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Research Article
Occupational noise exposure and hypertension: the
Dongfeng-Tongji Cohort Study
Dongming Wang, MDa,b,c,d, Min Zhou, MDa,b, Wenzhen Li, MDe, Weijia Kong, MDf,
Zhichao Wang, MDf, Yanjun Guo, MDa,b, Xiaomin Zhang, MDa,b, Meian He, MDa,b,
Huan Guo, MDa,b, and Weihong Chen, MD, PhDa,b,*
a
Department of Occupational & Environmental Health, School of Public Health, Tongji Medical College, Huazhong University of Science
and Technology, Wuhan, Hubei, China;
b
Key Laboratory of Environment and Health, Ministry of Education & Ministry of Environmental Protection, and State Key Laboratory of
Environmental Health (Incubating), School of Public Health, Tongji Medical College, Huazhong University of Science and Technology,
Wuhan, Hubei, China;
c
Department of Occupational Health, Wuhan Prevention and Treatment Center for Occupational Diseases, Wuhan, Hubei, China;
d
Hubei Province Key Laboratory of Occupational Hazard Identification and Control, Wuhan University of Science and Technology, Wuhan,
Hubei, China;
e
Department of Social Medicine and Health Management, School of Public Health, Tongji Medical College, Huazhong University of Science
and Technology, Wuhan, Hubei, China; and
f
Department of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan,
Hubei, China
Manuscript received August 8, 2017 and accepted November 7, 2017
Abstract
The association between occupational noise exposure and hypertension is unclear. We aimed to explore the association in a
Chinese population and to summarize our findings with previous published articles. The cross-sectional study included
22,450 participants from Dongfeng-Tongji Cohort Study. In a subsample of 10,636 subjects, we assessed the association be-
tween hearing loss and hypertension. For the meta-analysis, we searched PubMed and EMBASE until April 2017, and the
pooled odds ratio (OR) was combined using a random effect model. Compared with participants without occupational noise
exposure, the risk of hypertension was significantly higher for noise exposure duration 20 (OR ¼ 1.09, 95% confidence
interval [CI] ¼ 1.00–1.18). In the sex-specific analysis, the association was only significantly pronounced in males
(OR ¼ 1.16, 95% CI ¼ 1.03–1.31), but not in females (OR ¼ 1.01, 95% CI ¼ 0.88–1.14). In the subsample analyses, hearing
loss, which was an indicator for exposure to loud noise, was associated with a higher risk of hypertension, especially for
participants who were bilateral hearing loss (OR ¼ 1.39, 95% CI ¼ 1.24–1.54). In the meta-analysis, the pooled OR for
the association between occupational noise exposure and hypertension was 1.25 (95% CI ¼ 1.10–1.42). On the basis of
an indicator for exposure to occupational noise, the cross-sectional study and meta-analysis identified occupational noise
exposure as a potential risk factor for increased hypertension risk. J Am Soc Hypertens 2018;12(2):71–79. Ó 2017
American Society of Hypertension. All rights reserved.
Keywords: Hearing loss; hypertension; occupational noise exposure.
The study was supported by the National 111 Project in China Conflicts of interest: None.
(No.B12004), Innovative Research Team in University of Ministry *Corresponding author: Weihong Chen, MD, PhD, Department
of Education of China (No.IRT1246), the Fundamental Research of Occupational and Environmental Health, School of Public
Funds for the Central Universities, HUST2016YXZD044 and Health, Tongji Medical College, Huazhong University of Science
Open project of Hubei Province Key Laboratory of Occupational and Technology, No. 13 Hangkong Road, Wuhan, 430030, P. R.
Hazard Identification and Control (OHIC2017Y05). The funder China. Tel/Fax: þ86 27 83691677.
did not play any role in study design; in the collection, analysis, E-mail: wchen@mails.tjmu.edu.cn
and interpretation of data; in the writing of the report; nor in the
preparation, review, or approval of the article.
