Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study
Hereditary spastic paraplegias (HSP) are a composite and genetically heterogeneous group of conditions mainly expressed by the impairment of the central motor system ("pure" forms). The involvement of other components of the central nervous system or of other systems is described in the &q...
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creator | Martinuzzi, Andrea Montanaro, Domenico Vavla, Marinela Paparella, Gabriella Bonanni, Paolo Musumeci, Olimpia Brighina, Erika Hlavata, Hana Rossi, Giuseppe Aghakhanyan, Gayane Martino, Nicola Baratto, Alessandra D'Angelo, Maria Grazia Peruch, Francesca Fantin, Marianna Arnoldi, Alessia Citterio, Andrea Vantaggiato, Chiara Rizzo, Vincenzo Toscano, Antonio Bresolin, Nereo Bassi, Maria Teresa |
description | Hereditary spastic paraplegias (HSP) are a composite and genetically heterogeneous group of conditions mainly expressed by the impairment of the central motor system ("pure" forms). The involvement of other components of the central nervous system or of other systems is described in the "complicate" forms. The definition of an investigation protocol capable, by assembling clinical and paraclinical indicators to fully represent the extent of the motor system impairment, would help both the clinical handling of these conditions and contribute to our understanding of their pathogenesis.
We applied a clinical and paraclinical protocol which included tools exploring motor and non motor functioning, neurophysiology and MRI to a composite cohort of 70 molecularly defined HSP patients aged 3 to 65, to define for each indicator its significance in detailing the presence and the severity of the pathology.
Clinically increased deep tendon reflexes and lower limb (LL) weakness are constant findings in all patients. The "complicated" forms are characterized by peripheral motor impairment, cognitive and cerebellar involvement. The Spastic Paraplegia Rating Scale efficiently reflects the severity of functional problems and correlates with disease duration. Neurophysiology consistently documents the impairment of the central motor pathway to the LLs. Nevertheless, the upper extremities and sensory system involvement is a frequent finding. MRI diffusion tensor imaging (DTI) highlighted a significant alteration of FA and MD. Combining the sampling of the various portion of the cortico-spinal tract (CST) DTI consistently discriminated patients from controls.
We propose a graded clinical and paraclinical protocol for HSP phenotype definition, indicating for each tool the discriminative and descriptive capacity. Our protocol applied to 9 different forms of HSP showed that the functional impairment often extends beyond the CST. The novel DTI approach may add significant elements in disease recognition, staging and mapping. |
doi_str_mv | 10.1371/journal.pone.0153283 |
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We applied a clinical and paraclinical protocol which included tools exploring motor and non motor functioning, neurophysiology and MRI to a composite cohort of 70 molecularly defined HSP patients aged 3 to 65, to define for each indicator its significance in detailing the presence and the severity of the pathology.
Clinically increased deep tendon reflexes and lower limb (LL) weakness are constant findings in all patients. The "complicated" forms are characterized by peripheral motor impairment, cognitive and cerebellar involvement. The Spastic Paraplegia Rating Scale efficiently reflects the severity of functional problems and correlates with disease duration. Neurophysiology consistently documents the impairment of the central motor pathway to the LLs. Nevertheless, the upper extremities and sensory system involvement is a frequent finding. MRI diffusion tensor imaging (DTI) highlighted a significant alteration of FA and MD. Combining the sampling of the various portion of the cortico-spinal tract (CST) DTI consistently discriminated patients from controls.
We propose a graded clinical and paraclinical protocol for HSP phenotype definition, indicating for each tool the discriminative and descriptive capacity. Our protocol applied to 9 different forms of HSP showed that the functional impairment often extends beyond the CST. The novel DTI approach may add significant elements in disease recognition, staging and mapping.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0153283</identifier><identifier>PMID: 27077743</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adenosine Triphosphatases - genetics ; Adolescent ; Adult ; Aged ; Analysis ; Analysis of Variance ; Ataxia ; Biology and Life Sciences ; Brain research ; Central nervous system ; Cerebellum ; Cerebellum - physiopathology ; Child ; Child, Preschool ; Cognition - physiology ; Cognitive ability ; Cohort Studies ; Extremities ; Female ; GTP-Binding Proteins - genetics ; Heat shock proteins ; Hereditary spastic paraplegia ; Humans ; Impairment ; Indicators ; Influence ; Laboratories ; Lower Extremity - physiopathology ; Magnetic Resonance Imaging ; Male ; Medical imaging ; Medicine and Health Sciences ; Membrane Proteins - genetics ; Middle Aged ; Molecular biology ; Mutation ; Neurophysiology ; Neurosciences ; Paralysis ; Pathogenesis ; Patients ; Physiological aspects ; Pilot Projects ; Reflex, Stretch - physiology ; Reflexes ; Research and Analysis Methods ; Spastic paraplegia ; Spastic Paraplegia, Hereditary - diagnosis ; Spastic Paraplegia, Hereditary - genetics ; Spastic