Wenjun Li1, L Tugan Muftuler2, Gang Chen3, B Douglas Ward4, Matthew D Budde5, Jennifer L Jones6, Malgorzata B Franczak7, Piero G Antuono8, Shi-Jiang Li9, Joseph S Goveas10. 1. Department of Psychiatry and Behavioral Medicine, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: wli@mcw.edu. 2. Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: lmuftuler@mcw.edu. 3. Department of Biophysics, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: gachen@mcw.edu. 4. Department of Biophysics, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: ward@mcw.edu. 5. Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: mdbudde@mcw.edu. 6. Department of Neurology, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: JlJones@mcw.edu. 7. Department of Neurology, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: MFranczak@mcw.edu. 8. Department of Neurology, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: PAntuono@mcw.edu. 9. Department of Psychiatry and Behavioral Medicine, Medical College of Wisconsin, Milwaukee, WI, USA; Department of Biophysics, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: sjli@mcw.edu. 10. Department of Psychiatry and Behavioral Medicine, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: jgoveas@mcw.edu.
Abstract
BACKGROUND AND OBJECTIVE: Late-life depression (LLD) and amnestic mild cognitive impairment (aMCI) are associated with white matter (WM) disruptions of the fronto-limbic and interhemispheric tracts implicated in mood regulation and episodic memory functions. This work investigates the extent of these WM abnormalities in patients LLD and aMCI when these diseases occur alone and when they coexist. MATERIALS AND METHODS: Eighty-four subjects separated into cognitively normal (n=33), LLD (n=20), aMCI (n=18), and comorbid aMCI and LLD (n=13) completed Diffusion Tensor Imaging (DTI) scans. Tract-based spatial statistics was employed to skeletonize multiple DTI indices of the cingulum, corpus callosum, fornix and uncinate fasciculus. Analysis of covariance and post-hoc tests compared group differences. Multiple linear regressions were performed between DTI and behavioral measures for the whole sample and within individual patient groups. RESULTS: Divergent microstructural disruptions were identified in LLD- and aMCI-only groups, whereas the comorbid group showed widespread abnormalities especially in the hippocampal cingulum and fornix tracts. The LLD groups also showed significant disruptions in the uncinate fasciculus and corpus callosal tracts. Higher depressive symptom and lower episodic memory scores were associated with increased diffusivity measures in the fornix and hippocampal cingulum across all subjects. CONCLUSIONS: Widespread WM microstructural disruptions are present when LLD and aMCI are comorbid -especially in the medial temporal lobe tracts. These WM disruptions may be a marker of disease severity. Also, multiple DTI parameters should be used when evaluating the WM fiber integrity in LLD and aMCI.
BACKGROUND AND OBJECTIVE:Late-life depression (LLD) and amnestic mild cognitive impairment (aMCI) are associated with white matter (WM) disruptions of the fronto-limbic and interhemispheric tracts implicated in mood regulation and episodic memory functions. This work investigates the extent of these WM abnormalities in patients LLD and aMCI when these diseases occur alone and when they coexist. MATERIALS AND METHODS: Eighty-four subjects separated into cognitively normal (n=33), LLD (n=20), aMCI (n=18), and comorbid aMCI and LLD (n=13) completed Diffusion Tensor Imaging (DTI) scans. Tract-based spatial statistics was employed to skeletonize multiple DTI indices of the cingulum, corpus callosum, fornix and uncinate fasciculus. Analysis of covariance and post-hoc tests compared group differences. Multiple linear regressions were performed between DTI and behavioral measures for the whole sample and within individual patient groups. RESULTS: Divergent microstructural disruptions were identified in LLD- and aMCI-only groups, whereas the comorbid group showed widespread abnormalities especially in the hippocampal cingulum and fornix tracts. The LLD groups also showed significant disruptions in the uncinate fasciculus and corpus callosal tracts. Higher depressive symptom and lower episodic memory scores were associated with increased diffusivity measures in the fornix and hippocampal cingulum across all subjects. CONCLUSIONS: Widespread WM microstructural disruptions are present when LLD and aMCI are comorbid -especially in the medial temporal lobe tracts. These WM disruptions may be a marker of disease severity. Also, multiple DTI parameters should be used when evaluating the WM fiber integrity in LLD and aMCI.
Authors: Michelle M Mielke; Ozioma C Okonkwo; Kenichi Oishi; Susumu Mori; Sarah Tighe; Michael I Miller; Can Ceritoglu; Timothy Brown; Marilyn Albert; Constantine G Lyketsos Journal: Alzheimers Dement Date: 2012 Impact factor: 21.566
Authors: Serge Gauthier; Barry Reisberg; Michael Zaudig; Ronald C Petersen; Karen Ritchie; Karl Broich; Sylvie Belleville; Henry Brodaty; David Bennett; Howard Chertkow; Jeffrey L Cummings; Mony de Leon; Howard Feldman; Mary Ganguli; Harald Hampel; Philip Scheltens; Mary C Tierney; Peter Whitehouse; Bengt Winblad Journal: Lancet Date: 2006-04-15 Impact factor: 79.321
Authors: Claire E Sexton; Ukwuori G Kalu; Nicola Filippini; Clare E Mackay; Klaus P Ebmeier Journal: Neurobiol Aging Date: 2010-07-08 Impact factor: 4.673
Authors: Sean J Colloby; Michael J Firbank; Alan J Thomas; Akshya Vasudev; Steve W Parry; John T O'Brien Journal: J Affect Disord Date: 2011-08-20 Impact factor: 4.839
Authors: Joseph M Mettenburg; Tammie L Benzinger; Joshua S Shimony; Abraham Z Snyder; Yvette I Sheline Journal: Neuroimage Date: 2012-02-24 Impact factor: 6.556
Authors: Maria Giulia Preti; Maria Marcella Laganà; Francesca Baglio; Ludovica Griffanti; Raffaello Nemni; Pietro Cecconi; Giuseppe Baselli Journal: Conf Proc IEEE Eng Med Biol Soc Date: 2011
Authors: Stephen M Smith; Mark Jenkinson; Heidi Johansen-Berg; Daniel Rueckert; Thomas E Nichols; Clare E Mackay; Kate E Watkins; Olga Ciccarelli; M Zaheer Cader; Paul M Matthews; Timothy E J Behrens Journal: Neuroimage Date: 2006-04-19 Impact factor: 6.556
Authors: Wenjun Li; B Douglas Ward; Xiaolin Liu; Gang Chen; Jennifer L Jones; Piero G Antuono; Shi-Jiang Li; Joseph S Goveas Journal: J Neurol Neurosurg Psychiatry Date: 2014-11-28 Impact factor: 10.154
Authors: Benoit H Mulsant; Aristotle N Voineskos; Neda Rashidi-Ranjbar; Tarek K Rajji; Sanjeev Kumar; Nathan Herrmann; Linda Mah; Alastair J Flint; Corinne E Fischer; Meryl A Butters; Bruce G Pollock; Erin W Dickie; John A E Anderson Journal: Neuropsychopharmacology Date: 2020-05-18 Impact factor: 7.853
Authors: Melissa A Lancaster; Michael Seidenberg; J Carson Smith; Kristy A Nielson; John L Woodard; Sally Durgerian; Stephen M Rao Journal: J Int Neuropsychol Soc Date: 2016-11 Impact factor: 2.892