Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study.
A recent association scan using a genome-wide set of nonsynonymous coding single-nucleotide polymorphisms (nsSNPs) conducted in four diseases including Graves' disease (GD), identified nine novel possible regions of association with GD. We used a case-control approach in an attempt to replicate...
| Main Authors: | , , , , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2010
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| _version_ | 1826295068911206400 |
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| author | Newby, P Pickles, O Mazumdar, S Brand, O Carr-Smith, J Pearce, S Franklyn, J Evans, D Simmonds, M Gough, S |
| author_facet | Newby, P Pickles, O Mazumdar, S Brand, O Carr-Smith, J Pearce, S Franklyn, J Evans, D Simmonds, M Gough, S |
| author_sort | Newby, P |
| collection | OXFORD |
| description | A recent association scan using a genome-wide set of nonsynonymous coding single-nucleotide polymorphisms (nsSNPs) conducted in four diseases including Graves' disease (GD), identified nine novel possible regions of association with GD. We used a case-control approach in an attempt to replicate association of these nine regions in an independent collection of 1578 British GD patients and 1946 matched Caucasian controls. Although none of these loci showed evidence of association with GD in the independent data set, when combined with the original Wellcome Trust Case-Control Consortium study group, minor differences in allele frequencies (P>or=10(-3)) remained in the combined collection of 5924 subjects for four of the nsSNPs, present within HDLBP, TEKT1, JSRP1 and UTX. An additional 29 Tag SNPs were screened within these four gene regions to determine if further associations could be detected. Similarly, minor differences only (P=0.042-0.002) were detected in two HDLBP and two TEKT1 Tag SNPs in the combined UK GD collection. In conclusion, it is unlikely that the SNPs selected in this replication study have a significant effect on the risk of GD in the United Kingdom. Our study confirms the need for large data sets and stringent analysis criteria when searching for susceptibility loci in common diseases. |
| first_indexed | 2024-03-07T03:55:25Z |
| format | Journal article |
| id | oxford-uuid:c2b6658a-e2e6-4234-bb5e-1ade7798eebf |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T03:55:25Z |
| publishDate | 2010 |
| record_format | dspace |
| spelling | oxford-uuid:c2b6658a-e2e6-4234-bb5e-1ade7798eebf2022-03-27T06:10:52ZFollow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c2b6658a-e2e6-4234-bb5e-1ade7798eebfEnglishSymplectic Elements at Oxford2010Newby, PPickles, OMazumdar, SBrand, OCarr-Smith, JPearce, SFranklyn, JEvans, DSimmonds, MGough, SA recent association scan using a genome-wide set of nonsynonymous coding single-nucleotide polymorphisms (nsSNPs) conducted in four diseases including Graves' disease (GD), identified nine novel possible regions of association with GD. We used a case-control approach in an attempt to replicate association of these nine regions in an independent collection of 1578 British GD patients and 1946 matched Caucasian controls. Although none of these loci showed evidence of association with GD in the independent data set, when combined with the original Wellcome Trust Case-Control Consortium study group, minor differences in allele frequencies (P>or=10(-3)) remained in the combined collection of 5924 subjects for four of the nsSNPs, present within HDLBP, TEKT1, JSRP1 and UTX. An additional 29 Tag SNPs were screened within these four gene regions to determine if further associations could be detected. Similarly, minor differences only (P=0.042-0.002) were detected in two HDLBP and two TEKT1 Tag SNPs in the combined UK GD collection. In conclusion, it is unlikely that the SNPs selected in this replication study have a significant effect on the risk of GD in the United Kingdom. Our study confirms the need for large data sets and stringent analysis criteria when searching for susceptibility loci in common diseases. |
| spellingShingle | Newby, P Pickles, O Mazumdar, S Brand, O Carr-Smith, J Pearce, S Franklyn, J Evans, D Simmonds, M Gough, S Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. |
| title | Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. |
| title_full | Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. |
| title_fullStr | Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. |
| title_full_unstemmed | Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. |
| title_short | Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. |
| title_sort | follow up of potential novel graves disease susceptibility loci identified in the uk wtccc genome wide nonsynonymous snp study |
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