Title: Cerebral changes in post-polio syndrome: A quantitative MRI study
Author: Stacey Li Hi Shing, Jasmin Lope, Mary Clare McKenna, Rangariroyashe H. Chipika, Orla Hardiman, & Peter Bede
Affiliation: Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland
Journal: Journal of the Neurological Sciences
Citation: S.L.H. Shing, J. Lope, M.C. McKenna, et al., Cerebral changes in post-polio syndrome: A quantitative MRI study, Journal of the Neurological Sciences (2021), https://doi.org/10.1016/j.jns.2021.117361
Publication Year and Month: 2021 02
Abstract: BACKGROUND
Post-polio syndrome (PPS) has been traditionally considered a slowly progressive condition that affects polio survivors decades after their initial infection. Cerebral changes in PPS are poorly characterised and the few existing studies are strikingly conflicting.
OBJECTIVE
The overarching aim of this study is the comprehensive characterisation of cerebral grey and white matter alterations in post-polio syndrome with reference to healthy- and disease-controls using quantitative imaging metrics.
METHODS
Thirty-six patients with PPS, 88 patients with ALS and 117 healthy individuals were recruited in a prospective, single-centre neuroimaging study using uniform MRI acquisition parameters. All participants underwent standardised clinical assessments, T1-weighted imaging and diffusion tensor imaging. Whole-brain imaging and region-of-interest analyses were undertaken to evaluate patterns of grey matter changes. Tract-based spatial statistics were utilised to assess changes in diffusivity metrics in a study-specific whiter matter skeleton.
RESULTS
In contrast to healthy controls, PPS patients exhibited increased grey matter density in the brainstem, cerebellum and occipital lobe, accompanied by increased FA in the corticospinal tracts, cerebellum, bilateral mesial temporal lobes and inferior frontal tracts. PPS patients exhibited increased integrity metrics in the same anatomical regions where ALS patients showed degenerative changes.
CONCLUSIONS
Our findings suggests that PPS is associated with considerable cortical and white matter reorganisation which may be interpreted as compensatory, adaptive change in response to severe lower motor neuron injury in infancy.
Conclusions: Contrary to previous reports, we found no evidence of cerebral grey or white matter degeneration in a cohort of polio survivors using a validated quantitative neuroimaging protocol. Anatomical regions which are preferentially affected in ALS, such as the corticospinal tracts and the cerebellum exhibit superior integrity in PPS than in healthy controls.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any): KEYWORDS
Post-polio syndrome, Motor neuron disease, Neuroimaging, Pathology, Clinical trials
Link to Paper (if available): Click here to view full text or to download
Category: Brain, Late Effects of Polio, Post-Polio Motor Unit
Title: Imaging data indicate cerebral reorganisation in poliomyelitis survivors: Possible compensation for longstanding lower motor neuron pathology
Author: Stacey Li Hi Shing (a), Jasmin Lope (a), Rangariroyashe H. Chipika (a), Orla Hardiman (a), Peter Bede (a, b, ∗)
Affiliation: (a) Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland
(b) Pitié-Salpêtrière University Hospital, Sorbonne University, Paris, France
∗ Corresponding author: Peter Bede, Room 5.43, Computational Neuroimaging Group, Trinity Biomedical Sciences In- stitute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.
E-mail address: [email protected] (P.Bede).
Journal: NEW - PUT DETAILS IN CITATION FIELD
Citation: Journal of Neurological Sciences
424 (2021) 117361
DOI: https://doi.org/10.1016/j.jns.2021.117361
Publication Year and Month: 2021 05
Abstract: BACKGROUND
Post-polio syndrome (PPS) has been traditionally considered a slowly progressive condition that affects poliomyelitis survivors decades after their initial infection. Cerebral changes in poliomyelitis survivors are poorly characterised and the few existing studies are strikingly conflicting.
OBJECTIVE
The overarching aim of this study is the comprehensive characterisation of cerebral grey and white matter alterations in poliomyelitis survivors with reference to healthy- and disease-controls using quantitative imaging metrics.
METHODS
Thirty-six poliomyelitis survivors, 88 patients with ALS and 117 healthy individuals were recruited in a prospective, single-centre neuroimaging study using uniform MRI acquisition parameters. All participants underwent standardised clinical assessments, T1-weighted structural and diffusion tensor imaging. Whole-brain and region-of-interest morphometric analyses were undertaken to evaluate patterns of grey matter changes. Tract-based spatial statistics were performed to evaluate diffusivity alterations in a study-specific whiter matter skeleton.
RESULTS
In contrast to healthy controls, poliomyelitis survivors exhibited increased grey matter partial volumes in the brainstem, cerebellum and occipital lobe, accompanied by increased FA in the corticospinal tracts, cerebellum, bilateral mesial temporal lobes and inferior frontal tracts. Polio survivors exhibited increased integrity metrics in the same anatomical regions where ALS patients showed degenerative changes.
CONCLUSIONS
Our findings indicate considerable cortical and white matter reorganisation in poliomyelitis survivors which may be interpreted as compensatory, adaptive change in response to severe lower motor neuron injury in infancy.
Keywords
Post-polio syndrome, Motor neuron disease, Neuroimaging, Pathology, Poliomyelitis
Conclusions: Contrary to previous reports, we found no evidence of cerebral grey or white matter degeneration in a cohort of polio survivors using a validated quantitative neuroimaging protocol. The brainstem, corticospinal tracts and the cerebellum exhibit superior integrity in poliomyelitis survivors compared to healthy controls.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any):
Link to Paper (if available): Click here to view full text or to download
Category: Brain
Title: Parallels between Post Polio fatigue and chronic fatigue syndrome: a common pathophysiology?
Author: Bruno, R.L., Creange, S.J., and Frick, N.M
Affiliation: Kids' Fatigue Management Program and The Post-Polio Institute, Englewood Hospital and Medical Center, New Jersey
Journal:
Citation: Am J Med.
Publication Year and Month: 1998 09
Abstract: Fatigue is the most commonly reported and most debilitating of post-polio sequelae affecting the >1.8 million North American polio survivors. Post-polio fatigue is characterized by subjective reports of difficulty with attention, cognition, and maintaining wakefulness. These symptoms resemble those reported in nearly 2 dozen outbreaks of post-viral fatigue syndromes (PVFS) that have recurred during this century and that are related clinically, historically, anatomically, or physiologically to poliovirus infections. This article reviews recent studies that relate the symptoms of post-polio fatigue and chronic fatigue syndrome (CFS) to clinically significant deficits on neuropsychologic tests of attention, histopathologic and neuroradiologic evidence of brain lesions, impaired activation of the hypothalamic-pituitary-adrenal axis, increased prolactin secretion, and electroencephalogram (EEG) slow-wave activity. A possible common pathophysiology for post-polio fatigue and CFS, based on the Brain Fatigue Generator Model of PVFS, and a possible pharmacotherapy for PVFS based on replacement of depleted brain dopamine, will be described
Conclusions: There is evidence of severe brain lesions at the brain stem and less severe lesions in the cerebellum and cerebral cortex which could play a role in general and cognitive fatigue.
