DOI: https://doi.org/10.21203/rs.3.rs-42684/v1
Background: Previous studies have reported associations between hearing impairment (HI) and cognitive impairment, but the evidence is not conclusive while considering concurrent geriatric syndromes. Especially, evidence from previous studies rarely came from Asian studies. This study aimed to evaluate the independent effects of HI and hearing aid use on the incidence of cognitive impairment while considering most geriatric confounders.
Methods: This population-based, propensity-score matched cohort study used cohort from Waves IV–VII (1999–2011) survey of the Taiwan Longitudinal Study on Aging (TLSA). Cognitive impairment was identified based on Short Portable Mental Status Questionnaire (SPMSQ) scores. The hazard ratio (HR) was calculated using the Cox proportional hazard regression adjusting for age, sex, comorbidities, socioeconomic status, Center for Epidemiologic Studies Depression (CES-D) scores, the instrumental activities of daily living scale, mobility condition and quality of life. In addition, social support and participation were also considered as confounders in the analysis. To assess the robustness of our findings, we conducted a sensitivity analysis designed to access unmeasured confounding factors by calculating E-values.
Results: After 1:1 propensity-score matching, we included 709 participants in both the HI and non-HI groups with a mean age of 73.4 years and 39.4% of participants were female. The mean follow-up was 8.9±3.9 years. The HI group had a higher incidence of cognitive impairment than the non-HI group (74.5% vs. 69.1%, respectively), with an adjusted HR of 1.16 (95% confidence interval [CI], 1.03–1.32) based on a 12-year follow up. The E-value was 1.45 for the estimate, which provided evidence for this study’s robustness. Although, a subgroup analysis showed that hearing aid use was associated with lower incidences of cognitive impairment (66.3% vs. 75.6%) when compared to non-users in the HI group, the adjusted HR of 0.82 (95% CI, 0.61–1.09) revealed no significant differences.
Conclusions: HI was an independent risk factor of incident cognitive impairment on top of concurrent geriatric syndromes. Early HI detection may thus be effective for preventing cognitive decline. Further studies are needed to evaluate the effect of hearing aid use on the prevention of cognitive decline.
As it poses declines in memory and other cognitive functions, dementia creates high social and economic burdens for the ageing and those living in aged societies [1]. Many clinicians have therefore tried to identify modifiable risk factors for use in early interventions aimed at reducing the incidence of cognitive impairment. In this context, a variety of recent studies have focused on the association between age-related hearing impairment (HI) and cognitive impairment or dementia. This is because HI affects communication and can contribute to isolation, depression, and, possibly, dementia. Additionally, some types of HI is reversible with rehabilitative treatments such as hearing aid use and cochlear implantation [2].
In the United States, Lin and colleagues reported that HI was associated with 24% increased risk for incident cognitive impairment [3]. Deal and colleagues reported that moderate/severe HI was associated with increased risk of dementia (hazard ratio [HR], 1.55; 95% confidence interval [CI], 1.10–2.19) among older adults [4]. Similarly, Gurgel and colleagues demonstrated that HI was an independent predictor for developing dementia (HR, 1.27; 95%CI, 1.03–1.56) [5]. Further, the English Longitudinal Study of Ageing (ELSA) revealed that participants with self-reported HI had an odds ratio (OR) of 1.6 times (95%CI, 1.1–2.4) those with normal hearing in regard to developing dementia [6]. In Korea, Kim and colleagues found that both severe (adjusted HR, 1.17) and profound (adjusted HR, 1.51; 95% CI, 1.14–2.00) HI was associated with elevated dementia risks for middle- and older-aged individuals [7].
It is well-known that older adults often suffer from multi-morbidities. A study showed that among 2618 participants, 75.3%, 41.8%, and 22.5% had geriatric syndromes, multimorbidity, and disability, respectively, and 10.4% had all the three conditions" [8]. Recently, researchers have tried to use model adjustment or mediation analyses to assess possible mediating pathways between HI and cognitive impairment. For example, Fischer and colleagues attempted to prove that HI was independently associated with cognitive impairment (HR, 1.90; 95% CI, 1.11–3.26) while adjusting vision and olfaction impairments and frailty scores. However, there is residual confounding in the exposure-outcome relationship between HI and cognitive impairment as well-known confounders such as depression, physical function, and social support were not included in the analysis [9].
