38 +/- 17 years, range 15 to 72) with no known risk factors for atherosclerosis. The responses to reactive hyperemia (flow-mediated dilation, which is endothelium dependent) and to glyceryl trinitrate (an endothelium-independent dilator) were assessed for all the subjects and then for men and women separately. RESULTS: On multivariate analysis for the whole group, reduced flow-mediated dilation was related to older age (r = -0.34, p < 0.0001). In men, flow-mediated dilation was preserved in subjects aged < or = 40 years but declined thereafter at 0.21%/year. In women, flow-mediated dilation was stable until the early 50s, after which it declined at 0.49%/year (p = 0.002 compared with men). In contrast, there was no significant change in the glyceryl trinitrate response with aging in either gender. CONCLUSIONS: Aging is associated with progressive endothelial dysfunction in normal humans, and this appears to occur earlier in men than in women. In women, however, a steep decline commences at around the time of the menopause. This is consistent with a protective effect of estrogens on the arterial wall.
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Envejecimiento/fisiología , Endotelio Vascular/fisiología , Vasodilatación/fisiología , Adolescente , Adulto , Anciano , Endotelio Vascular/efectos de los fármacos , Endotelio Vascular/fisiopatología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Nitroglicerina/farmacología , Caracteres Sexuales , Vasodilatación/efectos de los fármacosRESUMEN
OBJECTIVES: This study sought to examine whether endothelial function is impaired in the large vessels of asymptomatic young adults with insulin-dependent diabetes and whether endothelial dysfunction is related to duration or control of diabetes, small-vessel disease or other vascular risk factors. BACKGROUND: Endothelial dysfunction is an early event in atherosclerosis, and large-vessel atherosclerotic disease is the major cause of morbidity and mortality in diabetes. METHODS: We compared 80 young adults with insulin-dependent diabetes (15 to 40 years old; mean [+/- SD] diabetes duration 13 +/- 8 years) with 80 matched nondiabetic control subjects. Using high resolution vascular ultrasound, we measured brachial artery responses to reactive hyperemia (with increased flow causing endothelium-dependent dilation) and sublingual glyceryltrinitrate (causing endothelium-independent dilation). RESULTS: Flow-mediated dilation was significantly impaired in diabetic subjects (5.0 +/- 3.7% vs. 9.3 +/- 3.8% in control subjects, p < 0.001). The ratio of flow-mediated dilation to glyceryltrinitrate-induced dilation was significantly lower in the diabetic subjects (p < 0.02), indicating that impaired dilation to increased flow was out of proportion to the impairment of the glyceryltrinitrate response in these subjects (15.6 +/- 5.6% vs. 19.7 +/- 6.6% in control subjects, p < 0.001). On multivariate analysis, flow-mediated dilation was inversely related to both duration of diabetes (r = -0.26, p < 0.05) and low density lipoprotein (LDL) cholesterol levels (r = -0.38, p < 0.005). CONCLUSIONS: Vascular reactivity is impaired in the systemic arteries of asymptomatic young adults with insulin-dependent diabetes and may represent early large-vessel disease. The degree of impairment is related to the duration of diabetes, and these patients appear particularly vulnerable to damage from LDL cholesterol, even at levels considered acceptable in nondiabetic subjects.
