Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2017 Apr 1.
Published in final edited form as: Am J Med. 2015 Nov 30;129(4):416–422. doi: 10.1016/j.amjmed.2015.11.014

Hypertension, Diuretic Use, and Risk of Hearing Loss

Brian M Lin a,b,f, Sharon G Curhan b,f, Molin Wang b,c,d, Roland Eavey g, Konstantina M Stankovic a,f, Gary C Curhan b,c,e,f
PMCID: PMC4792671  NIHMSID: NIHMS748813  PMID: 26656761

Abstract

Background

Hearing loss is highly prevalent among adults in the United States. Hypertension is also common and is often treated with diuretics. Hypertension may increase the risk of hearing loss by decreasing vascular supply to the stria vascularis. Use of thiazides has been anecdotally associated with hearing loss. In small studies, furosemide use has been associated with hearing loss that is usually reversible, but can be permanent. We investigated the relation between hypertension, diuretic use, and hearing loss in a prospective cohort of 54,721 women in Nurses’ Health Study I (NHSI), 1994–2012.

Methods

Eligible participants included 54,721 female nurses aged 48–73 years in 1994 who provided information on thiazide diuretic and furosemide use in 1994, answered the question on hearing loss over their lifetime in 2012, and did not report hearing loss with date of onset before date of onset of hypertension diagnosis or medication use. The outcome was self-reported hearing loss. Cox proportional hazards regression was used to adjust for potential confounders.

Results

During 774,096 person-years of follow-up, 19,296 cases of hearing loss were reported (incidence rate: 25 cases per 1000 person-years). At baseline in 1994, the mean age was 57.9 years and mean body mass index was 26.3 kg/m2. 30.8% of participants had a history of hypertension. History of hypertension was independently associated with a modestly higher risk of hearing loss (multivariable adjusted relative risk = 1.04 [1.01, 1.07]). Among women with a history of hypertension, neither thiazide diuretic (multivariable adjusted relative risk = 1.07 [0.99, 1.16]) nor furosemide use (multivariable adjusted relative risk = 0.91 [0.75, 1.09]) was significantly associated with risk of hearing loss, when compared with women not taking anti-hypertensive medications. There was no significant effect modification by age.

Conclusions

History of hypertension was associated with a small increased risk of hearing loss. Thiazide diuretic use and furosemide use were not associated with risk of hearing loss among women with a history of hypertension.

Keywords: Hearing loss, hypertension, thiazide diuretics, furosemide, prospective study

INTRODUCTION

Hearing loss is highly prevalent in adults in the United States. Approximately one-third of women in their fifties and approximately two-thirds of women in their sixties have hearing loss 1. As the life expectancy of individuals has increased, so has the prevalence of age-related hearing loss 2. Hearing loss can be disabling, therefore, identification of potential modifiable risk factors is an important public health issue 3, 4.

Hypertension is also common in the United States, and affects approximately 35% of women in their forties and fifties, and more than 65% of women older than sixty-five years of age 5. Hypertension may increase the risk of hearing loss via decreased vascular supply to the stria vascularis 7. However, current evidence regarding the relation between hypertension and risk of hearing loss is inconsistent, with cross-sectional studies suggesting a positive association 1, 8, and a prospective study suggesting no association 9.

The Joint National Committee (JNC) recommends thiazide diuretics as initial drug therapy for patients with uncomplicated hypertension 10. The relation between thiazides and hearing loss is largely anecdotal, with no published reports in the literature. Thus, the mechanism by which thiazides may alter hearing is unclear.

In small studies, furosemide use has been associated with sudden sensorineural hearing loss that is usually reversible but can be permanent 1113. The hearing loss is more likely to occur following intravenous drug administration but can also occur after oral dosing 11, 13. The mechanism by which furosemide may cause hearing loss in humans is unclear. Rodent models have shown that furosemide causes dysfunction of the stria vascularis, resulting in reduced endocochlear potential 1418. Chronically impaired endocochlear potential has been shown to reduce auditory nerve activity, thereby impairing hearing 19.

Although hypertension and diuretic use are common, the relation between hypertension, diuretic use, and hearing loss has not been prospectively studied in women. Therefore, we investigated the relation between hypertension, use of thiazide diuretics and furosemide, and hearing loss in a prospective cohort of 54,721 women in the Nurses’ Health Study I (NHS I). We also compared use of thiazide diuretics and furosemide with use of other hypertensive medications among hypertensive women to examine the relation between different hypertensive medications and risk of hearing loss.

MATERIALS AND METHODS

Study Participants

The Nurses Health Study I (NHS I) is a cohort of 121,700 female nurses aged 30–55 years when enrolled in 1976. Questionnaires are administered every 2 years, with an average follow-up rate of more than 90% of the eligible person-time. Participants were asked in 2012, “Do you have a hearing problem?” and, if so, “At what age did you first notice a change in your hearing?”. Of the 63,966 women who answered the long-form questionnaire in 2012, 47% reported having a hearing problem. We excluded women who reported a hearing problem that began before 1994 (baseline year of our study), those who had a history of non-melanoma skin cancer due to potential exposure to chemotherapeutic agents that can be ototoxic. After excluding these participants, our study population was 54,721 women.

