High-frequency rTMS treatment increases left prefrontal myo-inositol in young patients with treatment-resistant depression
High-frequency rTMS treatment increases left prefrontal myo-inositol in young patients with treatment-resistant depression
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高频 rTMS 治疗可增加年轻难治性抑郁症患者的左前额叶肌醇
DOI:
10.1016/j.pnpbp.2010.06.009
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发表时间:
2010-10
影响因子:
5.6
通讯作者:
Liu, Jun
中科院分区:
文献类型:
--
作者:
Zheng, Huirong;Zhang, Zhijun;Li, Zexuan;Men, Weiwei;Zhang, Li;Li, Lingjiang;Liu, Peng;Gao, Junling;Liu, Xiaoyun;Zou, Juan;Zhang, Yan;Liu, Jun
BACKGROUNDNeuroimaging studies suggest that the prefrontal cortex (PFC) is involved in the pathophysiology of major depression. Repetitive transcranial magnetic stimulation (rTMS) as an antidepressant intervention has increasingly been investigated in the last two decades. In this study metabolic changes within PFC of severely depressed patients before and after rTMS were evaluated by proton magnetic resonance spectroscopy (1H-MRS).METHODThirty-four young depressed patients with treatment-resistant unipolar depression were enrolled in a double-blind, randomized study[active ((n=19) vs. sham(n=15)), and the PFC was investigated before and after high-frequency (15Hz) rTMS using 3-tesla proton magnetic resonance spectroscopy. Response was defined as a 50% reduction of the Hamilton depression rating scale. The results were compared with 28 age- and gender-matched healthy controls.RESULTSIn depressive patients a significant reduction in myo-inositol (m-Ino) was observed pre-rTMS (p<0.001). After successful treatment, m-Ino increased significantly in left PFC and the levels no longer differed from those of age-matched controls. In addition to a positive correlation between clinical improvement and an increment in m-Ino ratio, a correlation between clinical improvement and early age onset was observed.CONCLUSIONSOur results support the notion that major depressive disorder is accompanied by state-dependent metabolic alterations, especially in myo-inositol metabolism, which can be partly reversed by successful rTMS.
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影响因子:
--
作者:
W. Drevets
通讯作者:
W. Drevets
DOI:
--
发表时间:
--
期刊:
--
影响因子:
--
作者:
D B Kearns;F. Chu;S. Branda;R. Kolter;R. Losick;F Chu;D. Kearns;P M Coutinho;E. Deleury;G. Davies;B. Henrissat;C Garinot-Schneider;A. Lellouch;R. Geremia;H. Blair;Berg;S. A. Lloyd;H. Tang;X. Wang;S. Billings;D. Blair;N. Thomas;C. Francis;D. J. Xu;Derosier;Irikura;M. Kihara;S. Yamaguchi;H. Sockett;R. Macnab;D L Marykwas;S. A. Schmidt;H. Berg;S M Block;Darnton;L. Turner;S. Rojevsky;G. Darnton;B. Glekas;A. Haldenwang;Y. Camp;S. Le Breton;S. Michaels;G. Mukhopadhyay;D. Ordal;Rudner;Ben-Shahar Yehuda;D. Blair;C. Fuqua;D. Higgins;P. Levin;S. Mukhopadhyay;J. Schummers;Hongbo Yu;M. Sur
通讯作者:
D B Kearns;F. Chu;S. Branda;R. Kolter;R. Losick;F Chu;D. Kearns;P M Coutinho;E. Deleury;G. Davies;B. Henrissat;C Garinot-Schneider;A. Lellouch;R. Geremia;H. Blair;Berg;S. A. Lloyd;H. Tang;X. Wang;S. Billings;D. Blair;N. Thomas;C. Francis;D. J. Xu;Derosier;Irikura;M. Kihara;S. Yamaguchi;H. Sockett;R. Macnab;D L Marykwas;S. A. Schmidt;H. Berg;S M Block;Darnton;L. Turner;S. Rojevsky;G. Darnton;B. Glekas;A. Haldenwang;Y. Camp;S. Le Breton;S. Michaels;G. Mukhopadhyay;D. Ordal;Rudner;Ben-Shahar Yehuda;D. Blair;C. Fuqua;D. Higgins;P. Levin;S. Mukhopadhyay;J. Schummers;Hongbo Yu;M. Sur
影响因子:
17.7
作者:
Kumar, A;Thomas, A;Toga, A
通讯作者:
Toga, A
影响因子:
11
作者:
Knable, MB;Barci, BM;Torrey, EF
通讯作者:
Torrey, EF
DOI:
10.1111/j.1600-0773.1990.tb02075.x
发表时间:
1990-03
期刊:
Pharmacology & toxicology
影响因子:
--
作者:
R. Belmaker;A. Livne;G. Agam;Moscovich Dg;N. Grisaru;G. Schreiber;S. Avissar;Abraham Danon;O. Kofman
通讯作者:
R. Belmaker;A. Livne;G. Agam;Moscovich Dg;N. Grisaru;G. Schreiber;S. Avissar;Abraham Danon;O. Kofman