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1.
Prenat Diagn ; 32(10): 933-42, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22763612

RESUMEN

OBJECTIVE: Our knowledge about miscarriages mainly concerns pregnancies of at least 8 weeks' gestation. Information about the morphology and the genetic determinants of early aborted embryos remains limited. In addition, it is known that aneuploidies account for less than half of recurrent spontaneous abortions. We hypothesized that (recurrent) early pregnancy losses might have other genetic causes. METHOD: Products of conception from 51 couples with at least one previous miscarriage were collected by hystero-embryoscopy. The extracted DNA was analyzed by low resolution array comparative genomic hybridization and high resolution single nucleotide polymorphism arrays to detect aneuploidies, polyploidies, submicroscopic copy number variants or copy neutral loss of heterozygosity. RESULTS: Chromosomal aberrations were identified in 65.6% (21/32) of miscarriages and in 89% (8/9) of anembryonic cases. Interestingly, 4/11 chromosomally euploid embryos contained regions of loss of heterozygosity >5 Mb, suggesting the miscarriages might be due to an underlying lethal recessive disease. CONCLUSION: Hystero-embryoscopic biopsy followed by array comparative genomic hybridization is a valuable diagnostic tool for early and recurrent miscarriages. Genome-wide high resolution single nucleotide polymorphism microarray analysis of a larger group of miscarriages could provide more insight into the genetic causes of recurrent spontaneous abortion.


Asunto(s)
Aborto Habitual/genética , Aborto Habitual/patología , Fetoscopía , Edad Gestacional , Histeroscopía , Adulto , Biopsia , Aberraciones Cromosómicas , Hibridación Genómica Comparativa , Femenino , Humanos , Pérdida de Heterocigocidad , Masculino , Polimorfismo de Nucleótido Simple , Embarazo
2.
Hum Reprod ; 24(2): 284-90, 2009 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19054781

RESUMEN

BACKGROUND: First trimester growth restriction may predict miscarriage or adverse outcome later in the pregnancy, but determinants of early growth are not well described. Our objective was to examine factors influencing fetal and gestational sac size in the first trimester. METHODS: Prospective observational study of 1828 singleton pregnancies before 12 weeks gestation. Maternal characteristics (ethnicity, maternal age, obstetric history, abdominal pain and vaginal bleeding), crown rump length (CRL) and mean gestational sac diameter (MSD) were recorded. A stepwise linear mixed effects analysis was performed to determine factors influencing rate of change in CRL and MSD. RESULTS: 1063 scans, in 464 women, were included. Rate of increase in CRL was higher in women of black ethnic origin (P = 0.0261) compared with white, and increased with advancing maternal age (P = 0.0046). Maternal age also influenced MSD: older women had gestational sacs which were 0.118 mm larger for each one year increase in maternal age (P = 0.0073). Bleeding, pain and prior obstetric history did not influence CRL or MSD. CONCLUSIONS: Rate of increase in CRL was greater in fetuses of black versus white women and increased with advancing maternal age. As CRL is used to date pregnancies, and this influences further growth assessment, consideration should be given to the use of individualized growth charts which take account of maternal factors found to influence first trimester growth.


Asunto(s)
Desarrollo Embrionario , Primer Trimestre del Embarazo/etnología , Adolescente , Adulto , Pueblo Asiatico , Población Negra , Largo Cráneo-Cadera , Femenino , Humanos , Edad Materna , Embarazo , Estudios Prospectivos , Factores de Riesgo , Ultrasonografía Prenatal , Población Blanca
3.
Biol Sex Differ ; 10(1): 48, 2019 09 09.
Artículo en Inglés | MEDLINE | ID: mdl-31500671

RESUMEN

BACKGROUND: According to the WHO Multicentre Growth Reference Study Group recommendations, boys and girls have different growth trajectories after birth. Our aim was to develop gender-specific fetal growth curves in a low-risk population and to compare immediate birth outcomes. METHODS: First, second, and third trimester fetal ultrasound examinations were conducted between 2002 and 2012. The data was selected using the following criteria: routine examinations in uncomplicated singleton pregnancies, Caucasian ethnicity, and confirmation of gestational age by a crown-rump length (CRL) measurement in the first trimester. Generalized Additive Model for Location, Scale and Shape (GAMLSS) was used to align the time frames of the longitudinal fetal measurements, corresponding with the methods of the postnatal growth curves of the WHO MGRS Group. RESULTS: A total of 27,680 complete scans were selected from the astraia© ultrasound database representing 12,368 pregnancies. Gender-specific fetal growth curves for biparietal diameter (BPD), head circumference (HC), abdominal circumference (AC), and femur length (FL) were derived. The HC and BPD were significantly larger in boys compared to girls from 20 weeks of gestation onwards (p < 0.001) equating to a 3-day difference at 20-24 weeks. Boys were significantly heavier, longer, and had greater head circumference than girls (p < 0.001) at birth. The Apgar score at 1 min (p = 0.01) and arterial cord pH (p < 0.001) were lower in boys. CONCLUSIONS: These longitudinal fetal growth curves for the first time allow integration with neonatal and pediatric WHO gender-specific growth curves. Boys exceed head growth halfway of the pregnancy, and immediate birth outcomes are worse in boys than girls. Gender difference in intrauterine growth is sufficiently distinct to have a clinically important effect on fetal weight estimation but also on the second trimester dating. Therefore, these differences might already play a role in early fetal or immediate neonatal management.


