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1.
Pediatr Nephrol ; 25(1): 129-34, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19705157

RESUMO

Data on urolithiasis (UL) in infancy are limited. The objective of this study was to increase awareness of infant UL and to investigate the influence of possible risk factors in this very specific age group. Nonfasting, second-voiding urine samples were obtained to test for urinary excretions of calcium, oxalate, citrate, magnesium, uric acid, and creatinine. Blood analysis included calcium, phosphate, magnesium, uric acid, creatinine, sodium, potassium, chloride, and alkaline phosphatase. Patients received follow-up testing every 1-2 months; serial ultrasonography was used to track UL status. Fifty infants with a median age of 5 months were enrolled in the study. Hypercalciuria was detected in 9/47, hyperoxaluria in 5/39, hypocitraturia in 4/31, and cystinuria in 2/50 infants. We identified at least one metabolic abnormality in 46% of our patients; no metabolic abnormality was identified in 27 infants. Within a mean follow-up period of 14 months, 17 infants became stone free, stones increased in number in ten patients and decreased in number in 16, and recurrence was detected in seven. This study showed that UL could be detected in very early life, even in the newborn period, and could be the source of late childhood/adulthood UL. Infants with nonspecific symptoms such as restlessness may have UL and should undergo ultrasonographic examination. Metabolic evaluation of UL in this specific age group carries some diagnostic challenges, e.g. unsatisfactory data regarding normal ranges of urinary mineral excretion, and collection of 24-h urine samples.


Assuntos
Doenças Metabólicas/diagnóstico , Urolitíase/diagnóstico , Análise Química do Sangue , Pré-Escolar , Ácido Cítrico/urina , Cistinúria/diagnóstico , Cistinúria/epidemiologia , Cistinúria/urina , Feminino , Humanos , Hipercalciúria/diagnóstico , Hipercalciúria/epidemiologia , Hipercalciúria/urina , Hiperoxalúria/diagnóstico , Hiperoxalúria/epidemiologia , Hiperoxalúria/urina , Lactente , Masculino , Doenças Metabólicas/epidemiologia , Doenças Metabólicas/urina , Valores de Referência , Estudos Retrospectivos , Fatores de Risco , Turquia/epidemiologia , Ultrassonografia , Urinálise , Urolitíase/epidemiologia , Urolitíase/urina
2.
Pediatr Transplant ; 13(6): 697-700, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18992046

RESUMO

The aim of this study was to analyze the semen variables and hormone profiles in kidney transplanted male adolescents. Eight post-pubertal male patients who underwent successful renal tx during the peripubertal period and who had ESRD during childhood were enrolled in the study. Patients who underwent tx before 14 yr old (group I) and patients who underwent tx after 14 yr old (group II) were evaluated separately. Semen was collected and analyzed. Serum levels of LH, FSH, and testosterone were measured and found to be normal in all patients except one. The mean age at the diagnosis of CKD was six yr and 13 yr in groups I and II, respectively. The mean age at the time of tx was 12 yr in the first and 17.8 yr in the second group. The patients in group I had received prednisone, cyclosporine A and azathioprine with a longer duration of time compared with patients in group II. Sperm counts (15.5 +/- 15.7 vs. 82.3 +/- 64.2 millions/mL) and sperm motilities (37.8 +/- 30.9 vs. 57.8 +/- 22.1%) were lower in group I than group II. Only one patient in group II had normal sperm parameters and azospermia was observed in one patient from group I. We conclude that the earlier onset and the longer duration of uremia, the more impairment of reproductive function. Also, it seems that duration of exposure to corticosteroids or cyclosporine combined with azathioprine contribute to sperm dysfunction in peripubertal transplanted boys.


Assuntos
Transplante de Rim/métodos , Sêmen/metabolismo , Adolescente , Corticosteroides/uso terapêutico , Azatioprina/uso terapêutico , Ciclosporina/uso terapêutico , Hormônio Foliculoestimulante/sangue , Humanos , Infertilidade Masculina/prevenção & controle , Transplante de Rim/efeitos adversos , Hormônio Luteinizante/sangue , Masculino , Prednisona/uso terapêutico , Contagem de Espermatozoides , Espermatozoides/patologia , Testosterona/sangue , Fatores de Tempo , Uremia/diagnóstico
3.
Pediatr Nephrol ; 24(6): 1173-80, 2009 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19224250

