Gray matter changes in late life depression - a structural MRI analysis

被引:120
作者
Andreescu, Carmen [1 ,2 ]
Butters, Meryl A. [1 ,2 ]
Begley, Amy [1 ,2 ]
Rajji, Tarek [3 ]
Wu, Minjie [4 ]
Meltzer, Carolyn C. [1 ,2 ,5 ,6 ,7 ,8 ]
Reynolds, Charles F., III [1 ,2 ]
Aizenstein, Howard [1 ,2 ,9 ]
机构
[1] Univ Pittsburgh, Sch Med, Adv Ctr Intervent & Serv Res Late Life Mood Disor, Dept Psychiat, Pittsburgh, PA 15213 USA
[2] John A Hartford Ctr Excellence Geriatr Psychiat, Pittsburgh, PA USA
[3] Univ Toronto, Ctr Addict & Mental Hlth, Toronto, ON, Canada
[4] Univ Pittsburgh, Dept Elect & Comp Engn, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15213 USA
[6] Emory Univ, Sch Med, Dept Radiol, Atlanta, GA 30322 USA
[7] Emory Univ, Sch Med, Dept Neurol, Atlanta, GA 30322 USA
[8] Emory Univ, Sch Med, Dept Psychiat & Behav Sci, Atlanta, GA USA
[9] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA 15213 USA
关键词
late-life depression; structural MRI; toxic-stress; prodromal dementia;
D O I
10.1038/sj.npp.1301655
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Multiple brain morphometric changes have been reported in late-life depression (LLD), mostly in studies comparing volumes of circumscribed brain areas. The aim of our study is to characterize the volumetric changes of multiple gray matter regions in relation to age of onset/duration of illness. We predicted that the association of gray matter volumes with total duration of illness and age of onset would differ depending on whether the region was susceptible to the toxic effects of chronic exposure to cortisol or to the vascular/neurodegenerative changes accompanying prodromal dementia. Seventy-one elderly depressed subjects were studied along with thirty-two comparison subjects. High-resolution T1-weighted brain MRIs were processed using an automated labeling pathway technique. To protect against type-I error, we combined the right and left hemisphere volume data. We sampled 24 regions of interest (ROIs). We used the primary visual cortex volume to normalize for individual variations in brain size. LLD Subjects had smaller volumes than non-depressed subjects in 17 of the 24 examined ROIs. Shorter duration of illness and later age of onset was correlated with smaller volumes of parahippocampal area and parietal inferior area. A later age of onset was also correlated with smaller volumes of several frontal and temporal areas, cingulum, and putamen. Our findings support a dementia prodrome model more strongly than a toxic stress model in this group of subjects. However, it remains likely that both processes as well as other factors contribute to the heterogeneity of volumetric brain changes in LLD.
引用
收藏
页码:2566 / 2572
页数:7
相关论文
共 45 条
[1]
ALEXOPOULOS GS, 1993, AM J PSYCHIAT, V150, P1693
[2]
Depression with late onset is associated with right frontal lobe atrophy [J].
Almeida, OP ;
Burton, EJ ;
Ferrier, N ;
McKeith, IG ;
O'Brien, JT .
PSYCHOLOGICAL MEDICINE, 2003, 33 (04) :675-681
[3]
[Anonymous], 2004, DEMENTIA RATING SCAL
[4]
Localizing gray matter deficits in late-onset depression using computational cortical pattern matching methods [J].
Ballmaier, M ;
Kumar, A ;
Thompson, PM ;
Narr, KL ;
Lavretsky, H ;
Estanol, L ;
DeLuca, H ;
Toga, AW .
AMERICAN JOURNAL OF PSYCHIATRY, 2004, 161 (11) :2091-2099
[5]
Brain morphometric abnormalities in geriatric depression: long-term neurobiological effects of illness duration [J].
Bell-McGinty, S ;
Butters, MA ;
Meltzer, CC ;
Greer, PJ ;
Reynolds, CF ;
Becker, JT .
AMERICAN JOURNAL OF PSYCHIATRY, 2002, 159 (08) :1424-1427
[6]
BREMNER J, 2005, DEPRESSION MIND BODY, V2, P38
[7]
Long-term benzodiazepine therapy does not result in brain abnormalities [J].
Busto, UE ;
Bremner, KE ;
Knight, K ;
terBrugge, K ;
Sellers, EM .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2000, 20 (01) :2-6
[8]
Chen M, 1999, 3 D DEFORMABLE REGIS
[9]
COFFEY CE, 1993, ARCH GEN PSYCHIAT, V50, P7
[10]
DREVETS WC, 1997, NATURE, V386, P827