TY - JOUR
T1 - Polymorphisms in toll-like receptor 4 are not associated with asthma or atopy-related phenotypes
AU - Raby, Benjamin A.
AU - Klimecki, Walter T.
AU - Laprise, Catherine
AU - Renaud, Yannick
AU - Faith, Janet
AU - Lemire, Mathieu
AU - Greenwood, Celia
AU - Weiland, Katherine M.
AU - Lange, Christoph
AU - Palmer, Lyle J.
AU - Lazarus, Ross
AU - Vercelli, Donata
AU - Kwiatkowski, David J.
AU - Silverman, Edwin K.
AU - Martinez, Fernando D.
AU - Hudson, Thomas J.
AU - Weiss, Scott T.
PY - 2002/12/1
Y1 - 2002/12/1
N2 - 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-disequilibrium 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.
AB - 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-disequilibrium 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.
KW - Asthma
KW - Genetic association
KW - Genetics
KW - Polymorphism
KW - Toll-like receptor 4
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U2 - 10.1164/rccm.200207-634OC
DO - 10.1164/rccm.200207-634OC
M3 - Article
C2 - 12406828
AN - SCOPUS:0036893595
SN - 1073-449X
VL - 166
SP - 1449
EP - 1456
JO - American journal of respiratory and critical care medicine
JF - American journal of respiratory and critical care medicine
IS - 11
ER -