Pure tone audiometry and otoacoustic emissions in hypertensive subjects

D. Korkmaz, M. Habeşoğlu, A. Yılmaz, A. Karaaslan, A. Tosun, Ç. Oysu
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Esparza et al. showed impairment in hearing thresholds in hypertensive patients with retinal vascular damage (4). However, Torre et al. reported no association between hypertension and sensorineural hearing loss in the DPOAE tests (5). Similarly, Parving et al. detected no relevant link between hypertension and hearing loss (9). In a study performed on 80 Wistar rats by Li S et al. it was shown that there were glycogenesis and an abnormal release of neurotransmitters caused by HT, resulting in aging of the cochlea (10). The result of the electrocochleographic tests was reported to be worse in rats with HT as compared with normotansive rats (11). In the literature, it was shown that glutathione, anti-oxidant enzyme, and Nacetyltransferase are found in the cochlea and these two enzymes are genetically scarce in presbyacusis (12). In this context, HT can lead to oxidative stress in the cochlea, thus, resulting in presbycusis. Our study has revealed that there was a significant increase of the subjective complaint of tinnitus in patients with HT compared to the control group. In pure tone audiological assessment, hearing thresholds were 33.08±13.09 and 40.85±19.83 dB at 4000 and 8000 Hz in the HT group, respectively, while 17.25±11.27 and 21.83±14.46 dB were measured in the control group, respectively. Audiometrically, a significant association appeared between presbycusis and HT in our study. The HT group had a statistically significant decrease in responses to DPOAE as compared with the control group at OAE tests performed especially at 6000 Hz frequencies. The results of our study, despite being different from those by Torre et al. were consistent with the ones by Esparza et al. In order to better understand the effect of HT on the cochlea, it is necessary to see the results of further studies on this issue in the literature. 5. Conclusion Systemic hypertension causes changes in a variety of target organs. Vascular physiodynamic changes have been implicated in HT induced target organ damage (2). The cochlea due to its contents vascular physiodynamic mechanisms is one of the target organs on which HT may have an effect. In studies performed so far, there have been conflicting results gained between HT and cochlear symptoms (4,5). Our results strongly suggest that HT can cause cochleopathologic changes, including dysfunction of outer hair cells, in cases with tinnitus, presbycusis and even in preclinical cases. The study was performed at the department of Ear, Nose and Throat Disorders of Umraniye Research and Training Hospital between January 2011 and December 2011. All patients gave their informed consent. The study included thirty patients with HT attending to our department for reasons other than hearing loss and ear diseases and thirty patients without HT whose ear and hearing were normal on examination. Subjects with acute or chronic middle or the external auditory canal disease, primary disorders of the inner ear or concomitant inner ear diseases (noise-induced hearing loss, inner ear damage due to ototoxicity, etc), diabetes mellitus or dyslipidemia, a neurological or renal problem, mental retardation, primary retinal damage or pregnancy were excluded. All patients underwent a thorough ENT and general systemic examination. Systemic blood pressures were measured; routine blood tests and audiological tests (pure tone audiometry and DPOAE) were performed. The HT group also underwent fundus examination; the Scheie classification of hypertensive retinopathy was also applied to the patients. 2.1. Audiology: (250-8000 Hz) pure tone audiometry was performed using a standard audiometer (Interacoustics AC40). DPOAE measurements were performed using the Otodynamics Echoport ILO292 USB-II. Stimuli were set at 75/75dB 2pts/oct. F2/f1 was set to be 1.22 and the frequency range was from 1 to 6 kHz. 2.2. Statistical investigations: Statistical analysis was performed with the use of NCSS (Number Cruncher Statistical System) 2007 & PASS (Power Analysis and Sample Size) 2008 Statistical Software (Utah, USA). Student's t-test was used in the descriptive statistics of the data (the mean and standard deviation) as well as in the comparisons. The Chi-square test and Yates Continuity Correction and Fisher’s Exact test were used for comparisons of quantitative data. P values of less than 0.05 and 0.01 were considered to indicate statistical significance. 1. Kim GH, Youn HJ, Kang S, Choi YS, Moon JI. Relation between grade II hypertensive retinopathy and coronary artery disease in treated essential hypertensives. 2010;32(7):469-73. 2. Guidelines Subcommitte of the WHO-International Society of Hypertension.Guidelines for the Management of Hypertension.J Hypertens 1999;17:151-83 3. Wong T.Y., Shankar A., Klein R. et al. Prospective cohort study of retinal vessel diameters and risk of hypertension. BMJ 2004; 329, 79–84 4. Esparza CM, Jauregui-Renaud K, Morelos CM, Muhl GE, Mendez MN, Carillo NS, Bello NS, Cardenas M. Systemic high blood pressure and inner ear dysfunction: a preliminary study. 2007; 32(3):173-8. 5. Torre P. Jr, Cruickshanks K.J., Klein R. et al. The association between cardiovascular disease and chochlear function in older adults. J. Speech. Lang. Hear. Res. 2005; 48, 473–481 6. Kemp Dt. Stimulated Acoustic Emissions from Within the Human Auditory System. Journal of Acoustic Society of America 1978; 64:1386-1391 7. Erdem T, Ozturan O, Miman Mc: Exploration of the Early Auditory Effects of Hyperlipoproteinemia and Diabetes Mellitus Using Otoacoustic Emissions. Eur Arch Otorhinolaryngol 2003; 260(2):62-6. Epub 2002 Sep 4 8. Markova M. The cochleovestibular syndrome in hypertension. Cesk. Otolaryngol. 1990; 39, 89–97 9. Parving A., Hein H.O., Suadicani P. et al. Epidemiology of hearing disorders. Some factors affecting hearing. The Copenhagen male study. Scand. Audiol. 1993; 22, 101–107 10. Li S., Gong S., Yang Y. et al. Effect of hypertension on hearing function, LDH and ChE of the cochlea in older rats. J. Huazhong. Univ. Sci. Technolog. Med. Sci. 2003; 23, 306–309 11. Tachibana M., Yamamichi I., Nakae S. et al. The site of involvement of hypertension within the cochlea. Acta. Otolaryngol. 