Sito in Italia dove è possibile acquistare la consegna acquisto Viagra a buon mercato e di alta qualità in ogni parte del mondo.


Human Reproduction, Vol.24, No.6 pp. 1330 – 1338, 2009 Advanced Access publication on February 26, 2009 Pregnancies conceived using assistedreproductive technologies (ART) havelow levels of pregnancy-associatedplasma protein-A (PAPP-A) leading toa high rate of false-positive resultsin first trimester screeningfor Down syndrome D.J. Amor1,2,3,4,8, J.X. Xu1,2, J.L. Halliday1,2, I. Francis3, D.L. Healy5,6, S. Breheny5,6, H.W.G. Baker4,7, and A.M. Jaques1 1Murdoch Childrens Research Institute, Royal Children’s Hospital, Parkville, Victoria, Australia 2Department of Paediatrics, University ofMelbourne, Melbourne, Victoria, Australia 3Victorian Clinical Genetics Services, Royal Children’s Hospital, Parkville, Victoria, Australia4 Melbourne IVF, East Melbourne, Victoria, Australia 5Department of Obstetrics and Gynaecology, Monash University, Clayton, Victoria, Australia 6Monash IVF, Richmond, Victoria, Australia 7Department of Obstetrics and Gynaecology, University of Melbourne, Royal Women’sHospital, Parkville, Victoria, Australia 8Correspondence Address. Murdoch Childrens Research Institute, Royal Children’s Hospital, Flemington Rd, Parkville 3052, Australia.
Tel: þ61-3-83-41-62-93; Fax: þ61-3-83-41-63-90; Email: background: First trimester screening (FTS) for Down syndrome combines measurement of nuchal translucency, free beta-humanchorionic gonadotrophin and pregnancy-associated plasma protein-A (PAPP-A). The aim of this study was to undertake a detailed analysisof FTS results in singleton pregnancies conceived using assisted reproductive technologies (ART) and non-ART pregnancies.
methods: A record linkage study compared outcomes in 1739 ART-conceived and 50 253 naturally conceived pregnancies.
results: Overall, significantly lower PAPP-A levels were detected in ART pregnancies (0.83 multiples of median, MoM) than in controls(1.00 MoM) (t-test P , 0.001). This difference remained after excluding complicated pregnancies. Analysis of factors affecting PAPP-A levelssuggested fresh compared with frozen embryo transfers and use of artificial cycles compared with natural cycles for frozen transfers wereassociated with lower values. The adjusted odds ratio (AdjOR) for receiving a false-positive result was 1.71 (95% CI 1.44 – 2.04; P , 0.001)for ART pregnancies compared with non-ART pregnancies, and this leads to a higher AdjOR (1.24, 95% CI 1.03 – 1.49; P ¼ 0.02) for having achorionic villous sampling (CVS) or amniocentesis.
conclusions: ART pregnancies have reduced FTS PAPP-A levels leading to an increased likelihood of receiving a false-positive resultand having a CVS/amniocentesis. Lower PAPP-A may reflect impairment of early implantation with some forms of ART.
Key words: ART / PAPP-A / pregnancy screening / pregnancy complications / hormonal stimulation based on maternal age alone was first described in 1988 (Wald et al.,1988). Over the last 10 years, second trimester serum screening has Pregnancy screening for Down syndrome (DS) and other chromo- been progressively replaced by first trimester combined screening.
some abnormalities has become part of routine antenatal care over The first trimester combined screen measures maternal serum levels the last 20 years. The measurement of second trimester biochemical markers in the blood of pregnant women to improve screening for DS pregnancy-associated plasma protein-A (PAPP-A) at 9 – 12 weeks & The Author 2009. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved.
For Permissions, please email: gestation and measures nuchal translucency (NT) by ultrasound at We hypothesized that in pregnancies conceived using ART, factors 11 – 13 weeks gestation. These measurements are combined with exist that are absent in natural conceptions, potentially influencing the maternal age, weight and gestational age to produce a risk estimate marker levels, and consequently, risk results of the first trimester com- of the fetus having DS or trisomy 18 (T18) (Wald et al., 2003). For bined screen. The aims of this study were to investigate in a large pregnancies at increased risk, prenatal diagnostic testing, CVS or population-based sample, the effect of ART on the individual amniocentesis, can be offered. In the Victorian population, the sensi- markers of the first trimester combined screen (fb-hCG, PAPP-A tivity of the first trimester combined screen for DS is 91% (using a risk and NT) and on the FPR. We also aimed to investigate the effect of threshold of 1 in 300 at the time of ultrasound), with the proportion of different ART modalities on these markers, and the impact of ART unaffected pregnancies receiving an increased risk result (false positive and screening results on the uptake of prenatal diagnostic testing rate, FPR) being 3.9% (Jaques et al., 2007).
(CVS and amniocentesis) following first trimester combined screening.
