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    Effect of adjunctive treatment with repetitive transcranial magnetic stimulation on exploratory eye movements and negative symptoms in schizophrenic patients:a randomized'double-blind'sham-controlled study

    2011-04-12 09:23:22HaiYingCHENZhiJuanZHANGJiJunWANGYueMinCHENZhiQingXIANGShenXunSHIJianHuaSHENG
    上海精神醫(yī)學(xué) 2011年4期
    關(guān)鍵詞:探索性經(jīng)顱眼球

    Hai Ying CHEN,Zhi Juan ZHANG,Ji Jun WANG,Yue Min CHEN,Zhi Qing XIANG,Shen Xun SHI,Jian Hua SHENG

    Effect of adjunctive treatment with repetitive transcranial magnetic stimulation on exploratory eye movements and negative symptoms in schizophrenic patients:a randomized'double-blind'sham-controlled study

    Hai Ying CHEN,Zhi Juan ZHANG,Ji Jun WANG,Yue Min CHEN,Zhi Qing XIANG,Shen Xun SHI,Jian Hua SHENG*

    Background:The left dorsolateral prefrontal cortex(DLPFC)is one of the crucial areas in ocular control that may be involved in the abnormal Exploratory Eye Movements(EEM)seen in schizophrenia.Repetitive Transcranial Magnetic Stimulation(rTMS)to this same region of the brain is a promising adjunctive therapy for the negative symptoms of schizophrenia.

    Objective:Assess the effects of rTMS stimulation on EEM abnormalities in schizophrenia and the relationship of changes in EEM to changes in the positive and negative symptoms of schizophrenia.

    Methods:46 inpatients with schizophrenia at the Shanghai Mental Health Center between June 2009 and February 2010 were randomly divided into an rTMS group(n=24)and a sham rTMS group(n=22).Both groups received standard antipsychotic medication.The rTMS group received five adjunctive rTMS treatments per week for four weeks using intermittent theta burst stimulation to the left dorsolateral prefrontal cortex.Patients were evaluated using blinded assessments of the Positive and Negative Syndrome Scale(PANSS)and tests of EEM[including number of eye fixations score(NEF),responsive search score(RSS),and the differentiation score(D)]before and after the course of treatment.

    Results:23 patients in the intervention group and 19 patients in the control group finished the study.Both groups had significant decreases in symptoms after four weeks of treatment but at the end of the treatment period both the total PANSS score and the PANSS negative symptom score were significantly lower in the group that received adjunctive rTMS.The NEF score increased significantly(i.e.,improved)in the real rTMS group after four weeks of treatment but not in the sham rTMS group;neither group had significant changes in the RSS or D scores.However,the median percent change in the NEF score for the real rTMS group(+10%)was not significantly greater than the median percent change in the sham rTMS group(-19%).

    Conclusion:Compared to standard antipsychotic therapy,a four-week course of antipsychotic medication with adjunctive rTMS was more effective in improving both the negative symptoms of schizophrenia and one component of the abnormal EEM seen in schizophrenia.High individual variability in responsiveness of EEM measures to treatment will necessitate relatively large samples to determine whether or not particular treatments are effective.

    Exploratory eye movement;Repetitive transcranial magnetic stimulation;Schizophrenia

    1 Introduction

    Abnormal eye movements in schizophrenia is a well documented phenomenon[1-3].Many studies assess these abnormal eye movements by evaluating Exploratory Eye Movements(EEM),specific ocular movements seen when gazing at static images.Abnormal EEM are common in persons with a diagnosis of schizophrenia[4-6].Kojima and colleagues[1]compared EEM in 145patientswith schizophrenia,116 patients with depression and 124 normal controls;they found that the sensitivity and specificity of EEM to schizophrenia were both higher than 80%and that the two components of EEM—the Responsive Search Score(RSS)and the Number of Eye Fixations(NEF)score—were significantly lower in schizophrenia than in the other two groups.Moreover,and RSS was a very stable indicator of a diagnosis of schizophrenia that was not influenced by the administration of antipsychotic medications or changes in patients'symptoms;though some studies report that EEM measures may changewithsymptomimprovement[7,8].Other studies that highlight the potential utility of EEM as biological markers of schizophrenia include the finding that parents of persons with schizophrenia have low RSS scores[9]and the finding of a correlation of EEM with chromosome 22q11—a heavily investigated candidate gene for schizophrenia[10].

