Source:http://linkedlifedata.com/resource/pubmed/id/11153913
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2001-1-10
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pubmed:abstractText |
Asthma is a complex disease involving genetic and environmental aetiology. The tumour necrosis factor-alpha (TNF-alpha) and angiotensin-converting enzyme (ACE) genes have been implicated in asthma pathogenesis. This study investigated the association of a G-308A variant of TNF-alpha and an insertion/deletion (I/D) variant of ACE with a self-reported history of childhood asthma, in two population groups. At Northwick Park Hospital, London, 1,811 pregnant women attending for antenatal care were recruited. Participants with a self-reported history of childhood asthma, determined by a researcher-administered questionnaire, and controls with no personal or family history of asthma, of UK/Irish (cases n=20; controls n=416) and South Asian (cases n=6; controls n=275) origin were used in this study. Participants were genotyped for the TNF-alpha-308 and ACE I/D variants by a PCR-RFLP and PCR approach. The TNF-alpha-308 allele 2 (-308A) was significantly associated with self-reported childhood asthma in the UK/Irish (Odds ratios (OR): 2.6; 95% confidence intervals (CI): 1.1-6.2; P=0.03) but not in the South Asian population. The ACE DD genotype was not associated with childhood asthma in either population group. Gametic phase disequilibrium between the TNF-alpha-308 and ACE I/D variants was significantly different from zero in UK/Irish cases (delta=0.09; P=0.034). The TNF-alpha308 allele 2 or a linked major histocompatibility complex (MHC) variant may be a genetic risk factor for childhood asthma in the UK/Irish sample.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0340-6717
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
107
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
591-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11153913-Adenine,
pubmed-meshheading:11153913-Asia,
pubmed-meshheading:11153913-Asthma,
pubmed-meshheading:11153913-Child,
pubmed-meshheading:11153913-Ethnic Groups,
pubmed-meshheading:11153913-Female,
pubmed-meshheading:11153913-Genotype,
pubmed-meshheading:11153913-Great Britain,
pubmed-meshheading:11153913-Guanine,
pubmed-meshheading:11153913-Humans,
pubmed-meshheading:11153913-Peptidyl-Dipeptidase A,
pubmed-meshheading:11153913-Point Mutation,
pubmed-meshheading:11153913-Polymorphism, Genetic,
pubmed-meshheading:11153913-Pregnancy,
pubmed-meshheading:11153913-Tumor Necrosis Factor-alpha
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pubmed:year |
2000
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pubmed:articleTitle |
Association of the TNF-alpha-308 (G-->A) polymorphism with self-reported history of childhood asthma.
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pubmed:affiliation |
Department of Medical and Community Genetics, Imperial College School of Medicine, Kennedy Galton Centre, Northwest London Hospitals NHS Trust, Harrow, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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