Home Email this page Print this page Bookmark this page Decrease font size Default font size Increase font size
Noise & Health  
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Email Alert *
Add to My List *
* Registration required (free)  

   Materials and me...
   Article Figures
   Article Tables

 Article Access Statistics
    PDF Downloaded25    
    Comments [Add]    
    Cited by others 1    

Recommend this journal


  Table of Contents    
Year : 2020  |  Volume : 22  |  Issue : 106  |  Page : 70-76
The effects of hyperinsulinemia on cochlear functions

1 Department of Internal Medicine, Başkent University Ankara Hospital, Ankara, Turkey
2 Department of Otorhinolaryngology, Başkent University Ankara Hospital, Ankara, Turkey
3 Department of Endocrinology and Metabolism, Başkent University Ankara Hospital, Ankara, Turkey

Click here for correspondence address and email
Date of Submission20-Jun-2020
Date of Decision24-Jul-2020
Date of Acceptance02-Oct-2020
Date of Web Publication31-Dec-2020

Context: Hyperinsulinemia is the most common metabolic change associated with cochleovestibular diseases. Aim: We aimed to investigate the auditory functions in hyperinsulinemic individuals. Settings and Design: A total of 164 patients were included in this case-control study. While 76 patients with insulin resistance (homeostasis model assessment of insulin resistance [HOMA-IR] of ≥2.5) constituted the case group, 88 patients with HOMA-IR values of <2.5 constituted the control group of the study. Material and Methods: The 75 g oral glucose tolerance test, blood biochemistry tests, hormonal analysis, audiological assessment, electrocochleography (EcochG), and transient evoked otoacoustic emissions (TEOAE) testing were performed. Statistical Analysis: One-way analysis of variance and Kruskal–Wallis analysis of variance were used for the comparison of the metabolic and ear parameters in the normal glucose tolerance (NGT), impaired fasting glucose (IFG), and impaired glucose tolerance (IGT) groups. The chi-square test was used to compare nominal variables. Spearman and Pearson correlation coefficients were used for the correlation analyses of continuous variables. Results: The pure tone audiometry at 0.5, 1, 2, and 4 kHz was better in the case group than in the control group. A positive correlation was found between HbA1c and right ear 0.5, 1, 4, and 8 kHz threshold values and left ear 2, 4, 6, and 8 kHz threshold values. A negative correlation was found between HbA1c and speech discrimination scores. The right ear 1.00 and 2.83 kHz TEOAE measurements in the individuals with NGT were found higher than those in patients with IGT, and the 1.42 kHz TEOAE measurements and reproducibility were found higher than those in patients with IFG. The left ear 1.00 and 1.42 kHz TEOAE measurements of the IGT patients were found lower than those of IFG and NGT patients. Conclusion: We showed that hearing was worsening in hyperinsulinemic patients and prediabetic conditions were related to hearing function impairment.

Keywords: Audiometry, Cochlea, HbA1c, hyperinsulinemia, prediabetes

How to cite this article:
Or Koca A, Koca HS, Anil C. The effects of hyperinsulinemia on cochlear functions. Noise Health 2020;22:70-6

How to cite this URL:
Or Koca A, Koca HS, Anil C. The effects of hyperinsulinemia on cochlear functions. Noise Health [serial online] 2020 [cited 2023 Dec 6];22:70-6. Available from: https://www.noiseandhealth.org/text.asp?2020/22/106/70/305703

  Introduction Top

Insulin resistance (IR) is generally defined as a decreased response to normal insulin concentrations. In clinical practice, it is considered as a low glucose response at a certain insulin concentration (endogenous or exogenous).[1],[2] Significant long-term results of IR are the development of type 2 diabetes mellitus (type 2 DM), cardiovascular diseases, obesity, and several malignancies related to IR (colon, breast, endometrial cancers, etc.).[3] Prediabetes has clinical significance in predicting the progression to type 2 diabetes and in detection and prevention of diabetic and prediabetic complications.

