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Hearing Research 384 (2019) 107827

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Hearing Research
journal homepage: www.elsevier.com/locate/heares

Research Paper

Association between shift work and hearing loss: The Dongfeng-Tongji


cohort study
Dongming Wang a, b, Yun Zhou a, b, Jixuan Ma a, b, Lili Xiao a, b, Limin Cao a, b, Min Zhou a, b,
Weijia Kong c, Zhichao Wang c, Wenzhen Li d, Meian He a, b, Xiaomin Zhang a, b,
Huan Guo a, b, Jing Yuan a, b, Weihong Chen a, b, *
a
Department of Occupational & Environmental Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology,
Wuhan, Hubei, 430030, China
b
Key Laboratory of Environment and Health, Ministry of Education & Ministry of Environmental Protection, State Key Laboratory of Environmental Health
(Incubating), School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China
c
Department of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Scienceand Technology, Wuhan, Hubei, 430030,
China
d
Department of Social Medicine and Health Management, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology,
Wuhan, Hubei, 430030, China

a r t i c l e i n f o a b s t r a c t

Article history: The association between shift work and hearing loss is unclear. We aimed to evaluate this association in a
Received 12 April 2019 Chinese population independently and in combination with occupational noise. A total of 11,196 par-
Received in revised form ticipants of the Dongfeng-Tongji cohort study were included. Shift work was self-reported and hearing
16 September 2019
loss was defined as a pure-tone mean of 25 dB or higher at 0.5, 1, 2, and 4 kHz in any ear. The Robust
Accepted 23 October 2019
Available online 26 October 2019
Poisson method were used to assess the relationship between shift work and hearing loss, and the
prevalence ratios (PRs) were calculated. Compared to individuals who reported no shift work, the PRs of
bilateral hearing loss were significantly higher for a shift work duration of fewer than 10 years in women,
Keywords:
Shift work
(PR ¼ 1.024, 95% confidence interval [CI] ¼ 1.002e1.053), but not in men (PR ¼ 1.016, 95% confidence
Hearing loss interval [CI] ¼ 0.998e1.035). The association between short duration of shift work and bilateral hearing
Occupational noise loss was just statistically significant in women when those with occupational noise exposure were
excluded (PR ¼ 1.067, 95%CI ¼ 1.015e1.122). When shift work and occupational noise exposure were
combined, the PRs for hearing loss were highest among individuals with the longest shift work (10
years) and longest noise exposure (20 years) durations, whether for bilateral (PR ¼ 1.114, 95%CI ¼ 1.068
e1.162) or any ear (PR ¼ 1.065, 95%CI ¼ 1.034e1.096). A short duration of shift work may be a risk factor
for hearing loss in women and could increase the prevalence of hearing loss when combined with
occupational noise.
© 2019 Published by Elsevier B.V.

1. Introduction of major public health concern. Irregular working hours and


different types of work schedules are associated with a range of
Shift work is common and often unavoidable with about 29% of adverse health outcomes such as sleep disturbance (Linton et al.,
workers in the United States experiencing this type of work 2015), diabetes mellitus (Pan et al., 2011), coronary heart disease
schedule (Alterman et al., 2013). Furthermore, about 22% of men (Vyas et al., 2012), metabolic disorders (Proper et al., 2016), and
and 11% of women work on shifts that including night work in other chronic health problems (Kecklund et al., 2016;
Europe (Hansen, 2017). The health consequences of shift work are Sigurdardottir et al., 2012).
Hearing loss is also a public health issue, it is reported that the
prevalence of unilateral and bilateral speech-frequency hearing
* Corresponding author. Department of Occupational and Environmental Health, loss was 6.6% and 7.5% in US adults aged 20e69 years in 2011e2012,
School of Public Health, Tongji Medical College, Huazhong University of Science and respectively (Hoffman et al., 2017). In occupational settings, Noise-
Technology, No. 13 Hangkong Road, Wuhan, 430030, PR China. induced hearing loss (NIHL) is one of the leading chronic health
E-mail address: wchen@mails.tjmu.edu.cn (W. Chen).