Pregnancies conceived using assisted reproductive technologies (ART) now account for 3% of all live births in Australia (Wang et al., 2007). Previous studies of second trimester serum screeninghave shown that serum markers in ART pregnancies differ from The effect of ART (IVF, ICSI, GIFT, embryo cryopreservation and natural conceptions, leading to an increased FPR (Barkai et al., 1996; hormone treatment) on the FPR of the first trimester combined screen Ribbert et al., 1996; Frishman et al., 1997; Wald et al., 1999; Raty and its three components (fb-hCG, PAPP-A, NT) was examined in et al., 2002; Lambert-Messerlian et al., 2006). The effect of ART on women with singleton pregnancies screened between February 2000 first trimester combined screening has been examined in 13 studies and June 2004 in Victoria, Australia. The pregnancies included did nothave a fetus or produce a child with a birth defect, and singleton pregnan- that have yielded contradictory and inconclusive results, largely due cies were defined as the presence of one fetus after 20 weeks gestation.
to small sample sizes. Some studies found that fb-hCG (Liao et al., Data from three separate databases were linked to obtain the study popu- 2001; Niemimaa et al., 2001; Ghisoni et al., 2003; Bersinger et al., lation (Fig. 1). A fourth prenatal diagnosis database was linked to the study 2004) and NT thickness (Maymon and Shulman, 2004; Hui population to investigate the uptake of CVS and amniocentesis. The four et al., 2005b) were increased in ART pregnancies, yet others found no differences in fb-hCG (Wojdemann et al., 2001; Maymon and The Victorian Perinatal Data Collection Unit (VPDCU) is responsible Shulman, 2002; Orlandi et al., 2002; Maymon and Shulman, 2004; for the collection of information on all Victorian births 20 weeks’ ges- Bellver et al., 2005; Lambert-Messerlian et al., 2006; Anckaert et al., tation or 400 g birthweight. Reporting to the VPDCU is mandatory 2008) or NT (Liao et al., 2001; Niemimaa et al., 2001; Wojdemann and data collected includes obstetric factors, neonatal outcomes, birth et al., 2001; Maymon and Shulman, 2002; Orlandi et al., 2002; defects and previous pregnancy history. A unique registration number isassigned to each newborn. During the study period there were Ghisoni et al., 2003; Lambert-Messerlian et al., 2006). PAPP-A levels 245 000 singleton births in Victoria.
have been decreased in some studies (Liao et al., 2001; Maymon The Victorian Birth Defects Register collects data on all pregnancies and Shulman, 2002; Orlandi et al., 2002; Bersinger et al., 2004; diagnosed with a birth defect, comprising live births, stillbirths, neonatal Maymon and Shulman, 2004; Hui et al., 2005a; Tul and Novak-Antolic, deaths and terminations. For this study, all pregnancies that resulted in a 2006; Anckaert et al., 2008), but unaltered in others (Niemimaa et al., birth defect were identified and excluded from the study population.
2001; Wojdemann et al., 2001; Ghisoni et al., 2003; Bellver et al., The Victorian Clinical Genetics Service (VCGS) conducts all first trime- 2005; Lambert-Messerlian et al., 2006).
ster combined screening tests in Victoria. The VCGS first trimester Figure 1 Flow diagram showing data linkage between three separate databases to obtain study population.
combined screening programme has been described elsewhere (Jaques before oocyte collection. Hormone treatment accompanying frozen – et al., 2006, 2007). Briefly, fb-hCG and PAPP-A measurements were per- thawed embryo transfers was defined as any combination of estradiol formed on a KRYPTOR analyser, and NT and crown– rump length (CRL) and progesterone for artificial cycles for oligomenorrhoea/amenorrhoea, measurements were made off-site by multiple ultrasonologists in accord- and clomiphene with or without HCG for ovulation induction to time to ance with the technique described by the Fetal Medicine Foundation (Nicolaides, 2004). NT and biochemistry values were calculated fromCRL in ART and non-ART pregnancies because this was the only way to directly compare ART and non-ART pregnancies, and because it has Ethics approval was obtained from the Human Research Ethics Commit- been shown that CRL and date of oocyte collection are practically equiv- tees of the Victorian Department of Human Services, Mercy Health and alent when calculating gestational age for first trimester screening (FTS) Aged Care, Royal Women’s Hospital, Freemasons Hospital, Epworth (Gjerris et al., 2008). The biochemistry and risk estimates were calculated Hospital, Monash University and Monash Surgical Private Hospital.
using software developed in house and results are monitored byUKNEQAS and audited by ascertaining pregnancy outcomes for calcu-lation of specificity and sensitivity as described elsewhere (Jaques et al., 2006, 2007).The VCGS prenatal screening database contains comprehen-sive data for all women who had first trimester combined screening in the Women in the non-ART and ART groups were similar in terms of maternal weight and gestational age at ultrasound (calculated from The data on ART in Victoria were obtained from the three major pro- CRL of the fetus) at the time of screening (Table I). Maternal viders: Melbourne IVF, Monash IVF and Melbourne Assisted Conception country of birth was Australia or Europe/UK for 91.7% of ART Centre, accounting for 98% of ART pregnancies in Victoria. The dataset mothers and 91.8% of non-ART mothers (P ¼ 0.90). The ART included detailed information on the ART cycles, including the type of group were older and more likely to be primigravid than the ART treatment, indication for ART, whether embryos were fresh or non-ART group. The measured CRL was less for fresh embryos frozen-thawed, the use of donor gametes or embryos and the number of fetal hearts present at ultrasound at 6 weeks gestation.
