RESUMEN
BACKGROUND: Childhood obesity is one of the major challenges of public health policies. The problem of fatty liver in childhood, known as MAFLD (metabolic dysfunction-associated fatty liver disease), is of particular interest as the gold standard diagnosis technique is invasive (liver biopsy). Hence, efforts are made to discover more specific biomarkers for the MAFLD signature. Therefore, the aim of the study was to evaluate Osteonectin and Hsp27 as biomarkers for MAFLD diagnosis and to assess their links with auxological and biochemical profiles of overweight and obese pediatric subjects. METHODS: A cross-sectional study in which we (re)analyzed data from the MR PONy cohort comprising 71 pediatric subjects. Auxological data, liver ultrasonography and biochemical serum profile were recorded. Lipid-derived indices and body composition indices were calculated. Nevertheless, serum Osteonectin and Hsp27 levels were assessed using an ELISA approach. RESULTS: MAFLD prevalence was 40.8%. Higher Osteonectin levels were noted in MAFLD subjects versus non-MAFLD subjects and in dyslipidemic children regardless of their liver function status. Lipid-derived indices had good diagnostic capacity for MAFLD. CONCLUSIONS: We confirm Osteonectin as a MAFLD diagnosis biomarker in children. Also, lipid-derived indices are useful as metabolic-associated organ impairment markers in children even before the onset of obesity.
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Enfermedades Cardiovasculares , Enfermedad del Hígado Graso no Alcohólico , Obesidad Infantil , Humanos , Niño , Animales , Caballos , Osteonectina , Estudios Transversales , Obesidad Infantil/diagnóstico , Proteínas de Choque Térmico HSP27 , Enfermedad del Hígado Graso no Alcohólico/diagnóstico , Biomarcadores , LípidosRESUMEN
Cunninghamella spp. is a group of fungi belonging to the Mucorales order. Cases of fungal endocarditis are sporadic, but more frequent in immunocompromised patients. COVID-19 (SARS-CoV-2 Infection Disease 2019) infections, prematurity, deferoxamine treatment, iron overload, neutropenia, diabetes, and malignant hemopathies proved to be risk factors for mucormycosis. We present the case of a 7-year-old boy who was treated every three weeks with blood transfusion for major beta-thalassemia, receiving deferoxamine for secondary hemochromatosis. After two weeks with nonspecific respiratory and digestive symptoms, he was admitted for fever, followed by lower limb ischemia and neurological signs. Echocardiography revealed massive endocarditis affecting the mitral and tricuspid valves with embolization phenomena in the brain, lungs, kidney, spleen, and lower limbs. As a particular finding, IgG antibodies for COVID-19 were positive. Emergency cardiac surgery was performed. The mitral valve necessitated replacement with CarboMedics prosthesis. Unfortunately, the patient did not survive. Cunninghamella spp. was confirmed via the PCR analysis of vegetations. Cunninghamella endocarditis in the context of a systemic infection presented as an opportunistic infection affecting a child who had several risk factors. Mucormycosis is challenging to treat, with high mortality. Prophylactic treatment in beta-thalassemia patients with iron-chelator deprivation drugs, such as deferiprone, may help in preventing these particular fungal infections.
RESUMEN
OBJECTIVE: Analysis of the results of screening for retinopathy of prematurity (ROP) in a sample of prematurely born babies evaluated in the Institute for Mother and Child Care, between September 2002 - 31st December 2007. MATERIALS AND METHOD: A data base of premies screened for retinopathy of prematurity in our clinic and also those referred sporadically from different neonatal units from other towns (1783 babies) was set up, and this was used to analyze aspects referring to the ROP incidence, as well as outcomes of laser treatment. RESULTS: A total of 1783 preterm babies were examined, overall incidence of ROP was 55%. Gestational age (GA) and birth weight (BW) are important factors associated with an increased risk of ROP). Of the 981 premies with various stages of ROF 124 (12.6%) had GA 32 - 34 weeks and 264/981 (26,1%) had BW 1500 - 2000g. 272/1783 (15.2%) had severe ROP which required laser photocoagulation. Favourable outcomes of laser photocoagulation was obtained in 86.7% of the total sample, with significant differences between those with zone II ROP vs those with zone I ROP (93.3% vs 76.9%, p = 0.002). CONCLUSIONS: ROP incidence in Romania is, for the time being, much higher than that reported in the developed countries. We believe that, at present, in our country the ROP inclusion screening criteria should be extended to GA < or = 34 weeks and/or BW < or = 2000g. Short term results of laser photocoagulation are similar to those reported in developed countries. In order to achieve a significant reduction in childhood blindness determined by ROP the current screening and treatment programme needs to be extended to the entire country.
