冰岛的ATTR心脏淀粉样变性:一项全国性的流行病学研究。

IF 1.9 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Cardiology Pub Date : 2025-01-24 DOI:10.1159/000543750
Hekla María Bergmann, Ævar Örn Úlfarsson, Hafsteinn Einarsson, Helena Xiang Jóhannsdóttir, Gunnar Thór Gunnarsson, Thórdís Jóna Hrafnkelsdóttir, Karl Andersen, Inga Jóna Ingimarsdóttir
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引用次数: 0

摘要

心脏淀粉样变性(CA)是由错误折叠的淀粉样蛋白沉积在心脏细胞外基质中引起的,可导致严重的心脏疾病。最近的数据表明,CA未被充分认识,治疗的进步增加了对这种疾病的关注,目的是尽早实施治疗以改善预后。关于甲状腺素转甲状腺素CA (atr -CA)在国家层面的流行情况,特别是在冰岛,了解有限。因此,这项研究代表了冰岛首次在全国范围内评估atr - ca的基线特征、诊断和治疗。方法:在冰岛雷克雅未克Landspitali大学医院心力衰竭(HF)专家于2023年创建的冰岛心脏淀粉样蛋白登记处(ICE-CAR)中,对2013年5月6日至2024年3月11日在冰岛诊断为atr - ca的所有患者进行回顾性研究。诊断是基于经胸超声心动图的不同组合,骨显像和心脏活检的升高的Perugini评分,以及自由轻链的测量,血液和尿液中的m成分测量。根据国家淀粉样变中心(NAC) atr - ca的预后分期系统对患者进行分组。结果:共发现atr - ca患者65例(男性60例,女性5例,中位年龄81.4岁[IQR 75.5-85.5岁]),均为野生型,无突变型。7例经心肌活检确诊。诊断时,83%的患者室间隔厚度≥15mm, 92%的患者后壁厚度≥12mm。大约57%的患者属于纽约心脏协会(NYHA)功能等级I-II。根据左室射血分数(LVEF), HF表型分布如下:降低(HFrEF) n = 24(37%),轻度降低(HFmrEF) n = 9(14%),保存(HFpEF) n = 29(44.5%),未知LVEF n = 3(4.5%)。共有54例患者报告了NAC分期:I期23例(35.4%),II期20例(30.8%),III期11例(16.9%)。约32%的患者接受了疾病改善治疗。结论:尽管在研究人群中观察到较低的NYHA等级,但我们在冰岛全国范围内对atr - ca的评估中发现,与其他研究相比,诊断时年龄更大,LVEF更低。这突出了早期发现和适当治疗干预治疗atr - ca的迫切需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unravelling ATTR Cardiac Amyloidosis in Iceland: A Nationwide Epidemiological Study.

Introduction: Cardiac amyloidosis (CA) arises from the deposition of misfolded amyloid proteins in the heart's extracellular matrix, leading to significant cardiac disease. Recent data suggest that CA is under-recognised, and advances in treatment have increased focus on this condition with the intention of implementing treatment earlier to improve prognosis. There is limited knowledge regarding the prevalence of transthyretin CA (ATTR-CA) on a national level, particularly in Iceland. Therefore, this study represents the first nationwide effort to evaluate the baseline characteristics, diagnostics, and treatment of ATTR-CA in Iceland.

Methods: A retrospective study of all patients diagnosed with ATTR-CA in Iceland from 6 May 2013 to 11 March 2024 was identified in the Icelandic Cardiac Amyloid Registry (ICE-CAR) created in 2023 by heart failure (HF) specialists at Landspitali University Hospital in Reykjavik, Iceland. Diagnosis was based on different combinations of transthoracic echocardiography, an elevated Perugini score on bone scintigraphy and heart biopsies, as well measurements of free light chains, M-component measurements in blood and urine. Patients were grouped according to the National Amyloidosis Centre (NAC) prognostic staging system for ATTR-CA.

Results: In total, 65 patients with ATTR-CA were identified (males n = 60, females n = 5, median age 81.4 years [IQR 75.5-85.5 years]), all wild-type and no mutant variant. Diagnosis was made with myocardial biopsy in 7 cases. Upon diagnosis, 83% of the patients had an interventricular septum thickness of ≥15 mm and 92% showed a posterior wall thickness of ≥12 mm. Approximately 57% of patients belonged to New York Heart Association (NYHA) functional class I-II. The HF phenotypes according to left ventricular ejection fraction (LVEF) were distributed as follows: reduced (HFrEF) n = 24 (37%), mildly reduced (HFmrEF) n = 9 (14%), preserved (HFpEF) n = 29 (44.5%), and unknown LVEF n = 3 (4.5%). A total of 54 patients had reported NAC stage: stage I 23 (35.4%), stage II 20 (30.8%), stage III 11 (16.9%). Around 32% received disease-modifying treatment.

Conclusion: Despite the low NYHA class observed in the study population, our findings in Iceland's nationwide assessment of ATTR-CA indicate more advanced age and lower LVEF at diagnosis compared to other studies. This highlights the critical need for early detection and appropriate therapeutic interventions in managing ATTR-CA.

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来源期刊
Cardiology
Cardiology 医学-心血管系统
CiteScore
3.40
自引率
5.30%
发文量
56
审稿时长
1.5 months
期刊介绍: ''Cardiology'' features first reports on original clinical, preclinical and fundamental research as well as ''Novel Insights from Clinical Experience'' and topical comprehensive reviews in selected areas of cardiovascular disease. ''Editorial Comments'' provide a critical but positive evaluation of a recent article. Papers not only describe but offer critical appraisals of new developments in non-invasive and invasive diagnostic methods and in pharmacologic, nutritional and mechanical/surgical therapies. Readers are thus kept informed of current strategies in the prevention, recognition and treatment of heart disease. Special sections in a variety of subspecialty areas reinforce the journal''s value as a complete record of recent progress for all cardiologists, internists, cardiac surgeons, clinical physiologists, pharmacologists and professionals in other areas of medicine interested in current activity in cardiovascular diseases.
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