Data for all CVS and amniocentesis tests performed in Victoria and their results are provided to the VPDCU by all four cytogenetic laboratories in the State. Information regarding the uptake of CVS and amniocentesis was PAPP-A levels were significantly lower (P , 0.001) in ART pregnancies available for the 41 756 pregnancies screened in 2002 – 2004. Excluded (0.83 MoM) compared with non-ART pregnancies (1.0 MoM) from this subset of analyses were 10 236 pregnancies screened in (Table II). A small increase in the NT was detected in the ART 2000 – 2002 because these pregnancies were not linked to the prenatal group (0.91 MoM) compared with the non-ART group (0.90 MoM) (P ¼ 0.004). Analyses of fb-hCG levels showed no significant differ-ence between ART (0.99 MoM) and non-ART (0.98 MoM) Data coding and statistical analyses were conducted using SPSS (version Adverse pregnancy complications, comprising pregnancies with 15; SPSS Inc., Chicago, IL, USA). Mann – Whitney U-tests were done to adverse perinatal outcomes (stillbirth, neonatal death, prematurity, test the difference between the characteristics (age, weight, CRL and birthweight ,2500 g) and/or obstetric complications (pre-eclampsia, gestational age of testing) of non-ART and ART groups, and chi-square pregnancy-induced hypertension, gestational diabetes) were more tests were performed to assess the difference in the proportion of common in the ART pregnancies (21.0%) compared with the women from the different groups who were primigravid. Independent non-ART pregnancies (13.9%). The PAPP-A levels were lower in samples t-tests were performed on the means of the log-transformed the complicated pregnancies overall but there was still a significant multiples of median (MoM) values for fb-hCG, PAPP-A and NT. Results difference between the ART and non-ART groups (Table II). Among were then back-transformed and are presented as geometric means.
uncomplicated pregnancies, PAPP-A levels remained significantly The statistical significance of differences in proportions between groups reduced in ART pregnancies (0.85 MoM) compared with non-ART and results were expressed as odds ratios (ORs) with 95% confidence pregnancies (1.02 MoM) (P , 0.001) (Table II).
intervals (CIs). Univariable logistic regression analysis was done toexplore associations between results and a number of covariables, e.g.
Analyses according to the aetiology of the infertility showed that maternal age, maternal country of birth, gravidity, parity, birthweight and PAPP-A levels were similarly reduced when the infertility was reported gestational age. Multivariable analysis was adjusted for maternal age and to be of female-only aetiology (0.82 MoM), male-only aetiology (0.85 gravidity as these were the only significant confounders.
MoM) and when a combination of male and female aetiologies was The ART study population was divided into subgroups to allow more present in the couple (0.82 MoM). The differences between these cat- in-depth analyses of the different exposures on outcome: (i) aetiology of egories were not statistically significant.
infertility (female-only aetiology, male-only aetiology, a combination of Further analysis of the effect of ART on marker levels was under- male and female aetiologies or unknown aetiology); (ii) ART procedure taken using the subset of pregnancies that did not have adverse peri- (IVF, ICSI or GIFT); (iii) embryo transfer (fresh or frozen – thawed); (iv) natal and obstetric complications (Table III). Comparison of PAPP-A presence or absence of exogenous hormone treatment and (v) presence levels between non-ART pregnancies (1.02 MoM) and each subtype of single or multiple fetal hearts at 6 weeks gestation. Although treat- of ART showed that the reduction in PAPP-A applied to all three ment protocols varied, hormone treatment accompanying fresh embryotransfers always was defined as follicle stimulating hormone (FSH) or clo- ART subtypes (IVF, 0.87 MoM; ICSI, 0.84 MoM; GIFT, 0.71 MoM).
miphene, with or without other drugs. All GIFT cycles were done with Compared with non-ART pregnancies (1.02 MoM), PAPP-A levels FSH. A small proportion (n ¼ 13) of fresh embryo transfers were done were reduced for both fresh embryos transfers (0.79 MoM, t-test without any hormone treatment to stimulate multifollicular development P , 0.001) and frozen – thawed embryo transfers (0.95 MoM, t-test Table I Characteristics of the study population Values are given as median (range) and Mann – Whitney tests were performed for P-value for maternal age, maternal weight, CRL at NT scan, gestation at NT scan and gestation at bloodsampling. Primigravid is given as a percent and chi-square tests were performed for P-values.*Denotes P-value of ,0.05 for the different ART groups (All, IVF, ICSI, GIFT, fresh and frozen)versus non-ART comparisons, # denotes P-value of ,0.05 for IVF versus ICSI comparison, ^ denotes P-value of ,0.05 for fresh versus frozen – thawed comparison.
aP-value based on the independent samples t-test, values are compared with the non-ART group.bIncludes pregnancies with adverse pregnancy outcomes [neonatal death, preterm (,37weeks) and low birthweight (,2.5 kg)] and pregnancies with obstetric complications (pre-eclampsia, pregnancy-induced hypertension and gestational diabetes).
P ¼ 0.001), however, fresh embryo transfers were associated with a Association between ART and false-positive significantly lower PAPP-A level when compared directly with frozen – thawed embryos (t-test P , 0.001).
