84 research outputs found
Influence of Power-to-Fuel Plant Flexibility Towards Power and Plant Utilization and Intermediate Hydrogen Buffer Size
Conversion of intermittent renewable energy into synthetic fuels and chemicals is required to secure longâdistance transport and feedstock for chemical industry. Due to the fluctuating energy generation, process intensification and feed flexibility are essential. This contribution investigates the importance of feed flexibility on the buffer size with applying a 20:80 scenario of wind/solar energy generation. The degree of power and plant utilization are calculated. With the capability to accept a lower load bound of 17â% after only 10âmin, a minimum tank capacity of only 1.3âh is calculated to avoid a fuel plant stop throughout a calendar year. Additional tank capacity for peak power compensation in the range of âŒ10âh is beneficial for the utilization degree of power and under the prerequisite of a loadâflexible fuel plant
Reliability of Intra-Retinal Layer Thickness Estimates
Purpose Measurement of intra-retinal layer thickness using optical coherence
tomography (OCT) has become increasingly prominent in multiple sclerosis (MS)
research. Nevertheless, the approaches used for determining the mean layer
thicknesses vary greatly. Insufficient data exist on the reliability of
different thickness estimates, which is crucial for their application in
clinical studies. This study addresses this lack by evaluating the
repeatability of different thickness estimates. Methods Studies that used
intra-retinal layer segmentation of macular OCT scans in patients with MS were
retrieved from PubMed. To investigate the repeatability of previously applied
layer estimation approaches, we generated datasets of repeating measurements
of 15 healthy subjects and 13 multiple sclerosis patients using two OCT
devices (Cirrus HD-OCT and Spectralis SD-OCT). We calculated each thickness
estimate in each repeated session and analyzed repeatability using intra-class
correlation coefficients and coefficients of repeatability. Results We
identified 27 articles, eleven of them used the Spectralis SD-OCT, nine Cirrus
HD-OCT, two studies used both devices and two studies applied RTVue-100.
Topcon OCT-1000, Stratus OCT and a research device were used in one study
each. In the studies that used the Spectralis, ten different thickness
estimates were identified, while thickness estimates of the Cirrus OCT were
based on two different scan settings. In the simulation dataset, thickness
estimates averaging larger areas showed an excellent repeatability for all
retinal layers except the outer plexiform layer (OPL). Conclusions Given the
good reliability, the thickness estimate of the 6mm-diameter area around the
fovea should be favored when OCT is used in clinical research. Assessment of
the OPL was weak in general and needs further investigation before OPL
thickness can be used as a reliable parameter
Global Crises and the Role of BISE
The COVID-19 pandemic has surprised the modern world and has presented challenges on an unprecedented scale. Within a few months of the first case being reported at the end of 2019, almost every country in the world is now affected (WHO 2020). Restrictions on public life were not made fast enough and, in some cases, were not sufficient to stop the global spread. Here we see the dark sides of globalization. The crisis is coming with an intensity undreamt of for todayâs generations, affecting all areas of life and, at least temporarily, fundamentally changing them. The social, economic and political effects are clearly noticeable and solutions are being sought everywhere to mitigate the crisis and both its direct and indirect consequences
Criteria for Blood Vessel Discrimination
Introduction The diagnostic potential of optical coherence tomography (OCT) in
neurological diseases is intensively discussed. Besides the sectional view of
the retina, modern OCT scanners produce a simultaneous top-view confocal
scanning laser ophthalmoscopy (cSLO) image including the option to evaluate
retinal vessels. A correct discrimination between arteries and veins
(labeling) is vital for detecting vascular differences between healthy
subjects and patients. Up to now, criteria for labeling (cSLO) images
generated by OCT scanners do not exist. Objective This study reviewed labeling
criteria originally developed for color fundus photography (CFP) images.
Methods The criteria were modified to reflect the cSLO technique, followed by
development of a protocol for labeling blood vessels. These criteria were
based on main aspects such as central light reflex, brightness, and vessel
thickness, as well as on some additional criteria such as vascular crossing
patterns and the context of the vessel tree. Results and Conclusion They
demonstrated excellent inter-rater agreement and validity, which seems to
indicate that labeling of images might no longer require more than one rater.
