在因主动脉瓣狭窄而进行瓣膜置换术切除的主动脉瓣中,隐匿性转甲状腺素和脂蛋白AI型淀粉样蛋白的出现频率很高。

IF 5.2 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kohei Honda, Masayoshi Tasaki, Tetsuhiro Yamano, Mitsuharu Ueda, Hironobu Naiki, Noriyuki Tanaka, Yukiko Morinaga, Aya Miyagawa-Hayashino
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引用次数: 0

摘要

背景:据报道,主动脉瓣狭窄(AS)患者瓣膜受淀粉样蛋白影响的发生率很高。由载脂蛋白AI(AApoAI)衍生的淀粉样蛋白可在主动脉瓣形成局部淀粉样沉积。尽管有报道称严重的主动脉瓣狭窄和心脏转甲状腺素型淀粉样变性(ATTR)并发症的发病率很高,但ATTR和载脂蛋白AApoAI累及瓣膜的发病率尚不清楚:方法:我们使用免疫染色法和质谱法分析了 2014 年至 2021 年期间京都府立医科大学因 AS 而进行瓣膜置换术的 97 个主动脉瓣中的淀粉样蛋白。同时还回顾了临床信息:44例(45%)发现淀粉样沉积物,其中30例(68%)涉及ATTR,33例(75%)涉及AApoAI。统计分析显示,与淀粉样蛋白阴性病例相比,淀粉样蛋白阳性病例的年龄和E/e'明显较低;与ATTR阴性病例相比,ATTR阳性病例的脑钠肽明显较低、骨折缩短率较高,左心室射血分数较高。最近有七名患者接受了骨闪烁成像检查,只有一例患者观察到了ATTR心肌病:结论:主动脉瓣内有淀粉样蛋白或ATTR沉积的患者,即使左心室功能保持不变,其强直性脊柱炎症状的表现也会早于无淀粉样蛋白或ATTR沉积的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High frequency of occult transthyretin and apolipoprotein AI-type amyloid in aortic valves removed by valve replacement for aortic stenosis.

Background: A high incidence of valvular involvement of amyloid in the setting of aortic stenosis (AS) has been reported. Amyloid derived from ApoAI (AApoAI) can form local amyloid deposits in the aortic valve. Although a high prevalence of concomitant severe AS and cardiac transthyretin-type amyloidosis (ATTR) has been reported, the prevalence of valvular involvement by ATTR and AApoAI is unclear.

Methods: Using immunostaining and mass spectrometry, we analysed amyloid proteins in 97 aortic valves removed for valve replacement due to AS at Kyoto Prefectural University of Medicine between 2014 and 2021. Clinical information was also reviewed.

Results: Amyloid deposits were found in 44 cases (45%), of which 30 cases (68%) involved ATTR and 33 cases (75%) AApoAI. Statistical analysis showed significantly lower age and E/e' among amyloid-positive cases compared with amyloid-negative cases and significantly lower brain natriuretic peptide, higher fractional shortening, and higher left ventricular ejection fraction among ATTR-positive cases compared with ATTR-negative cases. Seven recent patients underwent bone scintigraphy and ATTR cardiomyopathy was observed in only one case.

Conclusions: AS symptoms can manifest earlier in patients with amyloid or ATTR deposition in the aortic valve than in patients without such deposition, even though left ventricular function is preserved.

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来源期刊
Amyloid-Journal of Protein Folding Disorders
Amyloid-Journal of Protein Folding Disorders 生物-生化与分子生物学
CiteScore
10.60
自引率
10.90%
发文量
48
审稿时长
6-12 weeks
期刊介绍: Amyloid: the Journal of Protein Folding Disorders is dedicated to the study of all aspects of the protein groups and associated disorders that are classified as the amyloidoses as well as other disorders associated with abnormal protein folding. The journals major focus points are: etiology, pathogenesis, histopathology, chemical structure, nature of fibrillogenesis; whilst also publishing papers on the basic and chemical genetic aspects of many of these disorders. Amyloid is recognised as one of the leading publications on amyloid protein classifications and the associated disorders, as well as clinical studies on all aspects of amyloid related neurodegenerative diseases and major clinical studies on inherited amyloidosis, especially those related to transthyretin. The Journal also publishes book reviews, meeting reports, editorials, thesis abstracts, review articles and symposia in the various areas listed above.
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