Correlation Between Orofacial Pain and Sensory and Autonomic Neuropathies.

autonomic dysfunction dysautonomia idiopathic facial pain orofacial pain sensory neuropathic pain skin biopsy small fiber neuropathy temporomandibular disorders

Journal

Journal of pain research
ISSN: 1178-7090
Titre abrégé: J Pain Res
Pays: New Zealand
ID NLM: 101540514

Informations de publication

Date de publication:
2024
Historique:
received: 28 06 2024
accepted: 01 10 2024
medline: 14 10 2024
pubmed: 14 10 2024
entrez: 14 10 2024
Statut: epublish

Résumé

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. 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. 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. 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.

Identifiants

pubmed: 39399165
doi: 10.2147/JPR.S475528
pii: 475528
pmc: PMC11471112
doi:

Types de publication

Journal Article

Langues

eng

Pagination

3287-3295

Informations de copyright

© 2024 Handa et al.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work.

Auteurs

Shruti Handa (S)

Division of Oral and Maxillofacial Surgery, Department of Surgery, Massachusetts General Hospital and Harvard School of Dental Medicine, Boston, MA, USA.

Megan R Heffernan (MR)

Department of Neurology, Massachusetts General Hospital, Boston, MA, USA.

Summer Tan (S)

Department of Dentistry, Harvard School of Dental Medicine, Boston, MA, USA.

David A Keith (DA)

Division of Oral and Maxillofacial Surgery, Department of Surgery, Massachusetts General Hospital and Harvard School of Dental Medicine, Boston, MA, USA.

Annika Rosén (A)

Department of Oral and Maxillofacial Surgery, Eastman Institute, Stockholm, Sweden.
Department of Clinical Dentistry, University of Bergen, Bergen, Norway.
Department of Oral and Maxillofacial Surgery, Haukeland University Hospital, Bergen, Norway.

Hsinlin Thomas Cheng (HT)

Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Classifications MeSH