Functional improvement in chronic human spinal cord injury: Four years after acidic fibroblast growth factor

Abstract Few treatments have proven effective for patients with chronic spinal cord injury (SCI). This study aimed to evaluate the efficacy and safety of acidic fibroblast growth factor (aFGF) in human SCI. This was an open-label prospective clinical trial of aFGF with an extended follow-up to 48 mo...

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Main Authors: Chin-Chu Ko, Tsung-Hsi Tu, Jau-Ching Wu, Wen-Cheng Huang, Yun-An Tsai, Shih-Fong Huang, Hsueh-Chen Huang, Henrich Cheng
Format: Article
Language:English
Published: Nature Portfolio 2018-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-018-31083-4
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author Chin-Chu Ko
Tsung-Hsi Tu
Jau-Ching Wu
Wen-Cheng Huang
Yun-An Tsai
Shih-Fong Huang
Hsueh-Chen Huang
Henrich Cheng
author_facet Chin-Chu Ko
Tsung-Hsi Tu
Jau-Ching Wu
Wen-Cheng Huang
Yun-An Tsai
Shih-Fong Huang
Hsueh-Chen Huang
Henrich Cheng
author_sort Chin-Chu Ko
collection DOAJ
description Abstract Few treatments have proven effective for patients with chronic spinal cord injury (SCI). This study aimed to evaluate the efficacy and safety of acidic fibroblast growth factor (aFGF) in human SCI. This was an open-label prospective clinical trial of aFGF with an extended follow-up to 48 months. All patients were treated with aFGF 3 times, including once directly applied to the injured spinal cord during neurolysis surgery, and twice via lumbar punctures at 3- and 6-months post-operation. Every patient was evaluated with standardized measurements of neurological functions. The trial initially enrolled 60 patients (30 cervical and 30 thoracolumbar SCI), but only 46 (21 cervical- and 25 thoracolumbar-SCI) completed the follow-up. The ASIA impairment scales, motor, pin prick, light touch, and FIM motor subtotal scores were all improved in both groups, except that the ASIA scores of light touch only demonstrated tendency of increase in the cervical-SCI group. All patients had a decrease in dependence, and there were no major adverse events or other oncological problems throughout the follow-up. At 48 months, the study demonstrated that aFGF was safe, feasible, and could yield modest functional improvement in chronic SCI patients. Further randomized control investigations are warranted for validation of its optimal dosage.
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spelling doaj.art-f178265967004f39aa60c5e1b3e90f182022-12-21T18:00:36ZengNature PortfolioScientific Reports2045-23222018-08-018111010.1038/s41598-018-31083-4Functional improvement in chronic human spinal cord injury: Four years after acidic fibroblast growth factorChin-Chu Ko0Tsung-Hsi Tu1Jau-Ching Wu2Wen-Cheng Huang3Yun-An Tsai4Shih-Fong Huang5Hsueh-Chen Huang6Henrich Cheng7Jhong Jheng Spine & Orthopedic HospitalDepartment of Neurosurgery, Neurological Institute, Taipei Veterans General HospitalDepartment of Neurosurgery, Neurological Institute, Taipei Veterans General HospitalDepartment of Neurosurgery, Neurological Institute, Taipei Veterans General HospitalCenter for Neural Regeneration, Neurological Institute, Taipei Veterans General HospitalCenter for Neural Regeneration, Neurological Institute, Taipei Veterans General HospitalDepartment of Neurosurgery, Neurological Institute, Taipei Veterans General HospitalDepartment of Neurosurgery, Neurological Institute, Taipei Veterans General HospitalAbstract Few treatments have proven effective for patients with chronic spinal cord injury (SCI). This study aimed to evaluate the efficacy and safety of acidic fibroblast growth factor (aFGF) in human SCI. This was an open-label prospective clinical trial of aFGF with an extended follow-up to 48 months. All patients were treated with aFGF 3 times, including once directly applied to the injured spinal cord during neurolysis surgery, and twice via lumbar punctures at 3- and 6-months post-operation. Every patient was evaluated with standardized measurements of neurological functions. The trial initially enrolled 60 patients (30 cervical and 30 thoracolumbar SCI), but only 46 (21 cervical- and 25 thoracolumbar-SCI) completed the follow-up. The ASIA impairment scales, motor, pin prick, light touch, and FIM motor subtotal scores were all improved in both groups, except that the ASIA scores of light touch only demonstrated tendency of increase in the cervical-SCI group. All patients had a decrease in dependence, and there were no major adverse events or other oncological problems throughout the follow-up. At 48 months, the study demonstrated that aFGF was safe, feasible, and could yield modest functional improvement in chronic SCI patients. Further randomized control investigations are warranted for validation of its optimal dosage.https://doi.org/10.1038/s41598-018-31083-4
spellingShingle Chin-Chu Ko
Tsung-Hsi Tu
Jau-Ching Wu
Wen-Cheng Huang
Yun-An Tsai
Shih-Fong Huang
Hsueh-Chen Huang
Henrich Cheng
Functional improvement in chronic human spinal cord injury: Four years after acidic fibroblast growth factor
Scientific Reports
title Functional improvement in chronic human spinal cord injury: Four years after acidic fibroblast growth factor
title_full Functional improvement in chronic human spinal cord injury: Four years after acidic fibroblast growth factor
title_fullStr Functional improvement in chronic human spinal cord injury: Four years after acidic fibroblast growth factor
title_full_unstemmed Functional improvement in chronic human spinal cord injury: Four years after acidic fibroblast growth factor
title_short Functional improvement in chronic human spinal cord injury: Four years after acidic fibroblast growth factor
title_sort functional improvement in chronic human spinal cord injury four years after acidic fibroblast growth factor
url https://doi.org/10.1038/s41598-018-31083-4
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