GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • S. Karger AG  (2)
  • 2005-2009  (2)
  • 1
    In: Human Heredity, S. Karger AG, Vol. 65, No. 2 ( 2008), p. 105-118
    Abstract: 〈 i 〉 Objectives: 〈 /i 〉 A number of common non-synonymous single nucleotide polymorphisms (SNPs) in DNA repair genes have been reported to modify bladder cancer risk. These include: 〈 i 〉 APE1- 〈 /i 〉 Asn148Gln, 〈 i 〉 XRCC1- 〈 /i 〉 Arg399Gln and 〈 i 〉 XRCC1- 〈 /i 〉 Arg194Trp in the BER pathway, 〈 i 〉 XPD- 〈 /i 〉 Gln751Lys in the NER pathway and 〈 i 〉 XRCC3- 〈 /i 〉 Thr241Met in the DSB repair pathway. 〈 i 〉 Methods: 〈 /i 〉 To examine the independent and interacting effects of these SNPs in a large study group, we analyzed these genotypes in 1,029 cases and 1,281 controls enrolled in two case-control studies of incident bladder cancer, one conducted in New Hampshire, USA and the other in Turin, Italy. 〈 i 〉 Results: 〈 /i 〉 The odds ratio among current smokers with the variant 〈 i 〉 XRCC3- 〈 /i 〉 241 (TT) genotype was 1.7 (95% CI 1.0–2.7) compared to wild-type. We evaluated gene-environment and gene-gene interactions using four analytic approaches: logistic regression, Multifactor Dimensionality Reduction (MDR), hierarchical interaction graphs, classification and regression trees (CART), and logic regression analyses. All five methods supported a gene-gene interaction between 〈 i 〉 XRCC1- 〈 /i 〉 399/ 〈 i 〉 XRCC3- 〈 /i 〉 241 (p = 0.001) (adjusted OR for 〈 i 〉 XRCC1- 〈 /i 〉 399 GG, 〈 i 〉 XRCC3- 〈 /i 〉 241 TT vs. wild-type 2.0 (95% CI 1.4–3.0)). Three methods predicted an interaction between 〈 i 〉 XRCC1- 〈 /i 〉 399/ 〈 i 〉 XPD- 〈 /i 〉 751 (p = 0.008) (adjusted OR for 〈 i 〉 XRCC1- 〈 /i 〉 399 GA or AA, 〈 i 〉 XRCC3- 〈 /i 〉 241 AA vs. wild-type 1.4 (95% CI 1.1–2.0)). 〈 i 〉 Conclusions: 〈 /i 〉 These results support the hypothesis that common polymorphisms in DNA repair genes modify bladder cancer risk and highlight the value of using multiple complementary analytic approaches to identify multi-factor interactions.
    Type of Medium: Online Resource
    ISSN: 0001-5652 , 1423-0062
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2008
    detail.hit.zdb_id: 1482710-4
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Online Resource
    Online Resource
    S. Karger AG ; 2007
    In:  Human Heredity Vol. 63, No. 2 ( 2007), p. 120-133
    In: Human Heredity, S. Karger AG, Vol. 63, No. 2 ( 2007), p. 120-133
    Abstract: The workhorse of modern genetic analysis is the parametric linear model. The advantages of the linear modeling framework are many and include a mathematical understanding of the model fitting process and ease of interpretation. However, an important limitation is that linear models make assumptions about the nature of the data being modeled. This assumption may not be realistic for complex biological systems such as disease susceptibility where nonlinearities in the genotype to phenotype mapping relationship that result from epistasis, plastic reaction norms, locus heterogeneity, and phenocopy, for example, are the norm rather than the exception. We have previously developed a flexible modeling approach called symbolic discriminant analysis (SDA) that makes no assumptions about the patterns in the data. Rather, SDA lets the data dictate the size, shape, and complexity of a symbolic discriminant function that could include any set of mathematical functions from a list of candidates supplied by the user. Here, we outline a new five step process for symbolic model discovery that uses genetic programming (GP) for coarse-grained stochastic searching, experimental design for parameter optimization, graphical modeling for generating expert knowledge, and estimation of distribution algorithms for fine-grained stochastic searching. Finally, we introduce function mapping as a new method for interpreting symbolic discriminant functions. We show that function mapping when combined with measures of interaction information facilitates statistical interpretation by providing a graphical approach to decomposing complex models to highlight synergistic, redundant, and independent effects of polymorphisms and their composite functions. We illustrate this five step SDA modeling process with a real case-control dataset.
    Type of Medium: Online Resource
    ISSN: 0001-5652 , 1423-0062
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2007
    detail.hit.zdb_id: 1482710-4
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...