1984; 97, 257–265 12. Bared A, Ouyang X, Angeli S, Du LL, Hoang K, Yan D, Liu xz.: Antioxidant enzymes, presbycusis, and ethnic variability. Department of Otolaryngology, University of Miami, FL 33136, USA. 2010;143(2):263-8. Mehmet Habesoglu M.D. Umraniye Education and Research Hospital, Department of Otorhinolaryngology mhabesoglu@yahoo.com Objective: To find out the effect of systemic hypertension on 1) pure tone audiometry (PTA) 2) distortion product otoacoustic emissions (DPOAE) in adults. Material and methods: A clinical controlled prospective study was conducted between January 2011 and December 2011 at Umraniye Education and Research Hospital Otolaryngology Clinic. Thirty subjects with systemic hypertension and 30 controls were included in the study. All subjects underwent a physical exam including fundus examination, PTA and DPOAE. Results: Percentage of tinnitus in subjects with hypertension and in controls was 90% and 40% respectively (p= 0.001). PTA revealed a significantly higher sensorineural hearing loss at all frequencies above 500 Hz in the hypertensive subjects (p<0.05). In the right ear, DPOAE revealed response at 4000 and 6000 Hz in 80 and 20 %of hypertensive patients as well as 96,7 and 96,7% of the controls (p=0.103) and (p=0.001), respectively. In the left ear, DPOAE revealed response at 4000 and 6000 Hz in 73.3 and 26.7% of hypertensive patients as well as 96,7 and 93.3% of the controls (p=0.026) (p=0.001) respectively. Conclusion: Isolated hypertension affects vascular physiodynamics of cochlea and results in a hearing loss at ≥ 4000 Hz at pure tone audiometry and significant loss of distortion product otoacoustic emissions at 4000 to 6000 Hz. 3. RESULTS","PeriodicalId":312011,"journal":{"name":"The Medical Journal of Goztepe Training and Research Hospital","volume":"55 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2014-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Medical Journal of Goztepe Training and Research Hospital","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5222/J.GOZTEPETRH.2013.194","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

CONTACT Systemic hypertension causes changes in many target organs. The presence of stage-2 retinopathy detected by fundus examination is considered to be target organ damage. This damage occurs due to vascular physiodynamic changes (2). The cochlea is one of the target organs involved by HT due to its contents. Assessment of hearing as well as sounds induced by vibrations of the outer hair cells with OAE provides information about cochlear function. Conflicting results were reported by studies examining the effects of HT on the cochlea. Markov M et al delineated HT to be an important risk factor for the cochlea in the study of 50 patients with HT (8). Esparza et al. showed impairment in hearing thresholds in hypertensive patients with retinal vascular damage (4). However, Torre et al. reported no association between hypertension and sensorineural hearing loss in the DPOAE tests (5). Similarly, Parving et al. detected no relevant link between hypertension and hearing loss (9). In a study performed on 80 Wistar rats by Li S et al. it was shown that there were glycogenesis and an abnormal release of neurotransmitters caused by HT, resulting in aging of the cochlea (10). The result of the electrocochleographic tests was reported to be worse in rats with HT as compared with normotansive rats (11). In the literature, it was shown that glutathione, anti-oxidant enzyme, and Nacetyltransferase are found in the cochlea and these two enzymes are genetically scarce in presbyacusis (12). In this context, HT can lead to oxidative stress