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Dive into the research topics where Jakob Rath is active.

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Featured researches published by Jakob Rath.


NeuroImage | 2011

Clinical fMRI: Evidence for a 7 T benefit over 3 T

Roland Beisteiner; Simon Robinson; Moritz Wurnig; Markus Hilbert; K. Merksa; Jakob Rath; Ilse Höllinger; Nicolaus Klinger; Ch. Marosi; Siegfried Trattnig; Alexander Geißler

Despite there being an increasing number of installations of ultra high field MR systems (> 3 T) in clinical environments, no functional patient investigations have yet examined possible benefits for functional diagnostics. Here we performed presurgical localization of the primary motor hand area on 3 T and 7 T Siemens scanners with identical investigational procedures and comparable system specific sequence optimizations. Results from 17 patients showed significantly higher functional sensitivity of the 7 T system measured via percent signal change, mean t-values, number of suprathreshold voxels and contrast to noise ratio. On the other hand, 7 T data suffered from a significant increase of artifacts (ghosting, head motion). We conclude that ultra high field systems provide a clinically relevant increase of functional sensitivity for patient investigations.


Human Brain Mapping | 2010

How much are clinical fMRI reports influenced by standard postprocessing methods? An investigation of normalization and region of interest effects in the medial temporal lobe

Roland Beisteiner; Nicolaus Klinger; Ilse Höllinger; Jakob Rath; Susanne Gruber; Thomas Steinkellner; Thomas Foki; Alexander Geissler

Recent evidence has indicated that standard postprocessing methods such as template‐based region of interest (ROI) definition and normalization of individual brains to a standard template may influence final outcome of functional magnetic resonance imaging investigations. Here, we provide the first comprehensive investigation into whether ROI definition and normalization may also change the clinical interpretation of patient data. A series of medial temporal lobe epilepsy patients were investigated with a clinical memory paradigm and individually delineated as well as template‐based ROIs. Different metrics for activation quantification were applied. Results show that the application of template‐based ROIs can significantly change the clinical interpretation of individual patient data. This relates to sensitivity for brain activation and hemispheric dominance. We conclude that individual ROIs should be defined on nontransformed functional data and that use of more than one metric for activation quantification is beneficial. Hum Brain Mapp, 2010.


Experimental Neurology | 2010

FMRI correlates of apraxia in Parkinson's disease patients OFF medication

Thomas Foki; Walter Pirker; Nicolaus Klinger; Alexander Geißler; Jakob Rath; Thomas Steinkellner; I. Hoellinger; Susanne Gruber; Dietrich Haubenberger; Johann Lehrner; Gisela Pusswald; Siegfried Trattnig; Eduard Auff; Roland Beisteiner

Impairment of hand dexterity in Parkinsons disease (PD) is usually attributed to bradykinesia. Recently, behavioral studies illustrated that decreased dexterity might also be due to limb-kinetic apraxia (LkA), as demonstrated by impaired performance in a coin rotation task. Here, we provide a first investigation on whether functional magnetic resonance imaging (fMRI) may reveal specific brain activation patterns for PD patients with impaired performance in a coin rotation task. We compared coin rotation as an apraxia task to simple finger tapping as a bradykinesia task in ten PD patients OFF medication and matched healthy controls. In addition to a tendency for general overactivation, PD patients showed a perirolandic dissociation with precentral overactivation and postcentral underactivation. This finding significantly separated PD patients from healthy controls.


NeuroImage: Clinical | 2013

The benefits of skull stripping in the normalization of clinical fMRI data.

F.Ph.S. Fischmeister; Ilse Höllinger; Nicolaus Klinger; Alexander Geissler; Moritz Wurnig; Eva Matt; Jakob Rath; Simon Robinson; Siegfried Trattnig; Roland Beisteiner

Establishing a reliable correspondence between lesioned brains and a template is challenging using current normalization techniques. The optimum procedure has not been conclusively established, and a critical dichotomy is whether to use input data sets which contain skull signal, or whether skull signal should be removed. Here we provide a first investigation into whether clinical fMRI benefits from skull stripping, based on data from a presurgical language localization task. Brain activation changes related to deskulled/not-deskulled input data are determined in the context of very recently developed (New Segment, Unified Segmentation) and standard normalization approaches. Analysis of structural and functional data demonstrates that skull stripping improves language localization in MNI space — particularly when used in combination with the New Segment normalization technique.


