Evidence map›Paper›PMID 24918527›Full record

ArticleScientific reports2014

Genetic variations in IL1A and IL1RN are associated with the risk of preeclampsia in Chinese Han population.

Jing Li, Mengchun Liu, Jinbao Zong, Ping Tan, Jingli Wang, Xunfeng Wang, Yuanhua Ye, Shiguo Liu, Xuemei Liu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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  10. Evidence for shared molecular pathways of dysregulated decidualization in preeclampsia and endometrial disorders revealed by microarray data integration.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
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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 1 institution in 1 country.

Jing Li1] Department of clinical laboratory, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, 266003, China [2].
Mengchun Liu1] Nephrology department, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, 266003, China [2].
Jinbao ZongDepartment of clinical laboratory, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, 266003, China.
Ping TanObstetrical department, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, 266003, China.
Jingli WangGenetic Laboratory, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, 266003, China.
Xunfeng WangGenetic Laboratory, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, 266003, China.
Yuanhua YeObstetrical department, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, 266003, China.
Shiguo Liu1] Obstetrical department, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, 266003, China [2] Genetic Laboratory, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, 266003, China.
Xuemei LiuNephrology department, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, 266003, China.
Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preeclampsia (PE) is an excessive systemic inflammation response with dysfunction of endothelial. Our study was to investigate the association between genetic variations in IL-1 and the susceptibility to PE in Chinese Han population. 402 PE patients and 554 normal pregnant women of third trimester were enrolled. The polymorphisms of rs315952 in IL1RN and rs17561 in IL1A were genotyped by TaqMan allelic discrimination real-time PCR. Obviously statistic difference of the genotypic frequencies were found in both of IL1RN rs315952 and IL1A rs17561 between cases and controls (for rs315952, P = 0.001; for rs17561, P = 0.021.). For rs315952, the C allele was associated with development of PE (P = 0.003, OR = 1.319, 95%CI 1.099-1.583). Patients with CC or CT genotype were less likely to develop severe PE than patients carrying TT genotype(P < 0.001, OR = 0.24, 95%CI 0.15-0.40). For rs17561, the C allele was the risk factor for predisposition to PE (P = 0.012, OR = 1.496, 95%CI 1.089-2.055). Our results suggest IL1RN and IL1A may involve in the development of PE in Chinese Han population.

Indexed as

AdultAllelesAsian PeopleCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansInflammationInterleukin-1alphaInterleukin 1 Receptor Antagonist ProteinPolymorphism, GeneticPre-EclampsiaPregnancyRiskRisk FactorsIL1A protein, humanIL1RN protein, humanInterleukin-1alphaInterleukin 1 Receptor Antagonist Protein

Identifiers

PMID24918527
PMCPMC4052713
OpenAlexW1983877818

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.