1933-1711/$ - see front matter Ó 2017 American Society of Hypertension. All rights reserved.
https://doi.org/10.1016/j.jash.2017.11.001
72 D. Wang et al. / Journal of the American Society of Hypertension 12(2) (2018) 71–79
females and 66.8% aged >60 years. Overall, 8587 individ- exposed to occupational noise for 20 years were more in-
uals (38.2%) reported to expose to occupational noise dur- clined to having hypertension.
ing their work period, and the prevalence of hypertension
among all participants was 52.6% (11,799/22,450), 55.8% Occupational Noise Exposure and Hypertension
(5630/10,097) for males, and 49.9% (6169/12,353) for fe-
males. We observed pronounced differences in hyperten- The ORs and 95% CIs for the effect of occupational
sion prevalence by demographic characteristics. noise exposure on hypertension were presented in
Prevalence of hypertension was higher among men, indi- Table 2. Compared with participants not exposed to occu-
viduals aged >60 years, having a family history of hyper- pational noise, the risk of hypertension was significantly
tension, individuals who were overweight and obese, and higher in the group of 20 years noise exposure
the longest noise exposure duration group. Individuals (OR ¼ 1.09, 95% CI ¼ 1.00–1.18), after adjusting for
Table 1
Baseline characteristics of participants by hypertension categories
Variables Total Hypertension Normotension P Value
(N ¼ 22,450) (N ¼ 11,799) (N ¼ 10,651)
Age (y, mean SD) 62.6 7.8 64.2 7.4 60.9 7.8 <.001
Age (y) <.001
<60 7472 (33.3) 2996 (25.4) 4476 (42.0)
60 to w<70 13,396 (59.7) 7748 (65.7) 5648 (53.0)
70 1582 (7.1) 1055 (8.9) 527 (5.0)
Sex <.001
Male 10,097 (45.0) 5630 (47.7) 4467 (41.9)
Female 12,353 (55.0) 6169 (52.3) 6184 (58.1)
Shift work, n (%) 10,703 (47.7) 5500 (46.6) 5203 (48.9) .001
Current smokers, n (%) 4006 (17.8) 1999 (16.9) 2007 (18.8) <.001
Current drinkers, n (%) 4686 (20.9) 2413 (20.5) 2273 (21.3) .10
Family history of hypertension, n (%) 4963 (22.1) 3312 (28.1) 1651 (15.5) <.001
Physical activity, n (%) 19,982 (89.0) 10,527 (89.2) 9455 (88.8) .28
Life stress, n (%) 10,758 (47.9) 5873 (49.8) 4885 (45.9) <.001
Waist (cm, mean SD) 83.3 9.5 85.5 9.4 80.9 9.0 <.001
Tea consumption, n (%) 8207 (36.6) 4364 (37.0) 3843 (36.1) .16
Coffee consumption, n (%) 444 (2.0) 161 (1.4) 283 (2.7) <.001
Diabetes, n (%) 2688 (12.0) 1856 (15.8) 832 (7.8) <.001
TC, mmol/L 5.17 0.97 5.13 0.96 5.21 0.99 <.001
TG, mmol/L 1.46 1.15 1.32 1.08 1.59 1.20 <.001
HDL-C, mmol/L 1.44 0.41 1.47 0.40 1.41 0.41 <.001
LDL-C, mmol/L 3.02 0.84 2.99 0.83 3.05 0.85 <.001
BMI <.001
<18.5 604 (2.7) 192 (1.6) 412 (3.9)
18.5 to w<25 12,305 (54.8) 5557 (47.1) 6748 (63.3)
25w<28 6282 (28.0) 3749 (31.8) 2533 (23.8)
28 3259 (14.5) 2301 (19.5) 958 (9.0)
Occupational noise exposure, n (%) .003
No 13,863 (61.8) 7349 (62.3) 6514 (61.2)
1 y <10 1979 (8.8) 979 (8.3) 1000 (9.4)
10 y <20 2529 (11.3) 1283 (10.9) 1246 (11.7)
20 y 4079 (18.2) 2188 (18.5) 1891 (17.7)
Hearing loss, n (%)* <.001
No 2383 (22.4) 908 (17.6) 1475 (26.9)
Unilateral 1705 801 (15.5) 904 (16.5)
Bilateral 6548 3449 (66.9) 3099 (56.6)
Either 8253 (77.6) 4250 (82.4) 4003 (73.1)
BMI, body mass index; HDL-C, high-density lipoprotein cholesterol; LDL-C, low-density lipoprotein cholesterol; SD, standard devia-
tion; TC, total cholesterol; TG, triglyceride.
