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Introduction  115




           In  2016 they  had  data  for  6060 healthy volunteers  (admixed,  Caucasians,
           native Americans, Jews, and Afro-descendants) (Sosa-Macias et  al.,  2016).
           Other international initiatives that are carrying out pharmacogenetic research
           and promoting pharmacogenetics in Latin America are the Pharmacogenetics
           for Every Nation Initiative (PGENI) (http://www.pgeni.org) and The Golden
           Helix Institute of Biomedical Research (http://goldenhelix.org).
           Most of the regulatory agencies in Latin America do not enforce specific regula-
           tions for conducting pharmacogenetic research. Regulations may be inferred
           from general norms of clinical research and international regulations. In the
           case of new drugs, sponsors that perform pharmacogenetic studies are required
           to gain regulatory approval, and specific guidelines for pharmacogenetics eval-
           uation is needed in most Latin American countries (Quinones et al., 2014).
           Other international resources of interest are the Pharmacogenomics Research
           Network (PGRN) (www.pgrn.org), the Clinical Pharmacogenetics Implemen-
           tation Consortium (CPIC) (www.pharmgkb.org/page/cpic), and the Pharma-
           cogenomics Knowledge Base PharmGKB www.pharmgkb.org.

           Perspectives for Future Studies
           Several challenges remain for a broad implementation of genomic medicine
           into the care of NPDs in Latin American countries. In the last 20 years, we have
           learned that NPDs are complex and multifactorial entities, with the potential
           effect of hundreds of genetic and epigenetic factors interacting with multiple
           environmental variables, leading to particular individual susceptibilities to
           specific diseases (Burmeister et al., 2008).

           In Latin America, because of historical reasons, research initiatives into NPDs
           are usually not included in the top national priorities, leading to lack of
           adequate funding for the organization of the necessary clinical services and
           research infrastructure. There is the need for larger public and private funding
           for research into NPG in Latin American countries (Sharan et al., 2009). For
           this increase in funding, it will be fundamental that researchers develop more
           activities aimed to create a deeper awareness of the importance of research into
           NPG among the general public, regional and national governments, profes-
           sional and academic societies, and other key stakeholders. Data about preva-
           lence, heritability, and burden of NPDs will help to show that they should
           become key priorities for research in Latin America (Forero et al., 2014). Most
           of the epidemiological studies performed in Latin America have been cross-
           sectional works that did not include subsequent follow ups. The development
           of longitudinal cohort studies in the general population will open new ave-
           nues for research, both nationally and internationally.

           Collaborations  between laboratories are fundamental  for research projects
           in NPG and are vital for a deeper understanding of the pathophysiology of
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