Haugbøl Steven, Pinborg Lars H, Arfan Haroon M, Frøkjaer Vibe M, Madsen Jacob, Dyrby Tim B, Svarer Claus, Knudsen Gitte M
Neurobiology Research Unit, Centre for Integrated Molecular Brain Imaging, Copenhagen University Hospital, 9 Blegdamsvej, 2100, Copenhagen, Denmark.
Eur J Nucl Med Mol Imaging. 2007 Jun;34(6):910-5. doi: 10.1007/s00259-006-0296-y. Epub 2006 Dec 29.
To determine the reproducibility of measurements of brain 5-HT2A receptors with an [18F]altanserin PET bolus/infusion approach. Further, to estimate the sample size needed to detect regional differences between two groups and, finally, to evaluate how partial volume correction affects reproducibility and the required sample size.
For assessment of the variability, six subjects were investigated with [18F]altanserin PET twice, at an interval of less than 2 weeks. The sample size required to detect a 20% difference was estimated from [18F]altanserin PET studies in 84 healthy subjects. Regions of interest were automatically delineated on co-registered MR and PET images.
In cortical brain regions with a high density of 5-HT2A receptors, the outcome parameter (binding potential, BP1) showed high reproducibility, with a median difference between the two group measurements of 6% (range 5-12%), whereas in regions with a low receptor density, BP1 reproducibility was lower, with a median difference of 17% (range 11-39%). Partial volume correction reduced the variability in the sample considerably. The sample size required to detect a 20% difference in brain regions with high receptor density is approximately 27, whereas for low receptor binding regions the required sample size is substantially higher.
This study demonstrates that [18F]altanserin PET with a bolus/infusion design has very low variability, particularly in larger brain regions with high 5-HT2A receptor density. Moreover, partial volume correction considerably reduces the sample size required to detect regional changes between groups.
采用[18F]阿坦色林PET团注/输注法测定脑5-HT2A受体测量的可重复性。此外,估计检测两组之间区域差异所需的样本量,最后,评估部分容积校正如何影响可重复性和所需样本量。
为评估变异性,对6名受试者进行了两次[18F]阿坦色林PET检查,间隔时间少于2周。根据对84名健康受试者的[18F]阿坦色林PET研究估计检测20%差异所需的样本量。在配准的MR和PET图像上自动勾勒感兴趣区域。
在5-HT2A受体高密度的皮质脑区,结果参数(结合潜能,BP1)显示出高可重复性,两组测量值之间的中位数差异为6%(范围5-12%),而在受体低密度区域,BP1可重复性较低,中位数差异为17%(范围11-39%)。部分容积校正显著降低了样本的变异性。在高受体密度脑区检测20%差异所需的样本量约为27,而对于低受体结合区域,所需样本量则高得多。
本研究表明,采用团注/输注设计的[18F]阿坦色林PET变异性非常低,尤其是在5-HT2A受体密度高的较大脑区。此外,部分容积校正大大减少了检测组间区域变化所需的样本量。