in the cochlea, thus, resulting in presbycusis. Our study has revealed that there was a significant increase of the subjective complaint of tinnitus in patients with HT compared to the control group. In pure tone audiological assessment, hearing thresholds were 33.08±13.09 and 40.85±19.83 dB at 4000 and 8000 Hz in the HT group, respectively, while 17.25±11.27 and 21.83±14.46 dB were measured in the control group, respectively. Audiometrically, a significant association appeared between presbycusis and HT in our study. The HT group had a statistically significant decrease in responses to DPOAE as compared with the control group at OAE tests performed especially at 6000 Hz frequencies. The results of our study, despite being different from those by Torre et al. were consistent with the ones by Esparza et al. In order to better understand the effect of HT on the cochlea, it is necessary to see the results of further studies on this issue in the literature. 5. Conclusion Systemic hypertension causes changes in a variety of target organs. Vascular physiodynamic changes have been implicated in HT induced target organ damage (2). The cochlea due to its contents vascular physiodynamic mechanisms is one of the target organs on which HT may have an effect. In studies performed so far, there have been conflicting results gained between HT and cochlear symptoms (4,5). Our results strongly suggest that HT can cause cochleopathologic changes, including dysfunction of outer hair cells, in cases with tinnitus, presbycusis and even in preclinical cases. The study was performed at the department of Ear, Nose and Throat Disorders of Umraniye Research and Training Hospital between January 2011 and December 2011. All patients gave their informed consent. The study included thirty patients with HT attending to our department for reasons other than hearing loss and ear diseases and thirty patients without HT whose ear and hearing were normal on examination. Subjects with acute or chronic middle or the external auditory canal disease, primary disorders of the inner ear or concomitant inner ear diseases (noise-induced hearing loss, inner ear damage due to ototoxicity, etc), diabetes mellitus or dyslipidemia, a neurological or renal problem, mental retardation, primary retinal damage or pregnancy were excluded. All patients underwent a thorough ENT and general systemic examination. Systemic blood pressures were measured; routine blood tests and audiological tests (pure tone audiometry and DPOAE) were performed. The HT group also underwent fundus examination; the Scheie classification of hypertensive retinopathy was also applied to the patients. 2.1. Audiology: (250-8000 Hz) pure tone audiometry was performed using a standard audiometer (Interacoustics AC40). DPOAE measurements were performed using the Otodynamics Echoport ILO292 USB-II. Stimuli were set at 75/75dB 2pts/oct. F2/f1 was set to be 1.22 and the frequency range was from 1 to 6 kHz. 2.2. Statistical investigations: Statistical analysis was performed with the use of NCSS (Number Cruncher Statistical System) 2007 & PASS (Power Analysis and Sample Size) 2008 Statistical Software (Utah, USA). Student's t-test was used in the descriptive statistics of the data (the mean and standard deviation) as well as in the comparisons. The Chi-square test and Yates Continuity Correction and Fisher’s Exact test were used for comparisons of quantitative data. P values of less than 0.05 and 0.01 were considered to indicate statistical significance. 