Correlation Between Orofacial Pain and Sensory and Autonomic Neuropathies

被引:0
|
作者
Handa, Shruti [1 ,2 ]
Heffernan, Megan R. [3 ]
Tan, Summer [4 ]
Keith, David A. [1 ,2 ]
Rosen, Annika [5 ,6 ,7 ]
Cheng, Hsinlin Thomas [8 ,9 ]
机构
[1] Massachusetts Gen Hosp, Dept Surg, Div Oral & Maxillofacial Surg, Boston, MA USA
[2] Harvard Sch Dent Med, Boston, MA USA
[3] Massachusetts Gen Hosp, Dept Neurol, Boston, MA USA
[4] Harvard Sch Dent Med, Dept Dent, Boston, MA USA
[5] Eastman Inst, Dept Oral & Maxillofacial Surg, Stockholm, Sweden
[6] Univ Bergen, Dept Clin Dent, Bergen, Norway
[7] Haukeland Hosp, Dept Oral & Maxillofacial Surg, Bergen, Norway
[8] Massachusetts Gen Hosp, Dept Neurol, Boston, MA USA
[9] Harvard Med Sch, Boston, MA USA
来源
JOURNAL OF PAIN RESEARCH | 2024年 / 17卷
关键词
idiopathic facial pain; orofacial pain; temporomandibular disorders; skin biopsy; autonomic dysfunction; sensory neuropathic pain; dysautonomia; small fiber neuropathy; SMALL-FIBER NEUROPATHY; DIAGNOSTIC CHALLENGE; POLYNEUROPATHY; PREVALENCE; COMMON;
D O I
10.2147/JPR.S475528
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: Orofacial Pain (OFP) affects 15% of the general population. OFP conditions can be myofascial, also known as temporomandibular disorders (TMDs) or neuropathic. The underlying pathophysiology in several chronic OFP conditions, is unknown. Small fiber neuropathy (SFN) is a disorder of thinly myelinated A-delta and non-myelinated C-fibers and can manifest as sensory and autonomic neuropathies. SFN has been demonstrated in some OFP conditions. Our study aims to assess the presence of OFP in patients with sensory and autonomic neuropathies and assess the correlation between OFP, skin biopsy and autonomic dysfunction. Patients and Methods: This is a retrospective study (2018-2020) of patients from the SFN registry, Massachusetts General Hospital, Boston, USA, for the presence of OFP. All patients were included. Primary outcome: Prevalence of OFP in patients with chronic neuropathies. Secondary outcomes: Correlation between OFP and skin biopsy, dysautonomia, headaches, chronic nociceptive pain, psychological conditions, and patient factors, such as mean age and BMI. Results: Charts of 450 patients with sensory and autonomic neuropathies were reviewed. 22.67% (n=102) had OFP. The mean (range) age at biopsy in patients with OFP was 48.36 (20-81) years, female: male ratio 3.25:1. More OFP patients had negative skin biopsy results (p value<0.05) than those with sensory neuropathies. Patients with OFP had significantly higher prevalence of psychological conditions (p value 0.000), and higher BMI >30 (p value 0.025). Dysautonomia was significantly higher in patients with TMDs when compared to the ones without TMDs (p value 0.030). There was no significant difference in mean age, gender predilection, presence of headaches, peripheral neuropathies, and nociceptive pain between patients with and without OFP. Conclusion: OFP and sensory neuropathies can be overlapping conditions. Patients presenting with concomitant TMD and dysautonomia can be further tested for SFN. This can further help us understand a correlation if any, between idiopathic TMD/OFP conditions and SFN and further our understanding of the pathophysiology of these conditions.
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收藏
页码:3287 / 3295
页数:9
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