Bozovic, Ivo

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  • Bozovic, Ivo (2)
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Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2

Mijajlovic, Milija; Bozovic, Ivo; Pavlović, Aleksandra; Rakocevic-Stojanovic, Vidosava; Gluscevic, Sanja; Stojanovic, Amalija; Basta, Ivana; Meola, Giovanni; Peric, Stojan

(Elsevier, 2024)

TY  - JOUR
AU  - Mijajlovic, Milija
AU  - Bozovic, Ivo
AU  - Pavlović, Aleksandra
AU  - Rakocevic-Stojanovic, Vidosava
AU  - Gluscevic, Sanja
AU  - Stojanovic, Amalija
AU  - Basta, Ivana
AU  - Meola, Giovanni
AU  - Peric, Stojan
PY  - 2024
UR  - https://www.sciencedirect.com/science/article/pii/S2405844024028871
UR  - internal-pdf://2340/S2405844024028871.html
UR  - http://rfasper.fasper.bg.ac.rs/handle/123456789/5409
AB  - IntroductionMyotonic dystrophy type 1 (DM1) and 2 (DM2) are genetically determined progressive muscular disorders with multisystemic affection, including brain involvement. Transcranial sonography (TCS) is a reliable diagnostic tool for the investigation of deep brain structures. We sought to evaluate TCS findings in genetically confirmed DM1 and DM2 patients, and further correlate these results with patients’ clinical features.MethodsThis cross-sectional study included 163 patients (102 DM1, 61 DM2). Echogenicity of the brainstem raphe (BR) and substantia nigra (SN) as well as the diameter of the third ventricle (DTV) were assessed by TCS. Patients were evaluated using the Hamilton Depression Rating Scale, Fatigue Severity Scale and Daytime Sleepiness Scale.ResultsSN hyperechogenicity was observed in 40% of DM1 and 34% of DM2 patients. SN hypoechogenicity was detected in 17% of DM1 and 7% of DM2 patients. BR hypoechogenicity was found in 36% of DM1 and 47% of DM2 subjects. Enlarged DTV was noted in 19% of DM1 and 15% of DM2 patients. Older, weaker, depressive, and fatigued DM1 patients were more likely to have BR hypoechogenicity (p < 0.05). DTV correlated with age and disease duration in DM1 (p < 0.01). In DM2 patients SN hyperechogenicity correlated with fatigue. Excessive daytime sleepiness was associated with hypoechogenic BR (p < 0.05) and enlarged DVT (p < 0.01) in DM2 patients.ConclusionsTCS is an easy applicable and sensitive neuroimaging technique that could offer new information regarding several brainstem structures in DM1 and DM2. This may lead to better understanding of the pathogenesis of the brain involvement in DM with possible clinical implications.
PB  - Elsevier
T2  - Heliyon
T2  - HeliyonHeliyon
T1  - Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2
IS  - 5
SP  - e26856
VL  - 10
DO  - 10.1016/j.heliyon.2024.e26856
ER  - 
@article{
author = "Mijajlovic, Milija and Bozovic, Ivo and Pavlović, Aleksandra and Rakocevic-Stojanovic, Vidosava and Gluscevic, Sanja and Stojanovic, Amalija and Basta, Ivana and Meola, Giovanni and Peric, Stojan",
