4.1 Article

Unaltered Dopamine Transporter Availability in Drug-Naive Patients With Schizophrenia After 6 Months of Antipsychotics Treatment A Naturalistic Study

期刊

JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY
卷 37, 期 1, 页码 21-26

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/JCP.0000000000000632

关键词

antipsychotic; dopamine transporter; drug-naive schizophrenia; Positive and Negative Symptoms Scale; SPECT

资金

  1. National Science Council of Taiwan [NSC 95-2314-B-006-052, NSC 99-2314-B-006-019-MY3]
  2. Atomic Energy Council of Taiwan [NSC 91-NU-7-006-002]
  3. Ministry of Science and Technology, Republic of China [MOST 104-2314-B-006-032-MY2]
  4. Headquarters of University Advancement at the National Cheng Kung University [D102-35001, D103-35A09]
  5. Ministry of Education, Taiwan, Republic of China

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Background: Dopaminergic dysfunction, namely, dopamine transporter (DAT) availability variations in patients with drug-naive schizophrenia after long-term treatment, is still not well understood. The aims of the study were to explore (i) whether the DAT availability in patients with drug-naive schizophrenia differed after antipsychotic treatment and (ii) whether treatment with different generations of antipsychotics influenced the DAT availability after follow-up for 6 months. Methods: Twenty-four first-episode, drug-naive patients with schizophrenia were divided into first-and second-generation antipsychotic groups naturalistically. After 6 months of follow-up, 7 patients who received first-generation antipsychotic treatment and 17 patients who received second-generation antipsychotic treatment completed the study. The patients underwent premedication and 6-month follow-up measurements using single-photon emission computed tomography with technetium Tc 99m (Tc-99m) TRODAT-1. Psychopathological evaluations and adverse effects were recorded using appropriate scales. Results: Both of the treatment groups significantly improved according to Positive and Negative Symptoms Scale evaluation. However, no significant difference was noticed between the premedication and 6-month follow-up DAT scans. Nonsignificant differences existed even in the groups of different generations of antipsychotics. Conclusions: Improvements in psychotic symptoms in patients with schizophrenia may not be influenced by DAT availability, even under treatment with different antipsychotics for a sufficient treatment period.

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