Journal of the Society for Gynecologic Investigation

 

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Journal of the Society for Gynecologic Investigation, Vol. 13, No. 8, 531-541 (2006)
DOI: 10.1016/j.jsgi.2006.09.006


Reviews

Genetic Associations in Preterm Birth: A Primer of Marker Selection, Study Design, and Data Analysis

Ramkumar Menon, MS

Perinatal Research Center, Nashville, TN; North Atlantic Neuro-epidemiology Alliances (NANEA), Institute for Public Health, University of Aarhus, Aarhus, Denmark; Department of Medicine, Vanderbilt University, Nashville, TN; and the Center for Human Genetic Research, Vanderbilt University, Nashville, TN fortunat{at}edge.net

Stephen J. Fortunato, MD

Poul Thorsen, MD, PhD

Scott Williams, PhD

Perinatal Research Center, Nashville, TN; North Atlantic Neuro-epidemiology Alliances (NANEA), Institute for Public Health, University of Aarhus, Aarhus, Denmark; Department of Medicine, Vanderbilt University, Nashville, TN; and the Center for Human Genetic Research, Vanderbilt University, Nashville, TN

Spontaneous preterm birth (PTB; delivery before 37 weeks gestation) is a primary risk factor for infant morbidity and mortality. The etiology is unclear, but there is evidence that there is a genetic predisposition to PTB. Armed with the suggestion of genetic risk factors and the failure to identify useful biomarkers, investigators are starting to actively pursue the role of genetic predisposition in PTB. Several studies have been done to date assessing the role of single gene variants. However, positive findings have failed to replicate. We argue that heterogeneity in study designs, definition of phenotype, single-nucleotide polymorphism (SNP) selection, population selection, and sample size makes data interpretation difficult in complex phenotypes such as PTB. In this review, we introduce general concepts of study designs in genetic epidemiology, selection of candidate genes and markers for analysis, and analytical methodologies. We also introduce how the concept of gene-gene interactions (biologic epistatis) and gene-environment interactions may affect the predisposition to PTB.

Key Words: Genetic association • prematurity • single-nucleotide polymorphisms • multilocus analysis • MDR


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