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DOI 10.3233/npm-15814092

Медицинская библиотека · Journal of neonatal-perinatal medicine · 2015

Expression of cystathionine beta-synthase and histopathological observations in placentas of patients with Down syndrome.

Pinilla J Martínez, Ayala-Ramírez P, García-Robles R, Olaya-C M, Bermúdez M

Сравнительное исследованиеСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

UNLABELLED: Down syndrome is the most frequent aneuploidy in live births, with an overall frequency of 1/600-700 births. The overexpression of cystathionine β-synthase is thought to participate in the presentation of some phenotypes observed in Down syndrome.

OBJECTIVE

The aim of this study was to compare the expression levels of cystathionine β-synthase and histopathological observations from placentas of infants with Down syndrome and healthy newborns.

MATERIALS AND

METHODS

Six placentas of fetuses/infants with Down syndrome and sixteen placentas of healthy fetuses were studied. Cystathionine β-synthase mRNA and protein expression were performed by real-time PCR and immunohistochemistry, respectively.

RESULTS

We observed an increase in cystathionine β-synthase mRNA expression (p = 0.0465) and protein levels (p = 0.009) in placentas of fetus/infants with Down syndrome compared with controls. Significantly more circinate edges (p = 0.0007) and trophoblast inclusions (p = 0.0037) were observed in the group with Down syndrome compared with control group.

CONCLUSION

The results demonstrate overexpression of cystathionine β-synthase mRNA and protein in placentas of fetuses/infants with trisomy 21. Further histological abnormalities were found in placentas of patients with Down syndrome, suggesting an alteration in the development of placenta.

Для цитирования: Pinilla J Martínez, Ayala-Ramírez P, García-Robles R, Olaya-C M, Bermúdez M. Expression of cystathionine beta-synthase and histopathological observations in placentas of patients with Down syndrome.. Journal of neonatal-perinatal medicine. 2015. DOI: 10.3233/npm-15814092.

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