TY - JOUR
T1 - Diffuse Microstructural Abnormalities of Normal-Appearing White Matter in Late Life Depression
T2 - A Diffusion Tensor Imaging Study
AU - Shimony, Joshua S.
AU - Sheline, Yvette I.
AU - D'Angelo, Gina
AU - Epstein, Adrian A.
AU - Benzinger, Tammie L.S.
AU - Mintun, Mark A.
AU - McKinstry, Robert C.
AU - Snyder, Abraham Z.
N1 - Funding Information:
This work was supported by a NARSAD Independent Investigator Award (YIS), MH60697 (YIS), K24 MH079510 (YIS) and NIH K23 HD053212 (JSS). Neither the granting agencies nor any other funding entity had a role in any of the following aspects of this study: design and conduct of the study; collection, management, analysis and interpretation of the data; or preparation, review, or approval of the manuscript. Authors JSS and YIS are independent of any commercial provider, had full access to all of the data in this study, and take responsibility for the integrity of the data and the accuracy of the data analysis. We thank Anthony Durbin for help with data acquisition and data processing. Dr. Sheline serves on the advisory board and speaker's bureau of E. Lilly, Inc. All other authors report no biomedical financial interests or potential conflicts of interest.
PY - 2009/8/1
Y1 - 2009/8/1
N2 - Background: Many recent studies have identified white matter abnormalities in late life depression (LLD). These abnormalities include an increased volume of discrete white matter hyperintensities on T2-weighted imaging (WMH) and changes in the diffusion tensor properties of water. However, no study of LLD to date has examined the integrity of white matter outside of WMH (i.e., in normal-appearing white matter). Methods: We performed T1- and T2-weighted imaging as well as diffusion tensor imaging (DTI) in depressed elderly subjects (n = 73) and nondepressed control subjects (n = 23) matched for age and cerebrovascular risk factors. The structural images were segmented into white matter, gray matter, cerebrospinal fluid, and WMH. The DTI parameters were calculated in white matter regions of interest after excluding the WMH. Results: Compared with control subjects, in the LLD group there were widespread abnormalities in DTI parameters, particularly in prefrontal regions. From a comprehensive neuropsychological battery, the strongest correlations were observed between cognitive processing speed and DTI abnormalities. Conclusions: These results suggest that further investigation is warranted to determine potential reversibility and/or prognosis in LLD.
AB - Background: Many recent studies have identified white matter abnormalities in late life depression (LLD). These abnormalities include an increased volume of discrete white matter hyperintensities on T2-weighted imaging (WMH) and changes in the diffusion tensor properties of water. However, no study of LLD to date has examined the integrity of white matter outside of WMH (i.e., in normal-appearing white matter). Methods: We performed T1- and T2-weighted imaging as well as diffusion tensor imaging (DTI) in depressed elderly subjects (n = 73) and nondepressed control subjects (n = 23) matched for age and cerebrovascular risk factors. The structural images were segmented into white matter, gray matter, cerebrospinal fluid, and WMH. The DTI parameters were calculated in white matter regions of interest after excluding the WMH. Results: Compared with control subjects, in the LLD group there were widespread abnormalities in DTI parameters, particularly in prefrontal regions. From a comprehensive neuropsychological battery, the strongest correlations were observed between cognitive processing speed and DTI abnormalities. Conclusions: These results suggest that further investigation is warranted to determine potential reversibility and/or prognosis in LLD.
KW - Depression
KW - MRI
KW - diffusion tensor imaging
KW - geriatrics
KW - segmentation
UR - http://www.scopus.com/inward/record.url?scp=67649394199&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2009.02.032
DO - 10.1016/j.biopsych.2009.02.032
M3 - Article
C2 - 19375071
AN - SCOPUS:67649394199
SN - 0006-3223
VL - 66
SP - 245
EP - 252
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 3
ER -