small vessel diseases of the brain hereditary causes of hemiparesis

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SMALL VESSEL DISEASES OF THE BRAIN Hereditary causes of Hemiparesis

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Page 1: SMALL VESSEL DISEASES OF THE BRAIN Hereditary causes of Hemiparesis

SMALL VESSEL DISEASES OF THE BRAIN

Hereditary causes of Hemiparesis

Page 2: SMALL VESSEL DISEASES OF THE BRAIN Hereditary causes of Hemiparesis

Background

Hereditary, unrelated to arteriosclerosis or hypertensive disease

Cerebral autosomal dominant ateriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common form

Leads to cognitive decline and dementia from multiple small ischaemic lesions and lacunar infarcts

Yamamoto Y, Craggs L, Baumannt M, Kalimo H, Kalaria RN. Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain. Neuropathology and Applied Neurobiology. 2011;37:94-113.

Page 3: SMALL VESSEL DISEASES OF THE BRAIN Hereditary causes of Hemiparesis

Pathophysiology

Mutation in one of 4 different genes: NOTCH3, HTRA1, TREX1, COL4A1

Sucortical lesions Diffuse white matter

changes Lacunes Microinfarction

Yamamoto Y, Craggs L, Baumannt M, Kalimo H, Kalaria RN. Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain. Neuropathology and Applied Neurobiology. 2011;37:94-113.

Page 4: SMALL VESSEL DISEASES OF THE BRAIN Hereditary causes of Hemiparesis

Pathophysiology continued… Affects intracerebral small vessels including:

arteries, arterioles, capillaries, and small veins Arteriolar narrowing Thickened arterial walls with fibrosis Accumulation of eosinophilic material Pericyte degeneration Loss of vascular smooth muscle cells Arterial changes lead to reduction in cerebral

blood flow and blood volume in affected areas

Yamamoto Y, Craggs L, Baumannt M, Kalimo H, Kalaria RN. Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain. Neuropathology and Applied Neurobiology. 2011;37:94-113.

Page 5: SMALL VESSEL DISEASES OF THE BRAIN Hereditary causes of Hemiparesis

Signs & Symptoms

Mean age of onset (first stroke) is 46 y/o May be preceded by migraines Cognitive changes: deficits in attention,

processing speed, and executive function Dementia by the sixth decade of life Prognosis for disability and death worse for

men > women by 6 years

Yamamoto Y, Craggs L, Baumannt M, Kalimo H, Kalaria RN. Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain. Neuropathology and Applied Neurobiology. 2011;37:94-113.

Page 6: SMALL VESSEL DISEASES OF THE BRAIN Hereditary causes of Hemiparesis

Diagnostic tests and Imaging T2 weighted MRI Neuroimaging

Yamamoto Y, Craggs L, Baumannt M, Kalimo H, Kalaria RN. Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain. Neuropathology and Applied Neurobiology. 2011;37:94-113.

Page 7: SMALL VESSEL DISEASES OF THE BRAIN Hereditary causes of Hemiparesis

Small vessel disease compared to large vessel disease

Reference: Yamamoto Y, Craggs L, Baumannt M, Kalimo H, Kalaria RN. Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain. Neuropathology and Applied Neurobiology. 2011;37:94-113.

Page 8: SMALL VESSEL DISEASES OF THE BRAIN Hereditary causes of Hemiparesis

Types of Small Vessel Disease with hemiplegia

Hereditary Small Vessel Disease of the Brain (SVDB) – Autosomal Dominant- Age of onset: 36-52 y/o- Duration of disease: > 5 years- Key clinical features: Hemiplegia, motor and sensory deficits, memory impairments- Neuroimaging findings: diffuse white matter changes, deep cerebral infarcts, degeneration of pyramidal tract, and multiple micro bleeds

Reference: Yamamoto Y, Craggs L, Baumannt M, Kalimo H, Kalaria RN. Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain. Neuropathology and Applied Neurobiology. 2011;37:94-113.

Page 9: SMALL VESSEL DISEASES OF THE BRAIN Hereditary causes of Hemiparesis

Types of Small Vessel Disease with hemiplegia

COL4A1-related disorder (stroke syndrome) – Autosomal dominant- Age of onset: 14-49 y/o- Duration of disease: > 8 years- Key clinical features: infantile hemiparesis, migraines, intracerebral hemorrhages, seizures, Raynaud phenomenon, dementia- Neuroimaging findings: diffuse white matter changes, dilated perivasular changes, subcortical infarcts, microbleeds, and absence of porencephaly cavities

Reference: Yamamoto Y, Craggs L, Baumannt M, Kalimo H, Kalaria RN. Review: Molecular genetics and pathology of hereditary small vessel diseases of the brain. Neuropathology and Applied Neurobiology. 2011;37:94-113.