Abstract:Mexico faces important demographic and epidemiological transitions with significant implications to patterns of disease, disability, and death. On the one hand, there are problems of underdevelopment and, on the other, the emerging challenges of the chronic and degenerative diseases of the industrialized world. For these diseases, prevention becomes a key strategy for alleviating a major burden to the economy and health of the Mexican population. Genomic medicine has become a priority to the Mexican government… Show more
“…In addition, this information will increase our knowledge of genomic variability in Latino populations. The scientific and technological infrastructure derived from this project will significantly contribute to the development of genomic medicine in Mexico and Latin America (3,6).…”
Section: Discussionmentioning
confidence: 99%
“…Although the diversity of Latino populations poses several challenges for genetic studies (1), it makes them a powerful resource for analyzing the genetic bases of complex diseases (2). In the past 5 years, Mexico has been committed to develop a human and technological infrastructure for genomics with special emphasis on the development of a national platform of genomic medicine to improve healthcare of Mexicans (3)(4)(5)(6). This effort, together with a population of Ϸ105 million inhabitants including 60 Amerindian groups and a complex history of admixture, makes Mexico an ideal country in which to perform genomic analysis of common complex diseases.…”
Mexico is developing the basis for genomic medicine to improve healthcare of its population. The extensive study of genetic diversity and linkage disequilibrium structure of different populations has made it possible to develop tagging and imputation strategies to comprehensively analyze common genetic variation in association studies of complex diseases. We assessed the benefit of a Mexican haplotype map to improve identification of genes related to common diseases in the Mexican population. We evaluated genetic diversity, linkage disequilibrium patterns, and extent of haplotype sharing using genomewide data from Mexican Mestizos from regions with different histories of admixture and particular population dynamics. Ancestry was evaluated by including 1 Mexican Amerindian group and data from the HapMap. Our results provide evidence of genetic differences between Mexican subpopulations that should be considered in the design and analysis of association studies of complex diseases. In addition, these results support the notion that a haplotype map of the Mexican Mestizo population can reduce the number of tag SNPs required to characterize common genetic variation in this population. This is one of the first genomewide genotyping efforts of a recently admixed population in Latin America.admixture ͉ genetic variation ͉ population genetics ͉ SNP tagging
“…In addition, this information will increase our knowledge of genomic variability in Latino populations. The scientific and technological infrastructure derived from this project will significantly contribute to the development of genomic medicine in Mexico and Latin America (3,6).…”
Section: Discussionmentioning
confidence: 99%
“…Although the diversity of Latino populations poses several challenges for genetic studies (1), it makes them a powerful resource for analyzing the genetic bases of complex diseases (2). In the past 5 years, Mexico has been committed to develop a human and technological infrastructure for genomics with special emphasis on the development of a national platform of genomic medicine to improve healthcare of Mexicans (3)(4)(5)(6). This effort, together with a population of Ϸ105 million inhabitants including 60 Amerindian groups and a complex history of admixture, makes Mexico an ideal country in which to perform genomic analysis of common complex diseases.…”
Mexico is developing the basis for genomic medicine to improve healthcare of its population. The extensive study of genetic diversity and linkage disequilibrium structure of different populations has made it possible to develop tagging and imputation strategies to comprehensively analyze common genetic variation in association studies of complex diseases. We assessed the benefit of a Mexican haplotype map to improve identification of genes related to common diseases in the Mexican population. We evaluated genetic diversity, linkage disequilibrium patterns, and extent of haplotype sharing using genomewide data from Mexican Mestizos from regions with different histories of admixture and particular population dynamics. Ancestry was evaluated by including 1 Mexican Amerindian group and data from the HapMap. Our results provide evidence of genetic differences between Mexican subpopulations that should be considered in the design and analysis of association studies of complex diseases. In addition, these results support the notion that a haplotype map of the Mexican Mestizo population can reduce the number of tag SNPs required to characterize common genetic variation in this population. This is one of the first genomewide genotyping efforts of a recently admixed population in Latin America.admixture ͉ genetic variation ͉ population genetics ͉ SNP tagging
“…However, controversial results are reported (Bosron and Li, 1986;Vidal et al, 2004;Zintzaras et al, 2006) probably because heterogeneity and racial admixture is playing an important role, among other factors. Mexican population has been arisen by the admixture of indigenous, Spaniard, and African genes (Jimenez-Sanchez et al, 2008). Therefore, elucidation of the genomic structure of ethnic groups constitute significant contributions to this topic.…”
Background: Alcohol abuse represents the major identified etiological factor of cirrhosis in Me´xico. ADH1B, ALDH2, and CYP2E1 have been considered candidate genes in alcohol-related diseases. Controversial results probably due to ethnic differences, among other factors, have been reported. Mexican Mestizos (MES) derive from the combination of indigenous, Spaniard, and African genes. Huichols (HUI) constitute an indigenous group from western Mexico with no racial admixture. We determined ADH1B*2, ALDH2*2, and CYP2E1*c2 allele frequencies in healthy HUI and MES from western Mexico. Lipid and hepatic profile were also carried out.Methods: One hundred and one HUI and 331 MES subjects were studied. Genotype and allele frequency were assessed through polymerase chain reaction-restriction fragment length polymorphism after DNA isolation from peripheral leukocytes. Commercial kits for lipid and hepatic determinations were used.Results: Polymorphic allele distribution in HUI was: 0% ADH1B*2, 0.5% ALDH2*2, 51.5% CYP2E1*c2; in MES: 3.4% ADH1B*2, 0% ALDH2*2, 16.1% CYP2E1*c2. Frequency of ADH1B*2 was statistically (p < 0.001) lower in HUI than MES. CYP2E1*c2 polymorphic allele was significantly higher (p < 0.0001) in HUI than MES. Hepatic profile was normal in both groups. HUI showed a better lipid profile than MES independently of genotype.Conclusions: Huichols exhibited the highest CYP2E1*c2 allele frequency of the world documented up to this date; meanwhile, ADH1B*2 and ALDH2*2 were practically absent. This feature could be useful in the understanding of Mexican population gene composition, alcohol metabolism, and alcoholic liver disease development. However, further association studies are necessary. The heterogeneity of Mexican population was evidenced by the significantly different distribution of CYP2E1*c2 allele observed among different regions of the country. Lipid and hepatic values were not associated to genotype. This report constitutes the first study dealing with gene polymorphisms of alcohol metabolizing enzymes conducted in HUI.
“…Presently, many Rx companies supply medicines at a low cost to the developing world on the basis of onesize-fits-all, but low-cost Dx testing could soon make it possible to offer objective pretreatment testing in nontraditional markets. It is likely that Brazil, Russia, India and China (BRIC) countries, already viewed as emerging markets for various industries, including healthcare, will become early adopters of the personalized medicine paradigm [26]. In addition, the rise in distance-based telemedicine and patient monitoring may allow physicians to introduce Dx/Rx effectiveness to patients outside the hospital setting.…”
Acceptance and operation of a personalized medicine strategy within modern healthcare requires that all key stakeholders are able to understand and assess the benefits offered by the approach. In addition to the technological aspects of molecular diagnostics, as enablers of personalized medicine, stakeholders must also be apprised of the value-adding effects of the strategy in terms of improved treatment efficacy and health economics. This review attempts to cover these broad stakeholder interests by articulating the scientific feasibility, the beneficial medical outcomes and the commercial attractiveness offered by the integration of molecular diagnostics and personalized medicine into healthcare systems, principally by demonstrating how technology integration and value addition can be robustly assessed and represented.
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