* N ¼ 10,636 for audiometric data and hypertension data.
D. Wang et al. / Journal of the American Society of Hypertension 12(2) (2018) 71–79 75
Table 2
Odds ratios (95% confidence intervals) of hypertension by occupational noise exposure
Occupational Noise Exposure N Model 1* Model 2y Model 3z
Total
0 13,863 ref ref ref
1 y <10 1979 0.86 (0.78–0.94) 0.92 (0.84–1.02) 0.90 (0.79–1.01)
10 y <20 2529 0.91 (0.84–1.00) 0.96 (0.88–1.06) 0.94 (0.85–1.05)
20 y 4079 1.01 (0.94–1.08) 1.03 (0.96–1.11) 1.09 (1.00–1.18)
Male
0 5700 ref ref ref
1 y <10 857 0.89 (0.77–1.02) 0.89 (0.77–1.04) 0.84 (0.71–1.02)
10 y <20 953 0.95 (0.83–1.09) 0.95 (0.82–1.11) 0.92 (0.76–1.10)
20 y 2587 1.02 (0.93–1.12) 1.07 (0.97–1.18) 1.16 (1.03–1.31)
Female
0 8163 ref ref ref
1 y <10 1122 0.83 (0.73–0.93) 0.96 (0.84–1.09) 0.92 (0.81–1.06)
10 y <20 1576 0.90 (0.81–1.00) 0.97 (0.86–1.08) 0.96 (0.85–1.08)
20 y 1492 0.88 (0.79–0.98) 0.99 (0.88–1.11) 1.01 (0.88–1.14)
* Unadjusted.
y
Adjusted for age and body mass index.
z
Adjusted for age, sex, shift work, body mass index, waist, current smoking status (yes, no), current drinking status (yes, no), family
history of hypertension (yes, no), tea consumption (yes, no), coffee consumption (yes, no), physical activity (yes, no), life stress (yes,
no), diabetes (yes, no), total cholesterol, triglyceride, low-density lipoprotein, and high-density lipoprotein.
potential confounders. Stratified analyses revealed that the the random effects model. Overall, the polled OR of hyper-
association between the longest noise exposure duration tension for occupational noise exposure was 1.25 (95%
group (20 years) and hypertension was more pronounced CI ¼ 1.10–1.42, I2 ¼ 87.6%, Pheterogeneity < .001).
in males (OR ¼ 1.16, 95% CI ¼ 1.03–1.31), not in females Subgroup analysis by location, sex, study design, refer-
(OR ¼ 1.01, 95% CI ¼ 0.88–1.14). ence noise exposure group, number of participants, whether
controlling for BMI was conducted to test the stability of
Hearing Loss and Hypertension the results (Table S3). The associations between occupa-
tional noise exposure and the risk of hypertension were
In our different types of hearing loss study subgroup, par- similar in most subgroup analyses. But it implied that
ticipants with hearing loss had a significantly higher risk of different noise exposure reference group might be a
hypertension, compared with those with normal hearing possible source of heterogeneity. In addition, sensitivity
(Table 3). The ORs and CIs were 1.23 (1.07–1.41), 1.39 analysis excluded a single study, in turn, did not alter
(1.24–1.54), and 1.34 (1.20–1.50) for unilateral, bilateral, the combined OR, with a range from 1.16 (95%
and either ear hearing loss, respectively. In the stratified anal- CI ¼ 1.05–1.29) to 1.31 (95% CI ¼ 1.13–1.51; Figure S1).
