Second trimester maternal serum ADAM12 levels in Down's syndrome pregnancies.

Abstract:

OBJECTIVE:To estimate the utility of maternal serum ADAM12 as a Down's syndrome marker. METHODS:Samples from 71 Down's syndrome affected pregnancies were retrieved from - 20 degrees C storage together with 710 controls matched for gestation and storage time. ADAM12 was measured prior to identification of the affected pregnancies, and expressed in multiples of the gestation-specific median (MoM). RESULTS:The median ADAM12 level in the affected pregnancies was 1.36 MoM with a 10th-90th centile range of 0.90-1.94 MoM compared with 1.01 and 0.65-1.52 MoM in the unaffected control pregnancies (P = < 0.0001, two-side Wilcoxon Rank Sum Test). The Mahalanobis distance between the medians was 0.96 compared with 0.92, 1.18, 1.07 and 1.24 for alpha-fetoprotein, intact human chorionic gonadotrophin (hCG), unconjugated estriol and inhibin-A respectively in the same samples. In unaffected pregnancies there were highly statistically significant correlations between ADAM12 and each of the other markers; in the affected pregnancies the only significant correlations were with hCG (P< or =0.0001) and inhibin-A (P< or =0.05). Statistical modelling predicted that ADAM12 as a fifth marker could increase the detection rate by 2-3% or reduce the false-positive rate by 0.9-1.7%. CONCLUSIONS:ADAM12 is a second trimester marker of Down's syndrome, with discriminatory power similar to existing markers. It could be considered in multi-marker combinations.

journal_name

Prenat Diagn

journal_title

Prenatal diagnosis

authors

Donalson K,Turner S,Wastell H,Cuckle H

doi

10.1002/pd.2043

subject

Has Abstract

pub_date

2008-10-01 00:00:00

pages

904-7

issue

10

eissn

0197-3851

issn

1097-0223

journal_volume

28

pub_type

杂志文章
  • The influence of needle and syringe size on chorionic villus sampling of term placentae: a randomised trial.

    abstract:OBJECTIVE:To determine the effect of needle and syringe size on the amount of tissue obtained at chorionic villus sampling METHODS:Two needle sizes, 18 and 20 gauge, and two syringe sizes 5 mL and 20 mL, were used to assess samples from term post-partum placentae. Each of the four combinations was tested by 25 aspirat...

    journal_title:Prenatal diagnosis

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1002/pd.752

    authors: Cochrane L,Ainscough M,Alfirevic Z

    更新日期:2003-12-30 00:00:00

  • Microarray analysis: First-trimester maternal serum free β-hCG and the risk of significant copy number variants.

    abstract:OBJECTIVE:To determine whether abnormal levels of first-trimester maternal serum free β-hCG and PAPP-A are associated with significant copy number variants (CNVs) on chromosomal microarray analysis (CMA). METHODS:Retrospective cohort of singleton prenatal CMA studies (n = 2880). Cases with an abnormal karyotype, benig...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.5350

    authors: Bornstein E,Gulersen M,Krantz D,Cheung SW,Maliszewski K,Divon MY

    更新日期:2018-11-01 00:00:00

  • Reasons for accepting or declining participation in the ASPRE trial: A qualitative study with women at high risk of preterm pre-eclampsia.

    abstract:OBJECTIVE:To identify factors that affected the decision of pregnant women at high risk for pre-eclampsia (PE) in accepting or declining participation in a medicated clinical trial (ASPRE) for the prevention of preterm PE. METHOD:This was a qualitative, cross-sectional study. A purposive sample of 14 participants and ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章,多中心研究

    doi:10.1002/pd.5554

    authors: Nikčević AV,Dodd Z,Prior J,O'Gorman N,Poon LC,Nicolaides KH

    更新日期:2019-11-01 00:00:00

  • Trends in elective terminations of pregnancy between 1989 and 2000 in a French county (the Isère).

