Evidence map›Paper›PMID 39582021›Full record

ArticleJournal of human genetics2025

Preimplantation genetic testing for inborn errors of metabolism: observations from a reproductive genetic laboratory in China.

Xiaoli Li, Qiuxiang Huang, Fuchun Zhong, Yun Liu, Zhibiao Chen, Juan Lin, Zhongli Fan, Fenghua Lan, Zhihong Wang

Abstract read
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In one paragraph

Article in Journal of human genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Xiaoli Li *Department of Clinical Laboratory Medicine, Dongfang Hospital of Xiamen University, School of Medicine, Xiamen University, Fuzhou, Fujian, China.
Qiuxiang Huang *Center of Reproductive Medicine, Department of Obstetrics and Gynecology, Dongfang Hospital of Xiamen University, School of Medicine, Xiamen University, Fuzhou, Fujian, China.
Fuchun Zhong *Laboratory of Basic Medicine, Fujian Provincial Key Laboratory of Transplant Biology, Dongfang Hospital of Xiamen University, School of Medicine, Xiamen University, Fuzhou, Fujian, China.
Yun LiuCenter of Reproductive Medicine, Department of Obstetrics and Gynecology, Dongfang Hospital of Xiamen University, School of Medicine, Xiamen University, Fuzhou, Fujian, China.
Zhibiao ChenCenter of Reproductive Medicine, Department of Obstetrics and Gynecology, Dongfang Hospital of Xiamen University, School of Medicine, Xiamen University, Fuzhou, Fujian, China.
Juan LinLaboratory of Basic Medicine, Fujian Provincial Key Laboratory of Transplant Biology, Dongfang Hospital of Xiamen University, School of Medicine, Xiamen University, Fuzhou, Fujian, China.
Zhongli FanLaboratory of Basic Medicine, Fujian Provincial Key Laboratory of Transplant Biology, Dongfang Hospital of Xiamen University, School of Medicine, Xiamen University, Fuzhou, Fujian, China.
Fenghua LanLaboratory of Basic Medicine, Fujian Provincial Key Laboratory of Transplant Biology, Dongfang Hospital of Xiamen University, School of Medicine, Xiamen University, Fuzhou, Fujian, China.
Zhihong WangLaboratory of Basic Medicine, Fujian Provincial Key Laboratory of Transplant Biology, Dongfang Hospital of Xiamen University, School of Medicine, Xiamen University, Fuzhou, Fujian, China. xmzhwang@xmu.edu.cn.

Funding

Natural Science Foundation of Fujian Province (Fujian Provincial Natural Science Foundation) 2023J01134
6 · The paper itself

Abstract

In this study, we aimed to apply preimplantation genetic testing for monogenic disorders (PGT-M) based on mutated allele revealed by sequencing with aneuploidy and linkage analyses (MARSALA) to block the transmission of inborn errors of metabolism (IEMs). After the disease-causing variants were identified through genetic testing, four carrier couples having children affected with IEMs, including methylmalonic aciduria, glutaric acidemia type 1, beta-ketothiolase deficiency, and ornithine transcarbamylase deficiency, sought PGT-M. A series of PGT procedures involving intracytoplasmic sperm injection, blastocyst culture, biopsy of trophectoderm cells, and next-generation sequencing (NGS)-based MARSALA, was performed to provide comprehensive chromosome screening and variant gene analysis. Finally, embryos were selected for transfer, and prenatal diagnosis was conducted to confirm the PGT-M results. All four carrier couples obtained transferrable embryos after PGT. The results of the prenatal diagnosis were consistent with the PGT results, and all couples gave birth to healthy babies free of IEMs. The results of this study confirm that NGS-based MARSALA is an effective approach for families with IEMs to prevent the subsequent transmission of pathological genetic variants to the next generation.

Indexed as

Genetic TestingMetabolism, Inborn ErrorsPreimplantation DiagnosisAdultAneuploidyChinaEmbryo TransferFemaleHigh-Throughput Nucleotide SequencingHumansMalePregnancyPrenatal DiagnosisSperm Injections, Intracytoplasmic

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.