The results of several previous studies also conflict in regard to the effects of hearing aid interventions on cognitive function. For instances, Dawes and colleagues reported that hearing aid use was associated with better cognition independently of social isolation and depression [10]. Similarly, a population-based longitudinal cohort study showed that hearing aid use was positively associated with episodic memory scores [11]. On the other hand, Lin and colleagues indicated that self-reported hearing aid use was not associated with higher cognitive test scores among participants with hearing loss [12]. Moreover, another study found no significant differences between hearing-aid users and non-users in regard to cognitive issues, social engagement, or mental health outcomes among community-dwelling older adults with HI [13].
As such, this study aimed to evaluate the independent effects of HI and hearing aid use on the incidence of cognitive impairment among community-dwelling older adults while considering most geriatric confounders.
This study’s population included participants of the TLSA, which was a longitudinal, population-based survey initiated by the Health Promotion Administration, Ministry of Health and Welfare, Taiwan [14]. A three-stage systematic random sampling design was used to select an equal probability adult samples aged 60 or above. Data were collected through face-to-face personal interviews conducted by trained interviewers. Respondent follow-ups were then conducted every three to four years. A total of seven surveys were conducted in 1989, 1993, 1996, 1999, 2003, 2007, and 2011 (i.e., Waves I–VII). The details and design of the TLSA have been described elsewhere [15]. This study analyzed datasets from Waves IV–VII (i.e., 1999–2011).
First, of the 6,091 eligible older adults, we excluded 227 individuals who had only completed one wave of investigation (Fig. 1). Second, we excluded 384 individuals due to missing data for either the Short Portable Mental Status Questionnaire (SPMSQ) or sensory impairment items. Third, we excluded 156 individuals with a history of cancer. Finally, we excluded 1,672 individuals with cognitive impairments as defined by receiving SPMSQ scores ≤ 4 during their initial assessments [16]. Exclusion of older adults with cognitive impairments could ensure the accuracy of the responses in the initial assessments which may be influenced by cognitive status. Ultimately, data from 3,658 older adults without cognitive impairments were included for analysis. HI was defined by self-reported hearing loss or hearing aid use. The final sample was then divided into HI (n = 775) and non-HI (n = 2,883) groups.
We gathered subject data on age, sex, height, weight, level of education, marital status, living arrangement, self-rated health condition, health-related behaviors, self-reported economic pressure, concurrent comorbidities, and the use of assistive device (Table 1).
HI group n = 775 | Non-HI group n = 2,883 | P-Value | |
---|---|---|---|
Age*, year | 74.3 ± 8.1 | 66.2 ± 9.3 | < 0.001 |
Female sex, n (%) | 300 (38.7%) | 1317 (45.7%) | < 0.001 |
Height*, cm | 159.7 ± 8.8 | 160.1 ± 8.1 | 0.20 |
Weight*, kg | 59.2 ± 10.7 | 61.3 ± 10.7 | < 0.001 |
Body mass index*, kg/m2 | 23.2 ± 3.4 | 23.9 ± 3.4 | < 0.001 |
Assistive devices, n (%) | |||
Eyeglasses | 388 (50.1%) | 1809 (62.8%) | < 0.001 |
Hearing aids | 94 (12.1%) | NA | |
Dental prostheses | 584 (75.4%) | 2078 (72.1%) | 0.07 |
Crutches | 131 (16.9%) | 208 (7.2%) | < 0.001 |
Living arrangements, n (%) | < 0.001 | ||
Home | 758 (97.8%) | 2862 (99.3%) | |
