posted on 2022-09-09, 15:13authored byAlfredo De Giorgi, Alberto Maria Marra, Massimo Iacoviello, Vincenzo Triggiani, Giuseppe Rengo, Francesco Cacciatore, Ciro Maiello, Giuseppe Limongelli, Daniele Masarone, Francesco Perticone, Pasquale Perrone Filardi, Stefania Paolillo, Antonio Mancini, Maurizio Volterrani, Olga Vriz, Roberto Castello, Andrea Passantino, Michela Campo, Pietro Amedeo Modesti, Andrea Salzano, Roberta D’Assante, Michele Arcopinto, Valeria Raparelli, Fabio Fabbian, Angela Sciacqua, Annamaria Colao, Toru Suzuki, Eduardo Bossone, Antonio Cittadini, L Saccà, MG Monti, R Napoli, M Matarazzo, FM Stagnaro, A Schiavo, P Valente, F Ferrara, V Russo, M Malinconico, R Citro, E Guastalamacchia, M Leone, C Amarelli, I Mattucci, P Calabrò, R Calabrò, A D’Andrea, V Maddaloni, G Pacileo, R Scarafile, A Belfiore, A Cimellaro, L Casaretti, P Gargiulo, AMR Favuzzi, C Di Segni, C Bruno, E Vergani, A Frigo, MR Sorrentino, D Malandrino, R Manfredini, A Puzzo, L Ragusa, L Caliendo, L Carbone, A Frigiola, T Generali, F Giacomazzi, C De Vincentiis, A Ballotta, P Garofalo, G Malizia, Liam HeaneyLiam Heaney, D Bruzzese
<p>Introduction Data from the “Trattamento Ormonale nello Scompenso CArdiaco” (T.O.S.CA) registry showed that heart failure (HF) represents a complex clinical syndrome with different hormonal alterations. Renal failure represents a frequent complication in HF. We evaluated the relationship between renal function and insuline-like growth factor-1 (IGF-1) deficiency and its impact on cardiovascular mortality (CVM) in patients enrolled in the T.O.S.CA. registry. Methods At the enrolment, all subjects underwent chemistry examinations, including circulating hormones and cardiovascular functional tests. COX regression analysis was used to evaluate factors related to CVM during the follow-up period in all populations, in high-risk patients and in the young-adult population. Also, we evaluate the effects of renal function on the CVM. Results 337 patients (41 deceased) were analyzed. CVM was related to severe renal dysfunction (HR stages IV–V = 4.86), high-risk conditions (HR 2.25), serum IGF-1 (HR 0.42), and HF etiology (HR 5.85 and HR 1.63 for valvular and ischemic etiology, respectively). In high-risk patients, CVM was related to IGF-1 levels, severe renal dysfunction and valvular etiology, whereas in young patients CMV was related to the high-risk pattern and serum IGF-1 levels. Conclusions Our study showed the clinical and prognostic utility of the IGF-1 assay in patients with HF.</p>
This is an Open Access Article. It is published by Springer under the Creative Commons Attribution 4.0 International Licence (CC BY 4.0). Full details of this licence are available at: https://creativecommons.org/licenses/by/4.0/