JAMA Neurology | 2011

New Type of Cortical Neuroplasticity After Nerve Repair in Brachial Plexus Lesions

Roland Beisteiner; Ilse Höllinger; Jakob Rath; Moritz Wurnig; Markus Hilbert; Nicolaus Klinger; Alexander Geißler; Florian Ph.S. Fischmeister; Christian Wöber; Gerhard Klösch; Hanno Millesi; Wolfgang Grisold; Eduard Auff; Robert Schmidhammer

BACKGROUND In brachial plexus avulsion, a recent technique connects the ending of the disrupted musculocutaneous nerve to the side of the intact phrenic nerve to regain elbow flexion. This requires the phrenic nerve to perform a new double function: independent control of breathing and elbow flexion. Neuroplastic changes associated with acquisition of double nerve functions have not yet been investigated. OBJECTIVE To evaluate neuroplastic changes associated with acquisition of double nerve functions in a monofunctional nerve (phrenic nerve). DESIGN Clinical and functional magnetic resonance imaging investigations during arm movements, forced inspiration, and motor control tasks. SETTING Investigations at the Medical University of Vienna, Vienna, Austria. PARTICIPANTS Three healthy control subjects, 2 patients with phrenic nerve end-to-side coaptation, and 1 control patient with C7 end-to-end coaptation (same clinical presentation but phrenic nerve unchanged). RESULTS Clinical documentation showed that both patients with phrenic nerve end-to-side coaptation were able to control the diaphragm and the biceps independently via the same phrenic nerve. In contrast to all controls, both patients with phrenic nerve end-to-side coaptation activated the cortical diaphragm areas with flexion of the diseased arm. CONCLUSION Our functional magnetic resonance imaging data indicate that the patients cortical diaphragm areas reorganize in such a way that independent control of breathing and elbow flexion is possible with the same neuronal population.


Parkinsonism & Related Disorders | 2015

Finger dexterity deficits in Parkinson's disease and somatosensory cortical dysfunction

Thomas Foki; Walter Pirker; Alexander Geißler; Dietrich Haubenberger; Markus Hilbert; Ilse Hoellinger; Moritz Wurnig; Jakob Rath; Johann Lehrner; Eva Matt; Florian Ph.S. Fischmeister; Siegfried Trattnig; Eduard Auff; Roland Beisteiner

INTRODUCTION The patho-physiological basis for finger dexterity deficits in Parkinsons disease (PD) is controversial. Previously, bradykinesia was regarded as the major mechanism. However, recent research suggested limb-kinetic apraxia as an important component of impaired fine motor skills in PD. In contrast to bradykinesia, limb-kinetic apraxia only marginally responds to dopaminergic treatment. Here we investigate the novel hypothesis that the dexterity deficits are related to an intrinsic dysfunction of primary somatosensory cortex (S1), which is not reversible by dopaminergic medication. METHODS Applying a standard and approved dexterity task (coin rotation), brain activation networks were investigated using functional magnetic resonance imaging in PD patients both ON and OFF medication and matched healthy controls. RESULTS PD patients both ON and OFF medication showed impaired S1 activation relative to controls (p < 0.05; region of interest based analysis). The impaired S1 activation remained unchanged by dopaminergic medication. Despite the considerable clinical deficit, no other brain area showed impaired activation. In contrast, structures of the basal ganglia--motor cortex loop responded to dopaminergic medication. Behaviorally, dexterity performance both ON and OFF was significantly (p < 0.05) reduced relative to controls. CONCLUSIONS Our results provide first evidence that dexterity deficits in PD are related to an S1 dysfunction which is insensitive to dopaminergic treatment.


Journal of Magnetic Resonance Imaging | 2010

A population-specific symmetric phase model to automatically analyze susceptibility-weighted imaging (SWI) phase shifts and phase symmetry in the human brain

Günther Grabner; Dietrich Haubenberger; Jakob Rath; Roland Beisteiner; Eduard Auff; Siegfried Trattnig; Markus Barth

To create a population‐specific symmetric phase model and to evaluate the susceptibility‐weighted imaging (SWI) phase in terms of phase shift using different segmentation methods (manual and automatic) and phase shift symmetry, which is expected as a marker for lateralized Parkinsons disease (PD) symptoms.


Radiology | 2013

Variability of Clinical Functional MR Imaging Results: A Multicenter Study

Moritz Wurnig; Jakob Rath; Nicolaus Klinger; Ilse Höllinger; Alexander Geissler; Florian Ph.S. Fischmeister; Markus Aichhorn; Thomas Foki; Martin Kronbichler; Janpeter Nickel; Christian M. Siedentopf; Wolfgang Staffen; Michael Verius; Stefan Golaszewski; Florian Koppelstätter; Eduard Auff; Stephan Felber; Rüdiger J. Seitz; Roland Beisteiner

