جستجوی مقالات مرتبط با کلیدواژه "fetal blood" در نشریات گروه "پزشکی"
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Background
Umbilical cord blood serves as a potent source of hematopoietic stem cells, utilized in treating specific diseases and preserved in blood banks.
ObjectivesThis study aims to explore the ethical issues associated with these repositories.
MethodsThis qualitative research involved conducting 14 interviews with experts and the families of recipients or donors of umbilical cord blood. Participants were selected purposefully from May to November 2021.
ResultsThe investigation identified five principal ethical challenges: presentation of information, interpersonal relationships among involved parties, respect for human dignity, adherence to rules and regulations, and the handling of tissue samples. These challenges encompassed various categories and subcategories, including informed consent, communication and advertising of information, financial considerations, conflicts of interest, professional interactions, ownership rights concerning the child and parents, privacy and confidentiality issues, compliance with regulations and guidelines, and the clinical and research uses of the tissue samples.
ConclusionsThe study unveiled significant ethical concerns in the domain of umbilical cord blood stem cell banking. Addressing these ethical dilemmas necessitates the involvement of health policymakers and medical ethics experts, along with a comprehensive understanding of these banks' multifaceted nature by the community.
Keywords: Blood Banks, Blood Specimen Collection, Directive Counseling, Fetal Blood, Informed Consent, Ethics -
As widespread prophylaxis with anti-D Antibodies has dramatically diminished anti-D-associated hemolytic disease of the newborn (HDN), other antibodies-associated HDN has become relatively more significant. Two genes encode Rh proteins: the RhD gene coding for the D and the Rh CcEe gene coding for Cc Ee Antigens. D is a rare Rh phenotype in which RBCs lack Cc/Ee antigens while D antigen is strongly expressed. Anti R17 antibodies are important monomorphic antibodies acting against all previously mentioned antigens. It can pass through the placenta as a G immunoglobulin, leading to fetal or neonatal hemolysis. Here, we reported an immunized pregnant female with D- - phenotype and a history of intrauterine fetal death who had high titer of anti-Rh17 antibodies in her subsequent pregnancy. We would discuss our management strategy which led to good perinatal outcomes. To the best of our knowledge, this is the second case of HDN reported in English written literature in Iran.
Keywords: RH17 Antigen, Fetal Blood, Intrauterine transfusion, hemolytic disease of the fetal, newborn, Rh Isoimmunization -
Background
In addition to its short‑term effects, low birth weight increases the risk of noncommunicable diseases (NCDs) in adult life. The quality of maternal diet including the macronutrient intake is very important in this regard. This study aims to evaluate the possible associations between maternal zinc and neonatal anthropometric measures.
MethodThis cross‑sectional study was conducted on 226 pairs of mothers‑neonates in Isfahan, Iran. Maternal characteristics including the history of the disease, age, preconceptional weight, weight gain during pregnancy, as well as, anthropometric characteristics of neonates such as weight, height, length, and circumferences of head, belly, chest, and thigh were documented. Cord blood zinc was measured by atomic absorption spectrophotometer in three groups of neonates depending on their weights.
ResultsThe gestational age of neonates was 35 to 38 weeks with a mean weight of 3.13 ± 0.42 kg. The mean of zinc concentration was 0.81 ± 0.18 and it was higher in neonates with appropriate weight than in those with high or low birth weight (0.82 ± 0.18, 0.75 ± 0.19, and 0.65 ± 0.12 ng/ml, respectively). Bivariate correlation analysis showed significant weak correlation between cord blood zinc and neonatal weight (r = 0.16, P = 0.04).
ConclusionsThe cord blood zinc concentration of normal‑weight neonates was higher than others. Our findings suggest that maternal zinc may influence neonatal birth weight, and it should be considered in the primordial prevention of NCDs.
Keywords: Birth weight, fetal blood, preventive medicine, zinc -
International Journal of Occupational and Environmental Medicine, Volume:11 Issue: 1, Jan 2020, PP 15 -23Background
Birth weight is very important for long-term physical, mental, health, and brain development. Pesticide exposure is thought to interfere with fetal growth, among others, through disruption of the function of the insulin-like growth hormone-1 (IGF-1) hormone.
ObjectiveTo analyze the relationship between exposure to pesticides during pregnancy and low-birth weight (LBW) through the disruption of the IGF-1 hormone.
MethodsIn a case-control study, babies born with LBW (birth weight <2500 g) and those born later with normal birth weight (≥2500 g) at 2 hospitals in Brebes were chosen as cases and controls, respectively. Maternal pesticide exposure was measured by interview using a questionnaire. Umbilical serum IGF-I level was tested using the ELISA method.
