Genetic Polymorphisms of Infectious Diseases in Case-Control Studies
Author(s) -
Antônio Guilherme Pacheco,
Milton Ozório Moraes
Publication year - 2009
Publication title -
disease markers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 66
eISSN - 1875-8630
pISSN - 0278-0240
DOI - 10.1155/2009/685618
Subject(s) - genetic epidemiology , biology , genome wide association study , genetics , single nucleotide polymorphism , genetic association , epidemiology , snp , population , genetic diversity , disease , evolutionary biology , gene , genotype , medicine , environmental health , pathology
In the past decade, genetic epidemiological analyses in infectious diseases have increased drastically since the publication of human genome and all the subsequent projects analyzing human diversity at molecular level. The great majority of studies use classical epidemiological designs applied to genetic data, and more than 80% of published studies use population-based case-control designs with widely spread genetic markers in human genome, like short tandem repeats (STR) or single nucleotide polymorphisms (SNP), in genes chosen by their physiological association with the disease (candidate genes). Even though genetic data is less prone to several bias issues inherent to case-control studies, some care has to be taken when designing, performing, analyzing and interpreting results from such studies. Here we discuss some basic concepts of genetics and epidemiology as a departure to evaluate and review every step that should be followed to design, conduct, analyze, interpret and present data from those studies, using particularities of infectious diseases, especially leprosy and tuberculosis as models.
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