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1.
J. pediatr. (Rio J.) ; 89(1): 56-63, jan.-fev. 2013. tab
Article in Portuguese | LILACS | ID: lil-668826

ABSTRACT

OBJETIVO: O presente estudo objetivou identificar a prevalência do fenótipo cintura hipertrigliceridêmica (CHT) e avaliar sua associação com alterações metabólicas em adolescentes de baixa condição econômica. MÉTODO: Estudo transversal com amostra probabilística de 1.076 adolescentes entre 11 e 17 anos, de ambos os sexos, estudantes de escolas públicas. Os participantes foram submetidos à avaliação antropométrica (peso, altura e circunferência da cintura) e à dosagem dos níveis de colesterol total, LDL-C, HDL-C, colesterol não HDL, triglicérides (TG) e glicemia de jejum. Foram obtidas informações referentes às condições econômicas das famílias dos participantes.O fenótipo CHT foi definido pela presença simultânea da circunferência da cintura aumentada (> percentil 90 por idade e sexo) e dos níveis séricos de triglicérides elevados (> 100 mg/dL). A análise de regressão logística foi utilizada para avaliação das associações de interesse. RESULTADOS: A prevalência do fenótipo CHT foi de 7,2% entre os adolescentes, sendo mais elevada na presença de obesidade (63,4%), do colesterol não HDL (16,6%) e do LDL-C (13,7%) altos. A análise bivariada indicou que, das variáveis metabólicas, apenas a glicemia não se associou ao fenótipo CHT. A análise multivariada, ajustada por sexo e idade, indicou que o fenótipo CHT se associou positivamente com o colesterol não HDL alto (odds ratio, 7,0; IC 95% 3,9-12,6) e com o HDL-C baixo (odds ratio, 2,7; IC 95%, 1,5-4,8). CONCLUSÕES: Este estudo mostrou que o fenótipo CHT se associou com um perfil lipídico aterogênico e sugere esse fenótipo como uma ferramenta de screening que pode ser utilizada para identificar adolescentes com alterações metabólicas.


OBJECTIVE: This study aimed to identify the prevalence of hypertriglyceridemic waist (HTW) phenotype, and to evaluate its association with metabolic abnormalities in adolescents of low socioeconomic status. METHOD: This was a cross-sectional study with a random sample of 1,076 adolescents between 11 and 17 years, of both genders, from public schools. The participants underwent anthropometric measurements (weight, height, and waist circumference), and levels of total cholesterol, low-density-lipoprotein cholesterol (LDL-C), high-density-lipoprotein cholesterol (HDL-C), non-HDL cholesterol triglyceride (TG), and fasting glucose were measured. Information regarding the socioeconomic status of the participants' families was obtained. The HTW phenotype was defined by the simultaneous presence of increased waist circumference (> 90th percentile for age and gender) and serum triglyceride levels (> 100 mg/dL). A logistic regression analysis was used to evaluate the associations of interest. RESULTS: The prevalence of HTW phenotype was 7.2% among the adolescents, being higher in the presence of obesity (63.4%) and high levels of non-HDL cholesterol (16.6%) and LDL-C (13.7%). The bivariate analysis indicated that, of the metabolic variables, only blood glucose was not associated with the HTW phenotype. Multivariate analysis adjusted for age and gender indicated that the HTW phenotype was positively associated with high non-HDL cholesterol (odds ratio: 7.0; 95% CI: 3.9-12.6) and low HDL-C levels (odds ratio: 2.7; 95% CI: 1.5-4.8). CONCLUSIONS: This study demonstrated that the HTW phenotype was associated with an atherogenic lipid profile, and this phenotype is suggested as a screening tool to identify adolescents with metabolic alterations.