It was reported that 82% of patients with tinnitus complaints had a history of a glycemic disorder and hyperinsulinemia. Acute hyperinsulinemia causes cochlear function impairment related to the decrease in Na-K ATPase activity at the stria vascularis of the cochlea, with endocochlear potential loss.[4] Therefore, it is asserted that undiagnosed hearing loss is highly probable in prediabetic hyperinsulinemic individuals.[5] Hyperinsulinemia and hyperglycemia are the metabolic changes with the highest positive predictive value (96%) in cochleovestibular diseases.[6],[7]

Four basic extracellular potentials exist in the cochlea, which is situated in the inner ear and responsible for hearing: endolymphatic (endocochlear) potential, cochlear microphonics, summation potential (SP), and compound nerve action potential (AP). The electrocochleography (EcochG) test, used for monitoring the cochlea and cochlear nerve, can measure three potentials: cochlear microphonic, SP, and AP.[5]

Pure tone audiometry is the most frequently used testing technique in measuring hearing sensitivity. With this technique, the type of hearing loss and the frequencies of hearing loss varying between 250 and 8000 Hz can be determined routinely. There are three types of hearing loss: sensorineural, conductive, and mixed, as a combination of the first two. The impairment of the mechanisms involved in the formation of endolymph or endolymphatic potential due to aging or metabolic causes may result in hearing loss and this is called metabolic hypoacusis.[5]

Otoacoustic emission is defined as the acoustic energy produced by the outer hair cells with active movement in the organ of Corti. Otoacoustic emissions may be recorded spontaneously or evoked.[7] It has been determined that there is a decrease in the otoacoustic emission measurements of type 2 diabetics with hyperinsulinemia.

In this study, we aimed to investigate the effects of hyperinsulinemia, which is the early stage of type 2 diabetes, on inner ear functions using pure tone audiometry, transient evoked otoacoustic emission (TEOAE), and EcochG tests.

  Materials and methods Top

This research was designed as a prospective case-control, single-blind clinical study. Among the patients who had been admitted to the outpatient clinics of the Department of Endocrinology and Metabolism of the Başkent University Faculty of Medicine between May 2015 and March 2016, 76 consecutive patients between 18 and 64 years of age with IR [homeostasis model assessment of insulin resistance (HOMA-IR) value of ≥2.5] were enrolled in the case group, and 88 patients with HOMA-IR of <2.5 constituted the control group.

HOMA-IR was calculated using the following formula: [fasting plasma glucose (mg/dL) × fasting insulin level (μU/mL)]/405. Levels of ≥2.5 indicate IR.[8],[9],[10]

The patients were grouped as having normal glucose tolerance (NGT), impaired fasting glucose (IFG), impaired glucose tolerance (IGT), and DM with regard to their responses to the oral glucose tolerance test (OGTT). IFG was defined as fasting blood glucose (FBG) levels between 100 and 125 mg/dL, and IGT was defined as blood glucose levels between 140 and 199 mg/dL 2 hours after administering 75 g of oral glucose.[8] Patients who had levels of HbA1c of ≥6.5% or in the 75 g OGTT, patients with FBG levels of ≥126 mg/dL, and those with second-hour plasma glucose levels of ≥200 mg/dL after confirmation with repeat testing were diagnosed with DM.[9]

Patients with a history of hypertension, thyroid dysfunction, DM, chronic kidney disease, autoimmune or organic hearing loss, Meniere disease, neurodegenerative disorder, history of ear surgery, anatomic ear disorders, noise exposure, hematological or solid organ malignancy, or use of metformin or any other drugs with the potential to influence IR in the last 6 months were not included in the study.

Height, body weight, waist circumference, and right and left arm blood pressure measurements were performed via standard methods by the same physician and recorded. The body mass indices were calculated by dividing body weight (kg) by the square of height (m). Blood pressure was measured with a wall-mounted mercury sphygmomanometer device while the patients were in a sitting position after 30 minutes of resting. Blood pressure measurements were carried out on both arms with 10 minutes between the two measurements. Patients with average blood pressure of 140/90 mmHg or higher were excluded from the study.

