Research Article, J Aging Geriatr Med Vol: 2 Issue: 1
Relationship between Hearing Impairment and Frailty in Older Patients with Diabetes Mellitus
Sayuri Sable-Morita1, Saiko Sugiura2, Yasue Uchida2,3, Takahisa Tanikawa4,5, Haruhiko Tokuda5 and Hidenori Arai6*
1Nursing Department Nantional Center for Geriatric and Gerontology, Obu, Japan
2Department of Otorhinolaryngology, National center for Geriatric and Gerontology, Obu, Japan
3Department of Otorhinolaryngology, Aichi Medical Univeristy, Japan
4Department of Endocrinology, Metabolism and Diabetes, National center for Geriatric and Gerontology, Obu, Japan
5Department of Clinial Laboratory, National Center for Geriatrics and Gerontology, Obu, Japan
6Deputy Director, National Center for Geriatrics and Gerontology, Obu, Japan
*Corresponding Author : Hidenori Arai
National Center for Geriatrics and Gerontology 7-430, Morioka-cho Obu, Aichi, Japan, 474-8511
Tel: +81 562 46 2311
Fax: +81 562 87 0115
E-mail:harai@ncgg.go.jp
Received: January 15, 2018 Accepted: February 13, 2018 Published: February 19, 2018
Citation: Sable-Morita S, Sugiura S, Uchida Y, Tanikawa T, Tokuda H, et al. (2018) Relationship between Hearing Impairment and Frailty in Older Patients with Diabetes Mellitus. J Aging Geriatr Med 2:1. doi: 10.4172/2576-3946.1000114
Abstract
Aim: Hearing impairment, diabetes, and frailty have been increasingly prevalent in older people. Recently, the assessment of frailty has been recommended for older patients with diabetes mellitus. Diabetes increases the risk of hearing impairment, which in turn increases the risk of frailty. However, the relation between hearing impairment and frailty is still unclear in patients with diabetes. Thus, this study aimed to clarify the relationship between hearing impairment and frailty among older patients with diabetes mellitus.
Research design and methods: We used a finger friction test as a simple auditory screening for the assessment of hearing impairment and the Kihon Checklist (KCL for the assessment of frailty. The cognitive function was assessed using the Mini Mental State Examination (MMSE). A logistic regression analysis was used to investigate the cross-sectional associations between frailty and patient characteristics.
Results: This study involved 283 patients with diabetes with an average age of 75.3 years; the prevalence of frailty based on the scores of the KCL was 30%. Hearing impairment was present in 32.8% of patients without frailty and 57.6% of those with frailty (p<0.01). In multivariable analysis, frailty in patients with diabetes was associated with hearing impairment (odds ratio: 1.96, 95% confidence interval: 1.07-5.59].
Conclusions: These data suggest that hearing impairment as determined by a finger friction test is an important factor contributing to frailty among patients with diabetes.
Keywords: Diabetes; Older patients; Frailty; Prevalence
Introduction
Diabetes is a common chronic disease among older people, affecting approximately 20% of people over 65 years of age [1,2]. It increases mortality rate and significantly affects patient’s quality of life, socioeconomic vigor, and social security resources by inducing complications such as neuropathy, retinopathy, nephropathy, and diabetic foot. Frailty is a progressive condition in older people characterized by multisystem physiologic impairments and vulnerability to stressors; it is also a predictive factor for negative outcomes such as mortality, hospitalization, fall, bone fracture, and dementia [3,4] and is more prevalent in patients with diabetes. Therefore, the assessment of frailty is recommended in older patients with diabetes. Furthermore, it has been suggested that strict glycemic control may increase the risk of hypoglycemia for older people [5], which leads to falls, fracture, hospitalization, and frailty. On the other hand, frailty is also a risk factor for hypoglycemia; thus, the relationship between hypoglycemia and frailty is bidirectional. Accordingly, the management of frailty among older patients with diabetes is an important issue. However, the mechanisms leading to frailty in diabetes are not fully understood.