Ascertainment of hypertension

On the 1976 questionnaire and every 2 years thereafter, participants were asked whether a clinician had diagnosed them as having high blood pressure. Self-reported hypertension has been shown to be highly reliable in this cohort of women 20. We classified women who answered, “yes” to this question as having a history of hypertension from that time onwards.

Ascertainment of medication use

In 1994 and every two years thereafter, information on regular use of thiazide diuretics, furosemide, calcium channel blockers, and beta-blockers was obtained. In 1996, use of angiotensin-converting-enzyme inhibitors was first ascertained. We considered women who answered “yes” to have taken the indicated medication for the previous two years.

Ascertainment of hearing loss

The outcome examined in this study was self-reported hearing loss. The 2012 questionnaire inquired whether the women had hearing loss, and if so, the age of onset. Year and age of onset were calculated from participant responses. We defined incident cases of hearing loss as participants who reported a hearing problem first noticed after this study’s baseline of 1994.

The gold standard of evaluating hearing loss is pure-tone audiometry. However, it is logistically and financially challenging to obtain audiograms on all participants. Several studies have examined the correlation between self-reported hearing loss and hearing loss diagnosed by audiogram 2124. Studies found a single question on self-reported hearing loss to be a relatively reliable indicator of hearing loss 25 Significant associations between several factors and risk of self-reported hearing loss have been observed using this manner of assessment in Nurses’ Health Study II 2628.

Ascertainment of covariates

Covariates were selected based on previously reported risk factors for hearing loss. Factors considered included age 1, race 1, body mass index 26, 29, waist circumference 26, alcohol consumption 27, 30, folate 31, beta-carotene 32, trans fats 32, beta-cryptoxanthin 32, vitamin A, vitamin B12, vitamin C 32, vitamin E 32, omega-3 fatty acids 33, potassium 34, magnesium 35, physical activity 26, 36, smoking 30, diabetes 37, tinnitus 38, 39, and use of acetaminophen, aspirin, and ibuprofen 28. For covariate adjustment, body mass index was categorized as <21 kg/m2, 21–24 kg/m2, 25–29 kg/m2, 30–34 kg/m2, 35–40 kg/m2, and ≥40 kg/m2. We also adjusted for waist circumference (<71 cm, 71–79 cm, 80–88 cm, ≥89 cm). Body mass index and waist circumference were also adjusted for as continuous variables to assess for residual confounding by these variables. We performed age-stratified analysis to assess for possible effect modification by age. Hypertension was not adjusted for in our regression models for diuretic use to avoid over-adjustment.

Data on covariates was obtained from the biennial questionnaires. Women were asked in 2004 whether they described themselves as white, black/African-American, Asian, Native American/Alaska Native, Native Hawaiian/Pacific Islander, or other. Intake of alcohol, folate, vitamin B12, vitamin A, potassium, magnesium, vitamin E, trans fat, beta-carotene, and beta-cryptoxanthin was derived from semiquantitative food frequency questionnaires mailed to study participants every 4 years. Information derived from the semiquantitative food frequency questionnaires starting in 1994 was used in our analysis. The validity and reproducibility of these questionnaires has previously been reported 40, 41.

The other covariates have been shown to be valid measures for this cohort and other similar cohorts. For example, correlations for weight and physical activity were 0.97 and 0.79, respectively 4244.

Statistical analysis

All analyses were performed in a prospective manner using information on hypertension and medication use that was collected before the reported onset of hearing loss. We considered women who reported being diagnosed with hypertension in or prior to 1994 as having a history of hypertension. If on a subsequent questionnaire, participants reported having been diagnosed with hypertension, they were considered to have a history of hypertension from that point onward. Person-time contribution of each participant was assigned based on their response to questions regarding thiazide diuretic, furosemide, calcium channel blocker, and beta-blocker use on the 1994 questionnaire and every 2 years thereafter. Use of angiotensin-converting-enzyme inhibitors was first asked in 1996, and thus, person-time contribution of each participant was assigned based on their response to the question in 1996. Participants were censored at the time of onset of hearing loss or diagnosis of cancer. Multivariable-adjusted relative risks were calculated using Cox proportional hazards regression models. The Anderson-Gill data structure was used to handle left truncation and time-varying covariates efficiently 45. To control as finely as possible for confounding by age, we stratified the analysis jointly by age at start of follow-up and calendar year of the current questionnaire cycle. Duration of medication use was also used in our analyses. In these analyses, we excluded women who answered “yes” to use of the medication in question in the first year it was ascertained on the questionnaire to eliminate potential use of the medication beyond the two years preceding the baseline question. Answers in the affirmative on subsequent questionnaires for use of the medication were classified as two years of medication use. We examined the association between duration of medication use as continuous variables and categorical variables (no use, <2 years, 2–3 years, 4–5 years, 6–7 years, 8+ years). To examine whether the association between thiazide and furosemide use with hearing loss differed by history of hypertension, we performed analyses stratified by history of hypertension. We also tested for possible effect modification of the relation between use of thiazide diuretics, furosemide, and age (categorized by <60 years and ≥60 years). Because diuretic use may be associated with tinnitus, we also performed a secondary analysis that excluded participants who reported onset of tinnitus prior to onset of hearing loss. Covariate status from the 1994 questionnaire was updated on each subsequent questionnaire. All p-values are two-sided, with 95% confidence intervals calculated for all relative risks. SAS software, version 9.4 (SAS Institute Inc., Cary, North Carolina) was used to perform all statistical analyses. This study was approved by the Partners Healthcare IRB.

