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Vol. 47. Núm. 1.
Páginas 5-19 (enero 2004)
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Vol. 47. Núm. 1.
Páginas 5-19 (enero 2004)
Acceso a texto completo
Cribado bioquímico-ecográfico de las aneuploidías en el primer trimestre. Metodología y resultados
First-trimester biochemical-ultrasound aneuploidy screening. Methodology and results
Visitas
11985
C. Bacha, S. Torrenta, D. Cabrerob, J. Sabriàa,
Autor para correspondencia
jsabria@arrakis.es

Correspondencia: Servicio de Obstetricia y Ginecología. Hospital Universitario de Girona Doctor Josep Trueta. Ctra. de Francia, s/n. 17007 Girona. España
a Servicio de Obstetricia y Ginecología. Hospital Universitario de Girona Doctor Josep Trueta. Girona. España
b Laboratorio de Análisis Clínicos. Hospital Universitario de Girona Doctor Josep Trueta. Girona. España
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Resumen
Objetivo

Valorar la eficacia del cribado bioquímico-ecográfico de las aneuploidías en el primer trimestre de la gestación así como describir detalladamente la metodología utilizada.

Sujetos y métodos

Estudio prospectivo en 3.492 gestantes, portadoras de un feto único, en las que se realiza el cribado bioquímico mediante la fracción beta libre de la gonadotropina coriónica humana y la proteína plasmática A asociada al embarazo, entre las 8 y las 13 semanas de gestación, y el cribado ecográfico, entre las 11 y las 13 semanas, con la medición de la longitud cefalocaudal y del grosor de la translucencia nucal. Se exponen los procedimientos epidemiológico-matemáticos utilizados para estimar el riesgo de que una gestante sea portadora de un feto afectado de aneuploidía.

Resultados

El cribado bioquímico ecográfico del primer trimestre ha permitido detectar, en esta serie, el 83% (10 de 12) de las trisomías 21, el 86% (18 de 21) de las trisomías autosómicas y el 82% (23 de 28) de todas las aneuploidías, para una tasa de falsos positivos del 5,4%.

Conclusiones

Este tipo de cribado presenta una alta efectividad pero precisa una metodología adecuada para la obtención de resultados óptimos.

Palabras clave:
Cribado prenatal
Cribado bioquímico
Cribado ecográfico
Síndrome de Down
Primer trimestre
Abstract
Objective

To evaluate the effectiveness of first-trimester biochemical-ultrasound screening for aneuploidy and to describe the methodology used in detail.

Subjects and methods

We performed a prospective study of 3492 single pregnancies screened by means of two biochemical markers (free β subunit of human chorionic gonadotropin and pregnancy-associated plasma protein-A) between weeks 8 and 13 of gestation. Ultrasound screening was performed with measurement of nuchal translucency thickness and fetal crown-rump length between weeks 11 and 13. We describe the mathematical and epidemiological methods used to estimate the risk of aneuploidy in individual pregnancies.

Results

In our series, the detection rate of first-trimester biochemical-ultrasound screening was 83% (10 of 12) for trisomy 21, 86% (18 of 21) for autosomal trisomies and 82% (23 of 28) for all aneuploidies, with a false-positive rate of 5.4%.

Conclusions

This type of screening is highly effective but requires appropriate methodology to obtain optimal results.

