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Current Neurovascular Research

Editor-in-Chief

ISSN (Print): 1567-2026
ISSN (Online): 1875-5739

Research Article

Enlarged Perivascular Space in the Basal Ganglia is Associated with Cerebral Venous Reflux in Patients with Recent Small Subcortical Infarction

Author(s): Zhengrong Wu, Ke Zhang, Ce Zong, Hongbing Liu, Yanhong Wang, Yuming Xu and Yuan Gao*

Volume 21, Issue 2, 2024

Published on: 07 February, 2024

Page: [123 - 130] Pages: 8

DOI: 10.2174/0115672026299546240130092550

Price: $65

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Abstract

Background: Research has linked enlarged perivascular spaces (EPVS) to cerebral venous reflux (CVR) in patients with hypertensive intracerebral hemorrhage, but it is unclear whether this association exists in recent small subcortical infarct (RSSI) patients.

Objective: This study aimed to investigate the correlation between EPVS and CVR in patients with RSSI.

Method: This study included 297 patients, selected from patients with RSSI in the lenticulostriate artery admitted to the Department of Neurology of the First Affiliated Hospital of Zhengzhou University. CVR was assessed by time-of-flight magnetic resonance angiography (TOF-MRA). The relationship between EPVS and CVR was studied using multiple logistic regression analysis.

Results: This study included patients with an average age of 59.84±12.27 years, including 201 males (67.7%). CVR was observed in 40 (13.5%) patients. Compared to the group without CVR, the proportions of male patients and patients with a history of smoking and drinking were higher in the CVR group. The proportions of high-grade EPVS in the centrum semiovale region [23 cases (57.5%) vs. 108 cases (42.0%), p =0.067] and the basal ganglia region [30 cases (75.0%) vs. 133 cases (51.8%), p =0.006] were higher in the CVR group. After multiple logistic regression analysis, high-grade EPVS in the basal ganglia region was still associated with CVR (OR, 2.68; 95% CI, 1.22-5.87;p=0.014).

Conclusion: In the population with RSSI, EPVS in basal ganglia is significantly associated with CVR, suggesting a close relationship between venous dysfunction and the formation of EPVS.

Keywords: Recent small subcortical infarction, cerebral venous reflux, perivascular space, basal ganglia, cerebral small vessel disease, lenticulostriate artery territory.

