| 1. |
- Boen, Rune, et al.
(författare)
-
Beyond the global brain differences : intraindividual variability differences in 1q21.1 distal and 15q11.2 bp1-bp2 deletion carriers
- 2024
-
Ingår i: Biological Psychiatry. - 0006-3223 .- 1873-2402. ; 95:2, s. 147-160
-
Tidskriftsartikel (refereegranskat)abstract
- Background: Carriers of the 1q21.1 distal and 15q11.2 BP1-BP2 copy number variants exhibit regional and global brain differences compared with noncarriers. However, interpreting regional differences is challenging if a global difference drives the regional brain differences. Intraindividual variability measures can be used to test for regional differences beyond global differences in brain structure.Methods: Magnetic resonance imaging data were used to obtain regional brain values for 1q21.1 distal deletion (n = 30) and duplication (n = 27) and 15q11.2 BP1-BP2 deletion (n = 170) and duplication (n = 243) carriers and matched noncarriers (n = 2350). Regional intra-deviation scores, i.e., the standardized difference between an individual's regional difference and global difference, were used to test for regional differences that diverge from the global difference.Results: For the 1q21.1 distal deletion carriers, cortical surface area for regions in the medial visual cortex, posterior cingulate, and temporal pole differed less and regions in the prefrontal and superior temporal cortex differed more than the global difference in cortical surface area. For the 15q11.2 BP1-BP2 deletion carriers, cortical thickness in regions in the medial visual cortex, auditory cortex, and temporal pole differed less and the prefrontal and somatosensory cortex differed more than the global difference in cortical thickness.Conclusions: We find evidence for regional effects beyond differences in global brain measures in 1q21.1 distal and 15q11.2 BP1-BP2 copy number variants. The results provide new insight into brain profiling of the 1q21.1 distal and 15q11.2 BP1-BP2 copy number variants, with the potential to increase understanding of the mechanisms involved in altered neurodevelopment.
|
|
| 2. |
- Straube, Ulrich, et al.
(författare)
-
Operational radiation protection for astronauts and cosmonauts and correlated activities of ESA Medical Operations
- 2010
-
Ingår i: Acta Astronautica. - : Elsevier BV. - 0094-5765 .- 1879-2030. ; 66:7-8, s. 963-973
-
Forskningsöversikt (refereegranskat)abstract
- Since the early times of human spaceflight radiation has been, besides the influence of microgravity on the human body, recognized as a main health concern to astronauts and cosmonauts. The radiation environment that the crew experiences during spaceflight differs significantly to that found on earth due to particles of greater potential for biological damage. Highly energetic charged particles, such as protons, helium nuclei ("alpha particles") and heavier ions up to iron, originating from several sources, as well as protons and electrons trapped in the Earth's radiation belts, are the main contributors. The exposure that the crew receives during a spaceflight significantly exceeds exposures routinely received by terrestrial radiation workers. The European Space Agency's (ESA) Astronaut Center (EAC) in Cologne, Germany, is home of the European Astronaut Corps. Part of the EAC is the Crew Medical Support Office (CMSO or HSF-AM) responsible for ensuring the health and well-being of the European Astronauts. A sequence of activities is conducted to protect astronauts and cosmonauts health, including those aiming to mitigate adverse effects of space radiation. All health related activities are part of a multinational Medical Operations (MedOps) concept, which is executed by the different Space Agencies participating in the human spaceflight program of the International Space Station (ISS). This article will give an introduction to the current measures used for radiation monitoring and protection of astronauts and cosmonauts. The operational guidelines that shall ensure proper implementation and execution of those radiation protection measures will be addressed. Operational hardware for passive and active radiation monitoring and for personal dosimetry, as well as the operational procedures that are applied, are described.
|
|
| 3. |
|
|
| 4. |
- Bas-Hoogendam, Janna Marie, et al.
(författare)
-
Voxel-based morphometry multi-center mega-analysis of brain structure in social anxiety disorder
- 2017
-
Ingår i: NeuroImage. - : Elsevier BV. - 2213-1582. ; 16, s. 678-688
-
Tidskriftsartikel (refereegranskat)abstract
- Social anxiety disorder (SAD) is a prevalent and disabling mental disorder, associated with significant psychiatric co-morbidity. Previous research on structural brain alterations associated with SAD has yielded inconsistent results concerning the direction of the changes in gray matter (GM) in various brain regions, as well as on the relationship between brain structure and SAD-symptomatology. These heterogeneous findings are possibly due to limited sample sizes. Multi-site imaging offers new opportunities to investigate SAD-related alterations in brain structure in larger samples.An international multi-center mega-analysis on the largest database of SAD structural T1-weighted 3T MRI scans to date was performed to compare GM volume of SAD-patients (n = 174) and healthy control (HC)-participants (n = 213) using voxel-based morphometry. A hypothesis-driven region of interest (ROI) approach was used, focusing on the basal ganglia, the amygdala-hippocampal complex, the prefrontal cortex, and the parietal cortex. SAD-patients had larger GM volume in the dorsal striatum when compared to HC-participants. This increase correlated positively with the severity of self-reported social anxiety symptoms. No SAD-related differences in GM volume were present in the other ROIs. Thereby, the results of this mega-analysis suggest a role for the dorsal striatum in SAD, but previously reported SAD-related changes in GM in the amygdala, hippocampus, precuneus, prefrontal cortex and parietal regions were not replicated. Our findings emphasize the importance of large sample imaging studies and the need for meta-analyses like those performed by the Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium.
