Is fragmentary myoclonus on polysomnography (PSG) common in ankylosing spondylitis?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: November 16, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Fragmentary Myoclonus on PSG in Ankylosing Spondylitis

There is no established association between fragmentary myoclonus on polysomnography and ankylosing spondylitis, and this finding should not be considered common or expected in AS patients.

Evidence Base

The available evidence does not support a relationship between excessive fragmentary myoclonus (EFM) and ankylosing spondylitis:

  • No documented association exists in the literature. The major rheumatology guidelines for AS management from the American College of Rheumatology, Spondylitis Association of America, and Spondyloarthritis Research and Treatment Network make no mention of sleep-related movement disorders, fragmentary myoclonus, or polysomnographic findings as features of ankylosing spondylitis 1.

  • AS clinical features are well-characterized and do not include EFM. The spondyloarthropathies, including AS, are characterized by sacroiliitis, inflammatory arthritis, enthesitis, associations with inflammatory bowel disease or psoriasis, aortitis, and heart block—but not sleep-related movement disorders 1.

What EFM Actually Represents

Understanding the true nature of EFM is critical to avoid misattribution:

  • EFM is predominantly associated with peripheral nerve pathology, not rheumatologic disease. In a study of 98 patients with EFM detected incidentally on PSG, 50% had electrophysiological abnormalities, most commonly polyneuropathy (65.3%), followed by L5 nerve root lesions (26.5%) 2.

  • EFM occurs with specific sleep and neurological disorders. The phenomenon has been documented in association with sleep-related respiratory problems, periodic limb movements in sleep, narcolepsy, Parkinson's disease (62.7% prevalence), and Machado-Joseph disease (50% prevalence)—but not inflammatory arthropathies 3, 4, 5.

  • EFM is more common in older patients and males. A large prospective study found that patients with EFM had polyneuropathy and nerve root lesions significantly more frequently than controls (31.5% vs. 21%), and the finding was associated with advanced age 6, 5.

Clinical Implications

If EFM is found on PSG in an AS patient:

  • Investigate for peripheral nerve pathology. Patients with incidental EFM should undergo electrophysiological workup including motor nerve conduction studies of the peroneal and tibial nerves, F-wave recordings, sensory nerve conduction studies of the sural nerve, and needle electromyography 2.

  • Consider alternative explanations. EFM in an AS patient likely represents a coincidental finding related to age, peripheral neuropathy, obstructive sleep apnea, or periodic limb movements—not the AS itself 2, 6, 5.

  • Do not attribute EFM to AS pathophysiology. EFM is not primarily a sleep-related phenomenon but rather persists during sleep and points to peripheral nerve pathology in at least a portion of cases 2.

Common Pitfall

The major pitfall is assuming that any finding on PSG in an AS patient must be related to their rheumatologic disease. EFM has no established connection to inflammatory arthropathies and should prompt evaluation for the conditions with which it is actually associated: peripheral neuropathy, sleep apnea, and age-related changes 2, 6.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.