Abstract:ObjectivesThe comparison of treatment efficacy for cerebral cavernous malformations (CCMs) has not yet been well researched.DesignPubMed, Cochrane Library, Science Direct, ISI Web of Science, Embase and additional sources were searched to identify cohort studies about the treatment of CCMs published between 1990 and 2020. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines were followed; the Newcastle-Ottawa Scale was used to assess the risk of bias and to evaluate limitations bas… Show more
“…According to the most recent and largest meta-analysis from 2022, Bubenikova et al were able to assess and compare treatment approaches in 8994 patients suffering from a CCM. They found a higher prevention of (re)haemorrhage in patients undergoing surgical removal of their lesion, as well as additionally lower rates of morbidity compared to conservatively treated patients [26]. Their findings as well as further confirmation of our data could possibly affect treatment guidelines, leading to a more aggressive treatment after recurrent CM bleeding.…”
Section: External Validity and Clinical Relevancesupporting
confidence: 84%
“…Unfortunately, such studies are often limited to the assessment of initial and recurrent bleeding and the risk of a third bleeding has yet to be discovered [1,4,5,7,8,10,18,20]. Moreover, a significant number of trials analysing the outcome after treatments of such lesions exist [1,4,10,[24][25][26]. However, only a paucity of studies have tried to address the neurological impact of recurrent haemorrhagic events [4,9,14].…”
This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
“…According to the most recent and largest meta-analysis from 2022, Bubenikova et al were able to assess and compare treatment approaches in 8994 patients suffering from a CCM. They found a higher prevention of (re)haemorrhage in patients undergoing surgical removal of their lesion, as well as additionally lower rates of morbidity compared to conservatively treated patients [26]. Their findings as well as further confirmation of our data could possibly affect treatment guidelines, leading to a more aggressive treatment after recurrent CM bleeding.…”
Section: External Validity and Clinical Relevancesupporting
confidence: 84%
“…Unfortunately, such studies are often limited to the assessment of initial and recurrent bleeding and the risk of a third bleeding has yet to be discovered [1,4,5,7,8,10,18,20]. Moreover, a significant number of trials analysing the outcome after treatments of such lesions exist [1,4,10,[24][25][26]. However, only a paucity of studies have tried to address the neurological impact of recurrent haemorrhagic events [4,9,14].…”
This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
“…Cerebral cavernous malformations (CCMs) are hamartomatous vascular malformations characterized by intralesional hemorrhages [9 , 10] . The mean annual hemorrhage rate of CCMs is approximately 2.4% [11] .…”
“…Approximately 75% of patients with these cerebrovascular malformations have a high risk of intracranial hemorrhages, seizures, focal neurological deficits, and severe headaches secondary to CCM ( 5 ). Currently, surgery or radiosurgery of are possible interventional treatment options for patients with symptomatic CCM ( 6 ). Although genetic mutations in KRIT1/CCM1 , CCM2 , and PDCD10/CCM3 are known causes of CCM ( 7 ), factors influencing rates of disease severity and progression of CCM remain unknown.…”
AimNeuroinflammation plays a key role in both the pathogenesis and the progression of cerebral cavernous malformations (CCM). Flutriciclamide ([18F]GE-180) is a translocator protein (TSPO) targeting positron emission tomography (PET) tracer, developed for imaging neuroinflammation. The objectives of this study were to describe characteristics of flutriciclamide uptake in different brain tissue regions in CCM patients compared to controls, and to evaluate flutriciclamide uptake and iron deposition within CCM lesions.Materials and methodsFive patients with CCM and six controls underwent a 60 or 90 min continuous PET/MRI scan following 315 ± 68.9 MBq flutriciclamide administration. Standardized uptake value (SUV) and standardized uptake value ratio (SUVr) were obtained using the striatum as a pseudo-reference. Quantitative susceptibility maps (QSM) were used to define the location of the vascular malformation and calculate the amount of iron deposition in each lesion.ResultsIncreased flutriciclamide uptake was observed in all CCM lesions. The temporal pole demonstrated the highest radiotracer uptake; the paracentral lobule, cuneus and hippocampus exhibited moderate uptake; while the striatum had the lowest uptake, with average SUVs of 0.66, 0.55, 0.63, 0.55, and 0.33 for patient with CCM and 0.57, 0.50, 0.48, 0.42, and 0.32 for controls, respectively. Regional SUVr showed similar trends. The average SUV and QSM values in CCM lesions were 0.58 ± 0.23 g/ml and 0.30 ± 0.10 ppm. SUVs and QSM were positively correlated in CCM lesions (r = 0.53, p = 0.03).ConclusionThe distribution of flutriciclamide ([18F]GE-180) in the human brain and CCM lesions demonstrated the potential of this TSPO PET tracer as a marker of neuroinflammation that may be relevant for characterizing CCM disease progression along with QSM.
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