Diffusion-weighted MRI distinguishes Parkinson disease from the parkinsonian variant of multiple system atrophy: A systematic review and meta-analysis

被引:39
作者
Bajaj, Sweta [1 ]
Krismer, Florian [1 ]
Palma, Jose-Alberto [2 ]
Wenning, Gregor K. [1 ]
Kaufmann, Horacio [2 ]
Poewe, Werner [1 ,3 ]
Seppi, Klaus [1 ,3 ]
机构
[1] Med Univ Innsbruck, Dept Neurol, Innsbruck, Austria
[2] NYU, Sch Med, Dept Neurol, Dysauton Ctr, New York, NY USA
[3] Med Univ Innsbruck, Neuroimaging Res Core Facil, Innsbruck, Austria
来源
PLOS ONE | 2017年 / 12卷 / 12期
基金
美国国家卫生研究院;
关键词
DIFFERENTIAL-DIAGNOSIS; PUTAMINAL DEGENERATION; ACCURACY; MSA;
D O I
10.1371/journal.pone.0189897
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Putaminal diffusivity in brain magnetic resonance diffusion-weighted imaging (DWI) is increased in patients with the parkinsonian variant of multiple system atrophy (MSA-P) compared to Parkinson disease (PD) patients. Purpose We performed a systematic review and meta-analysis to evaluate the diagnostic accuracy of DWI to distinguish MSA-P from PD. Methods Studies on DWI were identified through a systematic PubMed and Clarivate Analytics((R))Web of Science((R)) Core Collection search. Papers were selected based on stringent inclusion criteria; minimum requirement was the inclusion of MSA-P and PD patients and documented true positive, true negative, false positive and false negative rates or overall sample size and reported sensitivity and specificity. Meta-analysis was performed using the hierarchical summary receiver operating characteristics curve approach. Results The database search yielded 1678 results of which 9 studies were deemed relevant. Diagnostic accuracy of putaminal diffusivity measurements were reported in all of these 9 studies, whereas results of other regions of interest were only reported irregularly. Therefore, a meta-analysis could only be performed for putaminal diffusivity measurements: 127 patients with MSA-P, 262 patients with PD and 70 healthy controls were included in the quantitative synthesis. The meta-analysis showed an overall sensitivity of 90% (95% confidence interval CI): 76.7%-95.8%) and an overall specificity of 93% (95% CI: 80.0%-97.7%) to distinguish MSA-P from PD based on putaminal diffusivity. Conclusion Putaminal diffusivity yields high sensitivity and specificity to distinguish clinically diagnosed patients with MSA-P from PD. The confidence intervals indicate substantial variability. Further multicenter studies with harmonized protocols are warranted particularly in early disease stages when clinical diagnosis is less certain.
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