Nursing home | 17 (2.2%) | 21 (0.7%) | |
Educational level, n (%) | < 0.001 | ||
Elementary school or below | 634 (81.8%) | 1903 (66.0%) | |
Junior high school | 62 (8.0%) | 346 (12.0%) | |
Senior high school | 64 (8.3%) | 464 (16.1%) | |
College or above | 15 (1.9%) | 170 (5.9%) | |
Marital status, n (%) | < 0.001 | ||
Married/Cohabitating | 456 (58.8%) | 2081 (72.2%) | |
Single/Divorced/Widowed | 319 (41.2%) | 802 (27.8%) | |
Living conditions, n (%) | 0.12 | ||
Living alone | 86 (11.1%) | 267 (9.3%) | |
Living with spouse or children | 689 (88.9%) | 2616 (90.7%) | |
Self-rated health condition, n (%) | < 0.001 | ||
Good or very good | 158 (20.4%) | 1223 (42.4%) | |
Okay | 300 (38.7%) | 1022 (35.5%) | |
Bad or very bad | 317 (40.9%) | 638 (22.1%) | |
Self-reported economic pressure, n (%) | 0.18 | ||
No | 527 (68.0%) | 1987 (68.9%) | |
Some | 158 (20.4%) | 624 (21.6%) | |
Heavy | 90 (11.6%) | 272 (9.4%) | |
Health-related behaviors, n (%) | |||
Smoking | 215 (27.7%) | 669 (23.2%) | 0.009 |
Alcohol | 196 (25.3%) | 894 (31.0%) | 0.22 |
Betel nuts | 54 (7.0%) | 154 (5.3%) | 0.08 |
Exercise habits, n (%) | 0.004 | ||
No | 288 (37.2%) | 897 (31.1%) | |
Exercise < 3 time/week | 57 (7.4%) | 265 (9.2%) | |
Exercise ≧ 3 times/week | 430 (55.5%) | 1721 (59.7%) | |
Comorbidities, n (%) | |||
Hypertension | 309 (39.9%) | 900 (31.2%) | < 0.001 |
Diabetes mellitus | 113 (14.6%) | 385 (13.4%) | 0.38 |
Heart disease | 171 (22.1%) | 434 (15.1%) | < 0.001 |
Stroke | 52 (6.7%) | 86 (3.0%) | < 0.001 |
COPD | 143 (18.5%) | 258 (9.0%) | < 0.001 |
Arthritis | 183 (23.6%) | 468 (16.2%) | < 0.001 |
Gastric ulcer | 169 (21.8%) | 503 (17.5%) | 0.005 |
Hepatobiliary disease | 64 (8.3%) | 220 (7.6%) | 0.56 |
Hip fracture | 23 (3.0%) | 41 (1.4%) | 0.004 |
Cataract | 219 (28.3%) | 608 (21.1%) | < 0.001 |
Chronic kidney disease | 69 (8.9%) | 230 (8.0%) | 0.40 |
Spine spondylosis | 71 (9.2%) | 271 (9.4%) | 0.84 |
Physical and psychosocial status* | |||
Social support score | 15.7 ± 3.2 | 16.4 ± 3.0 | < 0.001 |
Social participation | 0.42 ± 0.49 | 0.45 ± 0.50 | 0.14 |
Mobility score | 2.6 ± 2.5 | 1.2 ± 1.9 | < 0.001 |
IADL score | 0.75 ± 1.32 | 0.26 ± 0.85 | < 0.001 |
CES-D score | 4.5 ± 5.3 | 2.8 ± 4.3 | < 0.001 |
SPMSQ score | 8.3 ± 1.1 | 8.5 ± 0.9 | < 0.001 |
Quality of Life score | 7.5 ± 3.1 | 8.3 ± 2.9 | < 0.001 |
CES-D, Center for Epidemiologic Studies Depression; COPD, chronic obstructive pulmonary disease; HI, hearing impairment; IADL, instrumental activities of daily living scale; SPMSQ, short portable mental status questionnaire. * Values are given as means ± standard deviations, not no. (%). Higher total scores on the social support scale (0–20), social participation scale (0–6), SPMSQ (0–9), and Quality of Life scale (0–12) represented better condition. On the other hand, lower total scores on the mobility scale (0–8), IADL scale (0–5), and CES-D (0–24) represented better condition. Details are available in Methods section of the article. |
This study evaluated respondent physical and psychosocial status using multidimensional scores from the social support scale, social participation scale, mobility scores, instrumental activities of daily living (IADL) scale, Center for Epidemiologic Studies Depression (CES-D) scale, SPMSQ, and quality of life (QoL) scale [17–21]. Higher total scores for the social support scale (0–20), social participation scale (0–6), SPMSQ (0–9), and QoL scale (0–12) represented better condition. On the other hand, lower total scores for mobility scale (0–8), IADL scale (0–5), and CES-D (0–24) represented better condition. The details of each scales are given below.