Subject(s)
Adolescent , Child , Female , Humans , Male , Hypertriglyceridemia/epidemiology , Metabolic Syndrome/epidemiology , Obesity, Abdominal/epidemiology , Triglycerides/metabolism , Waist Circumference , Body Mass Index , Blood Glucose/analysis , Cross-Sectional Studies , Cholesterol/blood , Hypertriglyceridemia/diagnosis , Hypertriglyceridemia/metabolism , Lipoproteins, HDL/blood , Mass Screening , Metabolic Syndrome/genetics , Obesity, Abdominal/diagnosis , Phenotype , Prevalence , Risk Factors , Sex Factors , Socioeconomic Factors , Triglycerides/blood
3.
Braz. j. med. biol. res ; 40(3): 323-331, Mar. 2007. tab, graf
Article in English | LILACS | ID: lil-441760

ABSTRACT

The metabolic effects of carbohydrate supplementation in mice have not been extensively studied. In rats, glucose- and fructose-rich diets induce hypertriacylglycerolemia. In the present study, we compared the metabolic responses to two monosaccharide supplementations in two murine models. Adult male Wistar rats (N = 80) and C57BL/6 mice (N = 60), after 3 weeks on a standardized diet, were submitted to dietary supplementation by gavage with glucose (G) or fructose (F) solutions (500 g/L), 8 g/kg body weight for 21 days. Glycemia was significantly higher in rats after fructose treatment (F: 7.9 vs 9.3 mM) and in mice (G: 6.5 vs 10 and F: 6.6 vs 8.9 mM) after both carbohydrate treatments. Triacylglycerolemia increased significantly 1.5 times in rats after G or F supplementation. Total cholesterol did not change with G treatment in rats, but did decrease after F supplementation (1.5 vs 1.4 mM, P < 0.05). Both supplementations in rats induced insulin resistance, as suggested by the higher Homeostasis Model Assessment Index. In contrast, mice showed significant decreases in triacylglycerol (G: 1.8 vs 1.4 and F: 1.9 vs 1.4 mM, P < 0.01) and total cholesterol levels (G and F: 2.7 vs 2.5 mM, P < 0.05) after both monosaccharide supplementations. Wistar rats and C57BL/6 mice, although belonging to the same family (Muridae), presented opposite responses to glucose and fructose supplementation regarding serum triacylglycerol, free fatty acids, and insulin levels after monosaccharide treatment. Thus, while Wistar rats developed features of plurimetabolic syndrome, C57BL/6 mice presented changes in serum biochemical profile considered to be healthier for the cardiovascular system.


Subject(s)
Animals , Male , Mice , Rats , Dietary Carbohydrates/adverse effects , Fructose/administration & dosage , Glucose/administration & dosage , Hypertriglyceridemia/etiology , Insulin Resistance , Cholesterol/blood , Disease Models, Animal , Dietary Supplements/adverse effects , Fructose/adverse effects , Glucose/adverse effects , Hypertriglyceridemia/metabolism , Rats, Wistar , Triglycerides/blood
4.
Rev. cuba. med. gen. integr ; 13(4): 372-7, jul.-ago. 1997. graf
Article in Spanish | LILACS | ID: lil-223003

ABSTRACT

La hipetrigliceridemia es la dislipidemia más frecuente en el diabético, y la hipercolesterolemia es más frecuente que en las personas no diabéticas. Además, en el diabético se presentan alteraciones estructurales de las lipoproteínas que alteran la función plaquetaria y el sistema inmunológico, todo lo cual tiene en su conjunto un efecto que favorece el proceso aterogénico


Subject(s)
Fatty Acids/metabolism , Diabetes Mellitus, Type 1/metabolism , Diabetes Mellitus, Type 2/metabolism , Liver/metabolism , Hypercholesterolemia/metabolism , Hypertriglyceridemia/metabolism , Insulin/deficiency , Lipoproteins, VLDL/metabolism
6.
Arq. bras. cardiol ; 56(5): 407-412, maio 1991. tab
Article in Portuguese | LILACS | ID: lil-107861