|
|
| 5. |
- Groenewold, Nynke A., et al.
(författare)
-
Volume of subcortical brain regions in social anxiety disorder : mega-analytic results from 37 samples in the ENIGMA-Anxiety Working Group
- 2023
-
Ingår i: Molecular Psychiatry. - : Springer Nature. - 1359-4184 .- 1476-5578. ; 28:3, s. 1079-1089
-
Tidskriftsartikel (refereegranskat)abstract
- There is limited convergence in neuroimaging investigations into volumes of subcortical brain regions in social anxiety disorder (SAD). The inconsistent findings may arise from variations in methodological approaches across studies, including sample selection based on age and clinical characteristics. The ENIGMA-Anxiety Working Group initiated a global mega-analysis to determine whether differences in subcortical volumes can be detected in adults and adolescents with SAD relative to healthy controls. Volumetric data from 37 international samples with 1115 SAD patients and 2775 controls were obtained from ENIGMA-standardized protocols for image segmentation and quality assurance. Linear mixed-effects analyses were adjusted for comparisons across seven subcortical regions in each hemisphere using family-wise error (FWE)-correction. Mixed-effects d effect sizes were calculated. In the full sample, SAD patients showed smaller bilateral putamen volume than controls (left: d = −0.077, pFWE = 0.037; right: d = −0.104, pFWE = 0.001), and a significant interaction between SAD and age was found for the left putamen (r = −0.034, pFWE = 0.045). Smaller bilateral putamen volumes (left: d = −0.141, pFWE < 0.001; right: d = −0.158, pFWE < 0.001) and larger bilateral pallidum volumes (left: d = 0.129, pFWE = 0.006; right: d = 0.099, pFWE = 0.046) were detected in adult SAD patients relative to controls, but no volumetric differences were apparent in adolescent SAD patients relative to controls. Comorbid anxiety disorders and age of SAD onset were additional determinants of SAD-related volumetric differences in subcortical regions. To conclude, subtle volumetric alterations in subcortical regions in SAD were detected. Heterogeneity in age and clinical characteristics may partly explain inconsistencies in previous findings. The association between alterations in subcortical volumes and SAD illness progression deserves further investigation, especially from adolescence into adulthood.
|
|
| 6. |
|
|
| 7. |
- Sailer, Uta, et al.
(författare)
-
Impaired temporal prediction and eye-hand coordination in patients with cerebellar lesions.
- 2005
-
Ingår i: Behavioural Brain Research. - : Elsevier BV. - 0166-4328. ; 160:1, s. 72-87
-
Tidskriftsartikel (refereegranskat)abstract
- This study investigated the effect of cerebellar lesions on temporal prediction and coordination in eye and hand movements. Nine patients with cerebellar lesions were compared to controls while they made saccades with and without simultaneous pointing movements towards a target that was either temporally predictable or non-predictable. The direction and amplitude of the target step was always predictable. Patients made much more early and late saccades than controls, but an equal amount of visually triggered saccades. This suggests that inappropriate saccades could be suppressed during the preparation of a goal-directed saccade. Hand movement frequency did not differ between both groups. Thus, cerebellar lesions can induce inappropriate saccades more easily than inappropriate hand movements. Controls, but not patients, generated visually triggered saccades of shorter latencies when the target was temporally predictable. Thus, the patients could not use information about target timing to synchronise visually triggered saccades with the target. They could, however, use this information to improve the suppression of inappropriate saccades. Regarding coordination, patients showed impairments in synchronising saccades with hand movements. Nevertheless, hand movements led to an enhancement of anticipatory saccades in patients as in controls. Moreover, hand movements and temporal predictability affected saccadic accuracy in both groups similarly. These results suggest that cerebellar lesions do not generally prevent access to temporal information on the rhythm of a target sequence or the timing of a planned hand movement. More specifically, the cerebellum seems to be crucial for synchronizing saccades with such learned or planned temporal events.
|
|