Keywords:
Prenatal screening
Biochemical screening
Ultrasound screening
Down’s syndrome
First trimester
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Referencias bibliográficas
[1.]
H.S. Cuckle, N.J. Wald, S.G. Thompson.
Estimating a woman’s risk of having a pregnancy associated with Down’s syndrome using her age and serum alpha-fetoprotein level.
Br J Obstet Gynaecol, 94 (1987), pp. 387-392
[2.]
I.R. Merkatz, H.M. Nitowsky, J.N. Macri, W.E. Johnson.
An association between low maternal serum alphafetoprotein and fetal chromosome abnormalities.
Am J Obstet Gynecol, 148 (1984), pp. 886-894
[3.]
J.N. Macri, K. Spencer, D. Aitken, K. Garver, P.D. Buchanan, F. Muller, et al.
First-trimester free beta (hCG) screening for Down syndrome.
Prenat Diagn, 13 (1993), pp. 557-562
[4.]
K. Spencer, D.A. Aitken, J.A. Crossley, G. McCaw, E. Berry, R. Anderson, et al.
First trimester biochemical screening for trisomy 21: the role of free beta hCG, alpha fetoprotein and pregnancy associated plasma protein A.
Ann Clin Biochem, 31 (1994), pp. 447-454
[5.]
B. Brambati, M.C.M. Macintosh, B. Teisner.
Low maternal serum levels of pregnancy associated plasma protein A in the first trimester in association with abnormal karyotype.
Br Obstet Gynaecol, 100 (1993), pp. 324-326
[6.]
N.J. Wald, R. Stone, H.S. Cuckle.
Frist trimester concentrations of pregnancy associated plasma protein A and placental protein 14 in Down syndrome.
BMJ Xs, 305 (1992), pp. 28
[7.]
M.C. Macintosh, R. Iles, B. Teisner, K. Sharma, T. Chard, J.G. Grudzinskas, et al.
Maternal serum human chorionic gonadotrophin and pregnancy-associated plasma protein A, markers for fetal Down syndrome at 8-14 weeks.
Prenat Diagn, 14 (1994), pp. 203-208
[8.]
K. Spencer, N. Tul, K.H. Nicolaides.
Maternal serum free betahCG and PAPP-A in fetal sex chromosome defects in the first trimester.
Prenat Diagn, 20 (2000), pp. 390-394
[9.]
K. Spencer, C. Ong, H. Skentou, A.W. Liao, K. Nicolaides.
Screening for trisomy 13 by fetal nuchal translucency and maternal serum free β-hCG and PAPP-A at 10-14 weeks of gestation.
Prenat Diagn, 20 (2000), pp. 411-416
[10.]
N. Tul, K. Spencer, P. Noble, C. Chan, K. Nicolaides.
Screening for trisomy 18 by fetal nuchal translucency and maternal serum free beta-hCG and PAPP-A at 10-14 weeks of gestation.
Prenat Diagn, 19 (1999), pp. 1035-1042
[11.]
J. Szabo, J. Gellen.
Nuchal fluid accumulation in trisomy-21 detected by vaginosonography in first trimester.
Lancet, 336 (1990), pp. 1133
[12.]
R.J. Snijders, P. Noble, N. Sebire, A. Souka, K.H. Nicolaides.
UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10-14 weeks of gestation. Fetal Medicine Foundation First Trimester Screening Group.
[13.]
R. Zimmermann, A. Hucha, G. Savoldelli, F. Binkert, J. Achermann, J.G. Grudzinskas.
Serum parameters and nuchal translucency in first trimester screening for fetal chromosomal abnormalities.
Br J Obstet Gynaecol, 103 (1996), pp. 1009-1014
[14.]
N.J. Wald, A.K. Hackshaw.
Combining ultrasound and biochemistry in first-trimester screening for Down’s syndrome.
Prenat Diagn, 17 (1997), pp. 821-829
[15.]
K. Spencer, V. Souter, N. Tul, R. Snijders, K.H. Nicolaides.
A screening program for trisomy 21 at 10-14 weeks using fetal nuchal translucency, maternal serum free β-human chorionic gonadotropin and pregnancy-associated plasma protein-A.
Ultrasound Obstet Gynecol, 13 (1999), pp. 231-237
[16.]
I.M. De Graaf, E. Pajkrt, C.M. Bilardo, N.J. Leschot, H.S. Cuckle, M. Van Lith.
Early pregnancy screening for fetal aneuploidy with serum markers and nuchal translucency.
Prenat Diagn, 19 (1999), pp. 458-462
[17.]
D.A. Krantz, T.W. Hallahan, F. Orlandi, P. Buchanan, J.r. Larsen JW, J.N. Macri.