    Despite the fact that EEM abnormalities are one of the most well documented physical abnormalities seen in schizophrenia,few studies have assessed the biological basis for these abnormalities or the effect of treatment on EEM.Eye movements such as EEM are managed and regulated by the parietal,prefrontal and supplementary motor areas of the cerebrum.The dorsolateral prefrontal cortex (DLPFC)is one of the crucial areas in this ocular control[11];injuries in this area can lead to significant eye movement disorders[12].Thus,one might hypothesize that changes which affect the prefrontal cortex might influence EEM.

    Repetitive transcranial magnetic stimulate(rTMS) is a relatively new treatment in psychiatry that applies magnets to produce highly focused electrical currentsthatstimulatespecificpointsinthe brain[13].rTMS to the DLFPC has been used as an adjunctive treatment for the cognitive deficits of schizophrenia[14]and for the positive and negative symptoms in schizophrenia[15].To our knowledge no study has yet assessed the effect of rTMS on abnormal EEM and the relationship of rTMS-induced changes in EEM to clinical improvement.The present study aims to assess the effect of adjunctive treatment with rTMS to the left DLPFC on abnormal EEM in patients with schizophrenia who have prominent negative symptoms.We choose such subjects because of the relatively poor effectiveness of antipsychotic medications for negative symptoms and because some reports suggest that changes in the DLPFC are closely associated with the negative symptoms of schizophrenia[16].

    2 Methods

    2.1 Subjects

    Patients who took part in this study were all hospitalized patients with a diagnosis of schizophrenia at the Shanghai Mental Health Center of the Shanghai Jiao Tong University School of Medicine.ParticipantswererecruitedbetweenJune 2009 and February 2010.

    Inclusion criteria:1)meets diagnostic criteria for Schizophrenia using the Diagnostic and StatisticalManualforMentalDisorders,4thedition (DSM-Ⅳ);2)18 to 55 years of age;3)negative symptom factor score of the Positive and Negative Syndrome Scale(PANSS)≥20;4)on a stable medication regimen;and 5)had not previously participated in an EEM assessment.Exclusion criteria:1)prior suicidal or violent behavior;2)contraindications for rTMS treatment such as metal implants in the body or medical history of migraine,seizure,or abnormal EEG;3)diseases affecting eye movements;4)significant cardiac,pulmonary,or other serious illness;5)mental retardation;6)comorbid substance abuse;and 7)currently pregnant or breast feeding.(See Figure 1)

    Eligible subjects were randomized to rTMS therapy or sham rTMS therapy based on a computerized algorithm;the result for each subject was provided to the rTMS technician the first time the patient entered the rTMS treatment room.The treatment protocol was approved by the Ethics Committee of Shanghai Mental Health Center.All of the subjects or their accompanying family members signed informed consent for the treatment.

    2.2 Research Methods

    2.2.1 Repetitive transcranial magnetic stimulation

    The circular magnet version of the Magpro X100 transcranial magnetic stimulator produced by the Medtronic Company in Denmark was used in the study.The treatment protocol was based on that reported by Grossheinrich and colleagues[14]:the position for treatment was the left DLPFC;a treatment session involved administering a total of 2400 pulses over a 22-minute period using an intermittent theta burst stimulation pattern with a stimulus frequency of 50 Hz and strength of 80%of the patient's motor threshold;one treatment session was completed five days a week for four consecutive weeks(a total of 20 sessions).In the sham rTMS treatment patients were placed in the rTMS apparatus for 22 minutes and exposed to similar sounds as those experienced by rTMS but the magnets were not activated.

    2.2.2 EEM test method

    We assessed EEM using the DEM-2000 eye movement detector produced by the Shanghai Dikang Biotechnology Company,which automatically records the trajectory of eye movements and analyzes the data.Subjects sit comfortably in a chair and gaze at a small screen in front of them.The distance between the subject's eyes and the screen was 25 cm in order to keep the angle for moving the eyes from the left border to the right border at 33 degrees.The first S shaped figure(S1)was displayed on the screen for 15 s and subjects were asked to carefully observe the figure.The instrument automatically records the number of eye fixation(NEF)points in the 15 s.Subsequently two slightly different S shaped figures(S2 and S3)are displayed on the screen for 15 s,and the subject is again asked to carefully observe the figures and repeatedly asked"is there any other difference between this figure and the first figure"until the subject answers"no difference".The instrument divides S2 or S3 into seven regions,the number of regions the subject fixes on over a 5-second interval is recorded asthe‘responsivesearch score' (RSS).The highest RSS score for each image was seven and the maximum score for the two figures is 14[14].Higher NEF and RSS scores indicate better eye movement functioning.A discriminant score—the‘D score'—is also computed by combining the NEF and RSS results

    [D=10.265-(0.065*NEF+0.871*RSS)].The technician who conducted the EEM tests was blind to the treatment status of the patients.

