Author/Authors :
Heydari, Nahid School of Rehabilitation - Tehran University of Medical Sciences, Tehran, Iran , Hajiabolhassani, Fahimeh Department of Audiology - School of Rehabilitation - Tehran University of Medical Sciences, Tehran, Iran , Fatahi, Jamileh Department of Audiology - School of Rehabilitation - Tehran University of Medical Sciences, Tehran, Iran , Movaseghi, Shafieh Rheumatology Research Center - Imam Khomeini hospital - Tehran University of Medical Sciences, Iran , Jalaie, Shohreh Department of Biostatistics - School of Rehabilitation - Tehran University of Medical Sciences, Iran
Abstract :
Background: Rheumatoid arthritis (RA) is an autoimmune systemic disease. Most common autoimmune
diseases are multisystem disorders that may also present with otological manifestations, and
autoimmune inner ear disease accompanied by vestibular dysfunction. This study aimed to compare
the vestibular function between RA patients and normal subjects using cervical vestibular evoked
myogenic potentials (cVEMPs).
Methods: In this cross- sectional study, 25patients with RA (19 female and 6 male: mean (±SD)
age, 40.00 (±7.92) years) and 20 healthy subjects (15 female and 5 male: mean (±SD) age, 35.35
(±10.48) years) underwent cVEMPs, using 500 Hz-tone bursts at 95 dB nHL intensity level. Data
were analyzed using independent sample t-test through SPSS software v. 16.
Results: The mean peak latency of p13 was significantly higher in RA patients (p<0.001). The
mean peak latency of n23 was significantly higher in patients in the left ear (p=0.03). Vestibular
evoked myogenic potential (VEMP) responses were present in all (100%) of the participants. There
were no significant differences in mean peak to peak amplitude and amplitude ratio between the two
groups.
Conclusion: According to the prolonged latency of VEMP responses in RA patients, lesions in the
retrolabyrinthine, especially in the vestibulospinal tract are suspected.
Keywords :
Sternocleidomastoid muscle , Saccule , Vestibular evoked myogenic potentials , Rheumatoid arthritis