A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions
- PMID: 18319070
- PMCID: PMC2427295
- DOI: 10.1016/j.ajhg.2007.12.020
A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions
Abstract
Predictive genomic profiling used to produce personalized nutrition and other lifestyle health recommendations is currently offered directly to consumers. By examining previous meta-analyses and HuGE reviews, we assessed the scientific evidence supporting the purported gene-disease associations for genes included in genomic profiles offered online. We identified seven companies that offer predictive genomic profiling. We searched PubMed for meta-analyses and HuGE reviews of studies of gene-disease associations published from 2000 through June 2007 in which the genotypes of people with a disease were compared with those of a healthy or general-population control group. The seven companies tested at least 69 different polymorphisms in 56 genes. Of the 56 genes tested, 24 (43%) were not reviewed in meta-analyses. For the remaining 32 genes, we found 260 meta-analyses that examined 160 unique polymorphism-disease associations, of which only 60 (38%) were found to be statistically significant. Even the 60 significant associations, which involved 29 different polymorphisms and 28 different diseases, were generally modest, with synthetic odds ratios ranging from 0.54 to 0.88 for protective variants and from 1.04 to 3.2 for risk variants. Furthermore, genes in cardiogenomic profiles were more frequently associated with noncardiovascular diseases than with cardiovascular diseases, and though two of the five genes of the osteogenomic profiles did show significant associations with disease, the associations were not with bone diseases. There is insufficient scientific evidence to conclude that genomic profiles are useful in measuring genetic risk for common diseases or in developing personalized diet and lifestyle recommendations for disease prevention.
Figures
Comment in
-
Personalized genetics: a responsible approach.Am J Hum Genet. 2008 Jul;83(1):130; author reply 131. doi: 10.1016/j.ajhg.2008.06.002. Am J Hum Genet. 2008. PMID: 18606304 Free PMC article. No abstract available.
Similar articles
-
Personalized genetics: a responsible approach.Am J Hum Genet. 2008 Jul;83(1):130; author reply 131. doi: 10.1016/j.ajhg.2008.06.002. Am J Hum Genet. 2008. PMID: 18606304 Free PMC article. No abstract available.
-
Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics.Hum Mutat. 2010 Jun;31(6):631-55. doi: 10.1002/humu.21260. Hum Mutat. 2010. PMID: 20506564 Review.
-
The future of Cochrane Neonatal.Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12. Early Hum Dev. 2020. PMID: 33036834
-
Insights into genetics, human biology and disease gleaned from family based genomic studies.Genet Med. 2019 Apr;21(4):798-812. doi: 10.1038/s41436-018-0408-7. Epub 2019 Jan 18. Genet Med. 2019. PMID: 30655598 Free PMC article. Review.
-
Recommendations from the EGAPP Working Group: does genomic profiling to assess type 2 diabetes risk improve health outcomes?Genet Med. 2013 Aug;15(8):612-7. doi: 10.1038/gim.2013.9. Epub 2013 Mar 14. Genet Med. 2013. PMID: 23492873
Cited by
-
The genetics of cancer risk.Cancer J. 2011 Nov-Dec;17(6):416-22. doi: 10.1097/PPO.0b013e31823e5387. Cancer J. 2011. PMID: 22157285 Free PMC article. Review.
-
Health system implications of direct-to-consumer personal genome testing.Public Health Genomics. 2011;14(1):53-8. doi: 10.1159/000321962. Epub 2010 Nov 13. Public Health Genomics. 2011. PMID: 21071927 Free PMC article.
-
Pharmacogenetics of major depression: insights from level 1 of the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) trial.Mol Diagn Ther. 2008;12(5):321-30. doi: 10.1007/BF03256297. Mol Diagn Ther. 2008. PMID: 18803430 Free PMC article. Review.
-
Perceived impact of diabetes genetic risk testing among patients at high phenotypic risk for type 2 diabetes.Diabetes Care. 2011 Mar;34(3):568-73. doi: 10.2337/dc10-1960. Epub 2011 Feb 1. Diabetes Care. 2011. PMID: 21285385 Free PMC article.
-
How accurate can genetic predictions be?BMC Genomics. 2012 Jul 24;13:340. doi: 10.1186/1471-2164-13-340. BMC Genomics. 2012. PMID: 22827772 Free PMC article.
References
-
- Collins F.S., McKusick V.A. Implications of the Human Genome Project for medical science. JAMA. 2001;285:540–544. - PubMed
-
- Wallace H. GeneWatch UK; Buxton, UK: 2006. Your Diet Tailored to Your Genes: Preventing Diseases or Misleading Marketing?
-
- Hudson K., Javitt G., Burke W., Byers P., ASHG Social Issues Committee ASHG Statement on Direct-to-Consumer Genetic Testing in the United States. Am. J. Hum. Genet. 2007;81:635–637. - PubMed
-
- Vineis P., Christiani D.C. Genetic testing for sale. Epidemiology. 2004;15:3–5. - PubMed
-
- Government Accountability Office. (2006). Nutrigenetic testing: Tests purchased from four Web sites mislead consumers. (http://www.gao.gov/new.items/d06977t.pdf)
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical