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Selected Regional Changes in Brain Diffusivity in Isolated
Mild Fetal Ventriculomegaly
Ronen Bercovitz M.A, Gal Yaniv M.D. PhD, Eldad Katorza M.D,
Dafi Bergman B.Sc, Anat Biegon PhD, Chen Hoffmann M.D
Department of Diagnostic Imaging and Obstetrical & Gynecological
Sheba Medical Center, Sackler School of Medicine, Tel Aviv University
Stony Brook University School of Medicine, Stony Brook, NY, USA
Background
• Ventriculomegaly (VM) is a term used when the lateral
ventricles become dilated (Size>10 mm)
• The most common definition uses the atrium width
of the lateral ventricle
• VM occurs in around 1% of
pregnancies
Background
• Traditionally VM was divided
into three groups
Background
• Today it is also common
to divide VM severity
Background
• Isolated VM (IMVM) is defined as an enlargement
of ventricles without any additional pathology
Background
• There is no consensus about the clinical
significance of IMVM
• The reported incidence of associated neurological
pathology ranges from 0-36%
• We seek for imaging markers
for better understanding the
IMVM outcomes
Background
• Apparent Diffusion Coefficient (ADC) values gradually
change during fetal life with a typical pattern
• Fetal brain ADC does not change significantly
during the 3rd trimester
Background
• ADC values are a useful tool for assessing brain
pathology and development
Purpose
• To evaluate the impact of symmetric and asymmetric
Isolated Mild Ventriculomegaly (IMVM) on Apparent
Diffusion Coefficient (ADC) values in the fetal brain
Symmetric IMVMAsymmetric IMVM
Materials and methods
• 67 fetuses with IMVM were scanned
between 2009-2014
• MRI and – Ultrasound proven IMVM
• Compared to 38 normal feMRI scans
matched for gestational age (controls).
Materials and methods
• IMVM cases were divided into 3 groupes
• AVM- Asymmetrical ventriculomegaly
• SVM- Symmetrical ventriculomegaly
• AV1normal- Asymmetrical ventricles with one
normal-sized ventricle
Materials and methods
• ADC measurements
• ROI locations:
A: Frontal & Parietal lobe WM.B: Basal ganglia. C: Thalamus.
D: Temporal & Occipital lobe WM. E: Cerebellum. F: Pons
Results: Elevated ADC values
• ADC values were significantly elevated in the basal
ganglia (BG) of the AV1normal and SVM groups
• Results were compared to 38 normal feMRI scans matched for GA
38
42
17
P <0.003*
*
*
Results: Elevated ADC values
AV1normal Group
AV1normal group
• Results were compared to 38 normal feMRI scans matched for GA
• The ADC values in
the BG were elevated
only ipsilateral to the
enlarged atrium
Results: Reduced ADC values
AVM and SVM groups
• Frontal lobe ADC values were significantly reduced
• Results were compared to 38 normal feMRI scans matched for GA
38
8
17
P <0.003*
*
*
Results: Reduced ADC values
AVM group
• Temporal lobe ADC values were significantly reduced
• Results were compared to 38 normal feMRI scans matched for GA
38
8
P <0.001*
*
Discussion
• We identified distinct ADC value changes
in different brain regions in each IMVM group
basal ganglia Frontal lobe Temporal lobe
AV1normal
group
SVM
group
SVM
group
AVM
group
AVM
group
Discussion
• ADC value change analysis
ADC
Reduced ADC values
• Hyper-cellularity
• Acute ischemia
• Premature development
(premature myelin synthesis)
Frontal lobe
SVM
group
AVM
group
Temporal lobe
AVM
group
Discussion
• ADC value change analysis
ADC
Elevated ADC values
• Hypo-cellularity
• Edema
• Developmental delay
(delayed myelin synthesis)
basal ganglia
AV1normal
group
SVM
group
Conclusions
• Changes in ADC values may contribute to the
understanding of different IMVM significance
• A clinco-pathological correlation between ADC changes
and Vineland questioner score is needed
• Different IMVM subgroups are associated with
distinct ADC values in different brain regions
Thank You
Contact us :
chen.hoffmann@sheba.health.gov.il
ronen.bercovitz@sheba.health.gov.il
www.imaging.sheba.co.il
Discussion
ADC
Reduced ADC values
• Hyper-cellularity
• Acute ischemia
• Premature development
(premature myelin synthesis)
ADC
Elevated ADC values
• Hypo-cellularity
• Edema
• Developmental delay
(delayed myelin synthesis)
Limitations
• Some of our study groups are small
(AVM and SVM groups)
• Lack of clinical follow up of fetuses
• Lack of definitive explanation to results
38
8
17

