Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 8 de 8
Filtrar
Añadir filtros








Intervalo de año
1.
An. bras. dermatol ; 94(5): 561-566, Sept.-Oct. 2019. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1054858

RESUMEN

Abstract Background Rubeosis faciei diabeticorum is a persistent facial erythema in patients with diabetes mellitus. The actual pathogenesis has not been studied. However, it is speculated to be a cutaneous diabetic microangiopathy. Objective Examine the correlation between the severity of facial erythema and the possible causes of microvascular diabetic complications, namely oxidative stress, hyperglycemia, and cutaneous accumulation of advanced glycation end-products . Methods Patients diagnosed with Type 2 diabetes mellitus (n = 32) were enrolled in the study. The facial erythema index was measured using the Mexameter MX18; cutaneous accumulation of advanced glycation end-products was estimated by measuring skin auto fluorescence with the AGE Reader (DiagnOptics Technologies B.V. - Groningen, Netherlands). Glycated haemoglobin, total antioxidant status, and malondialdehyde were measured in blood by TBARS assay. The correlation between the selected variables was assessed by Spearman's rank test; p ≤ 0.05 was considered statistically significant. Results There was a statistically significant correlation between total antioxidant status and the facial erythema index (ρ = 0.398, p = 0.024). Malondialdehyde, skin autofluorescence, glycated haemoglobin, body mass index, duration of diabetes, and age did not demonstrate statistically significant correlation with the facial erythema index. Study limitations This is an observational study. Elevation of total antioxidant status could have been caused by several factors that might have also influenced the development of rubeosis faciei, including hyperbilirubinemia and hyperuricemia. Conclusions The results contradicted expectations. Total antioxidant status correlated positively with facial erythema index; however, there was no correlation with oxidative stress and skin autofluorescence. Further investigations should be conducted to reveal the cause of total antioxidant status elevation in patients with rubeosis faciei.


Asunto(s)
Humanos , Masculino , Femenino , Adulto , Persona de Mediana Edad , Anciano , Estrés Oxidativo , Angiopatías Diabéticas/metabolismo , Eritema/metabolismo , Dermatosis Facial/metabolismo , Valores de Referencia , Espectrofotometría , Hemoglobina Glucada/análisis , Índice de Masa Corporal , Estadísticas no Paramétricas , Diabetes Mellitus Tipo 2/complicaciones , Diabetes Mellitus Tipo 2/metabolismo , Angiopatías Diabéticas/complicaciones , Eritema/etiología , Dermatosis Facial/etiología , Fluorescencia , Malondialdehído/sangre , Antioxidantes/análisis
2.
Indian J Biochem Biophys ; 2014 Dec ; 51(6): 441-448
Artículo en Inglés | IMSEAR | ID: sea-156522

RESUMEN

The chronic diabetes mellitus (DM) is a major risk factor for cardiovascular disease. The incidence of cardiovascular disease might be a foremost cause of morbidity and mortality in patients afflicted with DM. In fact, DM is associated with multi-factorial cardiovascular signalling alterations via significant modulation of expression pattern, activation or release of PI3K, PKB, eNOS, EDRF, NADPH oxidase, EDHF, CGRP, adenosine, iNOS, ROCK, PKC-β2, CaMKII, microRNA (miR)-126 and miR-130a, which could result in inadequate maintenance of cardiovascular physiology and subsequent development of cardiovascular pathology. This review highlights the possible adverse implications of fundamental cardiovascular signalling alteration in DM-associated cardiovascular disease pathology.


