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3.
An. pediatr. (2003, Ed. impr.) ; 76(5): 279-284, mayo 2012. tab, graf
Artigo em Espanhol | IBECS | ID: ibc-99358

RESUMO

Introducción y objetivos: Conocer la prevalencia de sobrepeso en pacientes pediátricos con fibrosis quística (FQ) y su importancia como factor de resistencia insulínica diabetogénica y riesgo de hipertrigliceridemia. Material y métodos: Ciento nueve pacientes con FQ (47% varones) de 5-18 años se calificaron por su índice de masa corporal (IMC): desnutridos, normales o con sobrepeso. Se determinaron colesterol, triglicéridos y proteína C reactiva (PCR), glucohemoglobina y los índices HOMA-IR y QUICKI y en la sobrecarga oral de glucosa (SOG) su índice insulinogénico e ISI composite y áreas bajo la curva (ABC) de glucosa e insulina. Resultados: Seis pacientes (5,5%) tenían sobrepeso. Su edad, distribución sexual y base genética son similares al resto; aunque la proporción de suficientes pancreáticos (3/6; 50%) es superior (p=0,003). Los trastornos glucídicos no son más frecuentes que en el resto; pero la insulina basal, HOMA-IR, y la insulina durante la SOG (pico máximo y ABC) identifican su hiperinsulinismo, diferenciándolos de los otros dos grupos. Todos los pacientes muestran en la SOG respuesta insulínica tardía, sin diferencias en los índices derivados. Conclusiones: Entre los pacientes FQ con sobrepeso no hay mayor incidencia de trastornos glucídicos pero sí de hiperinsulinismo y resistencia insulínica, con el consiguiente riesgo añadido a la tendencia diabetogénica inherente a estos pacientes(AU)


Aim: To determine the prevalence of overweight in paediatric patients with cystic fibrosis (CF) and to analyse its role as diabetogenic insulin resistance factor and risk of hypertriglyceridaemia. Patients and methods: A total of 109 CF patients (47% males) between 5 and 18 years were divided into 3 groups according to body mass index (BMI): underweight, normal and overweight. Total cholesterol, triglycerides, C- reactive protein (CRP), glycosylated haemoglobin, HOMA-IR and QUICKI index were determined. Insulinogenic index, ISI composite and areas under the curve (AUC) for glucose and insulin were obtained by oral glucose tolerance test (OGTT). Results: Six patients (5.5%) were overweight. All groups had similar distribution by age, sex and CFTR mutation, although the proportion of pancreatic sufficient (3/6, 50%) was higher in overweight patients (P=.003). The prevalence of glycaemic disorders was similar between groups. Baseline insulin, HOMA-IR, and insulin during the OGTT (peak and AUC) were higher in overweight patients. All patients had a delayed insulin response in OGTT. Conclusions: Overweight CF patients do not have a higher incidence of glycaemic disorders, but their hyperinsulinism and insulin resistance may be additional diabetogenic risk factors(AU)


Assuntos
Humanos , Masculino , Feminino , Pré-Escolar , Criança , Adolescente , Resistência à Insulina , Fibrose Cística/complicações , Obesidade/complicações , Índice de Massa Corporal , Hiperinsulinismo/epidemiologia , Estudos Retrospectivos
4.
An Pediatr (Barc) ; 76(5): 279-84, 2012 May.
Artigo em Espanhol | MEDLINE | ID: mdl-22227349

RESUMO

AIM: To determine the prevalence of overweight in paediatric patients with cystic fibrosis (CF) and to analyse its role as diabetogenic insulin resistance factor and risk of hypertriglyceridaemia. PATIENTS AND METHODS: A total of 109 CF patients (47% males) between 5 and 18 years were divided into 3 groups according to body mass index (BMI): underweight, normal and overweight. Total cholesterol, triglycerides, C- reactive protein (CRP), glycosylated haemoglobin, HOMA-IR and QUICKI index were determined. Insulinogenic index, ISI composite and areas under the curve (AUC) for glucose and insulin were obtained by oral glucose tolerance test (OGTT). RESULTS: Six patients (5.5%) were overweight. All groups had similar distribution by age, sex and CFTR mutation, although the proportion of pancreatic sufficient (3/6, 50%) was higher in overweight patients (P=.003). The prevalence of glycaemic disorders was similar between groups. Baseline insulin, HOMA-IR, and insulin during the OGTT (peak and AUC) were higher in overweight patients. All patients had a delayed insulin response in OGTT. CONCLUSIONS: Overweight CF patients do not have a higher incidence of glycaemic disorders, but their hyperinsulinism and insulin resistance may be additional diabetogenic risk factors.


Assuntos
Fibrose Cística/complicações , Fibrose Cística/metabolismo , Resistência à Insulina , Sobrepeso/etiologia , Sobrepeso/metabolismo , Adolescente , Criança , Pré-Escolar , Estudos Transversais , Feminino , Humanos , Hipertrigliceridemia/complicações , Hipertrigliceridemia/metabolismo , Masculino , Sobrepeso/epidemiologia , Prevalência , Fatores de Risco
12.
An Esp Pediatr ; 38(5): 390-3, 1993 May.
Artigo em Espanhol | MEDLINE | ID: mdl-8503579

RESUMO

We have determined the blood lead levels of 1,242 children, from newborn to 14 years old, and 79 young mothers in a period of 10 months in Asturias (Spain). All of them were selected at random among those who consulted one of the three main hospitals in Asturias, but none were diagnosed as lead poisoning. We have found a mean blood lead level of 22.11 micrograms/dl; 23.55% had high levels (= 25 micrograms/dl). Sex was not significantly associated with blood lead levels either in the whole sample or in different age groups. Blood lead level increases rapidly from birth (19.3 micrograms/dl) to the age of one year (23.3 gamma/dl), fluctuating around this level until the age of 7. Then it declines with age until adolescence (19.6 micrograms/dl). From October (25.5 micrograms/dl) to July (20.9 micrograms/dl) the decrease in lead blood level was statistically significant. No difference has been found between urban and rural population. The decree of urbanization has not been found significant. The mean blood lead level in the mothers was 20.5 micrograms/dl.


Assuntos
Intoxicação por Chumbo/epidemiologia , Adolescente , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Chumbo/sangue , Intoxicação por Chumbo/sangue , Masculino , Mães , População Rural , Espanha/epidemiologia , População Urbana
13.
An Esp Pediatr ; 37(2): 118-20, 1992 Aug.
Artigo em Espanhol | MEDLINE | ID: mdl-1416535

RESUMO

Our objective was to investigate the pancreatic ultrasonographic size in diabetic children in order to compare in with a healthy population of children and to relate it to the characteristics of their disease. Fifty-four children (age 8.59 +/- 3.38 years) with insulin-dependent diabetes mellitus of short evolution and 23 healthy children of similar ages and sex were investigated. Anteroposterior measurement of pancreatic head, body and tail with real time ultrasonography were performed searching for a relationship of these factors with the acinar and residual insular function. The pancreatic measurements in the diabetic patients were sizeable smaller than in the healthy children with no relationship to age, height, weight or body surface. There were no differences in the pancreatic measurements in relationship to the evolution time or residual insular function in the diabetics.


Assuntos
Diabetes Mellitus Tipo 1/fisiopatologia , Pâncreas/diagnóstico por imagem , Estatura , Superfície Corporal , Peso Corporal , Criança , Pré-Escolar , Diabetes Mellitus Tipo 1/diagnóstico por imagem , Feminino , Humanos , Masculino , Pâncreas/anatomia & histologia , Pâncreas/fisiopatologia , Ultrassonografia
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