Biochemical examination

Blood samples were collected from all patients between 08:00 and 10:00 after 8 to 12 hours of fasting. FBG, fasting serum insulin, HbA1c, creatinine, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, triglyceride, thyroid-stimulating hormone (TSH), and free thyroxin (sT4) levels were measured. The patients then consumed 75 g of oral glucose solution and blood samples were taken 30, 60, and 120 minutes later for plasma glucose and insulin levels.

Glucose, creatinine, direct LDL, ultra HDL, and triglyceride kits were processed with the Abbott Architect c8000 device and free T4, TSH, and insulin kits were processed with the Abbott Architect i2000 device. The HbA1c kit was processed immunoturbidimetrically with the Abbott Architect c4000 device (Abbott®, Wiesbaden, Germany).

Audiological assessment

Pure tone audiometry, EcochG, and TEOAE tests were performed for all of the patients.

Pure tone air conduction (TDH-39P) and bone conduction audiometry at 125, 250, 500, 1000, 2000, 4000, 6000, and 8000 Hz were tested for all patients, as well as speech audiometry (AC 40, Interacoustics, Assens, Denmark). The speech recognition thresholds of the patients and speech discrimination test scores were assessed. The pure tone averages of 500, 1000, and 2000 Hz frequencies were calculated. Patients diagnosed with conductive hearing loss were excluded from the study.

The otoacoustic emission measurements were elicited by presenting nondirectional stimulus at 1.00, 1.42, 2.00, 2.83, and 4.00 kHz (Titan IMP440, Interacoustics, Assens, Denmark).

Among the otoacoustic emission measurements, those with reproducibility rates above 70 were considered significant.[7] The signal-to-noise ratio (SNR) values for both ears were included in the assessment.

EcochG (Audera, GSI, Eden Prairie, MN, USA) measurements were elicited by presenting a 95 dB nHL click stimulus with an external auditory canal electrode (gold tip trode electrode, 10 mm, Sanibel Supply, Assens, Denmark). Patients with SP, or AP ratios of ≥0.50, were considered to have cochlear hydrops, while individuals with ratios of <0.50 were considered normal.[5]

Statistical analysis

In the descriptive statistics for the continuous data, the mean, standard deviation, median, and minimum and maximum values were presented, and percentage values were presented for discrete data.

For the comparison of data obtained via measurements between case and control groups, the conformity of the data to normal distribution was tested using the t test and the Mann–Whitney U test.One-way analysis of variance and Kruskal–Wallis analysis of variance were used for the comparison of the metabolic and ear parameters in the NGT, IFG, and IGT groups.The chi-square test was used to compare nominal variables. Spearman and Pearson correlation coefficients were used for the correlation analyses of continuous variables.

For the assessment of differences among nominal variables (sex, glucose, 60th minute glucose, and NGT/IFG/IGT), the t test, Mann–Whitney U test, Kruskal–Wallis analysis of variance, and one-way analysis of variance were used.

SPSS 11.5 software (SPSS Inc., Chicago, IL, USA) was used for the calculations and P < 0.05 was considered as the limit for statistical significance.

  Results Top

A total of 185 patients were initially included in the study. Twenty-one patients were excluded (11 patients were diagnosed with DM, five patients had conductive hearing loss, five patients were lost to follow up for audiologic examination), 76 patients (46.3%) with HOMA-IR levels equal to or higher than 2.5 constituted the case group, and 88 patients (53.7%) with HOMA-IR levels below 2.5 constituted the control group.

There were 39 women in the case group and 56 women in the control group. The sex distributions of the case and control groups were similar (P = 0.11). It was found that 96.1% of the individuals in the case group and 98.9% of the control group were younger than 60 years. The mean age was 38.51 ± 10.28 years for the case group and 38.81 ± 9.40 for the control group (P > 0.05). Furthermore, 87.5% of the individuals in the control group and 81.7% in the case group were younger than 50 years. Ages of 50% of the individuals in the control group and 59.3% in the case group were under 40 years [Figure 1].
Figure 1 Comparison of right ear pure tone audiometry results of all patients with NGT, IFG and IGT. IFG, impaired fasting glucose; IGT, impaired glucose tolerance; NGT, normal glucose tolerance

Click here to view

The mean waist circumference, body mass index, HbA1c, LDL, and triglyceride levels were determined to be higher in the case group compared to the control group, and the mean HDL level was lower [Table 1].
Table 1 Comparison of the biochemical parameters of the case and control groups

Click here to view

The number of patients with first-hour post-glucose load plasma glucose level of ≥155 mg/dL was higher in the case group than the control group [Table 1].

A statistically significant difference was found between hearing levels in the groups for the right ear at 500, 1000, 2000, and 4000 Hz and for the left ear at 500, 1000, 2000, 4000, and 8000 Hz (for the right ear P < 0.001, P = 0.002, P = 0.001, and P = 0.006, respectively, and for the left ear P < 0.001, P = 0.003, P = 0.001, P < 0.001, and P = 0.044, respectively). Hearing levels (dBHL) were found lower in the case group than the control group. However, there was no significant difference in speech discrimination scores between the case and control groups (P > 0.05).

EcochG test findings showed no significant difference between groups. For the right ear, the SP/AP ratios were equal to or higher than 0.5 for 18.4% of the individuals in the case group and 15.9% in the control group, and for the left ear for 14.5% in the case group and 15.9% in the control group, respectively (P > 0.05).

In all patients, a positive correlation was detected between HbA1c levels and hearing levels for the right ear at 500, 1000, 4000, and 8000 Hz and for the left ear at 2000, 4000, 6000, and 8000 Hz (for the right ear r = 0.155 and P = 0.048, r = 0.159 and P = 0.043, r = 0.249 and P = 0.001, and r = 0.179 and P = 0.022, respectively, and for the left ear r = 0.192 and P = 0.014, r = 0.319 and P = 0.004, r = 0.226 and P = 0.004, and r = 0.159 and P = 0.042, respectively). A negative correlation was found between HbA1c levels and the speech discrimination scores for the right and the left ears (r = –0.219 and P = 0.005; r = –0.251 and P = 0.001).

Patients with NGT were found to have higher TEOAE measurements for the right ear at 1.00 and 2.83 kHz than the patients with IGT and higher TEOAE measurements at 1.42 kHz and higher reproducibility scores than the patients with IFG (P = 0.013, P = 0.035, P = 0.031, and P = 0.004, respectively).

Patients with IGT were determined to have lower TEOAE measurements for the left ear at 1.00 kHz than the patients with IFG and NGT and lower TEOAE measurements at 1.42 kHz than the IFG and NGT patients (P = 0.004 and P = 0.006, respectively).

The right ear 1000 and 4000 Hz audiometry thresholds of patients with NGT were found to be significantly lower than those of the patients with IFG (P < 0.05), and the 6000 and 8000 Hz threshold values were found to be significantly lower than those of the patients with IGT (P < 0.001).

The left ear 250 and 4000 Hz audiometry threshold values of patients with NGT were detected to be significantly lower than those of the patients with IFG and IGT (P < 0.05), whereas the 2000, 6000, and 8000 Hz threshold values were significantly lower than those of the patients with IGT (P < 0.05) [Figure 2]. The left ear speech discrimination scores of the patients with NGT were lower than the scores of the patients with IGT (P < 0.05).
Figure 2 Comparison of left ear pure tone audiometry results of all patients with NGT, IFG, and IGT. IFG, impaired fasting glucose; IGT, impaired glucose tolerance; NGT, normal glucose tolerance

Click here to view

  Discussion Top

In our study, it was shown that the hearing levels at 0.5 to 8 kHz frequencies among patients with NGT were lower than the levels of patients with IFG and IGT. Similarly, it was found that the NGT group scored better in the TEOAE testing than the prediabetes groups did (IFG and IGT). Moreover, these differences were also present when the parameters were considered separately for both ears and for both groups of patients.