https://doi.org/10.1016/j.heares.2019.107827
0378-5955/© 2019 Published by Elsevier B.V.
2 D. Wang et al. / Hearing Research 384 (2019) 107827

problems experienced by occupational populations and is one of arrangements that differed from a standard schedule through
the most recorded occupational diseases in Europe and other 0700/0800 to 1700/1800 at least three times per month for one
countries(Samant et al., 2008). Except for occupational noise, year. The participants who reported shift work were divided into
several other factors are reported to be associated with hearing two groups by the median duration of shift work; thus, shift work
loss, including age; sex; race; smoking; metabolic syndromes; and was divided into three categories: never (N ¼ 6244), 0-10y
chronic disease including hypertension, cardiovascular diseases, (N ¼ 2519), and 10y (N ¼ 2433).
and diabetes mellitus (Agrawal et al., 2009; Cruickshanks et al.,
1998). Besides, shift work is also reported to be associated with 2.4. Ascertainment of noise exposure assessment
metabolic syndromes, hypertension, cardiovascular diseases and
diabetes mellitus (Vetter et al., 2018; Wang et al., 2014). The occupational information of each subject was assessed by
Few studies have investigated the influence of shift work on the questionnaire, which contained employment and variables
hearing loss. Two previous studies mainly compared the effects of about the work, such as the corporation, job title, and duration of
different types of shift work on hearing loss with small samples to each job (Wang et al., 2018). The occupational noise levels for each
test the hypothesis that rotating shift work could affect the job title at each workplace were assessed by qualified institutions
continuous exposure time of occupational noise (Chou et al., 2009; according to the companies’ records. Noise exposure levels for
Holzmuller et al., 1990). However, these studies did not assess the workplaces outside of DMC were determined according to the job
independent effect of shift work on hearing loss after adjusting for description and in consultation with local occupational hygienists.
potential confounders. In addition, the potential joint effect of shift Occupational noise exposure was defined as exposure to normal-
work and occupational noise on hearing loss is not well ized continuous A-weighted sound pressure level equivalent to an
understood. 8-h per day of 80 dB (A) or above (LAeq, 8h  80 dB(A)) for at least
Thus, we conducted a study with large sample size to assess the one year. Noise exposure duration was also divided into four
effect of shift work on hearing loss, independently and in combi- groups: 0, 1-<10y, 10-<20y, 20y.
nation with occupational noise, based on the assumption that shift
work may affect hearing loss. 2.5. Ethical approval

2. Materials and methods The study was approved by the Ethics and Human Subject
committee of Tongji Medical College, and Dongfeng General Hos-
2.1. Study population pital, DMC. The written informed consents were obtained from all
of the participants.
The data used in this study were obtained from the Dongfeng-
Tongji Cohort Study, the details of which have been reported 2.6. Covariates
elsewhere (Wang et al., 2013). All participants were retired em-
ployees of Dongfeng Motor Corporation (DMC) with unique med- Information on sociodemographic characteristics (sex, race, and
ical insurance card numbers in the DMC’s health-care service age), smoking status, drinking status, hypertension, ototoxic med-
system. The cohort study began in 2008 and follow-up occurred ications, and chronic disease history were collected using a ques-
every five years. Finally, a total of 27,009 retired employees tionnaire in face-to-face interviews performed by trained
completed baseline questionnaires and medical examinations were interviewers. Individuals currently smoking at least one cigarette
included. Five years later, 25,978 individuals (96.2%) completed the per day for more than half a year were defined as current smokers;
follow-up until October 2013. In 2013, 11,513 participants from the otherwise they were regarded as non-smokers, including ever
baseline population underwent audiometric examinations. smokers and never smokers. Those who currently drank at least
In the present study, the 11,513 participants who underwent one time per week for more than half a year were defined as cur-
audiometric examinations in 2013 were included in our study, we rent drinkers; otherwise they were regarded as non-drinkers,
excluded individuals without auditory examination results (n ¼ 57) including ever drinkers and never drinkers. Hypertension was
and those who provided incomplete baseline information defined as a blood pressure of at least 140/90 mmHg, self-reported
(n ¼ 100), leaving 11,196 subjects in the present analysis. physician diagnosis of hypertension, or self-reported current use of
antihypertensive medication. Use of ototoxic medication was
2.2. Auditory measures and ascertainment of hearing loss defined as the self-reported use of loop diuretics, aminoglycosides,
or non-steroidal anti-inflammatory drugs. Chronic disease histories
Each participant first underwent a general physical and otologic diagnosed by a physician were reported by the participants,
examination. Pure-tone audiometry was then performed by certi- including diabetes mellitus, coronary heart disease, myocardial
fied audiologists in a sound-isolated room with a calibrated pure- infarction, and stroke.
tone audiometer (Micro-DSP ZD21). Air conduction thresholds
were determined for each ear at 0.5, 1, 2, 4 and 8 kHz across an 2.7. Statistical analysis
intensity range of 10 to 120 dB. Those who did not response at
maximum value were coded as the maximum value. Hearing loss at The sociodemographic characteristics of the participants were
the speech frequencies was defined as a pure-tone mean of 25 dB or reported as means (SD) for continuous variables and as numbers
higher at 0.5, 1, 2, and 4 kHz in any ear (Agrawal et al., 2008). (percentages) for categorical variables. The Robust Poisson method
was performed to evaluate the independent and combined asso-
2.3. Ascertainment of shift work ciations of shift work and occupational noise exposure with hearing
loss, and the prevalence ratios (PRs) were calculated, as the prev-
Shift work was assessed using a self-administrated question- alence of hearing loss is high in our study (Petersen et al., 2008).
naire. Participants were asked the following question: “Did you The associations were further evaluated with stratification by sex,
experience shift work during your work history?” Those who based on previous reports suggesting that sex may be an important
responded affirmatively were further asked about the duration of factor for hearing loss (Helzner et al., 2005). Models were con-
shift work. It was defined as any work schedule involving irregular structed using those who were non shift-workers and without
D. Wang et al. / Hearing Research 384 (2019) 107827 3

