Susceptibility to breast cancer and three polymorphisms of GSTZ1.

Glutathione S-transferases class zeta (GSTζ) is involved in the detoxification of xenobiotic compounds and catalyzes the biotransformation of a variety of α-haloacids including dichloroacetic acid and chlorofluoroacetic acid. It has been reported that, in mice, deficiency of Gstz1 (a member of GSTζ) resulted in the generation of a constant level of oxidative stress. The present study was carried out to investigate the association between genetic polymorphisms of GSTZ1 (in promoter site G-1002A and in coding sites Glu32Lys and Gly42Arg) and risk of breast cancer. We included 106 females with breast cancer and 106 healthy females frequency matched for age. The study polymorphisms were not associated with risk of breast cancer (p>0.05). The polymorphisms of GSTZ1 showed strong linkage disequilibrium among cancer patients and control subjects (p<0.0001). There was no significant difference between cancer patients and controls for frequencies of the GSTZ1 haplotypes (p>0.05). It seems there is no meaningful relationship between the genetic polymorphisms of GSTZ1 and risk of breast cancer.

Genetic polymorphisms of glutathione S-transferase Z1 in an Iranian population.

Genetic polymorphisms in gene encoding glutathione S-transferase Z1 (GSTZ1, a member of class zeta) have been defined. Previous studies have revealed that there was significant difference between populations for allelic frequency of several members of GSTs. In order to get more insight into the genetic structure of Iranian population the present study was done on Iranian Persian population who living in Shiraz (Fars province). The total study subjects consisted of 689 unrelated healthy individuals. Genetic polymorphisms for G-1002A, Glu32Lys and Gly42Arg of the GSTZ1 were detected by RFLP-PCR-based method. Allelic frequency of 32Lys, 42Arg, and -1002G was 0.2337, 0.0298 and 0.2184, respectively. The study population was at Hardy-Weinberg equilibrium for the polymorphisms of GSTZ1. Based on the complete dataset, these polymorphisms show significant linkage disequilibrium. Iranian gene pool showed intermediate frequency for alleles and haplotypes of GSTZ1 polymorphisms in comparison with European and Asian countries, which confirmed our previous reports for other genetic polymorphisms.

Effect of inbreeding on weight gain of offspring from birth to 12 months after birth: a study from Iran.

Consanguinity, the marriage between relatives, has been associated with adverse child health outcomes. The objective of the present study was to assess the effect of consanguinity on offspring weight gain from birth to 12 months after birth. Data were collected on 250 consecutive live-born singleton newborns referred to a local health centre in Shiraz (Fars province, southern Iran). Collected data covered socio-demographic characteristics (such as parental age at delivery and parental education), sex, birth order, weights from birth to 12 months after birth and consanguinity of marriages of parents. Considering the low prevalence of double first cousin, first cousin once removed, second cousin, and beyond second cousin marriages, only first cousin and unrelated marriages were included in the study. The study population consisted of a total of 207 newborns (57 offspring of first cousins, 150 offspring of unrelated marriages). Based on the results of repeated measurements analysis of variance, weight gain was associated with type of marriage (p=0.018), sex of offspring (p=0.001) and paternal education (p<0.001). There was no interaction between type of marriage and sex (p=0.831). Birth weight was not affected by type of marriage (p=0.46). There was significant interaction between inbreeding and time (p=0.034). Offspring of consanguineous marriages showed lower weight gain in comparison with those of unrelated marriages during 3-12 months after birth.