scholarly journals Using PCR Technician in Prenatal Diagnosis of Fetal Gender

2010 ◽  
Vol 4 (2) ◽  
pp. 84-90
Author(s):  
Abdulrahman A. Oleiwi

whole blood samples were obtained from 30 pregnant women at 15 –24 weeks of gestation. DNA was extracted from each plasma or serum sample. To detect the Y-chromosome specific marker DYS14 in the maternal blood, (Polymerase Chain Reaction) PCR were carried out for each DNA extract. The PCR products were analyzed by 1.5% agarose gel electrophoresis and ethidium bromide staining. The results compared with fetal gender after delivery. The result of delivery revealed that 13 pregnant women had a male fetus and the remaining 17 pregnant women had a female fetus and DYS14 was detected in all plasma and serum samples obtained from pregnant women and revealed that 13 pregnant women had a male fetus and the remaining 17 pregnant women had a female fetus. The PCR sensitivity for detecting the gender of fetus from maternal whole blood at 15–24 weeks of gestation was 100% in both plasma and serum, DYS14 was not detected in the DNA from any of the 17 pregnant women carrying a female fetus. The results showed that PCR analysis of maternal plasma and serum can be used to diagnose fetal gender.

2001 ◽  
Vol 47 (1) ◽  
pp. 41-46 ◽  
Author(s):  
Hiroshi Honda ◽  
Norio Miharu ◽  
Yoko Ohashi ◽  
Koso Ohama

Abstract Background: Fetal DNA has been found in maternal plasma and serum. Diagnosis of fetal gender using maternal plasma and serum has been attempted in an effort to develop a new noninvasive method of prenatal diagnosis. Methods: Peripheral blood samples were obtained from 61 pregnant women at 10–17 weeks of gestation before amniocentesis. DNA was extracted from 800 μL of each plasma or serum sample. To detect the Y-chromosome-specific sequences DYS14 and DYZ3 in the maternal plasma and serum, 40 cycles of PCR were carried out for each DNA extract. The PCR products were analyzed by 2.5% agarose gel electrophoresis and ethidium bromide staining, and the results were compared with the results of the cytogenetic analyses of amniocentesis. Results: Cytogenetic analysis of amniocentesis revealed that 31 pregnant women had a male fetus and the remaining 30 pregnant women had a female fetus. Both DYS14 and DYZ3 were detected in 27 of the 31 plasma samples obtained from pregnant women carrying a male fetus and in all of 31 serum samples obtained from the same women. Neither DYS14 nor DYZ3 was detected in either the plasma or serum samples obtained from any of the 30 pregnant women carrying a female fetus. Conclusion: PCR analysis of maternal serum can be used to diagnose fetal gender.


2005 ◽  
Vol 53 (3) ◽  
pp. 297-299 ◽  
Author(s):  
T.V. Zolotukhina ◽  
N.V. Shilova ◽  
E. Yu Voskoboeva

Sixty blood samples from pregnant women during gestational weeks 9–28 were investigated. Cell-free fetal DNA was extracted from maternal plasma or serum to be detected by nested PCR for determination of fetal gender. The SRY gene as a marker for fetal Y chromosome was detected in 34/36 women carrying a male fetus. In 3/24 women carrying female fetuses, the SRY sequence was also detected. Overall, fetal sex was correctly predicted in 91.7% of the cases. Therefore, the new, non-invasive method of prenatal diagnosis of fetal gender for women at risk of producing children with X-linked disorders is reliable, secure, and can substantially reduce invasive prenatal tests.


2012 ◽  
Vol 15 (2) ◽  
pp. 143-148 ◽  
Author(s):  
Elena Picchiassi ◽  
Gian Carlo Di Renzo ◽  
Federica Tarquini ◽  
Vittorio Bini ◽  
Michela Centra ◽  
...  

