Abstract
Hearing loss resulted from multiple intrinsic and extrinsic factors. Secondhand smoke (SHS) and obesity had been reported to be related to hearing loss. This study explored the possible associations of SHS and obesity with the hearing threshold. The relations between SHS and the hearing threshold in subjects from three different body mass index classes were analyzed. Our study included data from 1,961 subjects aged 20–69 years that were obtained from the National Health and Nutrition Examination Survey for the years 1999–2004. After adjusting for potential confounding factors, the subjects with the higher tertiles of serum cotinine levels tended to have higher hearing thresholds than those with the lowest tertile of serum cotinine levels (for both trends, p < 0.05). Notably, the obese subjects with the higher tertiles of serum cotinine levels had significantly higher hearing thresholds for high frequencies and low frequencies than those with the lowest tertile of serum cotinine levels (for both trends, p < 0.05). Our study showed a significant positive association between SHS exposure and hearing thresholds in the adult population, especially in obese individuals. Based on our findings, avoiding exposure to SHS, especially in obese adults, may decrease the risk of hearing loss.
Similar content being viewed by others
Introduction
Sensorineural hearing loss is an important public health problem with an estimated prevalence of 16.1% in the United States in adults aged 20 to 69 years1. When the aging of the population is taken into consideration, the prevalence can only be expected to increase2. Hearing loss can be a disabling condition that reduces the quality of life. Loss of hearing negatively affects cognitive and emotional status, work productivity and social interaction, leading to psychosocial problems such as depression, progressive isolation and withdrawal. Hearing loss can be result from multiple intrinsic and extrinsic factors which can be further classified as cochlear aging, environmental (e.g., noise exposure, ototoxic medications), genetic predisposition and health co-morbidities (e.g., tobacco smoking, hypertension, diabetes)2,3. Although aging and noise exposure are the leading causes of hearing loss in adults, other factors such as secondhand smoke (SHS) and obesity are also associated with loss of hearing4,5,6,7.
SHS is an important public health concern. SHS exposure increases the risk of cardiovascular disease to approximately 30% in nonsmoking individuals8. In the literature, there was a mountain of evidence regarding to smoking and hearing loss, but a little about the association between SHS and hearing loss. An active smoker is personally responsible for his/her own toxic exposures; however, involuntary exposures via SHS may place never smokers at increased risk for hearing loss4,5,9,10. A study by Fabry et al. examined a nationally representative cross-sectional dataset of 3307 individuals and found that SHS was significantly related with hearing loss in nonsmokers4. It merits a further investigation into the effect of SHS on hearing impairment.
Obesity is associated with increased risks of disease, disability, and death11. Obesity is considered to be a multifactorial metabolic disorder. Cardiovascular disease, cerebrovascular disease, hypertension, and diabetes are related with obesity. An association between obesity and hearing impairment has been observed in epidemiologic studies6,11,12. A multicenter European study of 4083 subjects found that higher body mass index (BMI) was related with hearing loss at both high frequencies and low frequencies12. In addition, the Nurses’ Health Study II of 116,430 women found that a higher BMI (≧40) and a larger waist circumference (WC; >88 cm) were associated with an increased risk of hearing loss11.
As these previous studies have shown, there is evidence indicating that SHS and obesity are related to hearing impairment. Moreover, these two distinct factors seem to share some possible mechanisms causing hearing impairment, such as atherosclerosis13, oxidative stress2,14,15,16,17, and inflammation16,17. It is reasonable to hypothesize that SHS and obesity together may have a combined effect that impairs hearing. From the viewpoint of public health, this investigation can help to set up more effective health education and public promotion campaigns to reduce SHS exposure and to introduce weight loss programs. The purpose of our study was to investigate the possible associations of SHS and obesity with the hearing threshold. We used data from the National Health and Nutrition Examination Survey (NHANES). In particular, we evaluated whether the relation between SHS and the hearing threshold was different for individuals with three different BMIs.
Results
Characteristics of the study population
Our study subjects were 1,961 participants from the NHANES 1999–2004 sample. The demographic distribution and clinical characteristics of our study group are presented according to the tertiles of the serum cotinine level (Table 1). Among the subjects, the mean age was 39.72 years (SD = 13.06) and 36.9% of the subjects were men. In the subjects with higher tertiles of serum cotinine concentration, WC, BMI, and uric acid levels were significantly higher, and age and HDL-C level were significantly lower; there were more males and fewer non-Hispanic whites.