Outcome of Research: More research required
Availability of Paper: Paid subscription required to view or download full text.
Comments (if any):
Link to Paper (if available): Click here to view Abstract
Category: Brain
Title: Physiology of the motor cortex in polio survivors.
Author: Lupu, V.D. et al.
Affiliation: EMG Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Building 10, CRC, 7-5680, 10 Center Drive, MSC-1404 Bethesda, Maryland 20892, USA.
Journal: Muscle & Nerve
Citation: Muscle Nerve. 2008;37(2):177-82.
DOI: 10.1002/mus.20913
Publication Year and Month: 2008 02
Abstract: We hypothesized that the corticospinal system undergoes functional changes in long-term polio survivors. Central motor conduction times (CMCTs) to the four limbs were measured in 24 polio survivors using transcranial magnetic stimulation (TMS). Resting motor thresholds and CMCTs were normal. In 17 subjects whose legs were affected by polio and 13 healthy controls, single- and paired-pulse TMS was used to assess motor cortex excitability while recording from tibialis anterior (TA) muscles at rest and following maximal contraction until fatigue. In polio survivors the slope of the recruitment curve was normal, but maximal motor evoked potentials (MEPs) were larger than in controls. MEPs were depressed after fatiguing exercise. Three patients with central fatigue by twitch interpolation had a trend toward slower recovery. There was no association with symptoms of post-polio syndrome. These changes occurring after polio may allow the motor cortex to activate a greater proportion of the motor neurons innervating affected muscles.
Conclusions:
Outcome of Research: More research required
Availability of Paper: Paid subscription required to view or download full text.
Comments (if any): There appear to be compensatory effects by the motor cortex to increase the strength of action potentials to innervate muscles that have fewer motor units (due to the polio virus). Surprisingly, this investigation did not find association between PPS or central fatigue with increased central recruitment patterns to innervate remaining muscle tissue.
Link to Paper (if available): Click here to view Abstract
Category: Brain, Diagnosis and Management, Late Effects of Polio, Post-Polio Motor Unit
Title: Spinal cord gray matter atrophy is associated with functional decline in post-polio syndrome
Author: Maria Janina Wendebourg (1,2), Matthias Weigel (1,2,3,4,5), Laura Richter (1), Vanya Gocheva (6), Patricia Hafner (6), Anna-Lena Orsini (6), Valentina Crepulja (1,2), Simone Schmidt (6), Antal Huck (4), Johanna Oechtering (1), Maria Blatow (7), Tanja Haas (3,4), Cristina Granziera (1,2,5), Ludwig Kappos (1,2,5), Philippe Cattin (4), Oliver Bieri (3,4) Dirk Fischer (6), Regina Schlaeger (1,2,5)
Affiliation: 1. Neurology Clinic and Policlinic, Department of Clinical Research, University Hospital Basel, University of Basel, Basel, Switzerland
2. Translational Imaging in Neurology (ThINk), Department of Biomedical Engineering, University of Basel, Basel, Switzerland
3. Division of Radiological Physics, Department of Radiology, University Hospital Basel, Basel, Switzerland
4. Department of Biomedical Engineering, University of Basel, Basel, Switzerland
5. MS Center and Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University of Basel, Basel, Switzerland
6. Division of Pediatric Neurology, University of Basel Children's Hospital, Basel, Switzerland
7. Department of Neuroradiology, Clinical Neuroscience Center, University Hospital Zurich, University of Zurich, Zurich,
Journal: European Journal of Neurology
Citation: Eur J Neurol. 2022;00:1–11.
DOI: 10.1111/ene.15261
Publication Year and Month: 2022 01
Abstract: Objective: To determine if patients with post- polio syndrome (PPS) show spinal cord gray matter (SCGM) atrophy and to assess associations between SCGM atrophy, muscle strength and patient- reported functional decline.
Methods: Twenty patients diagnosed with PPS (March of Dimes criteria) and 20 age- and sex- matched healthy controls (HC) underwent 3T axial 2D- rAMIRA magnetic resonance imaging at the intervertebral disc levels C2/C3–C6/C7, T9/T10 and the lumbar enlarge-ment level (Tmax) (0.5 × 0.5 mm2 in- plane resolution). SCGM areas were segmented manu-ally by two independent raters. Muscle strength, self-reported fatigue, depression and pain measures were assessed.
Results: Post- polio syndrome patients showed significantly and preferentially re-duced SCGM areas at C2/C3 (p= 0.048), C3/C4 (p= 0.001), C4/C5 (p< 0.001), C5/C6 (p= 0.004) and Tmax (p= 0.041) compared to HC. SCGM areas were significantly associated with muscle strength in corresponding myotomes even after adjustment for fatigue, pain and depression. SCGM areaTmax together with age and sex explained 68% of ankle dorsiflexion strength variance. No associations were found with age at or time since infection. Patients reporting PPS- related decline in arm function showed significant cervical SCGM atrophy compared to stable patients adjusted for initial disease severity.
Conclusions: Patients with PPS show significant SCGM atrophy that correlates with mus-cle strength and is associated with PPS- related functional decline. Our findings suggest a secondary neurodegenerative process underlying SCGM atrophy in PPS that is not ex-plained by aging or residua of the initial infection alone. Confirmation by longitudinal studies is needed. The described imaging methodology is promising for developing novel imaging surrogates for SCGM diseases.
Conclusions: The rAMIRA approach is a novel, promising, clinically feasible and sensitive method for segment-wise quantitation of GM atrophy in the cervical and thoracic SC in patients with lower motor neuron disorders. This study demonstrated its clinical applicability and vali-dated it in patients with PPS, a presumed pure, lower motor neuron disorder, which can serve as a model for other neurodegenerative, genetic or autoimmune diseases of the SCGM.
Patients with PPS show significant SCGM atrophy, particularly at levels close to the cervical and lumbar enlargements. Even after adjustment for the level of depression, fatigue and pain, potential confounding symptoms frequently observed in PPS, SCGM atrophy is significantly and segment-wise associated with muscle strength in corresponding myotomes. Moreover, SCGM atrophy is associated with patient-reported PPS-related functional decline. Secondary analyses suggest that SCGM atrophy is rather due to a second dis-ease phase than being a sole residuum of the initial infection or a pure aging effect. These observations support the hypothesis of a focally accentuated neurodegenerative process in the SC underlying PPS. Larger, ideally multicentric, longitudinal studies conducted over a sufficiently long timespan are an important next step to confirm our results and gain more insights into the development of SCGM atrophy over time and its correlation to clinical symptom evolution in patients with PPS.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any):
Link to Paper (if available): Click here to view full text or to download
There is currently 5 paper in this category.