    2.2.3 Assessment of psychotic symptoms

    The Chinese version of the PANSS was used to assess patients'psychotic symptoms at baseline and after 4 weeks of treatment.This instrument is used widely in China and has good internal consistency (Cronbach α=0.87[17]).The evaluating researchers were blind to the treatment status and EEM results of the subject they evaluated.

    2.3 Statistical analysis

    All data were analyzed using SPSS 15.0 software.Demographic data for the groups were compared using t-tests and Chi Square tests.Paired ttests were used to compare the before versus after changes in PANSS and the EEM test scores(NEF,RSS and D scores).Several of the before-versus-after percent change scores had skewed distributions so change scores were compared using median tests.

    3 Results

    3.1 Subjects

    In total 46 patients with schizophrenia satisfied inclusion criteria and 42 patients completed the 4-week trial.Four subjects dropped out in the first week of the trial;1 patient from the intervention group refused to continue rTMS because of transient headaches during the treatment sessions,2 control group subjects were discharged from the hospital by their family members for reasons unrelated to the rTMS treatment,and one control group subject stopped because of an exacerbation of hallucinations and delusions that required changing his medication regimen.The discontinuation rate in the two groups was not significantly different(4.1%vs. 13.6%,χ2=0.38,P>0.05).

    The 23 subjects in the intervention group who completed the trial included 16 males and 7 females;their mean(SD)age was 37.4(11.8)years (range 23-55);their mean duration of education was 12.0(2.2)years;their median(IQR)duration of illness was 17(6-23)years(range 1-34 years);and the median duration of their current hospitalization was 11(6-25)months(range 0.5-68 months).Their primary medication treatment was a follows:5 received a mean dose of 4.4(0.6) mg/d risperidone;5 received 20 mg/d olanzapine; 4 received a mean dose of 22.5(5.0)mg/d aripiprazole;2 received a mean dose of 550.0(70.7) mg/d quetiapine;and 7 received a mean dose of332.1(123.1)mg/d clozapine.

    The 19 subjects in the control group who completed the trial included 11 males and 8 females; their mean(SD)age was 39.7(13.3)years (range 18-52);their mean duration of education was 11.0(2.6)years;their median(IQR)duration of illness was 13(5-22)years(range 2-32 years);and the median duration of their current hospitalization was 12(5-26)months(range 0.5-58.5 months).Their medication treatment was a follows:9 received a mean dose of 4.0(1.0)mg/d risperidone;2 received 20 mg/d olanzapine;3 received a mean dose of 23.3(11.6)mg/d aripiprazole;2 received a mean dose of 550.0(70.7) mg/d quetiapine;and 4 received a mean dose of 312.5(25.0)mg/d clozapine.

    The differences in gender,age,years of education,duration of illness,length of hospital stay,category of antipsychotics,and calculated dosages of antipsychotics(using chlorpromazine equivalents) were not statistically different between the two groups.Seven subjects in the real rTMS group and eight subjects in the sham rTMS group also received a second antipsychotic(data provided on request).All subjects remained on the same dose of the same antipsychotic medication throughout the 4-week trial.

    3.2 Assessment of rTMS therapeutic efficacy

    As shown in Table 1,the total PANSS scores and the subscale scores in the real and sham rTMS groups were not significantly different at baseline. After four weeks of antipsychotic treatment with or without adjunctive rTMS treatment,the total PANSS scores and the positive symptoms score,negative symptoms score and general pathology score all decreased significantly in both groups.At the end of treatment the total PANSS score and the PANSS negative symptom score were significantly lower in the rTMS group than in the sham rTMS group;the PANSS general pathology score and the PANSS positive symptom score were also lower in the rTMS group but the differences did not reach statistical significance.The median percent change scores after the four weeks of treatment are shown in Table 2;the median drop in negative symptoms score and in the total PANSS score was significantly greater in the real rTMS group.

