Genetics in public health: Rarely explored
- PMID: 21031051
- PMCID: PMC2955951
- DOI: 10.4103/0971-6866.69326
Genetics in public health: Rarely explored
Abstract
The availability and the integration of genetic information into our understanding of normal and abnormal growth and development are driving important changes in health care. These changes have fostered the hope that the availability of genetic information will promote a better understanding of disease etiology and permit early, even pre-symptomatic diagnosis and preventive intervention to avoid disease onset. Hence, our aim was to review and provide the insight into the role of genetics in public health and its scope as well as barriers. The use of genetics along with their goals and essential public health functions are discussed. From the era of eugenics to the present era, this area has seen many turns in which geneticists have put through their effort to tie together the strings of both molecular genetics and public health. Though still the dark clouds of eugenics, the predictive power of genes, genetic reductionism, non-modifiable risk factors, individuals or populations, resource allocation, commercial imperative, discrimination and understanding and education are hanging above. The technological and scientific advances that have fundamentally changed our perception of human diseases fuel the expectations for this proactive health.
Keywords: Barriers; community genetics; genetics; public health.
Conflict of interest statement
Similar articles
-
Genetics and public health--evolution, or revolution?J Epidemiol Community Health. 2004 Nov;58(11):894-9. doi: 10.1136/jech.2003.018515. J Epidemiol Community Health. 2004. PMID: 15483303 Free PMC article. Review.
-
Genetic testing considerations for oral medicine.J Dent Educ. 2002 Oct;66(10):1185-202. J Dent Educ. 2002. PMID: 12449214 Review.
-
[The brave new world of prevention? On the prerequisites and scope of public health genetics].Gesundheitswesen. 2007 Feb;69(2):53-62. doi: 10.1055/s-2007-971057. Gesundheitswesen. 2007. PMID: 17405077 German.
-
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
-
[Advocacy for the establishment of a comprehensive strategy to reduce the "burden" of schizophrenic disorders].Encephale. 2016 Oct;42(5):476-483. doi: 10.1016/j.encep.2016.05.007. Epub 2016 Sep 9. Encephale. 2016. PMID: 27623121 Review. French.
Cited by
-
Integration of modern genetic knowledge and technology into public health in India.Indian J Hum Genet. 2010 May;16(2):45-6. doi: 10.4103/0971-6866.69325. Indian J Hum Genet. 2010. PMID: 21031050 Free PMC article. No abstract available.
-
Genetic Implications of HLA-DR and HLA-DQ Genotype on Tobacco Smoking and Oral Submucous Fibrosis.Oral Health Prev Dent. 2020 Jul 4;18(3):455-460. doi: 10.3290/j.ohpd.a44683. Oral Health Prev Dent. 2020. PMID: 32515416 Free PMC article.
-
Nutrigenomics research: a review.J Food Sci Technol. 2013 Jun;50(3):415-28. doi: 10.1007/s13197-012-0775-z. Epub 2012 Jul 19. J Food Sci Technol. 2013. PMID: 24425937 Free PMC article. Review.
-
Genetics in Dentistry: A Review of Advances and Implications.J Pharm Bioallied Sci. 2025 May;17(Suppl 1):S181-S183. doi: 10.4103/jpbs.jpbs_1758_24. Epub 2025 Feb 10. J Pharm Bioallied Sci. 2025. PMID: 40511121 Free PMC article. Review.
-
Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how?Pediatr Nephrol. 2019 Feb;34(2):195-210. doi: 10.1007/s00467-017-3838-6. Epub 2017 Nov 27. Pediatr Nephrol. 2019. PMID: 29181713 Free PMC article. Review.
References
-
- Collins FS, McKusick VA. Implications of the human genome project for medical science. JAMA. 2001;285:540–4. - PubMed
-
- van Ommen GJ, Bakker E, den Dunnen JT. The human genome project and the future of diagnostics, treatment and prevention. Lancet. 1999;354:5–19. - PubMed
-
- Wallace H. The need for independent scientific peer review of Biobank UK. Lancet. 2002;359:2282. - PubMed
-
- Pass K. Lessons learned from newborn screening for Phenylketonuria. In: Khoury M, Burke W, Thompson E, editors. Genetics and public health in the 21st century. Oxford: Oxford University Press; 2000. pp. 385–404.
LinkOut - more resources
Full Text Sources
Miscellaneous