Neurometabolic correlates of 6 and 16 weeks of treatment with risperidone in medication-naive first-episode psychosis patients

被引:6
|
作者
Birur, Badari [1 ]
Kraguljac, Nina Vanessa [1 ]
VerHoef, Lawrence [2 ]
Morgan, Charity J. [1 ]
Jindal, Ripu Daman [3 ]
Reid, Meredith Amanda [4 ]
Luker, Austin [1 ]
Lahti, Adrienne Carol [1 ]
机构
[1] Univ Alabama Birmingham, Dept Psychiat & Behav Neurobiol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Neurol, UAB Stn, Birmingham, AL 35294 USA
[3] Birmingham VA Med Ctr, Dept Neurol, Birmingham, AL USA
[4] Auburn Univ, Dept Elect & Comp Engn, MRI Res Ctr, Auburn, AL 36849 USA
关键词
MAGNETIC-RESONANCE-SPECTROSCOPY; N-ACETYL-ASPARTATE; PREFRONTAL CORTEX; PHARMACOLOGICAL-TREATMENT; ONSET HYPOTHESIS; DOPAMINE SYSTEM; BLOOD-FLOW; GLUTAMATE; SCHIZOPHRENIA; KETAMINE;
D O I
10.1038/s41398-020-0700-6
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Antipsychotic medications are the cornerstone of treatment in schizophrenia spectrum disorders. In first-episode psychosis, the recommended time for an antipsychotic medication trial is up to 16 weeks, but the biological correlates of shorter and longer antipsychotic treatment trials in these cohorts remain largely unknown. We enrolled 29 medication-naive first-episode patients (FEP) and 22 matched healthy controls (HC) in this magnetic resonance spectroscopy (MRS) study, examining the levels of combined glutamate and glutamine (commonly referred to as Glx) in the bilateral medial prefrontal cortex (MPFC) with a PRESS sequence (TR/TE = 2000/80 ms) before initiation of antipsychotic treatment, after 6 and 16 weeks of treatment with risperidone. Data were quantified in 18 HC and 20 FEP at baseline, for 19 HC and 15 FEP at week 6, and for 14 HC and 16 FEP at week 16. At baseline, none of the metabolites differed between groups. Metabolite levels did not change after 6 or 16 weeks of treatment in patients. Our data suggest that metabolite levels do not change after 6 or 16 weeks of treatment with risperidone in FEP. It is possible that our choice of sequence parameters and the limited sample size contributed to negative findings reported here. On the other hand, longer follow-up may be needed to detect treatment-related metabolic changes with MRS. In summary, our study adds to the efforts in better understanding glutamatergic neurometabolism in schizophrenia, especially as it relates to antipsychotic exposure.
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页数:8
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