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1.
Front Microbiol ; 9: 1230, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29946306

RESUMO

Gut microbiota is closely related to acute infectious diarrhea, one of the leading causes of mortality and morbidity in children worldwide. Understanding the dynamics of the recovery from this disease is of clinical interest. This work aims to correlate the dynamics of gut microbiota with the evolution of children who were suffering from acute infectious diarrhea caused by a rotavirus, and their recovery after the administration of a probiotic, Saccharomyces boulardii CNCM I-745. The experiment involved 10 children with acute infectious diarrhea caused by a rotavirus, and six healthy children, all aged between 3 and 4 years. The children who suffered the rotavirus infection received S. boulardii CNCM I-745 twice daily for the first 5 days of the experiment. Fecal samples were collected from each participant at 0, 3, 5, 10, and 30 days after probiotic administration. Microbial composition was characterized by 16S rRNA gene sequencing. Alpha and beta diversity were calculated, along with dynamical analysis based on Taylor's law to assess the temporal stability of the microbiota. All children infected with the rotavirus stopped having diarrhea at day 3 after the intervention. We observed low alpha diversities in the first 5 days (p-value < 0.05, Wilcoxon test), larger at 10 and 30 days after probiotic treatment. Canonical correspondence analysis (CCA) showed differences in the gut microbiota of healthy children and of those who suffered from acute diarrhea in the first days (p-value < 0.05, ADONIS test), but not in the last days of the experiment. Temporal variability was larger in children infected with the rotavirus than in healthy ones. In particular, Gammaproteobacteria class was found to be abundant in children with acute diarrhea. We identified the microbiota transition from a diseased state to a healthy one with time, whose characterization may lead to relevant clinical data. This work highlights the importance of using time series for the study of dysbiosis related to diarrhea.

2.
J Pak Med Assoc ; 67(5): 799-801, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28507377

RESUMO

Congenital nephrotic syndrome is a term used to describe a condition in babies who develop severe proteinuria and hypoalbuminaemia within their first three months of life. They generally have oedema and ascites from birth which, because of increased intra-abdominal pressure, can result in an umbilical hernia. The report presents a five-month old infant with congenital nephrotic syndrome who had spontaneous umbilical hernia rupture with evisceration. The approach to umbilical hernias is usually conservative, but in selected cases elective surgery may be indicated.


Assuntos
Hérnia Umbilical/cirurgia , Síndrome Nefrótica/complicações , Ruptura Espontânea/cirurgia , Colo , Edema/etiologia , Feminino , Hérnia Umbilical/etiologia , Humanos , Lactente , Intestino Delgado
3.
Int J Immunopathol Pharmacol ; 29(4): 626-631, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27272162

RESUMO

BACKGROUND: Asthma is a chronic inflammatory disorder of the airways which results in chronic hypoxia. Chronic hypoxia and inflammation can affect renal tubular function. OBJECTIVES: The aim of this study was to investigate renal tubular function and early kidney injury molecules such as urinary N-acetyl-betaglucosaminidase (NAG) and kidney injury molecule-1 (KIM-1) excretion in children with asthma. METHODS: Enrolled in the study were 73 children diagnosed with asthma and 65 healthy age- and gender-matched control subjects. Urine pH, sodium, phosphorus, potassium, microalbumin, creatinine, NAG, KIM-1, and serum creatinine, sodium, phosphorus were evaluated. The diagnosis of asthma and classification of mild or moderate were done according to the Global Initiative for Asthma guidelines. RESULTS: Serum sodium, phosphorus, creatinine, and urinary microalbumin were within normal levels in the both groups. Urinary pH, sodium, potassium, phosphorus, microalbumin, and KIM-1 excretions were similar between the control and study groups. Tubular phosphorus reabsorption was within normal limits in two groups. Urine NAG was elevated in the study group (P = 0.001). Urinary KIM-1 and NAG levels were positively correlated (r = 0.837; P = 0.001). When children with mild and moderate asthma were compared, all of the parameters were similar (P >0.05). CONCLUSIONS: This study showed that chronic asthma can lead to subtle renal impacts. We suggest that in children with asthma, urinary NAG level is a more valuable parameter to show degree of renal tubular injury than markers such as microalbumin and KIM-1. Chronic hypoxy and inflammation probably contributes to these subclinical renal effects.