occupational noise exposure as the reference group. We chose them, 77.6% (8688/11,196) had speech-frequency hearing loss,
covariates according to evidence from published literatures 44.2% (4592/11,196) were shift workers, and 34.6% (3878/11,196)
(Agrawal et al., 2009; Cruickshanks et al., 1998). The covariates were exposed to occupational noise. Compared to those with
included age, sex, race, smoking status, drinking status, hyperten- normal hearing, participants with speech-frequency hearing loss
sion, ototoxicity medicine, and chronic disease history (diabetes were older and they were more likely to be males; smokers;
mellitus, coronary heart disease, myocardial infarction, and stroke), drinkers; exposed to occupational noise; and have hypertension,
and all the covariates were adjusted in the statistical analyses. All diabetes mellitus, coronary heart disease, myocardial infarction, or
statistical analyses were performed using SAS version 9.2 software stroke. These features were more evident in those with bilateral
(SAS institute Inc., Cary, NC). The statistical tests were two sided, speech-frequency hearing loss.
and significance was set at P < 0.05.
3.1. Association between shift work and hearing loss
2.8. Sensitivity analysis
The effect of shift work on hearing loss was shown in Table S1.
To assess whether excluding participants with occupational Compared to that among participants without shift work, the
noise exposure could bias the results, a sensitivity analysis of the prevalence ratios (PRs) were higher among those with shift work,
effect of shift work on hearing loss was performed to test the sta- including bilateral (PR ¼ 1.034, 95% confidence interval
bility and robustness of the association. The prevalence of occu- [CI] ¼ 1.006e1.063) and any-ear (PR ¼ 1.023, 95%CI ¼ 1.003e1.043)
pational noise exposure was 34.7% (3891/11,196) among the speech-frequency hearing loss. In stratified analysis of sex, the PR
participants. for shift work and bilateral hearing loss was statistically significant
in women (PR ¼ 1.046, 95%CI ¼ 1.003e1.096), but not in men
3. Results (PR ¼ 1.021, 95%CI ¼ 0.988e1.056).
When shift work was categorized according to the duration
The characteristics of the participants included in the analysis (Table 2), the PRs of bilateral hearing loss was significantly higher
were reported by their categories of hearing loss (Table 1). Among for those with shift work (PR ¼ 1.021, 95%CI ¼ 1.005e1.038 for shift

Table 1
The characteristics of the participants by hearing loss categories.

Variables Participants (N ¼ 11196) Normal Hearing (N ¼ 2508) Speech-frequency hearing Loss (N ¼ 8688) Unilateral (N ¼ 1800) Bilateral (N ¼ 6888)

