2001Acta PharmaceuticaRequires access

Genotyping of á-antitrypsin S and Z alleles in deficient families in Croatia

Irena Žuntar, Elizabeta Topić, Zvonimir Jurčić

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Abstract

The aim of the study was to determine AAT genotype by the simple DNA-based method in a group of ten Croatian families. AAT genotype was determined by PCR-RFLP in samples taken from each member of the ten families (mother, father and child/children). In the group of parents, five normal genotypes, Pi MM and fifteen Pi MZ genotypes, were detected. In the group of children, particular genotypes followed the mode of inheritance. There were eight Pi MZ, and five Pi ZZ genotypes. PCR-RFLP was found to be the method of choice for AAT genotyping. Determination of AAT genotype in family studies enables the risk of deficient allele inheritance to be followed-up and assessed. Early diagnosis of a deficient AAT genotype contributes to the success of currently widely available AAT replacement therapy.

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What this paper is about

The aim of the study was to determine AAT genotype by the simple DNA-based method in a group of ten Croatian families. AAT genotype was determined by PCR-RFLP in samples taken from each member of the ten families (mother, father and child/children). In the group of parents, five normal genotypes, Pi MM and fifteen Pi MZ genotypes, were detected. In the group of children, particular genotypes followed the mode of inheritance. There were eight Pi MZ, and five Pi ZZ genotypes. PCR-RFLP was found to be the method of choice for AAT genotyping. Determination of AAT genotype in family studies enables the risk of deficient allele inheritance to be followed-up and assessed. Early diagnosis of a deficient AAT genotype contributes to the success of currently widely available AAT replacement therapy.

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Available abstract

The aim of the study was to determine AAT genotype by the simple DNA-based method in a group of ten Croatian families. AAT genotype was determined by PCR-RFLP in samples taken from each member of the ten families (mother, father and child/children). In the group of parents, five normal genotypes, Pi MM and fifteen Pi MZ genotypes, were detected. In the group of children, particular genotypes followed the mode of inheritance. There were eight Pi MZ, and five Pi ZZ genotypes. PCR-RFLP was found to be the method of choice for AAT genotyping. Determination of AAT genotype in family studies enables the risk of deficient allele inheritance to be followed-up and assessed. Early diagnosis of a deficient AAT genotype contributes to the success of currently widely available AAT replacement therapy.

Key concepts: Genotyping, Genotype, Genetics, Allele, Biology, Restriction fragment length polymorphism, Polymerase chain reaction, Gene

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