Development and integration of molecular genetic tests into clinical practice: the US experience

Expert Rev Mol Diagn. 2004 Jul;4(4):465-77. doi: 10.1586/14737159.4.4.465.

Abstract

The issues that arise in the development of genetic tests for prediction and diagnosis are described in the context of the authors' experience as laboratory directors in the USA. The goal is to identify gaps and weaknesses in the test validation process and to define the pivotal issues. Variables that influence a laboratory director's decision to develop a particular molecular genetic assay, including motivation, economics, intellectual property and the regulatory environment, are described. Issues of clinical and analytic validation are discussed, providing examples of tests with both good (cystic fibrosis carrier screening) and poor (apolipoprotein E genotyping for Alzheimer's disease) clinical utility. The decision-making process that occurs during the considered transition of a research-based molecular genetic assay into routine use in the clinical laboratory is summarized. Different factors will be weighted differently depending on the nature of the disease being tested, the complexity of its gene and mutations, the available technical platforms, potential regulatory and intellectual property restrictions, and whether the proposed test is to be offered by an academic or a commercial laboratory.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alzheimer Disease / diagnosis
  • Alzheimer Disease / genetics
  • Apolipoproteins E / metabolism
  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / genetics
  • Decision Making, Organizational
  • Genetic Diseases, Inborn / diagnosis*
  • Humans
  • Molecular Biology / methods*
  • Molecular Diagnostic Techniques* / economics
  • Patents as Topic
  • Reagent Kits, Diagnostic
  • Reproducibility of Results
  • United States
  • United States Food and Drug Administration

Substances

  • Apolipoproteins E
  • Reagent Kits, Diagnostic