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Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism

BACKGROUND: Certain loci on the human genome, such as glutathione S-transferase M1 (GSTM1), do not permit heterozygotes to be reliably determined by commonly used methods. Association of such a locus with a disease is therefore generally tested with a case-control design. When subjects have already...

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Autores principales: Buyske, Steven, Williams, Tanishia A, Mars, Audrey E, Stenroos, Edward S, Ming, Sue X, Wang, Rong, Sreenath, Madhura, Factura, Marivic F, Reddy, Chitra, Lambert, George H, Johnson, William G
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1382247/
https://www.ncbi.nlm.nih.gov/pubmed/16472391
http://dx.doi.org/10.1186/1471-2156-7-8
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author Buyske, Steven
Williams, Tanishia A
Mars, Audrey E
Stenroos, Edward S
Ming, Sue X
Wang, Rong
Sreenath, Madhura
Factura, Marivic F
Reddy, Chitra
Lambert, George H
Johnson, William G
author_facet Buyske, Steven
Williams, Tanishia A
Mars, Audrey E
Stenroos, Edward S
Ming, Sue X
Wang, Rong
Sreenath, Madhura
Factura, Marivic F
Reddy, Chitra
Lambert, George H
Johnson, William G
author_sort Buyske, Steven
collection PubMed
description BACKGROUND: Certain loci on the human genome, such as glutathione S-transferase M1 (GSTM1), do not permit heterozygotes to be reliably determined by commonly used methods. Association of such a locus with a disease is therefore generally tested with a case-control design. When subjects have already been ascertained in a case-parent design however, the question arises as to whether the data can still be used to test disease association at such a locus. RESULTS: A likelihood ratio test was constructed that can be used with a case-parents design but has somewhat less power than a Pearson's chi-squared test that uses a case-control design. The test is illustrated on a novel dataset showing a genotype relative risk near 2 for the homozygous GSTM1 deletion genotype and autism. CONCLUSION: Although the case-control design will remain the mainstay for a locus with a deletion, the likelihood ratio test will be useful for such a locus analyzed as part of a larger case-parent study design. The likelihood ratio test has the advantage that it can incorporate complete and incomplete case-parent trios as well as independent cases and controls. Both analyses support (p = 0.046 for the proposed test, p = 0.028 for the case-control analysis) an association of the homozygous GSTM1 deletion genotype with autism.
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spelling pubmed-13822472006-02-28 Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism Buyske, Steven Williams, Tanishia A Mars, Audrey E Stenroos, Edward S Ming, Sue X Wang, Rong Sreenath, Madhura Factura, Marivic F Reddy, Chitra Lambert, George H Johnson, William G BMC Genet Methodology Article BACKGROUND: Certain loci on the human genome, such as glutathione S-transferase M1 (GSTM1), do not permit heterozygotes to be reliably determined by commonly used methods. Association of such a locus with a disease is therefore generally tested with a case-control design. When subjects have already been ascertained in a case-parent design however, the question arises as to whether the data can still be used to test disease association at such a locus. RESULTS: A likelihood ratio test was constructed that can be used with a case-parents design but has somewhat less power than a Pearson's chi-squared test that uses a case-control design. The test is illustrated on a novel dataset showing a genotype relative risk near 2 for the homozygous GSTM1 deletion genotype and autism. CONCLUSION: Although the case-control design will remain the mainstay for a locus with a deletion, the likelihood ratio test will be useful for such a locus analyzed as part of a larger case-parent study design. The likelihood ratio test has the advantage that it can incorporate complete and incomplete case-parent trios as well as independent cases and controls. Both analyses support (p = 0.046 for the proposed test, p = 0.028 for the case-control analysis) an association of the homozygous GSTM1 deletion genotype with autism. BioMed Central 2006-02-10 /pmc/articles/PMC1382247/ /pubmed/16472391 http://dx.doi.org/10.1186/1471-2156-7-8 Text en Copyright © 2006 Buyske et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Buyske, Steven
Williams, Tanishia A
Mars, Audrey E
Stenroos, Edward S
Ming, Sue X
Wang, Rong
Sreenath, Madhura
Factura, Marivic F
Reddy, Chitra
Lambert, George H
Johnson, William G
Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism
title Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism
title_full Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism
title_fullStr Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism
title_full_unstemmed Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism
title_short Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism
title_sort analysis of case-parent trios at a locus with a deletion allele: association of gstm1 with autism
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1382247/
https://www.ncbi.nlm.nih.gov/pubmed/16472391
http://dx.doi.org/10.1186/1471-2156-7-8
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