Whole-exome sequencing-based carrier screening in Chinese Han infertile couples attempting assisted reproductive technology: an exploratory, single-center retrospective descriptive study

Background This study aimed to describe carrier findings, genetic counseling recommendations, and subsequent ART plan choices observed after untargeted whole-exome sequencing (WES)-based carrier screening in infertile Chinese Han couples attempting assisted reproductive technology (ART). Methods This retrospective, exploratory, single-center descriptive study included infertile couples who had undergone genetic counseling and WES for carrier screening in an in vitro fertilization (IVF) clinic affiliated with a university in Central China. Genetic findings, counseling recommendations, and ART plans documented after WES were summarized descriptively. No comparator group, validated decision-making survey instrument, or pre-specified before-after decision outcome was available. Results A total of 130 infertile or subfertile couples were enrolled. Overall, 82.7% (215/260; 95% CI 77.6-86.8%) of individuals carried at least one P/LP variant, including 77.7% (101/130; 95% CI 69.8-84.0%) of males and 87.7% (114/130; 95% CI 80.9-92.3%) of females. The carrier burden was 1.6038 variants per person. GJB2-associated deafness was the most prevalent finding, occurring in 13.8% (36/260) of individuals. After excluding somatic and autosomal-dominant secondary findings from the reproductive carrier-risk denominator, 7.7% (10/130; 95% CI 4.2-13.6%) of couples met the strict AR/XL at-risk-couple definition. Among these 10 couples, PGT-M was recorded as the post-WES ART plan for three couples (30.0%; 95% CI 10.8-60.3%). Conclusion In this retrospective descriptive cohort, WES-based carrier screening identified a high carrier burden and generated counseling recommendations that were followed by different ART plan choices among AR/XL at-risk couples. Genetic counseling before and after WES remains important for couples receiving positive carrier-screening results.

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Heliyon
Published
2026-08-28
DOI
https://doi.org/10.1016/j.heliyon.2026.e45369
Primary Topic
Cystic Fibrosis Research Advances
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article
Field-Weighted Citation Impact
0.00

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article

Whole-exome sequencing-based carrier screening in Chinese Han infertile couples attempting assisted reproductive technology: an exploratory, single-center retrospective descriptive study

Lei Jin, Bo Zhang, Meng Wang, Jing Yue et al.
Heliyon
Cystic Fibrosis Research Advances
article

Whole-exome sequencing-based carrier screening in Chinese Han infertile couples attempting assisted reproductive technology: an exploratory, single-center retrospective descriptive study

Lei Jin, Bo Zhang, Meng Wang, Jing Yue, Jiangshan Xie, Wen Chen, Wei Yang
article en

Abstract

Background This study aimed to describe carrier findings, genetic counseling recommendations, and subsequent ART plan choices observed after untargeted whole-exome sequencing (WES)-based carrier screening in infertile Chinese Han couples attempting assisted reproductive technology (ART). Methods This retrospective, exploratory, single-center descriptive study included infertile couples who had undergone genetic counseling and WES for carrier screening in an in vitro fertilization (IVF) clinic affiliated with a university in Central China. Genetic findings, counseling recommendations, and ART plans documented after WES were summarized descriptively. No comparator group, validated decision-making survey instrument, or pre-specified before-after decision outcome was available. Results A total of 130 infertile or subfertile couples were enrolled. Overall, 82.7% (215/260; 95% CI 77.6-86.8%) of individuals carried at least one P/LP variant, including 77.7% (101/130; 95% CI 69.8-84.0%) of males and 87.7% (114/130; 95% CI 80.9-92.3%) of females. The carrier burden was 1.6038 variants per person. GJB2-associated deafness was the most prevalent finding, occurring in 13.8% (36/260) of individuals. After excluding somatic and autosomal-dominant secondary findings from the reproductive carrier-risk denominator, 7.7% (10/130; 95% CI 4.2-13.6%) of couples met the strict AR/XL at-risk-couple definition. Among these 10 couples, PGT-M was recorded as the post-WES ART plan for three couples (30.0%; 95% CI 10.8-60.3%). Conclusion In this retrospective descriptive cohort, WES-based carrier screening identified a high carrier burden and generated counseling recommendations that were followed by different ART plan choices among AR/XL at-risk couples. Genetic counseling before and after WES remains important for couples receiving positive carrier-screening results.

HeliyonVol. 12(14)
Tongji Hospital (CN), Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China
Gender equality, Peace, Justice and strong institutions
Openalex Percentile: Top 11%
Cystic Fibrosis Research Advances
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