Virchow–Robin space

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A Virchow–Robin CSF space as seen on CT
CT image showing extensive low attenuation in the right hemispheric white matter due to dilated Type 2 Virchow–Robin spaces. This might be mistaken for vasogenic edema
Axial fat suppressed T2 weighted MRI image in the same patient as above demonstrating extensive dilated Type 2 Virchow–Robin spaces in the right hemisphere

Virchow–Robin spaces (VRS), also known as perivascular space, is the immunological space between the capillary and pia mater that can be expanded by leukocytes. The spaces are formed when large vessels take the pia mater with them when they dive deep into the brain. The pia mater is reflected from the surface of the brain onto the surface of blood vessels in the subarachnoid space. Perivascular cuffs are regions of leukocyte aggregation in VRS, usually found in patients with viral encephalitis.

VRS are extremely small and can usually only be seen on MR images when dilated. While many normal brains will show a few dilated VRS, an increase in dilated VRS has been shown to correlate with the incidence of several neurodegenerative diseases, making the spaces a popular topic of research.[1]

History[edit]

The appearance of Virchow–Robin spaces was first noted in 1843 by Durand Fardel.[2] In 1851, Rudolph Virchow was the first to provide a detailed description of these microscopic spaces between the outer and inner/middle lamina of the brain vessels. Charles-Philippe Robin confirmed these findings in 1859 and was the first to describe the perivascular spaces as channels that existed in normal anatomy. The immunological significance was discovered by Wilhelm His, Sr. in 1865 based on his observations of the flow of interstitial fluid over VRS to the lymphatic system.[3] For many years after VRS were first described, it was thought that they were in free communication with the cerebrospinal fluid in the subarachnoid space. It was later shown with the use of electron microscopy that pia mater serves as separation between the two. Upon the application of MRI, measurements of the differences of signal intensity between VRS and cerebrospinal fluid supported these findings.[3] As research technologies continued to expand, so too did information regarding the function, anatomy and clinical significance of VRS.

Anatomy[edit]

Virchow–Robin spaces are gaps containing interstitial fluid that span between blood vessels and the brain matter which they penetrate.[4] Like the blood vessels around which they form, Virchow–Robin spaces are found in both the subarachnoid space and the subpial space.[5] VRS surrounding arteries in the cerebral cortex and the basal ganglia are separated from the subpial space by one or two layers of leptomeninges, respectively, as well as the pia mater.[2] By virtue of the leptomeningeal cell layer, VRS belonging to the subarachnoid space are continuous with VRS of the subpial space. The direct communication between VRS of the subarachnoid space and the subpial space is unique to the brain’s arteries, as no leptomeningeal layers surround the brain’s veins.[2][5] Use of the scanning electron microscope has determined that VRS surrounding blood vessels in the subarachnoid space are not continuous with the subarachnoid space because of the presence of pia mater cells joined by desmosomes.[6]

Virchow–Robin spaces may be enlarged to a diameter of five millimeters in healthy humans and are usually harmless. When enlarged, they can disrupt the function of the brain regions into which they project.[4] Dilation can occur on one or both sides of the brain.[2]

Dilated Virchow–Robin spaces are categorized into three types:[2]

  • Type 1 dilated VRS are located on the lenticulostriate arteries projecting into the basal ganglia
  • Type 2 dilated VRS are located in the cortex following the path of the medullary arteries
  • Type 3 dilated VRS are located in the midbrain

Virchow–Robin spaces are most commonly located in the basal ganglia, thalamus, midbrain, cerebellum, hippocampus, insular cortex, the white matter of the cerebrum, and along the optic tract.[3] The ideal method used to visualize Virchow–Robin spaces is T2-weighted MRI. The MR images of dilated Virchow–Robin spaces must be distinguished from MR images of other neurological maladies that are similar in appearance. These illnesses are specifically:[2]

Virchow–Robin spaces are distinguished on an MRI by several key features. VRS appear as distinct round or oval entities with a signal intensity visually equivalent to that of cerebrospinal fluid in the subarachnoid space.[2][7][8] In addition, a Virchow–Robin space has no mass effect and is located along the blood vessel around which it forms.[7]

Function[edit]

One of the most basic roles of the VRS is the regulation of CNS fluid movement and drainage.[3] Virchow–Robin spaces ultimately drain fluid from neuronal cell bodies in the CNS to the cervical lymph nodes.[4] In particular, the “tide hypothesis” suggests that the cardiac contraction creates and maintains pressure waves to modulate the flow to and from the subarachnoid space and VRS.[9] By acting as a sort of sponge, the VRS are essential for signal transmission and maintenance of extracellular fluid (ECF).[9]