Age 67.1 ± 7.4 62.3 ± 6.6 68.5 ± 7.0 65.2 ± 6.4 69.3 ± 6.9
Sex
Male 5060(45.2) 668(26.6) 4392(50.6) 701(38.9) 3691(53.6)
Female 6136(54.8) 1840(73.4) 4296(49.4) 1099(61.1) 3197(46.4)
Race
Han 11025(98.5) 2472(98.6) 8553(98.4) 1756(97.6) 6797(98.7)
others 171(1.5) 36(1.4) 135(1.6) 44(2.4) 91(1.3)
Duration of shift work, year
No 6244(55.8) 1384(55.2) 4860(55.9) 993(55.2) 3867(56.1)
0 < x < 10 2519(22.5) 592(23.6) 1927(22.2) 419(23.3) 1508(21.9)
x  10 2433(21.7) 532(21.2) 1901(21.9) 388(21.5) 1513(22.0)
Smoking
Yes 1569(14.0) 239(9.5) 1330(15.3) 225(12.5) 1105(16.0)
No 9627(86.0) 2269(90.5) 7358(84.7) 1575(87.5) 5783(84.0)
Drinking
Yes 2616(23.4) 489(19.5) 2127(24.5) 413(22.9) 1714(24.9)
No 8580(76.6) 2019(80.5) 6561(75.5) 1387(77.1) 5174(75.1)
Hypertension
Yes 7739(69.1) 1518(60.5) 6221(71.6) 1189(66.1) 5032(73.0)
No 3457(30.9) 990(39.5) 2467(28.4) 611(33.9) 1856(27.0)
Diabetes mellitus
Yes 1759(15.7) 342(13.6) 1417(16.3) 272(15.1) 1145(16.6)
No 9437(84.3) 2166(86.4) 7271(83.7) 1528(84.9) 5743(83.4)
Coronary heart disease
Yes 2030(18.1) 335(13.4) 1695(19.5) 276(15.3) 1419(20.6)
No 9166(81.9) 2173(86.6) 6993(80.5) 1524(84.7) 5469(79.4)
Myocardial infarction
Yes 396(3.5) 46(1.8) 350(4.0) 44(2.4) 306(4.4)
No 10800(96.5) 2462(98.2) 8338(96.0) 1756(97.6) 6582(95.6)
Stroke
Yes 529(4.7) 80(3.2) 449(5.2) 58(3.2) 391(5.7)
No 10667(95.3) 2428(96.8) 8239(94.8) 1742(96.8) 6497(94.3)
Ototoxic medicine
Yes 2770(24.7) 615(24.5) 2155(24.8) 464(25.8) 1691(24.5)
No 8426(75.3) 1893(75.5) 6533(75.2) 1336(74.2) 5197(75.5)
Occupational noise exposure
Yes 3878(34.6) 841(33.5) 3037(35.0) 624(34.7) 2413(35.0)
No 7318(65.4) 1667(66.5) 5651(65.0) 1176(65.3) 4475(65.0)
Exposure duration of occupational noise
No 7305(65.3) 1666(66.4) 5639(64.9) 1176(65.3) 4463(64.8)
1  year<10 944(8.4) 253(10.1) 691(8.0) 184(10.2) 507(7.4)
10  year<20 1150(10.3) 271(10.8) 879(10.1) 194(10.8) 685(9.9)
year  20 1797(16.0) 318(12.7) 1479(17.0) 246(13.7) 1233(17.9)
4 D. Wang et al. / Hearing Research 384 (2019) 107827

Table 2
Prevalence ratios (95% CIs) of hearing loss by duration of shift work in total population (N ¼ 11196).

Shift work Unilateral(N ¼ 1800)a Bilateral(N ¼ 6888)b Any ear(N ¼ 8688)c

Total
No ref ref ref
1  year<10 0.984(0.937e1.033) 1.021(1.005e1.038) 1.013(1.002e1.024)
year  10 0.968(0.878e1.067) 1.043(1.011e1.077) 1.026(1.003e1.048)
Male
No ref ref ref
1  year<10 0.981(0.909e1.058) 1.016(0.998e1.035) 1.010(0.998e1.022)
year  10 0.962(0.827e1.120) 1.033(0.995e1.071) 1.019(0.995e1.045)
Female
No ref ref ref
1  year<10 0.981(0.920e1.046) 1.024(1.002e1.053) 1.013(0.994e1.032)
year  10 0.962(0.847e1.094) 1.049(0.993e1.108) 1.026(0.988e1.066)

Adjusted for age, sex, race, occupational noise exposure, smoking status, drinking status, hypertension, ototoxicity medicine, chronic diseases (diabetes mellitus,
coronary heart disease, myocardial infarction and stroke).
a
Pure-tone mean of 25 dB or higher at 0.5, 1, 2, and 4 kHz in one ear only.
b
Pure-tone mean of 25 dB or higher at 0.5, 1, 2, and 4 kHz in both ears.
c
Pure-tone mean of 25 dB or higher at 0.5, 1, 2, and 4 kHz in any ear, including one ear only and both ears.