Table IV shows the comparison between the non-ART and ART When examining the effect of hormone versus no hormone treat- groups for the proportion of women receiving a false-positive result ment irrespective of fresh or frozen – thawed embryo transfer, we from first trimester combined screening. Women conceiving using found that transfer cycles that included any hormone treatment ART had a significantly increased likelihood of receiving a false-positive resulted in lower PAPP-A levels (0.78 MoM) compared with those result (OR 2.71, 95% CI 2.19 – 3.35; P , 0.001) compared with without hormone treatment (0.99 MoM, t-test P , 0.001).
non-ART women. After adjusting for maternal age and gravidity, ART women were still more likely to receive a false-positive result[adjusted OR (AdjOR) 1.71, 95% CI 1.44 – 2.04; P , 0.001]. The like- lihood of receiving a false-positive result was higher for fresh embryo Of the 1739 singleton ART pregnancies, 1604 had one fetal heart, 123 transfers than for frozen – thawed embryo transfers.
had two or more fetal hearts and results for 12 were not available.
PAPP-A levels were 0.83 MoM for pregnancies with one fetal heart and 0.97 MoM for pregnancies with multiple fetal hearts. Results forfb-hCG were 0.99 MoM for one fetal heart and 1.03 MoM for multiple fetal hearts, and results for NT were 0.91 MoM for one fetal heart and A higher proportion of women who conceived using ART (10.6%) had a CVS or amniocentesis compared with their non-ART counterparts Table III Effect of ART on marker levels—excluding complicated pregnancies Fresh and frozen – thawed embryo transfer Fresh and frozen – thawed embryo transfer by hormone treatmentb Fresh without hormone treatment (n ¼ 11) Frozen – thawed with hormone treatment (n ¼ 118) Frozen – thawed without hormone treatment (n ¼ 455) All embryo transfers by hormone treatmentb aP-value based on the independent samples t-test, values are compared with the non-ART group.
bHormone treatment accompanying fresh embryo transfers always included FSH or clomiphene, often in combination with other drugs. All GIFT cycles were done with FSH. Hormonetreatment accompanying frozen – thawed embryo transfers comprised various combinations of estradiol, progesterone, clomiphene and HCG.
Table IV Comparison of false-positive results (5.3%) (OR 2.10, 95% CI 1.76 – 2.50; P , 0.001) (Table V). After adjust- accounted for, the OR of having a CVS or amniocentesis was reduced ing for maternal age, the ART group were still more likely to have a CVS to 0.78 (95% CI 0.60 – 1.00; P ¼ 0.054) for the ART group compared or amniocentesis compared with the non-ART group (OR 1.24, 95% CI with the non-ART group, suggesting that the higher false-positive rate 1.03 – 1.49; P ¼ 0.023). When the increased risk result was also was responsible for the higher uptake of invasive prenatal diagnosis in the ART group. When examining the effect of hormone versus nohormone treatment, we found that after controlling for maternal age, only women whose transfer cycles included hormone treatment were more likely than non-ART women to have a CVS or amniocentesis (AdjOR 1.38, 95% CI 1.11 – 1.71; P ¼ 0.003).
This is the largest and most comprehensive study to date on the influ- ence of ART conception on first trimester combined screening, and is important because of the increasing use of screening in all pregnancies.
This study comprises more than 1700 ART singleton pregnancies and more than 50 000 non-ART singleton pregnancies, representing almost as many ART pregnancies as all previous studies combined.
The primary effect of ART treatment was a significant reduction in the serum PAPP-A level compared with the non-ART conceptions, whereas fb-hCG was not significantly altered. A marginal increase in NT was observed in ART pregnancies, however, this very small differ- ence is likely due to operator effects, with ART pregnancies more likely to be scanned by a small subset of operators linked to ART clinics compared with non-ART pregnancies.
The pattern of markers observed in this study is similar to that observed in several previous studies (Liao et al., 2001; Maymon andShulman, 2002, 2004; Orlandi et al., 2002; Hui et al., 2005b; Anckaertet al., 2008), but differs from others that detected no effect of ART on PAPP-A levels (Niemimaa et al., 2001; Wojdemann et al., 2001; Ghisoni et al., 2003; Bellver et al., 2005; Lambert-Messerlian et al., 2006). Some studies have also suggested that ART results in an increase in fb-hCG (Niemimaa et al., 2001; Ghisoni et al., 2003; Ber-singer et al., 2004). A likely explanation for the contradictory findings of previous studies is their small sample sizes (sample size range 47 – We have also shown that as a result of the decreased PAPP-A in ART pregnancies, women conceiving using ART are more likely to receive a false-positive result from the first trimester combined screen and are therefore more likely to have CVS or amniocentesis.