Another role of the VRS is as an integral part of the blood–brain barrier (BBB).[10] While the BBB is often described as the tight junctions between the endothelial cells, this is an oversimplification that neglects the intricate role that perivascular spaces take in separating the venous blood from the parenchyma of the brain. Often, cell debris and foreign particles, which are impermeable to the BBB will get through the endothelial cells, only to be phagocytosed in the VR spaces. This holds true for many T and B cells, as well as monocytes, giving this small fluid filled space an important immunological role.[10]

VR spaces also play an important role in immunoregulation. VR spaces not only contain interstitial and cerebrospinal fluid, but they also have a constant flux of macrophages, which is regulated by blood-borne mononuclear cells, but do not pass the basement membrane of the glia limitans.[10] Similarly, as part of its role in signal transmission, perivascular spaces contain vasoactive neuropeptides (VNs), which, aside from regulating blood pressure and heart rate, have an integral role in controlling microglia.[11] VNs serve to prevent inflammation by activating the enzyme adenylate cyclase which then produces cAMP. The production of cAMP aids in the modulation of auto-reactive T cells by regulatory T cells. .[12] VRS is a susceptible space for VN compromise and when VN function is reduced in the VRS, immune response is adversely affected and the potential for degradation increases.[11][12] When inflammation by T cells begins, astrocytes begin to undergo apoptosis, due to their CD95 receptor, to open up the glia limitans and let T cells into the parenchyma of the brain.[10] Because this process is aided by the perivascular macrophages, these tend to accumulate during neuroinflammation and cause dilation of the VRS.[11]

Clinical significance[edit]

The clinical significance of Virchow–Robin spaces comes primarily from their tendency to dilate. The importance of dilation is hypothesized to be based on changes in shape rather than size.[3] Enlarged Virchow–Robin spaces have been observed most commonly in the basal ganglia, specifically on the lenticulostriate arteries. They have also been observed along the paramedial mesencephalothalamic artery and the substantia nigra in the mesencephalon, the brain region below the insula, the dentate nucleus in the cerebellum, and the corpus callosum, as well as the brain region directly above it, the cingulate gyrus.[4] Upon the clinical application of MRI, it was shown in several studies that VRS dilation and lacunar infracts are the most commonly observed histological correlates of signaling abnormalities.[3]

Senescence[edit]

Dilation is most commonly and closely associated with aging. Dilation of VRS has been shown to correlate best with age, even when accompanying factors including hypertension, dementia, and white matter lesions are considered.[13] In the elderly, VRS dilation has been correlated with many symptoms and conditions which often affect the arterial walls. Such conditions associated with VRS dilation in the elderly include vascular hypertension, arteriosclerosis, reduced cognitive capacity, dementia, and low post-mortem brain weight.[3] In addition to dilation among the elderly, dilation in young, healthy individuals can also be observed. This occurrence is rare and there has been no observed association in such cases with reduced cognitive function or white matter abnormalities.[3] When dilated VRS are observed in the corpus callosum, there is generally no neurological deficit associated. They are often observed in this region as cystic lesions with cerebrospinal-like fluid.[14]

Symptoms of dilated VRS[edit]

Extreme dilation has been associated with several specific clinical symptoms. In cases of severe dilation in only one hemisphere, symptoms reported include a non-specific fainting attack, hypertension, positional vertigo, headache, early recall disturbances, and hemifacial tics. Symptoms associated with severe bilateral dilation include ear pain (which was reported to have resolved on its own), dementia, and seizures. This data was compiled from case studies of individuals with severe VRS dilation.[3] Considering the anatomical abnormality presented in such cases, these findings were considered surprising in that the symptoms were relatively mild. In most cases there is in fact to mass effect associated with some VRS dilation. An exception to the mildness of clinical symptoms associated with VRS dilation is when there is extreme dilation in the lower mesencephalon at the junction between the substantia nigra and cerebral peduncle. In such cases, mild to moderate obstructive hydrocephalus was reported in most patients. Associated symptoms ranged from headaches to symptoms more severe than those just discussed in the cases of dilation in the cerebral hemispheres.[3] Other general symptoms associated with VRS dilation include headaches, dizziness, memory impairment, poor concentration, dementia, visual changes, oculomotor abnormality, tremors, seizures, limb weakness, and ataxia.[4]

Associated disorders[edit]

