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| Content Provider | PubMed Central |
|---|---|
| Author | Loeb, Mark Eskandarian, Sasha Rupp, Mark Fishman, Neil Gasink, Leanne Patterson, Jan Bramson, Jonathan Hudson, Thomas J. Lemire, Mathieu |
| Copyright Year | 2011 |
| Abstract | To determine genetic factors predisposing to neurological complications following West Nile virus infection, we analyzed a cohort of 560 neuroinvasive case patients and 950 control patients for 13 371 mostly nonsynonymous single-nucleotide polymorphisms (SNPs). The top 3 SNPs on the basis of statistical significance were also in genes of biological plausibility: rs2066786 in RFC1 (replication factor C1) (P = 1.88 × 10−5; odds ratio [OR], 0.68 [95% confidence interval {CI}, .56–.81]); rs2298771 in SCN1A (sodium channel, neuronal type I α subunit) (P = 5.87 × 10−5; OR, 1.47 [95% CI, 1.21–1.77]); and rs25651 in ANPEP (ananyl aminopeptidase) (P = 1.44 × 10−4; OR, 0.69 [95% CI, .56–.83]). Additional genotyping of these SNPs in a separate sample of 264 case patients and 296 control patients resulted in a lack of significance in the replication cohort; joint significance was as follows: rs2066786, P = .0022; rs2298771, P = .005; rs25651, P = .042. Using mostly nonsynonymous variants, we therefore did not identify genetic variants associated with neuroinvasive disease. |
| Related Links | http://dx.doi.org/10.1093/infdis/jir493 |
| Ending Page | 1037 |
| Page Count | 7 |
| Starting Page | 1031 |
| File Format | |
| ISSN | 00221899 |
| e-ISSN | 15376613 |
| Journal | The Journal of Infectious Diseases |
| Issue Number | 7 |
| Volume Number | 204 |
| Language | English |
| Publisher | Oxford University Press |
| Publisher Date | 2011-10-01 |
| Access Restriction | Open |
| Rights Holder | Oxford University Press |
| Subject Keyword | Immunology and Allergy Infectious Diseases Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Infectious Diseases Immunology and Allergy |
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