Different MRI-defined tuber types in tuberous sclerosis complex: Quantitative evaluation and association with disease manifestations

Brain Dev. 2018 Mar;40(3):196-204. doi: 10.1016/j.braindev.2017.11.010. Epub 2017 Dec 16.

Abstract

Background: Tuberous sclerosis complex (TSC) is a rare genetic disorder with multisystem involvement. A magnetic-resonance (MRI) based classification of tubers into types A, B and C has been proposed. However, the relationship between different tuber types and their quantitative characteristics, also the non-neurological manifestations of TSC remains unknown.

Aims: To quantitatively evaluate different MRI-defined tuber types and to explore their relationships with major disease manifestations in patients with tuberous sclerosis complex.

Methods: We performed quantitative manual assessment of tubers visible on T1W, T2W/FLAIR images and DW/ADC maps of 20 patients with TSC. Tubers were classified into types A, B and C based on their signal intensity on MRI. General clinical information and quantitative tuber characteristics were evaluated. Between-group comparisons were made using the nonparametric Mann-Whitney U test with Bonferroni correction.

Results: In total, 20 patients with 770 tubers were evaluated. Type A tubers were most numerous followed closely by Type B tubers, whereas Type C tubers were relatively rare. Tuber size was markedly different among the three tuber types: it increased from Type A to Type B to Type C. Infantile spasms, generalized-tonic clonic seizures, poor seizure control, cardiac rhabdomyomas, SEGA and developmental delay were not associated with quantitative tuber characteristics. Increased total Type B tuber load was associated with early onset epilepsy, while individually larger Type A and Type B tubers were associated with the presence angiomyolipoma (AML) and renal cysts.

Conclusions: MRI-defined tuber types differ significantly in their size and number. Larger total Type B tuber load and larger individual Type A and Type B tubers were found to be most associated with early seizure onset and renal angiomyolipomas, respectively. One possible explanation for the observed differences in the clinical phenotype based on MRI-defined tuber types is not the intrinsic qualitative distinctions between different tuber types, but rather their individual size and total tuber load.

Keywords: Angiomyolipoma; Cortical tubers; Epilepsy; Magnetic resonance imaging; Subependymal giant cell astrocytoma; Tuberous sclerosis complex.

MeSH terms

  • Adolescent
  • Cerebral Cortex / diagnostic imaging*
  • Cerebral Cortex / pathology
  • Child
  • Child, Preschool
  • Electroencephalography
  • Epilepsy / diagnostic imaging
  • Epilepsy / etiology
  • Female
  • Humans
  • Image Processing, Computer-Assisted*
  • Magnetic Resonance Imaging*
  • Male
  • Neurodevelopmental Disorders / diagnostic imaging
  • Neurodevelopmental Disorders / etiology
  • Retrospective Studies
  • Tuber Cinereum / diagnostic imaging*
  • Tuberous Sclerosis / classification
  • Tuberous Sclerosis / complications
  • Tuberous Sclerosis / diagnostic imaging*
  • Tuberous Sclerosis / genetics