Hippocampal 1H MRS in patients with bipolar disorder taking valproate versus valproate plus quetiapine

被引:39
作者
Atmaca, Murad [1 ]
Yildirim, Hanef
Ozdemir, Huseyin
Ogur, Erkin
Tezcan, Ertan
机构
[1] Firat Euphrates Univ, Firat Tip Merkezi, Sch Med, Dept Psychiat,Psikiyatri Anabilim Dali, TR-23119 Elazig, Turkey
[2] Firat Euphrates Univ, Firat Tip Merkezi, Sch Med, Dept Radiol,Psikiyatri Anabilim Dali, TR-23119 Elazig, Turkey
关键词
D O I
10.1017/S0033291706008968
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background. No study to date has examined the effects of mood stabilizer alone and the combination of mood stabilizer and atypical antipsychotic, quetiapine, on hippocampal neurochemical markers of bipolar disordered patients con currently. We therefore undertook a proton magnetic resonance spectroscopy ((1)H MRS) study of drug-free patients with bipolar disorder (drug-free group), patients undergoing valproate treatment (valproate group), patients administered valproate+quetiapine (valprote+quetiapine group) and healthy controls, focusing on the in vivo neuroanatomy of the hippocampus. Method. Thirty patients from the Firat University School of Medicine Department of Psychiatry and 10 healthy controls gave written informed consent to participate in the study. The patients and controls underwent proton magnetic resonance spectroscopic imaging ((1)H MRSI), and measures of N-acetylaspartate (NAA), choline-containing compounds (CHO), and creatine + phosphocreatine (CRE) in hippocampal regions were obtained. Results. The drug-free patients had significantly lower NAA/CRE and NAA/CHO ratios compared with the valproate and valproate+quetiapine groups and the healthy controls. The lower NAA/CRE and NAA/CHO ratios remained statistically significant even after covarying for age or whole brain volume compared with the valproate and valproate+quetiapine groups and healthy controls. In post hoe comparisons, a significant difference was found between the valproate+quetiapine group and the valproate group only with regard to NAA/CHO. Conclusion. Our findings suggest that valproate has a neuroprotective effect. In post hoc comparisons, a significant difference was found between the valproate+quetiapine and the valproate group with regard to NAA/CHO, indicating that the addition of quetiapine further increases the level of NAA and provides an additional neuroprotective effect.
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页码:121 / 129
页数:9
相关论文
共 38 条
[1]   Protective effects of atypical antipsychotic drugs on PC12 cells after serum withdrawal [J].
Bai, O ;
Wei, ZL ;
Lu, WF ;
Bowen, R ;
Keegan, D ;
Li, XM .
JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 69 (02) :278-283
[2]  
BAXTER LR, 1989, ARCH GEN PSYCHIAT, V46, P243
[3]  
Bertolino A, 1996, AM J PSYCHIAT, V153, P1554
[4]   Neuronal pathology in the hippocampal area of patients with bipolar disorder: A study with proton magnetic resonance spectroscopic imaging [J].
Bertolino, A ;
Frye, M ;
Callicott, JH ;
Mattay, VS ;
Rakow, R ;
Shelton-Repella, J ;
Post, R ;
Weinberger, DR .
BIOLOGICAL PSYCHIATRY, 2003, 53 (10) :906-913
[5]  
Blumberg HP, 1999, AM J PSYCHIAT, V156, P1986
[6]   1H magnetic resonance spectroscopy investigation of the dorsolateral prefrontal cortex in bipolar disorder patients [J].
Brambilla, P ;
Stanley, JA ;
Nicoletti, MA ;
Sassi, RB ;
Mallinger, AG ;
Frank, E ;
Kupfer, D ;
Keshavan, MS ;
Soares, JC .
JOURNAL OF AFFECTIVE DISORDERS, 2005, 86 (01) :61-67
[7]   Normalization of neuronal metabolic dysfunction after surgery for temporal lobe epilepsy - Evidence from proton MR spectroscopic imaging [J].
Cendes, F ;
Andermann, F ;
Dubeau, F ;
Matthews, PM ;
Arnold, DL .
NEUROLOGY, 1997, 49 (06) :1525-1533
[8]   Decreased N-acetylaspartate in children with familial bipolar disorder [J].
Chang, K ;
Adleman, N ;
Dienes, K ;
Barnea-Goraly, N ;
Reiss, A ;
Ketter, T .
BIOLOGICAL PSYCHIATRY, 2003, 53 (11) :1059-1065
[9]   Quetiapine - A review of its use in acute mania and depression associated with bipolar disorder [J].
Dando, TM ;
Keating, GM .
DRUGS, 2005, 65 (17) :2533-2551
[10]   Lower concentration of hippocampal N-acetylaspartate in familial bipolar I disorder [J].
Deicken, RF ;
Pegues, MP ;
Anzalone, S ;
Feiwell, R ;
Soher, B .
AMERICAN JOURNAL OF PSYCHIATRY, 2003, 160 (05) :873-882