Genetic polymorphisms of ESR1 and ESR2 that may influence estrogen activity and the risk of hypospadias.

Abstract

BACKGROUND:

The etiology of hypospadias is regarded as a complex disorder with both genetic and environmental contributions. Although alterations in androgen activity have been associated with hypospadias, few associations with estrogen activity have been documented. Here, we assessed genetic polymorphisms in estrogen receptor genes and their association with hypospadias.

METHODS:

Using a case-control study of 59 cases with hypospadias and 286 controls, we examined the association of hypospadias with the following polymorphisms: PvuII and XbaI in ESR1, and 2681-4A>G in ESR2.

RESULTS:

For the cases, we found a negative association with the G allele containing variants of ESR1 XbaI (OR = 0.52, P < 0.05), and a negative association with the G allele containing variants of ESR2 2681-4A>G (OR = 0.59, P < 0.05). For the cases, we also identified a negative association with the CG haplotype, and a positive association with the CA haplotype, defined by ESR1 PvuII and XbaI (P < 0.05).

CONCLUSIONS:

These findings suggest that the G allele containing variants of ESR1 XbaI and the G allele containing variants of ESR2 2681-4A>G may decrease the risk of hypospadias, whereas the ESR1 C-A haplotype may increase its risk.

• Authors: Susumu Ban, Fumihiro Sata, Norie Kurahashi, Setsuko Kasai, Kimihiko Moriya, Hidehiro Kakizaki, Katsuya Nonomura, Reiko Kishi
• Journal: Human reproduction (Oxford, England) (Hum Reprod) Vol. 23 Issue 6 Pg. 1466-71 (Jun 2008) ISSN: 1460-2350 [Electronic] England
• PMID: 18375409 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Estrogen Receptor alpha
• Estrogen Receptor beta
• Estrogens

Topics

• Alleles
• Case-Control Studies
• Child
• Estrogen Receptor alpha (genetics)
• Estrogen Receptor beta (genetics)
• Estrogens (physiology)
• Genetic Predisposition to Disease (epidemiology)
• Haplotypes
• Humans
• Hypospadias (genetics)
• Japan
• Male
• Polymorphism, Genetic
• Risk Factors