We applied a noninvasive prenatal test for the determination of fetal gender in multiple pregnancies by using free fetal DNA circulating in maternal blood in order to evaluate whether the quantification of male DNA could distinguish the fetal gender and the number of male and female fetuses in multiple pregnancies. We enrolled consecutively 44 women with twin pregnancies between 11–14 weeks of gestation. Peripheral maternal blood was collected, and genomic DNA was extracted from maternal plasma and analyzed for the multicopy DYS 14 sequence by using real-time PCR to quantify male DNA. Results showed that male DNA concentration was significantly higher in twin pregnancies with at least one male fetus, compared to twin pregnancies with only female fetuses. Comparing male DNA concentration in pregnancies with two male fetuses versus pregnancies with one female fetus and one male fetus, we did not obtain a significant difference between the two groups due to a slight overlapping of the range values. Therefore, our test correctly predicted fetal gender, distinguishing twin pregnancies with at least one male fetus from twin pregnancies with only female fetuses, with a diagnostic accuracy of 100%. For distinguishing pregnancies with two male fetuses from pregnancies with both female and male fetuses, a diagnostic accuracy of 76.1% was achieved.


1975 ◽  
Vol 80 (3) ◽  
pp. 569-576 ◽  
Author(s):  
B. Runnebaum ◽  
I. Stöber ◽  
J. Zander

ABSTRACT In 14 healthy pregnant women at term progesterone (P) and 20α-dihydroprogesterone (20α-DHP) were determined by radioimmunoassay both in the maternal and foetal compartments. The average concentrations were as follows (ng/ml blood or ng/g wet weight tissue): peripheral maternal blood P 56 ± 26, 20α-DHP 16 ± 8; placental tissue P 2514 ± 1516, 20α-DHP 429 ± 412; placental blood P 365 ± 160, 20α-DHP 35 ± 18; blood of the umbilical vein P 388 ± 121, 20α-DHP 33 ± 15; blood of the umbilical arteries P 162 ± 62, 20α-DHP 28 ± 10. In 5 healthy pregnant women at term progesterone (P), 20α-dihydroprogesterone (20α-DHP) and 20β-dihydroprogesterone (20β-DHP) were also determined by gas-liquid chromatography both in the maternal and foetal compartments. The average concentrations were as follows (ng/ml plasma or ng/g wet weight tissue): peripheral maternal plasma P 129 ± 49, 20α-DHP 15 ± 15, 20β-DHP 1.7 ± 0.9; placental tissue P 5060 ± 1435, 20α-DHP 230 ± 158, 20β-DHP 38 ± 30; placental plasma P 723 ± 245, 20α-DHP 24 ± 13, 20β-DHP 1.0 ± 0.1; plasma of the umbilical vein P 704 ± 227, 20α-DHP 17 ± 3, 20β-DHP 1.2 ± 0.3; plasma of the umbilical arteries P 324 ± 94, 20α-DHP 17 ± 5, 20β-DHP 2.6 ± 2.1 These results show that, contrary to the progesterone concentrations, no significant difference exists in the concentrations of 20α-DHP and 20β-DHP between the blood from the umbilical vein and arteries. Furthermore, no significant difference could be found in the concentrations of P and 20α-DHP between the sexes in either the blood from the umbilical vein or from the umbilical arteries.


Author(s):  
Zahra Moradi ◽  
Parvin Moradi ◽  
Mohamad Hassan Meshkibaf ◽  
Mehrnoosh Aleosfoor ◽  
Mehdi Sharafi ◽  
...  

Background: Preterm delivery is one of the main causes of infant death. Therefore, prediction of preterm delivery may eliminate a large number of prenatal complications. Objectives: The present study aimed to understand if preterm delivery can be predicted by assessing maternal plasma fibronectin concentration. Materials and Methods: Serum samples from 105 pregnant women participating in this study were collected. The plasma fibronectin were measured at 24-28 wk of gestation and again at 32-36 wk of gestation. Unfortunately, only 65 of the 105 pregnant women, returned for the second sampling. The plasma fibronectin was analyzed using ELISA method and its concentration in term and preterm deliveries was compared. The delivery dates of all the women were also recorded. Results: Out of 105 pregnant women, 28 delivered preterm (26.7%). The Plasma fibronectin concentrations in women with preterm delivery were higher than in those who delivered at term (p = 0.001). Accordingly, Plasma fibronectin concentrations were significantly higher in the second serum samples (p = 0.01). Plasma fibronectin concentrations was also higher in obese women and in those suffering from preeclampsia (p = 0.12) and gestational diabetes (p = 0.81). Conclusion: Plasma fibronectin concentrations test could be used as an optional screening test for preterm delivery at 28 to 34 wk of gestation in pregnant women who prefer to avoid vaginal sampling. Key words: Premature birth, Fibronectin, Maternal serum screening tests.


