Evidence map›Paper›PMID 31861421›Full record

ArticleInternational journal of molecular sciences2019

Association of Complement Factor D and H Polymorphisms with Recurrent Pregnancy Loss.

Hee Young Cho, Han Sung Park, Eun Ju Ko, Chang Soo Ryu, Jung Oh Kim, Young Ran Kim, Eun Hee Ahn, Woo Sik Lee, Nam Keun Kim

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  4. TNF-α-positive patients with recurrent pregnancy loss: The etiology and management.Technology and health care : official journal of the European Society for Engineering and Medicine · 2024
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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

9 authors at 2 institutions in 1 country.

Hee Young ChoDepartment of Obstetrics and Gynecology, CHA Bundang Medical Center, CHA University, Seongnam 13496, Korea.
Han Sung ParkDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
Eun Ju KoDepartment 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.
Jung Oh KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
Young Ran KimDepartment of Obstetrics and Gynecology, CHA Bundang Medical Center, CHA University, Seongnam 13496, Korea.
Eun Hee AhnDepartment of Obstetrics and Gynecology, CHA Bundang Medical Center, CHA University, Seongnam 13496, Korea.
Woo Sik LeeFertility Center of CHA Gangnam Medical Center, CHA University, Seoul 06125, Korea.
Nam Keun KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.
CHA University · KRCHA University Bundang Medical Center · KR

Funding

Korea Health Industry Development Institute HI18C19990200National Research Foundation of Korea 2017R1D1A1B03031542National Research Foundation of Korea 2018R1D1A1A09082764National Research Foundation of Korea 2018R1D1A1B07044096
6 · The paper itself

Abstract

Recurrent pregnancy loss (RPL) is defined as two or more consecutive pregnancy losses prior to 20 weeks of gestation, and the incidence of RPL is estimated at 1% of all pregnancies. While the etiologies of RPL are diverse, immune function is considered to be an important cause of RPL. In particular, the complement system is essential for stable development of the placenta and fetus. Moreover, complement factor D (

Indexed as

Genetic Predisposition to DiseasePolymorphism, GeneticAbortion, HabitualAdultAllelesCase-Control StudiesComplement Factor DComplement Factor HFemaleGene FrequencyGenetic Association StudiesGenotypeHumansCFD protein, humanCFH protein, humanComplement Factor DComplement Factor Hcomplement factor Dcomplement factor Hpolymorphismrecurrent pregnancy loss

Identifiers

PMID31861421
PMCPMC6981708
OpenAlexW2996298918

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.