Evidence map›Paper›PMID 31392662›Full record

ArticleJournal of assisted reproduction and genetics2019

Association of BMP15 and GDF9 variants to premature ovarian insufficiency.

Monise Santos, Emerson Barchi Cordts, Carla Peluso, Mayla Dornas, Felipe Heurre Vieira Neto, Bianca Bianco, Caio Parente Barbosa, Denise Maria Christofolini

Abstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Mutation analysis of theTurkish journal of obstetrics and gynecology · 2026
    Article
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  3. Article
  4. Article
  5. Review
  6. Article
  7. Relationship Between the Occurrence of Depression andInternational journal of molecular sciences · 2024
    Article
  8. Article
  9. Association of Polymorphisms inDiagnostics (Basel, Switzerland) · 2024
    Article
  10. Review
  11. Article
  12. Review
  13. Control of ovarian follicle development by TGFβ family signaling.Current opinion in endocrine and metabolic research · 2021
    Article
  14. Review
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.

Monise SantosInstituto Ideia Fértil, Avenida Príncipe de Gales, 821, Santo André, SP, 09060-650, Brazil.
Emerson Barchi CordtsInstituto Ideia Fértil, Avenida Príncipe de Gales, 821, Santo André, SP, 09060-650, Brazil.
Carla PelusoFaculdade de Medicina do ABC, Av. Lauro Gomes, 2000, Room 101, CEPES, Santo André, SP, 09060-870, Brazil.
Mayla DornasFaculdade de Medicina do ABC, Av. Lauro Gomes, 2000, Room 101, CEPES, Santo André, SP, 09060-870, Brazil.
Felipe Heurre Vieira NetoFaculdade de Medicina do ABC, Av. Lauro Gomes, 2000, Room 101, CEPES, Santo André, SP, 09060-870, Brazil.
Bianca BiancoInstituto Ideia Fértil, Avenida Príncipe de Gales, 821, Santo André, SP, 09060-650, Brazil.
Caio Parente BarbosaInstituto Ideia Fértil, Avenida Príncipe de Gales, 821, Santo André, SP, 09060-650, Brazil.
Denise Maria ChristofoliniInstituto Ideia Fértil, Avenida Príncipe de Gales, 821, Santo André, SP, 09060-650, Brazil. Denise.morf@gmail.com.ORCID http://orcid.org/0000-0001-9589-6417

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo identify genetic variation associated to premature ovarian insufficiency (POI).

methodsA total of 74 women with POI (group POI), 45 women with increased FSH levels (group high FSH), and 88 controls (non-POI) were studied. Genotyping of BMP15:c.-9C>G (rs3810682), BMP15:c.328+905A>G (rs3897937), and BMP15:c.852C>T (rs17003221); and GDF9:c.134-694G>A (rs4705974), GDF9:c.-31-951G>A (rs11748063), GDF9:c.-152G>C (rs30177), and GDF9:g.1073C>T (rs803224) was performed by the TaqMan methodology. Chi-square and Fisher's exact tests were performed to evaluate the distribution of genotypes, alleles, odds ratio, and the Hardy-Weinberg equilibrium of each variation. Haplotype analysis was performed for each gene considering the case and control groups. Bonferroni's correction was applied to chi-square and Fisher's exact test data, and p values < 0.007 for genotypes and alleles and < 0.006 for haplotypes were considered significant.

resultsIt was observed a statistically significant difference in genotype distribution of BMP15:c.852C>T between group POI and controls (p < 0.001). TT and TC genotypes were more frequently observed in group POI. Genotype distribution in case group POI, however, was not in the Hardy-Weinberg equilibrium, due to the increased number of heterozygotes in the sample. Concerning GDF9, no association was found among the studied genetic variants and POI or high FSH groups.

conclusionIt is concluded from the present study that the genotypes CT and TT from BMP15:c.852C>T variation may be risk factors for the development of POI.

Indexed as

Genetic Predisposition to DiseaseAdultAllelesBone Morphogenetic Protein 15FemaleGenetic Association StudiesGenotypeGrowth Differentiation Factor 9HumansPolymorphism, Single NucleotidePrimary Ovarian InsufficiencyBMP15 protein, humanBone Morphogenetic Protein 15GDF9 protein, humanGrowth Differentiation Factor 9BMP15GDF9Gene variantsInfertilityPremature ovarian insufficiency

Identifiers

PMID31392662
PMCPMC6823326

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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.