TY - JOUR
T1 - Neural correlates associated with cognitive decline in late-life depression
AU - Wang, Lihong
AU - Potter, Guy G.
AU - Krishnan, R. K.Ranga
AU - Dolcos, Florin
AU - Smith, Gwenn S.
AU - Steffens, David C.
N1 - Funding Information:
This research was supported by the Duke Silvio O. Conte Center for the Neuroscience of Depression (P50-MH60451) , the Paul B. Beeson Career Developmental Awards (K23-AG028982) , and a National Alliance for Research in Schizophrenia and Depression Young Investigator Award (LW). GGP is supported by NIA Career Developmental Awards (K23MH87741) , FD was supported by a Young Investigator Award from the National Alliance for Research on Schizophrenia and Depression and a CPRF Award from the Canadian Psychiatric Research Foundation, and DC is supported by a NIMH Mid-Career Development Award (K24 MH70027) .
PY - 2012/8
Y1 - 2012/8
N2 - OBJECTIVES: Persistent cognitive impairment (PCI) after remission of depressive symptoms is a major adverse outcome of late-life depression (LLD). The purpose of this study was to examine neural substrates associated with PCI in LLD. DESIGN: Longitudinal study. SETTING: Outpatient depression treatment study at Duke University. PARTICIPANTS: Twenty-three patients with LLD completed a 2-year follow-up study, and were in a remitted or partially remitted state at Year 2. METHODS: At first entry to the study (Year 0), all participants had a functional magnetic resonance imaging scan while performing an emotional oddball task. For the purpose of this report, the primary functional magnetic resonance imaging outcome was brain activation during target detection, which is a measure of executive function. The Consortium to Establish a Registry for Alzheimer's Disease neuropsychological battery was used to assess cognitive status yearly, and the Montgomery-sberg Depression Rating Scale was used to assess severity of depression at Year 0 and every 6 months thereafter for 2 years. We investigated changes in brain activation at Year 0 associated with PCI over 2 years. RESULTS: Patients with PCI at the 2-year follow-up date had significantly decreased activation at Year 0 in the dorsal anterior cingulate cortex, hippocampus, inferior frontal cortex, and insula compared to non-PCI patients. CONCLUSIONS: Our results suggest individuals who have LLD with PCI have decreased activation in the similar neural networks associated with the development of Alzheimer disease among nondepressed individuals. Measuring neural activity in these regions in individuals with LLD may help identify patients at-risk for cognitive impairment.
AB - OBJECTIVES: Persistent cognitive impairment (PCI) after remission of depressive symptoms is a major adverse outcome of late-life depression (LLD). The purpose of this study was to examine neural substrates associated with PCI in LLD. DESIGN: Longitudinal study. SETTING: Outpatient depression treatment study at Duke University. PARTICIPANTS: Twenty-three patients with LLD completed a 2-year follow-up study, and were in a remitted or partially remitted state at Year 2. METHODS: At first entry to the study (Year 0), all participants had a functional magnetic resonance imaging scan while performing an emotional oddball task. For the purpose of this report, the primary functional magnetic resonance imaging outcome was brain activation during target detection, which is a measure of executive function. The Consortium to Establish a Registry for Alzheimer's Disease neuropsychological battery was used to assess cognitive status yearly, and the Montgomery-sberg Depression Rating Scale was used to assess severity of depression at Year 0 and every 6 months thereafter for 2 years. We investigated changes in brain activation at Year 0 associated with PCI over 2 years. RESULTS: Patients with PCI at the 2-year follow-up date had significantly decreased activation at Year 0 in the dorsal anterior cingulate cortex, hippocampus, inferior frontal cortex, and insula compared to non-PCI patients. CONCLUSIONS: Our results suggest individuals who have LLD with PCI have decreased activation in the similar neural networks associated with the development of Alzheimer disease among nondepressed individuals. Measuring neural activity in these regions in individuals with LLD may help identify patients at-risk for cognitive impairment.
KW - Cognitive decline
KW - dorsal anterior cingulate cortex
KW - functional magnetic resonance imaging
KW - hippocampus
KW - late-life depression
UR - http://www.scopus.com/inward/record.url?scp=84864288043&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84864288043&partnerID=8YFLogxK
U2 - 10.1097/JGP.0b013e31823e2cc7
DO - 10.1097/JGP.0b013e31823e2cc7
M3 - Article
C2 - 22157280
AN - SCOPUS:84864288043
SN - 1064-7481
VL - 20
SP - 653
EP - 663
JO - American Journal of Geriatric Psychiatry
JF - American Journal of Geriatric Psychiatry
IS - 8
ER -