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LDL-Colesterol/sangre , Diabetes Mellitus Tipo 1/fisiopatología , Vasodilatación , Adolescente , Adulto , Velocidad del Flujo Sanguíneo , Arteria Braquial/diagnóstico por imagen , Arteria Braquial/fisiopatología , LDL-Colesterol/fisiología , Diabetes Mellitus Tipo 1/sangre , Endotelio Vascular/fisiopatología , Femenino , Humanos , Masculino , Músculo Liso Vascular/fisiopatología , Nitroglicerina/farmacología , Análisis de Regresión , Factores de Tiempo , Ultrasonografía Intervencional , Vasodilatación/efectos de los fármacos , Vasodilatadores/farmacologíaRESUMEN
OBJECTIVES: We sought to assess smooth muscle function in adults at risk for atherosclerosis. BACKGROUND: Previous studies in subjects at risk for atherosclerosis have demonstrated arterial endothelial dysfunction, with reduced vasodilator responses after pharmacologic or physiologic stimulation of endothelial nitric oxide (NO). Most have also shown a slight but nonsignificant impairment of vasodilation in response to exogenous sources of NO, such as nitroglycerin (NTG). We hypothesized that NTG responses might be reduced in a large number of consecutively studied adults at risk for atherosclerosis, independent of any impaired endothelium-dependent responses, consistent with concomitant smooth muscle dysfunction. METHODS: Using high resolution ultrasound, the dilator response of the brachial artery to 400 microg of sublingual NTG was measured in 800 asymptomatic subjects. Subjects were also assessed for a history of vascular risk factors, blood pressure, total serum cholesterol and flow-mediated endothelium-dependent dilation (EDD). RESULTS: We studied 317 men and 483 women, 38 +/- 17 years old (mean +/- SD, range 15 to 76). The mean cholesterol level was 5.2 +/- 1.3 mmol/liter, and there were 126 smokers and ex-smokers (16 +/- 9 mean pack-years) and 105 diabetic subjects. On univariate analysis, a reduced vasodilator response to NTG was associated with high cholesterol, cigarette smoking, diabetes mellitus, increasing age, male gender, larger vessel size and reduced EDD (p < or = 0.01 for all). On multivariate analysis, diabetes, larger vessel size and reduced EDD were all independently associated with impaired NTG-related vasodilation (p < or = 0.001 for all). In the 574 nondiabetic subjects who had never smoked cigarettes, the independent relation between EDD and NTG responses was still observed (r = 0.24, p = 0.01). CONCLUSIONS: The vasodilator response to exogenous NO is impaired in asymptomatic subjects with reduced EDD, consistent with smooth muscle dysfunction in adults at risk for atherosclerosis.
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Arteriosclerosis/fisiopatología , Endotelio Vascular/fisiopatología , Músculo Liso Vascular/fisiopatología , Administración Sublingual , Adolescente , Adulto , Anciano , Arteriosclerosis/diagnóstico , Angiopatías Diabéticas/diagnóstico , Angiopatías Diabéticas/fisiopatología , Femenino , Humanos , Hipercolesterolemia/diagnóstico , Hipercolesterolemia/fisiopatología , Masculino , Persona de Mediana Edad , Óxido Nítrico/agonistas , Óxido Nítrico/fisiología , Nitroglicerina/farmacología , Factores de Riesgo , Fumar/efectos adversos , Vasodilatación/fisiología , Vasodilatadores/farmacologíaRESUMEN
BACKGROUND: Patients with cyanotic congenital heart disease (CCHD) have a high prevalence of thrombosis, the most frequently described locations being the cerebral and pulmonary vessels. The reported prevalence of both cerebral infarction and pulmonary thrombosis has been highly variable. The aim of this study was to examine the prevalence of both cerebral and pulmonary thrombosis in CCHD according to medical history and imaging. In addition, the role of known erythrocytosis and haemostatic abnormalities as risk factors was evaluated. METHODS AND RESULTS: A cross-sectional descriptive study examining 98 stable adult patients with CCHD with a medical questionnaire, blood samples, MRI of the cerebrum (n=72), multidetector CT imaging (MDCT) of the thorax (n=76) and pulmonary scintigraphy (ventilation/perfusion/single-photon emission computerised tomography/CT) (n=66). The prevalence of cerebral infarction and pulmonary thrombosis according to imaging were 47% and 31%, respectively. Comparing the findings with previous medical history revealed a large under-reporting of thrombosis with only 22% of the patients having a clinical history of stroke and 25% of pulmonary thrombosis. There was no association between the degree of erythrocytosis or haemostatic abnormalities and the prevalence of thrombosis. CONCLUSIONS: Patients with CCHD have a prevalence of both cerebral and pulmonary thrombosis of around 30%-40%, which is much higher than that reported previously. Furthermore, there is a large discrepancy between clinical history and imaging findings, suggesting a high prevalence of silent thrombotic events. Neither erythrocytosis nor haemostatic abnormalities were associated with the prevalence of thrombosis in patients with CCHD. TRIAL REGISTRATION NUMBER: http://www.cvk.sum.dk/CVK/Home/English.aspx (H-KF-2006-4068).