    abstract:OBJECTIVES:This study was performed in order to provide a description of indications for induced elective terminations of pregnancy (ETOP), their characteristics (e.g. gestational age), and their evolution over time. DESIGN OF THE STUDY:This is an epidemiological study. The geographic area covered is the French county...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.711

    authors: Guillem P,Fabre B,Cans C,Robert-Gnansia E,Jouk PS

    更新日期:2003-11-01 00:00:00

  • Open fetal surgery for myelomeningocele.

    abstract::Despite efforts at prevention through the use of preconception folic acid, spina bifida remains one of the most common congenital anomalies of the central nervous system that is compatible with life. It is, however, associated with a significant degree of lifelong morbidity. The development of open fetal surgery for m...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章,评审

    doi:10.1002/pd.2805

    authors: Bebbington MW,Danzer E,Johnson MP,Adzick NS

    更新日期:2011-07-01 00:00:00

  • Karyotypes found in the population declared at increased risk of Down syndrome following maternal serum screening.

    abstract::Of the 65 328 pregnancies of South Australian mothers screened by the South Australian Maternal Serum Antenatal Screening (SAMSAS) Programme between 1 January 1991 and 31 December 1997, 3431 (5.25%) were declared at increased risk of fetal Down syndrome. Fetal or neonatal karyotype was determined in 2737/3431 (79.8%) ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.108

    authors: Ryall RG,Callen D,Cocciolone R,Duvnjak A,Esca R,Frantzis N,Gjerde EM,Haan EA,Hocking T,Sutherland G,Thomas DW,Webb F

    更新日期:2001-07-01 00:00:00

  • Prenatal diagnosis of mucopolysaccharidosis I: A special difficulty arising from an unusually low enzyme activity in mother's cells.

    abstract::We investigated a case (I.I.) of the severe form of mucopolysaccharidosis I (Hurler syndrome). Prenatal diagnosis was requested by the parents and the next pregnancy was monitored. We report here a special difficulty arising in this diagnosis due to the low enzyme activity in the mother's cells (10-15 per cent of cont...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970050209

    authors: Gatti R,Borrone C,Filocamo M,Pannone N,Di Natale P

    更新日期:1985-03-01 00:00:00

  • Early prenatal diagnosis of recurrent 46,XY partial gonadal dysgenesis.

    abstract:OBJECTIVES:We present a case of early prenatal diagnosis of recurrent 46,XY partial gonadal dysgenesis, by combining early genetic and sonographic evaluations. METHODS:The conceptus of a mother with a first child affected by 46,XY gonadal dysgenesis was sonographically evaluated at 21- and 23-mm BPD (12(+2) and 12(+6)...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.673

    authors: Mazza V,Ottolenghi C,Di Monte I,Baldassari F,Rivasi F,Volpe A,Forabosco A

    更新日期:2003-09-01 00:00:00

  • Applying decision analysis to facilitate informed decision making about prenatal diagnosis for Down syndrome: a randomised controlled trial.

    abstract:OBJECTIVE:To evaluate decision analysis as a technique to facilitate women's decision-making about prenatal diagnosis for Down syndrome using measures of effective decision-making. DESIGN:Randomised controlled trial in a UK hospital's prenatal diagnosis clinic. INTERVENTION:Routine versus routine consultation structu...

    journal_title:Prenatal diagnosis

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1002/pd.851

    authors: Bekker HL,Hewison J,Thornton JG

    更新日期:2004-04-01 00:00:00

  • Prenatal MR imaging of dural sinus malformation: a case report.

    abstract:OBJECTIVE:To describe prenatal magnetic resonance imaging (MRI) findings of dural sinus malformation (DSM), a very rare, congenital form of dural arteriovenous shunt (DAVS), typically affecting newborns. METHODS:Ultrasound (US) and MRI were performed at 34 weeks' gestation, and the findings of these examinations were ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1347

    authors: Rossi A,De Biasio P,Scarso E,Gandolfo C,Pavanello M,Morana G,Venturini PL,Tortori-Donati P