Audiovisual abilities change with advancing age and influence daily life. Hearing impairment is very common in older people, and diabetes may be a risk factor [6]. Uchida et al. reported the relationship between insulin use and hearing impairment in 90 middle-aged patients with diabetes and that hearing partially worsened with the length of diabetes [7]. In most cases, patients periodically visit eye clinics for retinopathy caused by diabetic complications as recommended by their physician; in contrast, few patients visit an ENT clinic for hearing impairment and may simply attribute hearing loss to aging. Some reports revealed that hearing impairment may be related to frailty [8,9]; however, no study has demonstrated such relationship in patients with diabetes. Finger friction test is a simple and useful method for the assessment of hearing ability. We have reported that even if the sound pressure of the friction test performed by speaking at a distance of 5 cm from an ear varies, it would be around 40 decibels [dB]. Detection of moderate or worse hearing impairment on pure tone audiometry had a sensitivity of 30% and specificity of 80% as per a self-administered questionnaire, while the finger friction test showed a much higher sensitivity of 70% with a specificity of 70%. Hence, the finger friction test is a more accurate screening method for hearing impairment in older people than interviews [10].
From these data, we hypothesized that hearing impairment is associated with frailty in older patients with diabetes and is detected by a friction test. In this study, we investigated frailty, diabetic complications, and hearing impairment in older patients with diabetes; in addition, we determined the factors influencing the presence of frailty in patients with diabetes.
Research Design and Methods
A cross-sectional study was conducted in 283 patients (130 men and 153 women) with diabetes mellitus aged over 65 years who attended a diabetic outpatient clinic of the National Center of Geriatrics and Gerontology in 2015. Patients who were certified for the long-term care insurance service were excluded from this study. Data regarding age, sex, body mass index (BMI), complications, and glycated hemoglobin (HbA1c) levels were obtained from the patients’ medical records. The cognitive function was assessed using the Japanese version of the Mini-Mental State Examination (MMSE), while nutritional status was evaluated using the Mini Nutritional Assessment (MNA). The finger friction test was used for the assessment of hearing impairment, and the Kihon Checklist (KCL) for the assessment of frailty. This study was approved by the Ethics and Conflict of Interest Committee of the National Center for Geriatrics and Gerontology. A written informed consent was obtained from all participants.
Finger friction test
After a trained examiner was able to create a constant finger rubbing noise stabilized around 40 dB as recorded by a decibel meter (Rion, NL-20, Tokyo, Japan), the finger friction test was performed. The test was individually conducted in a relatively quiet place (background noise: -35dB). The finger rubbing noise was made under dry conditions by softly rubbing the index finger with the thumb. Pursuant to the method of Richard et al. [11-13], the test was initiated with the following procedures. First, the finger rubbing noise was made in front of the older participant, and the participant was instructed to raise the right or left hand depending on the direction of the sound. After the participant understood the procedure, a noise was made behind the subject, and the reaction was recorded. The examiner then stood 30 cm behind the subject and made the noise 5 cm from each ear twice. The participant was considered as having hearing impairment if he or she was unable to hear the sound in both ears. The finger friction test is a simple and useful method for assessing patient’s hearing ability. In a previous study, pure tone audiometry and finger rub auditory screening tests were performed in 150 patients with diabetes aged 65 years or older. The efficacy of pure tone audiometry in detecting hearing impairment was examined in subjects who could not hear the finger rub on both ears. The sensitivity of the (Finger friction test) FFT in detecting moderate or higher levels of hearing loss was 71.4%, and specificity was 74.3%. The sensitivity was higher than that of the patient history inquiry, but specificity was lower.
As such, for elderly populations, the FFT is considered to be suitable to screen for moderate or higher hearing loss, due to its convenience and superior objectivity as compared to those of patient history inquiry [10]. Those participants who used a hearing aid in their daily life and were able to hear the sound while wearing the aid were considered as not having hearing impairment.
Frailty definition
The KCL was created by the Ministry of Health, Labour and Welfare to identify “potentially dependent elderly” and help determine desirable disability prevention programs. The check sheet has been used by community integrated care centers throughout the country since 2006 to evaluate the daily function of people aged over 65 years. This sheet consists of the following 25 items: exercise/fall (5 items), instrumental activities of daily living (3 items), cognition (3 items), mood (5 items), malnutrition (2 items), oral function (3 items), and social activities of daily living (4 items). Frailty was defined based on the total KCL score (frailty, 8 or higher; no frailty, 0-7). In comparison with Fried’s international criteria for frailty evaluation [14] and KCL total score, sensitivity and specificity were as high as 0.88 and 0.85, respectively, when the cutoff value was set at 7/8 points [15].
