Distortion product otoacoustic emission (2f1-f2) amplitude growth in human adults and neonates

被引:32
作者
Abdala, C [1 ]
机构
[1] House Ear Res Inst, Childrens Auditory Res & Evaluat Ctr, Los Angeles, CA 90057 USA
关键词
D O I
10.1121/1.428315
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Distortion product otoacoustic emissions (DPOAEs) are thought to be by-products of an active amplification process in the cochlea and thus serve as a metric for evaluating the integrity of this process. Because the cochlear amplifier functions in a level-dependent fashion, DPOAEs recorded as a function of stimulus level (i.e., a DPOAE growth function) may provide important information about the range and operational characteristics of the cochlear amplifier. The DPOAE growth functions recorded in human adults and neonates may provide information about the maturation of these active cochlear processes. Two experiments were conducted. Experiment I included normal-hearing adults and term-born neonates. The 2f1-f2 DPOAE growth functions were recorded for both age groups at three f2 frequencies. Experiment II, was an extension of the first experiment but added a subject group of premature neonates. The results of these studies indicate that DPOAE growth functions most often show amplitude saturation and nonmonotonic growth for all age groups. However, premature neonates show monotonic growth and the absence of amplitude saturation more often than adults. Those premature neonates who do show saturation also show an elevated threshold for amplitude saturation relative to adults. In contrast, term neonates are adultlike for most measures except that they show a larger percentage of nonsaturating growth functions than adults. These results may indicate immaturity in cochlear amplifier function prior to term birth in humans. Outer hair cell function and/or efferent regulation of outer hair cell function are hypothesized sources of this immaturity, although some contribution from the immature middle ear cannot be ruled out. (C) 2000 Acoustical Society of America. [S0001-4966(00)01201-7].
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页码:446 / 456
页数:11
相关论文
共 27 条
[1]   Maturation of medial efferent system function in humans [J].
Abdala, C ;
Ma, E ;
Sininger, YS .
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 1999, 105 (04) :2392-2402
[2]   Distortion product otoacoustic emission (2f(1)-f(2)) amplitude as a function of f(2)/f(1) frequency ratio and primary tone level separation in human adults and neonates [J].
Abdala, C .
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 1996, 100 (06) :3726-3740
[3]   A developmental study of distortion product otoacoustic emission (2f1-f2) suppression in humans [J].
Abdala, C .
HEARING RESEARCH, 1998, 121 (1-2) :125-138
[4]   Regional distribution of a creatine transporter in rat auditory brainstem: An in-situ hybridization study [J].
Hiel, H ;
Happe, HK ;
Warr, WB ;
Morley, BJ .
HEARING RESEARCH, 1996, 98 (1-2) :29-37
[5]  
Anson B. J., 1981, SURG ANATOMY HUMAN T
[6]  
Bredberg G., 1968, Acta Otolaryngol, V236, P1
[7]   ACOUSTIC DISTORTION PRODUCTS (ADP) FROM THE EARS OF TERM INFANTS AND YOUNG-ADULTS USING LOW STIMULUS LEVELS [J].
BROWN, AM ;
SHEPPARD, SL ;
RUSSELL, PT .
BRITISH JOURNAL OF AUDIOLOGY, 1994, 28 (4-5) :273-280
[8]   Comparison of distortion product otoacoustic emission (DPOAE) and auditory brain stem response (ABR) traveling wave delay measurements suggests frequency-specific synapse maturation [J].
Eggermont, JJ ;
Brown, DK ;
Ponton, CW ;
Kimberley, BP .
EAR AND HEARING, 1996, 17 (05) :386-394
[9]  
FEX J, 1962, ACTA PHYSIOL SCAND, V55, P1
[10]   ACOUSTIC DISTORTION PRODUCTS IN HUMANS - SYSTEMATIC CHANGES IN AMPLITUDE AS A FUNCTION OF F2/F1 RATIO [J].
HARRIS, FP ;
LONSBURYMARTIN, BL ;
STAGNER, BB ;
COATS, AC ;
MARTIN, GK .
JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA, 1989, 85 (01) :220-229