This algorithm extends the diagnostic possibilities offered by OCT
investigations
Investigation of Visual System Involvement in Spinocerebellar Ataxia Type 14
Spinocerebellar ataxia type 14 (SCA-PRKCG, formerly SCA14) is a rare, slowly progressive disorder caused by conventional mutations in protein kinase CÎł (PKCÎł). The disease usually manifests with ataxia, but previous reports suggested PRKCG variants in retinal pathology. To systematically investigate for the first time visual function and retinal morphology in patients with SCA-PRKCG. Seventeen patients with PRKCG variants and 17 healthy controls were prospectively recruited, of which 12 genetically confirmed SCA-PRKCG patients and 14 matched controls were analyzed. We enquired a structured history for visual symptoms. Vision-related quality of life was obtained with the National Eye Institute Visual Function Questionnaire (NEI-VFQ) including the Neuro-Ophthalmic Supplement (NOS). Participants underwent testing of visual acuity, contrast sensitivity, visual fields, and retinal morphology with optical coherence tomography (OCT). Measurements of the SCA-PRKCG group were analyzed for their association with clinical parameters (ataxia rating and disease duration). SCA-PRKCG patients rate their vision-related quality of life in NEI-VFQ significantly worse than controls. Furthermore, binocular visual acuity and contrast sensitivity were worse in SCA-PRKCG patients compared with controls. Despite this, none of the OCT measurements differed between groups. NEI-VFQ and NOS composite scores were related to ataxia severity. Additionally, we describe one patient with a genetic variant of uncertain significance in the catalytic domain of PKCÎł who, unlike all confirmed SCA-PRKCG, presented with a clinically silent epitheliopathy. SCA-PRKCG patients had reduced binocular vision and vision-related quality of life. Since no structural retinal damage was found, the pathomechanism of these findings remains unclear
Afferent Visual Pathway Affection in Patients with PMP22 Deletion-Related Hereditary Neuropathy with Liability to Pressure Palsies
Background The PMP22 gene encodes a protein integral to peripheral myelin. Its
deletion leads to hereditary neuropathy with liability to pressure palsies
(HNPP). PMP22 is not expressed in the adult central nervous system, but
previous studies suggest a role in CNS myelin development. The objective of
this study was to identify potential structural and functional alterations in
the afferent visual system in HNPP patients. Methods Twenty HNPP patients and
18 matched healthy controls (HC) were recruited in a cross-sectional study.
Participants underwent neurological examination including visual acuity,
visual evoked potential (VEP) examination, optical coherence tomography (OCT),
and magnetic resonance imaging with calculation of brain atrophy, regarding
grey and white matter, and voxel based morphometry (VBM), in addition answered
the National Eye Instituteâs 39-item Visual Functioning Questionnaire (NEI-
VFQ). Thirteen patients and 6 HC were additionally examined with magnetic
resonance spectroscopy (MRS). Results All patients had normal visual acuity,
but reported reduced peripheral vision in comparison to HC in the NEI-VFQ (p =
0.036). VEP latency was prolonged in patients (P100 = 103.7±5.7 ms) in
comparison to healthy subjects (P100 = 99.7±4.2 ms, p = 0.007). In OCT,
peripapillary retinal nerve fiber layer thickness RNFL was decreased in the
nasal sector (90.0±15.5 vs. 101.8±16.5, p = 0.013), and lower nasal sector
RNFL correlated with prolonged VEP latency (Rho = -0.405, p = 0.012). MRS
revealed reduced tNAA (731.4±45.4 vs. 814.9±62.1, p = 0.017) and tCr
(373.8±22.2 vs. 418.7±31.1, p = 0.002) in the visual cortex in patients vs.
HC. Whole brain volume, grey and white matter volume, VBM and metabolites in a
MRS sensory cortex control voxel did not differ significantly between patients
and HC. Conclusion PMP22 deletion leads to functional, metabolic and macro-
structural alterations in the afferent visual system of HNPP patients. Our
data suggest a functional relevance of these changes for peripheral vision,
which warrants further investigation and confirmation
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adultâonset disorder
Objectives: Genetic variant classification is a challenge in rare adult-onset disorders as in SCA-PRKCG (prior spinocerebellar ataxia type 14) with mostly private conventional mutations and nonspecific phenotype. We here propose a refined approach for clinicogenetic diagnosis by including protein modeling and provide for confirmed SCA-PRKCG a comprehensive phenotype description from a German multi-center cohort, including standardized 3D MR imaging.
Methods: This cross-sectional study prospectively obtained neurological, neuropsychological, and brain imaging data in 33 PRKCG variant carriers. Protein modeling was added as a classification criterion in variants of uncertain significance (VUS).
Results: Our sample included 25 cases confirmed as SCA-PRKCG (14 variants, thereof seven novel variants) and eight carriers of variants assigned as VUS (four variants) or benign/likely benign (two variants). Phenotype in SCA-PRKCG included slowly progressive ataxia (onset at 4-50 years), preceded in some by early-onset nonprogressive symptoms. Ataxia was often combined with action myoclonus, dystonia, or mild cognitive-affective disturbance. Inspection of brain MRI revealed nonprogressive cerebellar atrophy. As a novel finding, a previously not described T2 hyperintense dentate nucleus was seen in all SCA-PRKCG cases but in none of the controls.
