TY - JOUR
T1 - Pure tone hearing thresholds and speech recognition scores in Dutch patients carrying mutations in the USH2A gene
AU - Pennings, Ronald J.E.
AU - Huygen, Patrick L.M.
AU - Weston, Michael D.
AU - Van Aarem, Annelies
AU - Wagenaar, Mariette
AU - Kimberling, William J.
AU - Cremers, Cor W.R.J.
PY - 2003/1
Y1 - 2003/1
N2 - Objective: To establish the audiometric profile and speech recognition characteristics in 36 Usher IIa patients, carrying one (A) or two (B) pathogenic mutations in the USH2A gene. Study design: Family study. Setting: Tertiary referral center. Patients: Thirty six Usher IIa patients from 21 Dutch families. Methods: Ophthalmologic, vestibular, and audiometric examinations were performed on all patients. Cross-sectional analysis was performed on pure tone threshold data at 0.25 to 8 kHz and on speech phoneme recognition scores. Progression was evaluated using linear regression analysis on raw and presbyacusis corrected data. Results: A downsloping audiogram was found, with a mean threshold slope of -9 dB per octave, that was mildly progressive, i.e., by approximately 0.5 dB per year. Individual monaural maximum phoneme recognition scores (% correct) were analyzed in 30 patients in relation to the patient's age and level of hearing impairment characterized by a pure tone average (PTA1-4kHz). The speech recognition score started to deteriorate from a score of 90% at 38 years at a rate of 0.4% per year. The 90% level was attained at 69 dB hearing level (PTA1-4kHz); at higher levels of impairment, the score deteriorated at a slope of 0.6% per dB hearing level. There was no significant difference between group A and B in pure tone threshold, with or without presbyacusis correction, or phoneme recognition score as related to age or PTA1-4kHz. Conclusions: Patients with various mutations in USH2A have moderate to severe hearing impairment showing mild progression at approximately 0.5 dB hearing level per year.
AB - Objective: To establish the audiometric profile and speech recognition characteristics in 36 Usher IIa patients, carrying one (A) or two (B) pathogenic mutations in the USH2A gene. Study design: Family study. Setting: Tertiary referral center. Patients: Thirty six Usher IIa patients from 21 Dutch families. Methods: Ophthalmologic, vestibular, and audiometric examinations were performed on all patients. Cross-sectional analysis was performed on pure tone threshold data at 0.25 to 8 kHz and on speech phoneme recognition scores. Progression was evaluated using linear regression analysis on raw and presbyacusis corrected data. Results: A downsloping audiogram was found, with a mean threshold slope of -9 dB per octave, that was mildly progressive, i.e., by approximately 0.5 dB per year. Individual monaural maximum phoneme recognition scores (% correct) were analyzed in 30 patients in relation to the patient's age and level of hearing impairment characterized by a pure tone average (PTA1-4kHz). The speech recognition score started to deteriorate from a score of 90% at 38 years at a rate of 0.4% per year. The 90% level was attained at 69 dB hearing level (PTA1-4kHz); at higher levels of impairment, the score deteriorated at a slope of 0.6% per dB hearing level. There was no significant difference between group A and B in pure tone threshold, with or without presbyacusis correction, or phoneme recognition score as related to age or PTA1-4kHz. Conclusions: Patients with various mutations in USH2A have moderate to severe hearing impairment showing mild progression at approximately 0.5 dB hearing level per year.
KW - Genetic hearing impairment
KW - USH2A gene
KW - Usher syndrome Type IIa
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U2 - 10.1097/00129492-200301000-00013
DO - 10.1097/00129492-200301000-00013
M3 - Article
C2 - 12544030
AN - SCOPUS:0037261368
SN - 1531-7129
VL - 24
SP - 58
EP - 63
JO - Otology and Neurotology
JF - Otology and Neurotology
IS - 1
ER -