Superficial white matter microstructure affects processing speed in cerebral small vessel disease.
Superficial white matter microstructure affects processing speed in cerebral small vessel disease.
复制标题
浅层白质微结构影响脑小血管疾病的处理速度
DOI:
10.1002/hbm.26004
复制
发表时间:
2022-12-01
影响因子:
4.8
通讯作者:
中科院分区:
文献类型:
--
作者:
White matter hyperintensities (WMH) are a typical feature of cerebral small vessel disease (CSVD). This condition contributes to about 50% of dementias worldwide, a massive health burden in aging. Microstructural alterations in the deep white matter (DWM) have been widely examined in CSVD. However, little is known about abnormalities in the superficial white matter (SWM) and their relevance for processing speed, the main cognitive deficit in CSVD. In this paper, 141 patients with CSVD were studied. Processing speed was assessed by the completion time of the Trail Making Test Part A. White matter abnormalities were assessed by WMH burden (lesion volume on T2-FLAIR) and diffusion MRI, including DTI and free-water (FW) imaging microstructure measures. The results of our study indicate that the superficial white matter may play a particularly important role in cognitive decline in CSVD. SWM imaging measures resulted in a large contribution to processing speed, despite a relatively small WMH burden in the SWM. SWM FW had the strongest association with processing speed among all imaging markers and, unlike the other diffusion MRI measures, significantly increased between two patient subgroups with the lowest WMH burdens (possibly representing early stages of disease). When comparing two patient subgroups with the highest WMH burdens, the involvement of WMH in the SWM was accompanied by significant differences in processing speed and white matter microstructure. Given significant effects of WMH volume and regional FW on processing speed, we performed a mediation analysis. SWM FW was found to fully mediate the association between WMH volume and processing speed, while no mediation effect of DWM FW was observed. Overall, our findings identify SWM abnormalities in CSVD and suggest that the SWM has an important contribution to processing speed. Results indicate that FW in the SWM is a sensitive marker of microstructural changes associated with cognition in CSVD. This study extends the current understanding of CSVD-related dysfunction and suggests that the SWM, as an understudied region, can be a potential target for monitoring pathophysiological processes in future research.
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DOI:
10.1002/alz.12150
发表时间:
2020-11
期刊:
Alzheimer's & dementia : the journal of the Alzheimer's Association
影响因子:
--
作者:
Finsterwalder S;Vlegels N;Gesierich B;Araque Caballero MÁ;Weaver NA;Franzmeier N;Georgakis MK;Konieczny MJ;Koek HL;Dominantly Inherited Alzheimer Network (DIAN);Karch CM;Graff-Radford NR;Salloway S;Oh H;Allegri RF;Chhatwal JP;DELCODE study group;Jessen F;Düzel E;Dobisch L;Metzger C;Peters O;Incesoy EI;Priller J;Spruth EJ;Schneider A;Fließbach K;Buerger K;Janowitz D;Teipel SJ;Kilimann I;Laske C;Buchmann M;Heneka MT;Brosseron F;Spottke A;Roy N;Ertl-Wagner B;Scheffler K;Alzheimer's Disease Neuroimaging Initiative (ADNI);Utrecht VCI study group;Seo SW;Kim Y;Na DL;Kim HJ;Jang H;Ewers M;Levin J;Schmidt R;Pasternak O;Dichgans M;Biessels GJ;Duering M
通讯作者:
Duering M
影响因子:
5.2
作者:
Cedres, Nira;Ferreira, Daniel;Westman, Eric
通讯作者:
Westman, Eric
影响因子:
5.7
作者:
Gazes Y;Bowman FD;Razlighi QR;O'Shea D;Stern Y;Habeck C
通讯作者:
Habeck C
影响因子:
3.2
作者:
Bigham, Bahare;Zamanpour, Seyed Amir;Zare, Hoda
通讯作者:
Zare, Hoda
影响因子:
14.8
作者:
Bowie, Christopher R.;Harvey, Philip D.
通讯作者:
Harvey, Philip D.