RESULTS

Participant characteristics at baseline according to history of hypertension and medication use are shown in Table 1. Women who reported a history of hypertension or use of thiazide diuretics or furosemide tended to be older, had higher body mass index and waist circumference, were less physically active, and were more likely to have a history of smoking or diabetes compared with women who did not report a history of hypertension or medication use.

Table 1.

Baseline Characteristics of Participants According to Furosemide Use and Thiazide Use, Nurses’ Health Study I, 1994.

No History of Hypertension (n=34,523) History of Hypertension (n=15,401) Thiazide No (n=46,678) Thiazide Yes (n=3,246) Furosemide No (n=49,323) Furosemide Yes (n=601)
Age, years 57.2 (6.4) 59.4 (6.4) 57.8 (6.4) 59.4 (6.5) 57.9 (6.5) 59.8 (6.6)
Body mass index, kg/m2 25.5 (4.5) 28.2 (5.6) 26.2 (4.9) 28.8 (5.6) 26.3 (5.0) 30.0 (6.4)
Waist circumference, cm 84.1 (12.9) 90.4 (14.3) 85.6 (13.5) 91.4 (14.2) 85.9 (13.6) 93.1 (16.2)
White 95.0% 93.1% 94.6% 92.7% 94.5% 93.7%
Physical activity in 2001, METs 14.3 [5.4–28.5] 11.5 [4.0–25.0] 13.5 [5.0–27.5] 11.7 [4.0–25.0] 13.5 [5.0–27.4] 11.6 [3.3–25.1]
Smoking status
 Never smoker 46.5% 46.8% 46.6% 47.7% 46.7% 42.6%
 Past smoker 41.5% 44.5% 42.3% 43.6% 42.3% 50.2%
 Current smoker 12.0% 8.5% 10.9% 8.6% 10.8% 7.0%
Alcohol consumption, g/day 1.8 [0.0–6.5] 0.9 [0.0–5.3] 1.5 [0.0–6.2] 1.0 [0.0–5.8] 1.5 [0.0–6.1] 0.9 [0.0–3.5]
Daily nutrient intake
 Vitamin A, IU 1521 [840–2553] 1633 [861–2620] 1543 [847–2570] 1647 [860–2630] 1550 [847–2574] 1664 [849–2684]
 Vitamin B12, μg 8.0 [5.0–12.0] 8.0 [5.0–12.0] 8.0 [5.0–12.0] 8.0 [5.0–12.0] 8.0 [5.0–12.0] 8.0 [5.0–13.0]
 Vitamin C, mg 213 [136–433] 220 [143–438] 214 [138–433] 227 [147–463] 215 [138–435] 226 [155–417]
 Vitamin E, mg 14.7 [8.3–114.3] 15.7 [8.6–182.9] 14.9 [8.4–115.7] 16.6 [8.8–186.0] 15.0 [8.4–116.7] 17.0 [8.5–185.6]
 Folate, μg 404.7 [278.2–634.7] 414.7 [283.3–648.4] 406.8 [279.0–637.1] 422.1 [289.7–633.9] 408.0 [279.5–639.0] 408.9 [284.9–620.3]
 Potassium, mg 3200 [2571–3907] 3259 [2620–3999] 3207 [2577–3921] 3386 [2710–4171] 3214 [2583–3932] 3501 [2708–4283]
 Magnesium, mg 334 [266–412] 336 [267–413] 335 [266–413] 336 [270–413] 335 [267–413] 330 [260–410]
 Beta-Carotene, μg 4570 [3029–7014] 4695 [3108–7231] 4604 [3042–7064] 4759 [3215–7365] 4614 [3055–7079] 4626 [3123–7444]
 Beta-Cryptoxanthin, μg 155.7 [82.7–235.5] 170.7 [90.7–244.9] 159.1 [84.5–237.4] 178.2 [94.9–251.8] 160.2 [84.9–238.2] 176.8 [95.7–250.6]
 Trans-fats, gm 2.3 [1.6–3.2] 2.3 [1.6–3.2] 2.3 [1.6–3.2] 2.3 [1.6–3.2] 2.3 [1.6–3.2] 2.2 [1.5–3.2]
 Omega-3 fatty acids, gm 0.16 [0.09–0.27] 0.17 [0.10–0.28] 0.16 [0.09–0.27] 0.18 [0.10–0.29] 0.16 [0.10–0.27] 0.15 [0.09–0.27]
History of hypertension - - 27.0% 86.7% 30.4% 71.4%
History of diabetes 2.1% 7.3% 3.5% 6.7% 3.6% 12.5%
Aspirin use, days/week
 <1 77.6% 70.1% 75.8% 67.8% 75.4% 66.6%
 1–3 6.2% 5.6% 6.0% 5.9% 6.0% 5.2%
 4+ 16.0% 23.7% 17.8% 25.5% 18.2% 27.8%
Acetaminophen use, days/week
 <1 84.1% 79.5% 83.2% 75.7% 82.8% 71.2%
 1–3 8.4% 9.5% 8.6% 11.0% 8.7% 13.4%
 4+ 5.2% 7.8% 5.8% 9.5% 5.9% 11.3%
Ibuprofen use, days/week
 <1 76.9% 70.6% 75.7% 64.5% 75.1% 62.2%
 1–3 9.8% 9.8% 9.7% 11.5% 9.8% 9.2%
 4+ 7.6% 12.2% 8.6% 15.0% 8.9% 18.8%