Dilation is a typical characteristic of several diseases and disorders. These include diseases from metabolic and genetic disorders such as mannosidosis, myotonic dystrophy, Lowe syndrome, and Coffin-Lowry syndrome. Dilation is also a common characteristic of diseases or disorders of vascular pathologies, including CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy), hereditary infantile hemiparesis, retinal arteriolar tortuosity and leukoencephalopathy, migranes, and vascular dementia. A third group disorders typically associated with VRS dilation are neuroectodermal syndromes. This includes polycystic brains associated with ectodermal dysplasia, frontonasal dysplasia, and Joubert syndrome. There is a fourth miscellaneous group of disorders typically associated with dilation which include autism in children, Megalencephalopathy, Secondary Parkinson’s Disease, recent-onset Multiple Sclerosis and chronic alcoholism. Because dilation can be associated with several diseases but also observed in healthy patients, it is always important in the evaluation of VRS to study the tissue around the dilation via MRI and to consider the entire clinical context.[3]

Current research[edit]

Causes of dilated VRS[edit]

Much of the current research concerning Virchow–Robin spaces relates to their known tendency to dilate. Research is presently being performed in order to determine the exact cause of dilation in these perivascular spaces. Current theories include mechanical trauma resulting from cerebrospinal fluid pulsation, elongation of ectactic penetrating blood vessels, and abnormal vascular permeability leading to increased fluid exudation. Further research has implicated shrinkage or atrophy of surrounding brain tissue, perivascular demyelination, coiling of the arteries as they age, altered permeability of the arterial wall and obstruction of lymphatic drainage pathways.[3] In addition, insufficient fluid draining and injury to ischemic perivascular tissue resulting in an ex vacuo effect have been suggested as possible causes for dilated VRS.[4]

Association of dilated VRS and other diseases[edit]

Recent and ongoing research has found associations between enlarged VRS and several disorders.

Dementia[edit]

At one point in time, dilated Virchow–Robin spaces were so commonly noted in autopsies of persons with dementia, they were believed to cause the disease. However, additional research is currently being performed in order to confirm or refute a direct connection between dilation of VRS and dementia.[8]

Analysis of VRS may distinguish dementia caused by arteriosclerotic microvascular disease from dementia caused by neurodegenerative disease. A 2005 study has evidenced that a substantial amount of VRS in the substantia innominata, lentiform nucleus, and the caudate nucleus of the basal ganglia may implicate dementia due to arteriosclerotic microvascular disease, in particular Ischemic Vascular Dementia, as opposed dementia due to neurodegenerative disease, specifically Alzheimer’s disease and frontotemporal dementia. Thus, perhaps VRS dilation can be used to distinguish between diagnoses of vascular dementias and degenerative dementias.[15]

Alzheimer's disease[edit]

Some studies have assessed the spatial distribution and prevalence of VRS in people with Alzheimer's disease versus those without the disease. Researchers have found that while VRS appear to be correlated with natural aging, MR imaging reveals a greater prevalence of VRS in those with Alzheimer's.[16]

Cerebral amyloid angiopathy (CAA), a blood vessel failure often associated with Alheimer's disease, utilizes dilated VRS to spread inflammation to the parenchyma. Because the VRS often have an extra membrane in gray matter, the ischemic CAA response is often observed in white matter.[17]

It has been hypothesized that the structure of VRS in the cerebral cortex may contribute to the development of Alzheimer’s disease. In contrast to VRS of the basal ganglia, VRS in the cerebral cortex are surrounded by only one layer of leptomeninges. As such, VRS in the cerebral cortex may drain β-amyloid in interstitial fluid less effectively than VRS in the basal ganglia. The less-effective drainage may lead to the development of the β-amyloid plaques that characterize Alzheimer’s disease. In support of this hypothesis, studies have noted the greater frequency of β-amyloid plaques in the cerebral cortex than in the basal ganglia of Alzheimer’s disease patients.[6]

Stroke[edit]

Because dilated VRS are so closely correlated with cerebrovascular disease, there is much current research studying VRS as a diagnostic tool. In a recent study of 31 subjects, abnormal VRS dilation, along with irregular CSF pulsation, were correlated with those subjects with 3 or more risk factors for strokes. Therefore, VRS are a possible novel biomarker for hemorrhagic strokes.[18]

CADASIL syndrome (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome) is a hereditary stroke condition due to a Notch 3 gene mutation on Chromosome 19. Studies have noted that in comparison to family members lacking the affected haplotype that leads to the condition, an increased number of dilated VRS is observed in individuals with CADASIL. These VRS are localized primarily in the putamen and temporal subcortical white matter and they appear to correlate with age of the individual with the condition rather than severity of the disease itself.[19]