ysis, bilateral ear hearing loss got the highest risk of hyper- Visual inspection of funnel plots failed to identify sub-
tension in all the subgroups (OR: 1.29–1.58). Moreover, the stantial asymmetry (Figure S2). No evidence of publication
association between bilateral hearing loss and hypertension bias among these studies was found by Begg’s rank corre-
was particularly strong for participants who were females, lation test and Egger’s linear regression test (Begg’s test
aged 60 years, and exposed to occupational noise. Z ¼ 1.71, P ¼ .09; Egger’s test t ¼ 0.75, P ¼ .47).
Table 3
Odds ratios (95% confidence intervals) of hypertension by different types of hearing loss
Type of Hearing Loss N Model 1* Model 2y Model 3z
Total
No 2383 ref ref ref
Unilateral 1705 1.44 (1.27–1.64) 1.29 (1.13–1.46) 1.23 (1.07–1.41)
Bilateral 6548 1.81 (1.64–1.99) 1.41 (1.28–1.57) 1.39 (1.24–1.54)
Either 8253 1.73 (1.57–1.89) 1.38 (1.25–1.52) 1.34 (1.20–1.50)
Age (y)
<60
No 1436 ref ref ref
Unilateral 702 1.31 (1.08–1.58) 1.30 (1.08–1.57) 1.26 (1.02–1.55)
Bilateral 1414 1.46 (1.25–1.70) 1.43 (1.22–1.67) 1.32 (1.13–1.56)
Either 2116 1.41 (1.22–1.62) 1.38 (1.20–1.60) 1.30 (1.12–1.51)
60
No 947 ref ref ref
Unilateral 1003 1.24 (1.04–1.48) 1.26 (1.05–1.50) 1.19 (0.97–1.45)
Bilateral 5143 1.37 (1.20–1.58) 1.41 (1.23–1.62) 1.42 (1.21–1.65)
Either 6137 1.35 (1.18–1.55) 1.38 (1.21–1.59) 1.38 (1.17–1.61)
Sex
Male
No 641 ref ref ref
Unilateral 667 1.26 (1.02–1.57) 1.22 (0.98–1.51) 1.10 (0.85–1.42)
Bilateral 3513 1.47 (1.24–1.75) 1.36 (1.14–1.61) 1.34 (1.10–1.64)
Either 4180 1.44 (1.22–1.70) 1.33 (1.12–1.58) 1.30 (1.05–1.59)
Female
No 1742 ref ref ref
Unilateral 1038 1.48 (1.26–1.73) 1.32 (1.12–1.54) 1.28 (1.07–1.52)
Bilateral 3035 1.92 (1.71–2.17) 1.42 (1.25–1.62) 1.37 (1.19–1.56)
Either 4073 1.80 (1.60–2.02) 1.39 (1.23–1.57) 1.33 (1.17–1.53)
Occupational noise exposure
No 811 ref ref ref
Unilateral 595 1.39 (1.19–1.62) 1.21 (1.03–1.42) 1.31 (1.03–1.67)
Bilateral 2318 1.75 (1.55–1.97) 1.35 (1.19–1.53) 1.58 (1.31–1.92)
Either 2913 1.67 (1.49–1.87) 1.31 (1.16–1.48) 1.51 (1.24–1.82)
No occupational noise exposure
No 1572 ref ref ref
Unilateral 1110 1.56 (1.26–1.94) 1.44 (1.16–1.80) 1.20 (1.01–1.42)
Bilateral 4230 1.95 (1.65–2.30) 1.55 (1.30–1.85) 1.29 (1.12–1.49)
Either 5340 1.86 (1.58–2.19) 1.52 (1.28–1.81) 1.26 (1.11–1.44)
* Unadjusted.
y
Adjusted for age and sex.
z
Adjusted for age, sex, shift work, body mass index, waist, current smoking status (yes, no), current drinking status (yes, no), family
history of hypertension (yes, no), tea consumption (yes, no), coffee consumption (yes, no), physical activity (yes, no), life stress (yes,
no), diabetes (yes, no), total cholesterol, triglyceride, low-density lipoprotein cholesterol, and high-density lipoprotein cholesterol.