Values are mean (standard deviation), median [interquartile range], or percent

Abbreviations: METs = metabolic equivalents

Waist circumference values were taken from the 1996 questionnaire

At baseline, 15,401 women (31%) had a history of hypertension. Among women with hypertension, 2,813 (18%) were taking thiazide diuretics alone, 429 (3%) were taking furosemide alone, and 22 (0.1%) were taking both thiazide diuretics and furosemide.

The cumulative incidence of hearing loss among participants was 35%. During 774,096 person-years of follow-up time, 19,296 cases of hearing loss were reported (incidence rate: 25 cases per 1000 person-years). History of hypertension was independently associated with a modestly higher risk of hearing loss (multivariable adjusted relative risk = 1.04; 95% CI = 1.01, 1.07) (Table 2). Thiazide use was independently associated with higher risk of hearing loss (RR = 1.08; 95% CI = 1.04, 1.12), but furosemide use was not (RR = 1.01; 95% CI = 0.93, 1.08). After limiting the analysis to those women with a history of hypertension, none of the medications were significantly associated with risk of hearing loss when compared with women not taking medication (Table 3). Tests for effect modification by age for thiazide and furosemide use were not significant (p=0.61 and 0.11, respectively). Adjusting for waist circumference and body mass index as continuous variables did not significantly change the results. After excluding participants with a history of tinnitus, the results were not materially different (data not shown).

Table 2.

Age- and Multivariable-Adjusted Relative Risks of Incident Hearing Loss According to History of Hypertension, Nurses’ Health Study I, 1994–2012.

No. of Cases Person- Years Age-Adjusted RR 95% CI Multivariable-Adjusted RR* 95% CI
History of Hypertension
 No 8,289 417,000 1.00 Reference 1.00 Reference
 Yes 11,007 357,096 1.08 1.05, 1.12 1.04 1.01, 1.07

RR denotes relative risk

*

Adjusted for age, race, body mass index, waist circumference, alcohol consumption, physical activity, nutrient (folate, magnesium, potassium, vitamin A, vitamin B12, vitamin C, vitamin E, beta-carotene, beta-cryptoxanthin, trans-fat) intake, smoking status, hypertension, diabetes, tinnitus, and acetaminophen, aspirin, and ibuprofen use.

Table 3.

Age- and Multivariable-Adjusted Relative Risks of Incident Hearing Loss Among Women with a History of Hypertension, According to Anti-Hypertensive Medication Use, Nurses’ Health Study I, 1994–2012.