This finding is important because an increase in the uptake of CVS and amniocentesis in healthy pregnancies will lead to an increase inparental anxiety and in procedure-related morbidity, including miscar-riage. The increase in false-positive results and uptake of prenatal diag- nosis is seen for fresh and frozen – thawed embryo transfers, but only in the subset of embryo transfers where the mother was given hormone treatment around the time of embryo transfer. This study only examined the FPR and not other indicators of screening test per- formance such as sensitivity and specificity; therefore, no conclusion can be drawn in relation to whether adjustments for calculation of risk parameters need to be made. Following further investigation ofthe effectiveness of the first trimester combined screen in ART preg- nancies, it may be possible to modify screening protocols for ART pregnancies in order to reduce the FPR without reducing the sensi- The reduction in PAPP-A levels in ART pregnancies provides further evidence that ART pregnancies are different from non-ART pregnan- cies, an observation that may have implications beyond the combined screen. PAPP-A is a growth factor that promotes growth by cleaving insulin-like growth factor binding proteins (Lawrence et al., 1999)thereby increasing the bioavailability of insulin-like growth factors (IGFs) (Conover et al., 2004). PAPP-A is present at low concen- Novak-Antolic, 2006). We found significantly lower PAPP-A levels for trations in the blood of men and non-pregnant women, but is embryos transferred fresh compared with frozen – thawed embryos.
detected at high concentrations in the blood of pregnant women This finding is consistent with one previous study that separately exam- (Lin et al., 1974), with blood levels rising soon after implantation ined fresh and frozen – thawed embryo transfers and found a reduction and increasing with gestation, peaking in the third trimester (Guibour- in PAPP-A for fresh embryo transfers (Hui et al., 2005a). A second study denche et al., 2003). In pregnant women, circulating PAPP-A originates analysed PAPP-A levels in relation to the number of oocytes retrieved at the interface between the placenta and the endometrium, where it and found a greater reduction in PAPP-A following fresh embryo trans- is produced by placental trophoblasts and decidualized endometrial fers in stimulation cycles in which a greater number of oocytes were stromal cells, and is hypothesized to regulate IGF-II bioavailability in retrieved (Tul and Novak-Antolic, 2006), further suggesting that the placenta and to facilitate implantation (Giudice et al., 2002).
hormone stimulation and the woman’s response to hormone treatment Our data provide new insights into the possible mechanisms under- lying reduced PAPP-A in ART pregnancies.
In contrast to previous studies, we also detected significantly lower One consideration is whether the presence of a ‘vanished twin’ in PAPP-A levels for frozen – thawed embryos compared with non-ART some ART pregnancies might explain the difference in results pregnancies, indicating that the reduction in PAPP-A is not restricted between ART and non-ART pregnancies. However, in our ART popu- to fresh embryo transfers and prompting further analysis. The classifi- lation vanished twins appear to increase PAPP-A levels rather than cation of fresh versus frozen – thawed embryos has potential to mask decrease them; therefore, vanished twins are not responsible for an effect of hormone treatment because in our study population a sig- the observed reduced in PAPP-A levels in ART pregnancies. In fact, nificant proportion of frozen – thawed embryo transfers (20.6%) were vanished twins may have the opposite effect, suggesting that the accompanied by hormone treatment. When our data were stratified number of fetal hearts at early ultrasound should be considered in according to the presence or absence of any hormone treatment, any modification of screening protocols in ART pregnancies.
we found that reduced PAPP-A levels were seen only in the group It has previously been suggested that a reduction in PAPP-A in ART of pregnancies in which embryo transfer has been accompanied by pregnancies might be an artefact of testing being undertaken at an hormone treatment. In uncomplicated pregnancies where no earlier gestation in this group (Maymon and Shulman, 2002). In our hormone treatment was used, PAPP-A levels were normal.
population, there was no difference between the ART and non-ART The endocrine changes that occur during early pregnancy, including pregnancies in the timing of blood sampling or ultrasound. We did the production of PAPP-A by the endometrium and placenta, are the detect a slightly greater CRL for frozen – thawed embryos compared result of a complex and poorly understood set of interactions between with fresh embryos, equivalent to 1 day of gestational age. This the corpus luteum, endometrium, placenta and embryo. Our data difference may reflect a longer in vitro culture time for frozen – suggest that the administration of exogenous hormones, occurring in thawed embryos compared with fresh embryos, a difference that fresh and artificial frozen – thawed ART cycles, interferes with the would not affect the PAPP-A MoMs because these are adjusted for normal endocrine changes of early pregnancy, resulting in reduced PAPP-A levels are also known to be associated with adverse preg- The contribution of different types of hormone treatment to the nancy complications (hypertension, pre-eclampsia and gestational dia- reduced PAPP-A in ART pregnancies is more difficult to assess because betes) and adverse perinatal outcomes (prematurity, low birthweight treatment protocols are highly variable and more comprehensive treat- and neonatal death) (Ong et al., 2000; Dugoff et al., 2004; Smith et al., ment data were not available. It is, however, notable that similarly 2006). ART is associated with an overlapping spectrum of pregnancy reduced PAPP-A levels were seen for fresh embryo transfers that were and perinatal complications (Maman et al., 1998; Schieve et al., 2002; accompanied by FSH and/or clomiphene treatment, and for frozen– Helmerhorst et al., 2004; Shevell et al., 2005); therefore, lower thawed embryo transfers that were accompanied by treatment with PAPP-A in ART pregnancies might simply be a predictor of these com- various combinations of estradiol, progesterone, HCG and clomiphene.