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Cianosis/epidemiología , Cardiopatías Congénitas/epidemiología , Trombosis Intracraneal/epidemiología , Pulmón/irrigación sanguínea , Trombosis/epidemiología , Adulto , Estudios Transversales , Cianosis/diagnóstico , Dinamarca/epidemiología , Femenino , Cardiopatías Congénitas/diagnóstico , Humanos , Trombosis Intracraneal/diagnóstico , Imagen por Resonancia Magnética , Masculino , Registros Médicos , Persona de Mediana Edad , Tomografía Computarizada Multidetector , Imagen de Perfusión , Valor Predictivo de las Pruebas , Prevalencia , Factores de Riesgo , Encuestas y Cuestionarios , Trombosis/diagnóstico , Tomografía Computarizada de Emisión de Fotón ÚnicoRESUMEN
A projection from the subiculum to the retrosplenial cortex (area 29a and b) was studied by autoradiographic tracing of anterogradely transported proteins following injections of radioactive amino acids into ventral and dorsal parts of the subiculum. Only the dorsal parts of the subiculum projected to the retrosplenial cortex. The projection was exclusively ipsilateral, and topographically arranged along both the longitudinal septotemporal axis and the transverse plane of the subiculum. The termination in the retrosplenial cortex was confined to the relatively cell-free superficial layer (lamina 1) and the underlying cell-rich layers (laminae 3-4). Between these two terminations a narrow zone (lamina 2) was only weakly labeled. The projection constitutes an output route for hippocampal activity in addition to the fimbria-fornix system and the subicular projections to the parahippocampal areas.
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Corteza Cerebral/anatomía & histología , Hipocampo/anatomía & histología , Animales , Mapeo Encefálico , Femenino , Cobayas , Masculino , Vías Nerviosas/anatomía & histologíaRESUMEN
A study of the efferent projections of the entorhinal area in the guinea pig, by using anterograde (autoradiographic tracing of tritiated amino acids) and retrograde (fluorochrome tracing) methods, revealed the following projections: (1) to nonhippocampal cortices: retrosplenial cortex (area 29), cingulate cortex (areas 23, 24), prelimbic cortex (area 32), infralimbic cortex (area 25), perirhinal cortex (areas 35, 36), prepyriform cortex (area 51B), and insular cortex (areas 13-16). All received direct projection; (2) to subcortical targets: distinct terminations were observed in the lateral thalamic nucleus, the striatum, and the accumbens nucleus. In retrograde experiments, the cells giving rise to the projections to the hippocampus were found to lie in layers II and III, those projecting to the nonhippocampal cortical regions to originate in layer IV, and those projecting to the striatum and the accumbens to lie in layers V and VI. Many of the efferent projections to the cerebral cortical regions are associated with reciprocal projections from these regions to the superficial layers (I-III) of the entorhinal cortex. The entorhinal efferent projections generally terminate ipsilaterally. A weak termination is, however, present at the contralateral side. The efferent projections of the entorhinal area represent a route for important caudally directed, nonfornical hippocampal output.
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Corteza Cerebral/anatomía & histología , Cuerpo Estriado/anatomía & histología , Hipocampo/anatomía & histología , Núcleo Accumbens/anatomía & histología , Núcleos Septales/anatomía & histología , Animales , Autorradiografía , Vías Eferentes/anatomía & histología , Femenino , Cobayas , MasculinoRESUMEN
Projections from the subiculum to retrohippocampal areas were studied by reduced silver impregnation of anterograde degeneration and by autoradiographic tracing of transported proteins following injections of radioactive amino acids. The subiculum was found to project to the presubiculum and to the medial and lateral parts of the entorhinal area. The projections are exclusively ipsilateral, and arranged in a dorso-ventral topographical order with the terminations confined to the deep cortical layers. The projections form part of multisynaptic chains within the hippocampal region and must also be implicated in output routes for hippocampal activity additional to the fimbria-fornix system.
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Diencéfalo/anatomía & histología , Sistema Límbico/anatomía & histología , Vías Aferentes/anatomía & histología , Animales , Autorradiografía , Mapeo Encefálico , Vías Eferentes/anatomía & histología , Cobayas , Hipocampo/anatomía & histología , Terminología como AsuntoRESUMEN
The DD genotype is a polymorphism of the angiotensin-converting enzyme (ACE) gene, and is associated with a significantly increased risk of myocardial infarction. As endothelial dysfunction is an important event in both early atherogenesis and late atherosclerosis, we hypothesised that the adverse effect associated with the ACE/DD genotype might be mediated via endothelial damage. Using high resolution ultrasound, we studied the brachial arteries of 184 subjects aged 15-73 (mean 38 +/- 14) years, who were all normotensive, non-diabetic lifelong non-smokers. Arterial diameter was measured at rest, during reactive hyperaemia (with flow increase causing endothelium-dependent dilation) and after sublingual glyceryl trinitrate (GTN, an endothelium-independent vasodilator). The ACE genotype was determined in each case by DNA amplification; 49/184(27%) had DD, 89 (48%) had ID and 46 (25%) had II genotype. Flow-mediated dilation (FMD) was 8.5% +/- 3.9% in the DD, 7.8% +/- 4.1% in the ID and 7.8% +/- 4.1% in the II subjects (P = NS). GTN-induced dilation was also similar in the 3 groups. On multivariate analysis, endothelium-dependent dilation was inversely related to age (r = -0.33, P < 0.001), vessel size (r = -0.41, P < 0.001) but not ACE genotype (r = 0.002, P = 0.97). The ACE genotype is unrelated to endothelium-dependent dilation in the systemic arteries of clinically well adults. This suggests that the risk associated with this polymorphism may be mediated by other mechanisms.