PURPOSE To investigate intersite variability of clinical functional magnetic resonance (MR) imaging, including influence of task standardization on variability and use of various parameters to inform the clinician whether the reliability of a given functional localization is high or low. MATERIALS AND METHODS Local ethics committees approved the study; all participants gave written informed consent. Eight women and seven men (mean age, 40 years) were prospectively investigated at three experienced functional MR sites with 1.5- (two sites) or 3-T (one site) MR. Nonstandardized motor and highly standardized somatosensory versions of a frequently requested clinical task (localization of the primary sensorimotor cortex) were used. Perirolandic functional MR variability was assessed (peak activation variability, center of mass [COM] variability, intraclass correlation values, overlap ratio [OR], activation size ratio). Data quality measures for functional MR images included percentage signal change (PSC), contrast-to-noise ratio (CNR), and head motion parameters. Data were analyzed with analysis of variance and a correlation analysis. RESULTS Localization of perirolandic functional MR activity differed by 8 mm (peak activity) and 6 mm (COM activity) among sites. Peak activation varied up to 16.5 mm (COM range, 0.4-16.5 mm) and 45.5 mm (peak activity range, 1.8-45.5 mm). Signal strength (PSC, CNR) was significantly lower for the somatosensory task (mean PSC, 1.0% ± 0.5 [standard deviation]; mean CNR, 1.2 ± 0.4) than for the motor task (mean PSC, 2.4% ± 0.8; mean CNR, 2.9 ± 0.9) (P < .001, both). Intersite variability was larger with low signal strength (negative correlations between signal strength and peak activation variability) even if the task was highly standardized (mean OR, 22.0% ± 18.9 [somatosensory task] and 50.1% ± 18.8 [motor task]). CONCLUSION Clinical practice and clinical functional MR biomarker studies should consider that the center of task-specific brain activation may vary up to 16.5 mm, with the investigating site, and should maximize functional MR signal strength and evaluate reliability of local results with PSC and CNR.


Frontiers in Human Neuroscience | 2013

Comparing the microvascular specificity of the 3- and 7-T BOLD response using ICA and susceptibility-weighted imaging

Alexander Geißler; Florian Ph.S. Fischmeister; Günther Grabner; Moritz Wurnig; Jakob Rath; Thomas Foki; Eva Matt; Siegfried Trattnig; Roland Beisteiner; Simon Robinson

In functional MRI it is desirable for the blood-oxygenation level dependent (BOLD) signal to be localized to the tissue containing activated neurons rather than the veins draining that tissue. This study addresses the dependence of the specificity of the BOLD signal – the relative contribution of the BOLD signal arising from tissue compared to venous vessels – on magnetic field strength. To date, studies of specificity have been based on models or indirect measures of BOLD sensitivity such as signal to noise ratio and relaxation rates, and assessment has been made in isolated vein and tissue voxels. The consensus has been that ultra-high field systems not only significantly increase BOLD sensitivity but also specificity, that is, there is a proportionately reduced signal contribution from draining veins. Specificity was not quantified in prior studies, however, due to the difficulty of establishing a reliable network of veins in the activated volume. In this study we use a map of venous vessel networks extracted from 7 T high resolution Susceptibility-Weighted Images to quantify the relative contributions of micro- and macro-vasculature to functional MRI results obtained at 3 and 7 T. High resolution measurements made here minimize the contribution of physiological noise and Independent Component Analysis (ICA) is used to separate activation from technical, physiological, and motion artifacts. ICA also avoids the possibility of timing-dependent bias from different micro- and macro-vasculature responses. We find a significant increase in the number of activated voxels at 7 T in both the veins and the microvasculature – a BOLD sensitivity increase – with the increase in the microvasculature being higher. However, the small increase in sensitivity at 7 T was not significant. For the experimental conditions of this study, our findings do not support the hypothesis of an increased specificity of the BOLD response at ultra-high field.


Neurorehabilitation and Neural Repair | 2011

An fMRI Marker for Peripheral Nerve Regeneration

Jakob Rath; Nicolaus Klinger; Alexander Geißler; Ilse Höllinger; Susanne Gruber; Moritz Wurnig; Thomas Hausner; Eduard Auff; Robert Schmidhammer; Roland Beisteiner

Final outcome after surgical repair of peripheral nerve transections varies. Here, we present the first longitudinal functional magnetic resonance imaging (fMRI) obserof cortical somatosensory reorganization patterns after surgery. A 43-year-old man presented with isolated complete transecof the right median nerve and underwent immediate epineural end-to-end coaptation. Applying standardized vibrotactile median nerve stimulation, 3 T brain activation maps were evaluated at 1, 7, 15 weeks and 1 year after surgery. Initially, the affected hemisphere showed no primary activation but increased frontoparietal activity. After 1 year, primary activation had recovered, and frontoparietal activity was decreased relative to the nonaffected hemisphere. Based on these longitudinal fMRI patterns, we propose a new marker for restoration of somatosensory function, which may not be provided by electrophysiological methods.

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Roland Beisteiner

Medical University of Vienna

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Eduard Auff

Medical University of Vienna

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Nicolaus Klinger

Medical University of Vienna

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Thomas Foki

Medical University of Vienna

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Alexander Geissler

Medical University of Vienna

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Moritz Wurnig

Medical University of Vienna

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Siegfried Trattnig

Medical University of Vienna

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Alexander Geißler

Medical University of Vienna

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Ilse Höllinger

Medical University of Vienna

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