Statistical analysis
Continuous data were tested for normal distribution using the Kolmogorov-Smirnov test and were presented as mean ± SD in the case of normally distributed data and as the median and interquartile range in the case of non-normally distributed data. To compare the population characteristics by frailty status, the analysis of variance with t-test as well as the Mann-Whitney U test was used for the continuous variables, depending on the distribution of the variables, while chisquare test for the categorical variables. The logistic regression analysis was used to investigate the cross-sectional associations between frailty status and patient characteristics. P-values less than 0.05 were considered statistically significant. The data were analyzed using SPSS version 22.0.
Results
Among the study participants, 30% were frail and 70% were not. The clinical characteristics are summarized in Table 1. Patients in the frail group were older than those in the non-frail group. In the frail group, 57.6% were men and 42.3% were women. The BMI and HbA1c levels between the groups had no significant difference, but those in the frail group had a longer diabetes history and a higher prevalence of diabetic retinopathy and stroke. In the assessment of cognitive function and nutritional status, the frail group had lower MMSE and MNA scores. About 40.2% of the participants had hearing impairment. The proportion of hearing impairment in the frail group was 57.6%, which was higher than in the non-frail group. The results of the logistic regression analysis regarding factors associated with frailty are shown in Table 2. The table shows that frailty was associated with hearing impairment even after adjustment for age, sex, and BMI and other cofounders.
Non-frail (n=198) | Frail (n=85) | P value | |
---|---|---|---|
Age (years) | 73.1 ± 5.4 | 78.6 ± 5.6 | <0.001 |
BMI (kg/m2) | 23.2 (21.1-25.5) | 22.0 (19.7-25.9) | 0.16 |
Male sex, n (%) | 81 (40.9) | 49 (57.6) | 0.01 |
Duration of diabetes (yr) | 12 (8-19.3) | 18.4 (10-26) | 0.003 |
HbAlc (%) (mmol/mol) | 7.2 (6.6-7.8) | 7.5 (6.6-8.3) | 0.194 |
Insulin treatment, n (%) | 52 (26.3) | 31 (36.5) | 0.084 |
Neuropathy, n (%) | 106 (53.5) | 55 (64.7) | 0.082 |
Retinopathy, n (%) | 74 (37.4) | 46 (54.1) | 0.009 |
Nephropathy, n (%) | 113 (57.1) | 54 (63.5) | 0.311 |
Hypertension, n (%) | 106 (53.5) | 55 (64.7) | 0.082 |
Stroke, n (%) | 19 (9.6) | 25 (29.4) | <0.001 |
Coronary artery disease, n (%) | 25 (12.6) | 16 (18.8) | 0.175 |
Hearing impairment, n (%) | 65 (32.8) | 49 (57.6) | <0.001 |
MMSE (total points) | 28 (25-29) | 25 (22-28) | <0.001 |
MNA (total points) | 24 (13-27) | 13 (11-23.5) | <0.001 |
Table 1: Characteristics of patients with and without frailty.
Model 1 | Model 2 | Model 3 | |||||||
---|---|---|---|---|---|---|---|---|---|
OR | 95% CI | p | OR | 95% CI | p | OR | 95% CI | p | |
Hearing impairment | 2.79 | 1.65-4.69 | 0.001 | 2.05 | 1.17-3.62 | 0.01 | 2.02 | 1.085-3.76 | 0.027 |
Retinopathy | 1.170 | 0.610-2.244 | 0.637 | ||||||
Stroke | 2.023 | 0.934-4.382 | 0.074 | ||||||
Duration (Years) | 1.070 | 0.979-1.037 | 0.608 | ||||||
MNA | 0.922 | 0.880-0.966 | 0.001 | ||||||
MMSE | 0.891 | 0.803-0.988 | 0.029 |
Table 2: Logistic regression analysis of hearing impairment as risk factor for frailty in older diabetes patients.
Discussion
In this exploratory study, we examined the relationship between hearing impairment, frailty, and diabetic complications and found that hearing impairment was clearly related to frailty in diabetes. Some reports have shown that hearing impairment is associated with frailty in older people [8,9]. Moreover, individuals with hearing loss are more likely to have difficulties with communication, impaired activities of the daily living, and instrumental activities of the daily living and have reduced quality of life than those without [16]. Furthermore, hearing impairment has been associated with mortality [17], decline of cognitive function [18], depression [19], and reduced gait speed [20]. Therefore, hearing impairment may contribute to frailty through multidimensional pathways.
