Published online before print November 22, 2006, doi: 10.1161/01.STR.0000252121.56643.4a
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Stroke. 2007;38:6.)
© 2007 American Heart Association, Inc.
Editorials |
From Bench to Bedside and Back
The Value of Candidate Gene Association Studies in Translational Research
From the Department of Hematology/Oncology, Children’s Hospital & Research Center Oakland, Calif.
Correspondence to Carolyn Hoppe, MD, Department of Hematology/Oncology, Children’s Hospital & Research Center Oakland, 747 52nd Street, Oakland, CA 94609. E-mail choppe{at}mail.cho.org
See related article, pages 41–49
Key Words: pediatric stroke • risk factors • stroke • stroke in children • stroke in young adults • genetic modifiers
A major challenge in genetic association studies is the choice of appropriate candidate genes based on plausible biologically driven hypotheses. The current study by Voetsch and coworkers1 in this issue of Stroke illustrates how the integration of traditional epidemiological approaches, such as case-control studies, and experimental data from the laboratory can be used to assess the role of genetic factors in disease causation. Plasma glutathione peroxidase (GPx-3) is a selenocysteine-containing protein with antioxidant and antithrombotic properties. A familial deficiency in GPx-3 activity has been reported in children with idiopathic stroke, suggesting that polymorphisms in the plasma GPx-3 promoter gene may modify stroke risk.
The authors previously identified a novel, functional transcription start site in the GPx-3 gene with a promoter regulated by hypoxia2, prompting further analyses of this candidate gene. In the present study, the authors postulate that by influencing GPx-3 transcription and plasma GPx-3 enzyme levels, distinct variants in the GPx-3 gene may be influencing the pathogenesis of nonatherogenic stroke.
To test the hypothesis that GPx-3 promoter polymorphisms contribute to nonatherosclerotic stroke risk in children and young adults, the effect of GPx-3 polymorphisms on stroke risk was comprehensively assessed in 2 independent study populations. In the initial cohort, comprised of 123 young adult stroke patients and 123 healthy control subjects matched by age, gender and ethnicity, the frequencies of GPx-3 promoter variants were compared, and 2 common haplotypes, H1 and H2, were identified. The H2 haplotype (H2) was present in 13% of the affected and 7% of unaffected subjects, corresponding to a 2-fold increased risk of ischemic stroke associated with this haplotype. Interaction between the H2 haplotype and other vascular risk factors was also explored. Although subgroup analyses were limited by sample size, carriers of the H2 haplotype who had at least 1 other vascular risk factor had a >5-fold increased risk of ischemic stroke. These findings were then extended to an independent population of children with ischemic stroke, yielding virtually identical results: an increased prevalence of the H2 haplotype in affected children (13.4%) compared with unaffected controls (7.9%), with an OR of 2.13.
Recognizing that the identification of the H2 risk haplotype does not in itself provide insights into the physiological mechanisms affected by the genetic variant, the authors elegantly tested the functional significance of these results with gene reporter assays. Under hypoxic conditions, the GPx-3 promoter H2 haplotype was shown to reduce GPx-3 gene transcription, thereby attenuating the protective effect of this antioxidant enzyme.
As with most candidate gene association studies, this study is potentially limited by inadequate sample size, misclassification of stroke phenotypes and population stratification attributable to genetic admixture. However, confirmation of their findings in an independent cohort, together with the additional mechanistic studies performed to show the biological relevance of the candidate gene, strengthen the authors’ conclusion that the GPx-3 promotor gene is causally associated with stroke in children and young adults.
The next steps will continue to involve the integration of "bench" and "bedside" research. Additional experimental data from the laboratory are needed to understand the pathways regulated by the GPx-3 gene and how those are involved in stroke. At the same time, epidemiological and patient-centered research is also needed to determine the predictive value of this newly identified genetic risk factor for nonatherogenic stroke. Only through interdisciplinary approaches, of the type this study so well illustrates, will the gaps between bench and bedside be successfully bridged.
Acknowledgments
Disclosures
None.
Footnotes
The opinions in this editorial are not necessarily those of the editors or of the American Heart Association.
References
- Voetsch B, Jin RC, Bierl C, Benke KS, Kenet G, Simioni P, Ottaviano F, Damasceno BP, Annichino-Bizacchi JM, Handy DE, Loscalzo J. Promoter polymorphisms in the plasma glutathione peroxidase (GPx-3) gene: a novel risk factor for arterial ischemic stroke among young adults and children. Stroke. 2007; 38: 41–49.
- Bierl C, Voetsch B, Jin RC, Handy DE, Loscalzo J. Determinants of human plasma glutathione peroxidase (GPx-3) expression. J Biol Chem. 2004; 279: 26839–26845.
[Abstract/Free Full Text]
Related Article:
- Promoter Polymorphisms in the Plasma Glutathione Peroxidase (GPx-3) Gene: A Novel Risk Factor for Arterial Ischemic Stroke Among Young Adults and Children
- Barbara Voetsch, Richard C. Jin, Charlene Bierl, Kelly S. Benke, Gili Kenet, Paolo Simioni, Filomena Ottaviano, Benito P. Damasceno, Joyce M. Annichino-Bizacchi, Diane E. Handy, and Joseph Loscalzo
Stroke 2007 38: 41-49.[Abstract] [Full Text] [PDF]
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||