    3.3 EEM results

    Table 1 also shows that the differences in baseline NEF,RSS,and D scores between the two groups were not statistically significant.After four weeks of treatment the number of eye fixations (NEF)score increased(i.e.,improved)significantly in the group that received adjunctive rTMS but the RSS and D scores did not change significantly and none of the three measures changed significantly in the group that received sham rTMS. Table 2 shows that the real rTMS group had a median percent increase in the NEF score of 10%after four weeks of adjunctive rTMS treatment and the sham rTMS group had a median decrease of 19% in the NEF score over the same period;but this difference was not statistically significant due to the very wide range in the distribution of the percent change scores for the EEM measures.

    4 Discussion

    4.1 Main findings

    Similar to our previous report on adjunctive treatment of schizophrenia with rTMS[14],this study found that the addition of rTMS as an adjunctive treatment to standard antipsychotic treatment significantly improves the outcome for negative symptoms(as assessed by PANSS)after four weeks of treatment.

    We also found that after four weeks of adjunctive treatment with rTMS one of the measures of abnormal EEM in schizophrenia-number of eye fixations(NEF)—had improved significantly.But there was no improvement in the other measures of EEM(RRS and D scores)and the use of antipsychotic medications without adjunctive rTMS did not result in improvements in any of the measures of EEM.This result is relevant to the debate about whether or not abnormal EEM in schizophrenia can improve with treatment[1,8];it suggests that NEF is a state characteristic that can change over time while RSS is a trait characteristic that does not change over time.

    But our finding of improvement in NEF with adjunctive rTMS treatment needs to be replicated in larger samples.Despite a 29%difference in the before-versus-after percent change scores between the real and sham rTMS groups(+10%vs-19%),this difference was not statistically significant due to the very wide range in the percent change scores for the NEF measure.Thus the high individual variability in the responsiveness of these scores to treatmentnecessitateslargesamplestodetermine whether or not treatment is effective.This high variability in responsiveness may be one of the reasons for conflicting results in previous studies about abnormal EEM in schizophrenia.

    4.2 Limitations

    The major deficiency of the present study was the relatively small sample size and the relatively short duration of adjunctive rTMS treatment.Given the wide number of potential confounding factors simple randomization may not have adequately balanced the two groups.To minimize the effect of potentially imbalanced groups we also used the before versus after change scores to compare the efficacy of the two treatment modalities(antipsychotic medication with or without adjunctive rTMS).One subject withdrew from the intervention group forreasons apparently related to the rTMS treatment (reported headache during the treatment)and three other subjects were dropped from the control group for reasons unrelated to the rTMS treatment;given the small proportion of dropouts(8.7%)we did not include these‘treatment failure'results in the analysis.The drawings used for the EEM tests were the same at baseline and at four weeks after starting treatment;this could have affected the second evaluation but there is unlikely to be much carry-over‘learning effect'over the 4-week interval between the two tests and the use of similar procedures in both groups means that any learning effect would be similar in both groups and,thus,have little effect on the overall results about differences between the two treatment conditions.

    4.3 Implications

    The 5-day-per-week treatment schedule for rTMS used in this study may make this impractical in routine clinical care,but the importance of negative symptoms to the social dysfunction experienced by many patients with schizophrenia and the replicated effectiveness of rTMS in treating these difficult to treat symptoms justifies further research of this new treatment modality.Among several other issues,the optimal duration of treatment and interval between treatment sessions are yet to be determined.

    The fact that stimulation of the left dorsolateral prefrontal region was associated with increased NEF scores supports the notion that this region is involved in the EEM abnormalities seen in schizophrenia.Nemoto and colleagues[18]used fMRI to assess regional brain functioning during completion of a visual exploration task similar to the EEM test and detected a significant bilateral activation in the prefrontal cortex and thalamus in normal subjects that was deficient in patients with schizophrenia. Our findings are consistent with this result.Whether abnormal EEM is a byproduct of generalized dysfunction of the prefrontal cortex in schizophrenia or has a more specific etiologic relationship to schizophrenia remains to be determined.

    Funding

    Supported by National High-Tech Research and Development(863)Program of China(No. 2008AA02Z412);the Natural Science Foundation of China(No.30770773);the Janssen Science Foundation(2008);and the Shanghai Science Committee Foundation(No.10411966400).

