To investigate the association of the sarcopenia index (SI, serum creatinine value/cystatin C value × 100) with 3-year mortality and readmission among older inpatients, we reanalyzed a prospective study in the geriatric ward of a teaching hospital in western China. Older inpatients aged ≥ 60 years with normal kidney function were included. Survival status and readmission information were assessed annually during the 3-year follow-up. We applied Cox regression models to calculate the hazard ratio (HR) and 95% confidence intervals (CIs) of sarcopenia for predicting mortality and readmission. We included 248 participants (mean age: 81.2 ± 6.6 years). During the follow-up, 57 participants (23.9%) died, whereas 179 participants (75.2%) were readmitted at least one time. The SI was positively correlated with body mass index (BMI) (r = 0.214, p = 0.001), calf circumference (CC) (r = 0.253, p < 0.001), handgrip strength (r = 0.244, p < 0.001), and gait speed (r = 0.221, p < 0.001). A higher SI was independently associated with a lower risk of 3-year all-cause mortality after adjusting for potential confounders (HR per 1-SD = 0.80, 95% CI: 0.63–0.97). The SI was not significantly associated with readmission (HR per 1-SD = 0.97, 95% CI: 0.77–1.25). In conclusion, the SI is associated with 3-year all-cause mortality but not readmission in a study population of hospitalized older patients.
Sarcopenia was traditionally considered a geriatric syndrome characterized by low muscle mass and inadequate mass strength and/or physical performance1. It is prevalent in the population older than 65 years, especially in those who are hospitalized or institutionalized2, and is associated with an increased risk of adverse outcomes, such as functional decline, poor quality of life and death3,4,5.
Most recently, sarcopenia has been recognized as a disease with an international classification of disease, tenth revision, clinical modification (ICD-10-MC) Code6,7. This marks a substantial step forward in the understanding of sarcopenia and evokes the urgent need for a simple but accurate diagnostic method for the detection of sarcopenia.
Most of the current international consensuses agree that the diagnosis of sarcopenia should include low muscle mass and decreased muscle function6,8,9,10,11. Low muscle mass is usually measured with magnetic resonance imaging (MRI), computed tomography (CT), dual-energy X-ray absorptiometry (DXA) or bioelectrical impedance analysis (BIA). However, these methods are time-consuming, inconvenient, and device-reliable, and some of these methods are expensive and may induce radiation exposure. Decreased muscle function is usually estimated by handgrip strength and gait speed, which also need specific devices or experienced staff. To simplify the detection of sarcopenia, some efforts have been made, such as the SARC-F (a self-report questionnaire including five domains: strength, ambulation, rising from a chair, stair climbing, and history of falls)12 and the Ishii formula (a screening formula including three objective variables: age, handgrip strength and calf circumference [CC])13.
Several serum biomarkers have been applied as the indicators for sarcopenia as well. For example, serum creatinine is derived from creatine phosphate, its production is affected by muscle mass. Low serum creatinine value has been used as a surrogate of low muscle mass and is associated with adverse outcomes14,15. Conversely, cystatin C is a small protein originating from all nucleated cells, its production is relatively constant and less affected by skeletal muscle mass. Therefore, Kashani et al. recently used the two biomarkers to develop a novel sarcopenia index (SI, serum creatinine [mg/dl]/cystatin C [mg/l] × 100) for estimating skeletal muscle mass16. They reported that the SI was a fair measure for muscle mass and could modestly predict in-hospital mortality among intensive care unit (ICU) patients with normal kidney function. In another study from the same team, the authors reported that the SI was a potentially objective measure for estimating muscle mass among 28 lung transplant patients17.
Unlike other complex tools, the SI is only based on the serum concentration of creatinine and cystatin C, which is objective and routinely tested in older people. If the SI can accurately estimate sarcopenia in older people, it would be of great value for simplifying the diagnostic procedure of sarcopenia. Unfortunately, our team compared the SI with four classic diagnostic criteria of sarcopenia and found it could not accurately detect either low muscle mass or sarcopenia in community-dwelling older people18. However, most recently, Barreto et al.19 reported that the SI was a predictor of muscle mass and related to longer hospital length of stay and frailty among 171 ICU patients. This finding got us wondering: is the SI associated with the prognosis of non-ICU older inpatients? Therefore, we reanalyzed the data of a prospective study to evaluate whether the SI is associated with long-term mortality and readmission among hospitalized older adults.