Assuntos
Acetilglucosaminidase/urina , Asma/fisiopatologia , Asma/urina , Receptor Celular 1 do Vírus da Hepatite A/metabolismo , Nefropatias/urina , Túbulos Renais/metabolismo , Túbulos Renais/fisiopatologia , Albuminas/metabolismo , Asma/sangue , Asma/metabolismo , Biomarcadores/sangue , Biomarcadores/metabolismo , Biomarcadores/urina , Estudos de Casos e Controles , Criança , Creatinina/sangue , Feminino , Humanos , Concentração de Íons de Hidrogênio , Nefropatias/sangue , Nefropatias/metabolismo , Nefropatias/fisiopatologia , Masculino , Fósforo/sangue , Fósforo/urina , Potássio/urina , Sódio/sangue , Sódio/urina
4.
Ren Fail ; 38(4): 545-51, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26908058

RESUMO

Polymorphisms in the vitamin D receptor (VDR) gene have recently been reported to be associated with urinary calculi in pediatric and adult cases, but no studies have looked at the youngest period of life. The purpose of this study was to investigate the role of VDR gene polymorphisms in infantile urolithiasis in a Turkish population. We compared a study group of 104 infants (55 girls and 49 boys, mean age 6.94 ± 3.81 months) with a control group of 96 infants (51 girls and 45 boys, mean age 7.51 ± 3.23) to evaluate their demographics and metabolic risk factors. PCR-based restriction analysis of the polymorphisms on the VDR gene (BsmI and TaqI) showed statistically significant differences between study and control groups (p = 0.001 and 0.043, respectively). In addition, the prevalence of the BsmI genotype was significantly different between the hypercalciuric and normocalciuric stone formers (p = 0.007). Allelic frequencies were similar between the urolithiasis and control groups (p > 0.05). The B allele of BsmI and the A allele of ApaI were more prevalent in the hypercalciuric stone formers than in the normocalciuric stone formers (p = 0.018 vs.0.036, respectively). These results suggest that the BsmI and TaqI VDR genotypes could be candidate genes leading to infantile urolithiasis.


Assuntos
Polimorfismo Genético/genética , Receptores de Calcitriol/genética , Urolitíase/genética , Feminino , Genótipo , Humanos , Lactente , Masculino , Turquia
5.
Ital J Pediatr ; 41: 73, 2015 Oct 06.
Artigo em Inglês | MEDLINE | ID: mdl-26444536

RESUMO

BACKGROUND: This study aims to evaluate the children with chronic cough and to analyze their etiological factors according to the age groups. METHOD: Five hundred sixty-three children with chronic cough were included. The last diagnosis were established and were also emphasized according to the age groups. RESULTS: The mean age was 5.4 ± 3.8 years (2-months-17-years) and 52 % of them were male. The most common final diagnosis from all the participants were: asthma (24.9 %), asthma-like symptoms (19 %), protracted bacterial bronchitis (PBB) (11.9 %), and upper airway cough syndrome (9.1 %). However, psychogenic cough was the second most common diagnosis in the subjects over 6 years of age. CONCLUSION: Asthma and asthma-like symptoms were the most common diagnosis in children. Different age groups in children may have a different order of frequencies. Psychogenic cough should be thought of in the common causes especially in older children.


Assuntos
Algoritmos , Tosse/etiologia , Adolescente , Criança , Pré-Escolar , Doença Crônica , Tosse/epidemiologia , Feminino , Humanos , Lactente , Masculino , Turquia/epidemiologia
6.
Int J Biometeorol ; 59(11): 1685-90, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25732843

RESUMO

Variability in children's allergic sensitization has been detected not only among different countries but also among cities within the same nation but yet different climatic areas. The aim of this study was to investigate the sensitization pattern of asthmatic children who lived in different altitude areas: the two largest Turkish cities, Istanbul (sea level) and Erzurum (high altitude). Five hundred and twelve asthmatic children (6-15 years old) from Istanbul (western Turkey, at sea level) and 609 from Erzurum (eastern Turkey, at an altitude of 1800 m) were included in the study. All participants underwent skin testing with common inhalant allergens, spirometry, total IgE level, and clinical examination. The positive sensitization ratio to aeroallergens in children with asthma living at sea level was statistically higher than that in children living in the high altitude group [p = 0.001, OR (odds ratio) 4.9 (confidence interval (CI) 3.67-6.459)]. However, pollen sensitization in asthmatic children living in high altitudes was significantly higher than that in children living at sea level [p = 0.00, OR 2.6 (CI 1.79-3.87)]. Children with asthma who live at high altitudes are characterized by higher pollen but lower mite sensitization rates than those living at sea level in Turkey. Different climatic conditions and altitudes may affect aeroallergen sensitization in children with asthma.


