The response to beta2-agonist treatment shows large repeatability within individuals and may thus be determined by genetic influences. Here we present a systematic overview of the available genetic association and linkage data for beta2-agonist treatment response. Systematic searches identified 66 eligible articles, as of March 2007, pertaining either to B2AR gene polymorphisms and short-acting or long-acting beta2-agonists or to another 29 different genes. We systematize these study results according to gene, agent and type of outcomes addressed. The systematic review highlights major challenges in the field, including extreme multiplicity of analyses; lack of consensus for main phenotypes of interest; typically small sample sizes; and poor replicability of the proposed genetic variants. Future studies will benefit from standardization of analyses and outcomes, hypothesis-free genome-wide association testing platforms, potentially additional fine mapping around new discovered variants, and large-scale collaborative studies with prospective plans for replication among several teams, with transparent public recording of all data.
Foteini Chatzinasiou, Cinzia Lilli, K. Kypraiou, Irene Stefanaki, V. Nicolaou, George M. Spyrou, Εvangelos Εvangelou, Johannes T. Roehr, Elisavet Kodela, A. Katsambas, John P A Ioannidis, Lars Bertram, A. Stratigos
Rufus Cartwright, Altaf Mangera, Kari A.O. Tikkinen, Prabhakar Rajan, Jori S. Pesonen, Anna C. Kirby, Ganesh Thiagamoorthy, Chris Ambrose, Juan Gonzalez‐Maffe, Phillip R. Bennett, Tom Palmer, Andrew J. Walley, Paul M Ridker, Vik Khullar, Christopher R. Chapple
Emma Magavern, Harshal Deshmukh, Géraldine Asselin, Elizabeth Theusch, Stella Trompet, Xiaohui Li, Raymond Noordam, Y.-D. Ida Chen, Teresa E. Seeman, Kent D. Taylor, Wendy S. Post, Jean‐Claude Tardif, Dirk S. Paul, Emelia Benjamin, Nancy L. Heard‐Costa, Ramachandran S. Vasan, Jerome I. Rotter, Ronald M. Krauss, J. Wouter Jukema, Paul M. Ridker, Patricia B. Munroe, Mark J. Caulfield, Daniel I. Chasman,
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