ResultsThere was a significant relationship between pesticide exposure during pregnancy and LBW (OR 6.8; 95% CI 2.0 to 22.9) and low umbilical serum IGF-1 levels (OR 3.6; 95% CI 1.2 to 11.1). There was a significant relationship between low umbilical serum IGF-1 levels and LBW (OR 8.9; 95% CI 2.4 to 32.1).
ConclusionThere was a significant relationship between pesticide exposure during pregnancy and LBW through the umbilical serum IGF-1 reduction pathway
Keywords: Pesticides, Fetal blood, Infant, low birth weight, Organophosphates, Insulinlike growth factor I -
ObjectivesThe aim of this study was to investigate the relationship between umbilical cord blood gases and neonatal asphyxia as valuable criteria for fetal distress and labor compilations.Materials And MethodsIn this cross-sectional descriptive study of 150 deliveries (101 vaginal and 49 caesarean sections), singleton live-born infants between 34 and 42 weeks of gestation with no major anomalies. They were enrolled from November 2015 to March 2016, in delivery unit of obstetrics and gynecology ward, Imam Hossein Medical Center, Tehran, Iran. Blood samples were taken from umbilical vessels (arterial and venous) following delivery. All infants were monitored for Apgar scores at 1 and 5 minutes.ResultsThere were significant differences regarding venous blood lactate (PConclusionsThe results of the present study indicate that lactate analysis, as well as umbilical cord blood analysis, might be useful predictors of fetal asphyxia at delivery. Their potential role as a predictor of prenatal outcome should be evaluated further in future studies.Keywords: Fetal blood, Umbilical cord blood, Infant, Asphyxia, Prenatal diagnosis
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BackgroundUmbilical cord blood has been used for transplantation in regenerative medicine of hematological disorders. MicroRNAs are important regulators of gene expression that control both physiological and pathological processes such as development and cancer. Some studies have shown that miR-33, p53 and c-myc have critical roles in control of self-renewal cells.ObjectiveTo understand the effect of adipose-derived mesenchymal stem cells (ADSCs), as a feeder layer, on expansion of HSCs, the expression of p53 and miR-33a were evaluated.MethodsIsolated human ADSCs in passage 3 were cultured as a feeder layer. Ex vivo cultures of cord blood CD34 cells were performed in three culture conditions for 7 days: cytokines with ADSCs feeder layer, cytokines without ADSCs feeder layer, and co-culture with ADSCs without cytokine. Expression of genes p53, c-myc and miR-33 were analyzed by real-time PCR.ResultsThe expression of p53 was significantly down-regulated in HSCs directly cultured on ADSCs feeder layer compared to that cultured without feeder layer. The expression of miR-33a was significantly upregulated in HSCs directly cultured on feeder layer compare to that cultured without feeder layer.ConclusionDefining the role of ADSCs in controlling the HSC self-renewal through miR-33, p53 and c-myc may lead to the treatment and prevention of hematopoietic disorders.Keywords: Fetal blood, Cord blood stem cell transplantation, MicroRNAs, Mesenchymal stromal cells, Genes, p53, Genes, myc, MIRN33 microRNA, human [Supplementary Concept]
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BackgroundUmbilical cord blood (UCB) is believed to be a highly valuable source of hematopoietic stem cells for transplantation.ObjectiveTo investigate the prevalence of active and latent human cytomegalovirus (CMV) infection in UCB donors in Iranian population.MethodsA total of 825 UCB samples was collected under standard procedures and analyzed for the presence of CMV DNAs in buffy coat (latent infection) and plasma (active infection). DNA was extracted from buffy coat and plasma samples separately and tested with quantitative real-time PCR. All positive samples were checked by ELISA for IgG and IgM anti-CMV antibody.ResultsLatent CMV infection was detected in 17 (2%) buffy coat samples with a low level of viral load, which indicated the presence of latent viral infection in donors. None of the plasma samples were found positive for CMV DNA reflecting no active infection. In the 17 positive samples, CMV viral load was 91 104 (mean: 100) copies/mL. All samples positive for viral DNA were also found positive for CMV IgG antibody by ELISA. No CMV IgM antibody was detected in positive samples.ConclusionCMV is still the most important virus that infects hematopoietic stem cells and could be dangerous, especially for immunocompromized transplant recipients. We therefore suggest using real-time PCR for the detection and quantification of the viral DNA in buffy coat and plasma of UCB donors. PCR of plasma for detection of CMV and antibody assay for CMV infection add no more sensitivity for the detection of latent CMV infection in UCB donors.Keywords: Fetal blood, Cord blood stem cell Transplantation, Herpesviridae, Cytomegalovirus, Realtime polymerase chain reaction