plications that are known to be more common in the ART population We propose a model whereby hormone treatment accompanying (Maymon and Shulman, 2002; Bersinger et al., 2004). We were able to embryo transfers results in abnormal levels of ovarian steroid hor- analyse our data according to the presence or absence of these com- mones and other factors yet to be identified, which in turn cause a plications, and found that PAPP-A levels were reduced in ART preg- reduction in PAPP-A production. Although PAPP-A is produced by nancies with or without these complications.
the placenta, the reduction in PAPP-A is likely to be mediated via It has also been suggested that lower PAPP-A levels in ART preg- an effect of hormones on the endometrium because the effect is nancies might be the result of metabolic impairments related to infer- seen for hormone treatment administered prior to implantation and tility in the mother (Maymon and Shulman, 2002). This hypothesis is establishment of a placenta, possibly reflecting impairment of early partly refuted by our data that show that PAPP-A is similarly implantation with some forms of ART. Lower PAPP-A secretion reduced in male-factor infertility compared with female-factor inferti- should lower the availability of IGFs (Giudice et al., 2002) and lity. However, the difference in PAPP-A results between frozen – through this mechanism may directly contribute to low birthweight thawed embryos transferred with and without hormone treatment (Smith et al., 2002). It is well known that singleton babies born after may be related to underlying ovulatory disorders and defective endo- ART conception are at increased risk of being low birthweight or metrial development in the mother. This requires further study.
small for gestational age (Schieve et al., 2002; Halliday, 2007), and Our results support and extend the hypothesis that exogenous those with low PAPP-A from FTS are also at increased risk of low hormone treatment is the principal cause of reduced PAPP-A in ART birthweight (Dugoff et al., 2004; Barrett et al., 2008). Moreover, it pregnancies (Bersinger et al., 2004; Hui et al., 2005a; Tul and has been observed that babies born from fresh ART cycles are at increased risk of low birthweight and have a lower mean birthweight Bellver J, Lara C, Soares SR, Ramirez A, Pellicer A, Remohi J, Serra V. First compared with babies born from frozen – thawed cycles (Wada trimester biochemical screening for Down’s syndrome in singleton et al., 1994; Schieve et al., 2002; Wang et al., 2005; Belva et al., pregnancies conceived by assisted reproduction. Hum Reprod 2005; Belva F, Henriet S, Van den Abbeel E, Camus M, Devroey P, Van der Elst J, In conclusion, this study has provided conclusive evidence that first Liebaers I, Haentjens P, Bonduelle M. Neonatal outcome of 937 children trimester maternal serum levels of PAPP-A are decreased in ART born after transfer of cryopreserved embryos obtained by ICSI and IVF pregnancies, resulting in a much higher FPR on first trimester com- and comparison with outcome data of fresh ICSI and IVF cycles. Hum bined screening. Our results highlight the importance of pre- and post-test counselling for women carrying ART pregnancies. Further Bersinger NA, Wunder D, Vanderlick F, Chanson A, Pescia G, Janecek P, work should be undertaken to determine the viability of altering the Boillat E, Birkhauser MH. Maternal serum levels of placental proteins risk calculation for pregnancies conceived via ART, particularly those after in vitro fertilisation and their implications for prenatal screening.
that underwent hormone treatment. A recent trend towards ‘mild’ IVF with reduced hormone stimulation (Heijnen et al., 2007) might Conover CA, Bale LK, Overgaard MT, Johnstone EW, Laursen UH, have an additional benefit of reducing the number of false-positive results at first trimester combined screening. Hormone treatment pregnancy-associated plasma protein A is a critical growth regulatoryfactor during fetal development. Development 2004;131:1187 – 1194.
that accompanies many ART cycles appears to be strongly associated Dugoff L, Hobbins JC, Malone FD, Porter TF, Luthy D, Comstock CH, with the reduction in PAPP-A and the increased FPR, and may also Hankins G, Berkowitz RL, Merkatz I, Craigo SD et al. First-trimester contribute to the increased risk of low birthweight.
maternal serum PAPP-A and free-beta subunit human chorionicgonadotropin concentrations and nuchal translucency are associated with obstetric complications: a population-based screening study (theFASTER Trial). Am J Obstet Gynecol 2004;191:1446 – 1451.
A.M.J. and D.J.A. formulated the research question, performed the Frishman GN, Canick JA, Hogan JW, Hackett RJ, Kellner LH, Saller DN Jr.
data linkage/merging and analysis, interpreted the results and wrote Serum triple-marker screening in in vitro fertilization and naturally the paper. J.X.X. performed the statistical analyses, results interpret- conceived pregnancies. Obstet Gynecol 1997;90:98 – 101.
Ghisoni L, Ferrazzi E, Castagna C, Levi Setti PE, Masini AC, Pigni A.
ation and wrote the paper. I.F. provided the data from the maternal Prenatal diagnosis after ART success: the role of early combined screening lab, assisted with interpretation of the results and edited screening tests in counselling pregnant patients. Placenta 2003; the paper. J.L.H., D.L.H., H.W.G.B. and S.B. provided the ART data, oversaw the project, assisted with the interpretation of results Giudice LC, Conover CA, Bale L, Faessen GH, Ilg K, Sun I, Imani B, Suen LF, Irwin JC, Christiansen M et al. Identification and regulation ofthe IGFBP-4 protease and its physiological inhibitor in human regulation of IGF-II bioavailability in the placental bed during human implantation. J Clin Endocrinol Metab 2002;87:2359 – 2366.
