1H-magnetic resonance spectroscopy in obsessive-compulsive disorder: effects of 12 weeks of sertraline treatment on brain metabolites

被引:10
作者
Tukel, Rasit [1 ]
Aydin, Kubilay [2 ]
Ertekin, Erhan [1 ]
Ozyildirim, Seda Sahin [1 ]
Barburoglu, Mehmet [2 ]
机构
[1] Istanbul Univ, Istanbul Fac Med, Dept Psychiat, TR-34390 Istanbul, Turkey
[2] Istanbul Univ, Istanbul Fac Med, Dept Radiol, Neuroradiol Div, TR-34390 Istanbul, Turkey
关键词
Neuroimaging; Magnetic resonance spectroscopy; N-acetylaspartate; Obsessive-compulsive disorder; Sertraline; CEREBRAL GLUCOSE-METABOLISM; N-ACETYLASPARTATE; SYMPTOM PROVOCATION; ANTERIOR CINGULATE; BEHAVIOR-THERAPY; BLOOD-FLOW; RATES; ASPARTATE; SYSTEM; CORTEX;
D O I
10.1007/s00406-014-0545-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Several neuroimaging studies have investigated brain metabolite abnormalities in patients with obsessive-compulsive disorder (OCD) and also explored metabolic changes after OCD treatments using proton magnetic resonance spectroscopy (H-1-MRS). The main objective of this study was to investigate the effects of a selective serotonin re-uptake inhibitor (SSRI) treatment on the neurochemical levels in patients with OCD. In the present study, levels of N-acetylaspartate (NAA), choline, and myo-Inositol were measured in terms of their ratios with creatine (Cr) using H-1-MRS. The ratios of metabolite levels in the three brain regions for 19 unmedicated patients with OCD, including 10 who were drug-na < ve, at baseline and following 12 weeks of sertraline treatment and for 19 healthy control subjects were compared with ANOVA. In post hoc analysis, the NAA/Cr levels were significantly lower in patients with OCD at baseline than in healthy controls in the anterior cingulate and in the caudate. On the other hand, no significant differences were detected in terms of the NAA/Cr in the anterior cingulate, caudate, and putamen between the patients with OCD after 12 weeks of sertraline treatment and healthy controls. The paired t test revealed that NAA/Cr levels were significantly higher in patients with OCD after 12 weeks of sertraline treatment compared with those at baseline in the anterior cingulate and in the caudate. Our results suggest that reductions in NAA can be reversed with SSRI treatment, which may indicate an improvement in neuronal integrity.
引用
收藏
页码:219 / 226
页数:8
相关论文
共 42 条
[1]   fMRI of neuronal activation with symptom provocation in unmedicated patients with obsessive compulsive disorder [J].
Adler, CM ;
McDonough-Ryan, P ;
Sax, KW ;
Holland, SK ;
Arndt, S ;
Strakowski, SM .
JOURNAL OF PSYCHIATRIC RESEARCH, 2000, 34 (4-5) :317-324
[2]   Reduction of N-acetylaspartate in the medial prefrontal cortex correlated with symptom severity in obsessive-compulsive disorder: meta-analyses of 1H-MRS studies [J].
Aoki, Yuta ;
Aoki, Ai ;
Suwa, Hiroshi .
TRANSLATIONAL PSYCHIATRY, 2012, 2 :e153-e153
[3]   N-acetyl aspartate -: A neuronal marker? [J].
Barker, PB .
ANNALS OF NEUROLOGY, 2001, 49 (04) :423-424
[4]   A short echo 1H spectroscopy and volumetric MRI study of the corpus striatum in patients with obsessive-compulsive disorder and comparison subjects [J].
Bartha, R ;
Stein, MB ;
Williamson, PC ;
Drost, DJ ;
Neufeld, RWJ ;
Carr, TJ ;
Canaran, G ;
Densmore, M ;
Anderson, G ;
Siddiqui, AR .
AMERICAN JOURNAL OF PSYCHIATRY, 1998, 155 (11) :1584-1591
[5]   N-acetylaspartate in the vertebrate brain:: Metabolism and function [J].
Baslow, MH .
NEUROCHEMICAL RESEARCH, 2003, 28 (06) :941-953
[6]   Evidence supporting a role for N-acetyl-L-aspartate as a molecular water pump in myelinated neurons in the central nervous system -: An analytical review [J].
Baslow, MH .
NEUROCHEMISTRY INTERNATIONAL, 2002, 40 (04) :295-300
[7]   Evidence that the tri-cellular metabolism of N-acetylaspartate functions as the brain's "operating system": how NAA metabolism supports meaningful intercellular frequency-encoded communications [J].
Baslow, Morris H. .
AMINO ACIDS, 2010, 39 (05) :1139-1145
[8]  
BAXTER LR, 1988, AM J PSYCHIAT, V145, P1560
[9]  
BAXTER LR, 1992, ARCH GEN PSYCHIAT, V49, P681
[10]  
BAXTER LR, 1987, ARCH GEN PSYCHIAT, V44, P211