Identification of small fiber neuropathy in neuronal intranuclear inclusion disease: A clinicopathological study
INTRODUCTION Neuronal intranuclear inclusion disease (NIID) manifests as dementia combined with other neurological symptoms. However, small fiber neuropathy (SFN) and pathology remain unknown in NIID. METHODS A total of 294 subjects, including patients with NIID, Parkinson's disease, Alzheimer&...
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Published in | Alzheimer's & dementia Vol. 21; no. 2; pp. e14596 - n/a |
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Main Authors | , , , , , , , , , , , , , , , , , , , , |
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Language | English |
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John Wiley and Sons Inc
01.02.2025
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Abstract | INTRODUCTION
Neuronal intranuclear inclusion disease (NIID) manifests as dementia combined with other neurological symptoms. However, small fiber neuropathy (SFN) and pathology remain unknown in NIID.
METHODS
A total of 294 subjects, including patients with NIID, Parkinson's disease, Alzheimer's disease, diabetic peripheral neuropathy, and healthy controls (HCs), were included. Clinical scales, sensory and autonomic function testing, and skin biopsy were performed.
RESULTS
NIID patients had more severe sensory and autonomic dysfunction than other groups. Substantial reductions in intraepidermal, sweat gland, and pilomotor nerve fiber densities were observed in NIID patients, with a non–length dependent pattern. Detailed analysis revealed marked reductions in noradrenergic, cholinergic, peptidergic, and regenerative nerve fibers. Small fiber densities showed high diagnostic accuracy in distinguishing NIID from HCs and other diseases.
DISCUSSION
This study is the first to reveal wide and severe loss of small fibers in NIID, suggesting the involvement of SFN in the pathogenesis of NIID.
Highlights
Our study is the first to identify wide and severe non–length dependent small fiber neuropathy in neuronal intranuclear inclusion disease (NIID) patients.
Approximately 50% of NIID patients exhibited pure small fiber neuropathy without large fiber or mixed neuropathy.
NIID patients showed a significant reduction in noradrenergic, cholinergic, peptidergic, and regenerative fiber innervation.
Small fiber densities, especially intraepidermal nerve fiber density, demonstrated high diagnostic accuracy in distinguishing NIID patients from healthy controls and other disease groups.
Findings suggest that small fiber neuropathy may play a role in the pathogenesis of NIID. |
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AbstractList | INTRODUCTION
Neuronal intranuclear inclusion disease (NIID) manifests as dementia combined with other neurological symptoms. However, small fiber neuropathy (SFN) and pathology remain unknown in NIID.
METHODS
A total of 294 subjects, including patients with NIID, Parkinson's disease, Alzheimer's disease, diabetic peripheral neuropathy, and healthy controls (HCs), were included. Clinical scales, sensory and autonomic function testing, and skin biopsy were performed.
RESULTS
NIID patients had more severe sensory and autonomic dysfunction than other groups. Substantial reductions in intraepidermal, sweat gland, and pilomotor nerve fiber densities were observed in NIID patients, with a non–length dependent pattern. Detailed analysis revealed marked reductions in noradrenergic, cholinergic, peptidergic, and regenerative nerve fibers. Small fiber densities showed high diagnostic accuracy in distinguishing NIID from HCs and other diseases.
DISCUSSION
This study is the first to reveal wide and severe loss of small fibers in NIID, suggesting the involvement of SFN in the pathogenesis of NIID.
Highlights
Our study is the first to identify wide and severe non–length dependent small fiber neuropathy in neuronal intranuclear inclusion disease (NIID) patients.
Approximately 50% of NIID patients exhibited pure small fiber neuropathy without large fiber or mixed neuropathy.
NIID patients showed a significant reduction in noradrenergic, cholinergic, peptidergic, and regenerative fiber innervation.
Small fiber densities, especially intraepidermal nerve fiber density, demonstrated high diagnostic accuracy in distinguishing NIID patients from healthy controls and other disease groups.
