Calcium accumulation or iron deposition: Delving into the temporal sequence of amyotrophic lateral sclerosis pathophysiology in the primary motor cortex

Sadegh Ghaderi , Sana Mohammadi , Farzad Fatehi

Ibrain ›› 2024, Vol. 10 ›› Issue (3) : 375 -377.

PDF
Ibrain ›› 2024, Vol. 10 ›› Issue (3) : 375 -377. DOI: 10.1002/ibra.12168
LETTER

Calcium accumulation or iron deposition: Delving into the temporal sequence of amyotrophic lateral sclerosis pathophysiology in the primary motor cortex

Author information +
History +
PDF

Abstract

Amyotrophic lateral sclerosis (ALS) causes progressive motor neuron degeneration, but an in vivo understanding of its early pathology remains limited. A recent study used topographic layer imaging to investigate iron and calcium accumulation in the primary motor cortex (M1) of patients with ALS compared with controls. Despite the preserved cortical thickness, ALS patients showed increased iron in layer 6 and calcium accumulation in layer 5a and the superficial layer. Calcium accumulation was particularly prominent in the low-myelin borders, potentially preceding the demyelination. This study reveals a novel in vivo pathology in ALS, suggesting that calcium dysregulation may precede iron accumulation and contribute to early M1 cell degeneration. Further investigation using quantitative susceptibility mapping and complementary techniques, such as diffusion kurtosis imaging, along with ultrahigh-field magnetic resonance imaging, into the role of calcium and early intervention strategies is warranted.

Keywords

ALS / calcium / iron / primary motor cortex / QSM

Cite this article

Download citation ▾
Sadegh Ghaderi, Sana Mohammadi, Farzad Fatehi. Calcium accumulation or iron deposition: Delving into the temporal sequence of amyotrophic lateral sclerosis pathophysiology in the primary motor cortex. Ibrain, 2024, 10(3): 375-377 DOI:10.1002/ibra.12168

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Northall A, Doehler J, Weber M, et al. Multimodal layer modelling reveals in vivo pathology in amyotrophic lateral sclerosis. Brain. 2023;147:1087-1099.

[2]

Acosta-Cabronero J, Machts J, Schreiber S, et al. Quantitative susceptibility MRI to detect brain iron in amyotrophic lateral sclerosis. Radiology. 2018;289(1):195-203.

[3]

Udaka F, Kameyama M, Tomonaga M. Degeneration of Betz cells in motor neuron disease. A Golgi study. Acta Neuropathol. 1986;70(3-4):289-295.

[4]

Hammer RP, Tomiyasu U, Scheibel AB. Degeneration of the human Betz cell due to amyotrophic lateral sclerosis. Exp Neurol. 1979;63(2):336-346.

[5]

Kwan JY, Jeong SY, Van Gelderen P, et al. Iron accumulation in deep cortical layers accounts for MRI signal abnormalities in ALS: correlating 7 tesla MRI and pathology. PLoS One. 2012;7(4):e35241.

[6]

Costagli M, Donatelli G, Biagi L, et al. Magnetic susceptibility in the deep layers of the primary motor cortex in amyotrophic lateral sclerosis. NeuroImage: Clin. 2016;12:965-969.

[7]

Nolan M, Scott C, Gamarallage MP, et al. Quantitative patterns of motor cortex proteinopathy across ALS genotypes. Acta Neuropathol Commun. 2020;8(1):98.

[8]

Leal S, Gomes M. Calcium dysregulation links ALS defective proteins and motor neuron selective vulnerability. Front Cell Neurosci. 2015;9:225.

[9]

Welton T, Maller JJ, Lebel RM, Tan ET, Rowe DB, Grieve SM. Diffusion kurtosis and quantitative susceptibility mapping MRI are sensitive to structural abnormalities in amyotrophic lateral sclerosis. NeuroImage: Clin. 2019;24:101953.

[10]

Tan S, Hartono S, Welton T, et al. Utility of quantitative susceptibility mapping and diffusion kurtosis imaging in the diagnosis of early Parkinson’s disease. NeuroImage: Clini. 2021;32:102831.

RIGHTS & PERMISSIONS

2024 The Authors. Ibrain published by Affiliated Hospital of Zunyi Medical University (AHZMU) and Wiley-VCH GmbH.

AI Summary AI Mindmap
PDF

125

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/