Polymorphisms in toll-like receptor 4 are not associated with asthma or atopy-related phenotypes

BA Raby, WT Klimecki, C Laprise, Y Renaud, J Faith, M Lemire, C Greenwood, KM Weiland, C Lange, Lyle Palmer, R Lazarus, D Vercelli, DJ Kwiatkowski, EK Silverman, FD Martinez, TJ Hudson, ST Weiss

Research output: Contribution to journalArticlepeer-review

153 Citations (Scopus)


Toll-like receptor 4 (TLR4) is the principal receptor for bacterial endotoxin recognition, and functional variants in the gene confer endotoxin-hyporesponsiveness in humans. Furthermore, there is evidence that endotoxin exposure during early life is protective against the development of atopy and asthma, although this relationship remains poorly understood. It is therefore possible that genetic variation in the TLR4 locus contributes to asthma susceptibility. In this study we characterize the genetic diversity in the TLR4 locus and test for association between the common genetic variants and asthma-related phenotypes. In a cohort of 90 ethnically diverse subjects, we resequenced the TLR4 locus and identified a total of 29 single nucleotide polymorphisms. We assessed five common polymorphisms for evidence of association with asthma in two large family-based cohorts: a heterogeneous North American cohort (589 families), and a more homogenous population from northeastern Quebec, Canada (167 families). Using the transmission-disequilibrum test, we found no evidence of association for any of the polymorphisms tested, including two functional variants. Furthermore, we found no evidence for association between the TLR4 variants and four quantitative intermediate asthma- and atopy-related phenotypes. Based on these results, we found no evidence that genetic variation in TLR4 contributes to asthma susceptibility.
Original languageEnglish
Pages (from-to)1449-1456
JournalAmerican Journal of Respiratory and Critical Care Medicine
Publication statusPublished - 2002


Dive into the research topics of 'Polymorphisms in toll-like receptor 4 are not associated with asthma or atopy-related phenotypes'. Together they form a unique fingerprint.

Cite this