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Identification of messenger RNA of fetoplacental source in maternal plasma of women with normal pregnancies and pregnancies with intrauterine growth restriction / Identificacion de RNA mensajero de origen fetoplacentario en plasma materno de mujeres con embarazos normales y gestantes con restriccion de crecimiento intrauterino
Ayala Ramírez, Paola; García Robles, Reggie; Rojas, Juan Diego; Bermúdez, Martha; Bernal, Jaime.
  • Ayala Ramírez, Paola; s.af
  • García Robles, Reggie; s.af
  • Rojas, Juan Diego; s.af
  • Bermúdez, Martha; s.af
  • Bernal, Jaime; s.af
Colomb. med ; 43(3): 184-188, July-Sept. 2012. tab
Article in English | LILACS | ID: lil-663719
ABSTRACT

Objective:

to quantify placenta-specific RNA in plasma of women carrying foetuses with intrauterine growth restriction and pregnant women with normal pregnancies. Materials and

methods:

8 pregnant women with foetuses with intrauterine growth restriction were studied as well as 18 women with uncomplicated pregnancies in the third pregnancy trimester. Total free RNA was quantified in maternal plasma by spectrophotometry and the gene expression of hPL (Human Placental Lactogen) at the messenger RNA level through technical Real Time-Chain Reaction Polymerase.

Results:

plasma RNA of fetoplacental origin was successfully detected in 100% of pregnant women. There were no statistically significant differences between the values of total RNA extracted from plasma (p = 0.5975) nor in the messenger RNA expression of hPL gene (p = 0.5785) between cases and controls.

Conclusion:

messenger RNA of fetoplacental origin can be detected in maternal plasma during pregnancy.(AU)

Objective:

to quantify placenta-specific RNA in plasma of women carrying foetuses with intrauterine growth restriction and pregnant women with normal pregnancies. Materials and

methods:

8 pregnant women with foetuses with intrauterine growth restriction were studied as well as 18 women with uncomplicated pregnancies in the third pregnancy trimester. Total free RNA was quantified in maternal plasma by spectrophotometry and the gene expression of hPL (Human Placental Lactogen) at the messenger RNA level through technical Real Time-Chain Reaction Polymerase.

Results:

plasma RNA of fetoplacental origin was successfully detected in 100% of pregnant women. There were no statistically significant differences between the values of total RNA extracted from plasma (p = 0.5975) nor in the messenger RNA expression of hPL gene (p = 0.5785) between cases and controls.

Conclusion:

messenger RNA of fetoplacental origin can be detected in maternal plasma during pregnancy
RESUMEN

Objetivo:

cuantificar RNA específico de placenta en el plasma de mujeres con embarazos con fetos con Restricción de Crecimiento Intrauterino y gestantes con embarazos normales. Materiales y

métodos:

se estudiaron 8 mujeres con embarazos con fetos con Restricción de Crecimiento Intrauterino y 18 mujeres con embarazos sin complicaciones, en el tercer trimestre de embarazo. Se cuantificó el RNA total libre en plasma materno por espectrofotometría y la expresión del gen hPL (Lactógeno Placentario Humano) a nivel de RNA mensajero por medio de la técnica Reacción en Cadena de la Polimerasa en Tiempo Real.

Resultados:

se logró detectar RNA en plasma de origen fetoplacentario en el 100% de las gestantes. No se encontraron diferencias estadísticamente significativas entre los valores de RNA total extraído de plasma (p=0,5975) ni en la expresión del RNA mensajero del gen hPL (p=0,5785) entre casos y controles.

Conclusión:

es posible detectar RNA mensajero de origen fetoplacentario en plasma materno durante el embarazo.
Subject(s)

Full text: Available Index: LILACS (Americas) Main subject: RNA / Fetal Growth Retardation Type of study: Diagnostic study Limits: Pregnancy Language: English Journal: Colomb. med Journal subject: Medicine Year: 2012 Type: Article

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Full text: Available Index: LILACS (Americas) Main subject: RNA / Fetal Growth Retardation Type of study: Diagnostic study Limits: Pregnancy Language: English Journal: Colomb. med Journal subject: Medicine Year: 2012 Type: Article