First-trimester Down syndrome screening using dried blood biochemistry and nuchal translucency.
Obstet Gynecol, 96 (2000), pp. 207-213
[18.]
F. Orlandi, G. Damiani, T.W. Hallahan, D.A. Krantz, J.N. Macri.
First-trimester screening for fetal aneuploidy: biochemistry and nuchal translucency.
Ultrasound Obstet Gynecol, 10 (1997), pp. 381-386
[19.]
P. De Biasio, M. Siccardi, G. Volpe, L. Famularo, F. Santi, S. Canini.
First-trimester screening for Down syndrome using nuchal translucency measurement with free beta-hCG and PAPP-A between 10 and 13 weeks of pregnancy. The combined test.
Prenat Diagn, 19 (1999), pp. 360-363
[20.]
D.A. Krantz, T.W. Hallahan, F. Orlandi, P. Buchanan, J.r. Larsen JW, J.N. Macri.
First-trimester Down syndrome screening using dried blood biochemistry and nuchal translucency.
Obstet Gynecol, 96 (2000), pp. 207-213
[21.]
C. Bach, D. Cabrero, I. Vila, J. Sabria.
First-trimester fetal chromosomal defects screening in a low risk population by fetal nuchal translucency and maternal serum free β hCG and PAPP-A [abstract 055]. En: Abstracts’ book of the 10 International Conference on Prenatal Diagnosis and Therapy.
pp. 297
[22.]
K. Schuchter, E. Hafner, G. Stangl, M. Metzenbauer, D. Hofinger, K. Philipp.
The first trimester ‘ecombined test’ for the detection of Down syndrome pregnancies in 4939 unselected pregnancies.
Prenat Diagn, 22 (2002), pp. 211-215
[23.]
K. Spencer.
Accuracy of Down syndrome risks produced in a first-trimester screening programme incorporating fetal nuchal translucency thickness and maternal serum biochemistry.
Prenat Diagn, 22 (2002), pp. 244-246
[24.]
R. Bindra, V. Heath, A. Liao, K. Spencer, K.H. Nicolaides.
Onestop clinic for assessment of risk for trisomy 21 at 11-14 weeks: a prospective study of 15 030 pregnancies.
Ultrasound Obstet Gynecol, 20 (2002), pp. 219-225
[25.]
J. Sabria, D. Cabero, C. Bach.
Aneuploidy screening: ultrasound versus biochemistry.
Ultrasound Review Obstet Gynecol, 2 (2002), pp. 221-228
[26.]
K. Spencer, C.E. Spencer, M. Power, C. Dawson, K.H. Nicolaides.
Screening for chromosomal abnormalities in the first trimester using ultrasound and maternal serum biochemistry in a onestop clinic: a review of three years prospective experience.
Bjog, 110 (2003), pp. 281-286
[27.]
A. Fortuny, A. Borrell, Combining Ultrasound and Biochemistry. Two-step first trimester screening. International Down’s Syndrome Screening Group.
Abtracts of the Sixth International Congress, (2003),
[28.]
R. Wapner, E. Thom, J.L. Simpson, E. Pergament, R. Silver, K. Filkins, et al.
First-trimester screening for trisomies 21 and 18.
N Engl J Med, 349 (2003), pp. 1405-1413
[29.]
K.H. Nicolaides, R.J.M. Snijders, H.S. Cuckle.
Correct estimation of parameters for ultrasound nuchal translucency screening.
Prenat Diagn, 18 (1998), pp. 519-521
[30.]
N.J. Wald, C. Rodeck, A.K. Hackshaw, J. Walters, L. Chitty, A.M. Mackinson.
First and second trimester antenatal screening for Down’s syndrome: the results of the Serum, Urine and Ultrasound Screening Study (SURUSS).
Health Technol Assess, 7 (2003), pp. 1-77
[31.]
E.B. Hook, P.K. Cross, R.R. Regal.
The frequency of 47+21, 47+18, and 47+13 at the uppermost extremes of maternal ages: results on 56,094 fetuses studied prenatally and comparisons with data on livebirths.
Hum Genet, 68 (1984), pp. 211-220
[32.]
C.A. Hecht, E.B. Hook.
The imprecision in rates of Down syndrome by 1-year maternal age intervals: a critical analysis of rates used in biochemical screening.
Prenat Diagn, 14 (1994), pp. 729-738
[33.]
C.A. Hecht, E.B. Hook.
Rates of Down syndrome at livebirth by one-year maternal age intervals in studies with apparent close to complete ascertainment in populations of European origin: a proposed revised rate schedule for use in genetic and prenatal screening.
