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How to use an article about genetic association A: Background concepts

  • John Attia
  • , John P.A. Ioannidis
  • , Ammarin Thakkinstian
  • , Mark McEvoy
  • , Rodney J. Scott
  • , Cosetta Minelli
  • , John Thompson
  • , Claire Infante-Rivard
  • , Gordon Guyatt
  • University of Newcastle, College of Health, Medicine and Wellbeing
  • John Hunter Hospital
  • University of Ioannina
  • Tufts University School of Medicine
  • Hunter Area Pathology Service
  • University of Newcastle
  • Department of National Heart and Lung Institute
  • Universiry of Leicester
  • McGill University
  • McMaster University

Research output: Contribution to journalReview articlepeer-review

95 Citations (Scopus)

Abstract

This is the first in a series of 3 articles serving as an introduction to clinicians wishing to read and critically appraise genetic association studies. We summarize the key concepts in genetics that clinicians must understand to review these studies, including the structure of DNA, transcription and translation, patterns of inheritance, Hardy-Weinberg equilibrium, and linkage disequilibrium. We review the types of DNA variation, including single-nucleotide polymorphisms (SNPs), insertions, and deletions, and how these can affect protein function. We introduce the idea of genetic association for both single-candidate gene and genome-wide association studies, in which thousands of genetic variants are tested for association with disease. We use the APOE polymorphism and its association with dementia as a case study to demonstrate the concepts and introduce the terminology used in this field. The second and third articles will focus on issues of validity and applicability.

Original languageEnglish
Pages (from-to)74-81
Number of pages8
JournalJAMA
Volume301
Issue number1
DOIs
Publication statusPublished - 7 Jan 2009

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