Assuntos
Alérgenos/imunologia , Asma/imunologia , Adolescente , Altitude , Animais , Asma/sangue , Asma/epidemiologia , Asma/fisiopatologia , Criança , Cidades/epidemiologia , Feminino , Volume Expiratório Forçado , Humanos , Imunoglobulina E/sangue , Imunoglobulina E/imunologia , Masculino , Pólen/imunologia , Pyroglyphidae/imunologia , Testes Cutâneos , Turquia/epidemiologia
7.
J Pediatr Endocrinol Metab ; 28(1-2): 183-8, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25153579

RESUMO

OBJECTIVE: We aim to evaluate how vitamin D-containing supplements affect the vitamin D status of children 1-3 years old and to assess the variation of the vitamin D concentrations across different seasons. METHODS-MATERIAL: This retrospective study included a review of medical reports of 1035 patients (aged 1-3 years) who presented to our hospital between October 2011 and October 2013. The children were divided into 3 groups: Group 1: those supplemented with vitamin D3 (400 IU/day), Group 2: those supplemented with multivitamins, which included 200-400 IU/day of vitamin D2 or D3, and Group 3, the controls: those not supplemented with vitamin D. The groups were compared as to their biochemical findings and variation of vitamin D status with over four seasons. RESULTS: Gender distribution was not statistically different between the three groups (p=0.38). The children who had taken vitamin D-containing supplements had significantly higher vitamin D levels compared with the children who were given no vitamin D supplementation (p<0.001). Children with no vitamin D supplementation had significantly lower calcium and phosphorus levels compared with Groups 1 and 2. Vitamin D levels were affected by vitamin D supplementation (f=16.125, p<0.001) but not by season (f=0.699, p=0.650). CONCLUSION: The children aged 1-3 years who did not receive vitamin D-containing supplements had insufficient vitamin D and low levels of calcium and phosphorus. Vitamin D levels were affected by vitamin D supplementation but not by season.


Assuntos
Osso e Ossos/efeitos dos fármacos , Desenvolvimento Infantil/efeitos dos fármacos , Suplementos Nutricionais , Vitamina D/administração & dosagem , Osso e Ossos/fisiologia , Pré-Escolar , Feminino , Saúde , Nível de Saúde , Humanos , Lactente , Masculino , Admissão do Paciente/estatística & dados numéricos , Estudos Retrospectivos , Estações do Ano , Vitamina D/sangue , Vitaminas/administração & dosagem
8.
Brain Dev ; 37(6): 612-7, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25270981

RESUMO

AIM: SSPE is a rare progressive, invariably fatal long-term complication of measles infection. In this study, we assessed the demographic and prognostic characteristics of 64 consecutive SSPE patients diagnosed at a tertiary center. METHODS: The study had a retrospective design; data were obtained from patient records. RESULTS: The study includes 64 patients diagnosed with SSPE. There was history of consanguineous marriage in 27 (42.2%) patients. The average patient lifespan was 3.8years (45days-12years). The average patient age at diagnosis was 12.3 (range, 5-17)years. A statistically significant correlation was found between the age at diagnosis and lifespan (p=0.002). A statistically significant correlation was found between the incubation period and patient lifespan (p<0.001). No significant correlation was found between duration in the intensive care unit and lifespan (p=0.122). Routine physical therapy had no significant impact on the average lifespan (p=0.619). No significant difference was found between the vaccination dose and lifespan (p=0.651). CONCLUSIONS: High frequency of parental consanguinity in SSPE patients need to be evaluated as there might a genetic influence. Physical therapy and supportive treatments seems to have no affect on lifespan in SSPE patients. The age at diagnosis and incubation period might have an affect on prognosis and lifespan.


Assuntos
Panencefalite Esclerosante Subaguda/diagnóstico , Panencefalite Esclerosante Subaguda/epidemiologia , Adolescente , Criança , Pré-Escolar , Demografia , Feminino , Humanos , Masculino , Prognóstico , Panencefalite Esclerosante Subaguda/mortalidade , Turquia/epidemiologia
9.
Pediatr Nephrol ; 30(1): 139-44, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24801174

RESUMO

BACKGROUND: Obesity is an important health issue, the prevalence of which is increasing in childhood. The aim of this study was to examine urinary renal injury markers in order to determine the renal effect of obesity and its comorbidities in a pediatric population. METHODS: Eighty-four obese children and 64 healthy control subjects were enrolled in the study. We checked their urine using N-acetyl-beta-D-glucosaminidase (NAG), neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecule-1 (KIM-1), and microalbumin as renal injury markers. Associations of renal damage markers with hypertension, an impaired glucose tolerance test, and insulin resistance were assessed. RESULTS: Obese individuals had higher urinary NAG and KIM-1 values compared to those of healthy controls (p = 0.027, p = 0.026). There was no difference in urinary NGAL between obese and lean subjects (p = 0.885). Urinary renal injury markers were not statistically different in the obese group when checked for impaired glucose tolerance, insulin resistance, and hypertension (p > 0.05). CONCLUSIONS: This study shows that urinary NAG and KIM-1 could be used as a screening method for detection of early renal damage in obese children.


