<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(4)</volume><submitter>Santoro F</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Neurological disorders as a risk factor for Takotsubo syndrome (TTS) are not well characterized. The aim of the study was to evaluate TTS-associated neurological phenotypes and outcome.&lt;h4>Methods and results&lt;/h4>Patients with TTS enrolled in the international multicenter GEIST (German Italian Spanish Takotsubo) registry were analyzed. Prevalence, clinical characteristics, and short- and long-term outcomes of patients with TTS were recorded. A subgroup analysis of the 5 most represented neurological disorders was performed. In total, 400 (17%) of 2301 patients had neurological disorders. The most represented neurological conditions were previous cerebrovascular events (39%), followed by neurodegenerative disorders (30.7%), migraine (10%), epilepsy (9.5%), and brain tumor</pubmed_abstract><journal>Journal of the American Heart Association</journal><pagination>e032128</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11010100</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Neurological Disorders in Takotsubo Syndrome: Clinical Phenotypes and Outcomes.</pubmed_title><pmcid>PMC11010100</pmcid><pubmed_authors>Stiermaier T</pubmed_authors><pubmed_authors>Brunetti ND</pubmed_authors><pubmed_authors>Thiele H</pubmed_authors><pubmed_authors>Eitel I</pubmed_authors><pubmed_authors>Montisci R</pubmed_authors><pubmed_authors>Bartolomucci F</pubmed_authors><pubmed_authors>Vitale E</pubmed_authors><pubmed_authors>Guerra F</pubmed_authors><pubmed_authors>Akin I</pubmed_authors><pubmed_authors>Mariano E</pubmed_authors><pubmed_authors>Blanco E</pubmed_authors><pubmed_authors>El-Battrawy I</pubmed_authors><pubmed_authors>Caldarola P</pubmed_authors><pubmed_authors>Vedia O</pubmed_authors><pubmed_authors>Salamanca J</pubmed_authors><pubmed_authors>Novo G</pubmed_authors><pubmed_authors>Perez-Castellanos A</pubmed_authors><pubmed_authors>Santoro F</pubmed_authors><pubmed_authors>Cetera R</pubmed_authors><pubmed_authors>Martin A</pubmed_authors><pubmed_authors>Pais JL</pubmed_authors><pubmed_authors>Martino T</pubmed_authors><pubmed_authors>Ragnatela I</pubmed_authors><pubmed_authors>Musumeci B</pubmed_authors><pubmed_authors>Nunez Gil IJ</pubmed_authors><pubmed_authors>Cacciotti L</pubmed_authors><pubmed_authors>Arcari L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Neurological Disorders in Takotsubo Syndrome: Clinical Phenotypes and Outcomes.</name><description>&lt;h4>Background&lt;/h4>Neurological disorders as a risk factor for Takotsubo syndrome (TTS) are not well characterized. The aim of the study was to evaluate TTS-associated neurological phenotypes and outcome.&lt;h4>Methods and results&lt;/h4>Patients with TTS enrolled in the international multicenter GEIST (German Italian Spanish Takotsubo) registry were analyzed. Prevalence, clinical characteristics, and short- and long-term outcomes of patients with TTS were recorded. A subgroup analysis of the 5 most represented neurological disorders was performed. In total, 400 (17%) of 2301 patients had neurological disorders. The most represented neurological conditions were previous cerebrovascular events (39%), followed by neurodegenerative disorders (30.7%), migraine (10%), epilepsy (9.5%), and brain tumor</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-04-06T23:15:03.975Z</modification><creation>2025-04-06T23:15:03.975Z</creation></dates><accession>S-EPMC11010100</accession><cross_references><pubmed>38353238</pubmed><doi>10.1161/JAHA.123.032128</doi></cross_references></HashMap>