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1.
J Diabetes Complications ; 31(1): 186-194, 2017 01.
Artículo en Inglés | MEDLINE | ID: mdl-27742550

RESUMEN

AIM: To identify the prevalence and effect of hepatopathies of different etiologies among pediatric patients with type 1 diabetes mellitus (T1DM) using transient elastography (TE) and its relation to glycemic control. METHODS: One hundred T1DM patients were studied focusing on liver functions, fasting lipid profile, hemoglobin A1c (HbA1c), hepatitis C virus (HCV), serum immunoglobulins, autoimmune antibodies; anti-nuclear antibody (ANA), anti-smooth muscle antibody (ASMA), and anti-liver kidney microsomal antibody (anti-LKM). Abdominal ultrasound was performed and TE was done for patients with HCV, positive autoimmune antibody and/or abnormal ultrasound findings. RESULTS: Thirty-one patients were found to have one or more hepatic abnormalities; clinical hepatomegaly in 8%, elevated alanine aminotransferase (ALT) in 10%, HCV in 6%, autoimmune hepatitis (AIH) in 11% (10 were positive for ASMA and 2 were positive for ANA while anti-LKM antibodies were negative) and abnormal hepatic ultrasound in 20% (12 non-alcoholic fatty liver disease, 5 AIH, 2 HCV, 1 Mauriac syndrome). Mean liver stiffness in those 31 patients was 7.0±2.1kPa (range, 3.1-11.8kPa); 24 were Metavir F0-F1, 7 were F2-F3 while none was F4. Type 1 diabetic patients with abnormal hepatic ultrasound had higher fasting blood glucose, HbA1c and total cholesterol than those with normal findings. Liver stiffness was significantly higher in patients with abnormal liver ultrasound compared with normal sonography. Liver stiffness was positively correlated to HbA1c and ALT. CONCLUSIONS: Hepatic abnormalities are prevalent in T1DM and related to poor metabolic control. TE provides a non-invasive method for detection of hepatopathy-induced fibrosis.


Asunto(s)
Diabetes Mellitus Tipo 1/complicaciones , Insuficiencia Hepática/diagnóstico por imagen , Hiperglucemia/prevención & control , Hipoglucemia/prevención & control , Hígado/diagnóstico por imagen , Adolescente , Biomarcadores/sangre , Biopsia , Estudios Transversales , Diabetes Mellitus Tipo 1/sangre , Diabetes Mellitus Tipo 1/terapia , Egipto/epidemiología , Diagnóstico por Imagen de Elasticidad , Femenino , Hemoglobina Glucada/análisis , Hepacivirus/aislamiento & purificación , Insuficiencia Hepática/complicaciones , Insuficiencia Hepática/patología , Insuficiencia Hepática/virología , Hepatitis C/complicaciones , Hepatitis C/epidemiología , Hepatitis C/patología , Hepatitis C/virología , Hepatitis Autoinmune/complicaciones , Hepatitis Autoinmune/epidemiología , Hepatitis Autoinmune/patología , Hepatitis Autoinmune/virología , Hepatomegalia/complicaciones , Hepatomegalia/diagnóstico por imagen , Hepatomegalia/epidemiología , Hepatomegalia/patología , Humanos , Incidencia , Hígado/patología , Hígado/virología , Masculino , Prevalencia , Ultrasonografía
2.
Arch Med Res ; 47(7): 541-549, 2016 10.
Artículo en Inglés | MEDLINE | ID: mdl-28262196

RESUMEN

BACKGROUND AND AIMS: Chemerin plays an important role in metabolic syndrome (MetS) including nonalcoholic fatty liver disease (NAFLD). L-carnitine (LC) may reduce plasma glucose, lipid profile, and improve liver function. The aim of the study was to assess serum chemerin in obese children with suspected NAFLD, the effect of LC on NAFLD grade, chemerin and metabolic profile. METHODS: Fifty obese children were compared to 50 controls. All were subjected to anthropometric assessment, liver function, fasting lipid profile, glucose/insulin (G/I) ratio, homeostasis model assessment (HOMA) index, serum chemerin and abdominal ultrasonography before and after LC. RESULTS: Serum chemerin was higher in cases than controls. Eighty percent of cases had NAFLD with increase in chemerin as severity of NAFLD increased. There was a decrease in frequency of NAFLD and its severity after LC therapy. CONCLUSIONS: Noninvasive monitoring of serum chemerin in obese patients with suspected NAFLD could be used to diagnose NAFLD. LC supplementation is effective in treatment of NAFLD and reducing chemerin.


Asunto(s)
Antioxidantes/uso terapéutico , Carnitina/uso terapéutico , Quimiocinas/sangre , Péptidos y Proteínas de Señalización Intercelular/sangre , Síndrome Metabólico/sangre , Enfermedad del Hígado Graso no Alcohólico/tratamiento farmacológico , Obesidad/sangre , Adolescente , Biomarcadores/sangre , Estudios de Casos y Controles , Niño , Preescolar , Femenino , Humanos , Lactante , Lípidos/sangre , Masculino , Enfermedad del Hígado Graso no Alcohólico/sangre
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