Skip to main content
Log in

MRI of the normal brain from early childhood to middle age

I. Appearances on T2- and proton density-weighted images and occurrence of incidental high-signal foci

  • Paediatric and Developmental Neuroradiology
  • Published:
Neuroradiology Aims and scope Submit manuscript

Abstract

The magnetic resonance images of 67 healthy subjects aged 4–50 years were studied for differences in general signal intensity between the different brain structures, the frequency of focal intensity changes in the brain, and variations in size of the cerebrospinal fluid (CSF) spaces. In adults over 25 years of age the thalamus gave lower signal than the putamen or caudate nucleus. Definite periventricular high signal was found in the white matter of one third of subjects of all ages. Small (<5 mm in diameter) high signal foci were found in the cerebral white matter on T2-weighted images in 27% of subjects (20% of healthy children and adolescents and 34% of adults). They gave high signal on both short and long echoes in 11% of children and adolescents and in 22% of adults; 51% of all foci gave high signal with both echoes. This does not support the hypothesis that they are caused mainly by enlarged Virchow-Robin spaces. Of the high signal foci on T2-weighted images, 86% were in watershead areas. Two foci were found in one subject in the periventricular watershed area (beside the tips of the frontal horns) and they were never seen in the other deep white matter regions. In healthy, relatively young subjects with no known risk factors, high signal foci other than Virchow-Robin spaces, were common; neither their prevalence nor their number correlated with age in this series. A few slightly large sulci were found in some adults.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Lee B, Lipper E, Nass R, Ehrlich ME, de Ciccio-Bloom E, Auld P (1986) MRI of the central nervous system in neonates and young children. AJNR 7: 605–616

    Google Scholar 

  2. McArdle GB, Richardson J, Nicholas D, Mirfakhraee M, Hayden K, Amparo E (1987) Developmental features of the neonatal brain: MR imaging. Part I. Gray-white matter differentiation and myelination. Radiology 162: 223–229

    Google Scholar 

  3. Barkovich AJ, Kjos BO, Jackson DE, Norman D (1988) Normal maturation of the neonatal and infant brain: MR imaging at 1.5 T1. Radiology 166: 173–180

    Google Scholar 

  4. Awad IA, Spezler RF, Hodak JA, Awad CA, Carey R (1986) Incidental subcortical lesions identified on magnetic resonance imaging in the elderly. I. Correlation with age and cerebrovascular risk factors. Stroke 6: 1084–1089

    Google Scholar 

  5. Gerard G, Weisberg LA (1986) MRI periventricular lesions in adults. Neurology 36: 998–1001

    Google Scholar 

  6. Lechner H, Schmidt R, Bertha G, Justich E, Offenbacher H, Schneider G (1988) Nuclear magnetic resonance image white matter lesions and risk factors for stroke in normal individuals. Stroke 19: 263–265

    Google Scholar 

  7. Kertesz A, Black S, Tokar G, Benke T, Carr T, Nicholson L (1988) Periventricular and subcortical hyperintensities on magnetic resonance imaging. Arch Neurol 45: 404–408

    Google Scholar 

  8. Fazekas F (1989) Magnetic resonance signal abnormalities in asymptomatic individuals: their incidence and functional correlates. Eur Neurol 29: 164–168

    Google Scholar 

  9. Kobari M, Meyer JS, Ichijo M, Oravez W (1989) Leukoaraiosis: correlation of MR and CT findings with blood flow, atrophy, and cognition. AJNR 11: 273–281

    Google Scholar 

  10. Wahlund LO, Agartz I, Almqvist O, Basun H, Forssell L, Sääf J, Wetterberg L (1990) The brain in healthy aged individuals: MR imaging. Radiology 174: 675–679

    Google Scholar 

  11. van der Knaap MS, Valk J (1990) MR imaging of the various stages of normal myelination during the first year of life. Neuroradiology 31: 459–470

    Google Scholar 

  12. van Swieten J, van deer Hout H, van Ketel B, Hijdra A, Wokke H, van Gijn J (1991) Periventricular lesions in the white matter on magnetic resonance imaging in the elderly. A morphometric correlation with arterioclerosis and dilated perivascular spaces. Brain 114: 761–774

    Google Scholar 

  13. Meguro K, Yamaguchi T, Hishinuma T, Miyazawa H, Ono S, Yamada K, Matsuzava T (1993) Periventricular hyperintensity on magnetic resonance imaging correlated with brain ageing and atrophy. Neuroradiology 35: 125–129

    Google Scholar 

  14. Schmidt R, Fazekas F, Kleinert G, Offenbacher H, Gindl K, Payer F, Freidl W, Niederkorn K, Lechner H (1992) Magnetic resonance imaging signal hyperintensities in the deep and subcortical white matter. A comparative study between stroke patients and normal volunteers. Arch Neurol 49: 825–827

    Google Scholar 

  15. Horikoshi T, Yagi S, Fukamachi A (1993) Incidental high-intensity foci in the white matter on T2-weighted magnetic resonance imaging. Neuroradiology 35: 151–155

    Google Scholar 

  16. Meese W, Kluge W, Grumme T, Hopfenmyller W (1980) CT evaluation of the CSF spaces of healthy persons. Neuroradiology 19: 131–136

    Google Scholar 

  17. Gyldensted C (1977) Measurements of the normal ventricular system and hemispheric sulci of 100 adults with computed tomography. Neuroradiology 14: 183–192

    Google Scholar 

  18. Aoki S, Okada Y, Nishimura K, Barkovich AJ, Kjos B, Brasch RC, Norman D (1989) Normal deposition of brain iron in childhood and adolescence: MR imaging at 1.5 T. Radiology 172: 381–385

