Implementing Reproductive Carrier Screening to Include Diverse Asian Populations: Insights from Singapore
Bylstra, Y.; Yeo Juann, M.; Teo, J. X.; Goh, J.; Choi, C.; Chan, S.; Song, C.; Chew Yin Goh, J.; Chai, N.; Lieviant, J. A.; Toh, H. J.; Chan, S. H.; Blythe, R.; Menezes, M.; Yang, C.; Hodgson, J.; Graves, N.; Sng, J.; Lim, W. W.; Law, H. Y.; Amor, D.; Baynam, G.; Chan, J. K.; Chan, Y. H.; Tan, P.; Ng, I.; Lim, W. K.; Jamuar, S. S.
Show abstract
Background As part of Singapore's effort towards precision medicine tailored to Asian diversity, we describe the implementation of a nationwide reproductive carrier screening program. Using a customised 112-gene panel, incorporating population-specific recessive genetic diseases, we outline the overall program design, and initial efforts of community and stakeholder engagement, to inform culturally appropriate implementation. Methods Participants receive culturally tailored online education regarding our reproductive screening program and are provided results with genetic counselling and reproductive options. Community and stakeholder perspectives were assessed through questionnaires and consultations with religious leaders. Results Recruitment is nation-wide, and since initiation of our pilot phase in September 2024, 1,619 couples have registered interest, with 60% uptake of those deemed eligible. Among the 456 couples that have received results to date, four couples (0.9%) were identified to be at increased risk. Community questionnaire responses (n=1002), involving couples who participated in the program as well as the general public, indicated interest is high (59%) across the cohort but awareness, intent to participate and implications for reproductive options differed by sociodemographic factors such as ancestry and religion. Healthcare professional respondents (n=113) acknowledged carrier screening will be routine in medical care, but report limited confidence and resources. Engagement with religious leaders indicated support for the program. Conclusion These early program outcomes and community engagement are guiding the implementation of expanding population-based carrier screening in Singapore, contingent on addressing practical challenges through equitable outreach and professional training.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Defining the Critical Educational Components of Informed Consent for Genetic Testing: Views of US-Based Genetic Counselors and Medical Geneticists 95%
- A Qualitative Study Exploring the Consumer Experience of Receiving Self-Initiated Polygenic Risk Scores from a Third-Party Website 92%
- Benefits and barriers to implementing precision preventive care: results of a national physician survey 90%
Similar papers in this journal
- Development and evaluation of a novel educational program for providers on the use of polygenic risk scores 94%
- Systematic assessment of outcomes following a genetic diagnosis identified through a large-scale research study into developmental disorders 92%
- Comprehensive phenotyping of 3q29 deletion syndrome: recommendations for clinical care 92%
Similar papers in this journal
- Optical Genome Mapping And Single Nucleotide Polymorphism Microarray: An Integrated Approach For Investigating Challenging Cases Of Products Of Conception 92%
- Optical genome mapping as a next-generation cytogenomic tool for detection of structural and copy number variations for prenatal genomic analyses 91%
- Evaluation of optical genome mapping in clinical genetic testing of facioscapulohumeral muscular dystrophy 90%
Similar papers in this journal
- A Pooled Electronic Consultation Program to Improve Access to Genetics Specialists 91%
- Evaluation of DNA-poli: study protocol of a randomised controlled trial to assess a digital platform for family cascade genetic testing and predictive genetic counselling 91%
- Genetic Diagnosis of Facioscapulohumeral Muscular Dystrophy Type 1 Using Rare Variant Linkage Analysis and Long Read Genome Sequencing 89%
Similar papers in this journal
- Community Attitudes on Genetic Research of Gender Identity, Sexual Orientation, and Mental Health 94%
- Cohort profile: The Bristol IVF Study- A longitudinal study of women, their partners and treatment outcomes following assisted reproductive technologies 93%
- Feedback of Individual Genetic and Genomics Research Results: A Qualitative Study Involving Grassroots Communities in Uganda 92%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.