Findings suggest that small fiber neuropathy may play a role in the pathogenesis of NIID. Neuronal intranuclear inclusion disease (NIID) manifests as dementia combined with other neurological symptoms. However, small fiber neuropathy (SFN) and pathology remain unknown in NIID. A total of 294 subjects, including patients with NIID, Parkinson's disease, Alzheimer's disease, diabetic peripheral neuropathy, and healthy controls (HCs), were included. Clinical scales, sensory and autonomic function testing, and skin biopsy were performed. NIID patients had more severe sensory and autonomic dysfunction than other groups. Substantial reductions in intraepidermal, sweat gland, and pilomotor nerve fiber densities were observed in NIID patients, with a non-length dependent pattern. Detailed analysis revealed marked reductions in noradrenergic, cholinergic, peptidergic, and regenerative nerve fibers. Small fiber densities showed high diagnostic accuracy in distinguishing NIID from HCs and other diseases. This study is the first to reveal wide and severe loss of small fibers in NIID, suggesting the involvement of SFN in the pathogenesis of NIID. Our study is the first to identify wide and severe non-length dependent small fiber neuropathy in neuronal intranuclear inclusion disease (NIID) patients. Approximately 50% of NIID patients exhibited pure small fiber neuropathy without large fiber or mixed neuropathy. NIID patients showed a significant reduction in noradrenergic, cholinergic, peptidergic, and regenerative fiber innervation. Small fiber densities, especially intraepidermal nerve fiber density, demonstrated high diagnostic accuracy in distinguishing NIID patients from healthy controls and other disease groups. Findings suggest that small fiber neuropathy may play a role in the pathogenesis of NIID. Neuronal intranuclear inclusion disease (NIID) manifests as dementia combined with other neurological symptoms. However, small fiber neuropathy (SFN) and pathology remain unknown in NIID.INTRODUCTIONNeuronal intranuclear inclusion disease (NIID) manifests as dementia combined with other neurological symptoms. However, small fiber neuropathy (SFN) and pathology remain unknown in NIID.A total of 294 subjects, including patients with NIID, Parkinson's disease, Alzheimer's disease, diabetic peripheral neuropathy, and healthy controls (HCs), were included. Clinical scales, sensory and autonomic function testing, and skin biopsy were performed.METHODSA total of 294 subjects, including patients with NIID, Parkinson's disease, Alzheimer's disease, diabetic peripheral neuropathy, and healthy controls (HCs), were included. Clinical scales, sensory and autonomic function testing, and skin biopsy were performed.NIID patients had more severe sensory and autonomic dysfunction than other groups. Substantial reductions in intraepidermal, sweat gland, and pilomotor nerve fiber densities were observed in NIID patients, with a non-length dependent pattern. Detailed analysis revealed marked reductions in noradrenergic, cholinergic, peptidergic, and regenerative nerve fibers. Small fiber densities showed high diagnostic accuracy in distinguishing NIID from HCs and other diseases.RESULTSNIID patients had more severe sensory and autonomic dysfunction than other groups. Substantial reductions in intraepidermal, sweat gland, and pilomotor nerve fiber densities were observed in NIID patients, with a non-length dependent pattern. Detailed analysis revealed marked reductions in noradrenergic, cholinergic, peptidergic, and regenerative nerve fibers. Small fiber densities showed high diagnostic accuracy in distinguishing NIID from HCs and other diseases.This study is the first to reveal wide and severe loss of small fibers in NIID, suggesting the involvement of SFN in the pathogenesis of NIID.DISCUSSIONThis study is the first to reveal wide and severe loss of small fibers in NIID, suggesting the involvement of SFN in the pathogenesis of NIID.Our study is the first to identify wide and severe non-length dependent small fiber neuropathy in neuronal intranuclear inclusion disease (NIID) patients. Approximately 50% of NIID patients exhibited pure small fiber neuropathy without large fiber or mixed neuropathy. NIID patients showed a significant reduction in noradrenergic, cholinergic, peptidergic, and regenerative fiber innervation. Small fiber densities, especially intraepidermal nerve fiber density, demonstrated high diagnostic accuracy in distinguishing NIID patients from healthy controls and other disease groups. Findings suggest that small fiber neuropathy may play a role in the pathogenesis of NIID.HIGHLIGHTSOur study is the first to identify wide and severe non-length dependent small fiber neuropathy in neuronal intranuclear inclusion disease (NIID) patients. Approximately 50% of NIID patients exhibited pure small fiber neuropathy without large fiber or mixed neuropathy. NIID patients showed a significant reduction in noradrenergic, cholinergic, peptidergic, and regenerative fiber innervation. Small fiber densities, especially intraepidermal nerve fiber density, demonstrated high diagnostic accuracy in distinguishing NIID patients from healthy controls and other disease groups. Findings suggest that small fiber neuropathy may play a role in the pathogenesis of NIID. |
Author | Liu, Minglei Zhang, Ke Wang, Yanjiang Wang, Yanlin Xue, Yinge Xu, Yuming Liu, Han Yang, Tianyuan Yuan, Yanpeng Li, Shuo Liu, Chen Liu, Ruoyu Cheng, Lin Li, Lanjun Kong, Ying Wang, Yangyang Gao, Yuan Yang, Jing Yang, Ting Liu, Xiaojing Yuan, Jing |