The social support scale consisted of four questions designed to measure the four corresponding items of emotional support (What degree of care is received from family members, relatives, and/or friends?), instrumental support (Is someone available if you need help?), and information support (Do you feel that your family provides useful help? and Does your family consult your opinion when they make decisions?) [21]. Each item was scored from 1 to 5, with total scores ranging from 0 to 20.
Respondents answered the social participation scale to indicate whether they participated in group activities through one or more of six types of social organizations (i.e., hobby related clubs, religious or church groups, political groups, retired associations, elderly-related associations, and volunteer groups) [18]. Each type was coded as yes (score = 1) or no (score = 0), with total scores ranging from 0 to 6.
For physical function assessments, the mobility scale included the difficulty level of standing for 15 minutes, stooping, reaching overhead, grasping with fingers, lifting or carrying 25 pounds, running for 20–30 meters, walking 200–300 meters, and climbing stairs [19]. The IADL scale was used to assess five activities as proposed by Lawton and Brody [20]. Respondents who reported difficulty, were unable to carry out tasks, or received help and/or used equipment when performing tasks were coded as having difficulty (i.e., 1 = yes, 0 = no).
Depressive symptoms were measured using the shorter form of the CES-D scale [22]. This included the eight items of “my appetite was poor,” “everything I did took effort,” “my sleep was restless,” “felt depressed,” “felt lonely,” “people were unfriendly,” “felt sad,” and “could not get going.” Responses ranged from “rarely or none of the time” to “most or all of the time” to produce scores between 0 and 3, respectively, with total scores ranging from 0 to 24 [19].
The QoL scale consisted of 12 items proposed by Neugarten and colleagues [23], including “is your life better than that of most others?,” “are you satisfied with your life?,” “are you interested in the things in which you are engaged?,” “have the most recent years contained the best days of your life?,” “would you like to change your past life?,” “do you expect something good to happen in the future?,” “should your life be better than it is now?,” “are you bored with most things you do?,” “do you feel old and tired?,” “does most of your life meet your expectations?,” “do you feel that you are living in a safe environment?,” and “are you satisfied with your living environment?” Each item was rated as yes (1) or no (0), with total scores ranging from 0 to 12.
This study applied the modified version of SPMSQ to the exclusion criteria, propensity-score matching covariates, and primary outcome to constitute criteria for cognitive impairment. This study included responses to the nine following SPMSQ items: “where are you located now?,” “what is your home address?,” “what day is it?,” “what month is it?,” “what year is it?,” “how old are you?,” “who are the current and last presidents?,” and “subtract 3 from 20 four consecutive times” [16]. Participants with four or more errors were described as having cognitive impairment, which was our primary outcome, and several other cohort studies supported this cut-off point [24].
We assessed the robustness of our findings by conducting a sensitivity analysis designed to access unmeasured confounding factors related to the exposures and outcomes by calculating E-values [25]. The E-value is the minimum strength of association, on the risk ratio scale, that unmeasured confounders would need to have with both the exposure and outcome, conditional on the measured covariates, to fully explain away a specific exposure-outcome association.
Propensity-score matching was conducted through the PSMATCH procedure provided by SAS (Statistics Analysis System Institute Inc., Cary, NC, USA). This study used descriptive statistics to assess patient demographics. The adjusted HRs of incidences of cognitive impairment were calculated using the Cox proportional hazard model while adjusting for possible confounders. All analyses were conducted using SAS version 9.4.
Prior to the propensity-score matching process, the HI group contained 775 respondents, while the non-HI group contained 2,883 respondents (Fig. 1). HI respondents were significantly older (74.3 vs. 66.2 years). Further, the HI group was associated with lower self-rated health, less regular exercise, higher smoking rates, and higher prevalence rates for hypertension, heart disease, stroke, arthritis, gastric ulcers, hip fractures, and cataracts (Table 1). Most importantly, HI respondents generally had poorer physical and psychosocial status based on evaluations of social support, mobility, IADL, CES-D, SPMSQ, and QoL (Table 1).
After matching with the covariates, we included 709 participants in both the HI and non-HI groups for further analysis. All covariates were well-balanced between groups (Table 2). The mean follow-up was 8.9 ± 3.9 years. Respondent results for the mobility, IADL, CES-D, SPMSQ, and QoL scales showed that most had good physical and psychological function (Table 2).