    1. Kojima T,Matsushima E,Ohta K,Toru M,Han YH,Shen YC,et al.Exploratory eye movements as a marker of schizophrenia -a WHO multi-center study.World Health Organization. Schizophr Res,2001,52(3):203-213.

    2. Matsukawa Y,Takahashi S,Aoki M,Yamakami K,Nishinarita S,Horie T,et al.Patients with systemic lupus erythematosus show a normal responsive search score in exploratory eye movement analysis:comparisonwithschizophrenia.Ann Rheum Dis,2002,61(8):748-750.

    3. Matsushima E,Kojima T,Ohbayashi S,Ando H,Ando K,Shimazono Y.Exploratory eye movements in schizophrenic patients and patients with frontal lobe lesions.Eur Arch Psychiatry Clin Neurosci,1992,241(4):210-214.

    4. Xiang ZQ,Chen YM,Yan WW.The three sets of figures as stimulus for exploratory eye movement test in schizophrenia. Chinese Journal of Psychiatry,2006,39(4):205-208.(in Chinese)

    5. Avila MT,McMahon RP,Elliott AR,Thaker GK.Neurophysiological markers of vulnerability to schizophrenia:sensitivity and specificity of specific quantitative eye movement measures.J Abnorm Psychol,2002,111(2):259-267.

    6. Suzuki M,Takahashi S,Matsushima E,Tsunoda M,Kurachi M,Okada T,et al.Exploratory eye movement dysfunction as a discriminator for schizophrenia:a large sample study using a newly developed digital computerized system.Eur Arch Psychiatry Clin Neurosci,2009,259(3):186-194.

    7. Kojima T,Matsushima E,Nakajima K,Shiraishi H,Ando K,Ando H,et al.Eye movements in acute,chronic and remitted schizophrenia.Biol Psychiatry,1990,27(9):975-989.

    8. Xiang ZQ,Chen YM,Xu YF.Relationship between exploratory eye movements and clinical severity in schizophrenic patients.Shanghai Archives of Psychiatry,2008,20(6):321-324. (in Chinese)

    9. Xia ML,Takahashi S,Tanabe E,Matsuura M,Kojima T,Matsushima E.Eye movements studies on schizophrenics and their parents.Eur Neuropsychopharmacology,1996,6(Suppl 3):64.

    10. Takahashi S,Tanabe E,Yara K,Matsuura M,Matsushima E,Kojima T.Impairment of exploratory eye movement in schizophrenia patients and their siblings.Psychiatry Clin Neurosci,2008,62(5):487-493.

    11. Pierrot-Deseilligny C,Muri RM,Nyffeler T,Milea D.The role of the human dorsolateral prefrontal cortex in ocular motor behavior.Ann N Y Acad Sci,2005,1039:239-251.

    12. Guitton D,Buchtel HA,Douglas RM.Frontal lobe lesions in man cause difficulties in suppressing reflexive glances and in generating goal-directed saccades.Exp Brain Res,1985,58 (3):455-472.

    13. Rossi S,Hallett M,Rossini PM,Pascual-Leone A:A Safety of TMS consensus Group.Safety,ethical considerations,and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research.Clin Neurophysiol,2009,120(12):2008-2039.

    14. Grossheinrich N,Rau A,Pogarell O,Hennig-Fast K,Reinl M,Karch S,et al.Theta burst stimulation of the prefrontal cortex:safety and impact on cognition,mood,and resting electroencephalogram.Biol Psychiatry,2009,65(9):778-784.

    15. Zhang ZJ,Zhang XK,Li H,Zhong XL,Cheng ZW,Liao LW,et al.Double-blind randomized controlled trial of repetitive transcranial magnetic stimulation in the treatment of the negative symptoms of schizophrenia.Shanghai Archives of Psychiatry,2010,22(5):262-265.(in Chinese)

    16. 16.Molina V,Reig S,Pascau J,Sanz J,Sarramea F,Gispert JD,et al.Anatomical and functional cerebtral variables associated with basal symptoms but not risperidone response in minimally treated schizophrenia.Psychiatry Res,2003,124(3):163-175.