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Retinopatía de la Prematuridad/diagnóstico , Retinopatía de la Prematuridad/epidemiología , Peso al Nacer , Edad Gestacional , Humanos , Incidencia , Recién Nacido , Recien Nacido Prematuro , Coagulación con Láser/métodos , Tamizaje Neonatal/métodos , Retinopatía de la Prematuridad/cirugía , Estudios Retrospectivos , Factores de Riesgo , Rumanía/epidemiología , Índice de Severidad de la Enfermedad , Resultado del TratamientoRESUMEN
BACKGROUND AND AIMS: The aim of this study is to assess the lipid profile pattern of pediatric overweight and/or obese patients with Non-Alcoholic Fatty Liver Disease (NAFLD) in relation to IDF Consensus Criteria for Metabolic Syndrome (MetS). MATERIAL AND METHODS: We conducted a cross-sectional preliminary study on 45 consecutive pediatric patients. Overweight or obese children aged from 3 to 18 years were included. Standardized measurement of blood pressure and anthropometric parameters were performed. Biological evaluation included inflammatory status, lipid profile, glycemic profile, full blood count and liver function tests. Abdominal ultrasound was performed in all patients. RESULTS: Prevalence of MetS was 44.4%. A number of 21 patients (46.7%) had NAFLD. MetS patients had higher risk for NAFLD (OR = 9.5, 95% CI = 2.42-37.24). Also patients with positive familial history of type 2 diabetes had a 6.61 fold higher risk for NAFLD (OR = 6.61, 95% CI = 1.74-25.1). We performed a subgroup analysis in patients under ten years old. Patients under the age of ten which had both NAFLD and MetS met more frequently the hypertriglyceride criterion. After adjusting for age and MetS presence, triglyceride levels independently associated with NAFLD (adjusted R square = 0.46, unstandardized B coefficient = 34.51, 95% CI = 4.01-65.02, p = 0.02). CONCLUSION: NAFLD obese patients had higher prevalence of MetS, higher BMI and particular lipid profile pattern. Triglyceride levels independently associated with NAFLD after adjusting for age and MetS presence. According to our findings we suggest early triglyceride testing (even below the age of ten) in selected patients.
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Lípidos/sangre , Síndrome Metabólico/diagnóstico , Enfermedad del Hígado Graso no Alcohólico/complicaciones , Sobrepeso/sangre , Sobrepeso/complicaciones , Obesidad Infantil/sangre , Obesidad Infantil/complicaciones , Adolescente , Antropometría , Recuento de Células Sanguíneas , Glucemia/metabolismo , Niño , Preescolar , Estudios Transversales , Femenino , Humanos , Hígado/diagnóstico por imagen , Pruebas de Función Hepática , Masculino , Síndrome Metabólico/complicaciones , Enfermedad del Hígado Graso no Alcohólico/diagnóstico por imagen , Triglicéridos/sangre , UltrasonografíaRESUMEN
Echocardiography commonly represents the diagnostic clue in neonatal heart failure (HF). Congenital heart diseases are the most frequent causes of HF in this age group. Arterio-venous malformations are the most common noncardiac causes of HF. Normal cardiac structural findings on echocardiography require further investigations in order to exclude other causes of HF. We present three male patients admitted in the interval 2003-2007 with neonatal HF, systolic murmur, cardiomegaly, normal cardiac structure on echocardiography and intracranial bruit. All three cases were diagnosed with vein of Galen aneurysmal malformation (VGAM) by head ultrasound. According to age and malformation type, different presentation patterns were noticed: early neonatal intractable HF mimicking aortic coarctation, postnatal HF stabilized by drug treatment, and chronic HF in a VGAM with tendency to spontaneous regression. Both head ultrasound and cranial auscultation are mandatory in newborns or infants with no cardiac primary cause of HF.