Interpretation: In this largest cohort to date, SCA-PRKCG was characterized as a slowly progressive cerebellar syndrome with some clinical and imaging features suggestive of a developmental disorder. The observed non-ataxia movement disorders and cognitive-affective disturbance may well be attributed to cerebellar pathology. Protein modeling emerged as a valuable diagnostic tool for variant classification and the newly described T2 hyperintense dentate sign could serve as a supportive diagnostic marker of SCA-PRKCG
Temporal Retinal Nerve Fiber Loss in Patients with Spinocerebellar Ataxia Type 1
BACKGROUND: Autosomal dominant spinocerebellar ataxia type 1 is an adult onset progressive disorder with well characterized neurodegeneration in the cerebellum and brainstem. Beyond brain atrophy, few data exist concerning retinal and optic nerve involvement. OBJECTIVE: To evaluate retinal changes in SCA1 patients compared to age and gender matched healthy controls. METHODOLOGY/PRINCIPAL FINDINGS: Nine patients with SCA1 were prospectively recruited from the ataxia clinic and were compared to nine age and gender matched healthy controls. Both cohorts received assessment of visually evoked potentials and eye examination by optical coherence tomography to determine retinal nerve fiber layer thickness and total macular volume. While no differences were found in visually evoked potentials, SCA1 patients showed a significant reduction of mean retinal nerve fiber layer thickness (RNFLT) compared to healthy controls (84±13 ”m vs. 97±8 ”m, pâ=â0.004). Temporal areas showed the most prominent RNFLT reduction with high statistical significances (temporal-inferior: p<0.001, temporal: p<0.001, temporal-superior: pâ=â0.005) whereas RNFLT in nasal areas was in the range of the control group. From six SCA1 patients an additional macular scan was obtained. The comparison to the corresponding healthy control showed a slight but not significant reduction in TMV (8.22±0.68 mm(3) vs. 8.61±0.41 mm(3), pâ=â0.15). CONCLUSION: In SCA1 patients, we found evidence for degeneration of retinal nerve fibers. The temporal focus of the observed retinal nerve fiber layer reduction suggests an involvement of the papillo-macular bundle which resembles pathology found in toxic or mitochondrial optic nerve disease such as Leber's hereditary optic neuropathy (LHON) or dominant optic atrophy (DOA)
Optic Nerve Head Quantification in Idiopathic Intracranial Hypertension by Spectral Domain OCT
Objective: To evaluate 3D spectral domain optical coherence tomography (SDOCT) volume scans as a tool for quantification of optic nerve head (ONH) volume as a potential marker for treatment effectiveness and disease progression in idiopathic intracranial hypertension (IIH). Design and Patients: Cross-sectional pilot trial comparing 19 IIH patients and controls matched for gender, age and body mass index. Each participant underwent SDOCT. A custom segmentation algorithm was developed to quantify ONH volume (ONHV) and height (ONHH) in 3D volume scans. Results:Whereas peripapillary retinal nerve fiber layer thickness did not show differences between controls and IIH patients, the newly developed 3D parameters ONHV and ONHH were able to discriminate between controls, treated and untreated patients. Both ONHV and ONHH measures were related to levels of intracranial pressure (ICP). Conclusion: Our findings suggest 3D ONH measures as assessed by SDOCT as potential diagnostic and progression markers in IIH and other disorders with increased ICP. SDOCT may promise a fast and easy diagnostic alternative to repeated lumba
Methodik
Die vegetationskundliche und strukturelle Zuordnung der Lebensraumtypen erfolgt nach der vorrangig von Braun-Blanquet entwickelten Vegetationsklassifizierung, einer hierarchischen Gliederung der Vegetationstypen (Syntaxonomie), die die Ebenen der Assoziation, des Verbandes, der Ordnung und der Klasse umfasst. Hierbei ist die Assoziation die grundlegende Einheit, in der die Pflanzengesellschaften zusammengefasst werden, die sich durch gleiche charakteristische Arten(gruppen)kombinationen auszeichnen. Der Verband vereinigt Àhnliche Assoziationen. Das sind bereits umfassendere, jedoch standörtlich noch recht einheitliche Vegetationseinheiten. In Ordnungen werden Àhnliche VerbÀnde zusammengefasst. Die Klasse vereinigt Àhnliche Ordnungen
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