Anti-Hypertensive Medication No. of Cases Person-Years Age-Adjusted RR 95% CI Multivariable- Adjusted RR* 95% CI
No Medication 2,361 84,079 1.00 Reference 1.00 Reference
Thiazides 917 24,991 1.21 1.12, 1.31 1.07 0.99, 1.16
Furosemide 121 3,160 1.03 0.86, 1.24 0.91 0.75, 1.09
Calcium Channel Antagonists 694 24,040 1.03 0.94, 1.12 1.01 0.93, 1.10
Beta Blockers 1170 38,996 1.11 1.04, 1.19 1.01 0.94, 1.09
ACE Inhibitors 881 30.288 1.12 1.04, 1.21 1.04 0.96, 1.13
Other Anti-Hypertensive Medication 740 28,213 1.03 0.95, 1.12 1.00 0.92, 1.09
Multiple Anti-Hypertensive Medications 3,590 101,804 1.15 1.09, 1.21 1.03 0.97, 1.08

RR denotes relative risk

*

Adjusted for age, race, body mass index, waist circumference, alcohol consumption, physical activity, nutrient (folate, magnesium, potassium, vitamin A, vitamin B12, vitamin C, vitamin E, beta-carotene, beta-cryptoxanthin, trans fat) intake, smoking status, hypertension, diabetes, tinnitus, and acetaminophen, aspirin, and ibuprofen use, and all the antihypertensive medications in the table.

Duration of thiazide, furosemide, calcium channel blocker, beta-blocker, and angiotensin-converting-enzyme inhibitor use was not associated with risk of hearing loss (data not shown).

DISCUSSION

History of hypertension was associated with a very modest higher risk of hearing loss. After accounting for history of hypertension and adjusting for other antihypertensive medication use, there was no association between use of thiazide diuretics or furosemide and risk of hearing loss. There was also no association between duration of thiazide or furosemide use and risk of hearing loss. Use of other antihypertensive medications was not associated with risk of hearing loss.

The incidence rate of hearing loss in our cohort was 25 cases per 1000 person-years. In comparison, the approximate incidences of hearing loss in two previous prospective cohorts, where hearing loss was defined as a change in pure tone average of >25 decibels, were 72 cases per 1000 person-years among women 46, and 36 cases per 1000 person-years among men and women 47. Although the precise reasons for differing rates of hearing loss in these studies are unclear, potential explanations include differences in age and sex of the study populations and the method of outcome ascertainment.

The stria vascularis is located in the lateral cochlear wall and is responsible for sending auditory signals from the cochlea to the central nervous system 48. Vascular supply to the stria vascularis is derived from terminal arteries with no collateral supply. Therefore, it is particularly sensitive to events that compromise vascular supply, with animal studies showing reduced endocochlear potential and hearing loss occurring promptly after an anoxic event 49. It is hypothesized that hypertension may compromise the vascular supply to the stria vascularis thereby leading to hearing loss 7. There is limited evidence regarding the relation between hypertension and risk of hearing loss 1, 8, 9. Cross-sectional studies have shown higher prevalence of hearing loss among people with hypertension 1, 8, whereas a prospective study in men has suggested no association between hypertension and hearing loss 9. In our prospective cohort of women, hypertension was associated with a very slightly increased risk of hearing loss.

Given that we observed a small increased risk of hearing loss among women with a history of hypertension, we restricted our analysis of diuretic use to women with a history of hypertension. Despite anecdotal accounts that use of thiazides may be associated with risk hearing loss, we observed no association between thiazide diuretic use and hearing loss in our prospective study of women.

Furosemide use has been associated with risk of hearing loss in humans and rodent models 1113, 15. In humans, use of furosemide has been most commonly associated with hearing loss when administered intravenously and the hearing loss is usually reversible 11, 13. However, the hearing loss can be irreversible and has been reported with oral dosing 12. Although the mechanism by which this clinical hearing loss may occur unclear, rodent models suggest that it may occur via inhibition of the endocochlear potential and alteration of Organ of Corti mechanics 1418. Furthermore, long-term inhibition of the endocochlear potential has been associated with decreased auditory nerve activity 19, which may impair hearing. However, in our cohort of women, we found no association between furosemide use and risk of hearing loss.

Our study has limitations. The study population was predominantly white women. Further investigation is required to examine these associations in other populations. The outcome in our study was self-reported hearing loss. Although pure-tone audiometry is often considered the gold-standard for evaluating hearing loss, self-reported hearing loss has been shown to be reliable as an indicator for hearing loss 2124. In addition, a recent review done for the United States Preventative Services Task Force revealed that a single question about perceived hearing loss was almost as accurate as a more detailed questionnaire or a portable audiometric device for detection of hearing loss 50.

In conclusion, history of hypertension was associated with a small increased risk of hearing loss. Thiazide diuretic use and furosemide use were not associated with risk of hearing loss among women with a history of hypertension.

Clinical Significance.

  • Hypertension is independently associated with higher risk of hearing loss in women.

  • Use of thiazide diuretics and use of furosemide are not independently associated with risk of hearing loss in women.

Acknowledgments

Funding: This work was supported by grants U01 DC010811 and UM1 CA176726 from the National Institutes of Health. The sponsors of this study had no role in study design, data collection, data analysis, data interpretation, or writing of the manuscript.

Footnotes

All authors had access to the data and a role in writing the manuscript.

Ethical Approval: This study was approved by the Partners Healthcare IRB. Completion of the self-administered questionnaire was considered implied informed consent.

