Placental vascularization alterations in hypertensive disorders complicating pregnancy (HDCP) and small for gestational age with HDCP using three-dimensional power doppler in a prospective case control study
Yuan et al. BMC Pregnancy and Childbirth (2015) 15:240
DOI 10.1186/s12884-015-0666-1
RESEARCH ARTICLE
Open Access
Placental vascularization alterations in
hypertensive disorders complicating
pregnancy (HDCP) and small for gestational
age with HDCP using three-dimensional power
doppler in a prospective case control study
Ting Yuan, Ting Zhang and Zhen Han*
Abstract
Background: Hypertensive disorders complicating pregnancy (HDCP) continues to be a leading cause of maternal
and neonatal mortality and morbidity. The clinical value of placental three-dimensional power Doppler (3DPD) in
assessing HDCP requires further confirmation. The research was developed to assess changes of placental vascularity in
HDCP using 3DPD and to investigate the placental vascularity in small for gestational age (SGA) compared with not-SGA
in patients with HDCP.
Methods: There were 126 normotensive and 128 hypertensive pregnant women included in this prospective
case–control study from March 2011 to March 2013. Pregnant women underwent 3DPD. Vascularization index
(VI), flow index (FI) and vascularization flow index (VFI) were obtained. The placental 3DPD indices, umbilical
artery systolic and diastolic ratio (S/D) and pregnancy outcomes were compared between the groups.
Results: The placental VI and VFI were significantly lower in hypertensive women compared with normotensive women
(P < 0.001 and P = 0.014, respectively), and these parameters were significantly reduced in severe preeclampsia (P < 0.001
and P = 0.003, respectively). A weak correlation was found between VI and umbilical artery S/D in HDCP group (r = -0.277,
P = 0.001). In HDCP population, neonates who were postnatally diagnosed with SGA had lower VI (P = 0.041) and higher
S/D (P < 0.001).
Discussion: The placental vascularity indices decreased in hypertensive women and the reduction inplacental perfusion
was consistent with the severity of the hypertensive disorder. The associations betweenplacental vascularization and
umbilical artery impedance may be valuable for further researches and arerequired confirmation. The significant
differences in the 3DPD placental vascularization between SGA andnot-SGA in hypertensive pregnancy population may
show some clinical importance that we could use tobetter assess or predict the progression and adverse outcomes in the
future. Although 3DPD quantificationhas been widely used in multiple publications, we have to acknowledge its
limitations.
Conclusions: The intraplacental vascularization was poor in HDCP, and especially in severe preeclampsia. Neonates with
SGA had poor placental vascularization and higher umbilical artery S/D. Further studies should focus on the clinical
assessment of placental 3DPD as well as a combination of placental 3DPD and other fetal Doppler indices to better
predict the development and outcomes of preeclampsia.
Keywords: Hypertensive disorders complicating pregnancy (HDCP), Placenta, Small for gestational age (SGA),
Three-dimensional power Doppler (3DPD)
* Correspondence:
Department of Obstetrics and Gynecology, First Affiliated Hospital of Xi’an
Jiaotong University College of Medicine, Shaanxi, China
© 2015 Yuan et al. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0
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Yuan et al. BMC Pregnancy and Childbirth (2015) 15:240
Background
Hypertensive disorders complicating pregnancy (HDCP)
continues to be a leading cause of maternal and neonatal
mortality and morbidity [1]. The prevalence of HDCP is
approximately 5.22 % of all pregnancies in China and
8–10 % worldwide [2, 3]. In recent years, important
advances have been made in our understanding of the
pathogenesis and pathophysiology of preeclampsia, but
most of the factors that contribute to the disease remain
unclear. Multiple tests and combination tests have been
developed as screening methods for preeclampsia,
including maternal serum biomarkers and Doppler
parameters. To date, there is no effective screening test
for HDCP [4–6].
HDCP is currently considered as a chronic placental
disease. Placental dysfunction and hypo-perfusion play
an important role in HDCP pathophysiology and are
considered to be responsible for pathologic pregnancy
outcomes, such as fetal growth restriction and perinatal
loss [7–9]. Three-dimensional power Doppler (3DPD)
has been a focal point of recent placental research; it is
superior to 2D Doppler in several ways, including its
ability to detect the secondary and tertiary stem vessels
in the placenta and intraplacental vessel characteristics,
such as the vessel density, branching, caliber changes
and tortuosity, which can be shown using 3DPD [8, 10, 11].
Quantitative 3DPD analysis has been used to assess placental perfusion and vascularization indices, which potentially
reflect both utero-placental and feto-placental blood
perfusion [10].
Assessment of placental perfusion using 3DPD seems
to be more helpful in understanding HDCP pathophysiology. However, the clinical value of placental 3DPD in
assessing HDCP requires confirmation. The aim of our
study was to compare changes in placental vascularity
between HDCP and normotensive subjects using 3DPD,
and to assess whether placental vascularity changes presenting in small for gestational age (SGA) compared
with not-SGA in HDCP.
Patients and methods
Enrolment
This was a prospective case–control study that was conducted at the First Affiliated Hospital of Xi’an Jiaotong
University, ShaanXi, China, from March 2011 to March
2013. Women with HDCP were enrolled, and normotensive pregnant women were used as controls. HDCP and
normotensive pregnant subjects were individually matched
by maternal age ± 2 years and gestational week at
examination ±2 weeks.
The hypertensive group was further stratified into
the following subgroups: (1) gestational hypertension
(hypertension for the first time during pregnancy
without proteinuria); (2) severe preeclampsia (diastolic
Page 2 of 11
BP ≥110 mmHg, systolic BP ≥160 mmHg; proteinuria
from none to positive; elevated serum creatinine and
transaminase levels; obvious fetal growth restriction
(FGR); multi-organ disturbances, such as headache,
visual disturbance, upper abdominal pain, oliguria,
convulsion, thrombocytopenia and pulmonary edema);
(3) nonsevere preeclampsia (diastolic BP <110 mmHg,
systolic BP <160 mmHg; proteinuria from none to
positive; no multi-organ disturbances or only minimal
serum transaminase elevation). Nonsevere preeclampsia
includes “mild” and “moderate” (...truncated)