    更新日期:2006-01-01 00:00:00

  • Prenatal diagnosis of sex chromosome aneuploidy: possible reasons for high rates of pregnancy termination.

    abstract::Sex chromosome aneuploidy (SCA), when detected in amniocentesis, is usually an unexpected result of a test carried out for another purpose. For most SCAs, the prognosis is milder and less predictable than trisomy 21, and therefore parents are faced with a difficult decision regarding the option of pregnancy terminatio...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.78

    authors: Sagi M,Meiner V,Reshef N,Dagan J,Zlotogora J

    更新日期:2001-06-01 00:00:00

  • Prenatal diagnosis of holoprosencephaly in two fetuses with der (7)t(1;7)(q32;q32)pat inherited from the father with double translocations.

    abstract::The presence of two independent translocations in one person is rare. Herein, we report the prenatal diagnosis of two sibling fetuses with holoprosencephaly, whose father is a carrier of double translocations. The karyotype of the father is 46,XY, t(1;7) (q32;q32), t(14,15) (q32.1;q26.3). The two fetuses had variable ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.552

    authors: Chuang L,Kuo PL,Yang HB,Chien CH,Chen PY,Chang CH,Chang FM

    更新日期:2003-02-01 00:00:00

  • In utero acquired limb ischemia in monochorionic twins with and without twin-to-twin transfusion syndrome.

    abstract:OBJECTIVE:To report on the occurrence of in utero acquired limb ischemia in two referral institutions managing monochorionic (MC) twins with and without twin-to-twin transfusion syndrome (TTTS) and estimate its prevalence. METHODS:All MC twin pregnancies assessed at two referral units between 2002 and 2007 were retros...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章,多中心研究

    doi:10.1002/pd.2000

    authors: Lopriore E,Lewi L,Oepkes D,Debeer A,Vandenbussche FP,Deprest J,Walther FJ

    更新日期:2008-09-01 00:00:00

  • Prenatal diagnosis and obstetrical management of multicystic dysplastic kidney disease.

    abstract::Multicystic dysplastic kidney disease (MDKD) is one of the most common congenital renal anomalies. We report 16 consecutive cases of MDKD recognized in the antenatal period by sonography. Diagnosis is usually easy as MDKD has in the vast majority of cases a striking ultrasound appearance including enlargement of the k...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970070207

    authors: Rizzo N,Gabrielli S,Pilu G,Perolo A,Cacciari A,Domini R,Bovicelli L

    更新日期:1987-02-01 00:00:00

  • Elevation of glycosaminoglycans in the amniotic fluid of a fetus with mucopolysaccharidosis VII.

    abstract:OBJECTIVE:The aim of this study was to quantify glycosaminoglycans (GAGs) in amniotic fluid (AF) from an MPS VII fetus compared with age-matched fetuses obtained from normal pregnancies. METHOD:Disaccharides were measured by liquid chromatography tandem mass spectrometry, compared to age-matched controls. Enzyme assay...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.5028

    authors: Kubaski F,Brusius-Facchin AC,Mason RW,Patel P,Burin MG,Michelin-Tirelli K,Kessler RG,Bender F,Leistner-Segal S,Moreno CA,Cavalcanti DP,Giugliani R,Tomatsu S

    更新日期:2017-05-01 00:00:00

  • Aicardi syndrome: prenatal sonographic findings. A report of two cases.

    abstract::The prenatal sonographic findings in two children with Aicardi syndrome are reported. ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:

    authors: Bromley B,Krishnamoorthy KS,Benacerraf BR

    更新日期:2000-04-01 00:00:00

  • Current controversies in prenatal diagnosis 2: prediction and prevention of adverse pregnancy outcomes requires a genomic rather than proteomic solution.

    abstract::From both presentations, it is clear that understanding the APO associated with placental dysfunction represents one of the greatest challenges in the field of prenatal screening, diagnosis, and therapy. Their clinical impact on the health of the mother and child was well recognized by the debaters, and both have agre...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.4533

    authors: Chiu RW,Myatt L,Otaño L

    更新日期:2015-01-01 00:00:00

  • Fetal myelomeningocele surgery: Only treating the tip of the iceberg.