work duration of 1e10 years; PR ¼ 1.043, 95%CI ¼ 1.011e1.077 for CI ¼ 1.089e1.171). The results for any ear hearing loss were similar
shift work duration of more than 10 years), the results were similar as those for bilateral hearing loss.
for any ear hearing loss (PR ¼ 1.013, 95%CI ¼ 1.002e1.024 for shift
work duration of 1e10 years; PR ¼ 1.026, 95%CI ¼ 1.003e1.048 for
4. Discussion
shift work duration of more than 10 years). In stratified analysis of
sex, it was just statistically significant for a shift work duration of
This study identified a potential association between shift work
fewer than 10 in women (PR ¼ 1.024, 95%CI ¼ 1.002e1.053).
and hearing loss, especially bilateral hearing loss. This finding was
The results of a sensitivity analysis were nearly the same after
sex-specific, it was just statistically significant in women and only
excluding participants with occupational noise exposure (Table S2).
among women with a short duration of shift work. This result was
A shift work duration of fewer than 10 years was associated with
consistent with those obtained after excluding individuals with
bilateral (PR ¼ 1.057, 95%CI ¼ 1.015e1.101) and any-ear (PR ¼ 1.036,
occupational noise exposure. To confirm the results, we also
95%CI ¼ 1.007e1.066) hearing loss, and the association for bilateral
investigated the association between occupational noise exposure
hearing loss was just statistically significant in women (PR ¼ 1.067,
and hearing loss, and verified the positive relationship among both
95%CI ¼ 1.015e1.122).
men and women, which could explain the reliability of our study.
The underlying mechanism was not clear. Shift work is associ-
3.2. Combined effect of shift work and occupational noise exposure ated with diabetes mellitus (Vetter et al., 2018), metabolic syn-
on hearing loss drome (Wang et al., 2014), obesity (Sun et al., 2018), hypertension
(Manohar et al., 2017) and cardiovascular diseases (Torquati et al.,
We further explored the combined association of occupational 2017) through the endocrine pathway, as we have previously re-
noise exposure and shift work on any-ear and both-ear hearing loss ported (Guo et al., 2013, 2015). Recent published studies reported
(Fig. S1). Despite bilateral or any-ear hearing loss, the PRs were that diabetes mellitus (Kim et al., 2017), metabolic syndrome
highest among those exposed to occupational noise and shift work, (Aghazadeh-Attari et al., 2017), obesity (Curhan et al., 2013), hy-
compared to participants without shift work and no occupational pertension (Lin et al., 2016) and cardiovascular diseases (Tan et al.,
noise exposure. 2018) could increase the risk of hearing loss. The microvascular and
The effects of shift work duration and noise exposure duration neuropathic complications in multiple organ systems that affect
on bilateral and any-ear hearing loss were further assessed to test patients with diabetes mellitus may affect the inner ear (Friedman
the dose-response relationship (Table 3 and Table 4). The PRs were et al., 1975; Vinik et al., 2003), including microangiopathic changes
highest among individuals with the longest noise exposure (20 in the capillaries of the stria vascularis, such as narrowing of the
years) and shift work durations (10 years) (PR ¼ 1.114, 95% internal auditory artery, thickening of the basilar membrane,
CI ¼ 1.068e1.162, bilateral; PR ¼ 1.065, 95%CI ¼ 1.034e1.096, any demyelination of the auditory nerve and loss of spiral ganglion
ear). Sex-specific analyses revealed that the PR for bilateral hearing neurons and organ of Corti cells (Akinpelu et al., 2014; Fukushima
loss was higher in men (PR ¼ 1.117, 95%CI ¼ 1.064e1.173) than that et al., 2006). In addition, hypertension and cardiovascular dis-
in women (PR ¼ 1.101, 95%CI ¼ 1.023e1.185). eases may compromise the vascular supply to the stria vascularis
(Friedland et al., 2009). Moreover, shift work-induced obesity-
3.3. Association between occupational noise and hearing loss related oxidative stress and resultant damage to the auditory
epithelia may also contribute to hearing loss (Loffredo et al., 2012).
To confirm the results of our study, the associations between Further studies are warranted to investigate the potential biological
occupational noise exposure and hearing loss were also explored mechanism and difference between sexes.
(Table S3 and Table S4). Compared to those participants that were The sex-specific relationship between shift work and hearing
not exposed to occupational noise, the PR of bilateral hearing loss loss was an interesting finding, the reasons for which remain un-
increased with the increase of noise exposure duration and got the clear. The result implied that the association was statistically sig-
highest in the longest noise exposure duration group (PR ¼ 1.104, nificant for females, but not for males. This indicates that female
95%CI ¼ 1.067e1.141). Stratified analyses revealed that the PR be- shift workers should pay more attention to the prevention of
tween the longest noise exposure duration (20 years) and bilat- hearing loss, and provides a clue for future study of how the bio-
eral hearing loss was higher in men (PR ¼ 1.129, 95% logical mechanisms of shift work and hearing loss are affected by
D. Wang et al. / Hearing Research 384 (2019) 107827 5