Am J Med Genet, 24 (1996), pp. 376-385
[34.]
I. Bray, D.E. Wright, C. Davies, E.B. Hook.
Joint estimation of Down syndrome risk and ascertainment rates: a meta-analysis of nine published data sets.
Prenat Diagn, 18 (1998), pp. 9-20
[35.]
E.B. Hook.
Maternal age-specific rates of Down syndrome used in serum screening are biased low.
Prenat Diagn, 20 (2000), pp. 169
[36.]
J.G. Grudzinskas, R.H.T. Ward.
Screening for Down syndrome in the first trimester.
Epidemiology of Down syndrome,
[37.]
K.H. Nicolaides.
Screening for chromosomal defects.
Ultrasound Obstet Gynecol, 21 (2003), pp. 313-321
[38.]
J.K. Morris, N.J. Wald, H.C. Watt.
Fetal loss in Down syndrome pregnancies.
Prenat Diagn, 19 (1999), pp. 142-145
[39.]
R.J.M. Snijders, K. Nicolaides.
Ultrasound markers for fetal chromosomal defects.
The Parthenon Publishing Group, (1996),
[40.]
C. Wilson, N. Cuckle.
Risk at time of test.
DSNews, 8 (2001), pp. 41
[41.]
L.M. Neveux, G.E. Palomaki, D.A. Larivee, G.J. Knigth, J.E. Haddow.
Refinements in managing maternal weight adjustement for interpreting prenatal screening results.
[42.]
N.J. Wald, H.S. Cuckle, J.W. Densem, K. Nanchahal, P. Royston, T. Chard, et al.
Maternal serum screening for Down’s syndrome in early pregnancy.
Bmj, 297 (1988), pp. 883-887
[43.]
K. Spencer, C.Y. Ong, A.W. Liao, K.H. Nicolaides.
The influence of ethnic origin on first trimester biochemical markers of chromosomal abnormalities.
Prenat Diagn, 20 (2000), pp. 491-494
[44.]
K. Spencer.
The influence of smoking on maternal serum PAPP-A and free beta hCG levels in the first trimester of pregnancy.
Prenat Diagn, 18 (1999), pp. 1065-1066
[45.]
P. De Biasio, S. Canini, A. Crovo, F. Prefumo, P.L. Venturini.
Early vaginal bleeding and first-trimester markers for Down syndrome.
Prenat Diagn, 23 (2003), pp. 470-473
[46.]
N.J. Wald, N. White, J.K. Morris, W.J. Huttly, J.A. Canick.
Serum markers for Down’s syndrome in women who have had in vitro fertilisation: implications for antenatal screening.
Br J Obstet Gynaecol, 106 (1999), pp. 1304-1306
[47.]
S.O. Larsen, K.R. Wojdemann, A.C. Shalmi, K. Sundberg, M. Christiansen, A. Tabor.
Gender impact on first trimester markers in Down syndrome screening.
Prenat Diagn, 22 (2002), pp. 1207-1208
[48.]
G.E. Palomaki, J.E. Haddow.
Maternal serum alpha-fetoprotein, age, and Down syndrome risk.
Am J Obstet Gynecol, 156 (1987), pp. 460-463
[49.]
B. Nogaard-Petersen, S. Larsen, J. Arends, B. Svenstrup, A. Tabor.
Maternal serum markers in screening for Down syndrome.
Clin Genet, 37 (1990), pp. 35-43
[50.]
J.A. Crossley, D.A. Aitken, J.M. Connor.
Prenatal screening for chromosome abnormalities using maternal serum chorionic gonadotrophin, alpha-fetoprotein and age.
Prenat Diagn, 11 (1991), pp. 83-101
[51.]
T.M. Reynolds, M.D. Penney.
The mathematical basis of multivariate risk screening: with special reference to screening for Down’s syndrome associated pregnancy.
Ann Clin Biochem, 27 (1990), pp. 452-458
[52.]
J.E. Haddow, G.E. Palomaki, G.J. Knight, J. Williams, W.A. Miller, A. Johnson.
Screening of maternal serum for fetal Down’s syndrome in the first trimester.
N Engl J Med, 338 (1998), pp. 955-961
[53.]
F. Orlandi, G. Damiani, T.W. Hallahan, D.A. Krantz, J.N. Macri.
First-trimester screening for fetal aneuploidy: biochemistry and nuchal translucency.
Ultrasound Obstet Gynecol, 10 (1997), pp. 381-386
[54.]
N.J. Wald, H.C. Watt, A.K. Hackshaw.
Integrated screening for Down’s syndrome based on tests performed during the first and second trimesters.
N Engl J Med, 342 (1999), pp. 461-467
Copyright © 2004. Sociedad Española de Ginecología y Obstetricia
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