The objective of this study was to investigate whether mutations of the renin-angiotensin system genes are involved in primary vesicoureteric reflux (VUR) and VUR-associated renal scarring. The M235T polymorphism of the angiotensinogen ( ATG) gene, the I/D polymorphism of the angiotensin converting enzyme ( ACE) gene, and the A1166C polymorphism of the angiotensin II type 1 receptor ( AT1) gene were identified in 77 patients with primary VUR (aged 6.9+/-3.2 years, mean+/-SD) and 80 healthy controls (aged 33+/-7 years). Thirty-eight of the 77 VUR patients had low-grade VUR (grade I-III) and 39 had high-grade VUR (grade IV and V). Renal scarring was found in 43 VUR patients, while 34 patients had normal kidneys on dimercaptosuccinic acid scan. The ACE gene polymorphism was determined by polymerase chain reaction and the ATG and AT1 gene polymorphisms were determined by single-step LightCycler technology. We found significant over-representation of the DD genotype in patients with renal scarring (44 %) compared with normal controls (23%, P<0.05) and patients with no scar formation (21%, P<0.05). Significantly higher D and significantly lower I allele frequencies were present in VUR patients with scarred kidneys (D allele 0.64 and I allele 0.36) compared with controls (D allele 0.53 and I allele 0.47, P<0.05) and patients with unscarred kidneys (D allele 0.4 and I allele 0.6, P<0.05). No differences in the ATG and AT1 genotype distributions and allele frequencies were observed in VUR patients compared with the normal population. The DD genotype and D allele of ACE may be a genetic susceptibility factor contributing to scar formation in VUR. We detected no linkage of genetic polymorphisms of ATG and AT1 to VUR and VUR-associated renal scarring.

Salivirus (family Picornaviridae) may be associated with acute gastroenteritis in humans, but there have been no reports of salivirus outbreaks. Salivirus A1 infection with faecal virus concentrations of 2.1-2.6 × 10(9)/g were identified retrospectively in newborn babies, between the ages of 1.5 and 5 days, with apparent clinical symptoms of diarrhea (100 %), fever (40 %), vomiting (40 %), and loss of appetite (40 %) in a neonatal hospital unit in Hungary in July 2013. The complete genome sequence of the salivirus (including the 5'-terminal end) was determined. Salivirus mono-infection may be associated with gastroenteritis in babies who are a few days old. Salivirus testing should be done in public health laboratories in gastroenteritis outbreaks with unknown etiology.

Regional differences in morphometry (different prevalences of overweight and obesity) and the genetic background, disparate eating habits and other cultural factors may account for the differences in BP levels during childhood. As the prevalence of overweight and obesity is increasing worldwide, it is important that countries carefully monitor the weight and BP status of their children and adolescents.

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Background/Aims: Blood pressure (BP) during childhood is an established predictor of adult BP, which in turn predicts mortality in the event of cardiovascular disease. Reference data for systolic (SBP) and diastolic (DBP) BP are not available for Hungarian children (aged 11–14 years). The aim was to make up for this deficit. Methods: Analyses were performed on 14,504 Hungarian children aged 11–16 years. All measurements were made with a validated, automated device. Criteria described by international guidelines were used. Results: The 50th, 90th and 95th percentile BP values were defined by dividing the participating population into age-, gender- and height-specific subgroups. The SBP increased linearly with age to an apparent plateau at around the age of 15–16 years in both girls and boys, and there were similar increases in DBP and mean arterial pressure. Both the SBP and DBP revealed highly significant correlations in both genders with weight (SBP: r = 0.452, p < 0.01; DBP: r = 0.340, p < 0.01), height (SBP: r = 0.314, p < 0.01; DBP: r = 0.245, p < 0.01) and body mass index (SBP: r = 0.407, p < 0.01; DBP: r = 0.294, p < 0.01). Conclusion:The present study provides reference data on SBP and DBP, facilitating the diagnosis of essential hypertension in the 11- to 16-year age group.