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Abstract Details

Urinary Dysfunction in Myasthenia Gravis: Clinical Burden and Association with MG-ADL
Neuromuscular and Clinical Neurophysiology (EMG)
P4 - Poster Session 4 (8:00 AM-9:00 AM)
9-012
To assess the prevalence, predictors, and clinical significance of urinary dysfunction in myasthenia gravis (MG) patients compared with matched controls.

Myasthenia gravis primarily affects skeletal muscles, yet non-motor manifestations, particularly urinary incontinence (UI) and overactive bladder (OAB) symptoms, remain underexplored in MG. Given the impact of UI on quality of life, systematic investigation in MG is clinically important.

Eighty-six MG patients and 90 age- and sex-matched inpatient controls were evaluated in a cross-sectional, case-control study. All participants completed the International Consultation on Incontinence Questionnaire-Short Form (ICIQ-UI SF) and the Overactive Bladder Symptom Score (OABSS). MG severity was assessed using the Myasthenia Gravis Activities of Daily Living (MG-ADL) scale. MG patients were further categorized into early-onset (EOMG), late-onset (LOMG), and very late-onset (VLOMG) subgroups. Logistic regression identified predictors of UI, and Kaplan-Meier analysis was used to evaluate time to first recalled UI symptoms.

MG patients had over four times higher prevalence of UI symptoms (ICIQ-UI SF ≥6 in 52.3% vs. 12.2% in controls; p<0.001). LOMG patients exhibited the highest UI prevalence (63.2%) and progressed most rapidly to UI, while EOMG patients had the latest onset. OAB symptoms were also more prominent in MG, marked by higher OABSS (p<0.001), increased nocturia (≥3/night: 27.9% vs 11.1%; p=0.004), and greater urgency episodes (≥2/day: 38.4% vs 2.2%; p<0.001). MG-ADL score independently predicted UI (OR 2.38; 95% CI 1.04–5.46; p=0.041).

UI and OAB symptoms are more common in MG patients than in controls. Disease severity, as assessed by MG-ADL, is an independent predictor of UI, and age at disease onset may influence the timing of UI development. Routine screening and proactive management of UI in MG are warranted to improve patient quality of life and functional outcomes.

Authors/Disclosures
Alon Gorenshtein
PRESENTER
Mr. Gorenshtein has nothing to disclose.
Kamel Shihada, MD Mr. Shihada has nothing to disclose.
Gil I. Wolfe, MD, FAAN (Univ. At Buffalo, SUNY) Dr. Wolfe has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Grifols. Dr. Wolfe has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Alexion. Dr. Wolfe has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for ArgenX. Dr. Wolfe has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for UCB/Ra. Dr. Wolfe has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Janssen. Dr. Wolfe has received personal compensation in the range of $0-$499 for serving on a Scientific Advisory or Data Safety Monitoring board for Cartesian. Dr. Wolfe has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Grifols. The institution of Dr. Wolfe has received research support from UCB/Ra. The institution of Dr. Wolfe has received research support from Immunovant. The institution of Dr. Wolfe has received research support from Roche. Dr. Wolfe has received personal compensation in the range of $0-$499 for serving as a Advisor with FDA Advisory Panel for Cellular, Tissue and Genetic Therapies.
Shahar Shelly, MD (Rambam Medical Center) Dr. Shelly has or had stock in Remepy.