Association between serum cotinine level and hearing thresholds
The results of multiple linear regression analysis based on serum cotinine tertiles are shown in Table 2. Subjects in the higher tertiles of serum cotinine level tended to have a higher hearing threshold. In model 1, model 2, and model 3, positive associations between serum cotinine level and the hearing thresholds (high-PTA and low-PTA) were observed. In model 3, after subsequent adjustment with other covariates, the β coefficients of the high-PTA comparing the second and third tertiles of serum cotinine levels to the lowest tertile of serum cotinine levels were 0.012 and 0.049, respectively (p value for the trend = 0.002); the β coefficients of the low-PTA were −0.010 and 0.041, respectively, for the similar comparison of tertiles (p value for the trend = 0.013).
Associations among serum cotinine level, BMI and hearing thresholds
The analyses of the relations between the serum cotinine level, BMI and hearing thresholds are presented in Table 3. Obese subjects in the higher tertiles of serum cotinine levels had a higher hearing threshold. Among the three models, significant positive associations between the serum cotinine level and the hearing thresholds (high-PTA and low-PTA) were observed. In model 3, in obese subjects the β coefficients of the high-PTA comparing the second and third tertiles of serum cotinine levels to the lowest tertile of serum cotinine levels were 0.042 and 0.076, respectively (p value for the trend = 0.005); the β coefficients of the low-PTA were 0.028 and 0.068, respectively, for the similar comparison of tertiles (p value for the trend = 0.017).
Discussion
We studied a large and nationally representative group of nonsmoking adults in the United States who were exposed to SHS. On the basis of serum cotinine levels and self-reported information and consistent with a dose-dependent effect, we found that study subjects with the higher tertiles of serum cotinine levels had significantly higher high-frequency and low-frequency hearing thresholds compared with those with the lowest tertile of serum cotinine levels. Notably, this association was only observed in the obese subjects and was not found in normal weight subjects or overweight subjects. Among the obese subjects, those with higher tertiles of serum cotinine levels had significantly higher hearing thresholds than those with the lowest tertile of serum cotinine levels; this relation was not observed in the normal weight subjects or the overweight subjects. In other words, SHS did not seem to have a significant association with a hearing threshold shift in normal weight subjects or overweight subjects, but did have a significant positive association with a hearing threshold shift in obese subjects.
Previous studies have shown a correlation between SHS and hearing loss or cochlear auditory dysfunction4,5,9,10,20,21,22,23. In addition, our study results are in accord with the findings from previous studies that show a dose-response effect between the level of SHS exposure and the risk of hearing loss5,10,23. Cruickshanks et al. reported an association between smoking and hearing loss and also described a significant correlation between SHS and hearing loss. Nonsmokers who lived with a household member who smoked had a higher risk of hearing loss than those who did not live with a smoker (odds ratio, 1.94; 95% confidence interval, 1.01–3.74; P = 0.047)9. In a cross-sectional study of 164,770 adults aged between 40 and 69 years in the United Kingdom, Dawes et al. found that SHS exposure was associated with increased odds of hearing loss and a dose-response effect was observed5. Either prenatal or postnatal SHS exposure had a damaging effect on cochlear function in children. In mothers with prenatal SHS exposure, there were damaging effects on cochlear auditory function in neonates, as assessed by otoacoustic emissions testing21, and moreover, the increased risks of hearing loss still existed in adolescence and these risks were higher than in adolescents without prenatal SHS exposure22. Postnatal SHS exposure in children also had a negative effect on cochlear auditory function and increased the risk of hearing loss10,20,23.
The exact mechanism of ototoxicity due to smoking is not clear. It has been proposed that smoking may be deleterious to the inner ear due to a direct ototoxic effect of nicotine or another toxin or to vascular ischemia or hypoxemia in the cochlea from vasospasm, vasoconstriction, increased blood viscosity, production of carboxyhemoglobin, or blood vessel arteriosclerosis13,24,25,26,27. Oxidative stress caused by smoking also affects auditory function2,14,15. A previous study found nicotinic-like receptors in the cochlear hair cells, which may suggest that tobacco smoke has detrimental effects on hair cell function due to a possible action during the auditory neurotransmission28. Considering these possible mechanisms either collectively or separately, smokers or individuals exposed to SHS may be more susceptible to hearing impairment than nonsmokers or individuals not exposed to SHS. Furthermore, the impact of smoking could interact with other factors or with detrimental auditory exposures such as noise, causing synergic harmful effects on auditory function2,7,29,30.