HI group n = 709 | Non-HI group n = 709 | |
---|---|---|
Age*, year | 73.4 ± 7.7 | 73.5 ± 7.7 |
Female sex, n (%) | 279 (39.4%) | 279 (39.4%) |
Height*, cm | 159.7 ± 8.8 | 159.7 ± 8.4 |
Weight*, kg | 59.4 ± 10.7 | 59.8 ± 10.4 |
Body mass index*, kg/m2 | 23.2 ± 3.3 | 23.4 ± 3.6 |
Assistive devices, n (%) | ||
Eyeglasses | 366 (51.6%) | 377 (53.2%) |
Hearing aids | 83 (11.7%) | NA |
Dental prostheses | 534 (75.3%) | 536 (75.6%) |
Crutches | 109 (15.4%) | 114 (16.1%) |
Living arrangements, n (%) | ||
Home | 694 (97.9%) | 693 (97.7%) |
Nursing home | 15 (2.1%) | 16 (2.3%) |
Educational level, n (%) | ||
Elementary school or below | 570 (80.4%) | 557 (78.6%) |
Junior high school | 61 (8.6%) | 66 (9.3%) |
Senior high school | 64 (9.0%) | 66 (9.3%) |
College or above | 14 (2.0%) | 20 (2.8%) |
Marital status, n (%) | ||
Married/Cohabitating | 431 (60.8%) | 424 (59.8%) |
Single/Divorced/Widowed | 278 (39.2%) | 285 (40.2%) |
Living conditions, n (%) | ||
Living alone | 82 (11.6%) | 82 (11.6%) |
Living with spouse or children | 627 (88.4%) | 627 (88.4%) |
Self-rated health condition, n (%) | ||
Good or very good | 156 (22.0%) | 166 (23.4%) |
Okay | 280 (39.5%) | 266 (37.5%) |
Bad or very bad | 273 (38.5%) | 277 (39.1%) |
Self-reported economic pressure, n (%) | ||
No | 482 (68.0%) | 483 (68.1%) |
Some | 144 (20.3%) | 150 (21.2%) |
Heavy | 83 (11.7%) | 76 (10.7%) |
Health-related behaviors, n (%) | ||
Smoking | 195 (27.5%) | 186 (26.2%) |
Alcohol | 185 (26.1%) | 176 (24.8%) |
Betel nuts | 44 (6.2%) | 46 (6.5%) |
Exercise habits, n (%) | ||
No | 260 (36.7%) | 254 (35.8%) |
Exercise < 3 time/week | 48 (6.8%) | 36 (5.1%) |
Exercise ≧ 3 times/week | 401 (56.6%) | 419 (59.1%) |
Comorbidities, n (%) | ||
Hypertension | 273 (38.5%) | 279 (39.4%) |
Diabetes mellitus | 105 (14.8%) | 116 (16.4%) |
Heart disease | 155 (21.9%) | 156 (22.0%) |
Stroke | 44 (6.2%) | 45 (6.4%) |
COPD | 117 (16.5%) | 122 (17.2%) |
Arthritis | 161 (22.7%) | 155 (21.9%) |
Gastric ulcer | 152 (21.4%) | 150 (21.2%) |
Hepatobiliary disease | 56 (7.9%) | 61 (8.6%) |
Hip fracture | 19 (2.7%) | 17 (2.4%) |
Cataract | 199 (28.1%) | 204 (28.8%) |
Chronic kidney disease | 66 (9.3%) | 65 (9.2%) |
Spine spondylosis | 67 (9.5%) | 68 (9.6%) |
Physical and psychosocial status* | ||
Social support score | 15.8 ± 3.2 | 15.8 ± 3.4 |
Social participation | 0.42 ± 0.49 | 0.45 ± 0.50 |
Mobility score | 2.4 ± 2.5 | 2.4 ± 2.4 |
IADL score | 0.64 ± 1.23 | 0.65 ± 1.31 |
CESD score | 4.3 ± 5.2 | 4.1 ± 5.1 |
SPMSQ score | 8.3 ± 1.1 | 8.3 ± 1.2 |
Quality of Life score | 7.5 ± 3.0 | 7.5 ± 3.1 |
CES-D, Center for Epidemiologic Studies Depression; COPD, chronic obstructive pulmonary disease; HI, hearing impairment; IADL, instrumental activities of daily living scale; SPMSQ, short portable mental status questionnaire. * Values are given as means ± standard deviations, not no. (%). Higher total scores on the social support scale (0–20), social participation scale (0–6), SPMSQ (0–9), and Quality of Life scale (0–12) represented better condition. On the other hand, lower total scores on the mobility scale (0–8), IADL scale (0–5), and CES-D (0–24) represented better condition. Details are available in Methods section of the article. |
The incidence of cognitive impairment was statistically higher for the HI group (74.5% vs. 69.1%) based on the 12-year follow-up, with an adjusted HR of 1.16 (95% CI, 1.03–1.32) (Table 3). Further, there was no difference in risk of cognitive impairment between groups based on the 4- and 8-year follow-ups. A subgroup analysis revealed that HI respondents who used hearing aids had lower incidences of cognitive impairment (66.3% vs. 75.6%) when compared to those who did not use hearing aid during the 12-year follow-up (Table 4). However, the adjusted HR showed no significant decreases in hearing aid users when compared to non-users (Table 4).