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Enfermedad de la Arteria Coronaria/genética , Endotelio Vascular/fisiopatología , Peptidil-Dipeptidasa A/genética , Adolescente , Adulto , Anciano , Arteria Braquial/fisiopatología , Enfermedad de la Arteria Coronaria/fisiopatología , Femenino , Antebrazo/irrigación sanguínea , Genotipo , Humanos , Hiperemia/fisiopatología , Masculino , Persona de Mediana Edad , Nitroglicerina/farmacología , Factores de Riesgo , Vasodilatación/efectos de los fármacosRESUMEN
Quantification of variations in instantaneous heart rate (HR) can be used to evaluate cardiac autonomic function. A 24-hour standard deviation of all normal RR intervals less than 50 ms in survivors of myocardial infarction has been shown to be an independent marker of adverse prognosis. Twenty-four-hour HR variability in 140 healthy subjects aged 40 to 77 years was determined as (1) standard deviation, and (2) percentage of successive RR interval differences greater than 6%--an index of parasympathetic activity. The 24-hour standard deviation varied between 68 and 261 ms (median 139). Range for index of parasympathetic activity was 0.1 to 29.6% (median 4.4). Twenty percent of the interindividual variation in HR variability was explained by impact of risk factors. Standard deviation was uninfluenced by age, whereas parasympathetic activity decreased by increasing age. High physical training level was independently associated with significantly higher standard deviation (and parasympathetic activity) values during both day and night. Hourly figures of standard deviation decreased during the night, whereas parasympathetic activity increased and peaked early morning. Standard deviation values as low as those reported in high-risk patients were not observed, but comparable low values for, and lack of diurnal variation in, parasympathetic activity were seen in healthy subjects also. In conclusion, risk factors and, in particular, the physical training level have impact on 24-hour HR variability in healthy subjects. This may prove valuable for modification of cardiac autonomic activity in patients.
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Ritmo Circadiano/fisiología , Frecuencia Cardíaca/fisiología , Adulto , Anciano , Electrocardiografía Ambulatoria , Femenino , Humanos , Masculino , Persona de Mediana Edad , Educación y Entrenamiento Físico , Valores de Referencia , Factores de Riesgo , Fumar/fisiopatologíaRESUMEN
In addition to coronary vascular abnormalities, patients with syndrome X and variant angina often have systemic vascular symptoms. To determine whether these patients exhibit a generalized abnormality of vasoreactivity, we used high-resolution ultrasound to compare flow responses and endothelial function in the brachial artery in 21 patients with syndrome X, 15 patients with variant angina, and 20 healthy controls. Arterial diameter was measured at rest, after reactive hyperemia (endothelium-dependent flow-mediated vasodilation), and after sublingual glyceryl trinitrate (endothelium-independent vasodilation). The magnitude of hyperemic flow response was measured after transient forearm occlusion. Flow-mediated dilation in the brachial artery did not differ among patients with syndrome X, variant angina, and controls (2.7 +/- 2.3%, 3.8 +/- 3.5%, and 4.2 +/- 3.0%). Endothelium-independent vasodilation in the brachial artery was similar in the 3 groups (16.0 +/- 7.2%, 12.7 +/- 4.6%, and 14.8 +/- 4.9%). Despite a considerable overlap, reactive hyperemia was lower in patients with syndrome X than in patients with variant angina and controls (342+/-86% vs 466+/-184% and 452+/-104%; p < 0.05). These findings indicate that a substantial proportion of patients with syndrome X have a systemic microvascular abnormality, whereas variant angina is predominantly a segmental disorder of conduit vessels.