Evidence map›Paper›PMID 32224893›Full record

ArticleGenes2020

Study of the Association Between microRNA (miR-25T>C, miR-32C>A, miR-125C>T, and miR-222G>T) Polymorphisms and the Risk of Recurrent Pregnancy Loss in Korean Women.

Jeong Yong Lee, Jung Oh Kim, Han Sung Park, Chang Soo Ryu, Ji Hyang Kim, Young Ran Kim, Woo Sik Lee, Jung Ryeol Lee, Nam Keun Kim

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Genes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. miRNAs in decidual NK cells: regulators worthy of attention during pregnancy.Reproductive biology and endocrinology : RB&E · 2021
    Review
  6. Article
  7. Article
  8. The Impact of Leukemia Inhibitory Factor onReproductive medicine and biology
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Jeong Yong LeeDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
Jung Oh KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
Han Sung ParkDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
Chang Soo RyuDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
Ji Hyang KimDepartment of Obstetrics and Gynecology, CHA Bundang Medical Center, School of Medicine, CHA University, Seongnam 13496, Korea.
Young Ran KimDepartment of Obstetrics and Gynecology, CHA Bundang Medical Center, School of Medicine, CHA University, Seongnam 13496, Korea.
Woo Sik LeeDepartment of Obstetrics and Gynecology, CHA Gangnam Medical Center, School of Medicine, CHA University, Seoul 06135, Korea.
Jung Ryeol LeeDepartment of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seongnam 13590, Korea.
Nam Keun KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
CHA University · KRCHA University Bundang Medical Center · KRSeoul National University Bundang Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recurrent pregnancy loss (RPL), which is defined as two pregnancy losses that occur before 20 weeks of gestation, is relatively common, occurring in approximately 1-5% of women. The underlying cause is often unclear, although numerous factors may contribute to RPL, including environmental and immunological factors, blood coagulation disorders, and genetics. In particular, single nucleotide variants have been associated with RPL, including those found in microRNAs (miRNAs). We investigated the association between four miRNA polymorphisms, miR-25T>C, miR-32C>A, miR-125aC>T, and miR-222G>T, and RPL in a cohort consisting of 361 RPL patients and 272 controls. Subjects were genotyped at miRNA loci by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis, and genotype frequencies were calculated. We then performed allele and genotype combination analyses and measured the association between miRNA polymorphisms and clinical variables in both RPL patients and controls. We detected a statistically significant association between RPL and the miR-25T/miR-32C/miR-125aT/miR-222T allele combination (adjusted odds ratio (AOR), 4.361; 95% confidence interval (CI), 1.496-12.72;

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAbortion, HabitualCase-Control StudiesFemaleGene FrequencyHumansMicroRNAsPregnancyPrognosisMicroRNAsMIR222, humanMIRN125 microRNA, humanMIRN25 microRNA, humanMIRN32 microRNA, humanDNAgenemicroRNAmutationpregnancyvariant

Identifiers

PMID32224893
PMCPMC7231175
OpenAlexW3013906548

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.