Association of toll-like receptors polymorphisms with COPD risk in Chinese population

Background: Previous studies have reported that the Toll-like receptors (TLRs) are related with the progress of chronic obstructive pulmonary disease (COPD). We aimed to explore the association of TLRs single nucleotide polymorphisms (SNPs) and COPD risk. Methods: 170 COPD patients and 181 healthy c...

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Published inFrontiers in genetics Vol. 13; p. 955810
Main Authors Sun, Shulei, Shen, Yuehao, Feng, Jing
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 26.10.2022
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Summary:Background: Previous studies have reported that the Toll-like receptors (TLRs) are related with the progress of chronic obstructive pulmonary disease (COPD). We aimed to explore the association of TLRs single nucleotide polymorphisms (SNPs) and COPD risk. Methods: 170 COPD patients and 181 healthy controls were enrolled in this case-control study. MassARRAY platform was used for genotyping seven tagging SNPs ( TLR2 : rs3804100, rs4696480, rs3804099; TLR3 : rs3775290, rs3775291, rs5743305; TLR9 : rs352140) of TLRs. The correlations between the SNPs and COPD risk were determined using logistic regression. Results: We found that the rs3775291 of TLR3 significant decreased the risk of COPD (TT versus CC: non-adjusted OR = 0.329, 95% CI = 0.123–0.879, p = 0.027). In the genetic models analysis, the rs3775291 was associated with a decreased effect of COPD based on the recessive model (TT versus CC/CT: non-adjusted OR = 0.377, 95% CI = 0.144–0.988  p = 0.047). The rs4696480 of TLR2 gene was associated with a decreased risk of COPD after adjustment by age and gender (TA versus AA: adjusted OR = 0.606, 95% CI = 0.376–0.975, p = 0.039). Conclusion: Our study showed that genetic variants in TLRs were associated with risk of COPD. The rs3775291 and rs4696480 may act as a potential biomarker for predicting the risk of COPD in Chinese population.
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Reviewed by: Xiuqin Yang, Northeast Agricultural University, China
Ran Wang, Anhui Medical University, China
These authors have contributed equally to this work
This article was submitted to Human and Medical Genomics, a section of the journal Frontiers in Genetics
Edited by: Gilberto Vargas Alarcón, Instituto Nacional de Cardiologia Ignacio Chavez, Mexico
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2022.955810