Assuntos
Acetilglucosaminidase/urina , Biomarcadores/urina , Nefropatias/urina , Glicoproteínas de Membrana/urina , Obesidade/complicações , Proteínas de Fase Aguda/urina , Adolescente , Criança , Pré-Escolar , Estudos Transversais , Ensaio de Imunoadsorção Enzimática , Feminino , Receptor Celular 1 do Vírus da Hepatite A , Humanos , Nefropatias/etiologia , Lipocalina-2 , Lipocalinas/urina , Masculino , Proteínas Proto-Oncogênicas/urina , Receptores Virais
10.
Eur J Pediatr Surg ; 25(3): 299-304, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24705996

RESUMO

INTRODUCTION: The aim of the article is to investigate the beneficial effects of methylene blue (MB) on the acute phase of experimental corrosive esophageal burns. MATERIALS AND METHODS: A total of 21 male Sprague-Dawley rats were allocated into three groups with an equal number in each group. In Group 1 (control), the esophageal lumen was irrigated with saline. In Groups 2 (untreated) and 3 (MB treatment), the distal esophagus was burned with 30% NaOH solution. In Group 3, MB was applied locally on the distal esophageal lumen (30 mg/kg) 90 minutes after the burn. In all the groups, animals were humanely killed at the end of the 7th day. Distal esophageal specimens were obtained for histopathological and biochemical examinations. RESULTS: MB increased the tissue superoxide dismutase levels and the total antioxidant status, whereas it decreased the levels of the total oxidant status with significant attenuation of histopathological damage. CONCLUSION: MB might have reduced the tissue damage in corrosive esophagitis because of its antioxidant effects.


Assuntos
Queimaduras Químicas/patologia , Estenose Esofágica/prevenção & controle , Esofagite/patologia , Azul de Metileno/farmacologia , Estresse Oxidativo/efeitos dos fármacos , Animais , Queimaduras Químicas/complicações , Queimaduras Químicas/metabolismo , Catalase/metabolismo , Cáusticos , Modelos Animais de Doenças , Estenose Esofágica/induzido quimicamente , Esofagite/induzido quimicamente , Esofagite/complicações , Esofagite/metabolismo , Masculino , Oxidantes/metabolismo , Ratos Sprague-Dawley , Superóxido Dismutase/metabolismo
11.
Urology ; 82(2): 437-41, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23676358

RESUMO

OBJECTIVE: To investigate whether the child's and the parents' reports about lower urinary tract symptoms (LUTS) are reliable and correlate with each other. MATERIALS AND METHODS: A validated questionnaire, the International Consultation on Incontinence Questionnaire Pediatric Lower Urinary Tract Symptoms, including both children and parent versions, was completed by children (age 5-18 years) with and without LUTS (control) and their parents without assistance. All children were investigated with detailed history, bladder diary, urinalysis, and flowmetry with postvoid residual urine volume measurement. The data were stratified into 3 age groups (5-9, 10-13, and 14-18 years). The reliability of both versions was evaluated using Cronbach's α and ≥0.7 indicated acceptability. The correlation between the children's and parents' reports for each question was evaluated using Spearman correlation coefficients. The receiver operating characteristic curve was used to define the cutoff points, and the sensitivity and specificity were calculated. The principal component analysis method was used to explain the construct validity. RESULTS: A total of 272 children (147 with and 125 without LUTS) and their parents completed the questionnaire. The children and parent versions of the questionnaire were both reliable (Cronbach's α 0.709 and 0.710, respectively). The sensitivity and specificity was 82.4% and 80.0% for the children version and 87.8% and 78.4% for the parent version, respectively. The reliability and acceptability of the children's reports were insufficient for the 5-9 year age group, and the parents' answers were unreliable for the 10-13 year age group. The correlation between the parent and children reports was the lowest for the 10-13 year age group. CONCLUSION: The alteration in the reliability in the different age groups suggests that the combination of the parent and children versions is most appropriate for screening children with LUTS.


Assuntos
Sintomas do Trato Urinário Inferior/diagnóstico , Pais , Índice de Gravidade de Doença , Inquéritos e Questionários , Adolescente , Fatores Etários , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Análise de Componente Principal , Curva ROC , Reprodutibilidade dos Testes , Estatísticas não Paramétricas , Turquia
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