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A Multicenter MRI Protocol for the Evaluation and Quantification of Deep Vein Thrombosis
Published on: June 2, 2015
The relationship between deep medullary veins score and the severity and distribution of intracranial microbleeds
Ruiting Zhang1, Qingqing Li1, Ying Zhou1
1Department of Neurology, the Second Affiliated Hospital of Zhejiang University, School of Medicine, 88# Jiefang Road, Hangzhou, China.
Background:
Microbleeds are frequently detected in normal elderly population, and their presence is associated with an increased risk of intracerebral hemorrhage, ischemic stroke and cognitive impairment. Previous histopathologic findings mainly focused on arteries and capillaries. Nevertheless, few studies investigated the relationship between venous disruption and microbleeds.
Objective:
We aimed to evaluate the extent of venous disruption in vivo and assess the correlation between deep medullary veins (DMVs) disruption and the severity and distribution of intracranial microbleeds in patients with cerebral small vessel disease (cSVD).
Methods:
We retrospectively reviewed the clinical, laboratory and imaging data of the patients admitted to our department who received brain MRI and presented with CSVD imaging markers. Susceptibility weighted imaging (SWI) phase images were used to observe characteristics of DMVs and derive a brain region-based DMVs visual score. SWI magnitude images were used to evaluate microbleeds. We recorded the number and distribution (lobar or deep or infratentorial) of microbleeds. One-way ANOVA and logistic-regression analysis were used to examine the association between the DMVs score and microbleeds.
Results:
A total of 369 cSVD patients were analyzed, including 177 (48.0%) patients with microbleeds, among whom 81(45.8%) patients had 1-2 microbleeds and 96 (54.2%) patients had ≥3 microbleeds (extensive microbleeds). The patients' DMVs score ranged from 0 to18, with a median score of 8(6-12). Higher DMVs score was independently associated with extensive microbleeds (OR = 1.108, 95%Cl: 1.010-1.215, p = 0.03) after adjusting for gender, hypertension, hyperhomocysteinemia, Fazekas score and number of lacunas. According to the distribution, 38 (21.5%) patients were found with strict lobar microbleeds, while 139 (78.5%) patients had non-strict lobar microbleeds. Higher DMVs score was also independently associated with non-strict lobar microbleeds (OR = 1.106, 95% Cl: 1.019-1.200, p = 0.016) after adjusting for gender, hypertension, hyperhomocysteinemia, Fazekas score and number of lacunas. DMVs score was not associated with strict lobar microbleeds (p = 0.307).
Conclusion:
DMVs disruption might be involved in the development of extensive microbleeds, especially non-strict lobar cerebral microbleeds.
Insights
Deep medullary vein (DMV) disruption is linked to extensive microbleeds in patients with cerebral small vessel disease (cSVD). This finding highlights the role of venous changes in the development of non-strict lobar cerebral microbleeds.
Area of Science:
- Neurology
- Radiology
- Vascular Biology
Background:
- Cerebral microbleeds are common in the elderly, increasing risks for stroke and cognitive decline.
- Previous research on microbleeds primarily focused on arterial and capillary pathology.
- The link between venous disruption and microbleeds remains under-investigated.
Purpose of the Study:
- To assess deep medullary vein (DMV) disruption in vivo.
- To correlate DMV disruption with the severity and distribution of intracranial microbleeds in cerebral small vessel disease (cSVD) patients.
Main Methods:
- Retrospective analysis of 369 cSVD patients' clinical, laboratory, and MRI data.
- Utilized susceptibility-weighted imaging (SWI) for DMV assessment and microbleed evaluation.
- Calculated a brain region-based DMVs visual score and analyzed microbleed number and distribution.
Main Results:
- Higher DMVs scores were independently associated with extensive microbleeds (OR=1.108, p=0.03).
- DMVs disruption was also linked to non-strict lobar microbleeds (OR=1.106, p=0.016).
- No significant association was found between DMVs score and strict lobar microbleeds (p=0.307).
Conclusions:
- Deep medullary vein (DMV) disruption may contribute to the development of extensive microbleeds.
- This association is particularly evident for non-strict lobar cerebral microbleeds.
- Venous disruption is a potential factor in cSVD pathogenesis.
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