Table 3
Prevalence ratios (95% CIs) of hearing loss by combined categories of occupational noise exposure and duration of shift work (bilateral).

Shift work Noise

No 1  year<10 10  year<20 year20

Total
No ref 1.018(1.011e1.025) 1.027(1.017e1.038) 1.037(1.022e1.051)
1  year<10 1.057(1.015e1.101) 1.055(1.033e1.078) 1.065(1.039e1.092) 1.075(1.045e1.105)
year  10 1.028(0.997e1.049) 1.094(1.056e1.133) 1.104(1.062e1.148) 1.114(1.068e1.162)
Male
No ref 1.019(1.010e1.027) 1.028(1.016e1.041) 1.038(1.021e1.055)
1  year<10 1.015(0.982e1.049) 1.057(1.031e1.083) 1.067(1.037e1.098) 1.076(1.042e1.122)
year  10 1.030(0.963e1.101) 1.096(1.053e1.142) 1.107(1.058e1.157) 1.117(1.064e1.173)
Female
No ref 1.016(1.004e1.029) 1.024(1.006e1.043) 1.033(1.008e1.058)
1  year<10 1.067(1.015e1.122) 1.049(1.012e1.089) 1.058(1.014e1.104) 1.066(1.015e1.120)
year  10 1.033(0.998e1.059) 1.084(1.019e1.152) 1.092(1.021e1.169) 1.101(1.023e1.185)

Adjusted for age, sex, race, smoking status, drinking status, hypertension, ototoxicity medicine, chronic diseases (diabetes mellitus, coronary heart disease, myocardial
infarction and stroke).
Hearing loss was defined as pure-tone mean of 25 dB or higher at 0.5, 1, 2, and 4 kHz in both ears.

Table 4
Prevalence ratios (95% CIs) of hearing loss by combined categories of occupational noise exposure and duration of shift work (any ear).

Shift work Noise

No 1  year<10 10  year<20 year20

Total
No ref 1.011(1.006e1.016) 1.016(1.008e1.023) 1.021(1.011e1.031)
1  year<10 1.036(1.007e1.066) 1.032(1.017e1.047) 1.037(1.020e1.055) 1.043(1.023e1.063)
year  10 1.018(0.993e1.032) 1.054(1.028e1.080) 1.059(1.031e1.088) 1.065(1.034e1.096)
Male
No ref 1.009(1.004e1.015) 1.014(1.006e1.022) 1.019(1.008e1.030)
1  year<10 1.016(0.999e1.033) 1.028(1.012e1.045) 1.033(1.014e1.053) 1.038(1.016e1.061)
year  10 1.033(0.999e1.067) 1.048(1.020e1.076) 1.053(1.022e1.084) 1.058(1.024e1.092)
Female
No ref 1.011(1.003e1.020) 1.017(1.004e1.030) 1.022(1.005e1.040)
1  year<10 1.028(0.981e1.077) 1.034(1.008e1.060) 1.039(1.009e1.071) 1.045(1.010e1.081)
year  10 1.014(0.991e1.038) 1.057(1.013e1.102) 1.062(1.014e1.113) 1.068(1.015e1.124)

Adjusted for age, sex, race, smoking status, drinking status, hypertension, ototoxicity medicine, chronic diseases (diabetes mellitus, coronary heart disease, myocardial
infarction and stroke).
Hearing loss was defined as pure-tone mean of 25 dB or higher at 0.5, 1, 2, and 4 kHz in any ear, including one ear only and both ears.