Title: Parallels between Post Polio fatigue and chronic fatigue syndrome: a common pathophysiology?
Author: Bruno, R.L., Creange, S.J., and Frick, N.M
Affiliation: Kids' Fatigue Management Program and The Post-Polio Institute, Englewood Hospital and Medical Center, New Jersey
Journal:
Citation: Am J Med.
Publication Year and Month: 1998 09
Abstract: Fatigue is the most commonly reported and most debilitating of post-polio sequelae affecting the >1.8 million North American polio survivors. Post-polio fatigue is characterized by subjective reports of difficulty with attention, cognition, and maintaining wakefulness. These symptoms resemble those reported in nearly 2 dozen outbreaks of post-viral fatigue syndromes (PVFS) that have recurred during this century and that are related clinically, historically, anatomically, or physiologically to poliovirus infections. This article reviews recent studies that relate the symptoms of post-polio fatigue and chronic fatigue syndrome (CFS) to clinically significant deficits on neuropsychologic tests of attention, histopathologic and neuroradiologic evidence of brain lesions, impaired activation of the hypothalamic-pituitary-adrenal axis, increased prolactin secretion, and electroencephalogram (EEG) slow-wave activity. A possible common pathophysiology for post-polio fatigue and CFS, based on the Brain Fatigue Generator Model of PVFS, and a possible pharmacotherapy for PVFS based on replacement of depleted brain dopamine, will be described
Conclusions: There is evidence of severe brain lesions at the brain stem and less severe lesions in the cerebellum and cerebral cortex which could play a role in general and cognitive fatigue.
Outcome of Research: More research required
Availability of Paper: Paid subscription required to view or download full text.
Comments (if any):
Link to Paper (if available): Click here to view Abstract
Category: Brain
Title: Physiology of the motor cortex in polio survivors.
Author: Lupu, V.D. et al.
Affiliation: EMG Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Building 10, CRC, 7-5680, 10 Center Drive, MSC-1404 Bethesda, Maryland 20892, USA.
Journal: Muscle & Nerve
Citation: Muscle Nerve. 2008;37(2):177-82.
DOI: 10.1002/mus.20913
Publication Year and Month: 2008 02
Abstract: We hypothesized that the corticospinal system undergoes functional changes in long-term polio survivors. Central motor conduction times (CMCTs) to the four limbs were measured in 24 polio survivors using transcranial magnetic stimulation (TMS). Resting motor thresholds and CMCTs were normal. In 17 subjects whose legs were affected by polio and 13 healthy controls, single- and paired-pulse TMS was used to assess motor cortex excitability while recording from tibialis anterior (TA) muscles at rest and following maximal contraction until fatigue. In polio survivors the slope of the recruitment curve was normal, but maximal motor evoked potentials (MEPs) were larger than in controls. MEPs were depressed after fatiguing exercise. Three patients with central fatigue by twitch interpolation had a trend toward slower recovery. There was no association with symptoms of post-polio syndrome. These changes occurring after polio may allow the motor cortex to activate a greater proportion of the motor neurons innervating affected muscles.
Conclusions:
Outcome of Research: More research required
Availability of Paper: Paid subscription required to view or download full text.
Comments (if any): There appear to be compensatory effects by the motor cortex to increase the strength of action potentials to innervate muscles that have fewer motor units (due to the polio virus). Surprisingly, this investigation did not find association between PPS or central fatigue with increased central recruitment patterns to innervate remaining muscle tissue.
Link to Paper (if available): Click here to view Abstract
Category: Brain, Diagnosis and Management, Late Effects of Polio, Post-Polio Motor Unit
Title: Spinal cord gray matter atrophy is associated with functional decline in post-polio syndrome
Author: Maria Janina Wendebourg (1,2), Matthias Weigel (1,2,3,4,5), Laura Richter (1), Vanya Gocheva (6), Patricia Hafner (6), Anna-Lena Orsini (6), Valentina Crepulja (1,2), Simone Schmidt (6), Antal Huck (4), Johanna Oechtering (1), Maria Blatow (7), Tanja Haas (3,4), Cristina Granziera (1,2,5), Ludwig Kappos (1,2,5), Philippe Cattin (4), Oliver Bieri (3,4) Dirk Fischer (6), Regina Schlaeger (1,2,5)
Affiliation: 1. Neurology Clinic and Policlinic, Department of Clinical Research, University Hospital Basel, University of Basel, Basel, Switzerland
2. Translational Imaging in Neurology (ThINk), Department of Biomedical Engineering, University of Basel, Basel, Switzerland
3. Division of Radiological Physics, Department of Radiology, University Hospital Basel, Basel, Switzerland
4. Department of Biomedical Engineering, University of Basel, Basel, Switzerland
5. MS Center and Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University of Basel, Basel, Switzerland
6. Division of Pediatric Neurology, University of Basel Children's Hospital, Basel, Switzerland
7. Department of Neuroradiology, Clinical Neuroscience Center, University Hospital Zurich, University of Zurich, Zurich,
Journal: European Journal of Neurology
Citation: Eur J Neurol. 2022;00:1–11.
DOI: 10.1111/ene.15261
Publication Year and Month: 2022 01
Abstract: Objective: To determine if patients with post- polio syndrome (PPS) show spinal cord gray matter (SCGM) atrophy and to assess associations between SCGM atrophy, muscle strength and patient- reported functional decline.
Methods: Twenty patients diagnosed with PPS (March of Dimes criteria) and 20 age- and sex- matched healthy controls (HC) underwent 3T axial 2D- rAMIRA magnetic resonance imaging at the intervertebral disc levels C2/C3–C6/C7, T9/T10 and the lumbar enlarge-ment level (Tmax) (0.5 × 0.5 mm2 in- plane resolution). SCGM areas were segmented manu-ally by two independent raters. Muscle strength, self-reported fatigue, depression and pain measures were assessed.
Results: Post- polio syndrome patients showed significantly and preferentially re-duced SCGM areas at C2/C3 (p= 0.048), C3/C4 (p= 0.001), C4/C5 (p< 0.001), C5/C6 (p= 0.004) and Tmax (p= 0.041) compared to HC. SCGM areas were significantly associated with muscle strength in corresponding myotomes even after adjustment for fatigue, pain and depression. SCGM areaTmax together with age and sex explained 68% of ankle dorsiflexion strength variance. No associations were found with age at or time since infection. Patients reporting PPS- related decline in arm function showed significant cervical SCGM atrophy compared to stable patients adjusted for initial disease severity.
Conclusions: Patients with PPS show significant SCGM atrophy that correlates with mus-cle strength and is associated with PPS- related functional decline. Our findings suggest a secondary neurodegenerative process underlying SCGM atrophy in PPS that is not ex-plained by aging or residua of the initial infection alone. Confirmation by longitudinal studies is needed. The described imaging methodology is promising for developing novel imaging surrogates for SCGM diseases.
