Evidence map›Paper›PMID 25469124›Full record

ArticleIranian journal of reproductive medicine2014

The luteinizing hormone beta-subunit exon 3 (Gly102Ser) gene mutation and ovarian responses to controlled ovarian hyperstimulation.

Robab Davar, Nasim Tabibnejad, Seyed Mehdi Kalantar, Mohammad Hasan Sheikhha

Registry-linked trialAbstract read
In one paragraph

Article in Iranian journal of reproductive medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06486870 (Comparative Study Between Two Ovulation Induction Therapies and Laparoscopic Ovarian Drilling on Clinical Outcomes in Clomiphene Citrate-Resistant PCOS Women), which is not on this 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

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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.

NCT06486870 phase3completednot on this mapstarted 2020, after this paper: background citation

Comparative Study Between Two Ovulation Induction Therapies and Laparoscopic Ovarian Drilling on Clinical Outcomes in Clomiphene Citrate-Resistant PCOS Women

TypeinterventionalSponsorCairo UniversityRan2020 to 2024Enrolled183ConditionsPCOS (Polycystic Ovary Syndrome) of Bilateral OvariesArmsGonadotropin, Letrozole, laparoscopic ovarian drilling
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Pharmacogenomic of LH and its receptor: are we ready for clinical practice?Reproductive biology and endocrinology : RB&E · 2025
    Review
  2. Article
  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

4 authors.

Robab DavarResearch and Clinical Center for Infertility, Shahid Sdoughi University of Medical Sciences, Yazd, Iran.
Nasim TabibnejadResearch and Clinical Center for Infertility, Shahid Sdoughi University of Medical Sciences, Yazd, Iran.
Seyed Mehdi KalantarResearch and Clinical Center for Infertility, Shahid Sdoughi University of Medical Sciences, Yazd, Iran.
Mohammad Hasan SheikhhaResearch and Clinical Center for Infertility, Shahid Sdoughi University of Medical Sciences, Yazd, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite extensive progress in IVF techniques, one of the most difficult problems is the variability in the response to controlled ovarian hyperstimulation (COH). Recent studies show the effects of individual genetic variability on COH outcome.

objectiveTo evaluate the correlation between LHβ G1502A polymorphisms in exon 3 of the LH gene and ovarian response to COH. MATERIALS AND

methodsA total of 220 women treated with a long protocol for ovarian stimulation were studied. Three genotypes of GG, GA and AA were detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis.

resultsIn total, 34 (17%) patients were poor responders, 154 (77%) were normal responders and 12 (6%) were hyper responders. The most frequent genotype was GA (55.5%) whereas 44.5% of patients showed GG genotype and there was no patient with AA genotype. In total 54.5% of normal responders, 61.8% of poor responders and 50% of hyper responders showed GA genotype.

conclusionOur results did not establish a significant relationship between this polymorphism and the ovarian response. Therefore it is still very difficult to use the genotype of patients for prediction of the ovarian response to stimulation.

Indexed as

LHβgeneOvulationinductionSinglenucleotidepolymorphisms

Identifiers

PMID25469124
PMCPMC4248152

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