Literature DB >> 20230296

Absence of association between CD86 +1057G/A polymorphism and coronary artery disease.

Xiao-Na Ma1, Xia Wang, You-Yi Yan, Lin Yang, Da-Lei Zhang, Xin Sheng, Xiao-Min Liu, Hong Huang, Jing Dai, Ying-Jia Zhong, Lin-Chuan Liao.   

Abstract

CD86, one of the key costimulatory molecules, is not only involved in the initiation of T-cell immunity but also plays important roles in the development of cardiovascular diseases. The purpose of this study was to investigate the association between the CD86 polymorphism and the risk of coronary artery disease (CAD) in a Chinese population. We analyzed single-nucleotide polymorphism of CD86 +1057G/A (rs1129055) in 164 patients with CAD and 299 healthy controls by performing polymerase chain reaction-restriction fragment length polymorphism and DNA sequencing assay. No significant association was observed in the genotype and allele frequencies of +1057G/A polymorphism between cases and controls, indicating that CD86 +1057G/A polymorphism may not be associated with CAD in the Chinese population.

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Year:  2010        PMID: 20230296     DOI: 10.1089/dna.2009.0987

Source DB:  PubMed          Journal:  DNA Cell Biol        ISSN: 1044-5498            Impact factor:   3.311


  1 in total

1.  Association of co-stimulatory human B-lymphocyte antigen B7-2 (CD86) gene polymorphism with colorectal cancer risk.

Authors:  Pedram Azimzadeh; Sara Romani; Hanieh Mirtalebi; Seyed Reza Fatemi; Shabnam Kazemian; Mahsa Khanyaghma; Seyed Reza Mohebbi
Journal:  Gastroenterol Hepatol Bed Bench       Date:  2013
  1 in total

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