Womack Kyle B, Diaz-Arrastia Ramon, Aizenstein Howard J, Arnold Steven E, Barbas Nancy R, Boeve Bradley F, Clark Christopher M, DeCarli Charles S, Jagust William J, Leverenz James B, Peskind Elaine R, Turner R Scott, Zamrini Edward Y, Heidebrink Judith L, Burke James R, DeKosky Steven T, Farlow Martin R, Gabel Matthew J, Higdon Roger, Kawas Claudia H, Koeppe Robert A, Lipton Anne M, Foster Norman L
Department of Neurology, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd, Dallas, TX 75390-9129, USA.
Arch Neurol. 2011 Mar;68(3):329-37. doi: 10.1001/archneurol.2010.295. Epub 2010 Nov 8.
To evaluate the cause of diagnostic errors in the visual interpretation of positron emission tomographic scans with fludeoxyglucose F 18 (FDG-PET) in patients with frontotemporal lobar degeneration (FTLD) and patients with Alzheimer disease (AD).
Twelve trained raters unaware of clinical and autopsy information independently reviewed FDG-PET scans and provided their diagnostic impression and confidence of either FTLD or AD. Six of these raters also recorded whether metabolism appeared normal or abnormal in 5 predefined brain regions in each hemisphere-frontal cortex, anterior cingulate cortex, anterior temporal cortex, temporoparietal cortex, and posterior cingulate cortex. Results were compared with neuropathological diagnoses.
Academic medical centers.
Forty-five patients with pathologically confirmed FTLD (n=14) or AD (n=31).
Raters had a high degree of diagnostic accuracy in the interpretation of FDG-PET scans; however, raters consistently found some scans more difficult to interpret than others. Unanimity of diagnosis among the raters was more frequent in patients with AD (27 of 31 patients [87%]) than in patients with FTLD (7 of 14 patients [50%]) (P=.02). Disagreements in interpretation of scans in patients with FTLD largely occurred when there was temporoparietal hypometabolism, which was present in 7 of the 14 FTLD scans and 6 of the 7 scans lacking unanimity. Hypometabolism of anterior cingulate and anterior temporal regions had higher specificities and positive likelihood ratios for FTLD than temporoparietal hypometabolism had for AD.
Temporoparietal hypometabolism in FTLD is common and may cause inaccurate interpretation of FDG-PET scans. An interpretation paradigm that focuses on the absence of hypometabolism in regions typically affected in AD before considering FTLD is likely to misclassify a significant portion of FTLD scans. Anterior cingulate and/or anterior temporal hypometabolism indicates a high likelihood of FTLD, even when temporoparietal hypometabolism is present. Ultimately, the accurate interpretation of FDG-PET scans in patients with dementia cannot rest on the presence or absence of a single region of hypometabolism but rather must take into account the relative hypometabolism of all brain regions.
评估在额颞叶变性(FTLD)患者和阿尔茨海默病(AD)患者中,使用氟脱氧葡萄糖F 18(FDG-PET)进行正电子发射断层扫描视觉解读时诊断错误的原因。
12名对临床和尸检信息不知情的训练有素的评估者独立审查FDG-PET扫描,并给出他们对FTLD或AD的诊断印象和信心。其中6名评估者还记录了每个半球5个预定义脑区(额叶皮质、前扣带回皮质、颞前皮质、颞顶叶皮质和后扣带回皮质)的代谢是否正常或异常。将结果与神经病理学诊断进行比较。
学术医疗中心。
45例经病理证实为FTLD(n = 14)或AD(n = 31)的患者。
评估者在FDG-PET扫描解读中具有较高的诊断准确性;然而,评估者一致发现有些扫描比其他扫描更难解读。评估者之间的诊断一致性在AD患者(31例患者中的27例[87%])中比在FTLD患者(14例患者中的7例[50%])中更常见(P = 0.02)。FTLD患者扫描解读中的分歧主要发生在存在颞顶叶代谢减低时,14例FTLD扫描中有7例存在这种情况,7例缺乏一致性的扫描中有6例存在这种情况。与颞顶叶代谢减低对AD的情况相比,前扣带回和颞前区域的代谢减低对FTLD具有更高的特异性和阳性似然比。
FTLD中的颞顶叶代谢减低很常见,可能导致对FDG-PET扫描的解读不准确。在考虑FTLD之前,侧重于AD典型受累区域无代谢减低的解读模式可能会将很大一部分FTLD扫描误分类。即使存在颞顶叶代谢减低,前扣带回和/或颞前代谢减低也表明FTLD的可能性很大。最终,痴呆患者FDG-PET扫描的准确解读不能仅依赖于单个代谢减低区域的有无,而必须考虑所有脑区相对的代谢减低情况。