Conflicts of Interest: None declared

Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

References

  • 1.Agrawal Y, Platz EA, Niparko JK. Prevalence of hearing loss and differences by demographic characteristics among US adults: data from the National Health and Nutrition Examination Survey, 1999–2004. Archives of internal medicine. 2008;168:1522–1530. doi: 10.1001/archinte.168.14.1522. [DOI] [PubMed] [Google Scholar]
  • 2.Wallhagen MI, Strawbridge WJ, Cohen RD, Kaplan GA. An increasing prevalence of hearing impairment and associated risk factors over three decades of the Alameda County Study. American journal of public health. 1997;87:440–442. doi: 10.2105/ajph.87.3.440. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Cacciatore F, Napoli C, Abete P, Marciano E, Triassi M, Rengo F. Quality of life determinants and hearing function in an elderly population: Osservatorio Geriatrico Campano Study Group. Gerontology. 1999;45:323–328. doi: 10.1159/000022113. [DOI] [PubMed] [Google Scholar]
  • 4.Olusanya BO, Ruben RJ, Parving A. Reducing the burden of communication disorders in the developing world: an opportunity for the millennium development project. Jama. 2006;296:441–444. doi: 10.1001/jama.296.4.441. [DOI] [PubMed] [Google Scholar]
  • 5.Mozaffarian D, Benjamin EJ, Go AS, et al. Heart disease and stroke statistics--2015 update: a report from the American Heart Association. Circulation. 2015;131:e29–322. doi: 10.1161/CIR.0000000000000152. [DOI] [PubMed] [Google Scholar]
  • 6.Egan BM, Zhao Y, Axon RN. US trends in prevalence, awareness, treatment, and control of hypertension, 1988–2008. Jama. 2010;303:2043–2050. doi: 10.1001/jama.2010.650. [DOI] [PubMed] [Google Scholar]
  • 7.Friedland DR, Cederberg C, Tarima S. Audiometric pattern as a predictor of cardiovascular status: development of a model for assessment of risk. The Laryngoscope. 2009;119:473–486. doi: 10.1002/lary.20130. [DOI] [PubMed] [Google Scholar]
  • 8.Gates GA, Cobb JL, D’Agostino RB, Wolf PA. The relation of hearing in the elderly to the presence of cardiovascular disease and cardiovascular risk factors. Archives of otolaryngology--head & neck surgery. 1993;119:156–161. doi: 10.1001/archotol.1993.01880140038006. [DOI] [PubMed] [Google Scholar]
  • 9.Shargorodsky J, Curhan SG, Eavey R, Curhan GC. A prospective study of cardiovascular risk factors and incident hearing loss in men. The Laryngoscope. 2010;120:1887–1891. doi: 10.1002/lary.21039. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.James PA, Oparil S, Carter BL, et al. 2014 evidence-based guideline for the management of high blood pressure in adults: report from the panel members appointed to the Eighth Joint National Committee (JNC 8) Jama. 2014;311:507–520. doi: 10.1001/jama.2013.284427. [DOI] [PubMed] [Google Scholar]
  • 11.Wigand ME, Heidland A. Ototoxic side-effects of high doses of frusemide in patients with uraemia. Postgraduate medical journal. 1971;47(Suppl):54–56. [PubMed] [Google Scholar]
  • 12.Rifkin SI, de Quesada AM, Pickering MJ, Shires DL., Jr Deafness associated with oral furosemide. Southern medical journal. 1978;71:86–88. doi: 10.1097/00007611-197801000-00029. [DOI] [PubMed] [Google Scholar]
  • 13.Gallagher KL, Jones JK. Furosemide-induced ototoxicity. Annals of internal medicine. 1979;91:744–745. doi: 10.7326/0003-4819-91-5-744. [DOI] [PubMed] [Google Scholar]
  • 14.Ruggero MA, Rich NC. Furosemide alters organ of corti mechanics: evidence for feedback of outer hair cells upon the basilar membrane. The Journal of neuroscience : the official journal of the Society for Neuroscience. 1991;11:1057–1067. doi: 10.1523/JNEUROSCI.11-04-01057.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Chodynicki S, Kostrzewska A. Effect of furosemide and ethacrynic acid on endolymph potential in guinea pigs Otolaryngologia polska. The Polish otolaryngology. 1974;28:5–8. [PubMed] [Google Scholar]
  • 16.Brusilow SW. Propranolol antagonism to the effect of furosemide on the compostion of endolymph in guinea pigs. Canadian journal of physiology and pharmacology. 1976;54:42–48. doi: 10.1139/y76-007. [DOI] [PubMed] [Google Scholar]
  • 17.Kusakari J, Ise I, Comegys TH, Thalmann I, Thalmann R. Effect of ethacrynic acid, furosemide, and ouabain upon the endolymphatic potential and upon high energy phosphates of the stria vascularis. The Laryngoscope. 1978;88:12–37. doi: 10.1002/lary.1978.88.1.12. [DOI] [PubMed] [Google Scholar]
