Time slot's time in Taipei (GMT+8)
2025/11/23 08:00-10:00 Room 201 ABC
- SYMPOSIUM 13 Neuromuscular Disorders II
Peripheral Neurophysiology in Clinical Practice: Diagnostic and Therapeutic Surrogates?
- Time
- Topic
- Speaker
- Moderator
- 08:00-08:30
- Overview of pathophysiology and diagnosis for small fiber neuropathy
- Speaker:
Sung-Tsang Hsieh
- Moderator:
Jiann-Shing Jeng
- Sung-Tsang Hsieh
- MD, PhD
-
Professor, National Taiwan University Hospital
E-mail:shsieh@ntu.edu.tw
Executive Summary:
Dr Sung-Tsang Hsieh graduated from National Taiwan University for his MD and completed neurology resident training at National Taiwan University Hospital. He got Neuroscience PhD at Johns Hopkins University and did postdoc at Neurology of Johns Hopkins Hospital. Currently Dr Hsieh is an attending neurologist at National Taiwan University Hospital and holds professorship at Department of Anatomy and Cell Biology of National Taiwan University. Dr Hsieh is a pioneer in developing skin biopsy and quantifying skin nerves as a pathologic signature of small-diameter nociceptive nerve degeneration. This skin biopsy approach has become the gold standard to diagnose small fiber neuropathy. With this achievement, he is one of the members in the Skin Biopsy Task Force of European Federation of Neurological Societies and was elected as a Fellow of American Academy of Neurology. Since pain due to small fiber neuropathy is potentially attributed to maladaptive brain responses, over the last decade, Dr Hsieh and his team have developed integrated assessment system of small fiber neuropathy incorporating quantitative sensory testing, contact heat evoked potential (CHEP), and heat-activated functional MRI. Hereditary transthyreting amyloidosis (ATTRv) is one of the etiologies causing small fiber neuropathy and autonomic dysfunction and Dr Hsieh’s group identified a unique genotype of transthyretin (TTR) A97S as the major etiology of Taiwanese with ATTRv. Furthermore, Dr Hsieh and colleagues established the first brain bank in Taiwan to investigate the mechanisms and therapeutic targets of rare disease and neurodegneration.
Dr Sung-Tsang Hsieh graduated from National Taiwan University for his MD and completed neurology resident training at National Taiwan University Hospital. He got Neuroscience PhD at Johns Hopkins University and did postdoc at Neurology of Johns Hopkins Hospital. Currently Dr Hsieh is an attending neurologist at National Taiwan University Hospital and holds professorship at Department of Anatomy and Cell Biology of National Taiwan University. Dr Hsieh is a pioneer in developing skin biopsy and quantifying skin nerves as a pathologic signature of small-diameter nociceptive nerve degeneration. This skin biopsy approach has become the gold standard to diagnose small fiber neuropathy. With this achievement, he is one of the members in the Skin Biopsy Task Force of European Federation of Neurological Societies and was elected as a Fellow of American Academy of Neurology. Since pain due to small fiber neuropathy is potentially attributed to maladaptive brain responses, over the last decade, Dr Hsieh and his team have developed integrated assessment system of small fiber neuropathy incorporating quantitative sensory testing, contact heat evoked potential (CHEP), and heat-activated functional MRI. Hereditary transthyreting amyloidosis (ATTRv) is one of the etiologies causing small fiber neuropathy and autonomic dysfunction and Dr Hsieh’s group identified a unique genotype of transthyretin (TTR) A97S as the major etiology of Taiwanese with ATTRv. Furthermore, Dr Hsieh and colleagues established the first brain bank in Taiwan to investigate the mechanisms and therapeutic targets of rare disease and neurodegneration.
