Ernawati Ernawati

Dr. Ernawati Ernawati

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 December 2021 in American Journal of Obstetrics and Gynecology
Verified
Journal Article
Closed access
BEBrenda Eskenazi
Brenda Eskenazi
SRStephen Rauch
Stephen Rauch
EIEnrico Iurlaro
Enrico Iurlaro
RGRobert B. Gunier
Robert B. Gunier
ARAlbertina Rego
Albertina Rego
APAris T. Papageorghiou
Aris T. Papageorghiou

1 March 2023 in The Journal of Maternal-Fetal & Neonatal Medicine
Verified
Journal Article
Open access
LALetizia Alessandrini
Letizia Alessandrini
RARozi Aryananda
Rozi Aryananda
GAGrace Ariani
Grace Ariani
BABetty Agustina
Betty Agustina
MAMuhammad Ilham Aldika Akbar
Muhammad Ilham Aldika Akbar
EEErnawati Ernawati
Ernawati Ernawati
This study aims to further explore the role of angiogenic vs anti-angiogenic factors in placenta accreta spectrum (PAS).This cohort study included all patients with placenta previa and placenta acc...

30 April 2023 in Pharmacognosy Journal
Verified
Journal Article
Open access
PDF file
EEErnawati Ernawati
Ernawati Ernawati
AAAditiawarman Aditiawarman
Aditiawarman Aditiawarman
SRSalsabila Nabilah Rifdah
Salsabila Nabilah Rifdah
ASAgus Sulistyono
Agus Sulistyono

22 December 2025 in BMC Pregnancy and Childbirth
Verified
Journal Article
Open access
PDF file
EEErnawati Ernawati
Ernawati Ernawati
MAMuhammad I A Akbar
Muhammad I A Akbar
RARozi Aditya Aryananda
Rozi Aditya Aryananda
MBMuhammad Adrianes Bachnas
Muhammad Adrianes Bachnas
RIRima Irwinda
Rima Irwinda
HGHKFM Preeclampsia Research Group
HKFM Preeclampsia Research Group
HELLP syndrome, a severe complication of preeclampsia, is associated with increased maternal and neonatal morbidity and mortality. This study aims to evalu

22 October 2025 in Medical Sciences
Verified
Journal Article
Open access
PDF file
Khanisyah Erza GumilarKhanisyah Erza Gumilar
Khanisyah Erza Gumilar
AHAlexander Indra Humala
Alexander Indra Humala
MWManggala Pasca Wardhana
Manggala Pasca Wardhana
EEErnawati Ernawati
Ernawati Ernawati
ASAgus Sulistyono
Agus Sulistyono
GDGus Dekker
Gus Dekker
Background: Preeclampsia remains a leading cause of maternal and perinatal morbidity and mortality, yet its pathophysiology is not fully understood. Recent studies suggest that dysregulated maternal immune responses, particularly involving decidual Natural Killer (dNK) cells and immune checkpoint molecules such as B7-H3, may play a role in the pathogenesis of this heterogeneous syndrome, particularly in the development of early-onset preeclampsia (EOP). Objective: The aim of this study was to investigate the expression patterns of B7-H3 on extravillous trophoblasts (EVTs) and the abundance of dNK cells in preeclamptic versus normotensive pregnancies and to analyze the relationship between these two immune parameters. Methods: A cross-sectional study was conducted using 42 placental samples (21 preeclampsia, 21 controls). Immunohistochemistry (IHC) was performed to detect CD56 (dNK cells) and CD276 (B7-H3) expression. Expression was semi-quantitatively evaluated using the Remmele Immunoreactive Score (IRS). Statistical comparisons and correlation analyses were conducted. Results: Preeclamptic placentas exhibited significantly higher dNK cell expression (IRS 7.19 ± 2.16) and significantly lower B7-H3 expression (IRS 2.63 ± 0.90) compared to controls (p < 0.001 and p = 0.002, respectively). A positive correlation was found between B7-H3 and dNK cell expression in both groups, with a stronger correlation in normotensive pregnancies (r = 0.605; p = 0.004) and preeclampsia (r = 0.465; p = 0.034). Conclusions: The inverse expression pattern and reduction in B7-H3 expression compared to dNK cells in preeclampsia suggest a loss of immune tolerance at the maternal–fetal interface. These findings highlight the potential of B7-H3 as a biomarker and immunoregulatory target for early prediction and prevention of preeclampsia.

1 May 2024 in Journal of Pharmacy & Pharmacognosy Research
Verified
Journal Article
Open access
MAMuhammad Ilham Aldika Akbar
Muhammad Ilham Aldika Akbar
CWCitrawati Wungu
Citrawati Wungu
EEErnawati Ernawati
Ernawati Ernawati
GDGus Dekker
Gus Dekker
Context: Preeclampsia prevention is important for reducing maternal mortality and morbidity worldwide. Recent studies have explored the use of to prevent preeclampsia and improve maternal, perinatal, or neonatal outcomes. However, the results are still debatable. Aims: To evaluate the role of pravastatin in the prevention of preeclampsia in pregnant women. Methods: This study is a systematic review and meta-analysis of randomized controlled trials (RCTs) involving studies with healthy pregnant women receiving pravastatin vs. control to observe the risk of preeclampsia. Literature searching was conducted in PubMed, Science Direct, EBSCO/CINAHL, PROQUEST, and SCOPUS. Statistical analyses were performed using the Review Manager 5.4.1 software. Results: Five studies were initially identified for meeting the inclusion criteria; 2 studies were treatment studies and had to be excluded, and one small study only used pravastatin for a few weeks, leaving only two studies for statistical analysis. Administration of pravastatin was associated with a reduced risk of preeclampsia (OR: 0.51; 95% CI: 0.29-0.90; p= 0.02) and preterm delivery (OR: 0.31; 95% CI: 0.16-0.58; p<0.01). The risk of preeclampsia with severe features and small for gestational ages was not different. Only one study (INOVASIA) reported on preterm preeclampsia, prophylactic pravastatin was associated with a marked and significant reduction of preterm preeclampsia rates (OR: 0.034; 95% CI: 0.202-0.905). Pregnant women receiving pravastatin had better perinatal outcomes in terms of birthweight, Apgar scores, NICU admission, length of stay, and respiratory distress syndrome. Conclusions: Pravastatin has the potential to prevent the occurrence of preeclampsia, premature birth, and perinatal morbidity in pregnant women. However, it is necessary to conduct more RCTs with a larger sample size and appropriate follow-up of the offspring to further examine the efficacy of pravastatin in preeclampsia prevention.