  • 18.Rybak LP. Ototoxicity of loop diuretics. Otolaryngologic clinics of North America. 1993;26:829–844. [PubMed] [Google Scholar]
  • 19.Lang H, Jyothi V, Smythe NM, Dubno JR, Schulte BA, Schmiedt RA. Chronic reduction of endocochlear potential reduces auditory nerve activity: further confirmation of an animal model of metabolic presbyacusis. Journal of the Association for Research in Otolaryngology : JARO. 2010;11:419–434. doi: 10.1007/s10162-010-0214-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Colditz GA, Martin P, Stampfer MJ, et al. Validation of questionnaire information on risk factors and disease outcomes in a prospective cohort study of women. American journal of epidemiology. 1986;123:894–900. doi: 10.1093/oxfordjournals.aje.a114319. [DOI] [PubMed] [Google Scholar]
  • 21.Swanepoel de W, Eikelboom RH, Hunter ML, Friedland PL, Atlas MD. Self-reported hearing loss in baby boomers from the Busselton Healthy Ageing Study: audiometric correspondence and predictive value. Journal of the American Academy of Audiology. 2013;24:514–521. doi: 10.3766/jaaa.24.6.7. quiz 529. [DOI] [PubMed] [Google Scholar]
  • 22.Hannula S, Bloigu R, Majamaa K, Sorri M, Maki-Torkko E. Self-reported hearing problems among older adults: prevalence and comparison to measured hearing impairment. Journal of the American Academy of Audiology. 2011;22:550–559. doi: 10.3766/jaaa.22.8.7. [DOI] [PubMed] [Google Scholar]
  • 23.Salonen J, Johansson R, Karjalainen S, Vahlberg T, Isoaho R. Relationship between self-reported hearing and measured hearing impairment in an elderly population in Finland. International journal of audiology. 2011;50:297–302. doi: 10.3109/14992027.2010.549517. [DOI] [PubMed] [Google Scholar]
  • 24.Gomez MI, Hwang SA, Sobotova L, Stark AD, May JJ. A comparison of self-reported hearing loss and audiometry in a cohort of New York farmers. Journal of speech, language, and hearing research : JSLHR. 2001;44:1201–1208. doi: 10.1044/1092-4388(2001/093). [DOI] [PubMed] [Google Scholar]
  • 25.Kamil RJ, Genther DJ, Lin FR. Factors associated with the accuracy of subjective assessments of hearing impairment. Ear Hear. 2015;36:164–167. doi: 10.1097/AUD.0000000000000075. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Curhan SG, Eavey R, Wang M, Stampfer MJ, Curhan GC. Body mass index, waist circumference, physical activity, and risk of hearing loss in women. The American journal of medicine. 2013;126:1142, e1141–1148. doi: 10.1016/j.amjmed.2013.04.026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Curhan SG, Eavey R, Wang M, Stampfer MJ, Curhan GC. Prospective study of alcohol consumption and self-reported hearing loss in women. Alcohol. 2014 doi: 10.1016/j.alcohol.2014.10.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Curhan SG, Shargorodsky J, Eavey R, Curhan GC. Analgesic use and the risk of hearing loss in women. American journal of epidemiology. 2012;176:544–554. doi: 10.1093/aje/kws146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Seidman MD. Effects of dietary restriction and antioxidants on presbyacusis. The Laryngoscope. 2000;110:727–738. doi: 10.1097/00005537-200005000-00003. [DOI] [PubMed] [Google Scholar]
  • 30.Itoh A, Nakashima T, Arao H, et al. Smoking and drinking habits as risk factors for hearing loss in the elderly: epidemiological study of subjects undergoing routine health checks in Aichi, Japan. Public health. 2001;115:192–196. doi: 10.1038/sj.ph.1900765. [DOI] [PubMed] [Google Scholar]
  • 31.Durga J, Verhoef P, Anteunis LJ, Schouten E, Kok FJ. Effects of folic acid supplementation on hearing in older adults: a randomized, controlled trial. Annals of internal medicine. 2007;146:1–9. doi: 10.7326/0003-4819-146-1-200701020-00003. [DOI] [PubMed] [Google Scholar]
