Use of genomic panels to determine risk of developing type 2 diabetes in the general population: a targeted evidence-based review
| Autor: | Stephanie Melillo, Michael P. Douglas, Michael Marrone, Glenn E. Palomaki |
|---|---|
| Rok vydání: | 2013 |
| Předmět: |
Adult
Genotype Population Genome-wide association study Type 2 diabetes Risk Assessment White People Article Meta-Analysis as Topic Genetic variation medicine Humans Genetic Predisposition to Disease Genetic Testing Allele education Alleles Genetics (clinical) Genetic testing Genetics education.field_of_study medicine.diagnostic_test business.industry Genetic Variation Reproducibility of Results medicine.disease Diabetes Mellitus Type 2 business Risk assessment Transcription Factor 7-Like 2 Protein Genome-Wide Association Study |
| Zdroj: | Genetics in Medicine. 15:600-611 |
| ISSN: | 1098-3600 |
| DOI: | 10.1038/gim.2013.8 |
| Popis: | This evidence review addresses whether type 2 diabetes genomic risk panels improve health outcomes (e.g., reduce rates of developing type 2 diabetes) in low- or high-risk adults; two clinical scenarios promulgated by commercial companies offering such testing. Evidence for the analytic validity of available genomic profiles was inadequate. Clinical validity ranged from inadequate to convincing for 30 variants identified on five type 2 diabetes genomic panels and by genome-wide association studies. Eight common variants were identified for general population use; evidence credibility based on published criteria was strong for two variants, moderate for two variants, and weak for four variants. TCF7L2 had the largest per-allele odds ratio of 1.39 (95% confidence interval 1.33–1.46). Models combining the best four, best eight, and all 30 variants used summary effect sizes, reported genotype frequencies, and assumed independent effects. Areas under the curve were 0.547, 0.551, and 0.570, respectively. In high-risk populations, per-allele odds ratios for TCF7L2 alone were similar to those of the general population. TCF7L2, in combination with other variants, yielded minimal improvement in risk reclassification. Evidence on TCF7L2 clinical validity was adequate. Three studies addressed the clinical utility of intervention effectiveness, stratified by TCF7L2 genotype; none found significant interactions. Clinical utility evidence was inadequate. In addition to analytic validity and clinical utility knowledge gaps, additional gaps were identified regarding how to inform, produce, and evaluate models combining multiple variants. |
| Databáze: | OpenAIRE |
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