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利用[I]-间碘苄胍单光子发射计算机断层显像/计算机断层扫描对野生型转甲状腺素蛋白淀粉样变性心肌病心脏交感神经支配进行绝对定量和左心室分割的可行性:I-NERVE研究

Feasibility of the absolute quantification and left ventricular segmentation of cardiac sympathetic innervation in wild-type transthyretin amyloidosis cardiomyopathy with [I]-MIBG SPECT/CT: The I-NERVE study.

作者信息

Tubben Alwin, Prakken Niek H J, Ivashchenko Oleksandra V, Tingen Hendrea S A, Glaudemans Andor W J M, Noordzij Walter, Nienhuis Hans L A, van der Meer Peter, Slart Riemer H J A

机构信息

Department of Cardiology, University of Groningen, University Medical Center Groningen, the Netherlands; Amyloidosis Center of Expertise, University of Groningen, University Medical Center Groningen, the Netherlands.

Department of Radiology, University Medical Center Groningen, University of Groningen, the Netherlands.

出版信息

J Nucl Cardiol. 2025 Mar;45:102146. doi: 10.1016/j.nuclcard.2025.102146. Epub 2025 Feb 3.

Abstract

BACKGROUND

Cardiac sympathetic neuronal dysfunction is an early marker in wild-type transthyretin amyloidosis cardiomyopathy (ATTRwt-CM). Iodine-123-labeled norepinephrine analog meta-iodobenzylguanidine ([I]-MIBG) imaging evaluates cardiac sympathetic innervation but lacks volumetric activity quantification in current methods. This study aims to quantify cardiac sympathetic neuronal dysfunction in ATTRwt-CM using [I]-MIBG single-photon emission computed tomography/ computed tomography (SPECT/CT) and correlate findings with functional and structural cardiac parameters from echocardiogram and cardiac magnetic resonance imaging (CMR).

METHODS

We conducted a single-center, descriptive, cross-sectional study to quantify absolute myocardial sympathetic function in ATTRwt-CM using [I]-MIBG SPECT/CT. Retrospective reconstruction allowed for absolute tracer-uptake quantification of the left ventricle, overall and segmented, in kBq/mL, standard uptake value (SUV), and percentage of the injected dose (%ID). Echocardiography, CMR, and bone scintigraphy were performed according to clinical standards. Segmented [I]-MIBG SPECT/CT values were correlated with global longitudinal systolic strain (GLSS) on echocardiography, native-T1, and extracellular volume (ECV) on CMR using SPECT/CT fused with CMR.

RESULTS

Twenty-nine ATTRwt-CM patients (75.8 ± 6.6 years, 90% male) were prospectively included. All exhibited cardiac sympathetic neuronal dysfunction, with a median late heart-to-mediastinum ratio of 1.69 (1.45-1.89) and a washout rate of 22.7% (16.4%-27.3%). SUV, SUV, SUV, and %ID were 1.80 ± .78, 3.84 ± 1.41, 4.46 ± 1.68, and .46 ± .18, respectively, correlating with semiquantitative [I]-MIBG measures. No correlations were found with GLSS on echocardiography or native T1 and ECV on CMR.

CONCLUSIONS

The current study demonstrates the feasibility of volumetric quantification of [I]-MIBG SPECT/CT in ATTRwt-CM. SUV, SUV, SUV, and %ID correlate with semi-quantitative measures but not with key cardiac parameters on echocardiography or CMR. This confirms the sensitivity of [I]-MIBG SPECT/CT to different aspects of cardiac function or pathology.

TRIAL REGISTRATION

EudraCT ref. 2020-003350-72, retrospectively registered March 20, 2023. https://classic.

CLINICALTRIALS

gov/ct2/show/NCT05776212.

摘要

背景

心脏交感神经功能障碍是野生型转甲状腺素蛋白淀粉样变心肌病(ATTRwt-CM)的早期标志物。碘-123标记的去甲肾上腺素类似物间碘苄胍([I]-MIBG)成像可评估心脏交感神经支配情况,但目前的方法缺乏体积活性定量。本研究旨在使用[I]-MIBG单光子发射计算机断层扫描/计算机断层扫描(SPECT/CT)对ATTRwt-CM患者的心脏交感神经功能障碍进行定量,并将结果与超声心动图和心脏磁共振成像(CMR)的心脏功能和结构参数相关联。

方法

我们进行了一项单中心、描述性横断面研究,以使用[I]-MIBG SPECT/CT对ATTRwt-CM患者的绝对心肌交感神经功能进行定量。回顾性重建允许对左心室进行绝对示踪剂摄取定量,包括整体和分段的,以kBq/mL、标准摄取值(SUV)和注射剂量百分比(%ID)表示。根据临床标准进行超声心动图、CMR和骨闪烁显像。使用与CMR融合的SPECT/CT,将分段的[I]-MIBG SPECT/CT值与超声心动图上的整体纵向收缩应变(GLSS)、CMR上的固有T1和细胞外容积(ECV)相关联。

结果

前瞻性纳入了29例ATTRwt-CM患者(75.8±6.6岁,90%为男性)。所有患者均表现出心脏交感神经功能障碍,晚期心脏与纵隔比值的中位数为1.69(1.45-1.89),洗脱率为22.7%(16.4%-27.3%)。SUV、SUV、SUV和%ID分别为1.80±0.78、3.84±1.41、4.46±1.68和0.46±0.18,与半定量[I]-MIBG测量值相关。未发现与超声心动图上的GLSS或CMR上的固有T1和ECV相关。

结论

本研究证明了在ATTRwt-CM中对[I]-MIBG SPECT/CT进行体积定量的可行性。SUV、SUV、SUV和%ID与半定量测量值相关,但与超声心动图或CMR上的关键心脏参数无关。这证实了[I]-MIBG SPECT/CT对心脏功能或病理不同方面的敏感性。

试验注册

EudraCT编号2020-003350-72,于2023年3月20日进行回顾性注册。https://classic.

临床试验

gov/ct2/show/NCT05776212。

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