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1.
Int J Mol Sci ; 23(3)2022 Feb 08.
Artigo em Inglês | MEDLINE | ID: mdl-35163842

RESUMO

This work intends to describe the physical properties of red blood cell (RBC) membranes in obese adults. The hypothesis driving this research is that obesity, in addition to increasing the amount of body fat, will also modify the lipid composition of membranes in cells other than adipocytes. Forty-nine control volunteers (16 male, 33 female, BMI 21.8 ± 5.6 and 21.5 ± 4.2 kg/m2, respectively) and 52 obese subjects (16 male and 36 female, BMI 38.2± 11.0 and 40.7 ± 8.7 kg/m2, respectively) were examined. The two physical techniques applied were atomic force microscopy (AFM) in the force spectroscopy mode, which allows the micromechanical measurement of penetration forces, and fluorescence anisotropy of trimethylammonium diphenylhexatriene (TMA-DPH), which provides information on lipid order at the membrane polar-nonpolar interface. These techniques, in combination with lipidomic studies, revealed a decreased rigidity in the interfacial region of the RBC membranes of obese as compared to control patients, related to parallel changes in lipid composition. Lipidomic data show an increase in the cholesterol/phospholipid mole ratio and a decrease in sphingomyelin contents in obese membranes. ω-3 fatty acids (e.g., docosahexaenoic acid) appear to be less prevalent in obese patient RBCs, and this is the case for both the global fatty acid distribution and for the individual major lipids in the membrane phosphatidylcholine (PC), phosphatidylethanolamine (PE) and phosphatidylserine (PS). Moreover, some ω-6 fatty acids (e.g., arachidonic acid) are increased in obese patient RBCs. The switch from ω-3 to ω-6 lipids in obese subjects could be a major factor explaining the higher interfacial fluidity in obese patient RBC membranes.


Assuntos
Difenilexatrieno/análogos & derivados , Membrana Eritrocítica/fisiologia , Lipidômica/métodos , Obesidade/diagnóstico por imagem , Adolescente , Adulto , Fenômenos Biomecânicos , Estudos de Casos e Controles , Difenilexatrieno/administração & dosagem , Membrana Eritrocítica/metabolismo , Feminino , Polarização de Fluorescência , Humanos , Masculino , Microscopia de Força Atômica , Pessoa de Meia-Idade , Obesidade/metabolismo , Obesidade/fisiopatologia , Fosfatidilcolinas/metabolismo , Fosfatidiletanolaminas/metabolismo , Fosfatidilserinas/metabolismo , Adulto Jovem
2.
Matern Child Health J ; 21(7): 1488-1492, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28105546

RESUMO

Objectives To study if there is any relationship about higher cutoff values for 100 g oral glucose tolerance test and the need for insulin in women diagnosed with gestational diabetes. Materials and Methods This is a retrospective population-based study of 201 women diagnosed with Gestational Diabetes Mellitus (GDM) between January 2012 and June 2014 in the area of Oviedo, Asturias, Spain. According to diagnostic criteria recommended by GEDE, NDDG, gestational diabetes is diagnosed if two or more plasma glucose levels meet or exceed the following threshold: fasting glucose of 105 mg/dl, 1-h 190 mg/dl, 2-h 165 mg/dl, or 3-h 145 mg/dl. We aim to know if there is any relationship between higher cutoffs and insulin requirement. Results 36 out of 201 patients (17.91%) needed insulin to achieve the targets of blood glucose control. There were no differences in mean maternal age and birthweights. Fasting blood glucose levels were significantly higher in women with further need for insulin than those who only needed diet and exercise (p < 0.001). Also, blood glucose levels 2 h after the oral glucose intake were statistically different between the two groups (p 0.032). AUC for fasting glucose value was the highest according to ROC curve. Conclusions Fasting cutoff vales for 100 g oral glucose tolerance test are consistently higher in women diagnosed with Gestational Diabetes that further needed insulin to achieve adequate blood glucose control. The positive predictive value of fasting glucose value 105 mg/dl on OGTT was 81.1%, whereas for the cut-off 95 mg/dl it was 54.0%.


Assuntos
Glicemia/metabolismo , Diabetes Gestacional/diagnóstico , Teste de Tolerância a Glucose/normas , Hipoglicemiantes/administração & dosagem , Insulina/administração & dosagem , Adulto , Diabetes Gestacional/sangue , Diabetes Gestacional/terapia , Feminino , Humanos , Idade Materna , Pessoa de Meia-Idade , Guias de Prática Clínica como Assunto , Gravidez , Estudos Retrospectivos , Espanha
3.
J Clin Endocrinol Metab ; 108(11): e1341-e1346, 2023 10 18.
Artigo em Inglês | MEDLINE | ID: mdl-37207452

