Transcranial sonography in atypical parkinsonism: How reliable is it in real clinical practice? A multicentre comprehensive study

进行性核上麻痹 皮质基底变性 医学 帕金森病 帕金森病 萎缩 内科学 胃肠病学 预测值 病理 疾病
作者
Araceli Alonso‐Cánovas,José Ignacio Tembl Ferrairó,Irene Martínez‐Torres,José Luis López-Sendón Moreno,Isabel Parees-Moreno,Enric Monreal-Laguillo,Paula Pérez-Torre,Rafael Toledano Delgado,Guillermo García Ribas,Isabel Sastre Bataller,Jaime Masjuán,Juan Carlos Martínez-Castrillo,Uwe Walter
出处
期刊:Parkinsonism & Related Disorders [Elsevier]
卷期号:68: 40-45 被引量:13
标识
DOI:10.1016/j.parkreldis.2019.09.032
摘要

Introduction Substantia nigra hyperechogenicity (SN+) in transcranial sonography (TCS) is frequent in Parkinson's disease (PD), while lenticular nucleus hyperechogenicity (LN+) and 3rd ventricle enlargement (3V+) are typical of Atypical Parkinsonisms (AP). However, there are no studies assessing the diagnostic yield of all TCS biomarkers in the three AP (progressive supranuclear palsy, PSP, multiple system atrophy, MSA, corticobasal degeneration, CBD). Previous references lack homogeneous criteria and data are incomprehensive. Methods Analysis of TCS performed in routine clinical practice in AP and PD patients from two tertiary hospitals. Expert recommendations were strictly followed. Previous literature was critically analysed. Results 155 AP (98 PSP, 40 MSA, 14 CBD), 254 PD, 145 control subjects were included. We confirmed good sensitivity for SN+ in PD (80%), but specificity was lower than reported (61%). LN+ and 3V + had moderate sensitivity for AP and PSP diagnosis respectively (65%, 63%), but specificity was higher than reported (87%, 91%). We confirmed high specificity and positive predictive value of the combination SN/LN (98%, 93% AP; 83%, 86% PD). The combinations of two or three echofeatures, previously unreported, showed high specificity but lower sensitivity (SN/3V: 75% sensitivity, 87% specificity PD; 42% sensitivity, 98% specificity PSP) (SN + LN+: 79% sensitivity, 86% specificity CBD) (SN/3V/LN: 67% sensitivity, 89% specificity PD; 29% sensitivity, 99% specificity PSP; 41% sensitivity, 95% specificity MSA; 57% sensitivity 91% specificity CBD). Conclusions We present a large comprehensive study of TCS, confirming its usefulness and certain limitations in AP diagnosis. Adherence to consensus criteria is critical to implement TCS for clinical and research purposes.

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