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Published on: August 15, 2019
Impact of common genetic variation on neonatal disease and outcome
1University of Bristol, D Level, St Michael's Hospital, Bristol BS2 8EG, UK. david.harding@bristol.ac.uk
Insights
Identifying gene-environment interactions reveals disease mechanisms and patient vulnerabilities. This knowledge enables personalized treatments based on genetic susceptibility, particularly in neonates.
Area of Science:
- Genetics and Developmental Biology
- Neonatal Medicine
- Disease Mechanisms
Background:
- Gene-environment interactions are crucial for understanding disease etiology.
- Identifying genetic predispositions can inform targeted interventions.
- Neonatal conditions present unique challenges in studying genetic influences.
Purpose of the Study:
- To review the impact of common genetic variations on neonatal outcomes.
- To highlight the potential of genetic insights for personalized medicine in neonates.
- To discuss the strengths and limitations of genetic association studies in this field.
Main Methods:
- Literature review focusing on positive association studies.
- Analysis of common genetic variations and their effects on neonatal conditions.
- Discussion of methodologies in gene-environment interaction research.
Main Results:
- Common genetic variations can influence the outcome of various neonatal conditions.
- Association studies provide evidence for genetic susceptibility.
- Further research is needed to fully elucidate these interactions.
Conclusions:
- Understanding gene-environment interactions is key to unraveling disease development.
- Personalized treatment strategies can be developed based on inborn susceptibility.
- Genetic association studies, despite limitations, are valuable for future research and intervention in neonates.
Abstract:
The main aim of identifying gene-environment interactions is to provide insight into mechanisms of disease development and to identify patients with an inherent vulnerability to certain conditions. This in turn may allow patients to be targeted with individualised treatment based on the knowledge of their inborn susceptibility to specific conditions. This review describes the possible effects of common genetic variation on outcome in various conditions affecting the neonate. It focuses predominantly on studies of positive association rather than non-association to illustrate this potential influence and to highlight the potential for further study and intervention. The shortcomings of published association studies and the place of such studies in future research are also discussed.
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