    abstract:OBJECTIVE:Fetal myelomeningocele (fMMC) surgery improves infant outcomes when compared with postnatal surgery. Surgical selection criteria and the option of pregnancy termination, however, limit the number of cases that are eligible for prenatal surgery. We aimed to quantify what proportion of cases could ultimately be...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.5390

    authors: AlRefai A,Drake J,Kulkarni AV,Connor KL,Shannon P,Toi A,Chitayat D,Blaser S,Church PT,Abbasi N,Ryan G,Van Mieghem T

    更新日期:2019-01-01 00:00:00

  • Fetal capillary haemangioblastoma: an exceptional tumour. A review of the literature.

    abstract::We report a case of a fetal haemangioblastoma located in the cerebellopontine angle. On prenatal ultrasonographic examination a hyperechogenic and heterogeneous mass with a major vascularization on colour Doppler imaging was observed. It increased progressively and laminated the cerebellum. A neoplastic tumour was sus...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章,评审

    doi:10.1002/pd.452

    authors: Diguet A,Laquerrière A,Eurin D,Chanavaz-Lacheray I,Magdeleine Ruchoux M,Rossi A,Marpeau L

    更新日期:2002-11-01 00:00:00

  • QF-PCR: application, overview and review of the literature.

    abstract::Quantitative fluorescent polymerase chain reaction has been in diagnostic use in the UK for over 10 years and has proved to be a cost-effective, robust and accurate rapid prenatal test for common aneuploidies. Specific advantages include detection of triploidy, mosaicism and maternal cell contamination. Its applicatio...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章,评审

    doi:10.1002/pd.2945

    authors: Mann K,Ogilvie CM

    更新日期:2012-04-01 00:00:00

  • COFFEE: control-free noninvasive fetal chromosomal examination using maternal plasma DNA.

    abstract:OBJECTIVE:The aim of this study is to develop an approach for analyzing plasma DNA sequencing data for noninvasive fetal chromosomal aneuploidy testing that does not require the comparison with control samples or a series of selected genomic regions. RESULTS:We developed the control-free noninvasive fetal chromosomal ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.5016

    authors: Sun K,Chan KC,Hudecova I,Chiu RW,Lo YM,Jiang P

    更新日期:2017-04-01 00:00:00

  • Rapid genetic analysis of oculocutaneous albinism (OCA1) using denaturing high performance liquid chromatography (DHPLC) system.

    abstract:OBJECTIVES:To present the prenatal genetic diagnoses and counseling for two cases of oculocutaneous albinism (OCA) type I family by detection of mutations in the OCA1 gene by denaturing high performance liquid chromatography (DHPLC) system and a review of the literature. METHODS:All DNA samples were extracted from per...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1439

    authors: Lin SY,Chien SC,Su YN,Lee CN,Chen CP

    更新日期:2006-05-01 00:00:00

  • Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial.

    abstract::Cytogenetic microarray analysis (CMA) in prenatal testing detects chromosome abnormalities and new genetic syndromes that would be missed by conventional cytogenetics and has the potential to significantly enhance prenatal genetic evaluation. A large Eunice Kennedy Shriver National Institute Of Child Health and Human ...

    journal_title:Prenatal diagnosis

    pub_type: 临床试验,杂志文章

    doi:10.1002/pd.3863

    authors: Wapner RJ,Driscoll DA,Simpson JL

    更新日期:2012-04-01 00:00:00

  • Fetal brain-sparing after laser surgery for twin-twin transfusion syndrome appears associated with two-year neurodevelopmental outcomes.