Incidence of cognitive impairment | HI group N = 709 | Non-HI group N = 709 | Adjusted HR (95% CI) | P Value |
---|---|---|---|---|
4-year follow-up | 259 (36.5%) | 230 (32.4%) | 1.13 (0.94–1.35) | .18 |
8-year follow-up | 414 (58.4%) | 383 (54.0%) | 1.11 (0.97–1.28) | .14 |
12-year follow-up | 528 (74.5%) | 490 (69.1%) | 1.16 (1.03–1.32) | .02* |
CI, confidence interval; HI, hearing impairment; HR, hazard ratio. * Cox proportional hazard regression, p < 0.05. Hazard ratio was adjusted for all covariates listed in Table 2. |
Incidence of cognitive impairment | Hearing aid (+) N = 83 | Hearing aid (-) N = 626 | Adjusted HR (95% CI) | P Value |
---|---|---|---|---|
4-year follow-up | 27 (32.5%) | 232 (37.1%) | 0.93 (0.61–1.42) | .74 |
8-year follow-up | 45 (54.2%) | 369 (59.0%) | 0.81 (0.58–1.11) | .19 |
12-year follow-up | 55 (66.3%) | 473 (75.6%) | 0.82 (0.61–1.09) | .17 |
CI, confidence interval; HR, hazard ratio. * Cox proportional hazard regression, p < 0.05. Hazard ratio was adjusted for all covariates listed in Table 2. |
We used the formula to calculate the E-value for the effect estimate [25, 26]. For unmeasured confounders associated with HI and cognitive impairment during the 12-year follow-up, the E-value formula produced E = 1.45 for the estimate. The result could be interpreted that an unmeasured confounder that was associated with both the HI and cognitive impairment by a risk ratio of 1.45-fold each, above and beyond the measured confounders, but weaker confounding would not do so. As such, the E-value provided evidence for this study’s robustness.
To the best of our knowledge, this was the first study to demonstrate that HI elevated the risk of cognitive impairment among community-dwelling older adults while controlling for most concurrent geriatric confounders. Over 12 years, community-dwelling older adults with HI had significant increased risks for the incidence of cognitive impairment when compared to those without HI. By contrast, older adults with HI did not show an increased risk of cognitive impairment based on the 4- and 8-year follow-ups.
Previous cohort studies have demonstrated that older adults with HI have significantly increased HR of 1.55 over 9 years [4], 1.39–1.59 over 11 years [6], and 1.27 over 12.5 years of follow-up [5]. This study produced similar results, but with a lower HR of 1.16, because we matched and adjusted for most geriatric physical and psychosocial confounders known to increase the risk of cognitive impairment.
Age-related HI is characterized by high-frequency impairment (6000 and 8000 Hz), which may originate in the peripheral or central auditory systems [27]. However, most early-stage HI goes undetected for older adults. Further, those with self-reported HI often suffer from notably decreased decibels in hearing level (dB HL). A previous study showed that individuals with HI require 7.7 years on average to develop cognitive impairments, vs 10.9 years for individuals with normal hearing [3]. This study also showed that older adults with HI had an increased risk of cognitive impairment when compared to older adults without HI based on 12 years of follow-up. This has substantial public health policy implications. That is, there is a sufficient time period in which to detect and manage HI among these individuals, thus potentially preventing incidences of cognitive impairment.
