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Disease progression in cardiac transthyretin amyloidosis is indicated by serial calculation of National Amyloidosis Centre transthyretin amyloidosis stage

机译:疾病进展心脏ransthyretin淀粉样蛋白腺苷病的序列式淀粉蛋白淀粉样蛋白腺苷病阶段的连续计算表明

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摘要

Abstract Aims Cardiac transthyretin amyloidosis (ATTR‐CM) is a progressive and fatal condition. Prognosis can be determined at diagnosis according to the National Amyloidosis Centre (NAC) transthyretin amyloidosis (ATTR) stage. We sought to examine how NAC ATTR stage changes during follow‐up and whether it maintains its prognostic value throughout the disease course. Methods and results We performed a retrospective study of 945 patients with wild‐type ATTR‐CM (wtATTR‐CM) or hereditary ATTR‐CM associated with the V122I variant (V122I‐hATTR‐CM) who were diagnosed and serially evaluated at the UK NAC. Patients who commenced any disease‐modifying therapy for amyloidosis were censored at the time of doing so. Landmark Kaplan–Meier survival analyses were performed at diagnosis (n = 945) and at 6 ± 1 (n = 432), 12 ± 3 (n = 562), and 24 ± 3 (n = 316) months and stratified by recalculated NAC ATTR stage at the relevant time point. Cox regression analyses were performed to assess the prognostic significance during follow‐up of an increase in NAC ATTR stage from Stage I at diagnosis. Mortality in ATTR‐CM was predicted by NAC ATTR stage at each time point [Stage II vs. I, hazard ratios (HRs) 1.95–2.67; P < 0.001; Stage III vs. II, HRs 1.64–2.25; P < 0.001–0.013]. An increase from NAC ATTR Stage I, which occurred in 21%, 32%, and 44% of evaluable patients at 6, 12, and 24 months of follow‐up respectively, was highly predictive of ongoing mortality at each time point (HRs 2.58–3.22; P < 0.001) and in each genotypic subgroup (HRs 1.86–4.38; P < 0.05). Increase in NAC ATTR stage occurred earlier in V122I‐hATTR‐CM than in wtATTR‐CM (43% vs. 27% at 12 months of follow‐up; P = 0.003). Conclusions National Amyloidosis Centre ATTR stage predicts ongoing survival throughout the disease natural history in ATTR‐CM, and an increase from NAC ATTR Stage I at diagnosis to a higher NAC ATTR stage predicts mortality throughout follow‐up. Serial calculation of NAC ATTR stage suggests a more aggressive phenotype in V122I‐hATTR‐CM than in wtATTR‐CM.
机译:摘要AIMS心脏Transthyretin淀粉样蛋白症(attr-cm)是一种渐进性和致命的病症。根据国家淀粉样蛋白病中心(NAC)Transthyretin淀粉样蛋白症(attr)阶段,可以在诊断中确定预后。我们试图检查Nac attr阶段在随访期间如何变化,以及它是否在整个疾病过程中保持其预后价值。方法和结果我们对945例野生型attr-cm(WTATTR-cm)或遗传attr-cm进行了回顾性研究,与V122i变体(v122i-hatt-cm)诊断并在英国NAC诊断出来。在这样做时,开始对淀粉样症的任何疾病改性治疗的患者被审查。地标Kaplan-Meier存活分析在诊断(n = 945)和6±1(n = 432),12±3(n = 562),24±3(n = 316)个月,并通过重新计算的NAC分层attr阶段在相关的时间点。进行COX回归分析以评估从IS诊断阶段I阶段的NAC attr阶段的随访期间的预后显着性。在每个时间点的NAC attr阶段预测attr-cm的死亡率[阶段II与I,危险比(HRS)1.95-2.67; P <0.001; III阶段与II,HRS 1.64-2.25; P <0.001-0.013]。 NACattr阶段I的增加,其中21%,32%和44%的可评估患者分别在6,12和24个月的后续随访中,在每个时间点的持续死亡率高度预测(HRS 2.58 -3.22; p <0.001)和每个基因型亚组(HRS 1.86-4.38; P <0.05)。 NAC attr阶段的增加在V122I-Hattr-cm之前发生比WTATTR-CM(在12个月后的43%与27%的后续行动; P = 0.003)。结论国家淀粉样症中心attr阶段预测整个疾病自然历史的持续生存,从Nac attr阶段I增加诊断到更高的Nac attr阶段预测整个随访的死亡率。 NAC attr阶段的连续计算表明V122i-Hattr-cm中的侵略性表型比WTATTR-CM在。

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