Lecture Abstract:
Small fiber neuropathy, a unique type of peripheral nerve disorder, mainly affects small-diameter sensory nerves which are responsible for thermal and nociceptive functions. In small fiber neuropathy, there are two major manifestations: (1) negative symptoms, i.e. a loss of function, such as insensibility to noxious stimulus resulting in painless wounds and (2) positive symptoms, i.e. enhanced excitability of the neural axis causing neuropathic pain. During the last decade, we witnessed tremendous progress in the diagnosis of small fiber neuropathy and elucidation of the mechanisms of neuropathic pain in the context of (1) pathology: skin biopsy, (2) psychophysics: quantitative sensory testing (QST), (3) physiology: contact heat evoked potential (CHEP), laser evoked potential (LEP), and pain-related evoked potential (PREP), and (4) neuroimaging: functional MRI (fMRI), diffusion tensor imaging (DTI), connectome study). Small fibers are difficult to visualize under light microscopy and hence the diagnosis and confirmation of small-diameter nerve degeneration. The technique of punch skin biopsy together with sensitive immunohistochemistry and quantification of intraepidermal nerve fiber density (IENFd) provides objective and quantitative evidence of pathology for small fiber degeneration. Thermal thresholds measured by QST reflect functional capacity of small fibers. Noxious stimuli evoked potential including CHEP, LEP, and PREP offers physiological signatures of small fibers from different perspectives. Although small fiber neuropathy is a peripheral nerve degenerative disorder, peripheral sensitization could not fully account for the mechanism of neuropathic pain. We applied neuroimaging approaches including various sequencing and algorithms of resting-state and task-activated fMRI, structural connectome, and network analysis demonstrated concomitant central mechanism of maladaptive brain plasticity underlying neuropathic pain after nociceptive nerve degeneration. These observations lay down the foundations for designing medications and neuromodulation to treat the positive symptoms of neuropathic pain in small fiber neuropathy.
Small fiber neuropathy, a unique type of peripheral nerve disorder, mainly affects small-diameter sensory nerves which are responsible for thermal and nociceptive functions. In small fiber neuropathy, there are two major manifestations: (1) negative symptoms, i.e. a loss of function, such as insensibility to noxious stimulus resulting in painless wounds and (2) positive symptoms, i.e. enhanced excitability of the neural axis causing neuropathic pain. During the last decade, we witnessed tremendous progress in the diagnosis of small fiber neuropathy and elucidation of the mechanisms of neuropathic pain in the context of (1) pathology: skin biopsy, (2) psychophysics: quantitative sensory testing (QST), (3) physiology: contact heat evoked potential (CHEP), laser evoked potential (LEP), and pain-related evoked potential (PREP), and (4) neuroimaging: functional MRI (fMRI), diffusion tensor imaging (DTI), connectome study). Small fibers are difficult to visualize under light microscopy and hence the diagnosis and confirmation of small-diameter nerve degeneration. The technique of punch skin biopsy together with sensitive immunohistochemistry and quantification of intraepidermal nerve fiber density (IENFd) provides objective and quantitative evidence of pathology for small fiber degeneration. Thermal thresholds measured by QST reflect functional capacity of small fibers. Noxious stimuli evoked potential including CHEP, LEP, and PREP offers physiological signatures of small fibers from different perspectives. Although small fiber neuropathy is a peripheral nerve degenerative disorder, peripheral sensitization could not fully account for the mechanism of neuropathic pain. We applied neuroimaging approaches including various sequencing and algorithms of resting-state and task-activated fMRI, structural connectome, and network analysis demonstrated concomitant central mechanism of maladaptive brain plasticity underlying neuropathic pain after nociceptive nerve degeneration. These observations lay down the foundations for designing medications and neuromodulation to treat the positive symptoms of neuropathic pain in small fiber neuropathy.
- Time
- Topic
- Speaker
- Moderator
- 08:30-09:00
- Muscle excitability: resume the concept and update the clinical application
- Speaker:
Karl Ng
- Moderator:
Kongkiat Kulkantrakorn
- Karl Ng
- PhD
-
Senior Staff Specialist and Director Clinical Neurophysiology , Royal North Shore Hospital
Conjoint Associate Professor, University of Sydney
Editor in Chief, BMJ Neurology Open
E-mail:karl.ng@sydney.edu.au
Executive Summary:
Associate Professor Karl Ng is a neurologist and clinical neurophysiologist with the Royal North Shore Hospital and the University of Sydney. His special area of interest is in muscle and nerve excitability using threshold tracking techniques and Qtrac software, having commenced his PhD in Queen Square, London. He has published widely on this and has over 100 publications, including international consensus guidelines in Clinical Neurophysiology on the technique of muscle excitability. He is presently Editor in Chief of BMJ Neurology Open and Neurology editor for the Internal Medicine Journal.
