Proton magnetic resonance spectroscopic imaging in pediatric major depression

被引:78
作者
Farchione, TR
Moore, GJ
Rosenberg, DR
机构
[1] Wayne State Univ, Sch Med, Univ Hlth Ctr, Dept Psychiat & Behav Neurosci, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Dept Radiol, Detroit, MI USA
[3] Wayne State Univ, Sch Med, Dept Pediat, Detroit, MI 48201 USA
关键词
depression; pediatric; child; proton magnetic resonance spectroscopy; dorsolateral prefrontal cortex; brain;
D O I
10.1016/S0006-3223(02)01340-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Neurobiologic abnormalities in dorsolateral prefrontal cortex (DLPFC) are believed to be involved in the pathophysiology of major depressive disorder (MDD). Although MDD commonly emerges during childhood and adolescence, to out-knowledge, no prior study has examined the DLPFC in pediatric patients with MDD. Methods: In this study, choline compounds (Cho), N-acetylaspartate (NAA), and creatine/phosphocreatine (Cr) were measured in left and right DLPFC using a multislice proton magnetic resonance spectroscopic imaging sequence with validated phantom replacement methodology in 11 treatment-naive MDD patients, 10-16 years of age, and 11 case-matched healthy control subjects. Results: A significant increase in Cho was observed in left but not right DLPFC in MDD patients versus control subjects (32.5% higher). No significant differences in NAA or Cr were observed between case-control pairs. Conclusions: These results provide new evidence of localized functional neurochemical marker alterationsi in left DLPFC in pediatric MDD. Our results must be considered preliminary, however, given the small sample size.
引用
收藏
页码:86 / 92
页数:7
相关论文
共 59 条
[31]  
Lewinsohn PM, 1986, PSYCHOL AGING, V1, P63
[32]   Natural course of adolescent major depressive disorder in a community sample: Predictors of recurrence in young adults [J].
Lewinsohn, PM ;
Rohde, P ;
Seeley, JR ;
Klein, DN ;
Gotlib, LH .
AMERICAN JOURNAL OF PSYCHIATRY, 2000, 157 (10) :1584-1591
[33]  
LEWINSOHN PM, 1993, J ABNORM PSYCHOL, V102, P133, DOI 10.1037/0021-843X.102.1.133
[35]  
Mac Master FP, 1999, PROG NEURO-PSYCHOPH, V23, P601
[36]   In vivo H-1 MRS choline: Correlation with in vitro chemistry histology [J].
Miller, BL ;
Chang, L ;
Booth, R ;
Ernst, T ;
Cornford, M ;
Nikas, D ;
McBride, D ;
Jenden, DJ .
LIFE SCIENCES, 1996, 58 (22) :1929-1935
[37]   Choline, myo-inositol and mood in bipolar disorder: a proton magnetic resonance spectroscopic imaging study of the anterior cingulate cortex [J].
Moore, CM ;
Breeze, JL ;
Gruber, SA ;
Babb, SM ;
Frederick, BD ;
Villafuerte, RA ;
Stoll, AL ;
Hennen, J ;
Yurgelun-Todd, DA ;
Cohen, BM ;
Renshaw, PF .
BIPOLAR DISORDERS, 2000, 2 (03) :207-216
[38]   Prefrontal cortical volume in childhood-onset major depression - Preliminary findings [J].
Nolan, CL ;
Moore, GJ ;
Madden, R ;
Farchione, T ;
Bortoi, M ;
Lorch, E ;
Stewart, CM ;
Rosenberg, DR .
ARCHIVES OF GENERAL PSYCHIATRY, 2002, 59 (02) :173-179
[39]  
Nolte J., 1993, HUMAN BRAIN INTRO IT, P397
[40]   Glial reduction in the subgenual prefrontal cortex in mood disorders [J].
Öngür, D ;
Drevets, WC ;
Price, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13290-13295