Optimal DaTQUANT Thresholds for Diagnostic Accuracy of Dementia with Lewy Bodies (DLB) and Parkinson's Disease (PD).

IF 2.2 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Phillip H Kuo, Patrick Cella, Ying-Hui Chou, Alexander Arkhipenko, Julia M Fisher
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引用次数: 0

Abstract

Background: Quantitative thresholds are helpful to define an abnormal DaT SPECT in patients with suspected nigrostriatal degenerative diseases (NSDD). The optimal DaTQUANT threshold for diagnostic accuracy of DaT SPECT across combined movement and cognitive disorder populations has been previously described. Methods: We established optimal DaTQUANT thresholds that enhance the discrimination between dementia with Lewy bodies (DLB) and non-DLB dementia types, as well as between Parkinsonian syndromes (PS) and conditions not characterized by nigrostriatal degeneration (non-PS). Results: Data from a total of 303 patients were used in this retrospective analysis. Posterior putamen of the more affected hemisphere (MAH) was shown to be an accurate single-variable predictor for both DLB and PS and was comparable to the most accurate multi-variable models. Conclusions: Automated quantification with DaTQUANT can accurately aid in the differentiation of DLB from non-DLB dementias and PS from non-PS. Optimal thresholds for assisting a diagnosis of DLB are striatal binding ratio (SBR) ≤ 0.65, z-score ≤ -2.36, and a percent deviation ≤ -0.54 for the posterior putamen of the MAH. Optimal posterior putamen thresholds for assisting a diagnosis of PS are SBR ≤ 0.92, z-score ≤ -1.53, and a percent deviation ≤ -0.33, which are similar to our previously reported posterior putamen threshold values using a blended patient pool from multiple study populations.

诊断路易体痴呆症 (DLB) 和帕金森病 (PD) 的最佳 DaTQUANT 阈值。
背景:定量阈值有助于界定疑似黑质变性疾病(NSDD)患者的 DaT SPECT 异常。之前已描述了DaT SPECT诊断运动和认知障碍人群准确性的最佳DaTQUANT阈值。方法:我们确定了最佳 DaTQUANT 阈值,该阈值可提高路易体痴呆(DLB)和非路易体痴呆类型之间以及帕金森综合征(PS)和非黑质变性疾病(非 PS)之间的区分度。研究结果本次回顾性分析共使用了303名患者的数据。结果表明,受影响较大的大脑半球(MAH)的后部丘脑是DLB和PS的准确单变量预测因子,与最准确的多变量模型相当。结论使用 DaTQUANT 进行自动定量分析可准确帮助区分 DLB 和非 DLB 痴呆症以及 PS 和非 PS。辅助诊断 DLB 的最佳阈值是纹状体结合率 (SBR) ≤ 0.65、z-分数 ≤ -2.36、MAH 后部正中丘的百分比偏差 ≤ -0.54。辅助诊断 PS 的最佳后部丘脑阈值为:SBR ≤ 0.92,z-分数≤-1.53,百分比偏差≤-0.33,这与我们之前报道的使用来自多个研究人群的混合患者库的后部丘脑阈值相似。
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来源期刊
Tomography
Tomography Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
2.70
自引率
10.50%
发文量
222
期刊介绍: TomographyTM publishes basic (technical and pre-clinical) and clinical scientific articles which involve the advancement of imaging technologies. Tomography encompasses studies that use single or multiple imaging modalities including for example CT, US, PET, SPECT, MR and hyperpolarization technologies, as well as optical modalities (i.e. bioluminescence, photoacoustic, endomicroscopy, fiber optic imaging and optical computed tomography) in basic sciences, engineering, preclinical and clinical medicine. Tomography also welcomes studies involving exploration and refinement of contrast mechanisms and image-derived metrics within and across modalities toward the development of novel imaging probes for image-based feedback and intervention. The use of imaging in biology and medicine provides unparalleled opportunities to noninvasively interrogate tissues to obtain real-time dynamic and quantitative information required for diagnosis and response to interventions and to follow evolving pathological conditions. As multi-modal studies and the complexities of imaging technologies themselves are ever increasing to provide advanced information to scientists and clinicians. Tomography provides a unique publication venue allowing investigators the opportunity to more precisely communicate integrated findings related to the diverse and heterogeneous features associated with underlying anatomical, physiological, functional, metabolic and molecular genetic activities of normal and diseased tissue. Thus Tomography publishes peer-reviewed articles which involve the broad use of imaging of any tissue and disease type including both preclinical and clinical investigations. In addition, hardware/software along with chemical and molecular probe advances are welcome as they are deemed to significantly contribute towards the long-term goal of improving the overall impact of imaging on scientific and clinical discovery.
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