Petrich T, Börner A R, Otto D, Hofmann M, Knapp W H
Department of Nuclear Medicine, Medizinische Hochschule Hannover, Carl-Neuberg-Strasse 1, 30625 Hannover, Germany.
Eur J Nucl Med Mol Imaging. 2002 May;29(5):641-7. doi: 10.1007/s00259-001-0745-6. Epub 2002 Feb 27.
The influence of serum TSH levels on fluorine-18 fluorodeoxyglucose (FDG) uptake by recurrences or metastases of differentiated thyroid carcinomas has not yet been clarified. The aim of this study was to ascertain whether the administration of recombinant human thyrotropin (rhTSH) stimulates FDG uptake by such lesions. In this prospective study, 30 patients with positive or equivocal thyroglobulin (Tg) levels and negative or equivocal iodine-131 and/or morphological imaging results (ultrasound, MRI, CT) underwent FDG positron emission tomography (PET) under exogenous TSH suppression and under exogenous TSH stimulation of serum levels by injection of rhTSH. The mean interval between the FDG-PET studies under these two conditions was 9.3+/-8.8 weeks. Serum TSH levels and free thyroid hormones were determined on each occasion. FDG uptake was quantitated using tumour to background ratios (TBRs) and standardised uptake values (SUVs). Under TSH suppression there was focal FDG accumulation in nine subjects (22 tumour-like lesions). The total number of foci was 45. After exogenous TSH stimulation, the number of patients in whom FDG foci were detected was 19, and the number of foci identified was 82 (78 tumour-like lesions). TBR of regions showing positive FDG contrast with either of the modalities averaged 2.54+/-1.89, and under stimulated TSH levels, 5.51+/-2.99 ( P<0.0001). Corresponding SUVs were 2.05+/-1.45 versus 2.77+/-1.58 ( P<0.001). In a small number ( n=4) of foci related to inflammatory lymph nodes, TBR and SUV were only marginally increased under TSH stimulation (2.01+/-0.38 and 1.07+/-0.38, respectively), and the values did not differ significantly from those obtained under suppression. These results provide the first direct evidence that TSH stimulates FDG uptake by differentiated thyroid carcinoma and that, therefore, FDG-PET is more accurate under rhTSH than under suppression.
血清促甲状腺激素(TSH)水平对分化型甲状腺癌复发或转移灶摄取氟-18氟脱氧葡萄糖(FDG)的影响尚未明确。本研究的目的是确定重组人促甲状腺激素(rhTSH)的应用是否会刺激此类病灶摄取FDG。在这项前瞻性研究中,30例甲状腺球蛋白(Tg)水平呈阳性或可疑阳性,且碘-131和/或形态学成像结果(超声、MRI、CT)为阴性或可疑阴性的患者,在血清TSH受外源性抑制及通过注射rhTSH使血清水平受外源性刺激的情况下,接受了FDG正电子发射断层扫描(PET)检查。这两种情况下进行FDG-PET检查的平均间隔时间为9.3±8.8周。每次均测定血清TSH水平和游离甲状腺激素。使用肿瘤与本底比值(TBR)和标准化摄取值(SUV)对FDG摄取进行定量分析。在TSH受抑制的情况下,9例受试者(22个肿瘤样病灶)出现局灶性FDG积聚。病灶总数为45个。外源性TSH刺激后,检测到FDG病灶的患者有19例,发现的病灶数为82个(78个肿瘤样病灶)。两种检查方式下显示FDG阳性对比的区域的TBR平均为2.54±1.89,在TSH刺激水平下为5.51±2.99(P<0.0001)。相应的SUV分别为2.05±1.45和2.77±1.58(P<0.001)。在少数(n=4)与炎性淋巴结相关的病灶中,TSH刺激下TBR和SUV仅略有增加(分别为2.01±0.38和1.07±0.38),且这些值与抑制状态下获得的值无显著差异。这些结果提供了首个直接证据,即TSH刺激分化型甲状腺癌摄取FDG,因此,FDG-PET在rhTSH刺激状态下比抑制状态下更准确。