AuthorAffiliation | 5 Department of Neurology and Centre for Clinical Neuroscience Daping Hospital Third Military Medical University Chongqing China 3 Henan Key Laboratory of Cerebrovascular Diseases Zhengzhou China 2 NHC Key Laboratory of Prevention and treatment of Cerebrovascular Disease Zhengzhou China 1 Department of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China 4 Henan Medical Key Laboratory of Neurogenetic and Degenerative Diseases Zhengzhou China |
AuthorAffiliation_xml | – name: 1 Department of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China – name: 3 Henan Key Laboratory of Cerebrovascular Diseases Zhengzhou China – name: 5 Department of Neurology and Centre for Clinical Neuroscience Daping Hospital Third Military Medical University Chongqing China – name: 2 NHC Key Laboratory of Prevention and treatment of Cerebrovascular Disease Zhengzhou China – name: 4 Henan Medical Key Laboratory of Neurogenetic and Degenerative Diseases Zhengzhou China |
Author_xml | – sequence: 1 givenname: Minglei surname: Liu fullname: Liu, Minglei organization: The First Affiliated Hospital of Zhengzhou University – sequence: 2 givenname: Ruoyu surname: Liu fullname: Liu, Ruoyu organization: The First Affiliated Hospital of Zhengzhou University – sequence: 3 givenname: Yanpeng surname: Yuan fullname: Yuan, Yanpeng organization: NHC Key Laboratory of Prevention and treatment of Cerebrovascular Disease – sequence: 4 givenname: Xiaojing surname: Liu fullname: Liu, Xiaojing organization: Henan Key Laboratory of Cerebrovascular Diseases – sequence: 5 givenname: Lanjun surname: Li fullname: Li, Lanjun organization: Henan Medical Key Laboratory of Neurogenetic and Degenerative Diseases – sequence: 6 givenname: Yangyang surname: Wang fullname: Wang, Yangyang organization: NHC Key Laboratory of Prevention and treatment of Cerebrovascular Disease – sequence: 7 givenname: Jing surname: Yuan fullname: Yuan, Jing organization: NHC Key Laboratory of Prevention and treatment of Cerebrovascular Disease – sequence: 8 givenname: Ke surname: Zhang fullname: Zhang, Ke organization: NHC Key Laboratory of Prevention and treatment of Cerebrovascular Disease – sequence: 9 givenname: Shuo surname: Li fullname: Li, Shuo organization: Henan Medical Key Laboratory of Neurogenetic and Degenerative Diseases – sequence: 10 givenname: Ting surname: Yang fullname: Yang, Ting organization: Henan Key Laboratory of Cerebrovascular Diseases – sequence: 11 givenname: Yanlin surname: Wang fullname: Wang, Yanlin organization: Henan Key Laboratory of Cerebrovascular Diseases – sequence: 12 givenname: Yuan surname: Gao fullname: Gao, Yuan organization: NHC Key Laboratory of Prevention and treatment of Cerebrovascular Disease – sequence: 13 givenname: Han surname: Liu fullname: Liu, Han organization: Henan Key Laboratory of Cerebrovascular Diseases – sequence: 14 givenname: Yinge surname: Xue fullname: Xue, Yinge organization: The First Affiliated Hospital of Zhengzhou University – sequence: 15 givenname: Lin surname: Cheng fullname: Cheng, Lin organization: The First Affiliated Hospital of Zhengzhou University – sequence: 16 givenname: Tianyuan surname: Yang fullname: Yang, Tianyuan organization: The First Affiliated Hospital of Zhengzhou University – sequence: 17 givenname: Ying surname: Kong fullname: Kong, Ying organization: The First Affiliated Hospital of Zhengzhou University – sequence: 18 givenname: Chen surname: Liu fullname: Liu, Chen organization: The First Affiliated Hospital of Zhengzhou University – sequence: 19 givenname: Yanjiang surname: Wang fullname: Wang, Yanjiang organization: Third Military Medical University – sequence: 20 givenname: Yuming orcidid: 0000-0003-2689-9897 surname: Xu fullname: Xu, Yuming email: xuyuming@zzu.edu.cn organization: Henan Medical Key Laboratory of Neurogenetic and Degenerative Diseases – sequence: 21 givenname: Jing orcidid: 0000-0002-7356-5083 surname: Yang fullname: Yang, Jing email: yangjing9527@126.com, fccyangj1@zzu.edu.cn organization: Henan Medical Key Laboratory of Neurogenetic and Degenerative Diseases |
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Keywords | small fiber neuropathy dementia intraepidermal nerve fiber density autonomic dysfunction skin biopsy neuronal intranuclear inclusion disease |
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License | Attribution-NonCommercial-NoDerivs 2025 The Author(s). Alzheimer's & Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
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Snippet | INTRODUCTION
Neuronal intranuclear inclusion disease (NIID) manifests as dementia combined with other neurological symptoms. However, small fiber neuropathy... Neuronal intranuclear inclusion disease (NIID) manifests as dementia combined with other neurological symptoms. However, small fiber neuropathy (SFN) and... |
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SubjectTerms | Aged Aged, 80 and over Alzheimer Disease - pathology autonomic dysfunction dementia Female Humans intraepidermal nerve fiber density Intranuclear Inclusion Bodies - pathology Male Middle Aged Nerve Fibers - pathology Neurodegenerative Diseases - complications Neurodegenerative Diseases - pathology neuronal intranuclear inclusion disease Parkinson Disease - pathology skin biopsy small fiber neuropathy Small Fiber Neuropathy - diagnosis Small Fiber Neuropathy - etiology Small Fiber Neuropathy - pathology |
Title | Identification of small fiber neuropathy in neuronal intranuclear inclusion disease: A clinicopathological study |
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