Neurocognitive profiles in elderly patients with frontotemporal degeneration or major depressive disorder

被引:47
作者
Elderkin-Thompson, V
Boone, KB
Hwang, S
Kumar, A
机构
[1] Univ Calif Los Angeles, Neuropsychiat Res Inst, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles Hosp, Dept Psychiat & Biobehav Sci, Neuropsychiat Res Inst Biostat Core, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Harbor Med Ctr, Dept Psychiat, Los Angeles, CA 90024 USA
关键词
frontotemporal dementia; depression; cognition; elderly; neuropsychology;
D O I
10.1017/S1355617704105067
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Major depressive disorder (MDD) and frontotemporal dementia (FTD) are both disorders in elderly populations that involve the prefrontal cortex and appear to have similar neurocognitive deficits. This review examined whether there are testable deficits in cognition that are consistent across individuals within the same neuropathological condition that could be used to facilitate early diagnoses. Medline and PsychInfo databases were searched for cognitive studies of depressed and FTD patients that used a matched control group and reported findings with means and standard deviations (N = 312). Effect sizes for FTD patients with mild and moderately advanced disease were compared to effect sizes within subgroups of depressed patients, such as inpatients, outpatients and community volunteers. Moderately advanced FTD patients were more impaired than depressed patients over all domains. particularly in language ability, although depressed inpatients appeared similar to FTD patients in some domains. Effect sizes for FTD patients who were in the mild, or early, stage of thud disease (MMSE = 28) were similar to those of depressed outpatients but slightly worse than those of community volunteers in all domains except semantic memory and executive ability. In the latter two domains, even mild FTD patients had notably large deficits. All FTD patients showed more severe deficits in some domains relative to other domains. In contrast, depressed patients tended to vary by clinical presentation or disease severity. but the magnitude of impairment for each subgroup remained relatively consistent across domains and they did not have the severe focal deficits in one or two domains demonstrated by FTD patients.
引用
收藏
页码:753 / 771
页数:19
相关论文
共 131 条
[1]   NEUROPSYCHOLOGICAL DEFICITS AND CT SCAN CHANGES IN ELDERLY DEPRESSIVES [J].
ABAS, MA ;
SAHAKIAN, BJ ;
LEVY, R .
PSYCHOLOGICAL MEDICINE, 1990, 20 (03) :507-520
[2]   Executive dysfunction and long-term outcomes of geriatric depression [J].
Alexopoulos, GS ;
Meyers, BS ;
Young, RC ;
Kalayam, B ;
Kakuma, T ;
Gabrielle, M ;
Sirey, JA ;
Hull, J .
ARCHIVES OF GENERAL PSYCHIATRY, 2000, 57 (03) :285-290
[3]   Frontostriatal and limbic dysfunction in late-life depression [J].
Alexopoulos, GS .
AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY, 2002, 10 (06) :687-695
[4]  
[Anonymous], 1996, FUNDAMENTALS BEHAV S
[5]   Regional cerebral blood flow abnormalities in late-life depression: Relation to refractoriness and chronification [J].
Awata, S ;
Ito, H ;
Konno, M ;
Ono, S ;
Kawashima, R ;
Fukuda, H ;
Sato, M .
PSYCHIATRY AND CLINICAL NEUROSCIENCES, 1998, 52 (01) :97-105
[6]   Dual-task performance in dysexecutive and nondysexecutive patients with a frontal lesion [J].
Baddeley, A ;
DellaSala, S ;
Papagno, C ;
Spinnler, H .
NEUROPSYCHOLOGY, 1997, 11 (02) :187-194
[7]   Effects of experimentally-induced emotional states on frontal lobe cognitive task performance [J].
Bartolic, EI ;
Basso, MR ;
Schefft, BK ;
Glauser, T ;
Titanic-Schefft, M .
NEUROPSYCHOLOGIA, 1999, 37 (06) :677-683
[8]  
BAXTER LR, 1989, ARCH GEN PSYCHIAT, V46, P243
[9]   Cognitive performance in tests sensitive to frontal lobe dysfunction in the elderly depressed [J].
Beats, BC ;
Sahakian, BJ ;
Levy, R .
PSYCHOLOGICAL MEDICINE, 1996, 26 (03) :591-603
[10]   THE ANATOMY OF MELANCHOLIA - FOCAL ABNORMALITIES OF CEREBRAL BLOOD-FLOW IN MAJOR DEPRESSION [J].
BENCH, CJ ;
FRISTON, KJ ;
BROWN, RG ;
SCOTT, LC ;
FRACKOWIAK, RSJ ;
DOLAN, RJ .
PSYCHOLOGICAL MEDICINE, 1992, 22 (03) :607-615