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Glutathione-S-transferase genes and asthma phenotypes: a Human Genome Epidemiology (HuGE) systematic review and meta-analysis including unpublished data

Glutathione-S-transferase genes and asthma phenotypes: a Human Genome Epidemiology (HuGE) systematic review and meta-analysis including unpublished data
Glutathione-S-transferase genes and asthma phenotypes: a Human Genome Epidemiology (HuGE) systematic review and meta-analysis including unpublished data
Background: oxidative stress is thought to be involved in the pathogenesis of asthma. Glutathione-S-transferase (GST) enzymes, which play an important role in antioxidant defences, may therefore influence asthma risk. Two common deletion polymorphisms of GSTM1 and GSTT1 genes and the GSTP1 Ile105Val polymorphism have been associated with asthma in children and adults, but results are inconsistent across studies.

Methods: systematic review and meta-analysis of the effects of GST genes on asthma, wheezing and bronchial hyper-responsiveness (BHR), with inclusion of unpublished data from three studies, including the large Avon Longitudinal Study of Parents and Children (ALSPAC). Random effect or fixed effect models were used as appropriate, and sensitivity analyses were performed to assess the impact of study characteristics and quality on pooled results.

Results: the meta-analyses of GSTM1 (n = 22 studies) and GSTT1 (n = 19) showed increased asthma risk associated with the null genotype, but there was extreme between-study heterogeneity and publication bias and the association disappeared when meta-analysis was restricted to the largest studies. Meta-analysis of GSTP1 Ile105Val (n = 17) and asthma suggested a possible protective effect of the Val allele, but heterogeneity was extreme. Few studies evaluated wheezing and BHR and most reported no associations, although weak evidence was found for positive associations of GSTM1 null and GSTP1 Val allele with wheezing and a negative association of GSTP1 Val allele with BHR.

Conclusions: our findings do not support a substantial role of GST genes alone in the development of asthma. Future studies of large size should focus on interactions of GST genes with environmental oxidative exposures and with other genes involved in antioxidant pathways. Quality of study conduct and reporting needs to be improved to increase credibility of the evidence accumulating over time
meta-analysis, systematic review, glutathione-S-transferase genes, GSTM1 gene, GSTT1 gene, GSTP1 gene, asthma, wheezing, bronchial responsiveness, the avon longitudinal study of parents and children (ALSPAC)
0300-5771
539-562
Minelli, Cosetta
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Granell, Raquel
06e9e006-3754-4cc9-b3fc-42024bd05123
Newson, Roger
9630e35a-df9b-4379-91f1-0a9ee73dfe2d
Rose-Zerilli, Matthew J.
08b3afa4-dbc2-4c0d-a852-2a9f33431199
Torrent, Maties
d036c9a2-5560-46ef-a934-61ae70093a4a
Ring, Sue M.
034e91fc-505b-4005-bf5d-3b88a2488237
Holloway, John W.
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Shaheen, Seif O.
42e3b3fc-c70c-49e7-8c88-64f2606129ec
Henderson, John A.
03d06941-3f2c-4a2e-998b-8d18124049d1
Minelli, Cosetta
e9c228b2-b94c-4763-bb62-5acb94a7a50b
Granell, Raquel
06e9e006-3754-4cc9-b3fc-42024bd05123
Newson, Roger
9630e35a-df9b-4379-91f1-0a9ee73dfe2d
Rose-Zerilli, Matthew J.
08b3afa4-dbc2-4c0d-a852-2a9f33431199
Torrent, Maties
d036c9a2-5560-46ef-a934-61ae70093a4a
Ring, Sue M.
034e91fc-505b-4005-bf5d-3b88a2488237
Holloway, John W.
4bbd77e6-c095-445d-a36b-a50a72f6fe1a
Shaheen, Seif O.
42e3b3fc-c70c-49e7-8c88-64f2606129ec
Henderson, John A.
03d06941-3f2c-4a2e-998b-8d18124049d1

Minelli, Cosetta, Granell, Raquel, Newson, Roger, Rose-Zerilli, Matthew J., Torrent, Maties, Ring, Sue M., Holloway, John W., Shaheen, Seif O. and Henderson, John A. (2010) Glutathione-S-transferase genes and asthma phenotypes: a Human Genome Epidemiology (HuGE) systematic review and meta-analysis including unpublished data. International Journal of Epidemiology, 39 (2), 539-562. (doi:10.1093/ije/dyp337).

Record type: Article

Abstract

Background: oxidative stress is thought to be involved in the pathogenesis of asthma. Glutathione-S-transferase (GST) enzymes, which play an important role in antioxidant defences, may therefore influence asthma risk. Two common deletion polymorphisms of GSTM1 and GSTT1 genes and the GSTP1 Ile105Val polymorphism have been associated with asthma in children and adults, but results are inconsistent across studies.

Methods: systematic review and meta-analysis of the effects of GST genes on asthma, wheezing and bronchial hyper-responsiveness (BHR), with inclusion of unpublished data from three studies, including the large Avon Longitudinal Study of Parents and Children (ALSPAC). Random effect or fixed effect models were used as appropriate, and sensitivity analyses were performed to assess the impact of study characteristics and quality on pooled results.

Results: the meta-analyses of GSTM1 (n = 22 studies) and GSTT1 (n = 19) showed increased asthma risk associated with the null genotype, but there was extreme between-study heterogeneity and publication bias and the association disappeared when meta-analysis was restricted to the largest studies. Meta-analysis of GSTP1 Ile105Val (n = 17) and asthma suggested a possible protective effect of the Val allele, but heterogeneity was extreme. Few studies evaluated wheezing and BHR and most reported no associations, although weak evidence was found for positive associations of GSTM1 null and GSTP1 Val allele with wheezing and a negative association of GSTP1 Val allele with BHR.

Conclusions: our findings do not support a substantial role of GST genes alone in the development of asthma. Future studies of large size should focus on interactions of GST genes with environmental oxidative exposures and with other genes involved in antioxidant pathways. Quality of study conduct and reporting needs to be improved to increase credibility of the evidence accumulating over time

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Published date: April 2010
Keywords: meta-analysis, systematic review, glutathione-S-transferase genes, GSTM1 gene, GSTT1 gene, GSTP1 gene, asthma, wheezing, bronchial responsiveness, the avon longitudinal study of parents and children (ALSPAC)

Identifiers

Local EPrints ID: 72181
URI: http://eprints.soton.ac.uk/id/eprint/72181
ISSN: 0300-5771
PURE UUID: 70ff231e-4929-4b8e-a11b-3537b187907d
ORCID for Matthew J. Rose-Zerilli: ORCID iD orcid.org/0000-0002-1064-5350
ORCID for John W. Holloway: ORCID iD orcid.org/0000-0001-9998-0464

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Date deposited: 28 Jan 2010
Last modified: 14 Mar 2024 02:56

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Contributors

Author: Cosetta Minelli
Author: Raquel Granell
Author: Roger Newson
Author: Maties Torrent
Author: Sue M. Ring
Author: Seif O. Shaheen
Author: John A. Henderson

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