Evidence map›Paper›PMID 38695986›Full record

ArticleJournal of assisted reproduction and genetics2024

Stringent criteria needed for germline genome editing of human IVF embryos.

Alexis Heng Boon Chin, Jean-Didier Bosenge Nguma, Mohd Faizal Ahmad

Open access · greenAbstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

3 authors at 3 institutions in 3 countries.

Alexis Heng Boon ChinSingapore Fertility and IVF Consultancy Pvt Ltd, 531A Upper Cross Street, #04-95, Hong Lim Complex, Chinatown, 051531, Singapore. boonchinheng@yahoo.com.
Jean-Didier Bosenge NgumaDepartment of Obstetrics and Gynecology, Kisangani University Hospital, Kisangani, Democratic Republic of the Congo.
Mohd Faizal AhmadDepartment of Obstetrics & Gynecology, Faculty of Medicine, Advanced Reproductive Centre (ARC), Universiti Kebangsaan Malaysia, Jalan Yaacob Latif, Cheras, Kuala Lumpur, Malaysia. drmohdfaizal@ukm.edu.my.ORCID http://orcid.org/0000-0003-2541-3699
Singapore Clinical Research Institute · SGUniversité de Kisangani · CDUniversity Kebangsaan Malaysia Medical Centre · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Germline genome editing of IVF embryos is controversial because it is not directly health or lifesaving but is intended to prevent genetic diseases in yet-unborn future offspring. The following criteria are thus proposed for future clinical trials: (i) Due to medical risks, there should be cautious and judicious application while avoiding any non-essential usage, with rigorous patient counseling. (ii) Genome editing should only be performed on the entire batch of IVF embryos without initial PGT screening if all of them are expected to be affected by genetic disease. (iii) When there is a fair chance that some IVF embryos will not be affected by genetic diseases, initial PGT screening must be performed to identify unaffected embryos for transfer. (iv) IVF embryos with carrier status should not undergo germline genome editing. (v) If patients fail to conceive after the transfer of unaffected embryos, they should undergo another fresh IVF cycle rather than opt for genome editing of their remaining affected embryos. (vi) Only if the patient is unable to produce any more unaffected embryos in a fresh IVF cycle due to advanced maternal age or diminished ovarian reserves, can the genome editing of remaining affected embryos be permitted as a last resort.

Indexed as

Fertilization in VitroGene EditingGerm CellsPreimplantation DiagnosisEmbryo, MammalianEmbryo TransferFemaleHumansPregnancyCRISPR-Cas9EthicsGene therapyMonogenic disordersPatient enrolmentPreimplantation embryo

Identifiers

PMID38695986
PMCPMC11263300
OpenAlexW4396578494

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.