Clinical practice recommendations entail that hearing function should be tested during comprehensive geriatric assessments [28]. However, the importance of the Rinne tuning-fort test results are often underestimated in general practice when compared to cardiovascular risk factors. Moreover, only patients with significant HI (55 ~ 110 dBHL) are eligible for government subsidies to buy hearing aids. Notably, a previous study showed that moderate/severe HI (> 40 dBHL) was associated with incident dementia [4]. Although the benefits of hearing aids in regard to preventing cognitive impairments are not yet evident, these devices may still prevent social isolation and depression [10]. An ongoing randomized study, Aging and Cognitive Health Evaluation in Elders (ACHIEVE) trial, aims to determine efficacy of a best practices hearing (vs. successful aging) intervention on reducing cognitive decline in older adults with hearing loss [29]. Further trials are also needed to evaluate the cost-effectiveness of hearing aids in the dementia prevention and management contexts.
Although this study generated important findings, they should be interpreted with some cautions. First, although we used multiple strategies to minimize the effects of confounders through propensity-score matching, this observational study may entail residual confounding factors and thus cannot prove causality. Second, we did not evaluate HI severity among respondents, which is related to cognitive impairment. However, it is more important to detect HI during community screening than it is to determine severity. Third, compliance with hearing aids is often much less than with wearing glasses in the older adults [30]. Therefore, the effect of hearing aid on the prevention of cognitive decline might be underestimated. Finally, the sample size was relatively limited in regard to hearing aid users. Future clinical trials are therefore needed to confirm how hearing aid use may prevent cognitive decline.
This study found that HI was associated with an increased risk for the incidence of cognitive impairment while controlling for most geriatric confounders based on 12 years of follow-up data. Therefore, integration of hearing test into annual health prevention program was an effective way to screen HI and prevent HI-associated cognitive decline among community-dwelling older adults.
Center for Epidemiologic Studies Depression; CI:confidence interval; dB HL:decibels in hearing level; ELSA:English Longitudinal Study of Ageing; HR:hazard ratio; HI:hearing impairment; IADL:instrumental activities of daily living; QoL:quality of life; SPMSQ:Short Portable Mental Status Questionnaire; TLSA:Taiwan Longitudinal Study on Aging.
The current study was approved by the Institutional Review Board-II of the Kaohsiung Medical University Chung-Ho Memorial Hospital (approval no. KMUHIRB-E(II)-20190124) in 2019. Before recruitment, all participants received a proper explanation about the study and provided consent for inclusion in the study. Participants who could read and write signed the written consent documents; those who could not read nor write impressed the name stamps or handprint with the assistance of their family members. In addition, legal guardian/representative provided consent on behalf of the participants with cognitive decline or stroke.
Consent for publication
Not applicable.
Availability of data and materials
The datasets used and analyzed during the current study are not publicity available, but are available from the corresponding author on reasonable request with the permission of the Ministry of Health and Welfare, Taiwan.
Competing interests
The authors declare no conflicts of interest.
This work was supported by Ministry of Health and Welfare, Taiwan (Grant number: M06M2346 and M09M7269 awarded to M.-C. Lee). The study sponsor participated in the study design, but played no role in participant recruitment, data analysis, or paper preparation.
Study concept and design: C.-J.T., C.-Y.H., M.-C.L., and Y.-H.Y. developed study concept and designed the study. C.-J.T., and Y.-H.Y. performed data extraction and statistical analyses. T.-G.T., Y.-H.H., and C.-J.T. participated in drafting the article. M.-C.L., T.A.K., and Y.-H.Y. made critical revision of the manuscript. All authors approved the final version of the article, and ensured the accuracy and integrity of this work.
We thank our colleagues from the Center for Medical Informatics and Statistics, Kaohsiung Medical University, Kaohsiung, Taiwan for providing supports in statistical analysis. The sponsor has no role in the design, methods, subject recruitment, data collections, analysis and preparation of paper.