sex. These biological mechanisms are complex, and comprehensive that the independent effect of occupational noise on bilateral
research is needed. The possible adverse effect of circadian hearing loss was greater than that of shift work (1.055 vs 1.034).
disruption owing to shift work may influence the regulation of Furthermore, the relationship between occupational noise and
estrogens through the hypothalamic-pituitary-gonadal axis bilateral hearing loss in men was greater than that between shift
(Dumont et al., 2014; Gomez-Acebo et al., 2015; Papantoniou et al., work and bilateral hearing loss in women (1.080 vs 1.046), the
2015), which could contribute to the sex difference between shift special job may be a contributing factor, such as military service for
work and hearing loss. Furthermore, the increased risk in women males. This may explain the inverse sex-specific results of the
between shift work and obesity (Sun et al., 2018) and sex differ- combined effect of shift work and occupational noise and the in-
ences in insulin resistance could also contribute to this result (Qiu dependent effect of shift work on hearing loss. In addition, the
et al., 2018). Longer shift work was not significantly associated with association between the longest noise exposure duration (20
hearing loss, a finding that may be related to the continuous years) and bilateral hearing loss in men was also greater than that
adaption of the circadian system (Sun et al., 2018), resulting in a for a shorter shift work duration in women (1.129 vs 1.024),
gradually weakened effect of shift work on hearing loss. However, resulting in the highest combined PR for the longest noise exposure
the potential mechanism requires confirmation in future studies. (20 years) and longest shift work (10 years) durations. However,
As shift work and occupational noise exposure were not asso- the combined PR of shift work and occupational noise exposure was
ciated with unilateral hearing loss, we explored their joint effect on still higher than the independent effect of occupational noise,
bilateral and any-ear hearing loss. The combination of shift work which indicated that shift work could also increase the prevalence
and occupational noise resulted in the highest PRs among in- of hearing loss when combined with occupational noise.
dividuals with the longest noise exposure (20 years) and shift This study has some strengths. It evaluated the association be-
work (10 years) durations, regardless of bilateral or any-ear tween shift work and hearing loss in a large sample size, which has
hearing loss. Meanwhile, the PR was higher in men than that in rarely been assessed before. However, several limitations should be
women for bilateral hearing loss. The combined sex-specific results noted. Firstly, it was not a prospective study design; thus, we could
were almost the opposite of the independent association between not explore the causal relationship between shift work and hearing
shift work and hearing loss mentioned above. Occupational noise loss. Future follow-up is necessary to assess this association. Sec-
may be the most direct risk factor for hearing loss in occupational ondly, the shift work information was self-reported. However, the
settings and mainly induced bilateral hearing loss. It also indicated validity of self-reported exposure to shift work was verified in
6 D. Wang et al. / Hearing Research 384 (2019) 107827

