Evidence map›Paper›PMID 41384014›Full record

ArticleFrontiers in endocrinology2025

Incidence of miscarriages in women with children with 47,XXY, 48,XXXY, or 49,XXXXY.

Elizabeth Moser, Margaret Olaya, Andrea Gropman, Teresa Sadeghin, Carole Samango-Sprouse

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 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

5 authors.

Elizabeth MoserDepartment of Research, The Focus Foundation, Davidsonville, MD, United States.
Margaret OlayaDepartment of Research, The Focus Foundation, Davidsonville, MD, United States.
Andrea GropmanDepartment of Pediatric Medicine, St. Jude Children's Research Hospital, Memphis, TN, United States.
Teresa SadeghinDepartment of Research, The Focus Foundation, Davidsonville, MD, United States.
Carole Samango-SprouseDepartment of Research, The Focus Foundation, Davidsonville, MD, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: The management and the causes of miscarriages present challenges for the obstetrical community as well as for families. In families who have a child with an X and Y chromosomal disorder, the duress of pregnancy loss may be significantly exacerbated. A greater understanding of these mechanisms would inform medical providers and families of children with 47,XXY, or Klinefelter syndrome (KS), and variant disorders (48,XXXY and 49,XXXXY). This study investigates miscarriage incidences across a cohort of mothers of male offspring born with these disorders. Methods: Pregnancy history of mothers of male offspring with 47,XXY (KS) or variant disorders was collected. Statistical analyses were performed to determine if these mothers experienced higher incidences of miscarriage than the general population. Results: Mothers reporting miscarriage in the 47,XXY ( Conclusion: Mothers of children with 47,XXY (KS) and variant disorders are at increased risk of miscarriage compared to the general population based on the findings of this study.

Indexed as

Abortion, SpontaneousKlinefelter SyndromeAdultChildChromosomes, Human, XCohort StudiesFemaleHumansIncidenceMalePregnancy47,XXY48,XXXY49,XXXXYKlinefelter syndromemiscarriagesex chromosome aneuploidy

Identifiers

PMID41384014
PMCPMC12689414

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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 OpenQuestion graph.