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1.
Horm Res ; 70(6): 349-56, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18953172

RESUMEN

AIM: To evaluate if insulin resistance (IR) and metabolic syndrome (MS) were associated with poor cardiovascular fitness in very obese prepubertal Italian subjects. METHODS: Children referred to the Endocrinology and Diabetes Unit of Bambino Gesù Children's Hospital underwent an OGTT with glucose and insulin assays. QUICKI, ISI and HOMA-IR were calculated. Total and HDL cholesterol, triglycerides and percentage of body fat (DEXA) were determined. Cardiovascular fitness (maximal treadmill time) was evaluated using a treadmill protocol. The MS was defined as having 3 or more of following risk factors: obesity, impaired glucose tolerance, high blood pressure, low HDL-cholesterol, high triglycerides. RESULTS: Fifty-five very obese prepubertal Italian children were enrolled in the study. Unadjusted correlation revealed maximal treadmill time negatively related to fasting insulin (r = -0.53, p < 0.0001) and HOMA-IR (r = -0.57, p < 0.0001) and positively to QUICKI (r = 0.51, p < 0.0001) and ISI (r = 0.46, p = 0.0035). These relationships remained significant when in multivariate analysis age, gender, BMI SD and body composition were accounted for (all p < 0.01). The presence of the MS was independently associated with maximal treadmill time. CONCLUSION: Poorcardiovascular fitness, IR and MS were independently related, suggesting that the relationship between fitness and insulin action develops early in life.


Asunto(s)
Sistema Cardiovascular/fisiopatología , Síndrome Metabólico/epidemiología , Obesidad Mórbida/epidemiología , Aptitud Física , Factores de Edad , Composición Corporal , Niño , HDL-Colesterol/sangre , Prueba de Esfuerzo , Femenino , Humanos , Italia/epidemiología , Masculino , Obesidad Mórbida/fisiopatología , Factores Sexuales , Triglicéridos/sangre
2.
Acta Paediatr Suppl ; 95(452): 9-13, 2006 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-16801158

RESUMEN

UNLABELLED: Human growth hormone therapy is allowed in certain clinical conditions according to national healthcare criteria. Growth hormone, however, produces a wide spectrum of effects. Linear growth is only one of the many expected results, and there are interesting possibilities to explore which could provide additional means of improving the quality of life for the ever-increasing numbers of chronic paediatric patients. CONCLUSION: In this review, we discuss the rationale for and possibility of using growth hormone therapy in some conditions not strictly related to growth hormone deficiency.


Asunto(s)
Estatura , Huesos/efectos de los fármacos , Hormona del Crecimiento/uso terapéutico , Acondroplasia/tratamiento farmacológico , Acondroplasia/fisiopatología , Hiperplasia Suprarrenal Congénita/tratamiento farmacológico , Hiperplasia Suprarrenal Congénita/fisiopatología , Artritis Juvenil/tratamiento farmacológico , Artritis Juvenil/fisiopatología , Estatura/efectos de los fármacos , Quemaduras/tratamiento farmacológico , Quemaduras/fisiopatología , Niño , Fibrosis Quística/tratamiento farmacológico , Fibrosis Quística/fisiopatología , Edad Gestacional , Trastornos del Crecimiento/tratamiento farmacológico , Hormona del Crecimiento/farmacología , Humanos , Recién Nacido , Recién Nacido Pequeño para la Edad Gestacional , Síndrome del Intestino Corto/tratamiento farmacológico , Síndrome del Intestino Corto/fisiopatología , Cicatrización de Heridas/efectos de los fármacos
3.
Hum Mutat ; 25(2): 222, 2005 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-15643618

RESUMEN

We report the molecular findings in 14 patients (12 families) with X-linked adrenoleukodystrophy (X-ALD, MIM# 300100), a well-defined peroxisomal disorder attributed to mutations in the ABCD1 gene on chromosome Xq28. With the aims of determining the spectrum of mutations and developing an efficient molecular genetic test for analysis of at-risk women whose carrier status is unknown, and to offer molecular confirmation of their status to obligate heterozygotes, regardless of their clinical status, we carried out molecular screening by setting up a denaturing high-performance liquid chromatography (DHPLC)-based protocol. We identified eleven hemizygous base changes in ABCD1, including seven new mutations (c.145underscore;146ins4, c.264C>G, c.919C>T, c.994C>T, c.1027G>A, c.1508T>C, and c.1540A>C, resulting in the p.Pro193fs, p.Cys88Trp, p.Gln307X, p.Gln332X, p.Gly343Ser, p.Leu503Pro, and p.Ser514Arg changes, respectively). Adding new variants to the repertoire of ABCD1 mutations in X-ALD, our data provide an efficient, cost-effective, and reliable DHPLC detection protocol for mutation screening of X-ALD families.


Asunto(s)
Transportadoras de Casetes de Unión a ATP/genética , Adrenoleucodistrofia/genética , Análisis Mutacional de ADN/métodos , Mutación , Miembro 1 de la Subfamilia D de Transportador de Casetes de Unión al ATP , Transportadoras de Casetes de Unión a ATP/metabolismo , Adrenoleucodistrofia/diagnóstico , Adrenoleucodistrofia/metabolismo , Cromatografía Líquida de Alta Presión/métodos , Femenino , Humanos , Italia , Masculino
4.
J Pediatr Endocrinol Metab ; 16 Suppl 2: 317-20, 2003 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-12729410

RESUMEN

We describe peculiar aspects of growth and the pubertal growth spurt in dysmorphic syndromes, focusing our attention on the accelerated pubertal growth pattern in some dysmorphic syndromes leading to short stature (DSS). A normal pubertal growth spurt was observed in other dysmorphic syndromes leading to overgrowth (ODS).


Asunto(s)
Trastornos del Crecimiento/fisiopatología , Pubertad , Estatura , Niño , Femenino , Crecimiento , Trastornos del Crecimiento/patología , Humanos , Masculino
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