1. Kim GH, Youn HJ, Kang S, Choi YS, Moon JI. Relation between grade II hypertensive retinopathy and coronary artery disease in treated essential hypertensives. 2010;32(7):469-73. 2. Guidelines Subcommitte of the WHO-International Society of Hypertension.Guidelines for the Management of Hypertension.J Hypertens 1999;17:151-83 3. Wong T.Y., Shankar A., Klein R. et al. Prospective cohort study of retinal vessel diameters and risk of hypertension. BMJ 2004; 329, 79–84 4. Esparza CM, Jauregui-Renaud K, Morelos CM, Muhl GE, Mendez MN, Carillo NS, Bello NS, Cardenas M. Systemic high blood pressure and inner ear dysfunction: a preliminary study. 2007; 32(3):173-8. 5. Torre P. Jr, Cruickshanks K.J., Klein R. et al. The association between cardiovascular disease and chochlear function in older adults. J. Speech. Lang. Hear. Res. 2005; 48, 473–481 6. Kemp Dt. Stimulated Acoustic Emissions from Within the Human Auditory System. Journal of Acoustic Society of America 1978; 64:1386-1391 7. Erdem T, Ozturan O, Miman Mc: Exploration of the Early Auditory Effects of Hyperlipoproteinemia and Diabetes Mellitus Using Otoacoustic Emissions. Eur Arch Otorhinolaryngol 2003; 260(2):62-6. Epub 2002 Sep 4 8. Markova M. The cochleovestibular syndrome in hypertension. Cesk. Otolaryngol. 1990; 39, 89–97 9. Parving A., Hein H.O., Suadicani P. et al. Epidemiology of hearing disorders. Some factors affecting hearing. The Copenhagen male study. Scand. Audiol. 1993; 22, 101–107 10. Li S., Gong S., Yang Y. et al. Effect of hypertension on hearing function, LDH and ChE of the cochlea in older rats. J. Huazhong. Univ. Sci. Technolog. Med. Sci. 2003; 23, 306–309 11. Tachibana M., Yamamichi I., Nakae S. et al. The site of involvement of hypertension within the cochlea. Acta. Otolaryngol. 1984; 97, 257–265 12. Bared A, Ouyang X, Angeli S, Du LL, Hoang K, Yan D, Liu xz.: Antioxidant enzymes, presbycusis, and ethnic variability. Department of Otolaryngology, University of Miami, FL 33136, USA. 2010;143(2):263-8. Mehmet Habesoglu M.D. Umraniye Education and Research Hospital, Department of Otorhinolaryngology mhabesoglu@yahoo.com Objective: To find out the effect of systemic hypertension on 1) pure tone audiometry (PTA) 2) distortion product otoacoustic emissions (DPOAE) in adults. Material and methods: A clinical controlled prospective study was conducted between January 2011 and December 2011 at Umraniye Education and Research Hospital Otolaryngology Clinic. Thirty subjects with systemic hypertension and 30 controls were included in the study. All subjects underwent a physical exam including fundus examination, PTA and DPOAE. Results: Percentage of tinnitus in subjects with hypertension and in controls was 90% and 40% respectively (p= 0.001). PTA revealed a significantly higher sensorineural hearing loss at all frequencies above 500 Hz in the hypertensive subjects (p<0.05). In the right ear, DPOAE revealed response at 4000 and 6000 Hz in 80 and 20 %of hypertensive patients as well as 96,7 and 96,7% of the controls (p=0.103) and (p=0.001), respectively. In the left ear, DPOAE revealed response at 4000 and 6000 Hz in 73.3 and 26.7% of hypertensive patients as well as 96,7 and 93.3% of the controls (p=0.026) (p=0.001) respectively. Conclusion: Isolated hypertension affects vascular physiodynamics of cochlea and results in a hearing loss at ≥ 4000 Hz at pure tone audiometry and significant loss of distortion product otoacoustic emissions at 4000 to 6000 Hz. 3. RESULTS
