Assessment of Iron Deposition in the Brain in Frontotemporal Dementia and Its Correlation with Behavioral Traits.
Assessment of Iron Deposition in the Brain in Frontotemporal Dementia and Its Correlation with Behavioral Traits.
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DOI:
10.3174/ajnr.a5339
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发表时间:
2017-10
期刊:
影响因子:
--
通讯作者:
Mathuranath PS
中科院分区:
文献类型:
--
作者:
Sheelakumari R;Kesavadas C;Varghese T;Sreedharan RM;Thomas B;Verghese J;Mathuranath PS
Brain iron-deposition has been implicated as a major culprit in the pathophysiology of neurodegeneration. However, the quantitative assessment of iron in behavioralvariant frontotemporal dementia (bvFTD and primary progressive aphasia (PPA) brains has not been performed. The aim of our study was to investigate the characteristic iron levels in the FTD subtypes using susceptibility weighted imaging, and report its association with behavioural profiles. This prospective study included 46 FTD patients (34 bvFTD and 12 PPA) and 34 age-matched normal controls. We performed behavioural and neuropsychological assessment in all the subjects. The quantitative iron load was determined on SWI in the superior frontal gyrus and temporal pole, precentral gyrus, basal ganglia, anterior cingulate, frontal white matter, head and body of hippocampus, red nucleus, substantia nigra, insula and dendate nucleus. A linear regression analysis was performed to correlate between iron content and behavioural scores in patients. The iron content of bilateral superior frontal and temporal gyrus, anterior cingulate, putamen, right hemispheric precentral gyrus, insula, hippocampus and red nucleus was higher in bvFTD than controls. PPA patients had increased iron levels in the left superior temporal gyrus. In addition, right superior frontal gyrus iron deposition discriminated bvFTD from PPA. A significant correlation was found between apathy and iron content in superior frontal gyrus, and disinhibition and iron content in putamen. Quantitative assessment of iron deposition using SWI may serve as a new biomarker in the diagnostic work up of FTD and help distinguish FTD subtypes.