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Biomedical subjects

P Kozioł

Publications and source records attributed to P Kozioł.

8 recordsLinked to original sources

[Histocompatibility antigens in pregnant women with preeclampsia and in their husbands].

OBJECTIVES: Several pedigree and epidemiological studies have suggested that preeclampsia (PE) has an immunogenetic basis. Therefore, we have attempted to disclose a possible association between antigens of the HLA system (HLA-A, B and C) and development of PE. DESIGN AND METHODS: Peripheral blood lymphocytes were typed for HLA-A, B and C antigens by the two-stage microlymphocytotoxic test in 32 pregnant women with PE and in their husbands from south-east Poland. As a control population 411 healthy unrelated inhabitants of south-east Poland were studied. The obtained individual HLA antigens frequencies were compared with these in control individuals using Chi-square test and relative risk (RR) was computed as described by Svejgaard (1974). RESULTS: The frequency of B13 antigen occurrence was significantly higher in the women group with PE as compared to that in general population, and revealed significant association with the development of PE (0.02 < p < 0.05; RR = 2.733), while the frequency of Cw4 antigen was significantly lower (0.02 < p < 0.05; RR = 0.283). The frequency of B22 antigen occurrence in husbands group was significantly higher as compared with that in general population and this difference achieved very high statistical significance and strong association with the development of PE (p < 0.001; RR = 9.452). CONCLUSIONS: Results of our study point to the genetic transmission of susceptibility to PE. Typing for these antigens could be a potentially useful prenatal test for predicting which couples are at risk for PE.

Adult↗

Allele frequency distributions of D1S80 in the Polish population.

The polymorphism of the D1S80 locus has been analyzed in a population sample of 208 unrelated individuals in the Southeast Poland and 103 mother/child pairs. PCR amplified alleles were separated by a vertical discontinuous polyacrylamide gel electrophoresis system. Nineteen different alleles and 52 phenotypes could be distinguished. The alleles 18 (f = 0.267) and 24 (f = 0.300) were most common in Poland. D1S80 genotype frequencies of Poland population do not deviate from Hardy-Weinberg equilibrium. All mother/child pairs shared at least one D1S80 allele.

Adult↗

Rare phenotypes of the phosphoglucomutase locus 1 detectable by isoelectric focusing on Cellogel.

The rare phenotypes PGM1, determined by alleles PGM1(3), PGM1(4), PGM1(6), and PGM1(7) were examined by starch gel electrophoresis and cellulose acetate gel isoelectric focusing and were compared with the commonest phenotypes of PGM1. The frequencies of the rare genes found in the Polish populations were as follows: in Lublin, PGM1(3) = 0.0002, PGM1(4) = 0.0005, PGM1(6) = 0.0010, and PGM1(7) = 0.0005; in Wrocław, PGM1(3) = 0.0000, PGM1(4) = 0.0005, PGM1(6) = 0.0007, and PGM1(7) = 0.0002. The results suggest that the F and S type variants of the genes PGM1(4) and PGM1(7) probably do not occur. It is still possible that F and S variants exist for the genes PGM1(3) and PGM1(6).

Adult↗

Atypical segregation of esterase D: evidence of a rare "silent" allele EsD0.

Electrophoretic study of esterase D in 1027 mother-child pairs showed an atypical segregation of EsD alleles in one pair. The family analysis confirmed the evidence of a 'silent' gene (EsD0), which was observed in child, mother and grandfather. R banding of the metaphasal chromosomes revealed the normal appearance of the No. 13 pair, and no deletion of homologues No. 13 was observed in this family.

Adult↗

Subtypes of the phosphoglucomutase-1 (PGM1) locus detectable in Polish populations by isoelectric focusing on cellogel.

The technique of isoelectric focusing on methylated 'cellogel' strips (CAGIF) was used to confirm the presence of four alleles of PGM1 in human red cell lysates. The subtypes of PGM1 were determined in two Polish population samples, from Southwestern Poland (Wrocław region, n=321) and Southeastern Poland (Lubin region, n=212). Ten different phenotypes are considered as gene products of four alleles at PGM1, with the following frequencies: Wrocław: PGM1F, 0.1044; PGM1S, 0.5966; PGM2F, 0.0685; and PGM2S, 0.2305; Lublin: PGM1F, 0.1439; PGM1S, 0.6014; PGM2F, 0.0825; and PGM2S, 0.1722.

Electrophoresis, Cellulose Acetate↗

GLO polymorphism in two Polish population samples.

The red cell GLO phenotypes were determined in two Polish population samples. A total of 1310 people from the region of Lublin (Southeastern Poland, n = 797) and Wrocław (Southwestern Poland, n = 513) were investigated. The gene frequencies were calculated for GLO1 (= 0.4427) and GLO2 (= 0.5573). The evaluation of 372 mother-child pairs showed no deviation from a hereditary hypothesis.

Erythrocytes↗