TY - JOUR
T1 - The placental factor in spontaneous preterm birth in twin vs. singleton pregnancies
AU - Weiner, Eran
AU - Dekalo, Ann
AU - Feldstein, Ohad
AU - Barber, Elad
AU - Schreiber, Letizia
AU - Bar, Jacob
AU - Kovo, Michal
N1 - Publisher Copyright:
© 2017
PY - 2017/7/1
Y1 - 2017/7/1
N2 - Objective The association between infection and inflammatory response in singleton preterm birth (PTB) is well established, yet, less is known about PTB in twins. We aimed to compare the placental component and pregnancy outcome in pregnancies complicated with PTB of singletons vs. twin deliveries. We hypothesized that due to different underlying mechanisms, placental inflammatory lesions will be more prevalent in placentas derived from singleton pregnancies than twins. Study design Labor characteristics, neonatal outcome and placental histopathology reports of spontaneous PTB at 24–33 6 / 7 weeks, from 1/2008–12/2015, were reviewed. Results were compared between dichorionic-diamniotic twin deliveries (twins group) and singleton deliveries (singleton group) matched for gestational age. Excluded from the study medically indicated deliveries, due to preeclampsia or fetal growth restriction, and monochorionic twins. Placental lesions were classified to maternal vascular supply lesions, fetal vascular supply lesions, and maternal (MIR) and fetal (FIR) inflammatory responses. Composite neonatal outcome was defined as one or more of early complications: respiratory distress, necrotizing enterocolitis, sepsis, blood transfusion, ventilation, seizures, intra-ventricular hemorrhage, hypoglycemia, phototherapy, or death. Results The twins group (n = 72) was characterized by higher maternal BMI (p = 0.009), and higher rates of assisted reproductive techniques (56.2% vs. 17.8%, p < 0.001) and cesarean deliveries (75.3% vs. 32.8%, p < 0.001) as compared to the singleton group (n = 72). Placentas from the singleton group were characterized by higher rate of MIR, 58.9% vs. 19.2%, (p < 0.001), FIR, 31.5% vs. 3.4%, (p < 0.001), retro-placental hemorrhage, 26% vs. 8.9% (p < 0.001), and vascular lesions related to maternal malperfusion, 28.8% vs. 9.6%, (p < 0.001), as compared to placentas from the twins group. Higher rate of neonatal sepsis was observed in the singleton group as compared to the twins group, 24.7% vs. 4.1%, p < 0.001, respectively. By logistic regression analyses retro-placental hemorrhage, placental maternal vascular malperfusion lesions, MIR, FIR and neonatal sepsis were found to be independently associated with singleton PTB: aOR 3.4, 95% CI 2.1–6.9, p < 0.001, aOR = 3.1, 95% CI 1.8–7.2, p < 0.001, aOR = 2.9, 95% CI 1.4–7.8, p < 0.001, aOR = 4.9, 95% CI 2.3–6.9, p < 0.001, and aOR = 4.8, 95% CI 2.3–6.7, p < 0.001 respectively. Conclusion Placentas from singleton PTBs are characterized by higher rate of inflammatory and malperfusion lesions. The lack of these findings in twins PTBs suggests different factors that participate in the development of preterm birth in twins, such as over-distension of the uterus and up regulation of oxytocin receptors.
AB - Objective The association between infection and inflammatory response in singleton preterm birth (PTB) is well established, yet, less is known about PTB in twins. We aimed to compare the placental component and pregnancy outcome in pregnancies complicated with PTB of singletons vs. twin deliveries. We hypothesized that due to different underlying mechanisms, placental inflammatory lesions will be more prevalent in placentas derived from singleton pregnancies than twins. Study design Labor characteristics, neonatal outcome and placental histopathology reports of spontaneous PTB at 24–33 6 / 7 weeks, from 1/2008–12/2015, were reviewed. Results were compared between dichorionic-diamniotic twin deliveries (twins group) and singleton deliveries (singleton group) matched for gestational age. Excluded from the study medically indicated deliveries, due to preeclampsia or fetal growth restriction, and monochorionic twins. Placental lesions were classified to maternal vascular supply lesions, fetal vascular supply lesions, and maternal (MIR) and fetal (FIR) inflammatory responses. Composite neonatal outcome was defined as one or more of early complications: respiratory distress, necrotizing enterocolitis, sepsis, blood transfusion, ventilation, seizures, intra-ventricular hemorrhage, hypoglycemia, phototherapy, or death. Results The twins group (n = 72) was characterized by higher maternal BMI (p = 0.009), and higher rates of assisted reproductive techniques (56.2% vs. 17.8%, p < 0.001) and cesarean deliveries (75.3% vs. 32.8%, p < 0.001) as compared to the singleton group (n = 72). Placentas from the singleton group were characterized by higher rate of MIR, 58.9% vs. 19.2%, (p < 0.001), FIR, 31.5% vs. 3.4%, (p < 0.001), retro-placental hemorrhage, 26% vs. 8.9% (p < 0.001), and vascular lesions related to maternal malperfusion, 28.8% vs. 9.6%, (p < 0.001), as compared to placentas from the twins group. Higher rate of neonatal sepsis was observed in the singleton group as compared to the twins group, 24.7% vs. 4.1%, p < 0.001, respectively. By logistic regression analyses retro-placental hemorrhage, placental maternal vascular malperfusion lesions, MIR, FIR and neonatal sepsis were found to be independently associated with singleton PTB: aOR 3.4, 95% CI 2.1–6.9, p < 0.001, aOR = 3.1, 95% CI 1.8–7.2, p < 0.001, aOR = 2.9, 95% CI 1.4–7.8, p < 0.001, aOR = 4.9, 95% CI 2.3–6.9, p < 0.001, and aOR = 4.8, 95% CI 2.3–6.7, p < 0.001 respectively. Conclusion Placentas from singleton PTBs are characterized by higher rate of inflammatory and malperfusion lesions. The lack of these findings in twins PTBs suggests different factors that participate in the development of preterm birth in twins, such as over-distension of the uterus and up regulation of oxytocin receptors.
KW - Inflammatory lesions
KW - Multiple pregnancy
KW - Neonatal sepsis
KW - Placental pathology
KW - Preterm delivery
KW - Singletons
KW - Twins
UR - http://www.scopus.com/inward/record.url?scp=85018559904&partnerID=8YFLogxK
U2 - 10.1016/j.ejogrb.2017.04.035
DO - 10.1016/j.ejogrb.2017.04.035
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C2 - 28448801
AN - SCOPUS:85018559904
SN - 0301-2115
VL - 214
SP - 1
EP - 5
JO - European Journal of Obstetrics and Gynecology and Reproductive Biology
JF - European Journal of Obstetrics and Gynecology and Reproductive Biology
ER -