No abstract

Human cytomegalovirus (HCMV) is the most common congenital infection. HCMV strains display genetic variability in different regions. Distribution of HCMV genotypes in the population of congenitally infected newborns from Central Poland and viral load in newborns' blood is described and discussed. HCMV isolates were analysed by sequencing at three sites on the genome: the UL144 tumour necrosis factor-alpha (TNFα)-like receptor gene, the US28 beta-chemokine receptor gene and the UL55 envelope glycoprotein B (gB) gene. The newborns' blood was examined for HCMV DNA with a nested (UL144, UL55) or heminested (US28) polymerase chain reaction, and the genotypes were determined by sequence analysis. HCMV DNA was detectable in 25 out of 55 examined newborns born by HCMV-infected mothers (45.5%). The blood viral load in mother-infant pairs was determined. Most of the newborns had identical virus genotype, gB2 (96%), UL144 B1 (88%) and US28 A2 (84%). These genotypes were detected in all newborns with asymptomatic congenital infection. The occurrence of UL144 B1 or US28 A2 genotypes in the babies examined was significant in comparison to other genotypes (p=0.0002 and p=0.040 respectively). There was no association between specific gB subtypes in all patients groups (p=0.463). There was no correlation between HCMV genotypes and the outcome.

Introduction. Patients with psoriasis develop nonalcoholic fatty liver disease more often than healthy subjects. Objective. To estimate the level of basic parameters of liver function, compare these values between groups of patients with psoriasis and healthy individuals, and refer these values to selected risk factors of developing atherosclerosis. Material and methods. A case-control study in the dermatology department included 66 patients with psoriasis and 30 healthy volunteers. The two groups were comparable as regards age, sex and body mass index as well as abdominal circumference. In all subjects we estimated the parameters of liver function and selected the risk factors of atherosclerosis. Results. γ-Glutamyltransferase activity in patients with psoriasis was significantly higher than in the reference group individuals (p = 0.002) and it applies to men only (p = 0.0003). In women γ-glutamyltransferase activity was higher in patients with positive family history of psoriasis (p = 0.03). γ-Glutamyltransferase activity was also higher in smoking patients (p = 0.02). Activity and concentration of other liver function markers (alanine aminotransferase, aspartate aminotransferase, and bilirubin) did not differ significantly between healthy individuals and patients with psoriasis. There were no differences between patients with severe, moderate and mild psoriasis. A negative correlation between bilirubin concentration and age of patients (p = 0.02) and bilirubin and C-reactive protein concentration (p = 0.03) was observed. Activity of alanine aminotransferase correlated positively with abdominal circumference (p = 0.001), uric acid concentration (p = 0.004) and body mass index (p = 0.001). Activity of aspartate aminotransferase correlated positively with abdominal circumference (p = 0.001), uric acid concentration (p = 0.03) and body mass index (p = 0.001). Additionally, the increase in alanine aminotransferase activity was proportional to the increase in cholesterol (p = 0.01) and apolipoprotein B concentrations (p = 0.03). γ-Glutamyltransferase activity correlated positively with the concentration of uric acid (p = 0.008), cholesterol (p = 0.04), triglycerides (p = 0.04), and apolipoprotein B (p = 0.03). Conclusions. In patients with psoriasis increased activity of alanine aminotransferase and aspartate aminotransferase parameters probably result from liver diseases since they accompany dyslipidemia and obesity whereas the increase of γ-glutamyltransferase activity is probably associated mainly with psoriasis.