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selected regional changes ] Final4 (1)

  • 1. Selected Regional Changes in Brain Diffusivity in Isolated Mild Fetal Ventriculomegaly Ronen Bercovitz M.A, Gal Yaniv M.D. PhD, Eldad Katorza M.D, Dafi Bergman B.Sc, Anat Biegon PhD, Chen Hoffmann M.D Department of Diagnostic Imaging and Obstetrical & Gynecological Sheba Medical Center, Sackler School of Medicine, Tel Aviv University Stony Brook University School of Medicine, Stony Brook, NY, USA
  • 2. Background • Ventriculomegaly (VM) is a term used when the lateral ventricles become dilated (Size>10 mm) • The most common definition uses the atrium width of the lateral ventricle • VM occurs in around 1% of pregnancies
  • 3. Background • Traditionally VM was divided into three groups
  • 4. Background • Today it is also common to divide VM severity
  • 5. Background • Isolated VM (IMVM) is defined as an enlargement of ventricles without any additional pathology
  • 6. Background • There is no consensus about the clinical significance of IMVM • The reported incidence of associated neurological pathology ranges from 0-36% • We seek for imaging markers for better understanding the IMVM outcomes
  • 7. Background • Apparent Diffusion Coefficient (ADC) values gradually change during fetal life with a typical pattern • Fetal brain ADC does not change significantly during the 3rd trimester
  • 8. Background • ADC values are a useful tool for assessing brain pathology and development
  • 9. Purpose • To evaluate the impact of symmetric and asymmetric Isolated Mild Ventriculomegaly (IMVM) on Apparent Diffusion Coefficient (ADC) values in the fetal brain Symmetric IMVMAsymmetric IMVM
  • 10. Materials and methods • 67 fetuses with IMVM were scanned between 2009-2014 • MRI and – Ultrasound proven IMVM • Compared to 38 normal feMRI scans matched for gestational age (controls).
  • 11. Materials and methods • IMVM cases were divided into 3 groupes • AVM- Asymmetrical ventriculomegaly • SVM- Symmetrical ventriculomegaly • AV1normal- Asymmetrical ventricles with one normal-sized ventricle
  • 12. Materials and methods • ADC measurements • ROI locations: A: Frontal & Parietal lobe WM.B: Basal ganglia. C: Thalamus. D: Temporal & Occipital lobe WM. E: Cerebellum. F: Pons
  • 13. Results: Elevated ADC values • ADC values were significantly elevated in the basal ganglia (BG) of the AV1normal and SVM groups • Results were compared to 38 normal feMRI scans matched for GA 38 42 17 P <0.003* * *
  • 14. Results: Elevated ADC values AV1normal Group AV1normal group • Results were compared to 38 normal feMRI scans matched for GA • The ADC values in the BG were elevated only ipsilateral to the enlarged atrium
  • 15. Results: Reduced ADC values AVM and SVM groups • Frontal lobe ADC values were significantly reduced • Results were compared to 38 normal feMRI scans matched for GA 38 8 17 P <0.003* * *
  • 16. Results: Reduced ADC values AVM group • Temporal lobe ADC values were significantly reduced • Results were compared to 38 normal feMRI scans matched for GA 38 8 P <0.001* *
  • 17. Discussion • We identified distinct ADC value changes in different brain regions in each IMVM group basal ganglia Frontal lobe Temporal lobe AV1normal group SVM group SVM group AVM group AVM group
  • 18. Discussion • ADC value change analysis ADC Reduced ADC values • Hyper-cellularity • Acute ischemia • Premature development (premature myelin synthesis) Frontal lobe SVM group AVM group Temporal lobe AVM group
  • 19. Discussion • ADC value change analysis ADC Elevated ADC values • Hypo-cellularity • Edema • Developmental delay (delayed myelin synthesis) basal ganglia AV1normal group SVM group
  • 20. Conclusions • Changes in ADC values may contribute to the understanding of different IMVM significance • A clinco-pathological correlation between ADC changes and Vineland questioner score is needed • Different IMVM subgroups are associated with distinct ADC values in different brain regions
  • 21. Thank You Contact us : chen.hoffmann@sheba.health.gov.il ronen.bercovitz@sheba.health.gov.il www.imaging.sheba.co.il
  • 22. Discussion ADC Reduced ADC values • Hyper-cellularity • Acute ischemia • Premature development (premature myelin synthesis) ADC Elevated ADC values • Hypo-cellularity • Edema • Developmental delay (delayed myelin synthesis)
  • 23. Limitations • Some of our study groups are small (AVM and SVM groups) • Lack of clinical follow up of fetuses • Lack of definitive explanation to results 38 8 17

Editor's Notes

  1. D