Development and Validation of Staging Systems for AA Amyloidosis

医学 淀粉样变性 利钠肽 队列 内科学 胃肠病学 蛋白尿 肾脏疾病 淀粉样变性 泌尿科 心力衰竭 免疫学 抗体 免疫球蛋白轻链
作者
Marco Basset,Stefan Schönland,Laura Obici,Janine Günther,Eloísa Riva,Tobias Dittrich,Paolo Milani,Virginia Valeria Ferretti,Ettore Pasquinucci,Andrea Foli,Christoph Kimmich,Martina Nanci,Claudia Bellofiore,Francesca Benigna,Jörg Beimler,Pietro Benvenuti,F Fabris,Roberta Mussinelli,Mario Nuvolone,Catherine Klersy
出处
期刊:Journal of The American Society of Nephrology 卷期号:35 (6): 782-794 被引量:4
标识
DOI:10.1681/asn.0000000000000339
摘要

Key Points Patients with AA amyloidosis and age ≥65 years, eGFR <45 ml/min per 1.73 m 2 , and N -terminal type-B natriuretic peptide >1000 ng/L and/or type-B natriuretic peptide >130 ng/L at diagnosis have poorer survival. Proteinuria >3.0 g/24 hours and eGFR <35 ml/min per 1.73 m 2 identify patients at high risk of progression to end-stage kidney failure. Prognostic stratification in AA amyloidosis can be easily made by staging systems, similarly to AL and transthyretin amyloidosis. Background The kidney is involved in almost 100% of cases of AA amyloidosis, a rare disease caused by persistent inflammation with long overall survival but frequent progression to kidney failure. Identification of patients with advanced disease at diagnosis is difficult, given the absence of validated staging systems. Methods Patients with newly diagnosed AA amyloidosis from the Pavia ( n =233, testing cohort) and Heidelberg ( n =243, validation cohort) centers were included in this study. Cutoffs of continuous variables were determined by receiver operating characteristic analysis predicting death or dialysis at 24 months. Prognostic factors included in staging systems were identified by multivariable models in the testing cohort. Results Age ≥65 years, eGFR <45 ml/min per 1.73 m 2 , and elevated natriuretic peptides (type-B natriuretic peptide >130 ng/L and/or N -terminal type-B natriuretic peptide >1000 ng/L) were associated with overall survival and included in the staging system (all with simplified coefficients 1). Mean 36-month overall survival was lower with higher staging system scores (score 0–1: 92%; score 2: 72%; score 3: 32%). These results were confirmed in the validation cohort. For kidney failure, variables selected to enter in the staging system model were proteinuria >3 g/24 hour and eGFR <35 ml/min per 1.73 m 2 (both with simplified coefficients 1). The 36-month cumulative incidence of kidney failure was higher with higher staging system scores (score 0: 0%; score 1: 24%; score 2: 51%). Again, similar results were obtained in validation cohort. Conclusions We identified and validated biomarker-based staging systems for overall survival and kidney failure in AA amyloidosis.
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