Although obesity-related co-morbidities can impair hearing, obesity itself may have some specific associations with hearing impairment. In an animal study, obesity could exacerbate the hearing impairment with elevated hearing thresholds31. In humans, central obesity (i.e., either a higher amount of visceral adipose tissue or a greater WC), was found to be related to an elevated hearing threshold32,33. There is also evidence indicating that oxidative stress is a critical factor that links obesity with its associated complications16.
As far as we know, mechanisms of age-related hearing loss include hypoxia, atherosclerosis, inflammation, oxidative stress and production of reactive oxygen species, mitochondrial dysfunction, and subsequent apoptosis of the cochlear cells2. The two distinct factors, SHS and obesity, seem to share some possible mechanisms accelerating the process of hearing impairment, such as atherosclerosis13, oxidative stress2,14,15,16,17, and inflammation16,17. This might be the explanation why they have synergistic actions that impair hearing. Obesity and smoking-related atherosclerosis may lead to lumen narrowing in the internal auditory artery and reduce cochlear blood flow13. Reduced blood circulation to the cochlea, whether of microvascular or macrovascular origin, can cause dysfunction of the stria vascularis, diminished perfusion and hypoxia of cochlear hair cells and neurons, and can subsequently impact hearing function34,35,36. There is growing evidence that suggests that oxidative stress and inflammation are the important underlying factors connecting obesity with its related complications16, both of which could be aggravated by cigarette smoking17. A similar result was also observed in an animal study in which tobacco smoking was associated with worsening of the oxidative stress and subsequent chronic kidney injury in obese animals37. In a study that estimated the SHS exposure by measuring the nicotine level in hair, there was a significant relation between SHS exposure and oxidative stress in overweight subjects and obese subjects38. In other words, SHS exposure in obese individuals may worsen the existent oxidative stress and inflammation, which also could be exacerbated by hypoxia (associated with obesity and smoking-related atherosclerosis)2. They may synergistically cause hearing impairment. However, it needs further longitudinal study and laboratory research to investigate whether SHS and obesity have a synergistic effect that impairs hearing or not.
The tonotopic organization of the cochlea results that hair cells at the base of the cochlea respond to high frequencies and those at the apex to the low frequencies39. In our study analysis, we observe a significant positive association between secondhand smoke exposure and hearing thresholds of both high-frequency and low-frequency in the adult population of the United States, especially in obese individuals. The threshold elevation was across the frequency spectrum, affecting the cochlea from the base to the apex. Schuknecht characterized four categories of age-related hearing loss based on clinical and histopathologic changes within the cochlea: sensory, neural, strial, and cochlear conductive40. He described “strial” (also known as metabolic) hearing loss pathologically based on atrophy of the stria vascularis microvasculature throughout the cochlea. Individuals with this type of hearing loss tended to have relatively flat audiograms, i.e. similar losses in hearing sensitivity across the frequency range. We found that secondhand smoke exposure produce a similar broad-spectrum pattern of hearing impairment, like observations in other reports4,10, and this effect may be mediated by involvement of the stria vascularis. Although our results fit with that hypothesis, further study is needed to clarify whether the stria vascularis is the exact site of global cochlear injury.
Our study had several limitations. First, it is a cross-sectional study in which the serum cotinine levels and the hearing thresholds were measured at one timepoint, rather than a longitudinal study. Thus, causal inferences cannot be made. Second, no information regarding congenital or genetic hearing loss was available in the NHANES dataset. Third, a recall bias in the medical history data cannot be excluded. Fourth, our analysis dates were obtained from the 1999–2004 NHANES, so our present study focused on the participants aged 20–69. The interpretation of our results should be cautiously. Finally, misclassification of SHS was possible because the exposure estimate was based on the serum cotinine level that has an average half-life of 17 hours.
