In a recent study published in Nature Communications, researchers demonstrated a magnetic resonance imaging (MRI) method sensitive to the live brain’s iron homeostasis (the r1-r2 extent of rest or relaxivity).

Study: Non-invasive assessment of normal and impaired iron homeostasis within the brain. Image Credit: ORION PRODUCTION/Shutterstock.com

Background

Iron homeostasis is critical for brain function and is compromised in aging, neurodegenerative disorders, and cancer. Homeostasis of iron in live brain tissue is helpful for illness diagnosis, monitoring, treatment, and improving the understanding of disease causation. MRI, because of its paramagnetic characteristics, is a useful and non-invasive approach for assessing iron concentration in tissues of the brain. Understanding iron homeostasis within the brain is critical for accurate illness detection and therapy.

In regards to the study

In the current study, researchers proposed an MRI-based approach to iron rest in vivo that’s sensitive to the homeostasis of iron within the human brain.

The work employed MRI characteristics to investigate molecular iron habitats within the live brain in a non-invasive manner. The researchers used iron’s unique relaxivity property on the rates of magnetic resonance rest, R1 in addition to R2, to construct a biophysical framework of the linear interdependence, which was known as the r1-r2 relaxivity. The researchers employed the bottom-up approach to evaluate the relaxivity of varied environments of iron within the in vitro settings, followed by the top-down approach to evaluate the relaxivity within the human brain within the in vivo setting and relate it to the measurement of iron molecules and their genetic expression ex vivo.

The researchers examined the biological underpinnings of relaxivity in healthy individuals and compared them with other magnetic resonance contrasts. The researchers examined the contrast of relaxivity between non-pathological and diseased tissues amongst meningioma patients and compared the MR imaging results to tumor iron homeostasis calculations within the ex vivo environment. The sensitivity of R1 and R2 to myelin content was studied, and numerical simulations were run to account for the contributions of various brain tissue components to relaxivity assessment.

The researchers investigated the sensitivity of the relaxivity approach to the homeostasis of iron in normal and aged brains. They compiled previously published postmortem histology data characterizing iron, ferritin, and transferrin contents in various brain areas of young and elderly humans and evaluated iron mobilization ability using the postmortem dataset.

The researchers explored how the tumor features acquired by the relaxivity approach differed from the knowledge included in R1 in addition to R2. GSEA was used to discover molecular activities that were considerably linked with each MRI value. Finally, the researchers verified the relaxivity method’s sensitivity to iron homeostasis on the proteome level by comparing in vivo MRI results to ex vivo iron homeostasis calculation on the identical tissue.

Results

Within the in vitro environment, the MRI method was utilized to research the unique paramagnetic characteristics of ferrous, transferring, and ferritin ions. The technique was confirmed within the human brain in vivo versus ex vivo iron compound measurement and gene expression. The relaxivity method indicated iron homeostasis in tumors and distinguished neoplastic tissues from healthy tissues. The relaxivity model offered in vivo iron relaxivity data to assist within the identification of varied iron environments within the brain.

Each R1 in addition to R2 rose when the concentration of varied iron compounds increased, with the speed of this rise, termed the iron relaxivity, various depending on the iron environment. The iron relaxivity, which separated the iron environments and was consistent whether computed over samples with greater or lower amounts, might make clear the problem at hand.

The relaxivity was a good MRI estimate for the ratio of R1: R2 iron relaxivities. In comparison with iron-bound transferrin, apo-transferrin showed a considerably lower r1-r2 relaxivity, which accommodates paramagnetic characteristics that induce the relaxivity. The study findings indicated that the relaxivity method may be utilized to judge the extent of MR rest for iron in vivo to show the differential paramagnetic characteristics of varied molecular iron environments.

The outcomes also revealed that the relaxivity of r1 and r2 was less vulnerable to lipid content and composition than R1 in addition to R2. Within the human brains investigated in vivo, the relaxivity of r1 and r2 exhibited a statistically distinct MRI difference between R1 and R2. The R1 and R2 values demonstrated a substantial separation between gray-matter and white-matter areas, however the contrast observed by the relaxivity method across the brain exhibited a novel spatial pattern and highlighted distinctions across brain regions beyond the standard white-matter-gray matter divergence.

The r1-r2 relaxivity was connected to iron mobilization ability across the brain and in aging. R2 was highly linked with iron levels, indicating that the in vivo and postmortem datasets agreed. Iron mobilization ability was considerably linked with the relaxivity of r1 and r2 across brain areas and age groups, but not with R2 or R1. The relaxivity approach improved the differentiation between tumor and non-pathological tissue, with the impact of gadolinium (Gd)-free contrast equivalent in magnitude to that of Gd-based contrast. The findings provided support for the sensitivity of the relaxivity approach to iron homeostasis on the gene expression level.

The 2 most enriched pathways for r1-r2 relaxivity were “immunoglobulin complex” and “scavenging of heme from plasma.” The relaxivity indicated variations in iron homeostasis amongst tumor tissues, with relaxivity being considerably greater for tumors with a high transferrin/ferritin ratio in comparison with tumors with a low transferrin/ferritin ratio. The relaxivity evaluated in vivo revealed pathological disturbances in iron homeostasis that were previously only observed ex vivo, in line with gene expression and proteomics investigations.

Conclusion

Overall, the study findings showed that the strategy may enable non-invasive investigation and diagnosis of iron homeostasis in living human brains.