<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Guevara M</submitter><funding>Fondo Nacional de Innovación y Desarrollo Científico y Tecnológico (FONDOCYT)</funding><funding>Brazilian National Research Council (CNPq)</funding><funding>Instituto de Salud Carlos III (ISCIII) and European Union NextGeneration EU/Plan de Recuperación, Transformación y Resiliencia</funding><funding>AEXCID-Junta de Extremadura</funding><pagination>8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11768636</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(1)</volume><pubmed_abstract>&lt;b>Background/Objectives:&lt;/b> Genetic polymorphism of the dihydropyrimidine dehydrogenase gene (&lt;i>DPYD&lt;/i>) is responsible for the variability found in the metabolism of fluoropyrimidines such as 5-fluorouracil (5-FU), capecitabine, or tegafur. The &lt;i>DPYD&lt;/i> genotype is linked to variability in enzyme activity, 5-FU elimination, and toxicity. Approximately 10-40% of patients treated with fluoropyrimidines develop severe toxicity. The interethnic variability of &lt;i>DPYD&lt;/i> gene variants in Afro-Latin Americans is poorly studied, thereby establishing a barrier to the implementation of personalized medicine in these populations. Therefore, the present study aims to analyze the frequency of &lt;i>DPYD&lt;/i> variants with clinical relevance in the Dominican population and their association with g</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>The Frequency of &lt;i>DPYD&lt;/i> c.557A>G in the Dominican Population and Its Association with African Ancestry.</pubmed_title><pmcid>PMC11768636</pmcid><funding_grant_id>24IA001</funding_grant_id><funding_grant_id>312807/2022-8 and 200824/2024-4</funding_grant_id><funding_grant_id>PMP22/00099; BIOFRAM22</funding_grant_id><funding_grant_id>2020-201-2C5-204</funding_grant_id><pubmed_authors>Penas-Lledo E</pubmed_authors><pubmed_authors>Rodrigues-Soares F</pubmed_authors><pubmed_authors>LLerena A</pubmed_authors><pubmed_authors>Manochio C</pubmed_authors><pubmed_authors>Dorado P</pubmed_authors><pubmed_authors>de la Cruz CG</pubmed_authors><pubmed_authors>Rodriguez E</pubmed_authors><pubmed_authors>Guevara M</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Frequency of &lt;i>DPYD&lt;/i> c.557A>G in the Dominican Population and Its Association with African Ancestry.</name><description>&lt;b>Background/Objectives:&lt;/b> Genetic polymorphism of the dihydropyrimidine dehydrogenase gene (&lt;i>DPYD&lt;/i>) is responsible for the variability found in the metabolism of fluoropyrimidines such as 5-fluorouracil (5-FU), capecitabine, or tegafur. The &lt;i>DPYD&lt;/i> genotype is linked to variability in enzyme activity, 5-FU elimination, and toxicity. Approximately 10-40% of patients treated with fluoropyrimidines develop severe toxicity. The interethnic variability of &lt;i>DPYD&lt;/i> gene variants in Afro-Latin Americans is poorly studied, thereby establishing a barrier to the implementation of personalized medicine in these populations. Therefore, the present study aims to analyze the frequency of &lt;i>DPYD&lt;/i> variants with clinical relevance in the Dominican population and their association with g</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-04-22T03:25:57.23Z</modification><creation>2025-04-06T07:44:09.03Z</creation></dates><accession>S-EPMC11768636</accession><cross_references><pubmed>39861660</pubmed><doi>10.3390/pharmaceutics17010008</doi></cross_references></HashMap>