Imaging of dopamine transporters in Parkinson disease: a meta‐analysis of <sup>18</sup>F/<sup>123</sup>I‐FP‐CIT studies
Yanyan Kong, Chencheng Zhang, Kawai Liu, Aparna Wagle Shukla, Bomin Sun, Yihui Guan
Abstract
Abstract Objective 18 F‐FP‐CIT and 123 I‐FP‐CIT are widely used radiotracers in molecular imaging for Parkinson’s disease (PD) diagnosis. Compared with 123 I‐FP‐CIT, 18 F‐FP‐CIT has superior tracer kinetics. We aimed to conduct a meta‐analysis to assess the efficacy of using 18 F‐FP‐CIT positron emission tomography (PET) and 123 I‐FP‐CIT single‐photon emission computed tomography (SPECT) of dopamine transporters in patients with PD in order to provide evidence for clinical decision‐making. Methods We searched the PubMed, Embase, Wanfang Data, and China National Knowledge Infrastructure databases to identify the relevant studies from the time of inception of the databases to 30 April 2020. We identified six PET studies, including 779 patients with PD and 124 healthy controls, which met the inclusion criteria. Twenty‐seven SPECT studies with 1244 PD patients and 859 controls were also included in this meta‐analysis. Results Overall effect‐size analysis indicated that patients with PD showed significantly reduced 18 F‐FP‐CIT uptake in three brain regions [caudate nucleus: standardized mean difference (SMD) = −1.71, Z = −3.31, P = 0.0009; anterior putamen: SMD = −3.71, Z = −6.26, P < 0.0001; and posterior putamen: SMD = −5.49, Z = −5.97, P < 0.0001]. Significant decreases of 123 I‐FP‐CIT uptake were also observed in the caudate (SMD = −2.31, Z = −11.49, P < 0.0001) and putamen (SMD = −3.25, Z = −14.79, P < 0.0001). Interpretation In conclusion, our findings indicate that both 18 F‐FP‐CIT PET and 123 I‐FP‐CIT SPECT imaging of dopamine transporters can provide viable biomarkers for early PD diagnosis.