Age distribution and iron dependency of the T2 relaxation time in the globus pallidus and putamen

SummaryHeavily T2-weighted spin echo sequences of the brain show age-dependent low signal intensity in many extrapyramidal nuclei. Although it has been suggested that this low intensity results from non-haem iron, the specific influence of non-haem iron on the T2 relaxation time has not been quantified and remains controversial. The T2 relaxation times of the globus pallidus and putamen were measured from MRI at 1.5T in 27 healthy patients, by using a mathematical model. They were then plotted as a function of age and compared to the curve of age-dependent iron concentration determined post mortem. The curves of T2 relaxation time in the basal ganglia are congruent with published curves of iron concentration, indicating a high probability that the changes in T2 relaxation times and the low signal in the basal ganglia result from the local, age-dependent iron deposition. Individual measurements of T2 relaxation time show less variation before than after 45 years of age, indicating the influence of a second, more individual factor.

[1]  P. Burger,et al.  MR imaging of compact white matter pathways. , 1988, AJNR. American journal of neuroradiology.

[2]  L. Feinendegen,et al.  Trace element concentration in human brain. Activation analysis of cobalt, iron, rubidium, selenium, zinc, chromium, silver, cesium, antimony and scandium. , 1975, Brain : a journal of neurology.

[3]  V. Haughton,et al.  T1 and T2 measurements on a 1.5-T commercial MR imager. , 1989, Radiology.

[4]  W. Bradley,et al.  Iron accumulation in the basal ganglia following severe ischemic-anoxic insults in children. , 1988, Radiology.

[5]  C. McArdle,et al.  Developmental features of the neonatal brain: MR imaging. Part I. Gray-white matter differentiation and myelination. , 1987, Radiology.

[6]  J. Rowe,et al.  Human aging: usual and successful. , 1987, Science.

[7]  B. Drayer Basal ganglia: significance of signal hypointensity on T2-weighted MR images. , 1989, Radiology.

[8]  R. Henkelman,et al.  T2 values in the human brain: comparison with quantitative assays of iron and ferritin. , 1989, Radiology.

[9]  V M Haughton,et al.  Anterior commissure: anatomic-MR correlation and use as a landmark in three orthogonal planes. , 1986, Radiology.

[10]  B. Drayer,et al.  Imaging of the aging brain. Part I. Normal findings. , 1988, Radiology.

[11]  B. Drayer,et al.  Reduced signal intensity on MR images of thalamus and putamen in multiple sclerosis: increased iron content? , 1987, AJR. American journal of roentgenology.

[12]  D Gadian,et al.  Does signal-attenuation on high-field T2-weighted MRI of the brain reflect regional cerebral iron deposition? Observations on the relationship between regional cerebral water proton T2 values and iron levels. , 1989, Journal of neurology, neurosurgery, and psychiatry.

[13]  S. H. Koenig,et al.  Relaxometry of ferritin solutions and the influence of the Fe3+ core ions , 1986, Magnetic resonance in medicine.

[14]  G A Johnson,et al.  MRI of brain iron. , 1986, AJR. American journal of roentgenology.

[15]  S. Fahn,et al.  Study of movement disorders and brain iron by MR. , 1987, AJR. American journal of roentgenology.

[16]  B. Hallgren,et al.  THE EFFECT OF AGE ON THE NON‐HAEMIN IRON IN THE HUMAN BRAIN , 1958, Journal of neurochemistry.

[17]  R L Ehman,et al.  Reproducibility of T1 and T2 relaxation times calculated from routine MR imaging sequences: phantom study. , 1985, AJR. American journal of roentgenology.

[18]  G A Johnson,et al.  Parkinson plus syndrome: diagnosis using high field MR imaging of brain iron. , 1986, Radiology.

[19]  R A Brooks,et al.  Role of iron and ferritin in MR imaging of the brain: a study in primates at different field strengths. , 1990, Radiology.

[20]  R. Grossman,et al.  Intracranial hematomas: imaging by high-field MR. , 1985, Radiology.

[21]  A. Torvik,et al.  Ischaemic cerebrovascular diseases in an autopsy series , 1966 .