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Introduction  113




           behavior, hyperactivity, aggression, and executive function. Brazil, Colombia,
           and Mexico have made major contributions to the knowledge about genetics
           and endophenotypes in Latin American samples.

           Pharmacogenetics and Neuropsychiatric Disorders in Latin
           America
           Pharmacogenomics applied to NPDs will help to implement genomics in the
           care of neuropsychiatric patients in Latin America by predicting, based on the
           individual genetic profiles, whether a drug will treat the disease or whether a
           patient has a predisposition to adverse events (Suarez-Kurtz and Pena, 2006).
           In addition, this research will help with clinical decisions, such as the best drug
           and dosage for an individual, decreasing the time and costs of identifying the
           right pharmacological treatments. The first step in pharmacogenetics research
           is to identify the genetic variants that determine the response to a drug and to
           determine if the findings in other populations can be applied to the different
           samples of patients in the Latin America region (Suarez-Kurtz and Pena, 2006).
           As molecular genetic factors are important variables for the response to
           pharmacological  compounds  used  for  the  treatment  of  NPD,  several  stud-
           ies on pharmacogenetics have been carried out in Latin American countries
           (Table  6.5),  particularly  in  Mexico  and  Brazil.  These  studies  have  included
           ADHD, BP, MDD, OCD, and SZ patients, testing the effect of variants on candi-
           date genes (such as DRD1, SLC6A4, and MAOA, among others) to the response
           of drugs such as methylphenidate, clozapine, and lithium (Bruxel et al., 2015;
           Bruxel et al., 2013; Contini et al., 2011, 2010; Corregiari et al., 2012; da Silva
           et al., 2008; Gonzalez-Covarrubias et al., 2016; Guimaraes et al., 2009b; Kohl-
           rausch et al., 2008a,b; Kohlrausch et al., 2010, 2013; Michelon et al., 2006; Ota
           et al., 2012; Peñas-lledó et al., 2013; Polanczyk et al., 2007; Salatino-Oliveira
           et al., 2011; Zeni et al., 2007). Most of the studies on neurological disorders
           focused on epilepsy and aimed to estimate the allele and genotype frequencies
           of markers influencing the effects of antiepileptic drugs, evaluating if these fre-
           quencies were different between the Mexican-Mestizo populations and other
           reported samples (Fricke-Galindo et al., 2016). There are no studies on epigen-
           etic markers as possible predictors of response to pharmacological treatments
           on NPDs in Latin America (Reynolds and Fachim, 2016).
           To assess whether findings from other populations can be extrapolated to the
           samples from Latin America, there have been several studies and initiatives,
           which have estimated the frequency of the most relevant pharmacogenetic bio-
           markers for neuropsychiatric and metabolic phenotypes, in healthy volunteers
           from Latin American populations and have compared them to the frequen-
           cies observed in other samples around the world (Bonifaz-Pena et al., 2014;
           Cespedes-Garro et al., 2015; Rodeiro et al., 2012; Suarez-Kurtz, 2004).
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