Vestibular deterioration precedes hearing deterioration in the P51SCOCH mutation (DFNA9):: An analysis in 74 mutation carriers

被引:39
作者
Bischoff, AMLC
Huygen, PLM
Kemperman, MH
Pennings, RJE
Bom, SJH
Verhagen, WIM
Admiraal, RJC
Kremer, H
Cremers, CWRJ
机构
[1] Univ Nijmegen, Radboud Med Ctr, Dept Otorhinolaryngol, Nijmegen, Netherlands
[2] Canisius Wilhelmina Hosp, Dept Neurol, Nijmegen, Netherlands
关键词
COCH; Cochleovestibular impairment; DFNA9; Meniere's disease-p51S;
D O I
10.1097/01.mao.0000185048.84641.e3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: To analyze cochleovestibular impairment features in P51S COCH mutation carriers (n = 22) in a new, large Dutch family and to compare the results to those obtained in previously identified similar mutation carriers (n = 52). To evaluate age-related features between progressive hearing and vestibular impairment of all mutation carriers (n = 74). Study Design: Family study. Methods: Regression analysis was performed in relation to age to outline the development of hearing thresholds, speech recognition scores, and vestibulo-ocular reflex time constant as the key vestibular response parameter. Results: Pure tone thresholds, phoneme recognition scores, and vestibular responses of the mutation carriers in the new family were essentially similar to those previously established in all other mutation carriers. Hearing started to deteriorate in all mutation carriers from 43 years of age onwards, whereas deterioration of vestibular function started from age 34. Conclusion: Vestibular impairment starts earlier, progresses more rapidly, and, eventually, is more complete than hearing impairment in P51S COCH mutation carriers.
引用
收藏
页码:918 / 925
页数:8
相关论文
共 29 条
[1]   SOMATOSENSORY COMPENSATION FOR LOSS OF LABYRINTHINE FUNCTION [J].
BLES, W ;
DEJONG, JMBV ;
DEWIT, G .
ACTA OTO-LARYNGOLOGICA, 1984, 97 (3-4) :213-221
[2]   Cross-sectional analysis of hearing threshold in relation to age in a large family with cochleovestibular impairment thoroughly genotyped for DFNA9/COCH [J].
Bom, SJH ;
Kemperman, MH ;
Huygen, PLM ;
Luijendijk, MWJ ;
Cremers, CWRJ .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 2003, 112 (03) :280-286
[3]   Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9 [J].
Bom, SJH ;
Kemperman, MH ;
De Kok, YJM ;
Huygen, PLM ;
Verhagen, WIM ;
Cremers, FPM ;
Cremers, CWRJ .
LARYNGOSCOPE, 1999, 109 (09) :1525-1530
[4]   Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH [J].
Bom, SJH ;
De Leenheer, EMR ;
Lemaire, FX ;
Kemperman, MH ;
Verhagen, WIM ;
Marres, HAM ;
Kunst, HPM ;
Ensink, RJH ;
Bosman, AJ ;
Van Camp, G ;
Cremers, FPM ;
Huygen, PLM ;
Cremers, CWRJ .
ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 2001, 127 (09) :1045-1048
[5]   A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects [J].
de Kok, YJM ;
Bom, SJH ;
Brunt, TM ;
Kemperman, MH ;
van Beusekom, E ;
van der Velde-Visser, SD ;
Robertson, NG ;
Morton, CC ;
Huygen, PLM ;
Verhagen, WIM ;
Brunner, HG ;
Cremers, CWRJ ;
Cremers, FPM .
HUMAN MOLECULAR GENETICS, 1999, 8 (02) :361-366
[6]   PHYSIOLOGY OF PERIPHERAL NEURONS INNERVATING SEMICIRCULAR CANALS OF SQUIRREL MONKEY .2. RESPONSE TO SINUSOIDAL STIMULATION AND DYNAMICS OF PERIPHERAL VESTIBULAR SYSTEM [J].
FERNANDEZ, C ;
GOLDBERG, JM .
JOURNAL OF NEUROPHYSIOLOGY, 1971, 34 (04) :661-+
[7]   High prevalence of symptoms of Meniere's disease in three families with a mutation in the COCH gene [J].
Fransen, E ;
Verstreken, M ;
Verhagen, WIM ;
Wuyts, FL ;
Huygen, PLM ;
D'Haese, P ;
Robertson, NG ;
Morton, CC ;
McGuirt, WT ;
Smith, RJH ;
Declau, F ;
Van de Heyning, PH ;
Van Camp, G .
HUMAN MOLECULAR GENETICS, 1999, 8 (08) :1425-1429
[8]  
Huygen P L, 1989, Acta Otolaryngol Suppl, V468, P359
[9]  
HUYGEN PLM, 1991, EXP BRAIN RES, V87, P457
[10]  
International Standards Organization (ISO), 1984, 7029 ISO