Conclusions
Many epidemiologic studies about evaluating the possible risk factors of hearing impairment were conducted to find the preventable factors. They can give us inspiration of further laboratory research and an improved understanding of the etiologic risk factors related to hearing impairment which results in significant public health benefits. Noise-induced hearing loss is by far the most important preventable cause of hearing loss2,3,12. Other modifiable factors include smoking, ototoxic medication (aminoglycoside antibiotics, loop diuretics, cisplatin, or anti-inflammatory agents), diabetes, hypertension, and hyperlipidaemia2,3,5,12. Educating and advising patients to maintain good general health and fitness would have benefits on hearing preservation. Our study showed a significant positive association between SHS exposure (as assessed by higher serum cotinine levels) and hearing thresholds in the adult population of the United States, especially in obese individuals. In spite of previous studies showing a relation between SHS and hearing loss, our study is the first study to further indicate that SHS and obesity may have a synergic effect on hearing impairment. Based on our findings, avoiding exposure to SHS, especially in obese adults, may reduce the risk of hearing loss.
Methods
Study population
The NHANES is a large cross-sectional study that is designed to represent the non-institutionalized civilian population in the United States. This survey is annually conducted by the National Center for Health Statistics of the CDC. The survey includes an initial household interview and subsequent physical examinations and laboratory tests that are performed at a mobile examination center (MEC) to collect pertinent information.
We limited our study subjects to include NHANES participants who were nonsmokers exposed to SHS, as defined by both the personal questionnaire during the household interview and the self-reported questionnaire regarding smoking status that was administered at the MEC, as well as the nicotine level measured by a laboratory test. Our study examined data from 1,961 subjects aged 20–69 years that were obtained from the NHANES for the years 1999–2004 and included the following: demographic data, results of physical examinations, laboratory tests, questionnaire contents, and audiometric testing. Our study excluded individuals with current or ever occupational noise exposure or with incomplete data regarding either SHS exposure or other variables assessed in this study.
Audiometric measures
According to the NHANES protocol for 1999–2004, after the initial household interview and medical examination, half of the subjects were randomly scheduled for audiometric testing. Subjects who were eligible for testing were excluded if they could not take off their hearing aids or could not tolerate the auditory headphones. Audiometric testing was performed in the MEC sound-isolated room by technicians who were trained by a certified audiologist from the National Institute for Occupational Safety and Health. The audiometric instrumentation contained an interacoustics model AD226 audiometer equipped with standard TDH-39P headphones and EARTone 3A insert earphones. Both ears were tested across the frequencies of 500, 1,000, 2,000, 3,000, 4,000, 6,000, and 8000 Hz with an intensity range from −10 to 120 dB to measure the air-conduction pure tone hearing thresholds. The high-frequency pure-tone average (high-PTA) was calculated as the average of the pure-tone hearing level at 3,000, 4,000, 6,000, and 8,000 Hz. The low-frequency pure-tone average (low-PTA) was calculated as the average of pure tone hearing level at 500, 1,000, and 2,000 Hz. High-PTA and low-PTA were used for evaluation the high-frequency and low-frequency hearing impairment, respectively4,10. We chose the worse ear with the lower pure-tone average, for the regression analysis. More details of audiometric measures are available at http://www.cdc.gov/nchs/data/nhanes/au.pdf.
Definition of SHS exposure
Cotinine, a major proximal metabolite of nicotine, is extensively used as a biomarker of exposure to cigarette smoke for either active smoking or SHS18. A nonsmoker was defined as an individual who: (1) according to the personal questionnaire, had not smoked at least 100 cigarettes or had not smoked a pipe or a cigar or used snuff or chewing tobacco at least 20 times in their entire life and (2) and according to the MEC tobacco questionnaire, had not used tobacco or nicotine products in the past 5 days. Nonsmokers with serum cotinine levels that were detectable but <10 ng/mL were defined as having been exposed to SHS19. Due to the improvement of laboratory methods over time, the limit of detection (LOD) for cotinine was 0.050 ng/mL in the NHANES data for 1999–2000, but 0.015 ng/mL in the NHANES data for 2001–2004. However, for uniformity in using the 1999–2004 NHANES data, we used the LOD from the 1999–2000 NHANES data (0.050 ng/mL) for all individuals. For analysis purposes for values below the LOD, we used the equation of the LOD divided by the square root of two (0.035 ng/mL).
Definition of obesity
We classified subjects based on BMI according to the WHO definition, as follows: a BMI ≧ 30 is obese, a BMI of 25 to <30 is overweight, a BMI of 18.5 to <25 is normal weight, and a BMI < 18.5 is underweight. The BMI is defined as the body mass (in kilograms) divided by the square of the body height (in meters) and is expressed in units of kg/m2.