Gjerris AC, Loft A, Pinborg A, Tabor A, Christiansen M. First-trimester technology: significance of gestational dating by oocyte retrieval orsonographic measurement of crown-rump length. Ultrasound Obstet We gratefully acknowledge the assistance provided by Claire Garrett, Debbi Rushford, Susan Donath, John Carlin, Sharon Lewis, Veronica Guibourdenche J, Frendo JL, Pidoux G, Bertin G, Luton D, Muller F, Collins, Evelyne Muggli and Les Sheffield.
Porquet D, Evain-Brion D. Expression of pregnancy-associated plasmaprotein-A (PAPP-A) during human villous trophoblast differentiation invitro. Placenta 2003;24:532 – 539.
Halliday J. Outcomes of IVF conceptions: are they different? Best Pract Res Clin Obstet Gynaecol 2007;21:67 – 81.
We would like to thank the BUPA foundation funding this project.
Heijnen EM, Eijkemans MJ, De Klerk C, Polinder S, Beckers NG, Klinkert ER, Broekmans FJ, Passchier J, Te Velde ER, Macklon NS et al. A mild treatment strategy for in-vitro fertilisation: a randomisednon-inferiority trial. Lancet 2007;369:743 – 749.
Anckaert E, Schiettecatte J, Sleurs E, Devroey P, Smitz J. First trimester Helmerhorst FM, Perquin DA, Donker D, Keirse MJ. Perinatal outcome of screening for Down’s syndrome after assisted reproductive technology: singletons and twins after assisted conception: a systematic review of non-male factor infertility is associated with elevated free beta-human controlled studies. BMJ 2004;328:261.
chorionic gonadotropin levels at 10-14 weeks of gestation. Fertil Steril Hui PW, Lam YH, Tang MH, Ng EH, Yeung WS, Ho PC. Maternal serum pregnancy-associated plasma protein-A and free beta-human chorionic Barkai G, Goldman B, Ries L, Chaki R, Dor J, Cuckle H. Down’s syndrome gonadotrophin in pregnancies conceived with fresh and frozen-thawed screening marker levels following assisted reproduction. Prenat Diagn embryos from in vitro fertilization and intracytoplasmic sperm injection. Prenat Diagn 2005a;25:390 – 393.
Barrett SL, Bower C, Hadlow NC. Use of the combined first-trimester Hui PW, Tang MH, Lam YH, Yeung WS, Ng EH, Ho PC. Nuchal screen result and low PAPP-A to predict risk of adverse fetal translucency in pregnancies conceived after assisted reproduction outcomes. Prenat Diagn 2008;28:28 – 35.
technology. Ultrasound Obstet Gynecol 2005b;25:234 – 238.
Jaques AM, Collins VR, Haynes K, Sheffield LJ, Francis I, Forbes R, Halliday JL.
Ribbert LS, Kornman LH, De Wolf BT, Simons AH, Jansen CA, Using record linkage and manual follow-up to evaluate the Victorian Beekhuis JR, Mantingh A. Maternal serum screening for fetal Down maternal serum screening quadruple test for Down’s syndrome, trisomy syndrome in IVF pregnancies. Prenat Diagn 1996;16:35 – 38.
18 and neural tube defects. J Med Screen 2006;13:8–13.
Schieve LA, Meikle SF, Ferre C, Peterson HB, Jeng G, Wilcox LS. Low and Jaques AM, Halliday JL, Francis I, Bonacquisto L, Forbes R, Cronin A, very low birth weight in infants conceived with use of assisted Sheffield LJ. Follow up and evaluation of the Victorian first-trimester reproductive technology. N Engl J Med 2002;346:731 – 737.
combined screening programme for Down syndrome and trisomy 18.
Shevell T, Malone FD, Vidaver J, Porter TF, Luthy DA, Comstock CH, Hankins GD, Eddleman K, Dolan S, Dugoff L et al. Assisted Lambert-Messerlian G, Dugoff L, Vidaver J, Canick JA, Malone FD, Ball RH, reproductive technology and pregnancy outcome. Obstet Gynecol Comstock CH, Nyberg DA, Saade G, Eddleman K et al. First- and second-trimester Down syndrome screening markers in pregnancies Shih W, Rushford DD, Bourne H, Garrett C, McBain JC, Healy DL, achieved through assisted reproductive technologies (ART): a FASTER trial study. Prenat Diagn 2006;26:672 – 678.
reproduction technology: difference between transfer of fresh and Lawrence JB, Oxvig C, Overgaard MT, Sottrup-Jensen L, Gleich GJ, Hays LG, Yates JR III, Conover CA. The insulin-like growth factor collection. Hum Reprod 2008;23:1644 – 1653.