In our study, no significant difference between the case and control groups could be attributed to sex distribution or average age, and a homogeneous distribution was obtained. Only four patients (three from the case group and one from the control group) included in the study were older than 60 years. In order to determine whether these four patients had age-related presbycusis, the pure tone averages for both ears of those patients were compared to the ISO (International Organization for Standardization) 7029 standard values for the age range of 60-64 years and they were found to be below the median values; thus, any suspicion of presbycusis was eliminated.[11] Horikawa et al.[12] showed that the prevalence of hearing loss is 2.1 times higher in diabetic individuals than nondiabetics. It is known that aging plays a role in the development of both DM and hearing impairment. The possibility of aging affecting hearing functions should not be overlooked. However, their review supported the idea that diabetes-related hearing loss is independent of aging.[12] Our study was conducted with a relatively young to middle-aged group and showed that hearing function impairments developed in prediabetic individuals independently of aging.

The results of another review indicated that type 2 DM had a substantial relation with hearing loss. However, the contribution of DM to moderate and severe hearing loss could not be clarified.[13] This is an important issue since mild hearing loss does not require any aggressive clinical treatment, contrary to moderate and severe hearing loss. However, the mild hearing loss observed in diabetes might easily deteriorate due to external factors such as noise exposure. If prediabetes is effective in the loss of hearing functions, it should be determined, the required precautions should be taken, and hearing functions should be checked periodically.

Fowler et al.[14] showed in a study of monkeys that hearing functions were reduced in hyperinsulinemia, which is a prediabetic stage. In our study, the auditory brainstem response (BERA) test was not conducted. Audiological assessment was performed at 250 and 500 Hz and 1, 2, 4, 6, and 8 kHz frequencies; speech discrimination tests were administered for auditory perception; and TEOAE testing was conducted for assessing outer hair cell functions. It was found that hyperinsulinemia particularly affected the pure tone audiometry results, and the SNR values in TEOAE for the right and left ears showed similarity between the case and control groups. However, when the TEOAE measurements were examined in three separate groups with regard to glycemic level among the hyperinsulinemic group as NGT, IFG, and IGT, it was observed that the cochlear outer hair cell function loss was significantly higher in individuals with dysglycemic conditions accompanying hyperinsulinemia.

Angeli et al.[15] investigated the effect of acute hyperinsulinemia on the cochlea in sheep and showed with EcochG that cochlear functions were inhibited in hyperinsulinemia. In another study examining the effects of acute hyperinsulinemia in sheep with distortion product otoacoustic emission (DPOAE) testing, it was demonstrated that hyperinsulinemia was effective in cellular electrophysiology even in the acute phase, even though it had not been long enough to cause endolymphatic hydrops.[16] In our study, on the other hand, the cochlear functions were investigated in subjects with prediabetic conditions and hyperinsulinemia together with NGT. The case and control groups were compared in both an intragroup and an intergroup manner, but no difference was found in the electrocochleographic examination for both right and left ears. The hearing function impairment observed at frequencies above 1500 Hz in hyperinsulinemia was supported with pure tone audiometry in our study.