RESUMO

CONTEXT: Autoimmune diabetes can develop at any age, but unlike early-onset diabetes, adult onset is less well documented. We aimed to compare, over a wide age range, the most reliable predictive biomarkers for this pathology: pancreatic-autoantibodies and HLA-DRB1 genotype. METHODS: A retrospective study of 802 patients with diabetes (aged 11 months to 66 years) was conducted. Pancreatic autoantibodies at diagnosis: insulin autoantibodies (IAA), glutamate decarboxylase autoantibodies (GADA), islet tyrosine phosphatase 2 autoantibodies (IA2A), and zinc transporter-8 autoantibodies (ZnT8A) and HLA-DRB1 genotype were analyzed. RESULTS: Compared with early-onset patients, adults had a lower frequency of multiple autoantibodies, with GADA being the most common. At early onset, IAA was the most frequent in those younger than 6 years and correlated inversely with age; GADA and ZnT8A correlated directly and IA2A remained stable.The absence of HLA-DRB1 risk genotype was associated with higher age at diabetes onset (27.5 years; interquartile range [IQR], 14.3-35.7), whereas the high-risk HLA-DR3/DR4 was significantly more common at lower age (11.9 years; IQR, 7.1-21.6). ZnT8A was associated with DR4/non-DR3 (odds ratio [OR], 1.91; 95% CI, 1.15-3.17), GADA with DR3/non-DR4 (OR, 2.97; 95% CI, 1.55-5.71), and IA2A with DR4/non-DR3 and DR3/DR4 (OR, 3.89; 95% CI, 2.28-6.64, and OR, 3.08; 95% CI, 1.83-5.18, respectively). No association of IAA with HLA-DRB1 was found. CONCLUSION: Autoimmunity and HLA-DRB1 genotype are age-dependent biomarkers. Adult-onset autoimmune diabetes is associated with lower genetic risk and lower immune response to pancreatic islet cells compared with early-onset diabetes.


Assuntos
Autoanticorpos , Diabetes Mellitus Tipo 1 , Diabetes Mellitus Tipo 2 , Cadeias HLA-DRB1 , Adolescente , Adulto , Criança , Humanos , Adulto Jovem , Autoanticorpos/genética , Autoanticorpos/imunologia , Biomarcadores/metabolismo , Diabetes Mellitus Tipo 1/genética , Diabetes Mellitus Tipo 1/imunologia , Diabetes Mellitus Tipo 2/genética , Diabetes Mellitus Tipo 2/imunologia , Genótipo , Glutamato Descarboxilase , Antígeno HLA-DR4/genética , Cadeias HLA-DRB1/genética , Hormônios Pancreáticos , Estudos Retrospectivos , Lactente , Pré-Escolar , Pessoa de Meia-Idade , Idoso
4.
Sci Rep ; 11(1): 3016, 2021 02 04.
Artigo em Inglês | MEDLINE | ID: mdl-33542348

RESUMO

The aim of this study was to estimate the incidence of diabetes mellitus in the Basque Country and the risk factors involved in the disease by reassessing an adult population after 7 years of follow-up. In the previous prevalence study, 847 people older than 18 years were randomly selected from all over the Basque Country and were invited to answer a medical questionnaire, followed by a physical examination and an oral glucose tolerance test. In the reassessment, the same variables were collected and the resulting cohort comprised 517 individuals of whom 43 had diabetes at baseline. The cumulative incidence of diabetes was 4.64% in 7 years and the raw incidence rate was 6.56 cases/1000 person-years (95%CI: 4.11-9.93). Among the incident cases, 59% were undiagnosed. The most strongly associated markers by univariate analyses were age > 60 years, dyslipidaemia, prediabetes and insulin resistance. We also found association with hypertension, obesity, family history of diabetes and low education level. Multivariate analysis adjusted for age and sex showed that a set of risk factors assessed together (dyslipidaemia, waist-to-hip-ratio and family history of diabetes) had great predictive value (AUC-ROC = 0.899, 95%CI: 0.846-0.953, p = 0.942), which suggests the need for early intervention before the onset of prediabetes.


Assuntos
Doenças Cardiovasculares/epidemiologia , Diabetes Mellitus/epidemiologia , Hipertensão/epidemiologia , Obesidade/epidemiologia , Estado Pré-Diabético/epidemiologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Glicemia , Doenças Cardiovasculares/complicações , Doenças Cardiovasculares/genética , Doenças Cardiovasculares/patologia , Complicações do Diabetes/complicações , Complicações do Diabetes/epidemiologia , Complicações do Diabetes/genética , Complicações do Diabetes/patologia , Diabetes Mellitus/genética , Diabetes Mellitus/patologia , Feminino , Teste de Tolerância a Glucose , Humanos , Hipertensão/complicações , Hipertensão/genética , Hipertensão/patologia , Resistência à Insulina/genética , Masculino , Pessoa de Meia-Idade , Obesidade/complicações , Obesidade/genética , Obesidade/patologia , Estado Pré-Diabético/complicações , Estado Pré-Diabético/genética , Estado Pré-Diabético/patologia , Fatores de Risco , Espanha/epidemiologia , Relação Cintura-Quadril , Adulto Jovem
5.
PLoS One ; 12(12): e0189153, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29228058