    17. Si TM,Yang JZ,Shu L,Wang XL,Kong QM,Zhou M,et al. The reliability,validity of PANSS and its implications.Chinese Mental Health Journal,2004,18(1):45-47.(in Chinese)

    18. Nemoto Y,Matsuda T,Matsuura M.Neural circuits of eye movements during performance of the visual exploration task,which is similar to the responsive search score task,in schizophrenia patients and normal subjects.J Nihon Univ Med Ass,2004,63(7):352-359.(in Japanese) (received:2010-11-05;accepted:2011-03-09)

    重復(fù)經(jīng)顱磁刺激輔助治療對精神分裂癥患者探索性眼球運(yùn)動和陰性癥狀的影響:隨機(jī)、雙盲、偽刺激對照研究

    陳?,?張志娟 王繼軍 陳月敏 項志清 施慎遜 盛建華

    基金項目:國家高科技研究發(fā)展863計劃(2008AA02Z412);國家自然科學(xué)基金項目(30770773);楊森科學(xué)基金會(2008);上海市科學(xué)委員會基金項目(10411966400)。

    作者單位:上海交通大學(xué)醫(yī)學(xué)院附屬精神衛(wèi)生中心200030。通信作者:盛建華,電子信箱sjh-lyl@263.net

    背景左側(cè)前額葉背外側(cè)區(qū)(dorsolateral prefrontal cortex,DLPFC)是調(diào)控眼球運(yùn)動的關(guān)鍵區(qū)域,很可能與精神分裂癥的異常探索性眼球運(yùn)動(exploratory eye movement,EEM)有關(guān)。重復(fù)經(jīng)顱磁刺激(repetitive transcranial magnetic stimulation,rTMS)刺激大腦的這個區(qū)域有可能輔助治療精神分裂癥陰性癥狀。

    目的評估rTMS干預(yù)對精神分裂癥者EEM異常的影響,以及EEM變化與精神分裂癥陽性和陰性癥狀變化之間關(guān)系。

    方法在上海市精神衛(wèi)生中心住院的46位精神分裂癥患者于2009年6月至2010年2月參加本研究?;颊弑浑S機(jī)分為rTMS真刺激組(研究組,24例)和rTMS偽刺激組(對照組,22例)。兩組均接受標(biāo)準(zhǔn)抗精神病藥治療。rTMS真刺激組每周接受5次rTMS干預(yù),持續(xù)4周,應(yīng)用θ短陣快速脈沖刺激(intermittent theta burst stimulation,iTBS)模式刺激左側(cè)DLPFC。于治療前及治療4周末應(yīng)用陽性與陰性癥狀量表(Positive and Negative Syndrome Scale,PANSS)盲法評定患者的精神癥狀和進(jìn)行EEM檢查,EEM檢查指標(biāo)包含凝視點數(shù)(number of eye fixations score,NEF)、反應(yīng)探索分(the responsive search score,RSS)和判別值(differentiation score,D)。

    結(jié)果 研究組23例和對照組19例完成研究。經(jīng)rTMS干預(yù)4周后,兩組的癥狀均有明顯減輕,但是,接受rTMS輔助治療患者組的PANSS總分及PANSS陰性癥狀因子分明顯低于對照組。4周后,rTMS真刺激組的NEF分較治療前有明顯升高(改善),而rTMS偽刺激組的NEF分未見明顯升高;兩組治療前后RSS及D值的變化均不明顯。但是,rTMS真刺激組的NEF中位數(shù)變化的百分?jǐn)?shù)(+10%),并沒有顯著性高于rTMS偽刺激組的NEF中位數(shù)變化的百分?jǐn)?shù)(-19%)。

    結(jié)論與標(biāo)準(zhǔn)藥物治療相比,接受4周rTMS刺激左側(cè)前額葉背外側(cè)區(qū)輔助治療的精神分裂癥患者的陰性癥狀更輕,異常探索性眼球運(yùn)動EEM有一成份也有提高。EEM指標(biāo)對于治療的反應(yīng)方面存在高度個體化變異,這表明需要相對較大的樣本來判斷特殊治療是否有效。

    探索性眼球運(yùn)動 重復(fù)經(jīng)顱磁刺激 精神分裂癥

    10.3969/j.issn.1002-0829.2011.04.002

    Shanghai Mental Health Center,Shanghai Jiao Tong University School of Medicine,Shanghai,China 200030.*Correspondence:sjh-lyl@263.net

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