In the present study, the HbA1c value and pure tone audiometry thresholds were compared to examine any possible effect of chronic hyperinsulinemia on cochlear functions. Positive correlations were found between HbA1c and the measurements at 500, 1000, 4000, and 8000 Hz for the right ear and the measurements at 2000, 4000, 6000, and 8000 Hz for the left ear. It was shown that the thresholds at 4000, 6000, and 8000 Hz in pure tone audiometry for both right and left ears had increased significantly in individuals with HbA1c of ≥5.7%. When these data and the International Expert Committee classification on HbA1c are taken as a basis, it can be argued that the increase is more significant in hearing thresholds in pure tone audiometry in individuals with high potential for diabetes development.[17] Similar to our results, in a study by Kang et al.,[18] an increased risk of hearing loss was shown in the group with moderate and high HbA1c levels compared to the group with low HbA1c levels using pure tone audiometry. In 2008, Hirose[19] claimed that high concentrations of glucose in the endolymph, through diffusion related to the elevated plasma glucose levels, would cause cochlear impairment. Contrary to our study, they reported HbA1c to be the parameter showing the weakest correlation with hearing thresholds.

In the study of Hong and Kang[20] on mice, although there was hearing nerve dysfunction related to hyperglycemia, it was found that there was also functional impairment in central auditory pathways and cochlear outer hair cells due to IR-induced hyperinsulinemia in type 2 DM In our study, TEOAE testing was conducted to test the outer hair cell functions. However, BERA and central auditory pathway assessments were not conducted separately. Instead, the sensorial and neural pathways were assessed together using pure tone audiometry. Speech discrimination scores were used in the suprasegmental assessment of hearing. In particular, the comparisons on the basis of HbA1c levels demonstrated that the speech discrimination scores for both ears were significantly lower in the case group than the control group. Accordingly, it may be interpreted that the chronic effects of dysglycemic conditions may affect the central auditory processing and perception negatively. This needs to be proved with studies using objective central pathway assessment tests.

When all patients were grouped as NGT, IFG, and IGT and their EcochG-SP/AP measurements were considered, no differences were detected for either the right or the left ear. Similarly, there was no difference among NGT, IFG, and IGT groups with regard to the <0.50 and ≥0.50 limit values of the EcochG-SP/AP ratio for the left and right ears. It is known that EcochG measurements using external auditory canal electrodes do not yield reliable results. The EcochG method has low sensitivity in SP/AP ratio assessment and especially high specificity in cochlear hydrops diagnosis.[21] The contribution of EcochG is probably limited in indicating metabolic cochlear disease, unless cochlear hydrops has developed, and based on our findings, we believe that it is not beneficial to use it as a cochlear imaging test in hyperinsulinemia, one of the early diabetic stages.In our study, the chronic effects of hyperglycemia and hyperinsulinemia on the cochlea were presented. It was shown by Ryu et al.[22] that hyperglycemia could have an effect on the recovery of sudden idiopathic hearing loss. In this study, with a design similar to ours, the comparative assessment of individuals with impaired glucose disturbances such as prediabetic conditions and diabetes revealed significantly better treatment responses in the normoglycemic group.[22]

In a study by Horner[23] of induced hydrops in guinea pigs, effects on outer hair cells were seen at the apical turn of the cochlea and caused separation in neural connections, but the outer hair cells at the basal turn of the cochlea were intact. This could be explained by the cochlea protecting its basal turn, where more medial fibers end. The results of that study show similarities to the results of our study, and the elevated impairment especially in the medium frequencies in the audiological assessment in our study could be explained by this mechanism.

The female predominance of our study population may imply that the study represented men less. Due to the limited number of participants (n = 164), the validation of the findings of our study with larger populations would contribute to the generalizability of the data obtained. The balanced age distribution in the case and control groups, the exclusion of patients with hypertension, and the enrollment of a generally younger population enabled us to remove possible confounders and thus probably increased the reliability of the results.

Although the sensorial cell and cochlear neuron loss observed at the basal coil of the cochlea due to age-related hearing loss lowers the reliability of studies with older diabetic patients, age-related presbycusis was eliminated in our study by including patients based on the international standards for presbycusis thresholds. Therefore, we think that the reliability of pure tone audiometry is high in our study.

The euglycemic insulin clamp technique, the gold standard method for calculating IR, was not used in the present study due to difficulties in practicability. This might have influenced the sensitivity and authenticity of the results obtained.