The ratio of hearing impairment was 40.2% among all participants in the current study. Previously, Horikawa et al. reported that patients with diabetes have a higher incidence of hearing impairment compared with those without diabetes [21]. The Blue Mountains Hearing Study for Australia, a large-scale epidemiological survey, reported that adults with diabetes showed a significantly 2.7-fold higher prevalence of hearing impairment compared with those without diabetes [22]. Both type 1 and type 2 diabetes mellitus are risk factors for developing hearing impairment [23,24]. However, the mechanism of hearing impairment in diabetes is not clear. Some experimental animal models showed that microangiopathy affects the vascularization of the inner ear and degenerate its structures by interfering with nutrient transport [25,26]. In a histopathological study, several arteriosclerotic changes were observed in the temporal bones of a patient with type 1 diabetes [27]. Additionally, neuropathy is a diabetic complication and may cause auditory neural changes.
In several reports, the prevalence of frailty in diabetes ranges from 10% to 50%; this wide range is due to the various criteria used in defining frailty [28]. Despite the difference among studies, the rate of frailty in patients with diabetes is higher than that in older people without diabetes. However, the mechanisms leading to frailty in diabetes are not fully understood. This study reported the differences between frail and non-frail groups in terms of age, sex, duration of diabetes, prevalence of retinopathy and stroke, MMSE and MNA scores, and the prevalence of hearing impairment. The logistic regression analysis showed that hearing impairment was associated with frailty in diabetes.
A previous study has reported that hearing impairment tends to be underestimated and that there may be some differences between self-awareness and actual hearing test result [29,30]. In diabetes, complications related to micro- and macroangiopathy require a great deal of medical attention, but the evaluation of hearing impairment remains underestimated. Although this type of evaluation based on pure tones is a standard procedure, it is difficult to perform in an outpatient clinic. The present study evaluated hearing impairment using a finger friction test, a test that can be easily used to screen hearing impairments in older people [10].
In summary, hearing impairment is a poorly recognized diabetic complication and was associated with frailty in older patients with diabetes mellitus. This illustrates the necessity of adding a hearing test when evaluating older patients with diabetes. However, this study had several limitations, including the cross-sectional design. In addition, evaluation of hearing impairment was conducted using a finger friction test owing to its simplicity; nevertheless, future studies should consider these findings with a more accurate hearing ability test using an audiometer.
Acknowledgments
The authors thank the patients who took part in this study and the medical staff for their support with this project by recruiting the patients.
Funding
This study was supported by the Research Funding for Longevity Sciences from the National Center for Geriatrics and Gerontology (NCGG) 27-9, Japan.
References
- Kirkman MS, Biscoe VJ, Clark N, Florez H, Haas LB, et al. (2012) Diabetes in older adults. Diabetes Care 35: 2650-2664.
- Morley JE, Malmstrom TK, Rodriguez-Manas L, Sinclair AJ (2014) Frailty, sarcopenia and diabetes. J Am Med Dir Assoc 15:853-859.
- Ohkubo Y, Kishikawa H, Araki E, Miyata T, Isami S, et al. (1995) Intensive insulin therapy prevents the progression of diabetic microvascular complications in Japanese patients with non-insulin-dependent diabetes mellitus: a randomized prospective 6-year study. Diabetes Res Clin Pract 28: 103-117.
- The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group (2000) Retinopathy and Nephropathy in Patients with Type 1 Diabetes Four Years after a Trial of Intensive Therapy. N Engl J Med 6: 381-389.
- Nelson JM, Dufraux K, Cook P (2007) The relationship between glycemic control and falls in older adults. J Am Geriatr Soc 55: 2041-2044.
- Austin DF, Konrad-Martin D, Griest S, McMillan GP, McDermott D, et al. (2009) Diabetes-related changes in hearing. Laryngoscope 119: 1788-1796.
- Uchida Y, Sugiura S, Kishimoto M, Ueda H, Teranishi M, et al. (2012) Impact of diabetes-related factors on hearing in middle-aged and older patients of the inpatient diabetes education program. Audiology Japan 55: 182-189.
- Kamil RJ, Li L, Lin L (2014) Association of hearing impairment and frailty in older adults. J Am Geriatr Soc 62: 1186-1188.
- Kamil RJ, Betz J, Powers BB, Pratt S, Kritchevsky S, et al. (2015) Association of hearing impairment with incident frailty and falls in older adults. J Aging Health 28:644-660.
- Sable-Morita S, Sugiura S, Harasawa Y, Yamada K (2018) Investigating the use of the finger friction test in screening for moderate or higher hearing loss in elderly diabetes patients. Journal of Japan Academy of Gerontological Nursing in press.