RESUMO

Combinations of antiproteinurics, including angiotensin I-converting enzyme inhibitors + angiotensin II receptor antagonist + statins, are promising choices in the treatment of steroid-resistant nephrotic syndrome. We aimed to investigate the effects of high doses of immunoglobulin in addition to these combinations in rats with adriamycin-induced nephrosis. The study included 40 rats allocated into five groups: control, nephrotic syndrome without treatment, dual therapy (DT) with enalapril + losartan, triple therapy (TT) with enalapril + losartan + simvastatin, and quadruple therapy (QT) with enalapril + losartan + simvastatin + a high dose of immunoglobulin. The proteinuria levels were not statistically different between DT, TT and QT groups at weeks 5, 8, 12 and 16. At week 16, serum creatinine levels in the QT group were significantly lower than those in the control, DT and TT groups. The glomerulosclerosis index in the DT group was significantly lower than in the TT and QT groups. The scores for interstitial fibrosis and TGF-beta staining were similar among treatment groups. In conclusion, we showed that quadruple therapy including immunoglobulin had a beneficial effect on renal function in the late phase, but it had no additional effects in reducing proteinuria or in glomerulosclerosis score in experimental nephrotic syndrome. Further studies with angiotensin I-converting enzyme inhibitors (ACEIs), angiotensin II receptor antagonists (AIIRAs) and immunoglobulin combinations would offer some benefits in the treatment of nephrotic syndrome.


Assuntos
Enalapril/uso terapêutico , Imunoglobulinas/uso terapêutico , Fatores Imunológicos/uso terapêutico , Losartan/uso terapêutico , Síndrome Nefrótica/tratamento farmacológico , Sinvastatina/uso terapêutico , Animais , Anti-Hipertensivos/uso terapêutico , Pressão Sanguínea/efeitos dos fármacos , Creatinina/sangue , Quimioterapia Combinada , Masculino , Proteinúria , Ratos , Ratos Wistar , Fatores de Tempo , Resultado do Tratamento
4.
Nucl Med Commun ; 27(9): 715-21, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16894326

RESUMO

AIM: This prospective study aimed to investigate the diagnostic value of serum procalcitonin levels in children with acute pyelonephritis documented by Tc-dimercaptosuccinic acid (DMSA) scintigraphy. METHODS: We compared the symptoms and laboratory findings of fever, vomiting, abdominal/flank pain, leukocyte count, serum C-reactive protein and procalcitonin levels with the results of the DMSA scan obtained within the first 72 h after referral in children who were diagnosed as having acute pyelonephritis. Thirty-three children (31 female and two male) aged 1-11 years (mean 4.42 years) were enrolled in this prospective study. RESULTS: Twenty-one of 33 patients (64%) had positive DMSA scans. On the scans obtained after 6 months, five of 21 patients (23.8%) had renal scars. No correlation was found between clinical and laboratory parameters, alone or combined with each other, and positive DMSA scans. Serum procalcitonin levels were 0.767+/-0.64 and 1.23+/-1.17 ng . ml in children with normal and positive DMSA scans, respectively. The cut-off value for procalcitonin using receiver operating characteristic analysis was 0.9605 ng . ml, while sensitivity and specificity were 86.4% and 36.4%, respectively. However, if the cut-off value was chosen as 2 ng . ml, the sensitivity increased to 100% while specificity did not change markedly. CONCLUSION: The serum procalcitonin test, like other commonly used laboratory parameters, e.g. serum C-reactive protein and white blood cell count, was inadequate in distinguishing renal parenchymal involvement in acute febrile urinary tract infections.


Assuntos
Calcitonina/metabolismo , Precursores de Proteínas/metabolismo , Pielonefrite/diagnóstico , Compostos Radiofarmacêuticos , Ácido Dimercaptossuccínico Tecnécio Tc 99m , Doença Aguda , Proteína C-Reativa/metabolismo , Calcitonina/sangue , Peptídeo Relacionado com Gene de Calcitonina , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Rim/metabolismo , Contagem de Leucócitos , Masculino , Estudos Prospectivos , Precursores de Proteínas/sangue , Cintilografia
5.
Pediatr Nephrol ; 22(9): 1297-301, 2007 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17549524

RESUMO

The methodologies to diagnose hypercalciuria have not yet been standardized. The aims of this study were to assess the correlation between urinary calcium/creatinine ratio (UCa/Cr) > or = 0.21 (mg/mg) and 24 h urinary calcium excretions and to determine the reference values of the UCa/Cr ratio among a large population of schoolchildren in southern Turkey. Non-fasting, second morning urine samples were collected from 2,143 children aged 7-14 years. In children with suspected hypercalciuria [UCa/Cr > or = 0.21 (mg/mg)], 24 h urine samples were collected. The 95th percentile values of the UCa/Cr ratio for each age were calculated and showed a decrease in value with advancing age. In all, 269 (12.5%) of the children had UCa/Cr > or = 0.21 (mg/mg), of whom 66 (24.5%) had daily urinary calcium excretion > or =4 mg/kg per day. A weak correlation was found between spot UCa/Cr ratios and daily urinary calcium excretions in children with UCa/Cr > or = 0.21 (r = 0.27). We conclude that a spot UCa/Cr ratio of 0.21 (mg/mg) as the upper limit of normal cannot be used universally to define hypercalciuria. Age-specific reference values for UCa/Cr should be established for each population, to be used as a screening test for hypercalciuria, and the definite diagnosis should be established with 24 h urinary calcium excretion whenever possible.


Assuntos
Hipercalciúria/diagnóstico , Adolescente , Criança , Estudos Transversais , Feminino , Humanos , Masculino , Programas de Rastreamento
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