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DOI 10.1097/ede.0b013e3181c15a50

Медицинская библиотека · Epidemiology (Cambridge, Mass.) · 2010

Familial coaggregation of cryptorchidism and hypospadias.

Schnack Tine H, Poulsen Gry, Myrup Charlotte, Wohlfahrt Jan, Melbye Mads

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

It has been suggested that cryptorchidism and hypospadias may be the result of a common pathologic pathway that causes testicular dysgenesis during fetal life. To address the potential heritability of this pathway, we specifically examined to what extent a family history of cryptorchidism increases the risk of developing hypospadias and vice versa.

METHODS

By using Danish health registers, we identified 27,762 boys diagnosed with cryptorchidism and 4832 boys diagnosed with hypospadias in a cohort of 1,018,517 boys born during 1977-2005. Using binomial log-linear regression, we estimated risk ratios of cryptorchidism and hypospadias in male twin pairs and first-, second-, and third-degree relatives with a family history of hypospadias and cryptorchidism, respectively.

RESULTS

After adjusting for birth period and personal hypospadias/cryptorchidism status, there was little evidence of increased risk of cryptorchidism given a family history of hypospadias, and vice versa. However, cryptorchidism and hypospadias was associated on an individual level.

CONCLUSION

We found no persuasive evidence that a family history of hypospadias increases the risk of cryptorchidism and vice versa. Thus, we found no support for shared heritability of hypospadias and cryptorchidism.

Для цитирования: Schnack Tine H, Poulsen Gry, Myrup Charlotte, Wohlfahrt Jan, Melbye Mads. Familial coaggregation of cryptorchidism and hypospadias.. Epidemiology (Cambridge, Mass.). 2010. DOI: 10.1097/ede.0b013e3181c15a50.

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