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采用18F-多巴和正电子发射断层扫描对双胞胎帕金森病进行研究。

Parkinson's disease in twins studied with 18F-dopa and positron emission tomography.

作者信息

Burn D J, Mark M H, Playford E D, Maraganore D M, Zimmerman T R, Duvoisin R C, Harding A E, Marsden C D, Brooks D J

机构信息

MRC Cyclotron Unit, Hammersmith Hospital, London, UK.

出版信息

Neurology. 1992 Oct;42(10):1894-900. doi: 10.1212/wnl.42.10.1894.

Abstract

We used 18F-dopa PET to examine concordance for dysfunction of the nigrostriatal dopaminergic system in 18 co-twins of patients with Parkinson's disease (PD) and scanned one clinically concordant monozygotic (MZ) twin pair, 17 asymptomatic co-twins (10 MZ, 7 dizygotic [DZ]), and 13 twins with PD (8 MZ, 5 DZ). Mean 18F-dopa uptake of the twins with PD was significantly reduced in putamen to 38% and in caudate to 66% of normal. Mean putamen 18F-dopa uptake for the 17 asymptomatic co-twins was also significantly reduced (86% of normal), as was putamen tracer uptake for the 10 MZ (87% of normal) and seven DZ (83% of normal) asymptomatic co-twin subgroups. Four of 10 MZ and two of seven DZ asymptomatic co-twins had putamen 18F-dopa uptake reduced more than 2 SDs below the normal mean. Three of these four asymptomatic MZ co-twins had tremor on examination at the time of PET and one has now developed PD 2 years later. Our PET findings give concordances for nigral dysfunction of 45% in the MZ pairs and 29% in the DZ pairs at a 2-SD threshold, and 18% in MZ and 0% in DZ pairs at a 3-SD threshold of significance. These data suggest that the concordance for nigral pathology in PD twins may be higher than previously realized and that the presence of an isolated postural or rest tremor may be a phenotypic expression of PD.

摘要

我们使用18F-多巴PET检查了18例帕金森病(PD)患者的同卵双胞胎中黑质纹状体多巴胺能系统功能障碍的一致性,并对一对临床症状一致的同卵双胞胎、17例无症状的双胞胎(10例同卵双胞胎、7例异卵双胞胎)以及13例患PD的双胞胎(8例同卵双胞胎、5例异卵双胞胎)进行了扫描。患PD的双胞胎壳核的平均18F-多巴摄取量显著降低至正常水平的38%,尾状核降低至66%。17例无症状双胞胎的壳核平均18F-多巴摄取量也显著降低(为正常水平的86%),10例同卵双胞胎(为正常水平的87%)和7例异卵双胞胎(为正常水平的83%)无症状双胞胎亚组的壳核示踪剂摄取量同样显著降低。10例同卵双胞胎中有4例、7例异卵双胞胎中有2例无症状双胞胎的壳核18F-多巴摄取量比正常平均值低2个标准差以上。这4例无症状同卵双胞胎中有3例在PET检查时检查发现有震颤,其中1例在2年后已发展为PD。我们的PET研究结果显示,在2个标准差阈值时,同卵双胞胎对黑质功能障碍的一致性为45%,异卵双胞胎对为29%;在3个标准差显著性阈值时,同卵双胞胎对为18%,异卵双胞胎对为0%。这些数据表明,PD双胞胎中黑质病理的一致性可能比之前认识到的更高,孤立性姿势性或静止性震颤的存在可能是PD的一种表型表现。

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