Asunto(s)
Peso al Nacer , Desarrollo Fetal , Largo Cráneo-Cadera , Femenino , Humanos , Estudios Longitudinales , Masculino , Embarazo , Primer Trimestre del Embarazo , Segundo Trimestre del Embarazo , Tercer Trimestre del Embarazo , Caracteres Sexuales , Ultrasonografía Prenatal
4.
J Psychiatr Res ; 47(7): 880-91, 2013 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-23566423

RESUMEN

BACKGROUND: The methylation status of the human glucocorticoid receptor gene NR3C1 in newborns has been reported to be sensitive to prenatal maternal mood. This study investigates both the association between maternal cortisol and emotional state during pregnancy and the methylation state of the promoter region of NR3C1 gene. METHODS: We examined 83 pregnant women. Psychological data and diurnal cortisol data were assessed to evaluate maternal stress once each trimester. DNA methylation at different loci of the NR3C1 gene, including exon 1B, 1D and 1F, was analyzed in genomic DNA from cord blood mononuclear cells. RESULTS: Univariable analyses indicated pregnancy related anxiety to be the strongest psychological parameter throughout pregnancy. Most significant findings concerned 1F. Particularly the methylation state of CpG9 was significantly associated with maternal emotional wellbeing. In a multivariable model the proportion of variance in methylation state of F9 explained (PVE) by pregnancy related anxiety was 7.8% (p = 0.023) during T1. Furthermore different CpG-units located at the nerve growth factor inducible protein A (NGFI-A) binding sites of 1F were associated with maternal anxiety [(F20.21: PC PRAQ and fear of integrity in T1: respectively PVE:8.9% and PVE:9.0%; Fear of delivery T2: PVE:8.0%, Fear of integrity T2: PVE:6.0% and STAI T2: PVE:5.9%) - (F12.13: PC PRAQ T1: PVE:6.9%, fear of integrity T2: PVE:6.0% and fear of delivery T2: PVE:8.0%)] and cortisol (F38.39: PVE:8.9%) in T2. CONCLUSION: These data indicate that prenatal maternal emotional state, particularly pregnancy related anxiety, are associated with the methylation state of the NR3C1 gene in the child.


Asunto(s)
Ansiedad , Metilación de ADN , Emociones/fisiología , Hidrocortisona/metabolismo , Intercambio Materno-Fetal/genética , Regiones Promotoras Genéticas/genética , Receptores de Glucocorticoides/genética , Adulto , Ansiedad/sangre , Ansiedad/genética , Ansiedad/psicología , Área Bajo la Curva , Islas de CpG/genética , Epigenómica , Europa (Continente) , Femenino , Sangre Fetal/metabolismo , Edad Gestacional , Humanos , Embarazo , Escalas de Valoración Psiquiátrica , Receptores de Glucocorticoides/metabolismo , Estudios Retrospectivos , Saliva/metabolismo , Encuestas y Cuestionarios
5.
Curr Genomics ; 11(6): 397-401, 2010 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21358983

RESUMEN

Only 25 to 30% of conceptions result in a live birth. There is mounting evidence that the cause for this low fecundity is an extremely high incidence of chromosomal rearrangements occurring in the cleavage stage embryo. In this review, we gather all recent evidence for an extraordinary degree of mosaicisms in early embryogenesis. The presence of the rearrangements seen in the cleavage stage embryos can explain the origins of the placental mosaicisms seen during chorion villi sampling as well as the chromosomal anomalies seen in early miscarriages. Whereas these rearrangements often lead to implantation failure and early miscarriages, natural selection of the fittest cells in the embryo is the likely mechanism leading to healthy fetuses.

6.
Best Pract Res Clin Obstet Gynaecol ; 23(5): 691-709, 2009 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-19632900

RESUMEN

This article reviews serious clinical complications related to assisted reproductive technology (ART) procedures (ovarian stimulation and oocyte aspiration), including ovarian hyperstimulation syndrome (OHSS), bleeding and infection. These complications are rare, but can be severe and even life-threatening. It is important that general practitioners and gynaecologists are aware of these complications, because they will often be the first to be contacted by patients. Similarly, patients should be counselled before starting ART procedures that iatrogenic complications can be associated with ovarian stimulation and/or oocyte aspiration.


Asunto(s)
Síndrome de Hiperestimulación Ovárica/etiología , Técnicas Reproductivas Asistidas/efectos adversos , Enfermedades de los Anexos/etiología , Atención Ambulatoria , Anticoagulantes/uso terapéutico , Cuidados Críticos , Criopreservación , Electrólitos/uso terapéutico , Femenino , Fluidoterapia/métodos , Hemorragia , Hospitalización , Humanos , Mutación/genética , Recuperación del Oocito/métodos , Síndrome de Hiperestimulación Ovárica/prevención & control , Enfermedad Inflamatoria Pélvica/etiología , Receptores de HFE/genética , Sistema Renina-Angiotensina/fisiología , Factores de Riesgo , Tromboembolia/etiología , Anomalía Torsional/etiología , Factor A de Crecimiento Endotelial Vascular/fisiología , Vasodilatación/fisiología
7.
Curr Opin Anaesthesiol ; 16(3): 253-6, 2003 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-17021467

RESUMEN

PURPOSE OF THE REVIEW: The present manuscript reviews recent data on fetal intrapartum surveillance with special attention to new technologies. RECENT FINDINGS: Continuous fetal heart-rate monitoring, fetal blood sampling, intrapartum stimulation tests, fetal pulse oximetry and fetal electrocardiography will be reviewed. SUMMARY: From the available data it appears that to date the analysis of the sinus tachycardia segment of the fetal electrocardiography used in conjunction with continuous fetal heart-rate monitoring is the method of choice.

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