SYGNAL is built on a robust scientific foundation. Here you find MYCOR's own research and the key publications establishing the clinical context and unmet medical need.
Mahabadi AA, Knobeloch J, Backmann V, Michel L, Anker MS, Wakili R, Fach C, Anker SD, Rassaf T
ESC Heart Failure · 2025 · 12(4):2993–3002
We developed and validated a non-invasive screening tool for cardiac amyloidosis based on structured evaluation of three-dimensional ECGs. An AI algorithm was trained in a derivation cohort (n=66 amyloidosis cases, n=89 controls) and validated in an independent cohort (n=33 amyloidosis, n=67 controls). In the derivation cohort the algorithm achieved 85% sensitivity, 89% specificity, 91% PPV, and 87% NPV. In the independent validation cohort: 79% sensitivity, 82% specificity, 61% PPV, and 92% NPV — enabling reliable, non-invasive detection of cardiac amyloidosis from a standard ECG.
MYCOR Research Team · Universitätsklinikum Essen · Goethe-Universität Frankfurt
In preparation — target submission 2025/2026
Multi-center clinical validation of the SYGNAL algorithm for non-invasive cardiac amyloidosis screening in high-risk cohorts (HFpEF, TAVI). Primary endpoints: sensitivity, specificity, and diagnostic yield versus standard clinical workup.
Peer-reviewed publications establishing the scientific foundation of SYGNAL
Maurer MS, Schwartz JH, Gundapaneni B, et al.
New England Journal of Medicine · 2018 · 379:1007–1016
33% reduction in all-cause mortality, 32% reduction in hospitalizations (n=441)
Landmark ATTR-ACT trial establishing tafamidis as first ATTR therapy — underscoring the need for earlier diagnosis.
DOI: 10.1056/NEJMoa1805689Solomon SD, Vaduganathan M, Claggett BL, et al.
New England Journal of Medicine · 2024 · 391:1845–1855
28% risk reduction for death and CV events over 3.5 years (n=655)
HELIOS-B trial — supported EU approval of Vutrisiran for ATTR-CM (June 2025).
DOI: 10.1056/NEJMoa2409134Gillmore JD, Maurer MS, Falk RH, et al.
Circulation · 2016 · 133:2404–2412
Established the non-invasive diagnostic algorithm using ⁹⁹mTc-DPD scintigraphy + SPEP/FLC
Defining framework for non-invasive ATTR-CM diagnosis — the clinical standard SYGNAL is designed to complement.
DOI: 10.1161/CIRCULATIONAHA.116.021612Bhuiyan T, Helmke S, Patel AR, et al.
JACC: Heart Failure · 2018 · 6:781–790
Up to 13% of HFpEF patients >60 have ATTRwt — vastly underdiagnosed
Key epidemiology data establishing the magnitude of the undiagnosed ATTR-CM population in routine cardiology.
DOI: 10.1016/j.jchf.2018.05.020Nitsche C, Scully PR, Patel KP, et al.
Journal of the American College of Cardiology · 2021 · 77:128–139
ATTR-CM found in up to 16% of TAVI patients — most previously undiagnosed
Defines the TAVI population as a high-priority screening target for SYGNAL deployment.
DOI: 10.1016/j.jacc.2020.11.006Bishop C, Coelho-Filho OR, Shah RV, et al.
ESC Heart Failure · 2022 · 9:2491–2500
Delay >1 year correlates with higher NT-proBNP, PR prolongation, and conduction disorders
Quantifies the clinical cost of diagnostic delay — the exact problem SYGNAL is designed to solve.
DOI: 10.1002/ehf2.13986Witteles RM, Bokhari S, Damy T, et al.
JACC: Heart Failure · 2019 · 7:709–716
Systematic screening algorithms can 8-fold increase ATTR-CM detection rates
Establishes proof-of-concept for systematic ATTR-CM screening — validating SYGNAL's approach.
DOI: 10.1016/j.jchf.2019.04.010