Abstract
Iron can contribute to the pathogenesis and progression of multiple sclerosis (MS) due to its accumulation in the human brain. We focus on the thalamus as an information transmitter between various subcortical and cortical areas. Thalamic iron seems to follow different rules than iron in other deep gray matter structures and its relation to the clinical outcomes of MS is still indistinct. In our study, we investigated a connection between thalamic iron and patients' disability and course of the disease. The presence of paramagnetic substances in the tissues was tracked by T2* quantification. Twenty-eight subjects with definite MS and 15 age-matched healthy controls underwent MRI examination with a focus on gradient echo sequence. We observed a non-monotonous course of T2* values with age in healthy controls. Furthermore, T2* distribution in MS patients was significantly wider than that of age matched healthy volunteers (P<0.001). A strong significant correlation was demonstrated between T2* distribution spread and the expanded disability status scale (EDSS) (left thalamus:P<0.00005; right thalamus: P<0.005), and multiple sclerosis severity scale (MSSS) (left thalamus: P<0.05; right thalamus: P<0.005). The paramagnetic iron distribution in the thalamus in MS was not uniform and this inhomogeneity may be considered as an indicator of thalamic neurodegeneration in MS.
Highlights
There is a broad consensus that multiple sclerosis (MS) is more than an inflammatory disease; it involves some characteristic features of a classicalCLC number: R744.51, Document code: A The authors reported no conflict of interests
The forms of non-heme irons considered to be present in sufficient amounts to be detectable in MRI are ferritin and hemosiderin, which are found in various cell types[2,6]
The calculated T2* values ranged from 59.8 ms to 72.4 ms [mean 69.3 ms; 68.6 ms] and R2* ranged from 0.0137 ms–1 to 0.0167 ms–1 [mean 0.0144 ms–1 and 0.0145 ms–1]
Summary
There is a broad consensus that multiple sclerosis (MS) is more than an inflammatory disease; it involves some characteristic features of a classicalCLC number: R744.51, Document code: A The authors reported no conflict of interests. We investigated a connection between thalamic iron and patients' disability and course of the disease. We observed a non-monotonous course of T2* values with age in healthy controls.
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