» Articles » PMID: 25781024

Correlation Between Relaxometry and Diffusion Tensor Imaging in the Globus Pallidus of Huntington's Disease Patients

Overview
Journal PLoS One
Date 2015 Mar 18
PMID 25781024
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Huntington's disease (HD) is an inherited neurodegenerative disorder with progressive impairment of motor, behavioral and cognitive functions. The clinical features of HD are closely related to the degeneration of the basal ganglia, predominantly the striatum. The main striatal output structure, the globus pallidus, strongly accumulates metalloprotein-bound iron, which was recently shown to influence the diffusion tensor scalar values. To test the hypothesis that this effect dominates in the iron-rich basal ganglia of HD patients, we examined the globus pallidus using DTI and T2 relaxometry sequences. Quantitative magnetic resonance (MR), clinical and genetic data (number of CAG repeats) were obtained from 14 HD patients. MR parameters such as the T2 relaxation rate (RR), fractional anisotropy (FA) and mean diffusivity (MD) were analysed. A positive correlation was found between RR and FA (R2=0.84), between CAG and RR (R2=0.59) and between CAG and FA (R2=0.44). A negative correlation was observed between RR and MD (R2=0.66). A trend towards correlation between CAG and MD was noted. No correlation between MR and clinical parameters was found. Our results indicate that especially magnetic resonance FA measurements in the globus pallidus of HD patients may be strongly affected by metalloprotein-bound iron accumulation.

Citing Articles

Temporal dynamics of white and gray matter plasticity during motor skill acquisition: a comparative diffusion tensor imaging and multiparametric mapping analysis.

Emmenegger T, David G, Mohammadi S, Ziegler G, Callaghan M, Thompson A Cereb Cortex. 2024; 34(8.

PMID: 39214853 PMC: 11364465. DOI: 10.1093/cercor/bhae344.


Longitudinal assessment of early-life white matter development with quantitative relaxometry in nonhuman primates.

Moody J, Aggarwal N, Dean 3rd D, Tromp D, Kecskemeti S, Oler J Neuroimage. 2022; 251:118989.

PMID: 35151851 PMC: 8940652. DOI: 10.1016/j.neuroimage.2022.118989.


Nigral diffusivity, but not free water, correlates with iron content in Parkinson's disease.

Langley J, Huddleston D, Hu X Brain Commun. 2021; 3(4):fcab251.

PMID: 34805996 PMC: 8599079. DOI: 10.1093/braincomms/fcab251.


Neuroimaging, Urinary, and Plasma Biomarkers of Treatment Response in Huntington's Disease: Preclinical Evidence with the p75 Ligand LM11A-31.

Simmons D, Mills B, Butler Iii R, Kuan J, McHugh T, Akers C Neurotherapeutics. 2021; 18(2):1039-1063.

PMID: 33786806 PMC: 8423954. DOI: 10.1007/s13311-021-01023-8.


Diffusion imaging in Huntington's disease: comprehensive review.

Estevez-Fraga C, Scahill R, Rees G, Tabrizi S, Gregory S J Neurol Neurosurg Psychiatry. 2020; .

PMID: 33033167 PMC: 7803908. DOI: 10.1136/jnnp-2020-324377.


References
1.
Drayer B, Burger P, Darwin R, Riederer S, Herfkens R, Johnson G . MRI of brain iron. AJR Am J Roentgenol. 1986; 147(1):103-10. DOI: 10.2214/ajr.147.1.103. View

2.
Schenker C, Meier D, Wichmann W, Boesiger P, Valavanis A . Age distribution and iron dependency of the T2 relaxation time in the globus pallidus and putamen. Neuroradiology. 1993; 35(2):119-24. DOI: 10.1007/BF00593967. View

3.
Chen J, Hardy P, Kucharczyk W, Clauberg M, Joshi J, Vourlas A . MR of human postmortem brain tissue: correlative study between T2 and assays of iron and ferritin in Parkinson and Huntington disease. AJNR Am J Neuroradiol. 1993; 14(2):275-81. PMC: 8332933. View

4.
Zecca L, Youdim M, Riederer P, Connor J, Crichton R . Iron, brain ageing and neurodegenerative disorders. Nat Rev Neurosci. 2004; 5(11):863-73. DOI: 10.1038/nrn1537. View

5.
Smith S, Jenkinson M, Woolrich M, Beckmann C, Behrens T, Johansen-Berg H . Advances in functional and structural MR image analysis and implementation as FSL. Neuroimage. 2004; 23 Suppl 1:S208-19. DOI: 10.1016/j.neuroimage.2004.07.051. View