Evidence map›Paper›PMID 41283765›Full record

ArticleReproduction & fertility2025

Chromosomal miscarriage and pregnancy outcomes in recurrent pregnancy loss.

Yuxin Yang, Xiaoran Zhang, Yingying Zhang, Miaoxian Ou, Can Wang, Youhui Lu, Lu Luo, Qiong Wang

Abstract read
In one paragraph

Article in Reproduction & fertility, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Observational
  3. 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

8 authors.

Yuxin YangDepartment of Obstetrics and Gynecology, Reproductive Medical Center, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.ORCID 0009-0002-8677-624X
Xiaoran ZhangDepartment of Obstetrics and Gynecology, Reproductive Medical Center, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.ORCID 0009-0005-2032-762X
Yingying ZhangDepartment of Obstetrics and Gynecology, Reproductive Medical Center, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Miaoxian OuDepartment of Obstetrics and Gynecology, Reproductive Medical Center, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Can WangDepartment of Obstetrics and Gynecology, Reproductive Medical Center, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Youhui LuDepartment of Obstetrics and Gynecology, Reproductive Medical Center, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Lu LuoDepartment of Obstetrics and Gynecology, Reproductive Medical Center, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.ORCID 0000-0002-9151-6410
Qiong WangDepartment of Obstetrics and Gynecology, Reproductive Medical Center, First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.ORCID 0000-0001-9897-2120

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abstract: This prospective cohort study aimed to assess whether a history of embryonic chromosomal abnormality affects subsequent pregnancy outcomes in women with unexplained recurrent pregnancy loss. A total of 233 women with unexplained recurrent pregnancy loss who conceived naturally were included. Participants were categorized according to the chromosomal status of prior miscarriages. A multivariate logistic regression model was constructed to predict live birth based on these categories and observed pregnancy outcomes. Among the 233 included women, 171 (73.4%) had a live birth, while 62 (26.6%) experienced early pregnancy loss. Among women with one abnormal chromosomal miscarriage (n = 110), 94 (85.5%) had a live birth, accounting for 40.3% of the total cohort. In contrast, in the one normal chromosomal miscarriage group (n = 77), 47 (61.0%) achieved live birth, representing 20.2% of the total. The model identified a history of one chromosomally abnormal miscarriage (odds ratio = 3.88, 95% confidence interval: 1.87-8.06) and history of two chromosomally abnormal miscarriages (odds ratio = 8.93, 95% confidence interval: 1.07-74.55) as significant predictors of live birth. The predictive model achieved an area under the curve of 0.73 in the training dataset and 0.75 in the testing dataset. A history of embryonic chromosomal miscarriage may reflect improved pregnancy prospects and inform clinical counseling in unexplained recurrent pregnancy loss. Lay summary: Women with unexplained recurrent miscarriage often wonder whether their history will affect future natural pregnancies. Chromosomal abnormalities in embryos are a leading cause of miscarriage, but the impact of such a history on later outcomes has remained unclear. We studied 233 women with repeated unexplained losses and assessed their subsequent pregnancy results. Overall, 73.4% achieved a live birth, while 26.6% had another early miscarriage. Interestingly, among women who had one chromosomal abnormal miscarriage, 85.5% subsequently achieved a live birth. In contrast, the live birth rate was lower in the group who had a normal chromosomal miscarriage; only 61.0% went on to achieve a live birth. These results suggest that a history of abnormal chromosomal miscarriage may indicate better chances of future pregnancy and help guide clinical care.

Indexed as

Abortion, HabitualChromosome AberrationsPregnancy OutcomeAdultFemaleHumansLive BirthPregnancyProspective Studiesembryonic chromosomal abnormalitypredictive modelpregnancy outcomerecurrent pregnancy loss

Identifiers

PMID41283765
PMCPMC12694013

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.