85 dBA for more than 30 years had a significantly In the sex-specific estimates, we found the association
higher risk of hypertension in a retrospective cohort with a 16% increase in hypertension risk among males.
study with a sample size of 10,872.34 Moreover, the re- However, the relationship was not statistically significant
sults of the present study benefited from larger sample among female population. The gender difference may be
size and were based on models adjusting for individual related with different jobs between males and females.
risk factors, which were not conducted in previous study. Although exposed to occupational noise environment, fe-
The divergent outcomes among some studies may be male workers may experience relatively lower noise envi-
because of the different definition and category of occu- ronment, when compared with male workers.
pational noise, exposure duration, study design, exposure As we all know, occupational noise was one of the major
assessment, and sample size across different studies. causes of hearing loss,35 thus we use hearing loss as an
D. Wang et al. / Journal of the American Society of Hypertension 12(2) (2018) 71–79 77
Figure 1. The relationship between occupational noise exposure and risk of hypertension.
indicator to reflect the cumulative exposure of occupational could activate the hypothalamic-pituitary-adrenal and sym-
noise. Meanwhile, we also found it was significantly asso- pathetic nervous systems and then increase the level of
ciated with hypertension, and the bilateral ear hearing loss cortisol, adrenaline, and noradrenaline, which could result
got the highest risk. It could be explained that occupational in the change of blood pressure.37 Moreover, it could also
noise was usually supposed to bilateral and fairly symmet- affect the endocrine systems to disturb metabolic and hor-
rical.20,36 Besides, the association between bilateral hearing monal status of the human body, then increase the blood
loss and hypertension was more evident in the subgroup pressure, change hormones levels or other biochemical
subjects who exposed to occupational noise, which could levels (such as blood glucose and lipids), resulting in the
verify the result of occupational noise and hypertension occurrence of hypertension.38,39
in our study. Besides, unilateral hearing loss was also asso- The present study has several strengths. First, it revealed
ciated with higher risk of hypertension. We thought it may the independent cross-sectional study and selected a sub-
be related to the position of the work, one side face or sample subject with pure-tone audiometry to confirm the
closer to noise source, except for ear trauma or disease. results. Second, our study combined results with previously
We also searched the previously published studies and published articles simultaneously, which could benefit from
combined the results with our study. It showed that occupa- larger sample size. In addition, this is the first meta-analysis
tional noise exposure was associated with an increased risk to quantify the strength of association between occupa-
of hypertension when compared with no occupational noise tional noise exposure and hypertension, and we included
exposure. The meta-analysis including 181,700 partici- studies with a mean quality score of 7.1, which could
pants, substantially greater than previously published also increase the reliability of the findings.
studies, provides additional validity to our results. Besides, Some limitations should also be acknowledged. First, the
the association remained significant in most subgroup ana- cross-sectional design could restrict the evidence of causal
lyses, such as the subgroup of different study design, inferences. Second, although a range of confounders were
different number of participants, controlling for potential adjusted in our study, some other factors were still not
confounders or not, and different noise exposure reference included, such as leisure time noise exposure and individual
group. information on the use of hearing protection, which were
The mechanisms that underlie these associations are also reported to be associated with hypertension or noise
complex. Several potential biological mechanisms may exposure level. Third, occupational noise exposure outside
contribute to the association of occupational noise exposure of DMC was only based on the work history as reported by
and hypertension. Noise exposure, a psychosocial stressor, the workers or the job description. Fourth, different
78 D. Wang et al. / Journal of the American Society of Hypertension 12(2) (2018) 71–79
definitions for occupational noise exposure were used 10. van Kempen EE, Kruize H, Boshuizen HC,
across studies, which might introduce heterogeneity into Ameling CB, Staatsen BA, de Hollander AE. The asso-
the results. Finally, the limited information provided in ciation between noise exposure and blood pressure and
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occupational noise exposure workers. Studies with larger causes stroke or hypertension is still not known. BMJ
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Acknowledgments Am J Epidemiol 2013;177:818–25.
