Ingeborg Rasing

ORCID: 0000-0002-0953-7133
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About
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Research Areas
  • Intracerebral and Subarachnoid Hemorrhage Research
  • Alzheimer's disease research and treatments
  • Cerebrovascular and genetic disorders
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Neurosurgical Procedures and Complications
  • Acute Ischemic Stroke Management
  • Advanced Neuroimaging Techniques and Applications
  • Moyamoya disease diagnosis and treatment
  • Cerebrovascular and Carotid Artery Diseases
  • Intracranial Aneurysms: Treatment and Complications
  • Connective tissue disorders research
  • Dementia and Cognitive Impairment Research
  • Traumatic Brain Injury and Neurovascular Disturbances
  • Ophthalmology and Eye Disorders
  • Meningioma and schwannoma management
  • Congenital heart defects research
  • Vascular Malformations Diagnosis and Treatment
  • Kruppel-like factors research
  • Spinal Hematomas and Complications
  • Protease and Inhibitor Mechanisms
  • Advanced Glycation End Products research
  • Cerebrospinal fluid and hydrocephalus
  • MRI in cancer diagnosis

Leiden University Medical Center
2015-2025

University Medical Center Utrecht
2012-2015

Utrecht University
2013

Vascular amyloid β (Aβ) accumulation is the hallmark of cerebral angiopathy (CAA). The composition cerebrospinal fluid (CSF) CAA patients may serve as a diagnostic biomarker CAA. We studied potential peptides Aβ38, Aβ40, Aβ42, and Aβ43 in with sporadic (sCAA), hereditary Dutch-type (D-CAA), Alzheimer disease (AD).

10.1002/ana.26610 article EN cc-by Annals of Neurology 2023-01-27

Cerebral Amyloid Angiopathy (CAA) disease course is highly variable even in hereditary forms. Sex may be a possible modifying factor. We investigated biological sex differences clinical and magnetic resonance imaging-markers sporadic (sCAA) Dutch-type CAA (D-CAA).

10.1161/strokeaha.122.040823 article EN cc-by Stroke 2023-01-23

Neurofilament light chain (NFL) is a biomarker for neuroaxonal damage and glial fibrillary acidic protein (GFAP) reactive astrocytosis. Both processes occur in cerebral amyloid angiopathy (CAA), but studies investigating the potential of NFL GFAP as markers CAA are lacking. We aimed to investigate biomarkers astrocytosis CAA.

10.1186/s13195-024-01457-0 article EN cc-by Alzheimer s Research & Therapy 2024-04-23

Enlarged perivascular spaces (PVS) in the centrum semiovale are an important marker of Cerebral Amyloid Angiopathy (CAA) and thought to reflect brain clearance dysfunction. However, current golden standard for assessing PVS is limited a unilateral, single slice, qualitative analysis, which has disadvantage strong ceiling effect. We aim introduce whole-brain volume fraction (PVSvf) measurement assess cross-sectional longitudinal PVSvf differences between pre-symptomatic symptomatic Dutch-type...

10.1016/j.nicl.2025.103778 article EN cc-by NeuroImage Clinical 2025-04-01

Knowledge on the short-term progression of cerebral amyloid angiopathy (CAA) is important for clinical practice and design treatment trials. We investigated 1-year CAA-related MRI markers in sporadic (sCAA) Dutch-type hereditary (D-CAA). Participants were included from 2 prospective cohort studies. 3T-MRI was performed at baseline after 1 year. assessed macrobleeds, microbleeds (CMBs), cortical superficial siderosis (cSS), convexity subarachnoid hemorrhages (cSAHs), white matter...

10.1212/wnl.0000000000213546 article EN Neurology 2025-04-08

BACKGROUND: The temporal ordering of biomarkers for cerebral amyloid angiopathy (CAA) is important their use in trials and the understanding pathological cascade CAA. We investigated presence abnormality most common largest (pre)symptomatic Dutch-type hereditary CAA (D-CAA) cohort to date. METHODS: included cross-sectional data from participants with D-CAA controls without CAA-related small vessel disease markers on 3T-MRI, cerebrovascular reactivity functional 7T-MRI (fMRI) amyloid-β 40 42...

10.1161/strokeaha.123.044688 article EN cc-by Stroke 2024-03-06

Background and Purpose: Although evidence accumulates that the cerebellum is involved in cerebral amyloid angiopathy (CAA), cerebellar superficial siderosis not considered to be a disease marker. The objective of this study investigate frequency its relation hemorrhagic magnetic resonance imaging markers patients with sporadic Dutch-type hereditary CAA deep perforating arteriopathy–related intracerebral hemorrhage. Methods: We recruited from 3 prospective Tesla studies scored hemorrhages....

10.1161/strokeaha.121.035019 article EN Stroke 2021-09-20

Abstract Background The diagnosis of probable cerebral amyloid angiopathy (CAA) is currently mostly based on characteristics brain MRI. Blood biomarkers would be a cost-effective, easily accessible diagnostic method that may complement by MRI and aid in monitoring disease progression. We studied the potential plasma Aβ38, Aβ40, Aβ42 patients with hereditary Dutch-type CAA (D-CAA) sporadic (sCAA). Methods All Aβ peptides were quantified immunoassays discovery cohort (11 presymptomatic D-CAA...

10.1186/s13195-023-01245-2 article EN cc-by Alzheimer s Research & Therapy 2023-06-03

Abstract Background Neuropsychiatric symptoms (NPS) may affect cognition, but their burden in cerebral amyloid angiopathy (CAA), one of the main causes intracerebral hemorrhage (ICH) and dementia elderly, remains unclear. We investigated NPS, with emphasis on apathy irritability sporadic (sCAA) Dutch-type hereditary (D-)CAA. Methods included patients sCAA (pre)symptomatic D-CAA, controls from four prospective cohort studies. assessed NPS per group, stratified for history ICH, using...

10.1186/s13195-024-01445-4 article EN cc-by Alzheimer s Research & Therapy 2024-04-06

Peak width of skeletonized mean diffusivity (PSMD) is an emerging diffusion-MRI based marker to study subtle early alterations white matter microstructure. We assessed PSMD over the clinical continuum in Dutch-type hereditary CAA (D-CAA) and its association with other CAA-related MRI-markers cognitive symptoms. included (pre)symptomatic D-CAA mutation-carriers calculated from data. Associations between PSMD-levels, performance were linear regression models. 59 participants (25/34...

10.1177/0271678x241261771 article EN cc-by-nc Journal of Cerebral Blood Flow & Metabolism 2024-06-17

Abstract Background To evaluate the potential of cerebrospinal fluid (CSF) levels matrix metalloproteinases and tissue-type inhibitors (MMP; TIMP), ratios MMPs to TIMPs, function as biomarkers for sporadic or hereditary cerebral amyloid angiopathy (CAA). Methods CSF concentrations MMP-2, MMP-9 MMP-14, well tissue TIMP-1, TIMP-2 TIMP-3, were determined using immunoassays. These assays applied two, independent study groups CAA (sCAA) ( n = 28/43) control subjects 40/40), pre-symptomatic 11)...

10.1186/s13195-023-01171-3 article EN cc-by Alzheimer s Research & Therapy 2023-01-30

<h3>Background</h3> Smoking and hypertension increase the risk of aneurismal subarachnoid haemorrhage (SAH) two to threefold whereas a familial predisposition increases sixfold. We assessed additional smoking for presence an intracranial aneurysm (IA) in first-degree relatives patients with SAH. <h3>Methods</h3> studied SAH who were screened aneurysms. RRs corresponding 95% CIs IA calculated hypertension. <h3>Results</h3> The 1.5 (95% CI 0.7 3.2) smoking, 1.9 1.0 3.7) 2.7 1.4 5.3) plus...

10.1136/jnnp-2011-301147 article EN Journal of Neurology Neurosurgery & Psychiatry 2012-03-15

Background and Purpose— To determine whether migraine, which has often been described as an inaugural manifestation in monogenic cerebrovascular syndromes, is associated with cerebral amyloid pathology, we assessed migraine its correlation magnetic resonance imaging markers Hereditary Dutch-Type Cerebral Amyloid Angiopathy (D-CAA or Hemorrhage With Amyloidosis-Dutch type). Methods— All D-CAA mutation carriers who visited our clinic between 2012 2018 were included. Migraine was diagnosed by...

10.1161/strokeaha.119.028170 article EN cc-by-nc-nd Stroke 2020-03-18

Whether certain activities can trigger spontaneous intracerebral hemorrhage (ICH) remains unknown. Insights into factors that vessel rupture resulting in ICH improves knowledge on the pathophysiology of ICH. We assessed potential and their risk for onset.We included consecutive patients diagnosed with between July 1, 2013, December 31, 2019. interviewed exposure to 12 (eg, Valsalva maneuvers) (hazard) period soon before onset normal these year used case-crossover design calculate relative...

10.1161/strokeaha.121.036233 article EN Stroke 2021-12-16

We observed subarachnoid cerebrospinal fluid (CSF) hyperintensities at non-contrast 7-tesla (T) fluid-attenuated inversion recovery (FLAIR) MRI, frequently topographically associated with cortical superficial siderosis (cSS), in participants cerebral amyloid angiopathy (CAA). To systemically evaluate these CSF we investigated their frequency and anatomical temporal relationship cSS on 7T 3T MRI hereditary Dutch-type CAA (D-CAA), sporadic (sCAA), non-CAA controls.CAA were included from two...

10.1016/j.nicl.2023.103386 article EN cc-by-nc-nd NeuroImage Clinical 2023-01-01

Abstract Background Cerebral amyloid angiopathy (CAA) is a disease caused by the accumulation of amyloid-beta protein and major cause intracerebral hemorrhage (ICH) vascular dementia in elderly. The presence vessel wall may induce chronic state cerebral inflammation activating astrocytes, microglia, pro-inflammatory substances. Minocycline, an antibiotic tetracycline family, known to modulate inflammation, gelatinase activity, angiogenesis. These processes are suggested be key mechanisms CAA...

10.1186/s13063-023-07371-4 article EN cc-by Trials 2023-06-05

Cerebral amyloid angiopathy (CAA) is a main cause of cognitive dysfunction in the elderly. We investigated specific profiles, function stage before intracerebral hemorrhage (ICH), and association between magnetic resonance imaging (MRI) based cerebral small vessel disease (cSVD) burden CAA because data on these topics are limited.

10.1002/alz.14171 article EN cc-by-nc-nd Alzheimer s & Dementia 2024-10-10

Genetic risk factors for intracranial aneurysms may influence the size of aneurysms.To assess association between genetic and at time rupture.Genotypes 7 independent single-nucleotide polymorphisms (SNPs) 6 loci identified in genome-wide studies patients with were obtained from 700 Dutch an aneurysmal subarachnoid hemorrhage (1997-2007) previously genotyped studies; 255 additional (2007-2011) these SNPs. Aneurysms measured on computerized tomography angiography or digital subtraction...

10.1227/neu.0000000000000078 article EN Neurosurgery 2013-07-10

The revised Boston criteria v2.0 for cerebral amyloid angiopathy (CAA) add two radiological markers to the existing criteria: severe visible perivascular spaces in centrum semiovale and white matter hyperintensities (WMHs) a multispot pattern. This study aims determine sensitivity of updated mutation carriers with Dutch-type hereditary CAA (D-CAA) an early later disease stage.

10.1177/17474930241239801 article EN cc-by International Journal of Stroke 2024-03-06

Background and aim To investigate whether a striped occipital cortex intragyral hemorrhage, two markers recently detected on ultra-high-field 7-tesla-magnetic resonance imaging in hereditary cerebral amyloid angiopathy (CAA), also occur sporadic CAA (sCAA) or non-sCAA intracerebral hemorrhage (ICH). Methods We performed patients with probable sCAA non-sCAA-ICH. Striped (linear hypointense stripes perpendicular to the cortex) (hemorrhage restricted juxtacortical white matter of one gyrus)...

10.1177/1747493021991961 article EN cc-by-nc International Journal of Stroke 2021-02-03

<h3>Objective:</h3> The objective was to assess the risk of aneurysmal subarachnoid hemorrhage (aSAH) in initial 15 years after negative aneurysm screening persons with one first-degree relative aSAH. <h3>Methods:</h3> From a cohort relatives patients aSAH who underwent between 1995 and 1997 (n = 626), we included those 601). We retrieved all causes death sent questionnaire screenees were still alive. If reported, reviewed medical data. assessed incidence this survival analysis calculated an...

10.1212/wnl.0000000000001310 article EN Neurology 2015-01-31

Cortical calcifications have been reported in patients with cerebral amyloid angiopathy (CAA), although their prevalence and pathophysiology are unknown. We investigated the frequency of on computed tomography, association intracerebral hemorrhage (ICH) coexistence a striped pattern occipital cortex reflecting microcalcifications ultra-high-field 7T-magnetic resonance imaging Dutch-type hereditary CAA (D-CAA) sporadic CAA.We included D-CAA mutation carriers proven APP (amyloid precursor...

10.1161/strokeaha.120.033286 article EN Stroke 2021-04-05

Cerebral amyloid angiopathy (CAA) is a cerebrovascular disease affecting the small arteries in brain with hallmark depositions of amyloid-β vessel wall, leading to cognitive decline and intracerebral hemorrhage (ICH). An emerging MRI marker for CAA cortical superficial siderosis (cSS) as it strongly related risk (recurrent) ICH. Current assessment cSS mainly done on T2*- weighted using qualitative score consisting 5 categories severity which hampered by ceiling effects. Therefore, need more...

10.1016/j.nicl.2023.103447 article EN cc-by NeuroImage Clinical 2023-01-01

Cerebral Amyloid Angiopathy (CAA) is characterized by cerebrovascular amyloid-β accumulation leading to hallmark cortical MRI markers, such as vascular reactivity, but white matter also affected. By studying the relationship in different disease stages of Dutch-type CAA (D-CAA), we tested relation between reactivity and microstructural integrity loss. In a cross-sectional study D-CAA, 3 T was performed with Blood-Oxygen-Level-Dependent (BOLD) fMRI upon visual activation assess diffusion...

10.1177/0271678x231200425 article EN cc-by-nc Journal of Cerebral Blood Flow & Metabolism 2023-09-14

Objective Blood-brain barrier (BBB) dysfunction is implicated in the pathophysiology of cerebral small vessel disease (cSVD)-related intracerebral hemorrhage (ICH). The formation perihematomal edema (PHE) presumed to reflect acute BBB permeability following ICH. We aimed assess association between cSVD burden and PHE patients with spontaneous Methods selected ICH who underwent 3T MRI imaging within 21 days after symptom onset from a prospective observational multicenter cohort study. rated...

10.3389/fneur.2022.949133 article EN cc-by Frontiers in Neurology 2022-07-29
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