Corpus callosum macro and microstructure in late-life depression

被引:26
作者
Emsell, Louise [1 ,2 ,3 ]
Adamson, Christopher [4 ]
De Winter, Francois-Laurent [1 ]
Billiet, Thibo [2 ,3 ]
Christiaens, Daan [5 ,6 ,7 ]
Bouckaert, Filip [1 ,8 ]
Adamczuk, Katarzyna [3 ,9 ,10 ,11 ]
Vandenberghe, Rik [3 ,9 ]
Seal, Marc L. [4 ,12 ]
Sienaert, Pascal [8 ]
Sunaert, Stefan [2 ,3 ]
Vandenbulcke, Mathieu [1 ]
机构
[1] Univ Psychiat Ctr UPC KU Leuven, Old Age Psychiat, Leuven, Belgium
[2] Katholieke Univ Leuven, Translat MRI & Radiol, Leuven, Belgium
[3] Univ Hosp Leuven, Leuven, Belgium
[4] Murdoch Childrens Res Inst, Dev Imaging, Parkville, Vic, Australia
[5] Katholieke Univ Leuven, Dept Elect Engn ESAT Proc Speech & Images PSI, Med Image Comp, Leuven, Belgium
[6] Univ Hosp Leuven, Med Imaging Res Ctr, Leuven, Belgium
[7] Kings Coll London, Div Imaging Sci & Biomed Engn, London, England
[8] KU Leaven, Univ Psychiat Ctr KU Leuven, Acad Ctr ECT & Neurostimulat AcCENT, Kortenberg, Belgium
[9] Katholieke Univ Leuven, Dept Neurol, Lab Cognit Neurol, Leuven, Belgium
[10] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[11] Harvard Med Sch, Boston, MA USA
[12] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
关键词
Depression; Late-life; Corpus callosum; White matter; MRI; Diffusion; CONSTRAINED SPHERICAL DECONVOLUTION; WHITE-MATTER HYPERINTENSITIES; VASCULAR RISK-FACTORS; DIFFUSION-TENSOR MRI; GERIATRIC DEPRESSION; MAJOR DEPRESSION; BIPOLAR DISORDER; CROSSING FIBERS; OLDER-ADULTS; BRAIN;
D O I
10.1016/j.jad.2017.06.063
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Differences in corpus callosum (CC) morphology and microstructure have been implicated in late life depression and may distinguish between late and early-onset forms of the illness. However, a multimodal approach using complementary imaging techniques is required to disentangle microstructural alterations from macrostructural partial volume effects. Methods: 107 older adults were assessed: 55 currently-depressed patients without dementia and 52 controls without cognitive impairment. We investigated group differences and clinical associations in 7 sub-regions of the mid-sagittal corpus callosum using T1 anatomical data, white matter hyperintensity (WMH) quantification and two different diffusion MRI (dMRI) models (multi-tissue constrained spherical deconvolution, yielding apparent fibre density, AFD; and diffusion tensor imaging, yielding fractional anisotropy, FA and radial diffusivity, RD). Results: Callosal AFD was lower in patients compared to controls. There were no group differences in CC thickness, surface area, FA, RD, nor whole brain or WMH volume. Late-onset of depression was associated with lower FA, higher RD and lower AFD. There were no associations between any imaging measures and psychotic features or depression severity as assessed by the geriatric depression scale. WMH volume was associated with lower FA and AFD, and higher RD in patients. Limitations: Patients were predominantly treatment-resistant. Measurements were limited to the mid-sagittal CC. dMRI analysis was performed on a smaller cohort, n=77. AFD was derived from low b-value data. Conclusions: Callosal structure is largely preserved in LLD. WMH burden may impact on CC microstructure in late-onset depression suggesting vascular pathology has additional deleterious effects in these patients.
引用
收藏
页码:63 / 70
页数:8
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