Gene Solutions announces multi-centre study to develop next-generation prenatal genetic screening test that predicts for adverse pregnancy complications

Gene Solutions announced a multi-centre research collaboration with leading OBGYN centres in Vietnam, Singapore, Indonesia, and Philippines on the early prediction of pregnancy complications. This clinical study involving >10,000 women would be the first of its kind, focusing on maternal health, enabling earlier prediction of potential pregnancy complications.

At the workshop “Beyond the First-line Prenatal Screening” held in Singapore on March 15, 2024, 70 obstetricians and leading geneticists from Vietnam, Indonesia, the Philippines shared about the pathogenesis, clinical burden, and new evidence in prediction of Severe Pregnancy Syndromes.

Dr. Anna Belen I. Alensuela, Board Member of Philippine Obstetrical and Gynecology Society, cited studies where more than 15% of pregnancies suffer from great obstetrical syndromes causing severe adverse short and long-term outcomes for both the mother and fetus1.

“According to current guidelines, screening for the risk of premature birth, pre-eclampsia and gestational diabetes usually takes place in the later stages of pregnancy, while identifying high-risk patients early in the first trimester help in better identification and management of pregnancies under modern care model.” – shared Prof. Dr. Noroyono Wibowo, Head of Maternal Fetal Medicine of University of Indonesia.

Associate Professor Dr. Matthew Warren Kemp from the National University of Singapore presented research data demonstrating that biomarkers in maternal blood may be used as effective prediction models for pathological risks in severe pregnancy syndromes including preeclampsia and chorioamnionitis.

Gene Solutions announces multi-centre study to develop next-generation prenatal genetic screening test that predicts for adverse pregnancy complications

To address these considerations, Dr. Hoa from HCMC Medical Genetics Institute, co-founder of Gene Solutions shared preliminary data of multi-omic biomakers for early prediction of pregnancy complications and announced the multi-center research program “Building and Evaluating an Early Prediction Model for Pregnancy Complications: Pre-eclampsia, Preterm Birth, and Gestational Diabetes in Non-Invasive Prenatal Testing (NIPT)”. This two-phase study will run from 2024 to 2026, monitoring over 10,000 pregnant mothers across South-East Asia, laying the groundwork for next-generation NIPT as a triage screen in early prediction of pregnancy complications.

More than a million triSure NIPT tests for first trimester prenatal screening have been performed for pregnant women since 2018. Gene Solutions remains committed to bringing clinically relevant genomics solutions for a healthier population.

LATEST News

New Study Validates Gene Solutions’ Upgraded ctDNA Workflow Behind K-TRACK and K-4CARE

New Study Validates Gene Solutions’ Upgraded ctDNA Workflow Behind K-TRACK and K-4CARE

Peer-reviewed findings published in The Journal of Liquid Biopsy, an official journal of the International Society of Liquid Biopsy (ISLB), demonstrate broader ctDNA analysis, improved recurrence prediction, and greater flexibility with or without tumor tissue. SINGAPORE, 14 October 2026 – Gene Solutions announced the publication of a new peer-reviewed study validating the upgraded ctDNA workflow behind K-TRACK, K-4CARE, and K-TRACK Blood Only. Published in The Journal of Liquid Biopsy, an official journal of the International Society of Liquid Biopsy (ISLB), the study evaluated how Gene Solutions’ new hybrid-capture sequencing workflow and VarSURE bioinformatics pipeline improve upon its previous amplicon-based ctDNA method.

Read More

Biomarker and ctDNA Testing: A Personalized Approach to Cancer Care

Cancer diagnosis often brings many questions: Which treatment is most suitable for me? Is my treatment working? Has cancer changed? Could it come back? Every person’s cancer is different. Even when two people have the same type of cancer, their tumors may have different biological features. These differences can influence how the cancer behaves and how it responds to treatment. Biomarker and circulating tumor DNA, or ctDNA, testing may help doctors better understand these differences. Together, these tests may support more personalized treatment decisions and provide additional information as the cancer changes over time. Why can the same cancer respond

Read More
Gene Solutions NIPT preterm birth prenatal health

Gene Solutions Study Finds Preterm-Birth Signals in Routine triSure NIPT Data

A Gene Solutions study published in American Journal of Obstetrics & Gynecology (AJOG) Global Reports finds cell-free DNA fragmentomic patterns associated with spontaneous preterm birth, pointing to a potential path toward earlier pregnancy-risk assessment. SINGAPORE, Sept. 25, 2026 /PRNewswire/ — Gene Solutions, a global biotechnology company providing precision cell-free DNA solutions through multi-omics and artificial intelligence to improve pregnancy care, cancer detection and precision medicine, today announced the publication of a study showing the potential to assess the risk of spontaneous preterm birth from cell-free DNA fragmentomic signals already present in routine first-trimester non-invasive prenatal testing (NIPT) data. Published in AJOG Global Reports, the

Read More