[1]
Schaller B. Physiology of cerebral venous blood flow: From experimental data in animals to normal function in humans. Brain Res Brain Res Rev 2004; 46(3): 243-60.
[http://dx.doi.org/10.1016/j.brainresrev.2004.04.005] [PMID: 15571768]
[2]
Fulop GA, Tarantini S, Yabluchanskiy AJAJOP. Role of age-related alterations of the cerebral venous circulation in the pathogenesis of vascular cognitive impairment. Am J Physiol Heart Circ Physiol 2019; (5 Pt.2): 316.
[3]
Chung CP, Beggs C, Wang PN, et al. Jugular venous reflux and white matter abnormalities in Alzheimer’s disease: A pilot study. J Alzheimers Dis 2014; 39(3): 601-9.
[http://dx.doi.org/10.3233/JAD-131112] [PMID: 24217278]
[4]
Chung CP, Hu HH. Pathogenesis of leukoaraiosis: Role of jugular venous reflux. Med Hypotheses 2010; 75(1): 85-90.
[http://dx.doi.org/10.1016/j.mehy.2010.01.042] [PMID: 20172657]
[5]
Tsai HH, Lee BC, Chen YF, Jeng JS, Tsai LK. Cerebral venous reflux and dilated basal ganglia perivascular space in hypertensive intracerebral hemorrhage. J Stroke 2022; 24(3): 363-71.
[http://dx.doi.org/10.5853/jos.2022.01004] [PMID: 36221939]
[6]
Mestre H, Kostrikov S, Mehta RI, Nedergaard M. Perivascular spaces, glymphatic dysfunction, and small vessel disease. Clin Sci 2017; 131(17): 2257-74.
[http://dx.doi.org/10.1042/CS20160381] [PMID: 28798076]
[7]
Yu L, Hu X, Li H, Zhao Y. Perivascular spaces, glymphatic system and MR. Front Neurol 2022; 13: 844938.
[http://dx.doi.org/10.3389/fneur.2022.844938] [PMID: 35592469]
[8]
Ramaswamy S, Khasiyev F, Gutierrez J. Brain enlarged perivascular spaces as imaging biomarkers of cerebrovascular disease: A clinical narrative review. J Am Heart Assoc 2022; 11(24): e026601.
[http://dx.doi.org/10.1161/JAHA.122.026601] [PMID: 36533613]
[9]
Lee BC, Tsai HH, Liu CJ, et al. Cerebral venous reflux and cerebral amyloid angiopathy: An magnetic resonance imaging/positron emission tomography study. Stroke 2023; 54(4): 1046-55.
[http://dx.doi.org/10.1161/STROKEAHA.122.040503] [PMID: 36866674]
[10]
Kim JS, Yoon Y. Single subcortical infarction associated with parental arterial disease: Important yet neglected sub-type of atherothrombotic stroke. Int J Stroke 2013; 8(3): 197-203.
[http://dx.doi.org/10.1111/j.1747-4949.2012.00816.x] [PMID: 22568537]
[11]
Caton MT, Callen AL, Copelan AZ, Narsinh KH, Smith ER, Amans MR. Jugular venous reflux can mimic posterior fossa dural arteriovenous fistulas on MRI-MRA. AJR Am J Roentgenol 2021; 216(6): 1626-33.
[http://dx.doi.org/10.2214/AJR.20.24012] [PMID: 32876481]
[12]
Uchino A, Nomiyama K, Takase Y, et al. Retrograde flow in the dural sinuses detected by three-dimensional time-of-flight MR angiography. Neuroradiology 2007; 49(3): 211-5.
[http://dx.doi.org/10.1007/s00234-006-0186-9] [PMID: 17180368]
[13]
Jang J, Kim B, Kim B, et al. Reflux venous flow in dural sinus and internal jugular vein on 3D time-of-flight MR angiography. Neuroradiology 2013; 55(10): 1205-11.
[http://dx.doi.org/10.1007/s00234-013-1239-5] [PMID: 23868180]
[14]
Lee J, Lee JY, Lee YJ, et al. Differentiation of dural arteriovenous fistula from reflux venous flow on 3D TOF-MR angiography: Identifying asymmetric enlargement of external carotid artery branches. Clin Radiol 2020; 75(9): 714.e15-20.
[15]
Kim E, Kim JH, Choi BS, Jung C, Lee DH. MRI and MR angiography findings to differentiate jugular venous reflux from cavernous dural arteriovenous fistula. AJR Am J Roentgenol 2014; 202(4): 839-46.
[http://dx.doi.org/10.2214/AJR.13.11048] [PMID: 24660714]
[16]
Wardlaw JM, Smith EE, Biessels GJ, et al. Neuroimaging standards for research into small vessel disease and its contribution to ageing and neurodegeneration. Lancet Neurol 2013; 12(8): 822-38.
[http://dx.doi.org/10.1016/S1474-4422(13)70124-8] [PMID: 23867200]
[17]
Xu Z, Li F, Wang B, et al. New insights in addressing cerebral small vessel disease: Association with the deep medullary veins. Front Aging Neurosci 2020; 12: 597799.
[http://dx.doi.org/10.3389/fnagi.2020.597799] [PMID: 33335483]
[18]
Gregoire SM, Chaudhary UJ, Brown MM, et al. The microbleed anatomical rating scale (MARS): Reliability of a tool to map brain microbleeds. Neurology 2009; 73(21): 1759-66.
[http://dx.doi.org/10.1212/WNL.0b013e3181c34a7d] [PMID: 19933977]
[19]
Cordonnier C, Potter GM, Jackson CA, et al. improving interrater agreement about brain microbleeds: Development of the Brain Observer MicroBleed Scale (BOMBS). Stroke 2009; 40(1): 94-9.
[http://dx.doi.org/10.1161/STROKEAHA.108.526996] [PMID: 19008468]
[20]
Kapeller P, Barber R, Vermeulen RJ, et al. Visual rating of age-related white matter changes on magnetic resonance imaging: scale comparison, interrater agreement, and correlations with quantitative measurements. Stroke 2003; 34(2): 441-5.
[http://dx.doi.org/10.1161/01.STR.0000049766.26453.E9] [PMID: 12574557]
[21]
Jessen NA, Munk ASF, Lundgaard I, Nedergaard M. The glymphatic system: A beginner’s guide. Neurochem Res 2015; 40(12): 2583-99.
[http://dx.doi.org/10.1007/s11064-015-1581-6] [PMID: 25947369]
[22]
Gouveia-Freitas K, Bastos-Leite AJ. Perivascular spaces and brain waste clearance systems: Relevance for neurodegenerative and cerebrovascular pathology. Neuroradiology 2021; 63(10): 1581-97.
[http://dx.doi.org/10.1007/s00234-021-02718-7] [PMID: 34019111]
[23]
Brown R, Benveniste H, Black SE, et al. Understanding the role of the perivascular space in cerebral small vessel disease. Cardiovasc Res 2018; 114(11): 1462-73.
[http://dx.doi.org/10.1093/cvr/cvy113] [PMID: 29726891]
[24]
Waragai M, Takeuchi H, Fukushima T, Haisa T, Yonemitsu T. MRI and SPECT studies of dural arteriovenous fistulas presenting as pure progressive dementia with leukoencephalopathy: A cause of treatable dementia. Eur J Neurol 2006; 13(7): 754-9.
[http://dx.doi.org/10.1111/j.1468-1331.2006.01318.x] [PMID: 16834706]
[25]
Chung CP, Wang PN, Wu YH, et al. More severe white matter changes in the elderly with jugular venous reflux. Ann Neurol 2011; 69(3): 553-9.
[http://dx.doi.org/10.1002/ana.22276] [PMID: 21391231]
[26]
Tanaka T, Uemura K, Takahashi M, et al. Compression of the left brachiocephalic vein: Cause of high signal intensity of the left sigmoid sinus and internal jugular vein on MR images. Radiology 1993; 188(2): 355-61.
[http://dx.doi.org/10.1148/radiology.188.2.8327678] [PMID: 8327678]
[27]
Saiki K, Tsurumoto T, Okamoto K, Wakebe T. Relation between bilateral differences in internal jugular vein caliber and flow patterns of dural venous sinuses. Anat Sci Int 2013; 88(3): 141-50.
[http://dx.doi.org/10.1007/s12565-013-0176-z] [PMID: 23572397]

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