Guaraldi Pietro, Allegri Isabella, Ariatti Alessandra, Baldini Tommaso, Barbieri Andrea, Barocelli Federico, Bartolotti Michela, Biagini Elena, Bianchi Francesca, Borghi Annamaria, Borghi Claudia, Boriani Giuseppe, Cani Ilaria, Carigi Samuela, Codeluppi Luca, Currò Dossi Marco, Dalpozzo Francesca, D'Angelo Roberto, De Gennaro Riccardo, Di Spigno Francesco, Gardini Elisa, Lanati Gianluca, Leuzzi Chiara, Marzo Francesca, Masullo Marco, Mazzanti Gaia, Merli Elisa, Milandri Agnese, Monari Dennis, Perugini Enrica, Ponziani Alberto, Postiglione Emanuela, Rasia Marta, Rinaldi Rita, Scancarello Davide, Serafini Kevin, Serenelli Matteo, Sguazzotti Maurizio, Siena Ernesto, Simone Anna Maria, Terracciano Chiara, Valenti Chiara, Vitale Giovanni, Vitiello Maria, Longhi Simone
IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Department of Neurology, University Hospital of Parma, Parma, Italy.
Front Neurol. 2025 Aug 29;16:1666318. doi: 10.3389/fneur.2025.1666318. eCollection 2025.
Transthyretin amyloidosis (ATTR) is a rare disease caused by the extracellular accumulation of misfolded transthyretin (TTR) amyloid fibrils. ATTR can be either hereditary (ATTRv) or acquired (wtATTR). ATTRv is caused by a mutation in the transthyretin gene (TTR) with an autosomal dominant pattern of inheritance. In ATTRv amyloidosis, some patients primarily exhibit symptoms of polyneuropathy others mainly or exclusively present with symptoms of cardiomyopathy. However, many patients present with a multisystemic involvement that includes sensory, motor, autonomic, and cardiac symptoms. Early diagnosis and detection of disease progression are emerging as a crucial need for ATTR amyloidosis in order to significantly impact survival, patients' functions and quality of life. Currently, parameters to be monitored in ATTR patients in the real life might refer to some publicly available recommendations regarding the monitoring and assessment of disease progression in the real-world setting of patients with ATTRv. Nonetheless, a standardized disease monitoring protocol has not been established in Italy, posing a significant unmet need for a prompt and equal access to care. Therefore, in the Emilia-Romagna Region the "ATTR Working Group" has sought to tailor the recommendations to the Regional "real clinical setting" in order to optimize and standardize a monitoring protocol aimed at identifying disease progression. Patients' and carriers' access to uniform monitoring routes across the entire Region ensures optimal disease management and economic sustainability.
转甲状腺素蛋白淀粉样变性(ATTR)是一种罕见疾病,由错误折叠的转甲状腺素蛋白(TTR)淀粉样原纤维在细胞外积聚所致。ATTR可分为遗传性(ATTRv)或获得性(野生型ATTR,wtATTR)。ATTRv由转甲状腺素蛋白基因(TTR)突变引起,呈常染色体显性遗传模式。在ATTRv淀粉样变性中,一些患者主要表现为多发性神经病症状,另一些患者主要或仅表现为心肌病症状。然而,许多患者表现为多系统受累,包括感觉、运动、自主神经和心脏症状。早期诊断和疾病进展检测正成为ATTR淀粉样变性的关键需求,以便显著影响生存率、患者功能和生活质量。目前,现实生活中ATTR患者需要监测的参数可能参考一些关于在ATTRv患者现实世界环境中监测和评估疾病进展的公开可用建议。尽管如此,意大利尚未建立标准化的疾病监测方案,这对及时、平等获得医疗护理造成了重大需求缺口。因此,在艾米利亚 - 罗马涅大区,“ATTR工作组”试图根据地区“实际临床情况”调整建议,以优化和标准化旨在识别疾病进展的监测方案。患者和携带者在整个大区获得统一的监测途径可确保最佳的疾病管理和经济可持续性。