Assessment of covariates
Demographic data that included age, sex, race/ethnicity, status of smoking, and personal history were collected. Race was categorized as non-Hispanic black, non-Hispanic white, or other. Both the personal questionnaire and the self-reported questionnaire were used to determine smoking status. Participants were defined as having diabetes mellitus (DM) if they self-reported a diagnosis by a physician, had a fasting glucose level of ≥126 mg/dL, had a random glucose level of ≥200 mg/dL, or used diabetic medications. Heart disease was considered to be present if participants had experienced or had been diagnosed with angina, myocardial infarction, coronary artery disease, or congestive heart failure. Stroke was determined from self-reports. The current use of ototoxic medications including aminoglycosides, loop diuretics, non-steroidal anti-inflammatory drugs, or anticancer drugs, was ascertained from self-reports. Abnormal otoscopy was determined if there were abnormal results of an initial otoscopic screening examination of the eardrum and external acoustic canal before the audiometric testing. An audiometric impedance tympanometer was used for the tympanometry. Abnormal tympanometry was determined if the compliance was ≦0.3 ml or the middle-ear peak pressure was ≦−150 daPa. Body measurements, including height, weight, and WC (measured to the nearest 0.1 cm at the top of the hip bone after breathing out normally) were recorded from participants at the MEC. Uric acid data were determined using the Hitachi 737 analyzer. Levels of high-density lipoprotein cholesterol (HDL-C) were enzymatically measured using the Hitachi 704 analyzer. All measurements used standardized methods with documented accuracy that followed the CDC guidelines. All detailed information regarding biospecimen collection and processing protocols are available at the NHANES website.
Statistical analyses
SPSS (version 18.0 for Windows; SPSS, Inc., Chicago, IL, USA) was used to conduct the statistical analyses. Two-sided p-values < 0.05 were considered to indicate significant differences. Some covariates including age, WC, BMI, uric acid, and HDL-C were treated as continuous variables and were presented as the mean value ± standard deviation (SD). Some covariates such as sex and race were regarded as categorical variables and were presented as numbers with percentages. A log transformation was performed to normalize the distribution of the PTA hearing thresholds. Our study used tertile-based analysis that divided the serum cotinine level into tertiles with the individuals in the lowest tertile considered as the reference group. The three tertiles of the serum cotinine level were as follows: T1 < 0.0226 ng/mL, 0.0226 = T2 < 0.0719 ng/mL, and 0.0719 = T3 < 10 ng/mL. Linear regression analysis was used to assess the association of the tertiles of serum cotinine level with hearing threshold. A multiple-model approach was constructed for adjustments of covariates. Model 1 was adjusted for age, gender and race. Model 2 was model 1 after further adjustment for WC, BMI, HDL-C, and uric acid. Model 3 was model 2 after further adjustment for abnormal otoscopy and tympanometry, current use of ototoxic medications, history of DM, heart disease or stroke. The p-values for the trend tests were determined by treating the tertile of the serum cotinine level as a continuous variable (ranging from 1 to 3) to assess the associations across the increase in the tertile of the serum cotinine level with the PTA hearing threshold.
Ethics statement
The National Center for Health Statistics Institutional Review Board approved the NHANES study, and written informed consent was received from all participants prior to the study. However, our study was exempt from IRB review because we used a publicly available, unidentifiable dataset.
Additional Information
How to cite this article: Lin, Y.-Y. et al. Secondhand Smoke is Associated with Hearing Threshold Shifts in Obese Adults. Sci. Rep. 6, 33071; doi: 10.1038/srep33071 (2016).
References
Agrawal, Y., Platz, E. A. & Niparko, J. K. Prevalence of hearing loss and differences by demographic characteristics among US adults: data from the National Health and Nutrition Examination Survey, 1999–2004. Arch Intern Med 168, 1522–1530 (2008).
Yamasoba, T. et al. Current concepts in age-related hearing loss: epidemiology and mechanistic pathways. Hear Res 303, 30–38 (2013).
Gates, G. A. & Mills, J. H. Presbycusis. Lancet 366, 1111–1120 (2005).
Fabry, D. A. et al. Secondhand smoke exposure and the risk of hearing loss. Tob Control 20, 82–85 (2011).
Dawes, P. et al. Cigarette smoking, passive smoking, alcohol consumption, and hearing loss. J Assoc Res Otolaryngol 15, 663–674 (2014).
Lalwani, A. K., Katz, K., Liu, Y. H., Kim, S. & Weitzman, M. Obesity is associated with sensorineural hearing loss in adolescents. Laryngoscope 123, 3178–3184 (2013).
Cruickshanks, K. J. et al. Smoking, central adiposity, and poor glycemic control increase risk of hearing impairment. J Am Geriatr Soc 63, 918–924 (2015).
Benowitz, N. L. Cigarette smoking and cardiovascular disease: pathophysiology and implications for treatment. Prog Cardiovasc Dis 46, 91–111 (2003).
Cruickshanks, K. J. et al. Cigarette smoking and hearing loss: the epidemiology of hearing loss study. JAMA 279, 1715–1719 (1998).
Lalwani, A. K., Liu, Y. H. & Weitzman, M. Secondhand smoke and sensorineural hearing loss in adolescents. Arch Otolaryngol Head Neck Surg 137, 655–662 (2011).
Curhan, S. G., Eavey, R., Wang, M., Stampfer, M. J. & Curhan, G. C. Body mass index, waist circumference, physical activity, and risk of hearing loss in women. Am J Med 126, 1142 e1141–e1148 (2013).
Fransen, E. et al. Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study. J Assoc Res Otolaryngol 9, 264–276 (2008).
Makishima, K. Arteriolar sclerosis as a cause of presbycusis. Otolaryngology 86, ORL322–ORL326 (1978).
Ortigosa, S. M. et al. Oxidative stress induced in tobacco leaves by chloroplast over-expression of maize plastidial transglutaminase. Planta 232, 593–605 (2010).
Maffei, G. & Miani, P. Experimental tobacco poisoning. Resultant structural modifications of the cochlea and tuba acustica. Arch Otolaryngol 75, 386–396 (1962).
Rani, V., Deep, G., Singh, R. K., Palle, K. & Yadav, U. C. Oxidative stress and metabolic disorders: Pathogenesis and therapeutic strategies. Life Sci (2016).
Szulinska, M. et al. Evaluation of insulin resistance, tumor necrosis factor alpha, and total antioxidant status in obese patients smoking cigarettes. Eur Rev Med Pharmacol Sci 17, 1916–1922 (2013).
Benowitz, N. L. Cotinine as a biomarker of environmental tobacco smoke exposure. Epidemiol Rev 18, 188–204 (1996).
Pickett, M. S., Schober, S. E., Brody, D. J., Curtin, L. R. & Giovino, G. A. Smoke-free laws and secondhand smoke exposure in US non-smoking adults, 1999–2002. Tob Control 15, 302–307 (2006).
Durante, A. S. et al. Tobacco smoke exposure during childhood: effect on cochlear physiology. Int J Environ Res Public Health 10, 5257–5265 (2013).
Durante, A. S., Ibidi, S. M., Lotufo, J. P. & Carvallo, R. M. Maternal smoking during pregnancy: impact on otoacoustic emissions in neonates. Int J Pediatr Otorhinolaryngol 75, 1093–1098 (2011).
Weitzman, M., Govil, N., Liu, Y. H. & Lalwani, A. K. Maternal prenatal smoking and hearing loss among adolescents. JAMA Otolaryngol Head Neck Surg 139, 669–677 (2013).
Talaat, H. S., Metwaly, M. A., Khafagy, A. H. & Abdelraouf, H. R. Dose passive smoking induce sensorineural hearing loss in children? Int J Pediatr Otorhinolaryngol 78, 46–49 (2014).
Barone, J. A., Peters, J. M., Garabrant, D. H., Bernstein, L. & Krebsbach, R. Smoking as a risk factor in noise-induced hearing loss. J Occup Med 29, 741–745 (1987).
Hossain, M. et al. Tobacco smoke: a critical etiological factor for vascular impairment at the blood-brain barrier. Brain Res 1287, 192–205 (2009).
Browning, G. G., Gatehouse, S. & Lowe, G. D. Blood viscosity as a factor in sensorineural hearing impairment. Lancet 1, 121–123 (1986).
Lowe, G. D., Drummond, M. M., Forbes, C. D. & Barbenel, J. C. The effects of age and cigarette-smoking on blood and plasma viscosity in men. Scott Med J 25, 13–17 (1980).
Elgoyhen, A. B., Katz, E. & Fuchs, P. A. The nicotinic receptor of cochlear hair cells: a possible pharmacotherapeutic target? Biochem Pharmacol 78, 712–719 (2009).
Wild, D. C., Brewster, M. J. & Banerjee, A. R. Noise-induced hearing loss is exacerbated by long-term smoking. Clin Otolaryngol 30, 517–520 (2005).
Ahn, J. H. et al. Effects of cigarette smoking on hearing recovery from noise-induced temporary hearing threshold shifts in mice. Otol Neurotol 32, 926–932 (2011).
Hwang, J. H., Hsu, C. J., Yu, W. H., Liu, T. C. & Yang, W. S. Diet-induced obesity exacerbates auditory degeneration via hypoxia, inflammation, and apoptosis signaling pathways in CD/1 mice. PLoS One 8, e60730 (2013).
Kim, T. S. et al. Visceral adipose tissue is significantly associated with hearing thresholds in adult women. Clin Endocrinol (Oxf) 80, 368–375 (2014).
Hwang, J. H., Wu, C. C., Hsu, C. J., Liu, T. C. & Yang, W. S. Association of central obesity with the severity and audiometric configurations of age-related hearing impairment. Obesity (Silver Spring) 17, 1796–1801 (2009).
Liew, G. et al. Retinal microvascular abnormalities and age-related hearing loss: the Blue Mountains hearing study. Ear Hear 28, 394–401 (2007).
Gates, G. A., Cobb, J. L., D’Agostino, R. B. & Wolf, P. A. The relation of hearing in the elderly to the presence of cardiovascular disease and cardiovascular risk factors. Arch Otolaryngol Head Neck Surg 119, 156–161 (1993).
Nash, S. D. et al. The prevalence of hearing impairment and associated risk factors: the Beaver Dam Offspring Study. Arch Otolaryngol Head Neck Surg 137, 432–439 (2011).
Arany, I., Hall, S., Reed, D. K., Reed, C. T. & Dixit, M. Nicotine Enhances High-Fat Diet-Induced Oxidative Stress in the Kidney. Nicotine Tob Res (2016).
Groner, J. A. et al. Oxidative Stress in Youth and Adolescents With Elevated Body Mass Index Exposed to Secondhand Smoke. Nicotine Tob Res (2016).
Johnson, J. T. & Rosen, C. A. In Bailey’s Head and Neck Surgery-Otolaryngology (eds Weber, Peter C. & Khariwala, Samir ) Ch. Anatomy and Physiology of Hearing, 2253–2273 (Wolters Kluwer Health/Lippincott Williams & Wilkins, 2014).
Schuknecht, H. F. & Gacek, M. R. Cochlear pathology in presbycusis. Ann Otol Rhinol Laryngol 102, 1–16 (1993).
Author information
Authors and Affiliations
Contributions
Conceived and designed the experiments: Y.-Y.L. and W.-L.C. Performed the experiments: Y.-Y.L., L.-W.W., T.-W.K., C.-J.W., H.-F.Y., T.-C.P., Y.-J.L. and W.-L.C. Analyzed the data: Y.-Y.L., L.-W.W., T.-W.K., C.-J.W., H.-F.Y., T.-C.P., Y.-J.L. and W.-L.C. Contributed reagents/materials/analysis tools: Y.-Y.L., L.-W.W., T.-W.K., C.-J.W., H.-F.Y., T.-C.P., Y.-J.L. and W.-L.C. Prepared Tables 1–3: Y.-Y.L., L.-W.W., T.-W.K., C.-J.W., H.-F.Y., T.-C.P., Y.-J.L. and W.-L.C. Wrote the paper: Y.-Y.L. and W.-L.C.
Ethics declarations
Competing interests
The authors declare no competing financial interests.
Rights and permissions
This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
About this article
Cite this article
Lin, YY., Wu, LW., Kao, TW. et al. Secondhand Smoke is Associated with Hearing Threshold Shifts in Obese Adults. Sci Rep 6, 33071 (2016). https://doi.org/10.1038/srep33071
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/srep33071
This article is cited by
-
Self-reported and cotinine-verified smoking and increased risk of incident hearing loss
Scientific Reports (2021)
-
Exploring the association of Bone Alkaline Phosphatases And Hearing Loss
Scientific Reports (2020)
-
Urinary biomarkers of polycyclic aromatic hydrocarbons and the association with hearing threshold shifts in the United States adults
Environmental Science and Pollution Research (2020)
-
Air pollution increases the risk of SSNHL: A nested case-control study using meteorological data and national sample cohort data
Scientific Reports (2019)
-
Gender Differences in the Association between Moderate Alcohol Consumption and Hearing Threshold Shifts
Scientific Reports (2017)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.