There has been a high risk of stroke associated with VRS dilation in the elderly according to the Framingham Stroke Risk Score.[8] In contrast, other studies have concluded that VRS dilation is a normal phenomenon in aging with no association with arthrosclerosis. This remains, therefore, an important point of research in the field.[3]

Multiple sclerosis[edit]

Similar to the research concerning a potential connection between VRS and Alzheimer's, MRI scans of people recently diagnosed with multiple sclerosis have been studied. Larger, more prevalent VRS have been observed in those with MS.[20] Additional studies with similar findings have suggested that the inflammatory cells which contribute to the demyelination that characterizes MS also attack the VRS. Studies using advanced MRI techniques will be necessary to determine if VRS can be implicated as a potential marker of the disease.[21]

Autism[edit]

Dilated VRS are common among the elderly and are not common in children. Studies have noted the association between both developmental delay and non-syndromic autism and enlarged VRS.[22][23] Non-syndromic autism categorizes autistic patients for which there is no known cause.[22]

References[edit]

  1. ^ Esiri, MM; Gay, D (1990). "Immunological and neuropathological significance of the Virchow–Robin space". Journal of the Neurological Sciences 100: 3–8. doi:10.1016/0022-510X(90)90004-7. PMID 2089138. 
  2. ^ a b c d e f g Kwee, Robert M.; Kwee, Thomas C. (2007). "Virchow–Robin Spaces at MR Imaging". RadioGraphics 27: 1071–1086. doi:10.1148/rg.274065722. PMID 17620468. 
  3. ^ a b c d e f g h i j k l m Groeschel, S.; Chong, WK.; Surtees, R.; Hanefeld, F. (2006). "Virchow–Robin spaces on magnetic resonance images: normative data, their dilatation, and a review of the literature.". Neuroradiology 48: 745–754. doi:10.1007/s00234-006-0112-1. PMID 16896908. 
  4. ^ a b c d e f Fayeye, Oluwafikay; Pettorini, Benedetta Ludovica; Foster, Katharine; Rodrigues, Desiderio (2010). "Mesencephalic enlarged Virchow–Robin spaces in a 6-year-old boy: a case-based update". Child’s Nervous System 26: 1155–1160. doi:10.1007/s00381-010-1164-4. PMID 20437240. 
  5. ^ a b Zhang, E.T.; Inman, C.B.; Weller, R.O. (1990). "Interrelationships of the pia mater and the perivascular (Virchow–Robin) spaces in the human cerebrum". Journal of Anatomy 170: 111–123. PMC 1257067. PMID 2254158. 
  6. ^ a b Pollock, H.; Hutchings, M.; Weller, R.O.; Zhang, E.T. (1997). "Perivascular spaces in the basal ganglia of the human brain :their relationship to lacunes". Journal of Anatomy 191: 337–346. doi:10.1046/j.1469-7580.1997.19130337.x. PMC 1467691. PMID 9418990. 
  7. ^ a b Ogawa, Toshihide; Okudera, Toshio; Fukasawa, Hitoshi; Hashimoto, Manabu; Inugami, Atsushi; Fujita, Hideaki; Hatazawa, Jun; Noguchi, Kyo; Uemura, Kazuo; Nakajima, Shigeyoshi; Yasui, Nobuyuki (1995). "Unusual Widening of Virchow–Robin Spaces: MR Appearance". American Journal of Neuroradiology 6 (6): 1238–1242. PMID 7677015. 
  8. ^ a b c Mills, S.; Cain, J.; Purandare, N.; Jackson, A. (2007). "Biomarkers of cerebrovascular disease in dementia". British Journal of Radiology 80: S128–S145. doi:10.1259/bjr/79217686. 
  9. ^ a b Agnati, L.F.; Genedani, S.; Lenzi, P.L.; Leo, G.; Mora, F.; Fuxe, K. (2005). "Energy gradients for the homeostatic control of brain ECF composition and for VT signal migration: introduction of the tide hypothesis". Journal of Neural Transmission 112: 45–63. doi:10.1007/s00702-004-0180-5. PMID 15599604. 
  10. ^ a b c d Bechmann, Ingo; Galea, Ian; Perry, V Hugh (2007). "What is the blood–brain barrier (not)?". Trends in Immunology 28: 5–11. doi:10.1016/j.it.2006.11.007. 