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BackgroundManagement of hyperbilirubinemia remains a challenge for neonatal medicine because of the risk of neurological complications related to the toxicity of severe hyperbilirubinemia.ObjectivesThe purpose of this study was to examine the validity of cord blood alkaline phosphatase level for predicting neonatal hyperbilirubinemia. Patients andMethodsBetween October and December 2013 a total of 102 healthy term infants born to healthy mothers were studied. Cord blood samples were collected for measurement of alkaline Phosphatase levels immediately after birth. Neonates were followed-up for the emergence of jaundice. Newborns with clinical jaundice were recalled and serum bilirubin levels measured. Appropriate treatment based on serum bilirubin level was performed. Alkaline phosphatase levels between the non-jaundiced and jaundiced treated neonates were compared.ResultsThe incidence of severe jaundice that required treatment among followed-up neonates was 9.8%. The mean alkaline phosphatase level was 309.09 ± 82.51 IU/L in the non-jaundiced group and 367.80 ± 73.82 IU/L in the severely jaundiced group (P = 0.040). The cutoff value of 314 IU/L was associated with sensitivity 80% and specificity 63% for predicting neonatal hyperbilirubinemia requiring treatment.ConclusionsThe cord blood alkaline phosphatase level can be used as a predictor of severe neonatal jaundice.Keywords: Fetal Blood, Hyperbilirubinemia, Jaundice, Alkaline Phosphatese, Newborn
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سابقه و هدفیکی از راه های کنترل فرایند خون سازی، تنظیم به وسیله MicroRNA های مختلف می باشد. این RNAهای کوچک تنظیم کننده با تغییر در بیان ژن ها در مرحله پس از رونویسی، توانایی کنترل مراحل مختلف خون سازی را دارا می باشند. درمان بیماری های مختلف با استفاده از سلول های +CD-133 که از خون بند ناف جدا شده و در محیط آزمایش گاه تکثیر یافته اند در حال گسترش می باشد. هدف این مطالعه بررسی تغییرات ایجاد شده در بیان MicroRNA های شرکت کننده در فرایند خون سازی در مراحل مختلف تکثیر این سلول ها در in vitro بود.
مواد و روش هاسلول های بنیادی خون ساز +CD133 خون بند ناف به روش MACS جدا گردید. این سلول ها پس از شمارش و تایید توسط فلوسیتومتری، جهت بررسی اثر تکثیر بر بیان MicroRNA ها در دو گروه مورد مطالعه قرار گرفتند. در گروه اول RNA این سلول ها بلافاصله پس از جداسازی استخراج گردید و در گروه دوم سلول ها 12 روز پس از تکثیر در آزمایش گاه مورد مطالعه قرار گرفتند. جهت بررسی بیان MicroRNA ها از تکنیکqPCR Real time استفاده شد.
یافته هایافته ها نشان دادند که از مجموع 23 عدد MicroRNA بررسی شده در دو مرحله قبل و بعد از تکثیر، بیان 11 عدد از MicroRNA ها بدون تغییر بود. در حالی که در مرحله قبل نسبت به مرحله بعد از تکثیر، بیان 7 عدد از MicroRNA ها با افزایش و بیان 5 عدد از MicroRNA ها هم با کاهش هم راه بود.نتیجه گیرینتایج ما نشان دادند که تکثیر سلول های بنیادی خون ساز در محیط آزمایش گاه سبب تغییر در بیان MicroRNA های شرکت کننده در فرایند خون سازی می گردد. به طوری که این تغییرات سبب افزایش بیان MicroRNA های مسئول تمایز و کاهش بیان MicroRNA های شرکت کننده در همانند سازی این سلول ها می گرددکلید واژگان: خون سازی, میکرو آر ان آها, سلول بنیادی خون ساز+CD133, خون جنینKoomesh, Volume:15 Issue: 1, 2013, PP 11 -16IntroductionHematopoiesis is regulated by different microRNAs (miRNA). These small regulatory RNAs control hematopoiesis at different stages with changing in the expression of genes at post-transcriptional levels. Treatment of various diseases is increasing with using CD133+ hematopoietic cells isolated and in vitro expanded from the umbilical cord blood. This study was performed to show alteration of microRNAs levels involved in hematopoiesis in CD133+ hematopoietic cells isolated and invitro expanded from the umbilical cord blood.Materials And MethodsUmbilical cord blood CD133+ hematopoietic stem cells were isolated by MACS and then the cells confirmed and counted by using flowcytometery and finally were divided into two groups. In the first group RNA was extracted from the cells and the cells in the second group were cultured invitro for 12 days and then these cells were used to assess micoRNAs expression using qPCR real time.ResultsThe results showed that from 23 microRNAs، expression of 11 microRNAs was the same in two groups whereas expression of 7 and 5 microRNAs were respectively increased and decreased following in vitro culture.ConclusionBased on our results، in vitro expansion of the hematopoietic stem cells results in increased microRNAs levels which are responsible for differentiation and decreased microRNAs levels which are responsible for self- renewal.Keywords: Hematopoiesis, MicroRNAs, Hematopoietic Stem Cells+CD133, Fetal Blood
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