year = "2024",
abstract = "IntroductionMyotonic dystrophy type 1 (DM1) and 2 (DM2) are genetically determined progressive muscular disorders with multisystemic affection, including brain involvement. Transcranial sonography (TCS) is a reliable diagnostic tool for the investigation of deep brain structures. We sought to evaluate TCS findings in genetically confirmed DM1 and DM2 patients, and further correlate these results with patients’ clinical features.MethodsThis cross-sectional study included 163 patients (102 DM1, 61 DM2). Echogenicity of the brainstem raphe (BR) and substantia nigra (SN) as well as the diameter of the third ventricle (DTV) were assessed by TCS. Patients were evaluated using the Hamilton Depression Rating Scale, Fatigue Severity Scale and Daytime Sleepiness Scale.ResultsSN hyperechogenicity was observed in 40% of DM1 and 34% of DM2 patients. SN hypoechogenicity was detected in 17% of DM1 and 7% of DM2 patients. BR hypoechogenicity was found in 36% of DM1 and 47% of DM2 subjects. Enlarged DTV was noted in 19% of DM1 and 15% of DM2 patients. Older, weaker, depressive, and fatigued DM1 patients were more likely to have BR hypoechogenicity (p < 0.05). DTV correlated with age and disease duration in DM1 (p < 0.01). In DM2 patients SN hyperechogenicity correlated with fatigue. Excessive daytime sleepiness was associated with hypoechogenic BR (p < 0.05) and enlarged DVT (p < 0.01) in DM2 patients.ConclusionsTCS is an easy applicable and sensitive neuroimaging technique that could offer new information regarding several brainstem structures in DM1 and DM2. This may lead to better understanding of the pathogenesis of the brain involvement in DM with possible clinical implications.",
publisher = "Elsevier",
journal = "Heliyon, HeliyonHeliyon",
title = "Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2",
number = "5",
pages = "e26856",
volume = "10",
doi = "10.1016/j.heliyon.2024.e26856"
}
Mijajlovic, M., Bozovic, I., Pavlović, A., Rakocevic-Stojanovic, V., Gluscevic, S., Stojanovic, A., Basta, I., Meola, G.,& Peric, S.. (2024). Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2. in Heliyon
Elsevier., 10(5), e26856.
https://doi.org/10.1016/j.heliyon.2024.e26856
Mijajlovic M, Bozovic I, Pavlović A, Rakocevic-Stojanovic V, Gluscevic S, Stojanovic A, Basta I, Meola G, Peric S. Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2. in Heliyon. 2024;10(5):e26856.
doi:10.1016/j.heliyon.2024.e26856 .
Mijajlovic, Milija, Bozovic, Ivo, Pavlović, Aleksandra, Rakocevic-Stojanovic, Vidosava, Gluscevic, Sanja, Stojanovic, Amalija, Basta, Ivana, Meola, Giovanni, Peric, Stojan, "Transcranial brain parenchyma sonographic findings in patients with myotonic dystrophy type 1 and 2" in Heliyon, 10, no. 5 (2024):e26856,
https://doi.org/10.1016/j.heliyon.2024.e26856 . .
1

