Nerea Mora-Ayestaran
@NereMA
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Inherited Cardiac Diseases and Genetics.
Astigarraga, España
Joined January 2012
Rafael Sádaba, jefe del Servicio de Cirugía Cardíaca del HUN, nombrado presidente de la sociedad europea de su especialidad
diariodenavarra.es
Desempeñaba hasta ahora el cargo de vicepresidente de la European Association for Cardio-Thoracic Surgery (EACTS)
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Sex Differences in Prognosis of Patients with Genetic Dilated Cardiomyopathy @JonesLab_KUL @neallakdawala @Dr_Pavia @_antocannata
@fernidom @raafs_anne @jpocardio @NereMA @SikkingM @martijn_hoes #AHAJournals
https://t.co/WULgBOXmDD
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📰 Los genes asociados a muerte súbita elevan el riesgo de insuficiencia cardíaca en pacientes con miocardiopatía dilatada genética. Un nuevo estudio en el que ha participado nuestro compañero @jpocardio, ha demostrado que algunas alteraciones genéticas asociadas a la
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⏰ Just days left! Global leaders & KOLs live on HCM, amyloidosis & Fabry. In a few years you’ll ask why you missed this congress😉#HCM #Amyloidosis #Fabry
🗣️LATE-BREAKING NEWS: 🎥 VIRTUAL TICKETS NOW AVAILABLE!!! – join LIVE or ON DEMAND! 👉 Register today! https://t.co/jZZFnU2BRq 👉Don’t miss the 2025 HCM A CORUÑA meeting!🇪🇸 💡 Latest updates on HCM, Amyloidosis & Fabry Disease with leading experts 🇪🇺🇺🇸🇦🇷🇦🇺🇬🇧🇲🇽
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Teamwork made this study possible 🙌 Thanks to all my co-authors 👥 @esthglez @fernidom @cleaglez21 and especially to @dr_pavia for leading the project 👨⚕️🧬
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📖 Full open-access article in JACC: CardioOncology @JACCJournals: 👉 https://t.co/fH3HKhEiWx
jacc.org
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💡 Take-home message: Systematic cascade genetic screening in ATTRv families: 🧬 Identifies a median of 2 carriers per proband ❤️ Enables earlier diagnosis & treatment 👨👩👧 Provides counselling, reproductive planning & support
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⚠️ Still, 1 in 3 relatives did not undergo genetic screening. Independent predictors of absence of testing: 👴 Older age 🌍 Living in a different province/country 🧑 Male sex 👨👩👦 Distant family relationship We must bridge these gaps.
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⏱️ Earlier diagnosis & treatment Affected relatives were diagnosed and started disease-modifying therapy ~10 years earlier than probands (53 vs 66 years and 56.5 vs 66 years, both p<0.001). 📈🧬❤️ Timing matters!
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📊 Study population (2010–2023, @cardiopdh): 👨👩👧 749 at-risk relatives from 86 families 🧬464 relatives studied (5/family) 👉263 non-carriers discharged 👉201 carriers (2/family) 🧬 🔹134 healthy genetic carriers (🧬🤰 in 7 relatives) 🔹67 (33%) with ATTRv manifestations(❤️🧠👁️)
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🚨 Excited to share our latest work! “Impact of Genetic Testing & Family Screening in Hereditary Transthyretin Amyloidosis” 🧬❤️ Cascade genetic screening in ATTRv families 👨👩👧 enables earlier diagnosis, treatment & counselling. Here’s what we found 👇🧵
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.@CNIC_CARDIO Genes linked to sudden cardiac death increase the risk of heart failure in patients with genetic dilated cardiomyopathy https://t.co/FIHJSTbEvb
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Myocardial News Special Episode for the ESC 2025 congress is now available! #CardioTwitter #ESC2025
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#ESCCongress | time to put the badge down! This was a special one 💛Madrid 🇪🇸 was 🔝 set and it was great to host my 🇵🇹 friends So many 🔝 points: my #SoMe ambassador role, our unit @cardiopdh on 🔥 with 🔝 science and major #LBT! Great networking with mentors and friends 💛❤️
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Arrhythmic genotypes in dilated cardiomyopathy and risk of advanced heart failure. Discover more in #EHJ
#ESCCongress @escardio @ESC_Journals #genetics #heartfailure
https://t.co/GZJqFceyl7
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🚨 Live from #ESCCongress + now online in @CircAHA 🚨 https://t.co/KPsILAhJVT Honored to present our work on Intermediate-Effect Variants (IEVs) in HCM, selected for the Young Investigator Award. 🏆 60% of HCM cases G (-). Maybe we’ve been looking in the wrong place… 👇🧵
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I am very grateful to all my mentors @dr_pavia @esthglez @fernidom @jpocardio and to all the fellows who shared this journey with me @peiro_belen @Eva_Ce_Erre @fdefrutossemi @MSBBrandao #Dani #Clea
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