- Nakamura H, Arao H (1994) A Study on Finger Friction test. Audiology Japan 37 4: 322-329.
- Uhlmann RF, Larson EB, Koepsell TD (1986) Hearing impairment and cognitive decline in senile dementia of the Alzheimer’s type. J Am Geriatr Soc 34: 207-210.
- Uhlmann RF, Rees TS, Psaty BM, Duckert LG (1989) Validity and reliability of auditory screening tests in demented and non-demented older adults. J Am Gen Intern Med 4: 90-96.
- Fried LP, Tangen CM, Walston J, Newman AB, Hirsch C, et al. (2001) Cardiovascular Health Study Collaborative Research Group. Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci 56: 146-156.
- Satake S, Senda S, Hong YJ, Miura H, Endo H, et al. (2015) Validity of the Kihon Checklist for assessing frailty status. Geriatr Gerontol Int 14: 561-569.
- Torres-Russotto D, Landau GWM, Harding W, Bohne BA, Sun K, et al. (2009) Calibrated finger rub auditory screening test (CALFRAST). Neurology 18: 1595-1600.
- Dalton DS, Cruickshanks KJ, Kliein BE, Klein R, Wiley TL, et al. (2003) The impact of hearing loss on quality of life in older adults. Gerontologist 43: 661-668.
- Contrea KJ, Betz J, Genther DJ, Lin FR (2015) Association of hearing impairment and mortality in the National Health and Nutrition Examination Survey. JAMA Otolaryngol Head Neck Surg 141: 944-946.
- Sumi E, Takechi H, Wada T, Ishine M, Wakatsuki Y, et al. (2006) Comprehensive Geriatric Assessment for outpatients is important for the detection of functional disabilities and depressive symptoms associated with sensory impairment as well as for the screening of cognitive impairment. Geriatr Gerontol Int 6: 94-100.
- Lin FR, Yaffw K, Xia J, Xue QL, Harris TB, et al. (2013) Hearing loss and cognitive decline in older adults. JAMA Intern Med 173: 292-299.
- Sugiura S, Uchida Y, Nakashima T (2014) Hearing impairment and dementia. Geriat Med 52: 781-784.
- Mener DJ, Bets J, Genther DJ, Chen D, Lin FR (2013) Hearing loss and depression in older adults. J Am Geriatr Soc 61: 1627-1629.
- Lingstheng LI, Eleanor M, Simonsick, Lin FR (2013) Hearing loss and gait speed among older adults in the United States. Gait Posture 38: 25-29.
- Horikawa C, Kodama S, Tanaka S, Fujihara K, Hirasawa R, et al. (2013) Diabetes and risk of hearing impairment in adults, a meta-analysis. J Clin Endocrinol Metab 98: 51-58.
- Mitchell P, Gopinath B, McMahon CM, Rochtchina E, Wang JJ, et al. (2009) Relationship of type 2 diabetes to the prevalence, incidence and progression of age related hearing loss. Diabet Med 26: 483-488.
- Teng ZP, Tian R, Xing FL, Tang H, Xu JJ, et al. (2016) An association of type 1 diabetes mellitus with auditory dysfunction: A systematic review and meta-analysis. Laryngoscope.
- Akinpelu OV, Mujica-Mota M, Daniel SJ (2014) Is type 2 diabetes mellitus associated with alterations in hearing? A systematic review and meta-analysis. Laryngoscope 124: 767-776.
- Raynor E, Robinson WG, Garrett CG, McGuirt WT, Pillsbury HC, et al. (1995) Consumption of a high-galactose diet induces diabetic-like changes in the inner ear. Otolaryngol Head Neck Surg 113: 748-754.
- Smith TL, Raynor E, Prazma J, Buenting JE, Pillsbury HC (1995) Insulin-dependent diabetic microangiopathy in the inner ear. Laryngoscope 105: 236-240.
- Fukushima H, Cureoglu S, Schachern PA, Kusunoki T, Oktay MF, et al. (2005) Cochlear changes in patients with type 1 diabetes mellitus. Otolaryngol Head Neck Surg 105: 236-240.
- Uchida Y, Nakashima T, Ando F, Niino N, Shimokata H (2003) Prevalence of self-perceived auditory problems and their relation to audiometric thresholds in a middle-aged to elderly population. Acta Otolaryngol 123: 618-626.