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1.
J Perinat Med ; 48(8): 825-828, 2020 Oct 25.
Article in English | MEDLINE | ID: mdl-32769227

ABSTRACT

Objectives Assisted reproductive technologies (ART) may be associated with placental abnormalities including placenta previa, umbilical cord abnormalities, and placental abruption. Our study evaluates the relationship between ART and placental abnormalities compared with spontaneously conceived controls. Methods An IRB-approved cohort study was conducted including women who delivered between January 2013 and December 2018. We excluded delivery prior to 23 weeks and known fetal anomalies. Patients were matched with controls (2:1) for parity, age, and mode of delivery. Controls were women who had spontaneously conceived and delivered immediately preceding and following the index delivery. The primary outcome was placental abnormalities found on both antenatal ultrasound and pathology in ART gestations compared with spontaneously conceived gestations. Results There were 120 ART pregnancies and 240 matched control pregnancies identified. The groups were similar for parity, BMI, comorbidities, number of multiples, mode of delivery, and female newborns. The ART group had a higher maternal age (37.1±5 y vs. 30.0±5 y; p<0.001), greater preterm birth (29 vs. 6%; p<0.001), and lower BW (2,928±803 g vs. 3,273±586 g; p<0.001). The ART group had a higher incidence of placenta previa on ultrasound (4.0 vs. 0.4%, p=0.01), adherent placentas at delivery (3 vs. 0% p=0.014), placental abruption (2 vs. 0%; p=0.04), as well as an increased rate of velamentous cord insertion (12 vs. 3%, p<0.001) and marginal cord insertion (28 vs. 15%, p=0.002). ART demonstrated a two-fold likelihood of abnormal placental pathology. Conclusions ART is associated with increased rate of placental abnormalities, including abnormal umbilical cord insertion and increased rates of adherent placentation. This information may be beneficial in planning and surveillance in patients with ART pregnancies.


Subject(s)
Abruptio Placentae , Delivery, Obstetric , Placenta Previa , Reproductive Techniques, Assisted/statistics & numerical data , Ultrasonography, Prenatal/methods , Umbilical Cord , Abruptio Placentae/diagnosis , Abruptio Placentae/epidemiology , Adult , Body Mass Index , Comorbidity , Delivery, Obstetric/methods , Delivery, Obstetric/statistics & numerical data , Female , Humans , Infant, Newborn , Parity , Placenta/diagnostic imaging , Placenta Previa/diagnosis , Placenta Previa/epidemiology , Pregnancy , Pregnancy Outcome/epidemiology , Retrospective Studies , Risk Assessment/methods , Umbilical Cord/abnormalities , Umbilical Cord/diagnostic imaging , United States/epidemiology
2.
Pigment Cell Melanoma Res ; 31(1): 73-81, 2018 01.
Article in English | MEDLINE | ID: mdl-28786531

ABSTRACT

To determine the feasibility of liquid biopsy for monitoring of patients with advanced melanoma, cell-free DNA was extracted from plasma for 25 Stage III/IV patients, most (84.0%) having received previous therapy. DNA concentrations ranged from 0.6 to 390.0 ng/ml (median = 7.8 ng/ml) and were positively correlated with tumor burden as measured by imaging (Spearman rho = 0.5435, p = .0363). Using ultra-deep sequencing for a 61-gene panel, one or more mutations were detected in 12 of 25 samples (48.0%), and this proportion did not vary significantly for patients on or off therapy at the time of blood draw (52.9% and 37.5% respectively; p = .673). Sixteen mutations were detected in eight different genes, with the most frequent mutations detected in BRAF, NRAS, and KIT. Allele fractions ranged from 1.1% to 63.2% (median = 29.1%). Among patients with tissue next-generation sequencing, nine of 11 plasma mutations were also detected in matched tissue, for a concordance of 81.8%.


Subject(s)
Biomarkers, Tumor/genetics , Cell-Free Nucleic Acids/genetics , Melanoma/diagnosis , Mutation , Skin Neoplasms/diagnosis , Biomarkers, Tumor/blood , Cell-Free Nucleic Acids/blood , Feasibility Studies , Female , High-Throughput Nucleotide Sequencing , Humans , Male , Melanoma/blood , Melanoma/genetics , Middle Aged , Pilot Projects , Skin Neoplasms/blood , Skin Neoplasms/genetics
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