Cerebral Amyloid Angiopathy-Related Inflammation (CAA-rI): Three Heterogeneous Case Reports and a Focused Literature Review

Bozovic, Ivo; Jeremic, Marta; Pavlović, Aleksandra; Jovanovic, Carna; Kresojevic, Nikola; Vojvodic, Nikola; Jovanovic, Dejana; Sokic, Dragoslav; Mijajlovic, Milija

(MDPI [Commercial Publisher], 2023)

TY  - JOUR
AU  - Bozovic, Ivo
AU  - Jeremic, Marta
AU  - Pavlović, Aleksandra
AU  - Jovanovic, Carna
AU  - Kresojevic, Nikola
AU  - Vojvodic, Nikola
AU  - Jovanovic, Dejana
AU  - Sokic, Dragoslav
AU  - Mijajlovic, Milija
PY  - 2023
UR  - https://www.mdpi.com/2076-3425/13/5/747
UR  - C:\Users\FASPER\Zotero\storage\KN238T94\Bozovic et al. - 2023 - Cerebral Amyloid Angiopathy-Related Inflammation (.pdf
UR  - http://rfasper.fasper.bg.ac.rs/handle/123456789/5292
AB  - Cerebral amyloid angiopathy-related inflammation (CAA-rI) is a largely reversible, subacute encephalopathy, which is considered as a rare variant of cerebral amyloid angiopathy (CAA). Although the diagnosis of this inflammatory vasculopathy is generally clinico-pathologic, a probable or possible diagnosis can often be established based on current clinico-radiological diagnostic criteria. This is important since CAA-rI is considered as a treatable disorder, which most commonly occurs in the elderly population. Behavioral changes and cognitive deterioration are highlighted as the most common clinical signs of CAA-rI, followed by a heterogeneous spectrum of typical and atypical clinical presentations. However, despite the well-established clinical and radiological features incorporated in the current diagnostic criteria for this CAA variant, this rare disorder is still insufficiently recognized and treated. Here, we have shown three patients diagnosed with probable CAA-rI, with significant heterogeneity in the clinical and neuroradiological presentations, followed by different disease courses and outcomes after the introduction of immunosuppressive treatment. Moreover, we have also summarized up-to-date literature data about this rare, yet underdiagnosed, immune-mediated vasculopathy.
PB  - MDPI [Commercial Publisher]
T2  - Brain Sciences
T1  - Cerebral Amyloid Angiopathy-Related Inflammation (CAA-rI): Three Heterogeneous Case Reports and a Focused Literature Review
IS  - 5
SP  - 747
VL  - 13
DO  - 10.3390/brainsci13050747
ER  - 
@article{
author = "Bozovic, Ivo and Jeremic, Marta and Pavlović, Aleksandra and Jovanovic, Carna and Kresojevic, Nikola and Vojvodic, Nikola and Jovanovic, Dejana and Sokic, Dragoslav and Mijajlovic, Milija",
year = "2023",
abstract = "Cerebral amyloid angiopathy-related inflammation (CAA-rI) is a largely reversible, subacute encephalopathy, which is considered as a rare variant of cerebral amyloid angiopathy (CAA). Although the diagnosis of this inflammatory vasculopathy is generally clinico-pathologic, a probable or possible diagnosis can often be established based on current clinico-radiological diagnostic criteria. This is important since CAA-rI is considered as a treatable disorder, which most commonly occurs in the elderly population. Behavioral changes and cognitive deterioration are highlighted as the most common clinical signs of CAA-rI, followed by a heterogeneous spectrum of typical and atypical clinical presentations. However, despite the well-established clinical and radiological features incorporated in the current diagnostic criteria for this CAA variant, this rare disorder is still insufficiently recognized and treated. Here, we have shown three patients diagnosed with probable CAA-rI, with significant heterogeneity in the clinical and neuroradiological presentations, followed by different disease courses and outcomes after the introduction of immunosuppressive treatment. Moreover, we have also summarized up-to-date literature data about this rare, yet underdiagnosed, immune-mediated vasculopathy.",
publisher = "MDPI [Commercial Publisher]",
journal = "Brain Sciences",
title = "Cerebral Amyloid Angiopathy-Related Inflammation (CAA-rI): Three Heterogeneous Case Reports and a Focused Literature Review",
number = "5",
pages = "747",
volume = "13",
doi = "10.3390/brainsci13050747"
}
Bozovic, I., Jeremic, M., Pavlović, A., Jovanovic, C., Kresojevic, N., Vojvodic, N., Jovanovic, D., Sokic, D.,& Mijajlovic, M.. (2023). Cerebral Amyloid Angiopathy-Related Inflammation (CAA-rI): Three Heterogeneous Case Reports and a Focused Literature Review. in Brain Sciences
MDPI [Commercial Publisher]., 13(5), 747.
https://doi.org/10.3390/brainsci13050747
Bozovic I, Jeremic M, Pavlović A, Jovanovic C, Kresojevic N, Vojvodic N, Jovanovic D, Sokic D, Mijajlovic M. Cerebral Amyloid Angiopathy-Related Inflammation (CAA-rI): Three Heterogeneous Case Reports and a Focused Literature Review. in Brain Sciences. 2023;13(5):747.
doi:10.3390/brainsci13050747 .
Bozovic, Ivo, Jeremic, Marta, Pavlović, Aleksandra, Jovanovic, Carna, Kresojevic, Nikola, Vojvodic, Nikola, Jovanovic, Dejana, Sokic, Dragoslav, Mijajlovic, Milija, "Cerebral Amyloid Angiopathy-Related Inflammation (CAA-rI): Three Heterogeneous Case Reports and a Focused Literature Review" in Brain Sciences, 13, no. 5 (2023):747,
https://doi.org/10.3390/brainsci13050747 . .
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