ABSTRACT

Purpose - To compare the effects of lovastatin and gemfibrozil in patients with primary hyperlipidemias. Patients and Methods - Forty patients with cholesterolemia over 200 mgldl and triglyceridemia not higher than 350 mp/dl, excluded secondary causes, were selected. Twenty patients received lovastatin and 20 gemfibrozil. In order to establish the lipid profile, blood samples were taken after 2 months without medication, after 4 weeks of diet and placebo and after 6 and 12 weeks active treatment. Biochemic profile was determined before and after the treatment with active drug. Results - Thirty nine patients completed the study. Total and LDL-cholesterol were significantly reduced (p < 0.05) by both drugs but lovastatin had greater effect. Only gemfibrozil reduced triglycerides significantly. Neither drug had significant effects on HDL-cholesterol. The tolerance was satisfactory; only one patient (using gemfibrozil) needed to stop the treatment due to gastrointestinal side effects. The biochemic profïle did not present any significant alteration. Conclusion - Both drugs produced useful effects on the lipid profile. Lovastatin produced greater reductions of total and LDL-cholesterol, while gemfibrozil was more active reducing triglycerides. Neither drug changed significantly the HDL-cholesterol


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Lovastatin/therapeutic use , Gemfibrozil/therapeutic use , Hyperlipidemias/drug therapy , Lovastatin/metabolism , Gemfibrozil/metabolism , Hypertriglyceridemia/metabolism , Hypertriglyceridemia/drug therapy , Cholesterol/blood , Hypercholesterolemia/metabolism , Hypercholesterolemia/drug therapy , Hyperlipidemias/metabolism , Cholesterol, HDL/blood , Cholesterol, LDL/blood , Analysis of Variance , Triglycerides/blood
7.
Acta bioquím. clín. latinoam ; 24(2): 147-58, jun. 1990. ilus
Article in Spanish | LILACS | ID: lil-95763

ABSTRACT

En este trabajo se determinaron los valores promedio, desviación estándar y percentilos para el cociente Apo B/C-HDL y, por otra parte, se analizó el efecto de las lipoproteínas ricas en triglicéridos sobre la relación entre C-LDL y Apo B, determinada por electroinmunodifusión en suero total. Se estudiaron 74 individuos de 20 y más años, aparentemente sanos. Para Apo B/C-HDL se obtuvo un valor medio de 2,16+0,78. El percentilo 50 fue 2,00, el percentilo 75 fue 2,60 y el percentilo 95 fue 3,60. Los individuos con Apo B/C-HDL>3,60 estarían en riesgo respecto de la aterosclerosis coronaria. La relación entre C-LDL y Apo B, es importante para la detección de sujetos con hiperapo B, la cual está fuertemente relacionada con la aterosclerosis coronaria. Utilizando los triglicéridos como estimadores de masa de las lipoproteínas ricas en triglicéridos, se halló que mientras TG<160 mg/dl la correlación entre Apo B y C-LDL fue r= +0,65,P <0,001. Un 86% de los pacientes con C-LDL entre 80 y 165 mg/dl tenían Apo B entre 55 y 120 mg/dl, mientras que un 12% tenían Apo B por encima de 120 mg/dl. En estos pacientes se puede suponer la presencia de hiperapo B en estas condiciones experimentales. Cuando TG>160 mg/dl, la correlación entre Apo B y C-LDL disminuye a r=+0,39,P<0,1. Un 21% de los pacientes con C-LDL entre 80 y 165 mg/dl tenían Apo B entre 55 y 120 mg/dl, pero un 79% tenían Apo B por encima de 120 mg/dl. En estas condiciones experimentales no se podrían discriminar los pacientes con hiperapo B.


Subject(s)
Humans , Male , Female , Apolipoproteins B/blood , Apolipoproteins C/blood , Cholesterol, LDL , Coronary Disease/physiopathology , Immunodiffusion , Lipoproteins, HDL/blood , Risk Factors , Apolipoproteins B/biosynthesis , Apolipoproteins B/metabolism , Apolipoproteins C/biosynthesis , Apolipoproteins C/metabolism , Cholesterol, LDL/biosynthesis , Cholesterol, LDL/metabolism , Hypertriglyceridemia/diagnosis , Hypertriglyceridemia/metabolism , Lipoproteins, HDL/biosynthesis , Lipoproteins, HDL/metabolism
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