Purpose: To determine normal T2-relaxation values from different brain areas in healthy adults, assess age-related T2-relaxation changes in those sites, and evaluate potential gender-related T2-relaxation value differences.
Materials and Methods:We performed proton-density and T2-weighted imaging in 60 healthy adults (male: 38, age range ¼ 31-64 years, mean age 6 SD ¼ 46.1 6 9.3 years; female: 22, age range ¼ 37-66 years, mean age 6 SD ¼ 49.5 6 8.3 years), using a 3.0 Tesla MRI scanner. T2-relaxation values were calculated voxel-by-voxel from proton-density and T2-weighted images, and whole-brain T2-relaxation maps were constructed and normalized to a common space. A set of regions-of-interest were outlined within the basal ganglia, limbic, frontal, parietal, temporal, occipital, thalamic, hypothalamic, cerebellar, and pontine regions using mean background images derived from normalized and averaged T2-weighted images of all individuals, and regional T2-relaxation values were determined from these regions-of-interest and normalized T2-relaxation maps. Pearson's correlations were calculated between T2-relaxation values and age, and male-female differences evaluated with independent-samples t-tests.Results: T2-relaxation values typically increased with age in multiple brain sites; only a few regions showed declines, including the putamen and ventral pons. Sexrelated differences in T2-relaxation values appeared in basal ganglia, frontal, temporal, occipital, and cerebellar regions; males showed higher values over females in these sites.Conclusion: Establishment of normative adult T2-relaxation values over different brain areas, with age and sex as co-factors, offers baseline values against which diseaserelated tissue changes can be assessed. NONINVASIVE ASSESSMENT OF adult human brain changes resulting from neurologic, neuropsychological, and neurocognitive pathologies against normal age-related changes remains difficult (1-3). Myelin and neurons undergo slow degradation with age in adults (4,5), and these normative changes, as well as neurodegenerative processes inducing myelin and neuronal loss (6,7), increase free tissue water content. However, certain deep brain structures, including the basal ganglia, are known to show iron deposition with age in adult subjects (8), which can alter indications of normal progression of tissue changes in these sites. Pathological and treatment-related brain tissue alterations can be assessed accurately, but only after controlling for age-related changes, which mandates determination of normative values from gray and white matter regions over wide-spread brain areas.MR T2-relaxometry provides a quantitative surrogate marker of brain tissue changes in both health and disease by assessing free tissue water content (9) in the absence of diamagnetic and paramagnetic substances, which differs during pediatric development over normal patterns of aging in adult controls (5,10), and increases with disease processes (11). T2-relaxation values increase with increased free tissue water cont...