  11. ^ a b c Pantoni, Leonardo (2010). "Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges". Lancet Neurol 9: 689–701. doi:10.1016/S1474-4422(10)70104-6. PMID 20610345. 
  12. ^ a b Staines, D.R.; Brenu, E.W.; Marshall-Gradisnik, S. (2008). "Postulated role of vasoactive neuropeptide-related immunopathology of the blood brain barrier and Virchow–Robin spaces in the aetiology of neurological-related conditions.". Mediators of Inflammation 2008: 792428. doi:10.1155/2008/792428. PMC 2643053. PMID 19229345. 
  13. ^ Davis, Patricia C.; Mirra, Suzanne S.; Alazraki, Naomi (1994-06-01). "The brain in older persons with and without dementia: Findings on MR, PET, and SPECT images". American Journal of Roentgenology 162 (6): 1267–78. doi:10.2214/ajr.162.6.8191980. PMID 8191980. 
  14. ^ Uchino, A.; Takase, Y.; Nomiyama, K.; Egashira, R.; Kudo, S. (2005). "Acquired lesions of the corpus callosum: MR imaging". European Radiology 16 (4): 905–14. doi:10.1007/s00330-005-0037-9. PMID 16284771. 
  15. ^ Patankar, Toufail F.; Mitra, Dipayan; Varma, Anoop; Snowden, Julie; Neary, David; Jackson, Alan (2005). "Dilation of the Virchow–Robin Space Is a Sensitive Indicator of Cerebral Microvascular Disease: Study in Elderly Patients with Dementia". American Journal of Neuroradiology 26 (6): 1512–1520. PMID 15956523. 
  16. ^ Chen, W.; Song, X.; Zhang, Y. (2011). "Assessment of the Virchow–Robin Spaces in Alzheimer Disease, Mild Cognitive Impairment, and Normal Aging, Using High-Field MR Imaging.". American Journal of Neuroradiology 32: 1490–5. doi:10.3174/ajnr.A2541. PMID 21757525. 
  17. ^ Schrag, M; McAuley, G; Pomakian, J; Jiffry, A; Tung, S; Mueller, C; Vinters, HV; Haacke, EM; Holshouser, B; Kido, D; Kirsch, WM (2010). "Correlation of hypointesities in susceptibility-weighted images to tissue histology in dementia patients with cerebral amyloid angiopathy: a postmortem MRI study". European Radiology 119: 291–302. doi:10.1007/s00401-009-0615-z. PMC 2916065. PMID 19937043. 
  18. ^ Selvarajah, J; Scott, M; Stivaros, S; Hulme, S; Georgiou, R; Rothwell, N; Tyrrell, P; Jackson, A (2008). "Potential surrogate markers of cerebral microvascular angiopathy in asymptomatic subjects at risk of stroke". European Radiology 19: 1011–1018. doi:10.1007/s00330-008-1202-8. PMID 18987865. 
  19. ^ Cumurciuc, R.; Guichard, J.-P.; Reizine, D.; Gray, F.; Bousser, M. G.; Chabriat, H. (2006). "Dilation of Virchow–Robin spaces in CADASIL". European Journal of Neurology 13: 187–190. doi:10.1111/j.1468-1331.2006.01113.x. PMID 16490051. 
  20. ^ Etemadifar, M.; Hekmatnia, A.; Tayari, N.; Kazemi, M.; Ghazavi, A.; Akbari, M.; Maghzi, A. (2011). "Features of Virchow–Robin spaces in newly diagnosed multiple sclerosis patients.". European Journal of Radiology 80: 104–8. doi:10.1016/j.ejrad.2010.05.018. PMID 20650586. 
  21. ^ Achiron, A.; Faibel, M. (2002). "Sandlike appearance of Virchow–Robin spaces in early multiple sclerosis: a novel neuroradiologic marker.". American Journal of Neuroradiology 23 (3): 376–80. PMID 11901003. 
  22. ^ a b Boddaert, Nathalie; Zilbovicius, Mônica; Philipe, Anne; Robel, Laurence; Bourgeois, Marie; Barthélemy, Catherine; Seidenwurm, David; Meresse, Isabelle; Laurier, Laurence; Desguerre, Isabelle; Bahi-Buisson, Nadia; Brunelle, Francis; Munnich, Arnold; Samson, Yves; Mouren, Marie-Christine; Chabane, Nadia (2009). "MRI Findings in 77 Children with Non-Syndromic Autistic Disorder". PLoS ONE 4. doi:10.1371/journal.pone.0004415. PMC 2635956. PMID 19204795. 
  23. ^ Zeegers, Mijke; Van Der Grond, Jeroen; Durston, Sarah; Jan Nievelstein, Rutger; Witkamp, Theo; Van Daalen, Emma; Buitelaar, Jan; Van Engeland, Herman (2006). "Radiological findings in autistic and developmentally delayed children". Brain and Development 28 (8): 495–9. doi:10.1016/j.braindev.2006.02.006. PMID 16616445.