    abstract:OBJECTIVE:The cerebroplacental ratio (CPR) is a semi-quantitative marker for fetal brain-sparing. Our purpose was to measure the CPR at the time of treatment with selective laser photocoagulation of communicating vessels in gestations with twin-twin transfusion syndrome (TTTS) to test its association with neurological ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.4713

    authors: Chmait RH,Chon AH,Schrager SM,Llanes A,Hamilton A,Vanderbilt DL

    更新日期:2016-01-01 00:00:00

  • Antepartum management and obstetric outcomes among pregnancies with Down syndrome from diagnosis to delivery.

    abstract:OBJECTIVE:Little is known about the obstetric care of an ongoing pregnancy with trisomy 21. We sought to ascertain an obstetric profile for pregnancies with Down syndrome to help guide prenatal management. METHOD:Pregnancies managed for delivery with trisomy 21 between 2003 and 2014 were analyzed. We reviewed demograp...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.5054

    authors: Guseh SH,Little SE,Bennett K,Silva V,Wilkins-Haug LE

    更新日期:2017-07-01 00:00:00

  • Reference charts and equations of Korean fetal biometry.

    abstract:OBJECTIVE:To construct new reference charts and equations for fetal biparietal diameter (BPD), head circumference (HC), abdominal circumference (AC) and femur diaphysis length (FDL) from Korean fetuses at 12-40 weeks. METHOD:Prospective cross-sectional data obtained in one center for 5 years from a population of pregn...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1729

    authors: Jung SI,Lee YH,Moon MH,Song MJ,Min JY,Kim JA,Park JH,Yang JH,Kim MY,Chung JH,Cho JY,Kim KG

    更新日期:2007-06-01 00:00:00

  • Estimates for the sensitivity and false-positive rates for second trimester serum screening for Down syndrome and trisomy 18 with adjustment for cross-identification and double-positive results.

    abstract::Second trimester screening for fetal Down syndrome and trisomy 18 is available through separate protocols that combine the maternal age-specific risk and the analysis of maternal serum markers. We have determined the extent to which additional Down syndrome affected pregnancies may be identified through trisomy 18 scr...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:

    authors: Benn PA,Ying J,Beazoglou T,Egan JF

    更新日期:2001-01-01 00:00:00

  • Community attitudes to cystic fibrosis carrier testing in England: a pilot study.

    abstract::Inexpensive and accurate carrier testing for cystic fibrosis (CF) will be possible in the near future. There are no existing studies on the attitudes of English persons in the community to carrier testing for CF or any other recessive disorder. We have conducted a trial study of 166 persons at two schools, two doctors...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.1970091008

    authors: Williamson R,Allison ME,Bentley TJ,Lim SM,Watson E,Chapple J,Adam S,Boulton M

    更新日期:1989-10-01 00:00:00

  • The role of second trimester uterine artery Doppler in pregnancies with systemic lupus erythematosus.

    abstract:OBJECTIVE:The aim of this article is to assess the predictive value of second trimester mean uterine artery Doppler pulsatility index (mUtA PI) for pregnancy complications in women with systemic lupus erythematosus (SLE). METHODS:Cohort study of consecutive pregnancies complicated with SLE during a period of 12 years ...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.4517

    authors: Pagani G,Reggia R,Andreoli L,Prefumo F,Zatti S,Lojacono A,Tincani A,Frusca T

    更新日期:2015-05-01 00:00:00

  • Cell fusion phenomena detected after in utero transplantation of Ds-red-harboring porcine amniotic fluid stem cells into EGFP transgenic mice.

    abstract:OBJECTIVES:Amniotic fluid stem cells (AFSCs) are derived from the amniotic fluid of the developing fetus and can give rise to diverse differentiated cells of ectoderm, mesoderm, and endoderm lineages. Intrauterine transplantation is an approach used to cure inherited genetic fetal defects during the gestation period of...

    journal_title:Prenatal diagnosis

    pub_type: 杂志文章

    doi:10.1002/pd.4334

    authors: Peng SY,Chen YH,Chou CJ,Wang YH,Lee HM,Cheng WT,Shaw SW,Wu SC

    更新日期:2014-05-01 00:00:00