Evidence map›Paper›PMID 36631028›Full record

ArticleJournal of Korean medical science2022

Identification of Single Nucleotide Polymorphisms as Biomarkers for Recurrent Pregnancy Loss in Korean Women.

Hye In Kim, Eun A Choi, Eun Chan Paik, Soohyeon Park, Yu Im Hwang, Jae Hoon Lee, Seok Kyo Seo, SiHyun Cho, Young Sik Choi, Byung Seok Lee and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of Korean medical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

14 authors at 3 institutions in 1 country.

Hye In KimDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-7961-5988
Eun A ChoiDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-8846-4819
Eun Chan PaikBundang Cheil Women's Hospital, Seongnam, Korea.ORCID https://orcid.org/0000-0003-2321-1081
Soohyeon ParkBundang Cheil Women's Hospital, Seongnam, Korea.ORCID https://orcid.org/0000-0002-2158-2041
Yu Im HwangBundang Cheil Women's Hospital, Seongnam, Korea.ORCID https://orcid.org/0000-0001-6969-1362
Jae Hoon LeeInstitute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-4223-1395
Seok Kyo SeoDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-3404-0484
SiHyun ChoInstitute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-2718-6645
Young Sik ChoiDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-1157-4822
Byung Seok LeeDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-6001-2079
Jimyeong ParkSeoul Clinical Laboratories Healthcare Co., Ltd., Yongin, Korea.ORCID https://orcid.org/0000-0001-9245-6184
Sanghoo LeeSeoul Clinical Laboratories Healthcare Co., Ltd., Yongin, Korea. sprout30@scllab.co.kr.ORCID https://orcid.org/0000-0002-9980-8143
Kyoung-Ryul LeeSeoul Clinical Laboratories Healthcare Co., Ltd., Yongin, Korea.ORCID https://orcid.org/0000-0002-2802-2098
Bo Hyon YunDepartment of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-5703-797X
Yonsei University · KRDong-A Pharmaceutical (South Korea) · KRSeoul National University Bundang Hospital · KR

Funding

Seoul Clinical Laboratories Healthcare Co., Ltd
6 · The paper itself

Abstract

backgroundSingle nucleotide polymorphisms (SNPs) are reportedly associated with repeated abortion. Thus, genetic analysis based on race is the key to developing accurate diagnostic tests. This study analyzed the genetic polymorphisms of recurrent pregnancy loss (RPL) patients among Korean women compared to the controls.

methodsIn 53 women of RPL group and 50 controls, the genetic analysis was performed. The genotype distribution and allele frequency were analyzed statistically for the difference between the two groups. The association between each SNP marker and RPL risk was analyzed.

resultsThe genotypes of LEPR, endothelial nitric oxide synthase (eNOS), KDR, miR-27a, miR-449b, and tumor necrosis factor-alpha (TNF-α) were analyzed using odds ratio (OR) with 95% confidence intervals (CIs). Only the AG genotype of miR-449b (A>G) polymorphism showed significant association with the risk of RPL when compared to the AA genotype (OR, 2.39). The combination of GG/AG+GG/CA+AA genotypes for eNOS/miR-449b/TNF-α was associated with 7.36-fold higher risk of RPL (OR, 7.36). The GG/AG+GG combination for eNOS/miR-449b showed 2.43-fold higher risk for RPL (OR, 2.43). The combination of AG+GG/CA+AA genotypes for miR-449b/TNF-α showed a significant association with the risk of RPL (OR, 7.60). From the haplotype-based analysis, the G-G-A haplotype of eNOS/miR-449b/TNF-α and the G-A haplotype of miR-449b/TNF-α were associated with increased risk of RPL (OR, 19.31; OR, 22.08, respectively).

conclusionThere is a significant association between the risk of RPL and miR-449b/TNF-α combination, and therefore, genetic analysis for specific combined genotypes can be an important screening method for RPL in Korean women.

Indexed as

Abortion, HabitualMicroRNAsBiomarkersCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansPolymorphism, Single NucleotidePregnancyRepublic of KoreaTumor Necrosis Factor-alphaBiomarkersMicroRNAsTumor Necrosis Factor-alphaMicroRNAsMiscarriagePlasmaPregnancyRecurrent Pregnancy Loss

Identifiers

PMID36631028
PMCPMC9705206
OpenAlexW4312822709

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.