Differential effects of age on brain gray matter in bipolar patients and healthy individuals

被引:77
作者
Brambilla, P
Harenski, K
Nicoletti, M
Mallinger, AG
Frank, E
Kupfer, DJ
Keshavan, MS
Soares, JC
机构
[1] Univ Pittsburgh, Sch Med, Western Psychiat Inst & Clin, Neurochem Brain Imaging Lab,Dept Psychiat, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Pharmacol, Sch Med, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, Dept Psychol, Pittsburgh, PA 15260 USA
[4] Univ Pittsburgh, Dept Neurosci, Pittsburgh, PA 15260 USA
[5] Univ Pavia, Sch Med, IRCCS S Matteo, Dept Psychiat, I-27100 Pavia, Italy
关键词
neuroimaging; aging; affective disorders; mood disorders; magnetic resonance imaging;
D O I
10.1159/000054897
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This study examined possible differences in total gray and white matter brain content in bipolar patients and healthy individuals, and their relationship with age. 22 DSM-IV bipolar patients and 22 healthy controls underwent a 1.5-tesla Spoiled Gradient Recalled Acquisition (SPGR) MRI. Evaluators blind to patients' identities measured total brain, gray and white matter volumes using a semi-automated software. No differences were found for total brain volume, gray matter or white matter volumes between bipolar patients and healthy controls (MAN-COVA, age as covariate, p > 0.05). Age was inversely correlated with total gray matter volume in patients (r = -0.576, p = 0.005), but not in controls (r = -0.193, p = 0.388), Our findings suggest that any existing gray matter deficits in bipolar disorder are likely to be localized to specific brain regions, rather than generalized. The inverse correlation between age and brain gray matter volumes in bipolar patients, not present in healthy controls, in this sample of mostly middle-aged adults, could possibly indicate more pronounced age-related gray matter decline in bipolar patients, and may be of potential relevance for the pathophysiology of the disorder. Copyright (C) 2001S.KargerAG,Basel.
引用
收藏
页码:242 / 247
页数:6
相关论文
共 44 条
[11]   Relationship between prior course of illness and neuropsychological functioning in patients with bipolar disorder [J].
Denicoff, KD ;
Ali, SO ;
Mirsky, AF ;
Smith-Jackson, EE ;
Leverich, GS ;
Duncan, CC ;
Connell, EG ;
Post, RM .
JOURNAL OF AFFECTIVE DISORDERS, 1999, 56 (01) :67-73
[12]   NEURON LOSS IN THE AGING VISUAL-CORTEX OF MAN [J].
DEVANEY, KO ;
JOHNSON, HA .
JOURNALS OF GERONTOLOGY, 1980, 35 (06) :836-841
[13]  
DUPONT RM, 1990, ARCH GEN PSYCHIAT, V47, P55
[14]  
DUPONT RM, 1995, ARCH GEN PSYCHIAT, V52, P747
[15]   SUBCORTICAL SIGNAL HYPERINTENSITIES IN BIPOLAR PATIENTS DETECTED BY MRI [J].
DUPONT, RM ;
JERNIGAN, TL ;
GILLIN, JC ;
BUTTERS, N ;
DELIS, DC ;
HESSELINK, JR .
PSYCHIATRY RESEARCH, 1987, 21 (04) :357-358
[16]  
Figiel G S, 1991, J Neuropsychiatry Clin Neurosci, V3, P18
[17]   MRI PERIVENTRICULAR LESIONS IN ADULTS [J].
GERARD, G ;
WEISBERG, LA .
NEUROLOGY, 1986, 36 (07) :998-1001
[18]   VOLUMETRIC MRI MEASUREMENTS IN BIPOLARS COMPARED WITH SCHIZOPHRENICS AND HEALTHY CONTROLS [J].
HARVEY, I ;
PERSAUD, R ;
RON, MA ;
BAKER, G ;
MURRAY, RM .
PSYCHOLOGICAL MEDICINE, 1994, 24 (03) :689-699
[19]  
Horn J.L., 1982, AGING COGNITIVE PROC
[20]   A MAGNETIC-RESONANCE-IMAGING STUDY OF PUTAMEN NUCLEI IN MAJOR DEPRESSION [J].
HUSAIN, MM ;
MCDONALD, WM ;
DORAISWAMY, PM ;
FIGIEL, GS ;
NA, C ;
ESCALONA, PR ;
BOYKO, OB ;
NEMEROFF, CB ;
KRISHNAN, KRR .
PSYCHIATRY RESEARCH-NEUROIMAGING, 1991, 40 (02) :95-99