RESUMO

AIMS/HYPOTHESIS: Failure in glucose response to insulin is a common pathology associated with obesity. In this study, we analyzed the genome wide DNA methylation profile of visceral adipose tissue (VAT) samples in a population of individuals with obesity and assessed whether differential methylation profiles are associated with the presence of type 2 diabetes (T2D). METHODS: More than 485,000 CpG genome sites from VAT samples from women with obesity undergoing gastric bypass (n = 18), and classified as suffering from type 2 diabetes (T2D) or not (no type 2 diabetes, NT2D), were analyzed using DNA methylation arrays. RESULTS: We found significant differential methylation between T2D and NT2D samples in 24 CpGs that map with sixteen genes, one of which, HOOK2, demonstrated a significant correlation between differentially hypermethylated regions on the gene body and the presence of type 2 diabetes. This was validated by pyrosequencing in a population of 91 samples from both males and females with obesity. Furthermore, when these results were analyzed by gender, female T2D samples were found hypermethylated at the cg04657146-region and the cg 11738485-region of HOOK2 gene, whilst, interestingly, male samples were found hypomethylated in this latter region. CONCLUSION: The differential methylation profile of the HOOK2 gene in individuals with T2D and obesity might be related to the attendant T2D, but further studies are required to identify the potential role of HOOK2 gene in T2D disease. The finding of gender differences in T2D methylation of HOOK2 also warrants further investigation.


Assuntos
Tecido Adiposo/metabolismo , Metilação de DNA , Diabetes Mellitus Tipo 2/genética , Proteínas Associadas aos Microtúbulos/genética , Obesidade/genética , Estudos de Coortes , Feminino , Humanos , Masculino
6.
Endocrinol Diabetes Nutr ; 64(1): 44-56, 2017 Jan.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-28440770

RESUMO

There are some well known factors involved in the etiology of thyroid cancer, including iodine deficiency, radiation exposure at early ages, or some genetic changes. However, epigenetic modulators that may contribute to development of these tumors and be helpful to for both their diagnosis and treatment have recently been discovered. The currently known changes in DNA methylation, histone modifications, and non-coding RNAs in each type of thyroid carcinoma are reviewed here.


Assuntos
Transformação Celular Neoplásica/genética , Epigênese Genética , Neoplasias da Glândula Tireoide/genética , Adenocarcinoma Folicular/genética , Animais , Carcinoma Medular/genética , Carcinoma Papilar/genética , Ensaios Clínicos como Assunto , Ilhas de CpG/genética , Metilação de DNA , DNA de Neoplasias/genética , Código das Histonas , Inibidores de Histona Desacetilases/uso terapêutico , Humanos , Modelos Genéticos , Proteínas de Neoplasias/genética , Oncogenes , Regiões Promotoras Genéticas/genética , RNA Neoplásico/genética , RNA não Traduzido/genética , Neoplasias da Glândula Tireoide/tratamento farmacológico
7.
Nutr Hosp ; 31(4): 1874-8, 2015 Apr 01.
Artigo em Espanhol | MEDLINE | ID: mdl-25795983

RESUMO

We describe the case of a 23 year old man who had undergone laparoscopic surgery in order to remove a residual mass secondary to a testicular embryonal carcinoma. 15 days after he attended the emergency department complaining about abdominal bloating and copious drainage via the two laparoscopic surgery incisions. Biochemical analysis was consistent with chylous ascites. Although this is uncommon, it is well known that there is more likely to develop chylous ascites after oncologic surgery if retroperitoneal lymph nodes dissection is performed1. We decide to start with conservative treatment (dietary modifications) but, as it is not enough, then we decide stop any oral intake and treat him with parenteral nutrition, achieving then total resolution of the ascites.


Describimos el caso de un varón de 23 años operado mediante laparoscopia de una masa residual secundaria a un carcinoma embrionario testicular. 15 días después acude al servicio de Urgencias por distensión abdominal y drenaje de líquido lechoso por las dos incisiones de la cirugía laparoscópica. Tras el análisis bioquímico del líquido que reflejaba un aumento de triglicéridos se llegó al diagnóstico de ascitis quilosa. Aunque es infrecuente, se describe que existe mayor probabilidad de ascitis quilosa después de cirugías oncológicas si se lleva a cabo la disección de ganglios linfáticos retroperitoneales1. Se decide tratamiento conservador inicialmente con modificaciones dietéticas y posteriormente con nutrición parenteral, con resolución total de la ascitis.


Assuntos
Ascite Quilosa/etiologia , Laparoscopia/efeitos adversos , Complicações Pós-Operatórias/terapia , Ascite Quilosa/terapia , Humanos , Masculino , Neoplasias Embrionárias de Células Germinativas/cirurgia , Nutrição Parenteral , Neoplasias Testiculares/cirurgia , Adulto Jovem
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