Pirker W, Riedl M, Luger A, Czech T, Rössler K, Asenbaum S, Angelberger P, Kornhuber J, Deecke L, Podreka I, Brücke T
University Clinic for Neurology and Nuclear Medicine, Vienna, Austria.
J Nucl Med. 1996 Dec;37(12):1931-7.
Epidepride is a novel benzamide derivative with high affinity for D2 receptors. Epidepride, in its 123I-labeled form, can be used for SPECT imaging of striatal and extrastriatal dopamine D2 receptors. The present study evaluated the usefulness of epidepride and SPECT for in vivo imaging of dopamine receptors in pituitary adenomas.
SPECT imaging was performed in 19 patients with pituitary adenomas (among them 9 patients had prolactinoma, 4 acromegaly, 4 clinically nonfunctioning pituitary adenoma, 1 Cushing's disease and 1 Nelson's syndrome) and 7 control subjects 180 min after intravenous bolus injection of 3.9 +/- 1.1 mCi [123I]epidepride. The ratio target/cerebellum minus 1, reflecting specific/ nonspecific binding was used as semiquantitative measure of D2 receptor binding.
Eight of nine prolactinoma patients demonstrated specific binding within the adenoma. The adenoma/ cerebellum ratio 3 hr p.i. showed a wide variation with values from 2.5-33. In three prolactinomas, binding was higher than in the striatum. Specific binding within the lower range of prolactinomas (adenoma/cerebellum ratios 2 and 4.8) could be demonstrated in two of four GH-secreting adenomas. All four nonfunctioning tumors showed specific binding. The adenoma/cerebellum ratio was within the lower range of prolactinomas (5.2-7.5) in three of these patients but extremely high in one (52.3). No specific tracer uptake could be demonstrated in patients with Cushing's disease or Nelson's syndrome. The striatum/cerebellum ratio 3 hr p.i. in pituitary adenoma patients was not significantly different from control subjects (17.3 +/- 5.5 versus 17.8 +/- 6.6; patients versus control subjects).
Epidepride appears to be an excellent ligand for in vivo imaging of dopamine D2 receptors in pituitary adenomas. Epidepride SPECT could serve as a predictor for response to dopamine agonist treatment.
表哌立得是一种对D2受体具有高亲和力的新型苯甲酰胺衍生物。123I标记的表哌立得可用于纹状体和纹状体外多巴胺D2受体的单光子发射计算机断层扫描(SPECT)成像。本研究评估了表哌立得和SPECT在垂体腺瘤多巴胺受体体内成像中的应用价值。
19例垂体腺瘤患者(其中9例为催乳素瘤,4例为肢端肥大症,4例为临床无功能垂体腺瘤,1例库欣病和1例纳尔逊综合征)和7例对照受试者在静脉推注3.9±1.1毫居里[123I]表哌立得180分钟后进行SPECT成像。用反映特异性/非特异性结合的靶区/小脑比值减去1作为D2受体结合的半定量指标。
9例催乳素瘤患者中有8例在腺瘤内显示出特异性结合。注射后3小时的腺瘤/小脑比值变化很大,值在2.5至33之间。在3例催乳素瘤中,结合高于纹状体。在4例生长激素分泌型腺瘤中的2例中,可在较低范围的催乳素瘤内(腺瘤/小脑比值为2和4.8)显示出特异性结合。所有4例无功能肿瘤均显示出特异性结合。其中3例患者的腺瘤/小脑比值在催乳素瘤的较低范围内(5.2至7.5),但1例极高(52.3)。库欣病或纳尔逊综合征患者未显示出特异性示踪剂摄取。垂体腺瘤患者注射后3小时的纹状体/小脑比值与对照受试者无显著差异(分别为17.3±5.5和17.8±6.6;患者与对照受试者)。
表哌立得似乎是垂体腺瘤中多巴胺D2受体体内成像的优良配体。表哌立得SPECT可作为多巴胺激动剂治疗反应的预测指标。