We reanalyzed the data of a prospective observational study that was conducted in the acute ward of the Center of Gerontology and Geriatrics, West China Hospital of Sichuan University20. The study protocol was approved by the Research Ethics Committee of Sichuan University. All participants were fully informed and written informed consent was obtained from every participant or their legal proxies (for those who could not write their names). All the methods in this study were in accordance with the relevant guidelines and regulations.
Participants in baseline investigation
The detailed information of the study has been published previously20. In brief, between February and August 2012, we consecutively recruited patients aged 60 years and older and agreed to participate in the study. We excluded patients with cachexia or severe diseases that made them fail to communicate with the interviewers or to perform the walking test. Furthermore, for the current analysis, participants should have a record of serum creatinine and cystatin C measured upon admission. We excluded patients with an eGFR of <90 ml/min/1.73 m2 at admission from the current analysis as well.
Well-trained interviewers obtained baseline data from all participants through face-to-face interviews within 48 hours of admission. Well-trained technicians performed the anthropometric measurements. All interviewers and technicians received specific training and passed a training test prior to the formal investigation.
Measurement of cystatin C and creatinine, and the SI
Blood was drawn by experienced nurses in the morning after a fast of more than eight hours. Serum cystatin C concentration (mg/l) was measured with the cystatin C immunoturbidimetric assay (Sichuan Mike Biotechnology Co., Ltd., Chengdu, China), and serum creatinine concentration (mg/dl) was measured with the Roche enzymatic method (Creatinine Jaffe Gen.2 assay: Roche Diagnostics GmbH, Mannheim, Germany). The SI was calculated according to the following equation: serum creatinine value/cystatin C value × 100. According to the SI, all participants were separated into four groups, from Q1 corresponding to the first (lowest) quartile to Q4 corresponding to the fourth (highest) quantile. The quartile cut-off points were as follows: Q1 < 63.9, Q2 63.9–74.3, Q3 74.3–84.2, Q4 > 84.3.
Measurement of calf circumference (CC), gait speed, handgrip strength
Trained technicians measured the CC by using a millimeter-graded tape around the largest part of the calf to the nearest 0.1 cm, with the participants placed in the supine position, with the left knee raised and the calf placed at a right angle to the thigh. A 4-meter walking test was performed to measure the gait speed21. The participants were asked to walk a 4-meter distance with their usual speed on a flat level with no obstructions, and the consuming time was recorded by trained technicians to the nearest of 0.1 s. Gait speed was then calculated by the equation: gait speed (m/s) = 4/consuming time. The participants could use canes or walkers during the walking test, if necessary. The handgrip strength was measured by trained technicians using a handheld dynamometer based on train gauge sensors (EH101, Xiangshan Inc., Guangdong, China) to the nearest 0.1 kg. In a sitting position with the shoulder adducted, the elbow flexed at a 110° angle, the wrist placed in a neutral position, and the interphalangeal joint of the index finger positioned at a 90° angle, the participants were asked to grasp the dynamometer at their maximal power. Both hands were measured three times and the highest value of either hand was recorded for the analyses9.
Assessment of potential covariates
The following covariates were collected from the hospital information systems and the face-to-face interviews: age, sex, smoking status, alcohol drinking status, and comorbidities (hypertension, ischemic heart disease, respiratory disease, acute infection, liver disease, central nervous system [CNS] disease, diabetes, osteoarthritis, tumor of any type, falls in the previous 12 months). The participants’ nutritional status and cognitive function were also evaluated by using the revised version of Mini Nutritional Assessment short-form (MNA-SF)22 and the Chinese version of the Mini-Mental Status Examination (MMSE)23, respectively. The highest score for the MNA-SF is 14; a score between 8 and 11 indicates that the participant is ‘at risk of malnutrition’; and a score of ≤7 indicates that the participant has malnutrition22. Cognitive impairment is defined as an MMSE score of ≤17 for illiterates, ≤20 for primary school graduates, and ≤24 for high school graduates or individuals with higher education23. The Chinese version of the 30-item Geriatric Depression Scale (GDS-30) was applied to evaluate depression24. A GDS-30 score of ≥11 suggests depression24. In addition, hemoglobin and prealbumin were also tested for all participants.