  • 32.Curhan SG, Stankovic KM, Eavey RD, Wang M, Stampfer MJ, Curhan GC. Carotenoids, vitamin A, vitamin C, vitamin E, and folate and risk of self-reported hearing loss in women. The American journal of clinical nutrition. 2015 doi: 10.3945/ajcn.115.109314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Curhan SG, Eavey RD, Wang M, Rimm EB, Curhan GC. Fish and fatty acid consumption and the risk of hearing loss in women. The American journal of clinical nutrition. 2014;100:1371–1377. doi: 10.3945/ajcn.114.091819. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Wangemann P. Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential. The Journal of physiology. 2006;576:11–21. doi: 10.1113/jphysiol.2006.112888. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Haupt H, Scheibe F, Mazurek B. Therapeutic efficacy of magnesium in acoustic trauma in the guinea pig. ORL; journal for oto-rhino-laryngology and its related specialties. 2003;65:134–139. doi: 10.1159/000072250. [DOI] [PubMed] [Google Scholar]
  • 36.Li Y, Healy EW, Drane JW, Zhang J. Comorbidity between and risk factors for severe hearing and memory impairment in older Americans. Preventive medicine. 2006;43:416–421. doi: 10.1016/j.ypmed.2006.06.014. [DOI] [PubMed] [Google Scholar]
  • 37.Bainbridge KE, Hoffman HJ, Cowie CC. Diabetes and hearing impairment in the United States: audiometric evidence from the National Health and Nutrition Examination Survey, 1999 to 2004. Annals of internal medicine. 2008;149:1–10. doi: 10.7326/0003-4819-149-1-200807010-00231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Hasson D, Theorell T, Westerlund H, Canlon B. Prevalence and characteristics of hearing problems in a working and non-working Swedish population. Journal of epidemiology and community health. 2010;64:453–460. doi: 10.1136/jech.2009.095430. [DOI] [PubMed] [Google Scholar]
  • 39.Nondahl DM, Cruickshanks KJ, Wiley TL, Klein R, Klein BE, Tweed TS. Prevalence and 5-year incidence of tinnitus among older adults: the epidemiology of hearing loss study. Journal of the American Academy of Audiology. 2002;13:323–331. [PubMed] [Google Scholar]
  • 40.Rimm EB, Giovannucci EL, Stampfer MJ, Colditz GA, Litin LB, Willett WC. Reproducibility and validity of an expanded self-administered semiquantitative food frequency questionnaire among male health professionals. American journal of epidemiology. 1992;135:1114–1126. doi: 10.1093/oxfordjournals.aje.a116211. discussion 1127–1136. [DOI] [PubMed] [Google Scholar]
  • 41.Willett WC, Sampson L, Stampfer MJ, et al. Reproducibility and validity of a semiquantitative food frequency questionnaire. American journal of epidemiology. 1985;122:51–65. doi: 10.1093/oxfordjournals.aje.a114086. [DOI] [PubMed] [Google Scholar]
  • 42.Rimm EB, Stampfer MJ, Colditz GA, Chute CG, Litin LB, Willett WC. Validity of self-reported waist and hip circumferences in men and women. Epidemiology. 1990;1:466–473. doi: 10.1097/00001648-199011000-00009. [DOI] [PubMed] [Google Scholar]
  • 43.Willett W. Nutritional epidemiology. 3. Oxford; New York: Oxford University Press; 2013. [Google Scholar]
  • 44.Wolf AM, Hunter DJ, Colditz GA, et al. Reproducibility and validity of a self-administered physical activity questionnaire. International journal of epidemiology. 1994;23:991–999. doi: 10.1093/ije/23.5.991. [DOI] [PubMed] [Google Scholar]
  • 45.Therneau TM, Grambsch PM. Modeling survival data : extending the Cox model. New York: Springer; 2000. [Google Scholar]
  • 46.Cruickshanks KJ, Wiley TL, Tweed TS, et al. Prevalence of hearing loss in older adults in Beaver Dam, Wisconsin. The Epidemiology of Hearing Loss Study. American journal of epidemiology. 1998;148:879–886. doi: 10.1093/oxfordjournals.aje.a009713. [DOI] [PubMed] [Google Scholar]
  • 47.Mitchell P, Gopinath B, Wang JJ, et al. Five-year incidence and progression of hearing impairment in an older population. Ear Hear. 2011;32:251–257. doi: 10.1097/AUD.0b013e3181fc98bd. [DOI] [PubMed] [Google Scholar]
  • 48.Nin F, Hibino H, Doi K, Suzuki T, Hisa Y, Kurachi Y. The endocochlear potential depends on two K+ diffusion potentials and an electrical barrier in the stria vascularis of the inner ear. Proc Natl Acad Sci U S A. 2008;105:1751–1756. doi: 10.1073/pnas.0711463105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Morizane I, Hakuba N, Shimizu Y, et al. Transient cochlear ischemia and its effects on the stria vascularis. Neuroreport. 2005;16:799–802. doi: 10.1097/00001756-200505310-00004. [DOI] [PubMed] [Google Scholar]
  • 50.Chou R, Dana T, Bougatsos C, Fleming C, Beil T. Screening adults aged 50 years or older for hearing loss: a review of the evidence for the U.S. preventive services task force. Annals of internal medicine. 2011;154:347–355. doi: 10.7326/0003-4819-154-5-201103010-00009. [DOI] [PubMed] [Google Scholar]

RESOURCES