<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(19)</volume><submitter>Schwegel N</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Patients with transthyretin amyloid cardiomyopathy (ATTR-CM) represent a high-risk heart failure population with continued unmet therapeutic needs. Sodium-glucose co-transporter 2 inhibitors (SGLT2i) improve cardiovascular outcomes in patients with heart failure across the whole spectrum of ejection fraction, and first evidence regarding their safety and effectiveness in patients with ATTR-CM is arising. This study investigates the association between SGLT2i therapy and clinical outcomes in these patients. &lt;b>Methods:&lt;/b> This is an analysis of a prospective registry conducted at a referral centre for hypertrophic cardiomyopathies including 116 patients with confirmed ATTR-CM. Fifty-one patients (44%) were treated with SGLT2i while 65 patients (56%) remained SGLT2i-naïve. &lt;b>Results:&lt;/b> During a median follow-up of 2.6 (1.7-3.7) years, 38 patients (33%) died, of whom 11 patients (9%) received SGLT2i treatment and 27 patients (23%) were treatment-naïve. SGLT2i therapy was significantly associated with lower mortality (HR 0.457, 95%CI 0.227-0.922, &lt;i>p&lt;/i> = 0.029). This association persisted after adjusting for age and sex (HR 0.479, 95%CI 0.235-0.977, &lt;i>p&lt;/i> = 0.043) and after additional adjustment for eGFR, NT-proBNP, LVEF, and concomitant therapy with tafamidis (HR 0.328, 95%CI 0.141-0.760, &lt;i>p&lt;/i> = 0.009). However, when potential immortal time bias was considered, this association lost statistical significance (HR 1.075, 95%CI 0.524-2.206, &lt;i>p&lt;/i> = 0.843). No significant associations between SGLT2i therapy and worsening heart-failure hospitalization or cardiovascular mortality were observed. &lt;b>Conclusions:&lt;/b> In crude analysis, SGLT2i therapy associates with better survival in patients with ATTR-CM. However, after adjustment for immortal time, this association becomes statistically insignificant. Hence, to draw final conclusions on the effectiveness of SGLT2i therapy in these patients, a randomized controlled trial is warranted.</pubmed_abstract><journal>Journal of clinical medicine</journal><pagination>5966</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11477643</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of SGLT2-Inhibitor Therapy on Survival in Patients with Transthyretin Amyloid Cardiomyopathy: Analysis of a Prospective Registry Study.</pubmed_title><pmcid>PMC11477643</pmcid><pubmed_authors>Zach DK</pubmed_authors><pubmed_authors>Santner V</pubmed_authors><pubmed_authors>Wallner M</pubmed_authors><pubmed_authors>Aziz F</pubmed_authors><pubmed_authors>von Lewinski D</pubmed_authors><pubmed_authors>Gollmer J</pubmed_authors><pubmed_authors>Lugitsch J</pubmed_authors><pubmed_authors>Toferer C</pubmed_authors><pubmed_authors>Schwegel N</pubmed_authors><pubmed_authors>Zirlik A</pubmed_authors><pubmed_authors>Sourij H</pubmed_authors><pubmed_authors>Ablasser K</pubmed_authors><pubmed_authors>Verheyen N</pubmed_authors><pubmed_authors>Kolesnik E</pubmed_authors><pubmed_authors>Holler V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of SGLT2-Inhibitor Therapy on Survival in Patients with Transthyretin Amyloid Cardiomyopathy: Analysis of a Prospective Registry Study.</name><description>&lt;b>Background:&lt;/b> Patients with transthyretin amyloid cardiomyopathy (ATTR-CM) represent a high-risk heart failure population with continued unmet therapeutic needs. Sodium-glucose co-transporter 2 inhibitors (SGLT2i) improve cardiovascular outcomes in patients with heart failure across the whole spectrum of ejection fraction, and first evidence regarding their safety and effectiveness in patients with ATTR-CM is arising. This study investigates the association between SGLT2i therapy and clinical outcomes in these patients. &lt;b>Methods:&lt;/b> This is an analysis of a prospective registry conducted at a referral centre for hypertrophic cardiomyopathies including 116 patients with confirmed ATTR-CM. Fifty-one patients (44%) were treated with SGLT2i while 65 patients (56%) remained SGLT2i-naïve. &lt;b>Results:&lt;/b> During a median follow-up of 2.6 (1.7-3.7) years, 38 patients (33%) died, of whom 11 patients (9%) received SGLT2i treatment and 27 patients (23%) were treatment-naïve. SGLT2i therapy was significantly associated with lower mortality (HR 0.457, 95%CI 0.227-0.922, &lt;i>p&lt;/i> = 0.029). This association persisted after adjusting for age and sex (HR 0.479, 95%CI 0.235-0.977, &lt;i>p&lt;/i> = 0.043) and after additional adjustment for eGFR, NT-proBNP, LVEF, and concomitant therapy with tafamidis (HR 0.328, 95%CI 0.141-0.760, &lt;i>p&lt;/i> = 0.009). However, when potential immortal time bias was considered, this association lost statistical significance (HR 1.075, 95%CI 0.524-2.206, &lt;i>p&lt;/i> = 0.843). No significant associations between SGLT2i therapy and worsening heart-failure hospitalization or cardiovascular mortality were observed. &lt;b>Conclusions:&lt;/b> In crude analysis, SGLT2i therapy associates with better survival in patients with ATTR-CM. However, after adjustment for immortal time, this association becomes statistically insignificant. Hence, to draw final conclusions on the effectiveness of SGLT2i therapy in these patients, a randomized controlled trial is warranted.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2025-04-26T07:57:26.063Z</modification><creation>2025-04-06T12:31:12.128Z</creation></dates><accession>S-EPMC11477643</accession><cross_references><pubmed>39408026</pubmed><doi>10.3390/jcm13195966</doi></cross_references></HashMap>