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非心脏活检诊断转甲状腺素蛋白心脏淀粉样变性的阳性率。

Yield of noncardiac biopsy for the diagnosis of transthyretin cardiac amyloidosis.

机构信息

Division of Cardiovascular Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota.

Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.

出版信息

Am J Cardiol. 2014 May 15;113(10):1723-7. doi: 10.1016/j.amjcard.2014.02.030. Epub 2014 Mar 2.

Abstract

Transthyretin (ATTR) cardiac amyloidosis may be because of mutant transthyretin causing familial amyloid cardiomyopathy (FAC) or wild-type transthyretin causing systemic senile amyloidosis (SSA). Histologic confirmation is often challenging and may require endomyocardial biopsy (EMB). The purpose of this study was to determine the frequency of amyloid protein deposition in positive noncardiac organ biopsy or fat aspiration in patients with ATTR cardiac amyloidosis. The medical records of 286 patients (mean age 66 ± 11, 85% men) with a diagnosis of ATTR cardiac amyloidosis at our institution who underwent noncardiac biopsy or subcutaneous fat aspiration were reviewed, including 186 patients (65%) with FAC and 100 patients (35%) with SSA. One hundred and thirty-one patients (46%) had EMB, all of which were positive. There were 210 patients (73%) with positive noncardiac tissue sampling, including 175 patients (94%) with FAC and 35 patients (35%) with SSA (p <0.001). There were 141 patients (76%) with FAC and 84 patients (84%) with SSA who underwent fat aspiration, and 67% and 14% were positive, respectively, whereas 100 (54%) and 64 (64%) underwent bone marrow biopsy, and 41% and 30% were positive, respectively. Rectal and sural nerve biopsies were performed in 52 (28%) and 54 (29%) patients with FAC and were positive in 81% and 83%, respectively. Biopsy of other noncardiac sites was performed with relatively lower frequency. In conclusion, although EMB is more commonly required to establish the diagnosis of SSA than FAC, noncardiac biopsy or fat aspiration could be considered as initial testing in patients evaluated for ATTR cardiac amyloidosis with characteristic echocardiography findings.

摘要

转甲状腺素蛋白(ATTR)心脏淀粉样变可能是由于突变转甲状腺素蛋白导致家族性淀粉样心肌病(FAC)或野生型转甲状腺素蛋白导致系统性老年性淀粉样变性(SSA)。组织学确认通常具有挑战性,可能需要进行心肌内膜活检(EMB)。本研究旨在确定在具有特征性超声心动图表现的ATTR 心脏淀粉样变性患者中,阳性非心脏器官活检或脂肪抽吸中淀粉样蛋白沉积的频率。回顾了我院 286 例诊断为 ATTR 心脏淀粉样变性的患者的病历,这些患者接受了非心脏活检或皮下脂肪抽吸,其中 186 例(65%)为 FAC,100 例(35%)为 SSA。131 例(46%)患者进行了 EMB,均为阳性。210 例(73%)患者的非心脏组织样本呈阳性,其中 175 例(94%)为 FAC,35 例(35%)为 SSA(p<0.001)。141 例(76%)FAC 和 84 例(84%)SSA 患者进行了脂肪抽吸,阳性率分别为 67%和 14%,而 100 例(54%)和 64 例(64%)患者进行了骨髓活检,阳性率分别为 41%和 30%。52 例(28%)FAC 和 54 例(29%)患者进行了直肠和腓肠神经活检,阳性率分别为 81%和 83%。其他非心脏部位的活检进行的频率相对较低。总之,尽管与 FAC 相比,SSA 更常需要 EMB 来确诊,但对于具有特征性超声心动图表现的 ATTR 心脏淀粉样变性患者,非心脏活检或脂肪抽吸可作为初始检查。

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