高血压患者的纯音听力学和耳声发射
全身性高血压引起许多靶器官的改变。眼底检查发现的2期视网膜病变被认为是靶器官损害。这种损伤是由于血管生理动力学的改变而发生的(2)。耳蜗因其内容物而成为HT累及的靶器官之一。听力评估以及由外耳毛细胞振动引起的声音提供了有关耳蜗功能的信息。有关HT对耳蜗影响的研究报告了相互矛盾的结果。Markov M等人在对50例HT患者的研究中发现HT是耳蜗的一个重要危险因素(8)。Esparza等人发现伴有视网膜血管损伤的高血压患者的听力阈值受损(4)。然而,Torre等人在DPOAE测试中报告高血压与感音神经性听力损失之间没有关联(5)。Parving等人未发现高血压与听力损失之间存在相关联系(9)。Li S等人对80只Wistar大鼠的研究表明,HT引起的糖生成和神经递质的异常释放,导致耳蜗老化(10)。据报道,与正常电压的大鼠相比,HT大鼠的耳蜗检查结果更差(11)。文献显示耳蜗中存在谷胱甘肽、抗氧化酶和乙酰转移酶,而这两种酶在耳聋中是遗传上缺乏的(12)。在这种情况下,HT可导致耳蜗氧化应激,从而导致老年性耳聋。我们的研究显示,与对照组相比,HT患者对耳鸣的主诉明显增加。在纯音听力学评估中,HT组在4000和8000 Hz时的听力阈值分别为33.08±13.09和40.85±19.83 dB,对照组分别为17.25±11.27和21.83±14.46 dB。在我们的研究中,从听力学角度来看,老年性耳聋和HT之间存在显著的关联。在进行的OAE测试中,特别是在6000 Hz频率下,与对照组相比,HT组对DPOAE的反应有统计学意义上的显著降低。我们的研究结果虽然与Torre等人的研究结果不同,但与Esparza等人的研究结果一致。为了更好地了解HT对耳蜗的影响,有必要在文献中看到关于这一问题的进一步研究结果。5. 结论全身性高血压引起多种靶器官的改变。HT诱导的靶器官损伤与血管物理动力学变化有关(2)。耳蜗由于其内含物的血管物理动力学机制是HT可能产生作用的靶器官之一。在迄今为止进行的研究中,在高温疗法和耳蜗症状之间获得了相互矛盾的结果(4,5)。我们的研究结果强烈提示,在耳鸣、老年性耳聋甚至临床前病例中,HT可引起耳蜗病理改变,包括外毛细胞功能障碍。该研究于2011年1月至2011年12月在乌姆拉尼耶研究和培训医院耳鼻喉疾患科进行。所有患者均给予知情同意。本研究包括30例因听力损失和耳部疾病以外的原因到我科就诊的HT患者和30例耳部和听力检查正常的非HT患者。患有急性或慢性中耳道或外耳道疾病、内耳原发疾病或伴有内耳疾病(噪声性听力损失、耳毒性内耳损伤等)、糖尿病或血脂异常、神经系统或肾脏问题、智力低下、原发性视网膜损伤或妊娠的受试者被排除在外。所有患者都进行了彻底的耳鼻喉科和全身检查。测量全身血压;进行常规血液检查和听力学检查(纯音测听和DPOAE)。HT组同时行眼底检查;高血压视网膜病变的Scheie分型也适用于患者。2.1. 听力学:使用标准听力学计(Interacoustics AC40)进行(250- 8000hz)纯音听力学。DPOAE测量使用Otodynamics Echoport ILO292 USB-II进行。刺激设置为75/75dB 2pts/oct。F2/f1设为1.22,频率范围为1 ~ 6khz。2.2. 统计调查:使用NCSS (Number Cruncher统计系统)2007和PASS(功率分析和样本量)2008统计软件(美国犹他州)进行统计分析。在数据的描述性统计(均值和标准差)以及比较中使用了学生t检验。定量资料比较采用卡方检验和Yates连续性校正及Fisher精确检验。 P值小于0.05和0.01认为有统计学意义。1. 金根荣,尹海军,姜山,崔永元,文智。原发性高血压患者II级高血压视网膜病变与冠状动脉病变的关系2010年,32(7):469 - 73。2. 世卫组织-国际高血压学会指南小组委员会。高血压管理指南。[J]; journal of chengdu electromechanical college; 2009;17(1): 59 - 64。黄天耀,尚嘉安,李立文等。视网膜血管直径与高血压风险的前瞻性队列研究。BMJ 2004;[au:] [au:]Esparza CM, Jauregui-Renaud K, Morelos CM, Muhl GE, Mendez MN, Carillo NS, Bello NS, Cardenas M.系统性高血压与内耳功能障碍的初步研究。2007;32(3): 173 - 8。5. Torre P. Jr, Cruickshanks K.J, Klein R.等。老年人心血管疾病与耳蜗功能的关系j .演讲。朗。听到的。杂志2005;48, 473-481坎普Dt。人类听觉系统的受激声发射。美国声学学会学报1978;64:1386 - 1391 7。王晓明,王晓明,王晓明:高脂蛋白血症和糖尿病早期听觉效应的研究。欧洲耳鼻喉科2003;260(2): 62 - 6。Epub 2002年9月4日高血压的耳蜗前庭综合征。Cesk。Otolaryngol。1990;39, 89-97张建军,张建军,张建军,等。听力障碍的流行病学。影响听力的一些因素。哥本哈根男性研究。Scand。Audiol。1993;22, 101-107李松,龚松,杨宇等。高血压对老年大鼠听力功能及耳蜗LDH、ChE的影响。j .华中。大学,科学。技术。医学科学,2003;23, 306-309立花M,山道I, Nakae S.等。耳蜗内高血压受累的部位学报。Otolaryngol。1984;97, 257-265刘晓明,李建军,李建军,李建军,刘建军。抗氧化酶、老年性耳聋和种族差异。美国迈阿密大学耳鼻咽喉科,佛罗里达331362010年,143(2):263 - 8。Mehmet Habesoglu md . Umraniye教育与研究医院耳鼻咽喉科mhabesoglu@yahoo.com目的:探讨全身性高血压对成人纯音听力学(PTA)畸变产物耳声发射(DPOAE)的影响。材料和方法:2011年1月至2011年12月在Umraniye教育和研究医院耳鼻喉科诊所进行了一项临床对照前瞻性研究。30名全身性高血压患者和30名对照组纳入研究。所有受试者均进行了眼底检查、PTA和DPOAE检查。结果:高血压组和对照组耳鸣发生率分别为90%和40% (p= 0.001)。PTA显示高血压患者500hz以上所有频率的感音神经性听力损失显著增加(p<0.05)。右耳DPOAE在4000 Hz和6000 Hz时有应答的高血压患者分别为80%和20%,对照组分别为96%、7%和96.7% (p=0.103)和(p=0.001)。左耳DPOAE在4000 Hz和6000 Hz时有应答的高血压患者分别为73.3%和26.7%,对照组分别为96.6%、7%和93.3% (p=0.026) (p=0.001)。结论:孤立性高血压影响耳蜗血管物理动力学,导致纯音听力≥4000 Hz的听力损失和4000 ~ 6000 Hz的畸变产物耳声发射的显著损失。结果
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