Asunto(s)
Animales , Enfermedad de la Arteria Coronaria/metabolismo , Complicaciones de la Diabetes/metabolismo , Angiopatías Diabéticas/metabolismo , Humanos , Modelos Cardiovasculares , Proteoma/metabolismo , Transducción de Señal , /metabolismo
3.
Arq. bras. endocrinol. metab ; 52(2): 387-397, mar. 2008.
Artículo en Portugués | LILACS | ID: lil-481017

RESUMEN

O risco de doença arterial coronariana (DAC) nos pacientes com diabetes melito tipo 1 (DM1) é conhecido desde o final dos anos 1970, sendo atualmente a principal causa de mortalidade na população adulta com diabetes tipo 1 de longa duração. A patogênese do processo aterosclerótico nesta doença ainda é obscura, acreditando-se que a hiperglicemia desenvolva aí um papel importante, entretanto vários estudos epidemiológicos mostraram que a associação entre doença coronariana e glicemia, em pacientes com DM1 seja fraca. Dados recentes do estudo DCCT/EDIC mostram que o grupo que recebeu tratamento insulínico intensificado durante o DCCT desenvolveu graus menores de aterosclerose, relacionado aos valores reduzidos de HbA1c durante a fase ativa do estudo, com melhor proteção nos pacientes mais jovens e com menor duração da doença. Há também evidências de que os benefícios são maiores nos pacientes sem nefropatia quando comparados aos com doença renal. Outros fatores de risco importante para o desenvolvimento de DAC em pacientes com DM1 são os mesmos descritos para DM2, incluindo os componentes da síndrome metabólica e marcadores de resistência insulínica. Sugere-se que pacientes com DM1 devam ter o melhor controle glicêmico possível, desde o início da sua doença acrescido de vigilância e tratamento rígido dos fatores de riscos clássicos para DAC, principalmente naqueles com história familiar de DM2.


The association between type 1 diabetes and coronary heart disease has become very clear since the late 1970. It has been demonstrated that there is an important increased risk in morbidity and mortality caused by coronary artery disease in young adults with type 1 diabetes compared with the non diabetic population. The underlying pathogeneses is still poorly understood. While the role of glycemic control in the development of microvascular disease complication is well established its role in CVD in patients with DM1 remains unclear with epidemiologic studies reporting conflicting data. Recent findings from the DCCT/EDIC showed that prior intensive diabetes treatment during the DCCT was associated with less atherosclerosis, largely because of reduced level of HbA1c during the DCCT. The improvement of glycemic control itself appeared to be particularly effective in younger patients with shorter duration of the disease. Other analyses suggested the glycemia may have a stronger effect on CAD in patients without than in those with albuminúria. Other major determinants of coronary artery disease are the components of metabolic syndrome and the surrogate measure of insulin resistence: eGDR. It is proposed that patients with DM1 should have aggressive medical therapy, risk factor modification and careful monitoring not only of his blood sugar but also of the other processes involved in the atherosclerotic process, mostly the ones with family history of type 2 diabetes.


Asunto(s)
Adolescente , Adulto , Anciano , Niño , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Enfermedad de la Arteria Coronaria/etiología , Diabetes Mellitus Tipo 1/complicaciones , Angiopatías Diabéticas/etiología , Glucemia/análisis , Enfermedad de la Arteria Coronaria/epidemiología , Enfermedad de la Arteria Coronaria/metabolismo , Diabetes Mellitus Tipo 1/epidemiología , Angiopatías Diabéticas/epidemiología , Angiopatías Diabéticas/metabolismo , Hemoglobina Glucada/análisis , Hiperglucemia/complicaciones , Hiperglucemia/etiología , Hiperglucemia/metabolismo , Hipoglucemiantes/uso terapéutico , Resistencia a la Insulina , Insulina/uso terapéutico , Síndrome Metabólico/etiología , Síndrome Metabólico/metabolismo , Prevalencia , Adulto Joven
4.
Arq. bras. endocrinol. metab ; 51(2): 153-159, mar. 2007.
Artículo en Inglés | LILACS | ID: lil-449568