13. Chen S, Ni Y, Zhang L, Kong L, Lu L, Yang Z, et al.
The contributions of all the participants, staffs of the Noise exposure in occupational setting associated
Health Examination Center of the Dongfeng Central Hospi- with elevated blood pressure in China. BMC Public
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members of study team are greatly acknowledged. 14. Stokholm ZA, Bonde JP, Christensen KL, Hansen AM,
Kolstad HA. Occupational noise exposure and the risk
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Appendix
Gan
Souza
Chen
Chang
Liu Chiu
Liu jing
Inoue
Stokholm male
Stokholm female
1
log[or]
-1
0 .2 .4
s.e. of: log[or]
Table S1
Characteristics of studies included in meta-analysis
First Author Publication Year Country Study Design Sex of Population No of Participants
Attaichi et al 2013 Iran Cross-sectional Male 502
Gan et al 2010 US Cross-sectional Male and female 6307
Souza et al 2015 Brazil Cross-sectional Male and female 1729
Chen et al 2017 China Cross-sectional Male and female 2789
Chang et al 2013 Taiwan Cohort Male 578
Liu Chiu et al 2016 Taiwan Cohort Male and female 1002
Liu Jing et al 2016 China Cross-sectional Male and female 738
Inoue et al 2005 Japan Cross-sectional Male 415
Stokholm et al (male) 2013 Danish Cohort Male 108,402
Stokholm et al (female) 2013 Danish Cohort Female 36,788
This study (male) 2017 China Cross-sectional Male 10,097
This study (female) 2017 China Cross-sectional Female 12,353
79.e3
Table S2
Outcome and covariates of studies included in meta-analysis
First Author Noise Ascertainment Case Ascertainment Noise and Relative Risk Covariates in Fully Quality
(95% CI) Adjusted Model Assessment
Attaichi et al Measured by using a Measured by physicians with 61–72, 1.0 (reference); 77–83.5, 4.38 Age, work of duration, BMI, smoking, 7
CEL-440 sound a standard mercury (1.27–10.53); 86.5–97, 9.43 (2.81– dietary salt, regular exercise, shift
level meter sphygmomanometer 23.46); 88–102, 14.22 (3.21–40.84) working, nature of job, and family
history of hypertension
D. Wang et al. / Journal of the American Society of Hypertension 12(2) (2018) 71–79
Gan et al Questionnaire Self-reported or measured 0, 1.0 (reference); 0–0.3 y, 1.16 (0.83– Age, sex, ethnicity, BMI, educational 6
using a mercury 1.63); 0.4–1.5 y, 1.29 (0.80–2.07); level, physical activity, smoking and
sphygmomanometer 1.6–18.8 y, 1.09 (0.79–1.51) diabetes, annual family income,
pack-years of smoking, passive
smoking in the workplace or at
home, alcohol drinking, waist
circumference, and total cholesterol
Souza et al Measured using a Self-reported or measured by 75, 1.0 (reference); 75–85, 1.56 Age, gender, BMI 7
digital audio physicians (1.13–2.17); 85, 1.58 (1.10–2.26)
dosimeter
Chen et al Determined by a Self-reported or measured by 80,1.0 (reference); 80–90, 1.11 (0.71– Age, smoking, and drinking status 7
noise statistical physicians 1.72); 90–95, 1.99 (1.38–2.87); 95–
analyzer 100, 2.26 (1.54–3.33); 100, 2.83
(1.87–4.28)
Chang et al Measured using Self-reported or measured by <80, 1.0 (reference); 80–<85, 1.75 Age, BMI, employment duration, 8
a sound analyzer nurse with an automated (1.09–2.81); 85, 1.93 (1.15–3.22) alcohol intake, cigarette use,