    Google Scholar 

  19. Drayer B (1988) Imaging of the aging brain. Part I. Normal findings. Radiology 166: 785–796

    Google Scholar 

  20. Milton WJ, Atlas SW, Lexa FJ, Mozley DP, Gur RE (1991) Deep gray matter hypointensity with aging in healthy adults: MR imaging at 1.5 T. Radiology 181: 715–719

    Google Scholar 

  21. Drayer B, Burger P, Hurwitz B, Dawson D, Cain J (1987) Reduced signal intensity on MR images of thalamus and putamen in multiple sclerosis: increased iron content? AJNR 8: 413–419

    Google Scholar 

  22. Schenker C, Meier D, Wichmann W, Boesiger P, Valavanis A (1993) Age distribution and iron dependency of the T2 relaxation time in the globus pallidus and putamen. Neuroradiology 35: 119–124

    Google Scholar 

  23. Drayer B, Burger P, Darwin R, Riederer S, Hefkens R, Johnson GA (1986) Magnetic resonance imaging of brain iron. AJNR 7: 373–380

    Google Scholar 

  24. Drayer BD (1989) Basal ganglia: significance of signal hypointensity on T2-weighted MR images. Radiology 173: 311–312

    Google Scholar 

  25. Bizzi A, Brooks RA, Brunett A, Hill J, Alger J, Miletisch R, Francavilla T, Di Chiro G (1990) Role of iron and ferritin in MR imaging of the brain: a study in primates at different field strengths. Radiology 177: 59–65

    Google Scholar 

  26. Chen JC, Hardy PA, Clauberg M et al (1989) T2 values in the human brain: comparison with quantitative assays of iron and ferritin. Radiology 173: 521–526

    Google Scholar 

  27. Brooks DJ, Luthert P, Gadian D, Marsden CD (1989) 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. J Neurol Neurosurg Psychiatry 52: 108–111

    Google Scholar 

  28. Chen J, Hardy P, Kucharczyk W, Clauberg M, Joshi J, Vourlas A, Dhar M, Henkelman M (1993) MR of human postmortem brain tissue: correlative study between T2 assays of iron and ferritin in Parkinson and Huntington disease. AJNR 14: 275–281

    Google Scholar 

  29. Zimmerman R, Fleming C, Lee B, Saint-Louis L, Deck M (1986) Periventricular hyperintensity seen by magnetic resonance. AJNR 7: 13–20

    Google Scholar 

  30. Braffman BH, Trojanowski JQ, Atlas SW (1991) The aging and neurodegenerative disorders. In: Atlas SW, (ed.) Magnetic resonance imaging of the brain and spine. New York: Raven Press, pp 567–624

    Google Scholar 

  31. Rubenstein, J., Kim J, Morava-Protzner I, Stanchev P, Henkelman RM (1993) Effects of collagen orientation on MR imaging characteristics of bovine articular cartilage. Radiology 188: 219–226

    Google Scholar 

  32. Kinosada Y, Ono M, Okuda Y, Tanaka N, Hattori T, Nakagawa T (1993) MR tractography. New visualizing technique of anatomical structures of nerve fiber system from diffusion-weighted images using maximum projection methods (1993). Proc Soc Magn Reson Med. Twelfth Annual Scientific Meeting. New York, pp 290

  33. Stanisz G, Kim JK, Bronskill MJ, Henkelman RM (1993) NMR anisotrophy in tissue: T2 relaxation, diffusion and magnetization transfer. Proc Soc Magn Reson Med Twelfth Annual Scientific Meeting. New York, pp 1287

  34. Heier LA, Bauer CJ, Schwartz L, Zimmerman RD, Morgello S, Deck MDF (1989) Large Virchow-Robin spaces: MR-clinical correlation. AJNR 10: 929–936

    Google Scholar 

  35. Jungreis C, Kanal E, Hirch W, Martinez A, Moossy J (1988) Normal perivascular spaces mimicking lacunar infarction: MR imaging. Radiology 169: 101–104

    Google Scholar 

  36. Rao SM, Mittenberg W, Bernardin L, Haughton V, Leo GJ (1989) Neuropsychological test findings in subjects with leukoaraiosis. Arch Neurol 46: 40–44

    Google Scholar 

  37. Awad IA, Spetzler RF, Hodak JA (1986). Incidental subcortical lesions identified on magnetic resonance imaging in the elderly. II. Postmortem pathological correlations. Stroke 17: 1090–1099

    Google Scholar 

  38. Kirkpatrick JB, Hayman LA (1987) White matter lesions in MR imaging of clinically healthy brains of elderly subjects: possible pathologic basis. Radiology 162: 509–511

    Google Scholar 

  39. Fazekas F, Kleinert R, Offenbacher H, Payer F, Schmidt R, Kleinert G, Radner H, Lechner H (1990) The morphologic correlate of incidental punctate white matter hyperintensities on MR images. AJNR 12: 915–921

    Google Scholar 

  40. Braffman BH, Zimmerman RA, Trojanowsky JQ, Gonatas NK, Hickey WF, Schlaepfer WW (1988) Brain MR: pathologic correlation with gross and histopathology. 1. Lacunar infarction and Virchow-Robin spaces. AJNR 9 621–628

    Google Scholar 

  41. Marshall VG, Bradley WG, Marshall CE, Bhoopat T, Rhodes RH (1988) Deep white matter infarction: correlation of MR imaging and histopathologic findings. Radiology 167: 517–522

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Autti, T., Raininko, R., Vanhanen, S.L. et al. MRI of the normal brain from early childhood to middle age. Neuroradiology 36, 644–648 (1994). https://doi.org/10.1007/BF00600431

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00600431

Key words

Navigation