previous studies (Harma et al., 2017). Thirdly, some other con- index, waist circumference, physical activity, and risk of hearing loss in women.
Am. J. Med. 126, 1142 e1-8.
founders were still not included in the analyses, such as recrea-
Dumont, M., Paquet, J., 2014. Progressive decrease of melatonin production over
tional noise exposure, hearing protection devices, etc. However, consecutive days of simulated night work. Chronobiol. Int. 31, 1231e1238.
most of the employers might not wear hearing protection devices Friedland, D.R., Cederberg, C., Tarima, S., 2009. Audiometric pattern as a predictor of
according to the company records, as the protection consciousness cardiovascular status: development of a model for assessment of risk. The
Laryngoscope 119, 473e486.
of the workers may be poor in the past. Friedman, S.A., Schulman, R.H., Weiss, S., 1975. Hearing and diabetic neuropathy.
Arch. Intern. Med. 135, 573e576.
Fukushima, H., Cureoglu, S., Schachern, P.A., Paparella, M.M., Harada, T., Oktay, M.F.,
5. Conclusions
2006. Effects of type 2 diabetes mellitus on cochlear structure in humans. Arch.
Otolaryngol. Head Neck Surg. 132, 934e938.
In summary, our data provide evidence that shift work was Gomez-Acebo, I., Dierssen-Sotos, T., Papantoniou, K., Garcia-Unzueta, M.T., Santos-
Benito, M.F., Llorca, J., 2015. Association between exposure to rotating night
independently associated with bilateral hearing loss in this large
shift versus day shift using levels of 6-sulfatoxymelatonin and cortisol and
sample study of middle-aged and elderly Chinese adults, a finding other sex hormones in women. Chronobiol. Int. 32, 128e135.
that was just statistically significant among women. When com- Guo, Y., Liu, Y., Huang, X., Rong, Y., He, M., Wang, Y., Yuan, J., Wu, T., Chen, W., 2013.
bined with occupational noise exposure, shift work could increase The effects of shift work on sleeping quality, hypertension and diabetes in
retired workers. PLoS One 8, e71107.
the prevalence of noise-induced hearing loss. Future studies are Guo, Y., Rong, Y., Huang, X., Lai, H., Luo, X., Zhang, Z., Liu, Y., He, M., Wu, T., Chen, W.,
needed to evaluate the potential mechanisms of these findings. 2015. Shift work and the relationship with metabolic syndrome in Chinese aged
workers. PLoS One 10, e0120632.
Hansen, J., 2017. Night shift work and risk of breast cancer. Curr. Environ. Health
Funding Rep. 4, 325e339.
Harma, M., Koskinen, A., Ropponen, A., Puttonen, S., Karhula, K., Vahtera, J.,
Kivimaki, M., 2017. Validity of self-reported exposure to shift work. Occup.
The study was supported by the National Natural Science
Environ. Med. 74, 228e230.
Foundation of China (81903291), China Postdoctoral Science Helzner, E.P., Cauley, J.A., Pratt, S.R., Wisniewski, S.R., Zmuda, J.M., Talbott, E.O., de
Foundation (2019T120666, 2018M640705, 2019T120665) and the Rekeneire, N., Harris, T.B., Rubin, S.M., Simonsick, E.M., Tylavsky, F.A.,
Fundamental Research Funds for the Central Universities, Newman, A.B., 2005. Race and sex differences in age-related hearing loss: the
health, aging and body composition study. J. Am. Geriatr. Soc. 53, 2119e2127.
HUST2016JCTD116. The funder did not play any role in study Hoffman, H.J., Dobie, R.A., Losonczy, K.G., Themann, C.L., Flamme, G.A., 2017.
design; in the collection, analysis, and interpretation of data; in the Declining prevalence of hearing loss in US adults aged 20 to 69 years. JAMA
writing of the report; nor in the preparation, review, or approval of Otolaryngol. Head Neck Surg. 143, 274e285.
Holzmuller, M., Seibt, A., Jakubowski, A., Friedrichsen, G., 1990. Studies on the
the manuscript. combined effects of shift work and noise on permanent hearing loss. Z. Gesamte
Hyg. 36, 501e502.
Declaration of competing interest Kecklund, G., Axelsson, J., 2016. Health consequences of shift work and insufficient
sleep. BMJ 355, i5210.
Kim, M.B., Zhang, Y., Chang, Y., Ryu, S., Choi, Y., Kwon, M.J., Moon, I.J., Deal, J.A.,
None. Lin, F.R., Guallar, E., Chung, E.C., Hong, S.H., Ban, J.H., Shin, H., Cho, J., 2017.
Diabetes mellitus and the incidence of hearing loss: a cohort study. Int. J. Epi-
demiol. 46, 717e726.
Acknowledgments Lin, B.M., Curhan, S.G., Wang, M., Eavey, R., Stankovic, K.M., Curhan, G.C., 2016.
Hypertension, diuretic use, and risk of hearing loss. Am. J. Med. 129, 416e422.
Linton, S.J., Kecklund, G., Franklin, K.A., Leissner, L.C., Sivertsen, B., Lindberg, E.,
The contributions of all the participants, staffs of the Health
Svensson, A.C., Hansson, S.O., Sundin, O., Hetta, J., Bjorkelund, C., Hall, C., 2015.
Examination Center of the Dongfeng Central Hospital and the The effect of the work environment on future sleep disturbances: a systematic
Medical Insurance Center of DMC, and all members of study team review. Sleep Med. Rev. 23, 10e19.
are greatly acknowledged. Loffredo, L., Martino, F., Carnevale, R., Pignatelli, P., Catasca, E., Perri, L.,
Calabrese, C.M., Palumbo, M.M., Baratta, F., Del Ben, M., Angelico, F., Violi, F.,
2012. Obesity and hypercholesterolemia are associated with NOX2 generated
Appendix A. Supplementary data oxidative stress and arterial dysfunction. J. Pediatr. 161, 1004e1009.
Manohar, S., Thongprayoon, C., Cheungpasitporn, W., Mao, M.A., Herrmann, S.M.,
2017. Associations of rotational shift work and night shift status with hyper-
Supplementary data to this article can be found online at tension: a systematic review and meta-analysis. J. Hypertens. 35, 1929e1937.
https://doi.org/10.1016/j.heares.2019.107827. Pan, A., Schernhammer, E.S., Sun, Q., Hu, F.B., 2011. Rotating night shift work and
risk of type 2 diabetes: two prospective cohort studies in women. PLoS Med. 8,
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