Associate Professor Karl Ng is a neurologist and clinical neurophysiologist with the Royal North Shore Hospital and the University of Sydney. His special area of interest is in muscle and nerve excitability using threshold tracking techniques and Qtrac software, having commenced his PhD in Queen Square, London. He has published widely on this and has over 100 publications, including international consensus guidelines in Clinical Neurophysiology on the technique of muscle excitability. He is presently Editor in Chief of BMJ Neurology Open and Neurology editor for the Internal Medicine Journal.
Lecture Abstract:
Muscle excitability employing the Qtrac excitability protocol will be shown. Concepts surrounding the physiology of sarcolemmal properties will be demonstrated, and a review of selected studies in normal physiology and disease states will be covered. Possible clinical applications will also be discussed.
Muscle excitability employing the Qtrac excitability protocol will be shown. Concepts surrounding the physiology of sarcolemmal properties will be demonstrated, and a review of selected studies in normal physiology and disease states will be covered. Possible clinical applications will also be discussed.
- Time
- Topic
- Speaker
- Moderator
- 09:00-09:30
- Clinical and neurophysiological assessment for sarcopenia
- Speaker:
Hsueh-Wen Hsueh
- Moderator:
Li-Kai Tsai
- Hsueh-Wen Hsueh
- MD, MS
-
Visiting Neurologist, Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan
Visiting Neurologist, Department of Neurology, National Taiwan University Hospital Hsin-Chu Branch, Hsinchu, Taiwan.
E-mail:b93401044@ntu.edu.tw
Executive Summary:
Dr. Hsueh-Wen Hsueh started his residency in Department of Neurology in National Taiwan University Hospital and accomplished the training in 2017. He became the attending physician in Department of Neurology of National Taiwan University Hospital at the same year. His research interest is imaging and histopathological studies in different neuromuscular disorders. He established the neuromuscular ultrasound and MRI with several published articles in the Department of Neurology of National Taiwan University Hospital. He also engaged in several clinical trials of neuromuscular disorders.
Dr. Hsueh-Wen Hsueh started his residency in Department of Neurology in National Taiwan University Hospital and accomplished the training in 2017. He became the attending physician in Department of Neurology of National Taiwan University Hospital at the same year. His research interest is imaging and histopathological studies in different neuromuscular disorders. He established the neuromuscular ultrasound and MRI with several published articles in the Department of Neurology of National Taiwan University Hospital. He also engaged in several clinical trials of neuromuscular disorders.
Lecture Abstract:
Sarcopenia is a functional diagnosis that reflects muscle impairment. Unlike etiological diagnoses, which focus on the underlying cause, sarcopenia is defined by functional decline in skeletal muscle performance. Several assessment tools have been developed to diagnose and monitor the severity of sarcopenia. Interestingly, when these diagnostic criteria are applied to neuromuscular disorders such as amyotrophic lateral sclerosis or inclusion body myositis, these conditions often also meet the definition of sarcopenia.
In this presentation, I will begin by introducing the concept of sarcopenia and the current diagnostic tools used to assess it. I will then broaden the discussion to include various methods for evaluating skeletal muscle, encompassing clinical assessments, electrophysiological testing, and imaging techniques.
Sarcopenia is a functional diagnosis that reflects muscle impairment. Unlike etiological diagnoses, which focus on the underlying cause, sarcopenia is defined by functional decline in skeletal muscle performance. Several assessment tools have been developed to diagnose and monitor the severity of sarcopenia. Interestingly, when these diagnostic criteria are applied to neuromuscular disorders such as amyotrophic lateral sclerosis or inclusion body myositis, these conditions often also meet the definition of sarcopenia.
In this presentation, I will begin by introducing the concept of sarcopenia and the current diagnostic tools used to assess it. I will then broaden the discussion to include various methods for evaluating skeletal muscle, encompassing clinical assessments, electrophysiological testing, and imaging techniques.