Conclusions: The rAMIRA approach is a novel, promising, clinically feasible and sensitive method for segment-wise quantitation of GM atrophy in the cervical and thoracic SC in patients with lower motor neuron disorders. This study demonstrated its clinical applicability and vali-dated it in patients with PPS, a presumed pure, lower motor neuron disorder, which can serve as a model for other neurodegenerative, genetic or autoimmune diseases of the SCGM.
Patients with PPS show significant SCGM atrophy, particularly at levels close to the cervical and lumbar enlargements. Even after adjustment for the level of depression, fatigue and pain, potential confounding symptoms frequently observed in PPS, SCGM atrophy is significantly and segment-wise associated with muscle strength in corresponding myotomes. Moreover, SCGM atrophy is associated with patient-reported PPS-related functional decline. Secondary analyses suggest that SCGM atrophy is rather due to a second dis-ease phase than being a sole residuum of the initial infection or a pure aging effect. These observations support the hypothesis of a focally accentuated neurodegenerative process in the SC underlying PPS. Larger, ideally multicentric, longitudinal studies conducted over a sufficiently long timespan are an important next step to confirm our results and gain more insights into the development of SCGM atrophy over time and its correlation to clinical symptom evolution in patients with PPS.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any):
Link to Paper (if available): Click here to view full text or to download
Category: Brain, Late Effects of Polio, Post-Polio Motor Unit
Title: Imaging data indicate cerebral reorganisation in poliomyelitis survivors: Possible compensation for longstanding lower motor neuron pathology
Author: Stacey Li Hi Shing (a), Jasmin Lope (a), Rangariroyashe H. Chipika (a), Orla Hardiman (a), Peter Bede (a, b, ∗)
Affiliation: (a) Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland
(b) Pitié-Salpêtrière University Hospital, Sorbonne University, Paris, France
∗ Corresponding author: Peter Bede, Room 5.43, Computational Neuroimaging Group, Trinity Biomedical Sciences In- stitute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.
E-mail address: [email protected] (P.Bede).
Journal: NEW - PUT DETAILS IN CITATION FIELD
Citation: Journal of Neurological Sciences
424 (2021) 117361
DOI: https://doi.org/10.1016/j.jns.2021.117361
Publication Year and Month: 2021 05
Abstract: BACKGROUND
Post-polio syndrome (PPS) has been traditionally considered a slowly progressive condition that affects poliomyelitis survivors decades after their initial infection. Cerebral changes in poliomyelitis survivors are poorly characterised and the few existing studies are strikingly conflicting.
OBJECTIVE
The overarching aim of this study is the comprehensive characterisation of cerebral grey and white matter alterations in poliomyelitis survivors with reference to healthy- and disease-controls using quantitative imaging metrics.
METHODS
Thirty-six poliomyelitis survivors, 88 patients with ALS and 117 healthy individuals were recruited in a prospective, single-centre neuroimaging study using uniform MRI acquisition parameters. All participants underwent standardised clinical assessments, T1-weighted structural and diffusion tensor imaging. Whole-brain and region-of-interest morphometric analyses were undertaken to evaluate patterns of grey matter changes. Tract-based spatial statistics were performed to evaluate diffusivity alterations in a study-specific whiter matter skeleton.
RESULTS
In contrast to healthy controls, poliomyelitis survivors exhibited increased grey matter partial volumes in the brainstem, cerebellum and occipital lobe, accompanied by increased FA in the corticospinal tracts, cerebellum, bilateral mesial temporal lobes and inferior frontal tracts. Polio survivors exhibited increased integrity metrics in the same anatomical regions where ALS patients showed degenerative changes.
CONCLUSIONS
Our findings indicate considerable cortical and white matter reorganisation in poliomyelitis survivors which may be interpreted as compensatory, adaptive change in response to severe lower motor neuron injury in infancy.
Keywords
Post-polio syndrome, Motor neuron disease, Neuroimaging, Pathology, Poliomyelitis
Conclusions: Contrary to previous reports, we found no evidence of cerebral grey or white matter degeneration in a cohort of polio survivors using a validated quantitative neuroimaging protocol. The brainstem, corticospinal tracts and the cerebellum exhibit superior integrity in poliomyelitis survivors compared to healthy controls.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any):
Link to Paper (if available): Click here to view full text or to download
Category: Brain
Title: Cerebral changes in post-polio syndrome: A quantitative MRI study
Author: Stacey Li Hi Shing, Jasmin Lope, Mary Clare McKenna, Rangariroyashe H. Chipika, Orla Hardiman, & Peter Bede
Affiliation: Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland
Journal: Journal of the Neurological Sciences
Citation: S.L.H. Shing, J. Lope, M.C. McKenna, et al., Cerebral changes in post-polio syndrome: A quantitative MRI study, Journal of the Neurological Sciences (2021), https://doi.org/10.1016/j.jns.2021.117361
Publication Year and Month: 2021 02
Abstract: BACKGROUND
Post-polio syndrome (PPS) has been traditionally considered a slowly progressive condition that affects polio survivors decades after their initial infection. Cerebral changes in PPS are poorly characterised and the few existing studies are strikingly conflicting.
OBJECTIVE
The overarching aim of this study is the comprehensive characterisation of cerebral grey and white matter alterations in post-polio syndrome with reference to healthy- and disease-controls using quantitative imaging metrics.
METHODS
Thirty-six patients with PPS, 88 patients with ALS and 117 healthy individuals were recruited in a prospective, single-centre neuroimaging study using uniform MRI acquisition parameters. All participants underwent standardised clinical assessments, T1-weighted imaging and diffusion tensor imaging. Whole-brain imaging and region-of-interest analyses were undertaken to evaluate patterns of grey matter changes. Tract-based spatial statistics were utilised to assess changes in diffusivity metrics in a study-specific whiter matter skeleton.
RESULTS
In contrast to healthy controls, PPS patients exhibited increased grey matter density in the brainstem, cerebellum and occipital lobe, accompanied by increased FA in the corticospinal tracts, cerebellum, bilateral mesial temporal lobes and inferior frontal tracts. PPS patients exhibited increased integrity metrics in the same anatomical regions where ALS patients showed degenerative changes.
CONCLUSIONS
Our findings suggests that PPS is associated with considerable cortical and white matter reorganisation which may be interpreted as compensatory, adaptive change in response to severe lower motor neuron injury in infancy.
Conclusions: Contrary to previous reports, we found no evidence of cerebral grey or white matter degeneration in a cohort of polio survivors using a validated quantitative neuroimaging protocol. Anatomical regions which are preferentially affected in ALS, such as the corticospinal tracts and the cerebellum exhibit superior integrity in PPS than in healthy controls.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any): KEYWORDS
Post-polio syndrome, Motor neuron disease, Neuroimaging, Pathology, Clinical trials
Link to Paper (if available): Click here to view full text or to download
There is currently 5 paper in this category.
Title: Parallels between Post Polio fatigue and chronic fatigue syndrome: a common pathophysiology?