RESUMEN

Diabetic patients have a 3-fold higher risk of developing atherosclerosis and its clinical complications as compared to non-diabetic individuals. Part of the cardiovascular risk associated with diabetes is probably due to genetic determinants influencing both glucose homeostasis and the development of atherosclerosis. However, type 2 diabetes frequently coexists with other cardiovascular risk factors like arterial hypertension, central obesity and dyslipidemia. Genetic variability affecting many areas such as lipid and energy metabolisms, hypertension and haemodynamic mechanisms, blood clotting homeostasis, inflammation, and matrix turnover in the vascular wall will have an impact on the development of macrovascular complications in diabetic patients. Adiponectin is abundantly secreted by adipocytes. It plays important roles in lipid and glucose metabolisms and has direct anti-inflammatory and anti-atherogenic effects. In this review, we summarize recent data from the literature suggesting an implication of allelic variations of the adiponectin gene (ADIPOQ) in the genetic determinants of cardiovascular disease in diabetic subjects.


Os pacientes com diabetes apresentam risco três vezes maior de desenvolverem aterosclerose e suas complicações quando comparados a indivíduos sem hiperglicemia. Parte desse risco associado ao diabetes é provavelmente relacionado a determinantes genéticos que influenciam tanto a homeostase glicídica quanto o desenvolvimento da aterosclerose. Entretanto, o diabetes tipo 2 freqüentemente coexiste com outros fatores de risco cardiovascular, tais como hipertensão arterial, obesidade central e dislipidemia. A variabilidade genética interfere em várias áreas tais como o metabolismo lipídico, o metabolismo energético, hipertensão, mecanismos hemodinâmicos, mecanismos de coagulação, inflamação e na formação da matriz na parede vascular, que podem estar envolvidos nas complicações macrovasculares dos pacientes com diabetes. A adiponectina é secretada com abundância pelos adipócitos. Apresenta importante papel no metabolismo lipídico e glicídico, tendo ação direta tanto antiinflamatória quanto anti-aterogênica. Na atual revisão, nós resumimos os dados recentes da literatura que sugerem uma implicação de variantes alélicas do gene da adiponectina (ADIPOQ) que podem estar envolvidos na determinação genética da doença cardiovascular em indivíduos com diabetes.


Asunto(s)
Humanos , Alelos , Adiponectina/genética , Enfermedad de la Arteria Coronaria/genética , /complicaciones , Angiopatías Diabéticas/genética , Variación Genética , Enfermedad de la Arteria Coronaria/metabolismo , /metabolismo , Angiopatías Diabéticas/metabolismo , Metabolismo Energético , Predisposición Genética a la Enfermedad , Metabolismo de los Lípidos , Lipoproteínas/metabolismo , Factores de Riesgo
6.
Rev. mex. oftalmol ; 67(3): 101-4, mayo-jun. 1993. tab
Artículo en Español | LILACS | ID: lil-124665

RESUMEN

Varios modelos experimentales reproducen las manifestaciones oculares de la diabetes mellitus, así es el caso del modelo no diabético de suplemento de sacarosa en la rata, el cual es un modelo no diabético que reproduce la nagiopatía diabética, con secreción de insulina normal. Durante seis meses de experimentación, encontramos cambios oculares importantes como cataratas bilaterales, despoblación de las células ganglionares de la retina, así como hipoagregabilidad plaquetaria in vitro. Todo esto, en ausencia de niveles altos de glucosa en la sangre, indica una alta disponibilidad metabólica de la glucosa, lo que determina las lesiones en el cristalino y retina encontradas en este estudio. Este modelo experimental tambien confirma el desarrollo de la hipoagregabilidad plaquetaria in vitro, la cual puede ser atribuída a la estimulación de las plaquetas in vivo.


Asunto(s)
Animales , Ratas , Sacarosa/efectos adversos , Sacarosa/metabolismo , Hiperglucemia/inducido químicamente , Hiperglucemia/metabolismo , Retinopatía Diabética/fisiopatología , Retinopatía Diabética/metabolismo , Ratas/metabolismo , Enfermedades Vasculares/fisiopatología , Enfermedades Vasculares/metabolismo , Activación Plaquetaria/fisiología , Angiopatías Diabéticas/fisiopatología , Angiopatías Diabéticas/metabolismo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA