Objective To examine whether the existence and severity of diabetic retinopathy (DR) could be associated with the prevalent sarcopenia and muscle quality in patients with type 2 diabetes.
Research design and methods This is a cross-sectional study of 316 patients with type 2 diabetes (mean age 65±12 years; 38% female). Body compositions were measured by the dual-energy X-ray absorptiometry. Patients were divided into three groups: patients without DR (NDR), with non-proliferative DR (NPDR) and proliferative DR (PDR). Sarcopenia was diagnosed according to the criteria for Asians, using both skeletal muscle index (SMI) and grip strength (kg). Muscle quality was also determined by the grip strength divided by SMI. Logistic regression analyses were carried out to assess the cross-sectional association of the severity of DR with sarcopenia. In addition, linear regression analyses were performed to determine the associations between DR and muscle quality. Selection of covariates in the multivariate logistic and linear regression analyses was done by a stepwise procedure.
Results Among the patients examined, NDR, NPDR and PDR were diagnosed in 261, 38 and 17 patients, respectively. The prevalence of sarcopenia significantly increased along with the progression of DR. Multivariate logistic regression analysis showed that PDR is significantly associated with sarcopenia (OR 7.78, 95% CI 1.52 to 39.81, p=0.014) and low muscle strength (OR 6.25, 95% CI 1.15 to 33.96, p=0.034). Multivariate linear regression analysis additionally showed that the existence of DR was significantly associated with the muscle quality (standardized β −0.136, p=0.005 for NPDR, standardized β −0.146, p=0.003 for PDR).
Conclusions This study provides evidence that PDR is significantly associated with sarcopenia, and the existence of DR increases the risk for low muscle quality in patients with type 2 diabetes.
- Diabetic retinopathy
- Type 2 diabetes
- Dual-energy x-ray absorptiometry
- Muscle quality.
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Significance of the study
What is already known about this subject?
Several recent studies have reported that diabetes contributes to the burden of sarcopenia and diabetic microvascular complications are associated with sarcopenia. However, the association between diabetic retinopathy and sarcopenia remains largely unknown.
What are the new findings?
In this study, the prevalence of sarcopenia significantly was increased along with the progression of diabetic retinopathy in patients with type 2 diabetes. In the multivariate models, proliferative diabetic retinopathy was significantly associated with sarcopenia, and the existence of diabetic retinopathy was significantly associated with the low muscle quality.
How might these results change the focus of research or clinical practice?
Patients with diabetic retinopathy may be regarded as a high-risk group for sarcopenia and low muscle quality.
Diabetic retinopathy (DR) is one of the common microvascular complications in patients with diabetes and a leading cause of the visual impairment and blindness.1–3 DR is associated with an increased risk for albuminuria, cardiovascular events, and all-cause mortality in patients with diabetes.4 5
Sarcopenia is deﬁned as the loss of skeletal muscle mass and strength with aging and contributes to both physical disability and mobility limitations.6 7 In addition to aging, many chronic diseases are also associated with sarcopenia.8 Of the chronic disease, diabetes has been reported to be one of the significant contributors to the exacerbation of sarcopenia.9 The Health, Aging, and Body Composition (ABC) Study revealed that diabetes is associated with the rapid loss of skeletal muscle strength and mass.10 Interestingly, this study also demonstrated that muscle quality, defined as muscle strength standardized for muscle mass, declined more rapidly in patients with diabetes than in subjects without diabetes. Similarly, Volpato et al reported in a cross-sectional analysis of 835 participants that patients with diabetes have a lower muscle strength in lower extremities, despite having a larger muscle mass, and diabetes might cause mobility limitations via impaired muscle quality.11 In addition, either longer duration of diabetes or poor glycemic control were reported to be associated with the low muscle quality.12 Given these findings, sarcopenia and low muscle quality may be considered as one of the chronic complications related to diabetes.
Several recent studies have reported that the association was between diabetic microvascular complications and sarcopenia. Andersen et al demonstrated that both diabetic neuropathy (DN) and DR are significantly associated with muscle weakness of lower extremities (ankle and knee) in the univariate models and the statistical significance of DN but not DR remained unchanged in the multivariate models.13 Andreassen et al reported that DN could be involved in the accelerated muscle atrophy of lower extremities, but no difference was observed for the muscle quality between neuropathic and non-neuropathic patients.14 These findings suggest that DN may have an adverse effect on mobility through sarcopenia in patients with diabetes. Also, DR may be a cause for mobility limitations, and the association between visual impairment and sarcopenia has been reported.15 However, it remains unknown the association between the severity of DR and sarcopenia in patients with diabetes. In addition, no study has investigated the association of DR with muscle quality so far. We therefore examined whether the existence and the severity of DR could be associated with the prevalent sarcopenia and muscle quality in patients with type 2 diabetes.
Materials and methods
Patients with type 2 diabetes who regularly visited to the outpatient clinic at Tokyo Medical and Dental University Hospital participated in this study. Patients were eligible, if they were aged 20 years or older, and patients who had been taken a funduscopy, measured a grip strength, and undergone the whole body dual-energy X-ray absorptiometry (DXA) between 1 July 2012 and 31 October 2016 were enrolled. Patients with severe renal impairment (estimated glomerular filtration rate (eGFR) <15 mL/min/1.73 m2 or undergoing renal replacement therapy), pregnant women, and those with infectious or malignant diseases were excluded. Type 2 diabetes was diagnosed according to the criteria of the Japan Diabetes Society (JDS).16 This study complies with the principles laid by the Declaration of Helsinki and has been approved by the ethical committee of Tokyo Medical and Dental University (M2016-220).
Clinical and biochemical analysis
Standardized questionnaires were used to obtain information on medication and medical history. HbA1c was measured using the latex agglutination method. HbA1c levels were expressed in accordance with the National Glycohemoglobin Standardization Programs recommended by the JDS.16 The GFR was estimated using the following equation for the Japanese, as proposed by the Japanese Society of Nephrology17: GFR=194 × SCr−1.094 × age−0.287((if female)×0.739), where SCr stands for serum creatinine in mg/dL, measured by an enzymatic method. Urinary albumin and creatinine excretion were measured by the turbidimetric immunoassay and enzymatic method, in a spot urine collection. Urinary albumin-to-creatinine ratio (ACR) was used for the assessment of albuminuria. The body mass index (BMI) was calculated as the weight divided by the square of height (kg/m2). Regional fat and lean mass including android and gynoid were measured by the whole body DXA (Lunar iDXA, GE Healthcare, Madison, Wisconsin, USA), as described previously.18 Patients were positioned for whole-body scans in accordance with the manufacturer’s protocol. The whole-body fat and fat-free mass was divided into several regions, such as arms, legs, and the trunk. Appendicular lean mass was estimated as the sum of fat-free mass of the two upper limbs and two lower limbs. The skeletal muscle index (SMI) was calculated as the appendicular lean mass divided by the square of the height (kg/m2). The average of bilateral grip strength (kg) measured by a hand dynamometer Grip-D (TKK5401, Takei, Niigata, Japan) was used for the assessment of muscle strength. In accordance with the criteria for Asians proposed by consensus report of the Asian Working Group for Sarcopenia (AWGS),7 a low muscle strength was defined as a hand grip strength <26.0 kg in male and <18.0 kg female, and a low muscle mass was defined as an SMI of <7.0 in male and <5.4 in female. Patients with both low muscle strength and low muscle mass were diagnosed as having a sarcopenia. The muscle quality was defined as the muscle strength per unit of the muscle mass. The ratio of grip strength to SMI (kg/kg/m2) was used to assess the muscle quality in this study.
Assessment of DR
The presence and severity of DR were determined by qualified ophthalmologists in our hospital. The patients were grouped into three groups: patients without diabetic retinopathy (NDR), patients with non-proliferative diabetic retinopathy (NPDR), and patients with proliferative diabetic retinopathy (PDR), according to the medical record. The information on retinopathy obtained at the nearest date to DXA examination was used.
Statistical analysis was performed using SPSS V.21.0 statistical package. Data were presented as either mean±SD, median with IQR or percentages as appropriate according to data distribution. Comparisons among the groups were analyzed by either one-way analysis of variance (continuous variables) or the χ2test (categorical variables). Logistic regression analyses were carried out to assess the cross-sectional association of the severity of DR with sarcopenia. The OR with 95% CI was calculated in the logistic regression models. Next, both univariate and multivariate linear regression analyses were performed to determine the associations between DR and muscle quality. The selection of covariates in the multivariate logistic and linear regression analyses was done by a stepwise procedure. Differences were considered to be statistically significant at p value less than 0.05.
Characteristics of study participants
A total of 316 Japanese patients with type 2 diabetes (mean age 65±12 years; 38% female) were enrolled in this study. As shown in table 1, 38 and 17 patients were diagnosed as having NPDR and PDR, respectively. Patients with PDR were significantly older, had a lower grip strength, longer duration of diabetes and higher level of logarithmic-transformed ACR and were more frequently receiving insulin therapy and angiotensin receptor blockers (ARBs) than those with either NDR or NPDR. In addition, there was a significant difference in the frequency of receiving calcium channel blockers among the three groups.
Association of DR with sarcopenia and its components
As shown in figure 1, the prevalence of sarcopenia significantly increased along with the progression of DR. When comparing the association between components of sarcopenia and severity of DR, the prevalence of low muscle strength significantly increased along with the progression of DR. In contrast, no significant difference in the prevalence of low muscle mass was observed among the three groups. PDR was significantly associated with the prevalent sarcopenia (OR 3.58, 95% CI 1.19 to 10.72, p=0.023) in a univariate model (table 2). After adjustment for other covariates including age, gender, BMI, body fat and the use of ARBs selected by a stepwise regression, the association between PDR and sarcopenia remained signiﬁcant (OR 7.78, 95% CI 1.52 to 39.81, p=0.014). In addition to PDR, age (OR 1.12, 95% CI 1.06 to 1.18, p<0.001) was positively associated with sarcopenia and BMI (OR 0.67, 95% CI 0.55 to 0.81, p<0.001) and the use of ARBs (OR 0.25, 95% CI 0.09 to 0.69, p=0.007) were negatively associated with the risk for prevalent sarcopenia. The similar findings were observed in the association of PDR with a low muscle strength; ORs of PDR for the prevalence of low muscle strength were 14.6 (95% CI 3.17 to 67.21, p<0.001) in a univariate and 6.25 (95% CI 1.15 to 33.96, p=0.034) in a multivariate model. Other selected covariates were age (OR 1.09, 95% CI 1.06 to 1.13, p<0.001), the use of insulin (OR 2.14, 95% CI 1.06 to 4.33, p=0.034), history of cardiovascular disease (CVD) (OR 2.22, 95% CI 0.93 to 5.29, p=0.073) and male sex (OR 0.28, 95% CI 0.15 to 0.55, p<0.001). In contrast, PDR was not significantly associated with a low muscle mass in both the univariate and multivariate models (table 2). Age (OR 1.06, 95% CI 1.02 to 1.11, p=0.004), male sex (OR 6.87, 95% CI 2.73 to 15.03, p<0.001) and body fat (OR 1.26, 95% CI 1.14 to 1.39, p<0.001) were positively associated with a low muscle mass and BMI (OR 0.41, 95% CI 0.31 to 0.54, p<0.001) and the use of ARBs (OR 0.41, 95% CI 0.17 to 0.98, p=0.044) were negatively associated with a low muscle mass.
Association between DR and muscle quality
Figure 2 showed that the muscle quality was lower in patients with PDR than that in patients with either NDR or NPDR. In the univariate linear regression model (table 3), the existence of DR was significantly associated with a low muscle quality (standardised β −0.189, p=0.002 for NPDR, standardised β −0.235, p<0.001 for PDR). The existence of DR remained to be significantly associated with a low muscle quality after adjustment for covariates including age and gender (standardised β −0.141, p=0.006 for NPDR, standardised β −0.145, p=0.005 for PDR). Further adjustment for body fat and history of CVD did not attenuate the significant association between DR and the muscle quality (standardised β −0.136, p=0.005 for NPDR, standardised β −0.146, p=0.003 for PDR).
In the present study, we demonstrated for the first time that type 2 diabetic patients with DR, especially those with PDR, are at a high risk for the prevalent sarcopenia and the increased risk of sarcopenia in patients with DR could be attributable mainly to the impairment of muscle strength. Furthermore, we also revealed that the existence of DR is significantly associated with a low muscle quality in patients with type 2 diabetes.
Although sarcopenia is diagnosed with both low muscle mass and strength,6 7 several studies have documented that a low muscle strength is more strongly associated with both physical disability and mobility limitations than a low muscle mass.19 20 Regarding the muscle strength, it is well established that the muscle weakness of lower extremities is associated with mobility limitations21 22 and a low handgrip strength is also associated with the muscle weakness of lower extremities, muscle strength, and mobility limitations.23 Moreover, recent community-based studies revealed that a low handgrip strength was a significant predictor of CVD and mortality.24 25 In our data, PDR was significantly associated with a low muscle strength in the multivariate logistic regression analyses (table 2), suggesting that the association of PDR with incident CVD and mortality in patients with diabetes might be partly explained by the coexistence of sarcopenia.
The reduction of muscle strength with aging can be partly explained by the parallel decline in muscle mass.26 However, the reduction of muscle strength with aging occurred more rapidly than that is expected by the decline in muscle mass, and the contradiction between muscle mass and strength was thought to be caused by a decline in muscle quality.20 In a 12-year longitudinal study of a community-dwelling population in Japan, the age-related decrease in muscle mass was relatively small, but the muscle quality significantly decreased with aging.27 Other than aging, the Health ABC study reported that the decline in muscle quality was accelerated by the presence of diabetes.10 Another recent study demonstrated that diabetic patients with a poor glycemic control (HbA1c≥8.5%) were at a significantly increased risk for the decline in muscle quality and the impaired functional ability (assessed using Short Physical Performance Battery) compared with either patients with a HbA1c of <8.5% or subjects without diabetes.28 Those studies implied that a muscle quality plays a key role in the relationship between diabetes and mobility limitations. We revealed for the first time in this study that DR is strongly associated with a low muscle quality (table 3), presumably suggesting that the screening of DR would be useful to estimate the risks for the low muscle quality in patients with diabetes.
Among diabetic patients, some investigators have recently focused on the association of diabetic microvascular complications with a muscle mass, strength, and quality. In a cross-sectional study comprising 36 patients with type 2 diabetes and 36 control subjects, Andersen et al reported that the existence of both DN and DR was associated with a muscle weakness of lower extremities in a univariate analysis.13 In a multivariate analysis, there was a significant association between DN and a muscle weakness of lower extremities, whereas the statistical significance of DR disappeared. It is assumed that the impact of DN on the muscle strength of lower extremities may be stronger than that of DR; however, no information was available regarding the association between muscle mass and the severity of DR. In addition, the sample size of the study was small; therefore, concluding insufficient evidence for whether DR could be associated with a sarcopenia defined as both low muscle mass and strength. In this regard, we believe that our data in this study is the first to show evidence for the clinical relevance of DR with both sarcopenia and muscle quality in patients with type 2 diabetes.
As shown in table 2, we revealed apparent differences in the impact of gender on a low muscle strength and low muscle mass (male were protective against the decline of grip strength as were female against the low muscle mass). Both low muscle strength and low muscle mass were defined by the criteria for Asians, proposed by consensus report of the AWGS.7 However, the cut-off values were established on the basis of the data obtained mainly from subjects without diabetes, and it has still been unclear whether the criteria could be applied for patients with diabetes. Further studies may be needed to identify cut-off values for the diagnosis of sarcopenia in patients with diabetes.
We also found a significant association of ARBs with sarcopenia in patients with diabetes (table 2). Previous reports showed the potential of renin angiotensin aldosterone system inhibitors to protect against the decline of muscle strength.29 30 Onder et al reported that ACE inhibitors can prevent the decline in muscle strength in elderly women with hypertension in a 5-year longitudinal observational study.29 In the cross-sectional survey of 2431 participants from the Health ABC Study, the use of ACE inhibitors was significantly associated with a larger muscle mass in lower extremities.30 Our data are consistent with the results of these previous studies29 30 and suggest the possibility that ARBs may prevent the progression of sarcopenia in patients with diabetes.
This study has several limitations. First, it is impossible to infer causality because of its cross-sectional design, although we revealed the significant association between DR and sarcopenia in patients with type 2 diabetes. Second, the characteristics of subjects in this study were homogenous; therefore, the generalization of our findings might be limited. Third, information on diet, exercise and visual acuity that could affect both muscle mass and strength was unavailable. Visual impairment may lead to lack of exercise, resulting in the progression of sarcopenia or the decline in muscle quality. Finally, we were unable to obtain information on DN. DN was recently reported to be strongly associated with a low muscle strength, low muscle mass and decline in muscle quality.13 14 31 Therefore, further studies are needed in order to reveal the association of both DR and DN with sarcopenia and/or muscle quality.
In conclusion, this is the first study to investigate the association of DR, especially PDR with sarcopenia, which is defined as both low muscle mass and strength. Our data further suggest that type 2 diabetic patients with either NPDR or PDR are at a high risk for the low muscle quality compared with patients with NDR.
The authors would like to thank all the staff of the Department of Molecular Endocrinology and Metabolism, Tokyo Medical and Dental University for their contributions.
Contributors RB and TF designed the study, researched data, and wrote and edited the manuscript. RB, IM, TY, and YO contributed to intellectual discussion and reviewed and edited the manuscript. TT, YN, MM, HI, and KH researched data. As the corresponding author and guarantor of this manuscript, RB is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Funding This work was partially supported by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan, Grants-in-Aid from the Ministry of Health, Labor, and Welfare of Japan (Comprehensive Research on Lifestyle-Related Diseases Including Cardiovascular Diseases and Diabetes Mellitus) and Grants-in-Aid from Astellas Foundation for Research on Metabolic Disorders.
Competing interests None declared.
Ethics approval The ethical committee of Tokyo Medical and Dental University (M2016-220).
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement No additional data are available.
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