Author: Bruno, R.L., Creange, S.J., and Frick, N.M
Affiliation: Kids' Fatigue Management Program and The Post-Polio Institute, Englewood Hospital and Medical Center, New Jersey
Journal:
Citation: Am J Med.
Publication Year and Month: 1998 09
Abstract: Fatigue is the most commonly reported and most debilitating of post-polio sequelae affecting the >1.8 million North American polio survivors. Post-polio fatigue is characterized by subjective reports of difficulty with attention, cognition, and maintaining wakefulness. These symptoms resemble those reported in nearly 2 dozen outbreaks of post-viral fatigue syndromes (PVFS) that have recurred during this century and that are related clinically, historically, anatomically, or physiologically to poliovirus infections. This article reviews recent studies that relate the symptoms of post-polio fatigue and chronic fatigue syndrome (CFS) to clinically significant deficits on neuropsychologic tests of attention, histopathologic and neuroradiologic evidence of brain lesions, impaired activation of the hypothalamic-pituitary-adrenal axis, increased prolactin secretion, and electroencephalogram (EEG) slow-wave activity. A possible common pathophysiology for post-polio fatigue and CFS, based on the Brain Fatigue Generator Model of PVFS, and a possible pharmacotherapy for PVFS based on replacement of depleted brain dopamine, will be described
Conclusions: There is evidence of severe brain lesions at the brain stem and less severe lesions in the cerebellum and cerebral cortex which could play a role in general and cognitive fatigue.
Outcome of Research: More research required
Availability of Paper: Paid subscription required to view or download full text.
Comments (if any):
Link to Paper (if available): Click here to view Abstract
Category: Brain, Diagnosis and Management, Late Effects of Polio, Post-Polio Motor Unit
Title: Spinal cord gray matter atrophy is associated with functional decline in post-polio syndrome
Author: Maria Janina Wendebourg (1,2), Matthias Weigel (1,2,3,4,5), Laura Richter (1), Vanya Gocheva (6), Patricia Hafner (6), Anna-Lena Orsini (6), Valentina Crepulja (1,2), Simone Schmidt (6), Antal Huck (4), Johanna Oechtering (1), Maria Blatow (7), Tanja Haas (3,4), Cristina Granziera (1,2,5), Ludwig Kappos (1,2,5), Philippe Cattin (4), Oliver Bieri (3,4) Dirk Fischer (6), Regina Schlaeger (1,2,5)
Affiliation: 1. Neurology Clinic and Policlinic, Department of Clinical Research, University Hospital Basel, University of Basel, Basel, Switzerland
2. Translational Imaging in Neurology (ThINk), Department of Biomedical Engineering, University of Basel, Basel, Switzerland
3. Division of Radiological Physics, Department of Radiology, University Hospital Basel, Basel, Switzerland
4. Department of Biomedical Engineering, University of Basel, Basel, Switzerland
5. MS Center and Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University of Basel, Basel, Switzerland
6. Division of Pediatric Neurology, University of Basel Children's Hospital, Basel, Switzerland
7. Department of Neuroradiology, Clinical Neuroscience Center, University Hospital Zurich, University of Zurich, Zurich,
Journal: European Journal of Neurology
Citation: Eur J Neurol. 2022;00:1–11.
DOI: 10.1111/ene.15261
Publication Year and Month: 2022 01
Abstract: Objective: To determine if patients with post- polio syndrome (PPS) show spinal cord gray matter (SCGM) atrophy and to assess associations between SCGM atrophy, muscle strength and patient- reported functional decline.
Methods: Twenty patients diagnosed with PPS (March of Dimes criteria) and 20 age- and sex- matched healthy controls (HC) underwent 3T axial 2D- rAMIRA magnetic resonance imaging at the intervertebral disc levels C2/C3–C6/C7, T9/T10 and the lumbar enlarge-ment level (Tmax) (0.5 × 0.5 mm2 in- plane resolution). SCGM areas were segmented manu-ally by two independent raters. Muscle strength, self-reported fatigue, depression and pain measures were assessed.
Results: Post- polio syndrome patients showed significantly and preferentially re-duced SCGM areas at C2/C3 (p= 0.048), C3/C4 (p= 0.001), C4/C5 (p< 0.001), C5/C6 (p= 0.004) and Tmax (p= 0.041) compared to HC. SCGM areas were significantly associated with muscle strength in corresponding myotomes even after adjustment for fatigue, pain and depression. SCGM areaTmax together with age and sex explained 68% of ankle dorsiflexion strength variance. No associations were found with age at or time since infection. Patients reporting PPS- related decline in arm function showed significant cervical SCGM atrophy compared to stable patients adjusted for initial disease severity.
Conclusions: Patients with PPS show significant SCGM atrophy that correlates with mus-cle strength and is associated with PPS- related functional decline. Our findings suggest a secondary neurodegenerative process underlying SCGM atrophy in PPS that is not ex-plained by aging or residua of the initial infection alone. Confirmation by longitudinal studies is needed. The described imaging methodology is promising for developing novel imaging surrogates for SCGM diseases.
Conclusions: The rAMIRA approach is a novel, promising, clinically feasible and sensitive method for segment-wise quantitation of GM atrophy in the cervical and thoracic SC in patients with lower motor neuron disorders. This study demonstrated its clinical applicability and vali-dated it in patients with PPS, a presumed pure, lower motor neuron disorder, which can serve as a model for other neurodegenerative, genetic or autoimmune diseases of the SCGM.
Patients with PPS show significant SCGM atrophy, particularly at levels close to the cervical and lumbar enlargements. Even after adjustment for the level of depression, fatigue and pain, potential confounding symptoms frequently observed in PPS, SCGM atrophy is significantly and segment-wise associated with muscle strength in corresponding myotomes. Moreover, SCGM atrophy is associated with patient-reported PPS-related functional decline. Secondary analyses suggest that SCGM atrophy is rather due to a second dis-ease phase than being a sole residuum of the initial infection or a pure aging effect. These observations support the hypothesis of a focally accentuated neurodegenerative process in the SC underlying PPS. Larger, ideally multicentric, longitudinal studies conducted over a sufficiently long timespan are an important next step to confirm our results and gain more insights into the development of SCGM atrophy over time and its correlation to clinical symptom evolution in patients with PPS.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any):
Link to Paper (if available): Click here to view full text or to download
Category: Brain
Title: Cerebral changes in post-polio syndrome: A quantitative MRI study
Author: Stacey Li Hi Shing, Jasmin Lope, Mary Clare McKenna, Rangariroyashe H. Chipika, Orla Hardiman, & Peter Bede
Affiliation: Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland
Journal: Journal of the Neurological Sciences
Citation: S.L.H. Shing, J. Lope, M.C. McKenna, et al., Cerebral changes in post-polio syndrome: A quantitative MRI study, Journal of the Neurological Sciences (2021), https://doi.org/10.1016/j.jns.2021.117361
Publication Year and Month: 2021 02
Abstract: BACKGROUND
Post-polio syndrome (PPS) has been traditionally considered a slowly progressive condition that affects polio survivors decades after their initial infection. Cerebral changes in PPS are poorly characterised and the few existing studies are strikingly conflicting.