Administration of EcochG as the only electrophysiological assessment limits the possibility of supporting our study with more objective data. The EcochG test plays an important role in the differential diagnosis of endolymphatic hydrops and metabolic ear diseases, and the difference found between the case group and the control group in our study supported this fact. However, the EcochG test could not provide sufficient information as it is not certain whether metabolic exposure could cause hydrops or not.

Although high-frequency audiometry was not performed in our study, significant findings were obtained in the 1.125 to 8 kHz range in hyperinsulinemic and especially dysglycemic individuals. Also, since acoustic trauma exposure, especially exposure over 4 kHz, would decrease the strength of the study, patients with unilateral hearing loss and with noise exposure history were excluded and this risk was reduced substantially.

Although the audiological assessments were conducted under optimal conditions for all patients, the administration of the TEOAE and EcochG measurements in a room without sound isolation decreased the reliability of these tests. The TEOAE testing was preferred instead of DPOAE in our study since it is a practice in clinical studies.

  Conclusion Top

Our study shows that prediabetic conditions (IFG and IGT) are associated with hearing function impairment before hearing loss occurs.

In dysglycemic conditions, the TEOAE, pure tone audiometry, and speech discrimination scores yield significant findings, and they can be used clinically for hearing screening in prediabetic patient groups.

Strategies intended to reduce hyperinsulinemia and to prevent diabetes may help to ameliorate hearing dysfunctions, and it is seen that further studies in this respect are required.

This research was funded by the Başkent University Clinical Research Fund.

This study was approved with Decision No. 15/18 dated 08/05/2015 by the Başkent University Faculty of Medicine’s Clinical Research Ethics Committee (Project No: KA15/124).

Ethical Approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Declaration of Helsinki and its later amendments or comparable ethical standards.

Informed Consent

Oral and written informed consent was obtained from all individual participants included in the study.

