Imaging CXCR4 expression in patients with suspected primary hyperaldosteronism
Purpose It is challenging to differentiate unilateral aldosterone-producing adenoma (APA) from bilateral idiopathic adrenal hyperplasia (IAH) and nonfunctional adrenal adenoma (NFA) in primary aldosteronism (PA). In a first primarily ex vivo study detection, CXC chemokine receptor type 4 (CXCR4) exp...
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Veröffentlicht in: | European journal of nuclear medicine and molecular imaging 2020-10, Vol.47 (11), p.2656-2665 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Purpose
It is challenging to differentiate unilateral aldosterone-producing adenoma (APA) from bilateral idiopathic adrenal hyperplasia (IAH) and nonfunctional adrenal adenoma (NFA) in primary aldosteronism (PA). In a first primarily ex vivo study detection, CXC chemokine receptor type 4 (CXCR4) expression has been shown to be a valuable tool for the detection of APA. In this study, we aimed to clinically evaluate CXCR4 imaging with
68
Ga-pentixafor PET/CT for detecting APA.
Methods
We prospectively recruited 36 patients with clinical suspicion of PA. All patients underwent
68
Ga-pentixafor PET/CT. Positive lesions were defined based on higher tracer uptake in adrenal nodular(s) shown on CT than the normal adrenal. These lesions were referred for adrenalectomy subsequently. All patients received clinical follow-up. Semi-quantitative analysis using maximum standardized uptake value (SUV
max
), lesion-to-liver ratio (LLR), and lesion-to-contralateral ratio (LCR) has also been performed. PET/CT results were correlated with clinical presentation and follow-up.
Results
Thirty-nine adrenal lesions in 36 patients were found; 25 APA, 4 IAH, and 10 NFA according to histopathology and clinical assessment. Sensitivity, specificity, and accuracy of
68
Ga-pentixafor PET/CT in distinguishing APA by visualization were 100%, 78.6%, and 92.3% respectively. The SUV
max
of APA (21.34 ± 9.41,
n
= 25) was significantly higher than that of non-APA lesions (6.29 ± 2.10,
n
= 14,
P
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ISSN: | 1619-7070 1619-7089 |
DOI: | 10.1007/s00259-020-04722-0 |