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A genetic variant in the placenta-derived MHC class I chain-related gene A increases the risk of preterm birth in a Chinese population

Overview of attention for article published in Human Genetics, September 2017
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Title
A genetic variant in the placenta-derived MHC class I chain-related gene A increases the risk of preterm birth in a Chinese population
Published in
Human Genetics, September 2017
DOI 10.1007/s00439-017-1834-3
Pubmed ID
Authors

Junjiao Song, Jing Li, Han Liu, Yuexin Gan, Yang Sun, Min Yu, Yongjun Zhang, Fei Luo, Ying Tian, Weiye Wang, Jun Zhang, Julian Little, Haidong Cheng, Dan Chen

Abstract

Preterm birth (PTB) is a predominant contributor to neonatal mortality and morbidity worldwide. However, the pathophysiology of PTB is not well-understood. We tested the hypothesis that single-nucleotide polymorphisms (SNPs) in the placenta-derived MHC class I chain-related gene A (MICA) could disrupt placental development and hence result in PTB. Nineteen selected SNPs in MICA were genotyped in a case-control study of 127 premature infants and 634 term controls in a Chinese Han population. We found that significantly increased PTB risk was associated with homozygosity for the A variant of rs2256318 (adjusted odds ratio = 6.97 and 95% confidence interval = 2.34-20.74 for A/A, compared with G/G genotype, P = 0.001). In addition, the A/A genotype of rs2256318 was associated with decreased placental weight of neonates (β = -25.331; P = 0.033). Furthermore, stratified analysis demonstrated that the A/A genotype of rs2256318 was associated with increased PTB risk in female group. In addition, we observed statistical interaction between the polymorphism rs2516448 and sex (P = 0.04). No significant differences in the distribution of haplotypes between cases and controls were detected. Our results indicate that the polymorphism of rs2256318 in MICA may contribute to the etiology of PTB through interfering with placental development. These findings need to be further validated in larger and multi-ethnic populations.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 22 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 22 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 5 23%
Researcher 3 14%
Student > Bachelor 3 14%
Unknown 11 50%
Readers by discipline Count As %
Medicine and Dentistry 4 18%
Agricultural and Biological Sciences 2 9%
Biochemistry, Genetics and Molecular Biology 1 5%
Nursing and Health Professions 1 5%
Sports and Recreations 1 5%
Other 1 5%
Unknown 12 55%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 01 September 2017.
All research outputs
#15,478,452
of 23,001,641 outputs
Outputs from Human Genetics
#2,547
of 2,958 outputs
Outputs of similar age
#198,321
of 316,305 outputs
Outputs of similar age from Human Genetics
#10
of 13 outputs
Altmetric has tracked 23,001,641 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,958 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 6.2. This one is in the 10th percentile – i.e., 10% of its peers scored the same or lower than it.
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We're also able to compare this research output to 13 others from the same source and published within six weeks on either side of this one. This one is in the 23rd percentile – i.e., 23% of its contemporaries scored the same or lower than it.