OBJECTIVE
The overarching aim of this study is the comprehensive characterisation of cerebral grey and white matter alterations in post-polio syndrome with reference to healthy- and disease-controls using quantitative imaging metrics.
METHODS
Thirty-six patients with PPS, 88 patients with ALS and 117 healthy individuals were recruited in a prospective, single-centre neuroimaging study using uniform MRI acquisition parameters. All participants underwent standardised clinical assessments, T1-weighted imaging and diffusion tensor imaging. Whole-brain imaging and region-of-interest analyses were undertaken to evaluate patterns of grey matter changes. Tract-based spatial statistics were utilised to assess changes in diffusivity metrics in a study-specific whiter matter skeleton.
RESULTS
In contrast to healthy controls, PPS patients exhibited increased grey matter density in the brainstem, cerebellum and occipital lobe, accompanied by increased FA in the corticospinal tracts, cerebellum, bilateral mesial temporal lobes and inferior frontal tracts. PPS patients exhibited increased integrity metrics in the same anatomical regions where ALS patients showed degenerative changes.
CONCLUSIONS
Our findings suggests that PPS is associated with considerable cortical and white matter reorganisation which may be interpreted as compensatory, adaptive change in response to severe lower motor neuron injury in infancy.
Conclusions: Contrary to previous reports, we found no evidence of cerebral grey or white matter degeneration in a cohort of polio survivors using a validated quantitative neuroimaging protocol. Anatomical regions which are preferentially affected in ALS, such as the corticospinal tracts and the cerebellum exhibit superior integrity in PPS than in healthy controls.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any): KEYWORDS
Post-polio syndrome, Motor neuron disease, Neuroimaging, Pathology, Clinical trials
Link to Paper (if available): Click here to view full text or to download
Category: Brain
Title: Physiology of the motor cortex in polio survivors.
Author: Lupu, V.D. et al.
Affiliation: EMG Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Building 10, CRC, 7-5680, 10 Center Drive, MSC-1404 Bethesda, Maryland 20892, USA.
Journal: Muscle & Nerve
Citation: Muscle Nerve. 2008;37(2):177-82.
DOI: 10.1002/mus.20913
Publication Year and Month: 2008 02
Abstract: We hypothesized that the corticospinal system undergoes functional changes in long-term polio survivors. Central motor conduction times (CMCTs) to the four limbs were measured in 24 polio survivors using transcranial magnetic stimulation (TMS). Resting motor thresholds and CMCTs were normal. In 17 subjects whose legs were affected by polio and 13 healthy controls, single- and paired-pulse TMS was used to assess motor cortex excitability while recording from tibialis anterior (TA) muscles at rest and following maximal contraction until fatigue. In polio survivors the slope of the recruitment curve was normal, but maximal motor evoked potentials (MEPs) were larger than in controls. MEPs were depressed after fatiguing exercise. Three patients with central fatigue by twitch interpolation had a trend toward slower recovery. There was no association with symptoms of post-polio syndrome. These changes occurring after polio may allow the motor cortex to activate a greater proportion of the motor neurons innervating affected muscles.
Conclusions:
Outcome of Research: More research required
Availability of Paper: Paid subscription required to view or download full text.
Comments (if any): There appear to be compensatory effects by the motor cortex to increase the strength of action potentials to innervate muscles that have fewer motor units (due to the polio virus). Surprisingly, this investigation did not find association between PPS or central fatigue with increased central recruitment patterns to innervate remaining muscle tissue.
Link to Paper (if available): Click here to view Abstract
Category: Brain, Late Effects of Polio, Post-Polio Motor Unit
Title: Imaging data indicate cerebral reorganisation in poliomyelitis survivors: Possible compensation for longstanding lower motor neuron pathology
Author: Stacey Li Hi Shing (a), Jasmin Lope (a), Rangariroyashe H. Chipika (a), Orla Hardiman (a), Peter Bede (a, b, ∗)
Affiliation: (a) Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland
(b) Pitié-Salpêtrière University Hospital, Sorbonne University, Paris, France
∗ Corresponding author: Peter Bede, Room 5.43, Computational Neuroimaging Group, Trinity Biomedical Sciences In- stitute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.
E-mail address: [email protected] (P.Bede).
Journal: NEW - PUT DETAILS IN CITATION FIELD
Citation: Journal of Neurological Sciences
424 (2021) 117361
DOI: https://doi.org/10.1016/j.jns.2021.117361
Publication Year and Month: 2021 05
Abstract: BACKGROUND
Post-polio syndrome (PPS) has been traditionally considered a slowly progressive condition that affects poliomyelitis survivors decades after their initial infection. Cerebral changes in poliomyelitis survivors are poorly characterised and the few existing studies are strikingly conflicting.
OBJECTIVE
The overarching aim of this study is the comprehensive characterisation of cerebral grey and white matter alterations in poliomyelitis survivors with reference to healthy- and disease-controls using quantitative imaging metrics.
METHODS
Thirty-six poliomyelitis survivors, 88 patients with ALS and 117 healthy individuals were recruited in a prospective, single-centre neuroimaging study using uniform MRI acquisition parameters. All participants underwent standardised clinical assessments, T1-weighted structural and diffusion tensor imaging. Whole-brain and region-of-interest morphometric analyses were undertaken to evaluate patterns of grey matter changes. Tract-based spatial statistics were performed to evaluate diffusivity alterations in a study-specific whiter matter skeleton.
RESULTS
In contrast to healthy controls, poliomyelitis survivors exhibited increased grey matter partial volumes in the brainstem, cerebellum and occipital lobe, accompanied by increased FA in the corticospinal tracts, cerebellum, bilateral mesial temporal lobes and inferior frontal tracts. Polio survivors exhibited increased integrity metrics in the same anatomical regions where ALS patients showed degenerative changes.
CONCLUSIONS
Our findings indicate considerable cortical and white matter reorganisation in poliomyelitis survivors which may be interpreted as compensatory, adaptive change in response to severe lower motor neuron injury in infancy.
Keywords
Post-polio syndrome, Motor neuron disease, Neuroimaging, Pathology, Poliomyelitis
Conclusions: Contrary to previous reports, we found no evidence of cerebral grey or white matter degeneration in a cohort of polio survivors using a validated quantitative neuroimaging protocol. The brainstem, corticospinal tracts and the cerebellum exhibit superior integrity in poliomyelitis survivors compared to healthy controls.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any):
Link to Paper (if available): Click here to view full text or to download
There is currently 5 paper in this category.