During the 3-year follow-up, we obtained the survival status and readmission information of the participants by annual telephone interviews. The death events were further confirmed by the data retrieved from the Local Death Registry (but the readmission information was not). The period from the first investigation to the date of death was recorded for the participants who died during the follow-up. The period from the first investigation to the end of the last follow-up was recorded for the participants who did not die. The first readmission time was recorded for the individuals who were readmitted to hospitals several times during the 3-year period of follow-up.
First, the normality of continuous data was investigated using the Kolmogorov–Smirnov test. Then, the data were presented as number (percentage) for categorical variables and mean (standard deviation [SD]) for continuous variables.
For continuous variables, a one-way ANOVA was used to detect differences across groups, and Fisher’s Least Significant Difference (LSD) post hoc analysis was used to determine the difference between every two groups. For categorical variables, the chi-squared test was used to detect the difference across groups. When a significant difference was identified across groups, column proportions tests (z-tests) with Bonferroni correction were performed to determine the difference between every two groups.
Univariate and multivariate Cox proportional-hazard models were applied to calculate the unadjusted and adjusted hazard ratio (HR) and 95% confidence interval (CI) of the SI for mortality and readmission, respectively. The SI was treated as either a continuous variable (per 1-SD) or a categorical variable (using the quartile cut-off points as mentioned above). Age, sex, and other confounders which were significantly different between the quartile groups of SI were adjusted for in the multivariate Cox models. In addition, survival and readmission curves were estimated using the Kaplan-Meier method to determine the impact of quartile of SI on mortality and readmission, respectively. The differences between the curves were compared using log-rank tests.
All data analyses were performed using SPSS version 20.0 (SPSS Inc., Chicago, IL, USA). During most testing, p < 0.05 was considered statistically significant, however, p-values were corrected for the z-tests with the Bonferroni correction (with the statistical significance set at p < 0.008, where 0.008 = 0.05/6).
Characteristics of the study population
A total of 313 participants agreed to participate in this study, 65 of them were excluded due to different reasons (Fig. 1). As a result, 248 participants (201 men and 47 women; mean age: 81.2 ± 6.6 years) were included in the current baseline analyses. Ten of the 248 participants lost to follow-up during the 3-year follow-up, which led to a final sample size of 238 participants (Fig. 1).
The baseline characteristics of participants according to the quartiles of SI are shown in Table 1. The mean age of the participants in the Q4 group was significantly lower than the other three groups. The prevalence of depression, cognitive impairment, and malnutrition was significantly higher in the Q1 group than in the other three groups, whereas body mass index (BMI), CC in men, gait speed in women, handgrip strength in men, and hemoglobin were the lowest in the Q1 group.
Correlation between the SI and BMI, CC, handgrip strength, and gait speed
The SI was positively correlated with BMI (r = 0.214, p = 0.001), CC (r = 0.253, p < 0.001), handgrip strength (r = 0.244, p < 0.001), and gait speed (r = 0.221, p < 0.001) (Fig. 2).
Association between the SI and 3-year all-cause mortality
During the 3-year follow-up, a total of 57 participants (23.9%) died. The mortality according to the quartiles of the SI was 32.2%, 25.0%, 23.3% and 15.3% in the Q1, Q2, Q3, and Q4 groups, respectively.
When the SI was treated as a continuous variable (per 1-SD), a higher SI was independently associated with a lower risk of 3-year all-cause mortality after adjusting for potential confounders (HR per 1-SD = 0.80, 95% CI: 0.63–0.97) (Table 2).
We also evaluated the association between different quartiles of SI and 3-year all-cause mortality. After adjusting for potential confounders, the Q1 group and the Q2 group were associated with 3-year all-cause mortality (HR = 1.85, 95% CI: 1.10–4.21; and HR = 1.28, 95% CI: 1.03–3.11, respectively) when using the Q4 group as the reference. The Q3 group was not significantly associated with 3-year all-cause mortality (HR = 1.25, 95% CI: 0.78–2.56) (Table 2).