Data Availability Statement

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

  References Top

Kahn CR, Rosenthal AS. Immunologic reactions to insulin: insulin allergy, insulin resistance, and the autoimmune insulin syndrome. Diabetes Care 1979;2:283-95.  Back to cited text no. 1
Esteghamati A, Ashraf H, Khalilzadeh O, Zandieh A, Nakhjavani M, Rashidi A et al. Optimal cut-off of homeostasis model assessment of insulin resistance (HOMA-IR) for the diagnosis of metabolic syndrome: third national surveillance of risk factors of non-communicable diseases in Iran (SuRFNCD-2007). Nutr Metab (Lond) 2010;7:26.  Back to cited text no. 2
McLaughlin T, Abbasi F, Cheal K et al. Use of metabolic markers to identify overweight individuals who are insulin resistant. Ann Intern Med 2003;139:802.  Back to cited text no. 3
Mangabeira Albernaz PL, Fukuda Y. Glucose, insulin and inner ear pathology. Acta Otolaryngol 1984;97:496-501.  Back to cited text no. 4
Mills JH, Khariwala SS, Weber PC. İşitmenin Anatomi ve Fizyolojisi. In: Bailey BJ, Johnson JT, Newlands SD, (Eds). Baş Boyun Cerrahisi-Otolarengoloji. 4. Baskı, Ankara, Türkiye: Lippincott Williams & Wilkins; 2011. pp. 1883-1903.  Back to cited text no. 5
Elbarbary NS, El-Kabarity RH, Desouky ED. Cochleopathy in Egyptian adolescents with type 1 diabetes mellitus. Int J Pediatr Otorhinolaryngol 2012;76:1558-64.  Back to cited text no. 6
Hall JW. Handbook of Otoacoustic Emissions. San Diego, CA: Singular Publishing Group; 1999. p. 245.  Back to cited text no. 7
Abdul-Ghani MA, DeFronzo RA. Pathophysiology of prediabetes. Curr Diab Rep 2009;9:193-9.  Back to cited text no. 8
American Diabetes Association. Standards of medical care in diabetes 2015. Diabetes Care 2015;38:S8-16.  Back to cited text no. 9
American Diabetes Association. Classification and diagnosis of diabetes: standards of medical care in diabetes-2018. Diabetes Care 2018;41(Suppl 1):S13-27.  Back to cited text no. 10
Stenklev NC, Laukli E. Presbycusis-hearing thresholds and the ISO 7029. Int J Audiol 2004;43:295-306.  Back to cited text no. 11
Horikawa C, Kodama S, Tanaka S, Fujihara K, Hirasawa R, Yachi Y et al. Diabetes and risk of hearing impairment in adults: a meta-analysis. J Clin Endocrinol Metab 2013;98;51-58.  Back to cited text no. 12
Olubunmi V, Akinpelu XX. Is type 2 diabetes mellitus associated with alterations in hearing? A systematic review and meta-analysis. Laryngoscope 2014;124:767-76.  Back to cited text no. 13
Fowler CG, Chiasson KB, Colman RJ, Kemnitz JW, Beasley TM, Weindruch RH. Hyperinsulinemia/diabetes, hearing, and aging in the University of Wisconsin calorie restriction monkeys. Hear Res 2015;328:78-86.  Back to cited text no. 14
Roberto Dihl Angeli, Luiz Lavinsky, Alexandre Dolganov. Alterations in cochlear function during induced acute hyperinsulinemia in an animal model. Braz J Otorhinolaryngol 2009;75:760-4.  Back to cited text no. 15
Francisco Carlos Zuma e Maia, Luiz Lavinsky. Distortion product otoacoustic emissions in an animal model of induced hyperinsulinemia. Int Tinnitus J 2006;12:133-9.  Back to cited text no. 16
Lipska KJ, De Rekeneire N, Van Ness PH, Johnson KC, Kanaya A, Koster A et al. Identifying dysglycemic states in older adults: implications of the emerging use of hemoglobin A1c. J Clin Endocrinol Metab 2010;95:5289-95.  Back to cited text no. 17
Kang SH, Jung da J. Association between HbA1c level and hearing impairment in a nondiabetic adult population. Metab Syndr Relat Disord 2016;14:129-134.  Back to cited text no. 18
Hirose K. Hearing loss and diabetes: you might not know what you’re missing. Ann Intern Med 2008;149:54-55.  Back to cited text no. 19
Bin Na Hong, Tong Ho Kang. Distinction between auditory electrophysiological responses in type 1 and type 2 diabetic animal models. Neurosci Lett 2014;566:309-14.  Back to cited text no. 20
Won-Ho Chung, Do-Yeon Cho. Clinical usefulness of extratympanic electrocochleography in the diagnosis of Ménie‘re’s disease. Otol Neurotol 2004;25:144-9.  Back to cited text no. 21
Ryu OH, Choi MG, Park CH, Kim DK, Lee JS, Lee JH. Hyperglycemia as a potential prognostic factor of idiopathic sudden sensorineural hearing loss. Otol Neurotol 2014;150:853-8.  Back to cited text no. 22
Horner CK. Hypersensitivity of hydropic ears, at frequencies with normal thresholds, to temporary threshold shifts. Hear Res 1990;48:281-6.  Back to cited text no. 23

Correspondence Address:
Arzu Or Koca
Keçiören Health Administration and Research Center, Department of Endocrinology and Metabolism, Kuşcağız, 06010, Keçiören, Ankara
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/nah.NAH_41_20

Rights and Permissions


  [Figure 1], [Figure 2]

  [Table 1]

This article has been cited by
1 Sex-specific associations between diabetes mellitus and hearing loss in the middle-aged and elderly: a national cohort study of Chinese adults
Weiwei Wang, Chen Zhang, Ruogu Meng, Siyan Zhan, Shengfeng Wang, Lei Feng, Yongfeng Song
Endocrine Practice. 2022;
[Pubmed] | [DOI]