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Association of polymorphisms in the beta2-adrenoreceptor gene with higher levels of parasitic infection.

Authors :
Ramsay CE
Hayden CM
Tiller KJ
Burton PR
Hagel I
Palenque M
Lynch NR
Goldblatt J
LeSouëf PN
Source :
Human genetics [Hum Genet] 1999 Mar; Vol. 104 (3), pp. 269-74.
Publication Year :
1999

Abstract

The diminishing incidence of parasitic infection in westernised societies has been suggested to result in an increased prevalance of asthma. Asthma is a polygenic disease and genome screens have shown that genes on chromosome 5q31-33 are strongly linked to the disease. The gene for the beta2-adrenoreceptor is located in this region and two polymorphisms have been identified that result in amino acid changes at positions 16 (ArgGly) and 27 (GlnGlu). To determine whether these polymorphisms influence asthma and parasitic infection, a genotype/phenotype study has been performed on a cohort of 126 children from Coche Island in Venezuela. There is a high incidence of asthma on the island and intestinal helminthiasis is endemic. Genotyping for both polymorphisms was carried out by using the polymerase chain reaction and allele-specific oligonucleotide hybridisation. Genotype frequencies in this cohort were consistent with other studies and both polymorphisms were in significant linkage disequilibrium. Individuals who were homozygous for Arg16 had significantly higher levels of specific IgE to Ascaris lumbricoides (P=0.002), significantly higher A. lumbricoides egg counts (P<0.001) and significantly larger wheal sizes following skin-prick testing with A. lumbricoides allergen (P=0.008). There was no association between either polymorphism and total serum IgE or asthma in this population. A combination of mast cell degranulation and the lung migratory phase of A. lumbricoides larvae may result in bronchoconstriction in infected individuals. These results suggest that the Gly 16 allele confers resistance to high levels of parasitic infection in this population. An alternative explanation for the association is that it may be the result of linkage disequilibrium with other genes in the chromosome 5q31-33 region.

Details

Language :
English
ISSN :
0340-6717
Volume :
104
Issue :
3
Database :
MEDLINE
Journal :
Human genetics
Publication Type :
Academic Journal
Accession number :
10323253
Full Text :
https://doi.org/10.1007/s004390050947