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Background and objectives <p>Neuropathic facial pain (NFP) is linked to lesions of trigeminal nerves, distinguishing it from persistent idiopathic facial pain (PIFP) which is clinically similar but without neurological abnormalities and without clinically objectifiable cause. Our recent brainstem imaging studies have demonstrated that abnormal central pain processing plays a role in the pathophysiology of PIFP.</p> Methods <p>Using the identical brainstem imaging protocol this current study aims to investigate the trigeminal pain processing mechanisms in patients with peripheral NFP using functional magnetic resonance imaging (fMRI).</p> <p>Twenty patients with NFP and 20 healthy control subjects (HC) participated in a well-established protocol of trigeminal nociceptive stimulation using gaseous ammonia. Functional images were acquired with a 3T MRI scanner, utilizing an optimized protocol designed for high-resolution echoplanar imaging of the brainstem. In a further step, using the same protocol, the imaging data from our database of patients with PIFP characterized by specific clinical features of persistent facial pain without detectable neurological damage, were incorporated into the analyses.</p> Results <p>Patients with NFP exhibited stronger activation in the spinal trigeminal nucleus (sTN) and other pain transmitting areas in response to painful stimulation when compared to HC. This finding is similar to a previous study in PIFP patients using the same imaging parameters. When contrasting patients with PIFP from this earlier study with NFP patients, a network of overactive brain areas further distinguished PIFP patients.&#xa0;</p> Discussion <p>Our findings indicate that altered central pain processing contributes to the pathophysiology of PIFP, possibly as a sign for nociplastic changes. Integrating these results into facial pain models could enhance the overall understanding of mechanisms underlying NFP and PIFP.</p>

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Visualizing nociplastic pain: functional hyperexcitability in neuropathic and idiopathic facial pain syndromes

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年10月13日

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  • Arne May,
  • Vanessa Ciancia,
  • Hauke Basedau

摘要

Background and objectives

Neuropathic facial pain (NFP) is linked to lesions of trigeminal nerves, distinguishing it from persistent idiopathic facial pain (PIFP) which is clinically similar but without neurological abnormalities and without clinically objectifiable cause. Our recent brainstem imaging studies have demonstrated that abnormal central pain processing plays a role in the pathophysiology of PIFP.

Methods

Using the identical brainstem imaging protocol this current study aims to investigate the trigeminal pain processing mechanisms in patients with peripheral NFP using functional magnetic resonance imaging (fMRI).

Twenty patients with NFP and 20 healthy control subjects (HC) participated in a well-established protocol of trigeminal nociceptive stimulation using gaseous ammonia. Functional images were acquired with a 3T MRI scanner, utilizing an optimized protocol designed for high-resolution echoplanar imaging of the brainstem. In a further step, using the same protocol, the imaging data from our database of patients with PIFP characterized by specific clinical features of persistent facial pain without detectable neurological damage, were incorporated into the analyses.

Results

Patients with NFP exhibited stronger activation in the spinal trigeminal nucleus (sTN) and other pain transmitting areas in response to painful stimulation when compared to HC. This finding is similar to a previous study in PIFP patients using the same imaging parameters. When contrasting patients with PIFP from this earlier study with NFP patients, a network of overactive brain areas further distinguished PIFP patients. 

Discussion

Our findings indicate that altered central pain processing contributes to the pathophysiology of PIFP, possibly as a sign for nociplastic changes. Integrating these results into facial pain models could enhance the overall understanding of mechanisms underlying NFP and PIFP.