Decreased thalamic glutamate level in unmedicated adult obsessive-compulsive disorder patients detected by proton magnetic resonance spectroscopy

被引:33
作者
Zhu, Yajing [1 ,2 ]
Fan, Qing [3 ]
Han, Xu [4 ]
Zhang, Haiyin [3 ]
Chen, Jue [3 ]
Wang, Zhen [3 ]
Zhang, Zongfeng [3 ]
Tan, Ling [5 ]
Xiao, Zeping [3 ]
Tong, Shanbao [1 ,2 ]
Maletic-Savatic, Mirjana [4 ]
Li, Yao [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Med X Res Inst, Shanghai 200030, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Biomed Engn, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Shanghai Mental Hlth Ctr, Shanghai 200030, Peoples R China
[4] Texas Childrens Hosp, Jan & Dan Duncan Neurol Res Inst, Baylor Coll Med, Dept Pediat,Neurosci, Houston, TX 77030 USA
[5] Shanghai Jiao Tong Univ, Ruijin Hosp, Sch Med, Dept Radiol, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
Obsessive-compulsive disorder; Magnetic resonance spectroscopy; Glutamate; Thalamus; Medial prefrontal cortex; Multivariate analysis; MAJOR DEPRESSIVE DISORDER; MEDIAL PREFRONTAL CORTEX; CEREBRAL-BLOOD-FLOW; OCD-LIKE BEHAVIORS; ANTERIOR CINGULATE; METABOLITE CONCENTRATIONS; PEDIATRIC-PATIENTS; N-ACETYLASPARTATE; SYMPTOM SEVERITY; ABNORMALITIES;
D O I
10.1016/j.jad.2015.03.008
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Previous neuroimaging studies implied that the dysfunction of cortico-striato-thalamo-cortical (CSTC) circuit served as the neural basis for the pathophysiology of obsessive-compulsive disorder (OCD). The imbalances in neuronal metabolite and neurotransmitter within CSTC circuit have been shown as the leading reasons of the OCD onset. The aim of this study is to investigate the metabolic alterations, especially the glutamatergic signal dysfunction within CSTC circuit, and the relationships between neural metabolites and the symptom severity of OCD patients. Methods: Single voxel magnetic resonance spectroscopy (MRS) was conducted in medial prefrontal cortex (mPFC) and bilateral thalamus areas for thirteen unmedicated adult OCD patients with age-, gender-, and education matched healthy controls. Quantification and multivariate analysis were performed to identify vital metabolic biomarkers for patients and healthy controls group differentiation. Moreover, we performed Spearman's rank correlation analysis for OCD patients to examine the relationship between the metabolite concentration level and OCD symptomatology. Results: Patients with OCD showed significantly decreased glutamate level in mPFC (p=0.021) and right thalamus (p=0.039), and significantly increased choline compounds in left thalamus (p=0.044).The glutamate in right thalamus was shown as the most important metabolite for group separation from multivariate analysis (Q(2)=0.134) and was significantly correlated with the patients' compulsion scores (Spearman r= -0.674, p=0.016). Limitations: Limited sample size, the use of creatine and phosphocreatine (Cr) ratios rather than absolute concentrations and unresolved glutamine (Gin) are limitations of the present study. Conclusion: Our study results consolidated the hypothesis about glutamatergic signaling dysfunction in OCD. To our knowledge, it is the first finding about a reduced thalamic glutamate level in adult unmedicated OCD patients. The dysregulation of glutamate serves as a potential target for the OCD pharmacotherapy and the detailed mechanisms underlying the glutamate alterations within CSTC circuits merit further investigations. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:193 / 200
页数:8
相关论文
共 80 条
[1]   PARALLEL ORGANIZATION OF FUNCTIONALLY SEGREGATED CIRCUITS LINKING BASAL GANGLIA AND CORTEX [J].
ALEXANDER, GE ;
DELONG, MR ;
STRICK, PL .
ANNUAL REVIEW OF NEUROSCIENCE, 1986, 9 :357-381
[2]   Tc-99m HMPAO brain perfusion SPECT in drug-free obsessive-compulsive patients without depression [J].
Alptekin, K ;
Degirmenci, B ;
Kivircik, B ;
Durak, H ;
Yemez, B ;
Derebek, E ;
Tunca, Z .
PSYCHIATRY RESEARCH-NEUROIMAGING, 2001, 107 (01) :51-56
[3]  
[Anonymous], J NEUROPSYCHIATRY CL
[4]   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
[5]   Pathophysiology of obsessive-compulsive disorder - A necessary link between phenomenology, neuropsychology, imagery and physiology [J].
Aouizerate, B ;
Guehl, D ;
Cuny, E ;
Rougier, A ;
Bioulac, B ;
Tignol, J ;
Burbaud, P .
PROGRESS IN NEUROBIOLOGY, 2004, 72 (03) :195-221
[6]   Glutamate transporter gene SLC1A1 associated with obsessive-compulsive disorder [J].
Arnold, Paul Daniel ;
Sicard, Tricia ;
Burroughs, Eliza ;
Richter, Margaret A. ;
Kennedy, James L. .
ARCHIVES OF GENERAL PSYCHIATRY, 2006, 63 (07) :769-776
[7]   Glutamate receptor gene (GRIN2B) associated with reduced anterior cingulate glutamatergic concentration in pediatric obsessive-compulsive disorder [J].
Arnold, Paul Daniel ;
MacMaster, Frank P. ;
Richter, Margaret A. ;
Hanna, Gregory L. ;
Sicard, Tricia ;
Burroughs, Eliza ;
Mirza, Yousha ;
Easter, Phillip C. ;
Rose, Michelle ;
Kennedy, James L. ;
Rosenberg, David R. .
PSYCHIATRY RESEARCH-NEUROIMAGING, 2009, 172 (02) :136-139
[8]   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
[9]  
Baxter L. R., 1992, PSYCHIAT CLIN N AM
[10]  
BAXTER LR, 1988, AM J PSYCHIAT, V145, P1560