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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Veröffentlicht in:PloS one 2016-04, Vol.11 (4), p.e0153283-e0153283
Hauptverfasser: 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
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container_issue 4
container_start_page e0153283
container_title PloS one
container_volume 11
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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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. 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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. 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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 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genetics</subject><subject>Spastic Paraplegia, Hereditary - physiopathology</subject><subject>Spastin</subject><subject>Tendons - physiopathology</subject><subject>Young 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Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; 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 &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; 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>
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1932-6203
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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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