<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(9)</volume><submitter>Ain QT</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Empagliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, improves outcomes in heart failure (HF) patients, yet inter-individual variability in response remains unclear. Genetic variants in Brain-Derived Neurotrophic Factor &lt;i>BDNF&lt;/i> (rs6265) and ATPase Sarcoplasmic/Endoplasmic Reticulum Ca&lt;sup>2+&lt;/sup> Transporting 2 ATP2A2 (rs1860561) may influence the treatment efficacy. &lt;b>Objective:&lt;/b> To assess the association of &lt;i>BDNF&lt;/i> and &lt;i>ATP2A2&lt;/i> polymorphisms with the response to low-dose empagliflozin (10 mg) in Pakistani patients with heart failure and a reduced ejection fraction (HFrEF). &lt;b>Methods:&lt;/b> In this prospective study, 120 HF patients with an ejection fraction of 25-45% who had been on stable standard heart failure therapy for at least 3 mont</pubmed_abstract><journal>Biomedicines</journal><pagination>2095</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12467674</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Personalized Response to Empagliflozin in Heart Failure: Association of BDNF and ATP2A2 Variants in a South Asian Cohort.</pubmed_title><pmcid>PMC12467674</pmcid><pubmed_authors>Hasan A</pubmed_authors><pubmed_authors>Khan AA</pubmed_authors><pubmed_authors>Ahmed S</pubmed_authors><pubmed_authors>Azam F</pubmed_authors><pubmed_authors>Usman M</pubmed_authors><pubmed_authors>Ain QT</pubmed_authors><pubmed_authors>Ijaz U</pubmed_authors><pubmed_authors>Ahmed R</pubmed_authors><pubmed_authors>Ali M</pubmed_authors><pubmed_authors>Shaheen A</pubmed_authors><pubmed_authors>Ahmed M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Personalized Response to Empagliflozin in Heart Failure: Association of BDNF and ATP2A2 Variants in a South Asian Cohort.</name><description>&lt;b>Background:&lt;/b> Empagliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor, improves outcomes in heart failure (HF) patients, yet inter-individual variability in response remains unclear. Genetic variants in Brain-Derived Neurotrophic Factor &lt;i>BDNF&lt;/i> (rs6265) and ATPase Sarcoplasmic/Endoplasmic Reticulum Ca&lt;sup>2+&lt;/sup> Transporting 2 ATP2A2 (rs1860561) may influence the treatment efficacy. &lt;b>Objective:&lt;/b> To assess the association of &lt;i>BDNF&lt;/i> and &lt;i>ATP2A2&lt;/i> polymorphisms with the response to low-dose empagliflozin (10 mg) in Pakistani patients with heart failure and a reduced ejection fraction (HFrEF). &lt;b>Methods:&lt;/b> In this prospective study, 120 HF patients with an ejection fraction of 25-45% who had been on stable standard heart failure therapy for at least 3 mont</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-06-30T03:24:08.686Z</modification><creation>2026-06-30T03:16:37.13Z</creation></dates><accession>S-EPMC12467674</accession><cross_references><pubmed>41007658</pubmed><doi>10.3390/biomedicines13092095</doi></cross_references></HashMap>