2017 ◽  
Vol 10 (1) ◽  
pp. 1-4
Author(s):  
Rubina Tamrakar Gurung ◽  
P Sharma

Introduction: Animal and pathologic models have provided evidence for a fetal influence on the labor process; however, the potential impact of fetal gender on the labor curve has gone largely unstudied.Objectives: To determine the association between fetal gender and first stage labor curve at term.Methods: This was a retrospective study. There were 330 patients en­rolled in this study, who gave birth from January 2011 to December 2012 by reviewing the charts. A total of 500 charts were reviewed.Results: There were three hundred thirty (330) patients, out of which a total of 179 (54.2%) patients gave birth to males and 151 (45.8%) gave birth to females. Women who had a male fetus had a longer first stage of labor than women who carried a female fetus. The difference in the birth weight of the infants is statistically significant, male newborns were heavier at birth than female newborns.Conclusions: Term labor in the first stage was found to be slower in women who carried a male fetus compared with those with female fe­tus which is not statistically significant.Journal of Gandaki Medical College  Vol. 10, No. 1, 2017, page: 1-4


2017 ◽  
Vol 41 (S1) ◽  
pp. S169-S169
Author(s):  
E. Toffol ◽  
A.P. Elomaa ◽  
V. Glover ◽  
P. Kivimäki ◽  
M. Pasanen ◽  
...  

IntroductionAnxiety symptoms are frequent during pregnancy, and they adversely affect pregnancy outcomes and offspring development. The underlying biological mechanisms are not known, but may in part be explained by alterations in certain maternal metabolic pathways. No metabolomic studies have investigated possible metabolic alterations in anxious pregnant women.ObjectiveThis pilot study compared the metabolic profiles of anxious and non-anxious pregnant women using a mass spectrometry-based quantitative metabolomics system.MethodsCases were 20 participants of the Kuopio birth cohort study (www.kubico.fi) with first and third trimester symptoms of anxiety (Edinburgh postnatal depression scale, anxiety subscale – EPDS-3A ≥ 4), but no depression (EPDS ≤ 12). Controls were 20 participants with low anxiety (EPDS–3A ≤ 3) and depression (total EPDS ≤ 9) in both the first and third trimester. Maternal metabolic profiles were analyzed from serum samples drawn when the mothers arrived at the delivery hospital.ResultsMetabolic pathway analyses revealed significant enrichment in the glycine, serine and threonine metabolism (P = 0.046), as well as in the betaine (P = 0.048) metabolism pathways. Homocysteine was the only metabolite to significantly differentiate between cases and controls (VIP score 3.3), with lower concentrations in cases (P = 0.003) even when excluding non-users of folic acid supplementation (n = 5; P = 0.002), C-sections (n = 5; P = 0.013), or samples taken immediately postpartum (n = 2; P = 0.004). No other metabolites significantly differed between the groups.ConclusionsPhysiological adaptation induced by pregnancy, which may have homogenized the study populations, could explain the only minor metabolic differences between the two groups. Further research in larger samples, comparing metabolic alterations in umbilical cord blood and maternal blood is warranted.Disclosure of interestThe authors have not supplied their declaration of competing interest.


2012 ◽  
Vol 413 (5-6) ◽  
pp. 600-604 ◽  
Author(s):  
Shin Young Kim ◽  
Ji Hyae Lim ◽  
So Yeon Park ◽  
Moon Young Kim ◽  
June Seek Choi ◽  
...  