Paraplegia, Hereditary - physiopathology ; Spastin ; Tendons - physiopathology ; Young Adult</subject><ispartof>PloS one, 2016-04, Vol.11 (4), p.e0153283-e0153283</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Martinuzzi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2016 Martinuzzi et al 2016 Martinuzzi et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c725t-23203db4b65ed83661c0c5c73f022c1fdd4fe91f3b3c7b64839564d77173bec43</citedby><cites>FETCH-LOGICAL-c725t-23203db4b65ed83661c0c5c73f022c1fdd4fe91f3b3c7b64839564d77173bec43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831837/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831837/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27077743$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Toft, Mathias</contributor><creatorcontrib>Martinuzzi, Andrea</creatorcontrib><creatorcontrib>Montanaro, Domenico</creatorcontrib><creatorcontrib>Vavla, Marinela</creatorcontrib><creatorcontrib>Paparella, Gabriella</creatorcontrib><creatorcontrib>Bonanni, Paolo</creatorcontrib><creatorcontrib>Musumeci, Olimpia</creatorcontrib><creatorcontrib>Brighina, Erika</creatorcontrib><creatorcontrib>Hlavata, Hana</creatorcontrib><creatorcontrib>Rossi, Giuseppe</creatorcontrib><creatorcontrib>Aghakhanyan, Gayane</creatorcontrib><creatorcontrib>Martino, Nicola</creatorcontrib><creatorcontrib>Baratto, Alessandra</creatorcontrib><creatorcontrib>D'Angelo, Maria Grazia</creatorcontrib><creatorcontrib>Peruch, Francesca</creatorcontrib><creatorcontrib>Fantin, Marianna</creatorcontrib><creatorcontrib>Arnoldi, Alessia</creatorcontrib><creatorcontrib>Citterio, Andrea</creatorcontrib><creatorcontrib>Vantaggiato, Chiara</creatorcontrib><creatorcontrib>Rizzo, Vincenzo</creatorcontrib><creatorcontrib>Toscano, Antonio</creatorcontrib><creatorcontrib>Bresolin, Nereo</creatorcontrib><creatorcontrib>Bassi, Maria Teresa</creatorcontrib><title>Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Hereditary spastic paraplegias (HSP) are a composite and genetically heterogeneous group of conditions mainly expressed by the impairment of the central motor system ("pure" forms). The involvement of other components of the central nervous system or of other systems is described in the "complicate" forms. The definition of an investigation protocol capable, by assembling clinical and paraclinical indicators to fully represent the extent of the motor system impairment, would help both the clinical handling of these conditions and contribute to our understanding of their pathogenesis.
We applied a clinical and paraclinical protocol which included tools exploring motor and non motor functioning, neurophysiology and MRI to a composite cohort of 70 molecularly defined HSP patients aged 3 to 65, to define for each indicator its significance in detailing the presence and the severity of the pathology.
Clinically increased deep tendon reflexes and lower limb (LL) weakness are constant findings in all patients. The "complicated" forms are characterized by peripheral motor impairment, cognitive and cerebellar involvement. The Spastic Paraplegia Rating Scale efficiently reflects the severity of functional problems and correlates with disease duration. Neurophysiology consistently documents the impairment of the central motor pathway to the LLs. Nevertheless, the upper extremities and sensory system involvement is a frequent finding. MRI diffusion tensor imaging (DTI) highlighted a significant alteration of FA and MD. Combining the sampling of the various portion of the cortico-spinal tract (CST) DTI consistently discriminated patients from controls.
We propose a graded clinical and paraclinical protocol for HSP phenotype definition, indicating for each tool the discriminative and descriptive capacity. Our protocol applied to 9 different forms of HSP showed that the functional impairment often extends beyond the CST. The novel DTI approach may add significant elements in disease recognition, staging and mapping.</description><subject>Adenosine Triphosphatases - genetics</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Analysis</subject><subject>Analysis of Variance</subject><subject>Ataxia</subject><subject>Biology and Life Sciences</subject><subject>Brain research</subject><subject>Central nervous system</subject><subject>Cerebellum</subject><subject>Cerebellum - physiopathology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cognition - physiology</subject><subject>Cognitive ability</subject><subject>Cohort Studies</subject><subject>Extremities</subject><subject>Female</subject><subject>GTP-Binding Proteins - genetics</subject><subject>Heat shock proteins</subject><subject>Hereditary spastic paraplegia</subject><subject>Humans</subject><subject>Impairment</subject><subject>Indicators</subject><subject>Influence</subject><subject>Laboratories</subject><subject>Lower Extremity - physiopathology</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Medicine and Health Sciences</subject><subject>Membrane Proteins - genetics</subject><subject>Middle Aged</subject><subject>Molecular biology</subject><subject>Mutation</subject><subject>Neurophysiology</subject><subject>Neurosciences</subject><subject>Paralysis</subject><subject>Pathogenesis</subject><subject>Patients</subject><subject>Physiological aspects</subject><subject>Pilot Projects</subject><subject>Reflex, Stretch - physiology</subject><subject>Reflexes</subject><subject>Research and Analysis Methods</subject><subject>Spastic paraplegia</subject><subject>Spastic Paraplegia, Hereditary - diagnosis</subject><subject>Spastic Paraplegia, Hereditary - genetics</subject><subject>Spastic Paraplegia, Hereditary - physiopathology</subject><subject>Spastin</subject><subject>Tendons - physiopathology</subject><subject>Young 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and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study</title><author>Martinuzzi, Andrea ; Montanaro, Domenico ; Vavla, Marinela ; Paparella, Gabriella ; Bonanni, Paolo ; Musumeci, Olimpia ; Brighina, Erika ; Hlavata, Hana ; Rossi, Giuseppe ; Aghakhanyan, Gayane ; Martino, Nicola ; Baratto, Alessandra ; D'Angelo, Maria Grazia ; Peruch, Francesca ; Fantin, Marianna ; Arnoldi, Alessia ; Citterio, Andrea ; Vantaggiato, Chiara ; Rizzo, Vincenzo ; Toscano, Antonio ; Bresolin, Nereo ; Bassi, Maria Teresa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c725t-23203db4b65ed83661c0c5c73f022c1fdd4fe91f3b3c7b64839564d77173bec43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adenosine Triphosphatases - genetics</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Analysis</topic><topic>Analysis of 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Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martinuzzi, Andrea</au><au>Montanaro, Domenico</au><au>Vavla, Marinela</au><au>Paparella, Gabriella</au><au>Bonanni, Paolo</au><au>Musumeci, Olimpia</au><au>Brighina, Erika</au><au>Hlavata, Hana</au><au>Rossi, Giuseppe</au><au>Aghakhanyan, Gayane</au><au>Martino, Nicola</au><au>Baratto, Alessandra</au><au>D'Angelo, Maria Grazia</au><au>Peruch, Francesca</au><au>Fantin, Marianna</au><au>Arnoldi, Alessia</au><au>Citterio, Andrea</au><au>Vantaggiato, Chiara</au><au>Rizzo, Vincenzo</au><au>Toscano, Antonio</au><au>Bresolin, Nereo</au><au>Bassi, Maria Teresa</au><au>Toft, Mathias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-04-14</date><risdate>2016</risdate><volume>11</volume><issue>4</issue><spage>e0153283</spage><epage>e0153283</epage><pages>e0153283-e0153283</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Hereditary spastic paraplegias (HSP) are a composite and genetically heterogeneous group of conditions mainly expressed by the impairment of the central motor system ("pure" forms). The involvement of other components of the central nervous system or of other systems is described in the "complicate" forms. The definition of an investigation protocol capable, by assembling clinical and paraclinical indicators to fully represent the extent of the motor system impairment, would help both the clinical handling of these conditions and contribute to our understanding of their pathogenesis.
We applied a clinical and paraclinical protocol which included tools exploring motor and non motor functioning, neurophysiology and MRI to a composite cohort of 70 molecularly defined HSP patients aged 3 to 65, to define for each indicator its significance in detailing the presence and the severity of the pathology.
Clinically increased deep tendon reflexes and lower limb (LL) weakness are constant findings in all patients. The "complicated" forms are characterized by peripheral motor impairment, cognitive and cerebellar involvement. The Spastic Paraplegia Rating Scale efficiently reflects the severity of functional problems and correlates with disease duration. Neurophysiology consistently documents the impairment of the central motor pathway to the LLs. Nevertheless, the upper extremities and sensory system involvement is a frequent finding. MRI diffusion tensor imaging (DTI) highlighted a significant alteration of FA and MD. Combining the sampling of the various portion of the cortico-spinal tract (CST) DTI consistently discriminated patients from controls.
We propose a graded clinical and paraclinical protocol for HSP phenotype definition, indicating for each tool the discriminative and descriptive capacity. Our protocol applied to 9 different forms of HSP showed that the functional impairment often extends beyond the CST. The novel DTI approach may add significant elements in disease recognition, staging and mapping.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>27077743</pmid><doi>10.1371/journal.pone.0153283</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2016-04, Vol.11 (4), p.e0153283-e0153283 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1781147724 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science (PLoS) Journals Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Adenosine Triphosphatases - genetics Adolescent Adult Aged Analysis Analysis of Variance Ataxia Biology and Life Sciences Brain research Central nervous system Cerebellum Cerebellum - physiopathology Child Child, Preschool Cognition - physiology Cognitive ability Cohort Studies Extremities Female GTP-Binding Proteins - genetics Heat shock proteins Hereditary spastic paraplegia Humans Impairment Indicators Influence Laboratories Lower Extremity - physiopathology Magnetic Resonance Imaging Male Medical imaging Medicine and Health Sciences Membrane Proteins - genetics Middle Aged Molecular biology Mutation Neurophysiology Neurosciences Paralysis Pathogenesis Patients Physiological aspects Pilot Projects Reflex, Stretch - physiology Reflexes Research and Analysis Methods Spastic paraplegia Spastic Paraplegia, Hereditary - diagnosis Spastic Paraplegia, Hereditary - genetics Spastic Paraplegia, Hereditary - physiopathology Spastin Tendons - physiopathology Young Adult |
title | Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study |
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