Title: Spinal cord gray matter atrophy is associated with functional decline in post-polio syndrome
Author: Maria Janina Wendebourg (1,2), Matthias Weigel (1,2,3,4,5), Laura Richter (1), Vanya Gocheva (6), Patricia Hafner (6), Anna-Lena Orsini (6), Valentina Crepulja (1,2), Simone Schmidt (6), Antal Huck (4), Johanna Oechtering (1), Maria Blatow (7), Tanja Haas (3,4), Cristina Granziera (1,2,5), Ludwig Kappos (1,2,5), Philippe Cattin (4), Oliver Bieri (3,4) Dirk Fischer (6), Regina Schlaeger (1,2,5)
Affiliation: 1. Neurology Clinic and Policlinic, Department of Clinical Research, University Hospital Basel, University of Basel, Basel, Switzerland
2. Translational Imaging in Neurology (ThINk), Department of Biomedical Engineering, University of Basel, Basel, Switzerland
3. Division of Radiological Physics, Department of Radiology, University Hospital Basel, Basel, Switzerland
4. Department of Biomedical Engineering, University of Basel, Basel, Switzerland
5. MS Center and Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University of Basel, Basel, Switzerland
6. Division of Pediatric Neurology, University of Basel Children's Hospital, Basel, Switzerland
7. Department of Neuroradiology, Clinical Neuroscience Center, University Hospital Zurich, University of Zurich, Zurich,
Journal: European Journal of Neurology
Citation: Eur J Neurol. 2022;00:1–11.
DOI: 10.1111/ene.15261
Publication Year and Month: 2022 01
Abstract: Objective: To determine if patients with post- polio syndrome (PPS) show spinal cord gray matter (SCGM) atrophy and to assess associations between SCGM atrophy, muscle strength and patient- reported functional decline.
Methods: Twenty patients diagnosed with PPS (March of Dimes criteria) and 20 age- and sex- matched healthy controls (HC) underwent 3T axial 2D- rAMIRA magnetic resonance imaging at the intervertebral disc levels C2/C3–C6/C7, T9/T10 and the lumbar enlarge-ment level (Tmax) (0.5 × 0.5 mm2 in- plane resolution). SCGM areas were segmented manu-ally by two independent raters. Muscle strength, self-reported fatigue, depression and pain measures were assessed.
Results: Post- polio syndrome patients showed significantly and preferentially re-duced SCGM areas at C2/C3 (p= 0.048), C3/C4 (p= 0.001), C4/C5 (p< 0.001), C5/C6 (p= 0.004) and Tmax (p= 0.041) compared to HC. SCGM areas were significantly associated with muscle strength in corresponding myotomes even after adjustment for fatigue, pain and depression. SCGM areaTmax together with age and sex explained 68% of ankle dorsiflexion strength variance. No associations were found with age at or time since infection. Patients reporting PPS- related decline in arm function showed significant cervical SCGM atrophy compared to stable patients adjusted for initial disease severity.
Conclusions: Patients with PPS show significant SCGM atrophy that correlates with mus-cle strength and is associated with PPS- related functional decline. Our findings suggest a secondary neurodegenerative process underlying SCGM atrophy in PPS that is not ex-plained by aging or residua of the initial infection alone. Confirmation by longitudinal studies is needed. The described imaging methodology is promising for developing novel imaging surrogates for SCGM diseases.
Conclusions: The rAMIRA approach is a novel, promising, clinically feasible and sensitive method for segment-wise quantitation of GM atrophy in the cervical and thoracic SC in patients with lower motor neuron disorders. This study demonstrated its clinical applicability and vali-dated it in patients with PPS, a presumed pure, lower motor neuron disorder, which can serve as a model for other neurodegenerative, genetic or autoimmune diseases of the SCGM.
Patients with PPS show significant SCGM atrophy, particularly at levels close to the cervical and lumbar enlargements. Even after adjustment for the level of depression, fatigue and pain, potential confounding symptoms frequently observed in PPS, SCGM atrophy is significantly and segment-wise associated with muscle strength in corresponding myotomes. Moreover, SCGM atrophy is associated with patient-reported PPS-related functional decline. Secondary analyses suggest that SCGM atrophy is rather due to a second dis-ease phase than being a sole residuum of the initial infection or a pure aging effect. These observations support the hypothesis of a focally accentuated neurodegenerative process in the SC underlying PPS. Larger, ideally multicentric, longitudinal studies conducted over a sufficiently long timespan are an important next step to confirm our results and gain more insights into the development of SCGM atrophy over time and its correlation to clinical symptom evolution in patients with PPS.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any):
Link to Paper (if available): Click here to view full text or to download
Category: Brain, Late Effects of Polio, Post-Polio Motor Unit
Title: Imaging data indicate cerebral reorganisation in poliomyelitis survivors: Possible compensation for longstanding lower motor neuron pathology
Author: Stacey Li Hi Shing (a), Jasmin Lope (a), Rangariroyashe H. Chipika (a), Orla Hardiman (a), Peter Bede (a, b, ∗)
Affiliation: (a) Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland
(b) Pitié-Salpêtrière University Hospital, Sorbonne University, Paris, France
∗ Corresponding author: Peter Bede, Room 5.43, Computational Neuroimaging Group, Trinity Biomedical Sciences In- stitute, Trinity College Dublin, Pearse Street, Dublin 2, Ireland.
E-mail address: [email protected] (P.Bede).
Journal: NEW - PUT DETAILS IN CITATION FIELD
Citation: Journal of Neurological Sciences
424 (2021) 117361
DOI: https://doi.org/10.1016/j.jns.2021.117361
Publication Year and Month: 2021 05
Abstract: BACKGROUND
Post-polio syndrome (PPS) has been traditionally considered a slowly progressive condition that affects poliomyelitis survivors decades after their initial infection. Cerebral changes in poliomyelitis survivors are poorly characterised and the few existing studies are strikingly conflicting.
OBJECTIVE
The overarching aim of this study is the comprehensive characterisation of cerebral grey and white matter alterations in poliomyelitis survivors with reference to healthy- and disease-controls using quantitative imaging metrics.
METHODS
Thirty-six poliomyelitis survivors, 88 patients with ALS and 117 healthy individuals were recruited in a prospective, single-centre neuroimaging study using uniform MRI acquisition parameters. All participants underwent standardised clinical assessments, T1-weighted structural and diffusion tensor imaging. Whole-brain and region-of-interest morphometric analyses were undertaken to evaluate patterns of grey matter changes. Tract-based spatial statistics were performed to evaluate diffusivity alterations in a study-specific whiter matter skeleton.
RESULTS
In contrast to healthy controls, poliomyelitis survivors exhibited increased grey matter partial volumes in the brainstem, cerebellum and occipital lobe, accompanied by increased FA in the corticospinal tracts, cerebellum, bilateral mesial temporal lobes and inferior frontal tracts. Polio survivors exhibited increased integrity metrics in the same anatomical regions where ALS patients showed degenerative changes.
