4.7 Article

Examining endogenous dopamine in treated schizophrenia using [11C]-(+)-PHNO positron emission tomography: A pilot study

期刊

CLINICA CHIMICA ACTA
卷 449, 期 -, 页码 60-62

出版社

ELSEVIER
DOI: 10.1016/j.cca.2015.03.020

关键词

PET; Dopamine; D2/3R; Schizophrenia

资金

  1. Canadian Institutes of Health Research [MOP-114989]
  2. U.S. National Institutes of Health [R01MH084886-01A2]
  3. Canadian Institutes of Health Research
  4. U.S. National Institutes of Health
  5. Mexico Institut de Ciencia y Tecnologia para la Capital del Conocimiento en el Distrito Federal (ICyTDF)
  6. Janssen

向作者/读者索取更多资源

Background: Using positron emission tomography (PET) it is possible to estimate endogenous dopamine (DA) occupying D-2/3 receptors (D2/3R) in the living human brain. Persons with schizophrenia (SZ) (previously medicated and nave) have increased endogenous DA occupying D2/3R in the caudate. It is unknown whether currently medicated patients demonstrate increased DA levels at D2/3R. Moreover, DA levels have not been estimated in SZ using agonist radiotracers, which may offer a more sensitive quantification over antagonists. Methods: Using the agonist radiotracer [C-11]-(+)-PHNO, DA levels were estimated at D2/3R (Delta BPND) in three patients with SZ (male, mean age = 30 +/- 16). Patients were currently being treated long-term with Olanzapine (147 +/- 88 nmol/L). Results were compared to ten healthy controls (HCs). Results: Medicated persons with SZ had greater ABPND in the left caudate (U = 2, Z = -2.20, p = .03) and right putamen (U = 2, Z = 220, p = .03). No differences were observed in the ventral striatum or globus pallidus. Conclusions: It is possible to estimate endogenous DA at D2/3R in SZ patients currently taking antipsychotics. Despite medication, patients continue to have increased endogenous DA at D2/3R This lends more biological support to the clinical observation that relapses in symptoms can occur in the face of complete antipsychotic discontinuation. Future studies with larger samples are warranted. (C) 2015 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据