Clinical Chemistry Link to Randox Laboratories Web Site
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 50: 1498-1499, 2004; 10.1373/clinchem.2004.037515
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an electronic Letter to
the Editor about this paper
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via ISI Web of Science (1)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Valdes, R.
Right arrow Articles by Linder, M. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Valdes, R., Jr
Right arrow Articles by Linder, M. W.
Related Collections
Right arrow Molecular Diagnostics and Genetics
Right arrow Drug Monitoring and Toxicology
(Clinical Chemistry. 2004;50:1498-1499.)
© 2004 American Association for Clinical Chemistry, Inc.


Editorials

Fine-Tuning Pharmacogenetics: Paradigm for Linking Laboratory Results to Clinical Action

Roland Valdes, Jra and Mark W. Linder

1 University of Louisville School of Medicine, Louisville, KY 40202

aAuthor for correspondence.

The first 20% of the full text of this article appears below.

Pharmacogenetics (PGx) is the study of the relationship between gene-based markers and pharmacology as it relates to the processing and/or function of drugs. The clinical utility of PGx is embodied principally in the ability to predict either the most appropriate dosing of a medicine or the selection of a particular medicine for a given individual. This expectation has led to the concept of "personalized medicine". Although the science and clinical application of PGx seem to be rapidly converging, the horizon remains a bit fuzzy, partly because the evidence needed to establish its clinical application to patient care is just now beginning to surface.

The clinical laboratory is the principal vehicle for providing PGx testing services to the medical community (1). These services include providing access to the testing, selecting appropriate testing profiles, and among other responsibilities, providing the evidence required to formulate decisions on medical applications (2). From this perspective, advances in laboratory medicine, as with most medical disciplines, are typically achieved in incremental steps. Each step provides a basis on which to build consensus for accepting a standard for the practice. Often however, new information gets substantially ahead of the commonly accepted medical practice and an element of confusion, perhaps driven by high expectations, sets in. To avoid this dilemma, a reasonable strategy must be developed to establish pathways for . . . [Full Text of this Article]







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by the American Association for Clinical Chemistry.