sphygmomanometer education level, regular exercise
Liu Chiu et al Measured using a Self-reported or measured by <75, 1.0 (reference); 75–79, 0.98 Age, sex, triglyceride level, the use of 8
sound level meter physicians (0.68–1.42); 80, 1.38 (1.02–1.85) hearing-protective devices, BMI,
smoking status, alcohol
consumption, regular exercise, and
family history of hypertension
Liu Jing et al Measured using a Measured by physicians 85, 1.0 (reference); >85, 1.52 (1.07– Age 6
sound pressure with an automated 2.15)
noise meter sphygmomanometer
Inoue et al Measured using a Self-reported or measured by 75, 1.0 (reference); 92, 0.48 (0.28– Age, BMI, smoking, alcohol drinking, 7
sound pressure physicians 0.81) exercise, diet, and family history of
noise meter hypertension
Stokholm et al Measured by personal Self-reported or a hospital <75, 1.0 (reference); 75–79, 1.03 Age, socioeconomic status, calendar 8
(male) dosimeters discharge diagnosis of (0.90–1.18); 80–84, 1.00 (0.88– year, and employment status
hypertension 1.14); 85–89, 1.04 (0.91–1.18); 90–
94, 1.06 (0.92–1.22); 95–99, 0.98
(0.84–1.15); >100, 0.99 (0.75–1.31)
(continued)
Table S2 (continued )
First Author Noise Ascertainment Case Ascertainment Noise and Relative Risk Covariates in Fully Quality
(95% CI) Adjusted Model Assessment
Stokholm et al 75, 1.0 (reference); 75–79, 1.03 (0.89–
(female) 1.18); 80–84, 1.10 (0.96–1.25); 85–
89, 1.12 (0.97–1.28); 90–94, 1.21
(1.03–1.42); 95–99, 1.29 (1.03–1.60)
This study Came from the Self-reported <80, 1.0 Age, sex, shift work, BMI, waist, 7
D. Wang et al. / Journal of the American Society of Hypertension 12(2) (2018) 71–79
(male) company records or measured (reference); 80, current smoking status, current
which were measured by physicians 1.05 (0.95–1.16) drinking status, family history of
This study by qualified institutions, <80, 1.0 (reference); 80, 0.97 (0.89– hypertension, tea consumption,
(female) or consulted with 1.05) coffee consumption, physical
local industrial activity, life stress
hygienists
BMI, body mass index; CI, confidence interval.
79.e4
79.e5 D. Wang et al. / Journal of the American Society of Hypertension 12(2) (2018) 71–79
Table S3
Stratified analyses on associations of occupational noise exposure and risk of hypertension
Variables No. RR 95% CI I2 (%) P*
Location
Asia 8 1.39 1.08–1.79 90.60 <.001
Europe 2 1.07 0.97–1.17 74.70 <.002
USA 2 1.33 0.98–1.81 72.70 .056
Sex
Male 2 1.03 0.97–1.09 0 .631
Female 2 1.04 0.91–1.20 85.80 .008
Combined 8 1.55 1.11–2.15 87 <.001
Study design
Cross-sectional 8 1.35 1.07–1.70 90.70 <.001
Cohort 4 1.14 1.00–1.30 77.50 .004
Reference group
<75 dB(A) 5 1.15 1.01–1.30 78.00 .003
<80/85 dB(A) 4 1.31 1.06–1.62 86.00 <.001
Others 3 1.6 0.47–5.38 95.50 <.001
No. of participants
5000 7 1.64 1.10–2.43 87.50 <.001
>5000 5 1.05 0.99–1.11 53.70 .071
Controlling family history of hypertension in models
Yes 5 1.19 0.89–1.60 91.80 <.001
No 7 1.31 1.14–1.51 82.80 <.001
Controlling BMI in models
Yes 7 1.3 1.03–1.62 90.10 <.001
No 5 1.2 1.03–1.40 83.20 <.001
BMI, body mass index; CI, confidence interval; RR, relative risk.
P* for heterogeneity.