Author(s):  
Najmeh Davoodian ◽  
Ali Kadivar ◽  
Heidar Heidari Khoie ◽  
Sima Hematian Khayat ◽  
Mahboobeh Heidari Nasirabadi

Background and Aims: New advances in the use of cell-free fetal DNA (cffDNA) in maternal plasma of pregnant women has provided the possibility of applying cffDNA in prenatal diagnosis as a non-invasive method. One of the applications of prenatal diagnosis is fetal gender determination. Early prenatal determination of fetal sex is required for pregnant women at risk of X-linked and some endocrine diseases. The present study was carried out to perform an efficient polymerase chain reaction (PCR) method in order to improve sensitivity, specificity and accuracy of non-invasive fetal gender detection using fetal DNA in maternal plasma during 8th -12th weeks of pregnancy. Materials and Methods: Thirty-five pregnant women with 8 to 12 weeks of pregnancy were selected for prenatal fetal sex determination. Maternal peripheral blood was collected and cffDNA was extracted from 3-ml of maternal plasma. Two multi copy Y-chromosome-specific region (DYS and DAZ) and a single copy gene (SRY) were amplified by real-time quantitative PCR. Amplification was labeled as positive, negative, or inconclusive according to a stringent algorithm. Results: Using this method, the sensitivity and specificity of the real-time PCR assay was 100% and 93.8% for prenatal fetal sex detection, respectively. Conclusions: It is concluded that fetal sex can be determined with a high level of accuracy by our algorithm, after 8 weeks of gestation with cffDNA analysis.


Blood ◽  
2013 ◽  
Vol 122 (21) ◽  
pp. 2405-2405
Author(s):  
Nancy Rodriguez ◽  
Pilar Noguerol ◽  
Lutgardo García ◽  
Hada Macher ◽  
Magdalena Carmona ◽  
...  

Abstract A protocol-based and multidisciplinary follow-up of the pregnant woman including Primary Care, Hematology Deparment, and Fetal Medicine, is required for the appropriate prophylaxis and treatment of the hemolytic disease of the newborn (HDN). The combined application of new monitoring techniques, such as the study of the fetal D antigen (RhD) by PCR in maternal blood and the determination of the blood flow of the middle cerebral artery (MCA) in the fetus by Doppler ultrasonography allows the child’s prenatal follow up without invasive procedures. Objectives To evaluate the results obtained using this strategy of combined monitorization in our institution from 2009. Secondary aims were: To review all cases of immunized pregnant women and to analyze the outcomes of selective anti D prophylaxis at week 28, according to fetal RHD analyzed by PCR in maternal blood. Patients and Method s 38,000 pregnant women are included in the analysis. Antibody (Ab) screening is made during the first 3 months of pregnancy, and titer is evaluated using agglutination tests in immunized women with clinically significant (CS) Ab. RhD negative women immunized against RhD undergo fetal RHD and SRY determination using a new multiplex RT-PCR assay for fetal cell-free DNA in maternal plasma as soon as possible. In addition, in patients with CS-Ab and previous obstetric complications or antibody titer >1/32 or rising, MCA Doppler is performed to assess the degree of fetal anemia and evaluate the need for intrauterine transfusion (IUT), or to advance childbirth to week 34. On the other hand, non-immunized RhD negative, women are controlled again in the 28th week to re-assess the presence of antibodies and well as fetal RHD and SRY determination and only those with RHD positive fetuses receive anti D gammaglobulin. Results Ab were found in 290 pregnant women. 116 were not clinically significant and did not require further control. 174 women had CS-Ab against Rh, Kell, Jk, Fy, and Lu antigen systems. Out of them, 29 RhD negative women were immunized against anti D (all of them due to previous incomplete or no prophylaxis). The study of fetal RHD revealed that 9 of these 29 women had RHD- fetuses and were released from hospital. The remaining 20 RhD- patients together with those 145 women with other CS-Ab underwent obstetric history assessment as wellas antibody titers assay, and MCA Doppler, according to the criteria mentioned above. Remarkably, after these assessments only 11 IUTs were required in 6 pregnant women, all of them were performed without any complications. Involved antibodies in these 6 patients were: Rh, Kell and Jk. Fetal RHD testing in 4,064 RhD negative women at the 28thweek detected 1,423 who had RHD- fetuses which did not require prophylaxis. There were no false negatives among the newborns. Conclusions 1. A combined monitorization strategy of the pregnant woman avoids unnecessary controls and invasive procedures. 2. Anti D prophylaxis has 100% efficacy in all pregnant women requiring it. 3. Those women immunized against RhD, who had RHD- fetuses, can have a quiet gestation since week 12 without further immunohematologic assessments. Disclosures: No relevant conflicts of interest to declare.


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