CONCLUSIONS
Our findings indicate considerable cortical and white matter reorganisation in poliomyelitis survivors which may be interpreted as compensatory, adaptive change in response to severe lower motor neuron injury in infancy.
Keywords
Post-polio syndrome, Motor neuron disease, Neuroimaging, Pathology, Poliomyelitis
Conclusions: Contrary to previous reports, we found no evidence of cerebral grey or white matter degeneration in a cohort of polio survivors using a validated quantitative neuroimaging protocol. The brainstem, corticospinal tracts and the cerebellum exhibit superior integrity in poliomyelitis survivors compared to healthy controls.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any):
Link to Paper (if available): Click here to view full text or to download
Category: Brain
Title: Cerebral changes in post-polio syndrome: A quantitative MRI study
Author: Stacey Li Hi Shing, Jasmin Lope, Mary Clare McKenna, Rangariroyashe H. Chipika, Orla Hardiman, & Peter Bede
Affiliation: Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Ireland
Journal: Journal of the Neurological Sciences
Citation: S.L.H. Shing, J. Lope, M.C. McKenna, et al., Cerebral changes in post-polio syndrome: A quantitative MRI study, Journal of the Neurological Sciences (2021), https://doi.org/10.1016/j.jns.2021.117361
Publication Year and Month: 2021 02
Abstract: BACKGROUND
Post-polio syndrome (PPS) has been traditionally considered a slowly progressive condition that affects polio survivors decades after their initial infection. Cerebral changes in PPS are poorly characterised and the few existing studies are strikingly conflicting.
OBJECTIVE
The overarching aim of this study is the comprehensive characterisation of cerebral grey and white matter alterations in post-polio syndrome with reference to healthy- and disease-controls using quantitative imaging metrics.
METHODS
Thirty-six patients with PPS, 88 patients with ALS and 117 healthy individuals were recruited in a prospective, single-centre neuroimaging study using uniform MRI acquisition parameters. All participants underwent standardised clinical assessments, T1-weighted imaging and diffusion tensor imaging. Whole-brain imaging and region-of-interest analyses were undertaken to evaluate patterns of grey matter changes. Tract-based spatial statistics were utilised to assess changes in diffusivity metrics in a study-specific whiter matter skeleton.
RESULTS
In contrast to healthy controls, PPS patients exhibited increased grey matter density in the brainstem, cerebellum and occipital lobe, accompanied by increased FA in the corticospinal tracts, cerebellum, bilateral mesial temporal lobes and inferior frontal tracts. PPS patients exhibited increased integrity metrics in the same anatomical regions where ALS patients showed degenerative changes.
CONCLUSIONS
Our findings suggests that PPS is associated with considerable cortical and white matter reorganisation which may be interpreted as compensatory, adaptive change in response to severe lower motor neuron injury in infancy.
Conclusions: Contrary to previous reports, we found no evidence of cerebral grey or white matter degeneration in a cohort of polio survivors using a validated quantitative neuroimaging protocol. Anatomical regions which are preferentially affected in ALS, such as the corticospinal tracts and the cerebellum exhibit superior integrity in PPS than in healthy controls.
Outcome of Research: More research required
Availability of Paper: The full text of this paper has been generously made available by the publisher.
Comments (if any): KEYWORDS
Post-polio syndrome, Motor neuron disease, Neuroimaging, Pathology, Clinical trials
Link to Paper (if available): Click here to view full text or to download
Category: Brain
Title: Physiology of the motor cortex in polio survivors.
Author: Lupu, V.D. et al.
Affiliation: EMG Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Building 10, CRC, 7-5680, 10 Center Drive, MSC-1404 Bethesda, Maryland 20892, USA.
Journal: Muscle & Nerve
Citation: Muscle Nerve. 2008;37(2):177-82.
DOI: 10.1002/mus.20913
Publication Year and Month: 2008 02
Abstract: We hypothesized that the corticospinal system undergoes functional changes in long-term polio survivors. Central motor conduction times (CMCTs) to the four limbs were measured in 24 polio survivors using transcranial magnetic stimulation (TMS). Resting motor thresholds and CMCTs were normal. In 17 subjects whose legs were affected by polio and 13 healthy controls, single- and paired-pulse TMS was used to assess motor cortex excitability while recording from tibialis anterior (TA) muscles at rest and following maximal contraction until fatigue. In polio survivors the slope of the recruitment curve was normal, but maximal motor evoked potentials (MEPs) were larger than in controls. MEPs were depressed after fatiguing exercise. Three patients with central fatigue by twitch interpolation had a trend toward slower recovery. There was no association with symptoms of post-polio syndrome. These changes occurring after polio may allow the motor cortex to activate a greater proportion of the motor neurons innervating affected muscles.
Conclusions:
Outcome of Research: More research required
Availability of Paper: Paid subscription required to view or download full text.
Comments (if any): There appear to be compensatory effects by the motor cortex to increase the strength of action potentials to innervate muscles that have fewer motor units (due to the polio virus). Surprisingly, this investigation did not find association between PPS or central fatigue with increased central recruitment patterns to innervate remaining muscle tissue.
Link to Paper (if available): Click here to view Abstract
Category: Brain
Title: Parallels between Post Polio fatigue and chronic fatigue syndrome: a common pathophysiology?
Author: Bruno, R.L., Creange, S.J., and Frick, N.M
Affiliation: Kids' Fatigue Management Program and The Post-Polio Institute, Englewood Hospital and Medical Center, New Jersey
Journal:
Citation: Am J Med.
Publication Year and Month: 1998 09
Abstract: Fatigue is the most commonly reported and most debilitating of post-polio sequelae affecting the >1.8 million North American polio survivors. Post-polio fatigue is characterized by subjective reports of difficulty with attention, cognition, and maintaining wakefulness. These symptoms resemble those reported in nearly 2 dozen outbreaks of post-viral fatigue syndromes (PVFS) that have recurred during this century and that are related clinically, historically, anatomically, or physiologically to poliovirus infections. This article reviews recent studies that relate the symptoms of post-polio fatigue and chronic fatigue syndrome (CFS) to clinically significant deficits on neuropsychologic tests of attention, histopathologic and neuroradiologic evidence of brain lesions, impaired activation of the hypothalamic-pituitary-adrenal axis, increased prolactin secretion, and electroencephalogram (EEG) slow-wave activity. A possible common pathophysiology for post-polio fatigue and CFS, based on the Brain Fatigue Generator Model of PVFS, and a possible pharmacotherapy for PVFS based on replacement of depleted brain dopamine, will be described
Conclusions: There is evidence of severe brain lesions at the brain stem and less severe lesions in the cerebellum and cerebral cortex which could play a role in general and cognitive fatigue.
Outcome of Research: More research required
Availability of Paper: Paid subscription required to view or download full text.
Comments (if any):
Link to Paper (if available): Click here to view Abstract
There is currently 5 paper in this category.