(IGF)-dependent IGF binding protein-4 protease secreted by human Smith GC, Stenhouse EJ, Crossley JA, Aitken DA, Cameron AD, fibroblasts is pregnancy-associated plasma protein-A. Proc Natl Acad Connor JM. Early-pregnancy origins of low birth weight. Nature 2002; Liao AW, Heath V, Kametas N, Spencer K, Nicolaides KH. First-trimester Smith GCS, Shah I, Crossley JA, Aitken DA, Pell JP, Nelson SM, screening for trisomy 21 in singleton pregnancies achieved by assisted Cameron AD, Connor MJ, Dobbie R. Pregnancy-associated plasma reproduction. Hum Reprod 2001;16:1501 – 1504.
protein A and alpha-fetoprotein and prediction of adverse perinatal Lin TM, Galbert SP, Kiefer D, Spellacy WN, Gall S. Characterization of outcome. Obstet Gynecol 2006;107:161 – 166.
four human pregnancy-associated plasma proteins. Am J Obstet Gynecol Tul N, Novak-Antolic Z. Serum PAPP-A levels at 10-14 weeks of gestation are altered in women after assisted conception. Prenat Diagn 2006; Maman E, Lunenfeld E, Levy A, Vardi H, Potashnik G. Obstetric outcome of singleton pregnancies conceived by in vitro fertilization and ovulation Wada I, Macnamee MC, Wick K, Bradfield JM, Brinsden PR. Birth induction compared with those conceived spontaneously. Fertil Steril characteristics and perinatal outcome of babies conceived from cryopreserved embryos. Hum Reprod 1994;9:543 – 546.
Maymon R, Shulman A. Serial first- and second-trimester Down’s Wald NJ, Cuckle HS, Densem JW, Nanchahal K, Royston P, Chard T, Haddow JE, Knight GJ, Palomaki GE, Canick JA. Maternal serum singletons. Hum Reprod 2002;17:1081 – 1085.
screening for Down’s syndrome in early pregnancy. BMJ 1988;297: Maymon R, Shulman A. Integrated first- and second-trimester Down syndrome screening test among unaffected IVF pregnancies. Prenat Wald NJ, White N, Morris JK, Huttly WJ, Canick JA. Serum markers for Down’s syndrome in women who have had in vitro fertilisation: Nicolaides KH. The 11-13þ6 Weeks Scan. London: Fetal Medicine implications for antenatal screening. BJOG 1999;106:1304 – 1306.
Wald NJ, Rodeck C, Hackshaw AK, Walters J, Chitty L, Mackinson AM.
Niemimaa M, Heinonen S, Seppala M, Hippelainen M, Martikainen H, First and second trimester antenatal screening for Down’s syndrome: Ryynanen M. First-trimester screening for Down’s syndrome in in the results of the Serum, Urine and Ultrasound Screening Study vitro fertilization pregnancies. Fertil Steril 2001;76:1282 – 1283.
(SURUSS). Health Technol Assess 2003;7:1 – 77.
Ong CY, Liao AW, Spencer K, Munim S, Nicolaides KH. First trimester Wang YA, Sullivan EA, Black D, Dean J, Bryant J, Chapman M. Preterm maternal serum free beta human chorionic gonadotrophin and birth and low birth weight after assisted reproductive technology- pregnancy associated plasma protein A as predictors of pregnancy related pregnancy in Australia between 1996 and 2000. Fertil Steril complications. BJOG 2000;107:1265 – 1270.
Orlandi F, Rossi C, Allegra A, Krantz D, Hallahan T, Orlandi E, Macri J.
Wang YA, Dean J, Sullivan EA. Assisted Reproduction Technology in Australia First trimester screening with free beta-hCG, PAPP-A and nuchal and New Zealand 2005. Sydney: AIHW National Perinatal Statistics Unit, translucency in pregnancies conceived with assisted reproduction.
Wojdemann KR, Larsen SO, Shalmi A, Sundberg K, Christiansen M, Raty R, Virtanen A, Koskinen P, Anttila L, Forsstrom J, Laitinen P, Tabor A. First trimester screening for Down syndrome and assisted Morsky P, Tiitinen A, Ekblad U. Serum free beta-HCG and alpha- reproduction: no basis for concern. Prenat Diagn 2001;21:563 – 565.
fetoprotein levels in IVF, ICSI and frozen embryo transfer pregnancies Submitted on October 7, 2008; resubmitted on January 15, 2009; accepted on in maternal mid-trimester serum screening for Down’s syndrome.


3412 red - far red meter

Red/Far-Red Light Meter PRODUCT MANUAL Thank you for purchasing a Field ScoutTM Red / Far Red Me- ter. This manual describes its features and operation. Using the Meter 1. Press the ON/OFF button to turn the meter on or off. When first turned on, the display will show the current battery level. 2. Press the READ button to take a light reading. The meter will measure the inciden

Microsoft word - d-lyte-08.doc

Douglas R. Adler, M.D. Ronald A. Bloom, M.D. Kenneth D. Chi, M.D. Ruven Levitan, M.D. Nina H. Merel, M.D. Alan B. Shapiro, M.D. 847-677-1170 Procedure Scheduler Ext. 17 --- Nurse Line Ext. 51 Please read ALL instructions before your colonoscopy examination and MARK CALENDAR of anychanges you need to make. Please call with any problems or questions.  Obtain one of the

Copyright © 2010-2014 Medicament Inoculation Pdf