Figure 3 shows the survival curves of the participants in different quartile groups according to the SI. The log-rank test indicated that the survival curves of the participants in different quartile groups were significantly different (p < 0.001).
Association between the SI and readmission
During the 3-year follow-up, a total of 179 participants (75.2%) were readmitted at least one time. The readmission rate according to the quartiles of SI was 84.7%, 78.3%, 71.7% and 66.1% in the Q1, Q2, Q3, and Q4 groups, respectively.
Table 3 shows the association between the SI and readmission according to Cox Regression Models. The SI was not significantly associated with readmission no matter it was treated as either a continuous variable (HR per 1-SD = 0.97, 95% CI: 0.77–1.25) or a categorical data (Q1: HR = 1.23, 95% CI: 0.77–1.99; Q2: HR = 0.97, 95% CI: 0.58–1.61; Q3: HR = 1.10, 95% CI: 0.68–1.76; Q4: reference).
Figure 4 shows the Kaplan-Meier curves for readmission of the participants in different quartile groups according to the SI. The log-rank test indicated that this difference between the curves was not statistically significant (p = 0.198).
As we aforementioned, due to the defects of current diagnostic methods for sarcopenia, the validation of a specific biomarker as the surrogate marker of sarcopenia is an attractive method25. As a newcomer in this field, the SI and a very similar biomarker (serum creatinine/cystatin C ratio) are of low cost, high accessibility, and repeatability26, therefore, they have been studied in different populations since being introduced in 201516,17,18,19,27.
Only two previous studies addressed the association between the SI and mortality16,27. In a retrospective study conducted in adult ICU patients, the SI was related to in-hospital and 90-day mortality16. Recently, another retrospective study also found that a lower SI was associated with a significantly higher risk of mortality among adult ICU patients27. Our finding that the SI was associated with long-term mortality among hospitalized older patients was in line with these findings. However, more prospective studies are needed before a robust conclusion can be drawn.
No previous study addressed the association between the SI and readmission. Our study showed that the SI was not associated with readmission in older inpatients for the first time. However, a recent prospective study demonstrated that the SI can be used as a predictor of hospitalization among patients with chronic obstructive pulmonary disease28.
Moreover, the serum creatinine/cystatin C ratio has been applied for other purposes in different populations. For example, in a retrospective study, Suzuki et al.29 reported that serum creatinine/cystatin C ratio appeared to be a predictive marker for chemotherapy-related adverse effects in patients with lung cancer. In another multicenter prospective study, Komorita et al.30 applied serum creatinine/cystatin C ratio in patients with type 2 diabetes and regularly attending teaching hospitals or diabetes clinics. They found that a lower creatinine/cystatin C ratio was a significant risk factor for fractures.
Putting all these findings together, we may argue that the SI (or serum creatinine/cystatin C ratio) might serve as a potentially valuable biomarker for predicting various adverse outcomes in different populations. However, it is noteworthy that the predictive value of the SI for adverse outcomes does not necessarily mean that it can be applied as a surrogate marker of sarcopenia. In fact, the SI was applied as a malnutrition screening tool in a retrospective study conducted in Mayo Clinic ICU patients27. A previous study demonstrated that the SI correlated with CT-derived skeletal muscle mass in adult ICU patients19. Similarly, the serum creatinine/cystatin C ratio correlated with DXA-derived skeletal muscle mass in kidney transplant recipients31. Furthermore, the serum creatinine/cystatin C ratio was recommended by Osaka et al.32 as a surrogate screening marker for sarcopenia in patients with type 2 diabetes. However, in a recent prospective study, our team reported that the SI cannot accurately detect either BIA-defined skeletal muscle mass or sarcopenia in urban community-dwelling older people with normal kidney function18. The discrepancy of these findings may due to the heterogeneity of the study populations and the methods to measure skeletal muscle mass. It seems that the SI is more sensitive in patients with more serious diseases and with a higher pretest probability of sarcopenia. However, based on the current evidence, whether the SI can be applied to estimate skeletal muscle mass (or sarcopenia) or not (especially among older adults) remains unclear, further studies are therefore warranted.
Interestingly, our study found a positive correlation between the SI and handgrip strength (or gait speed). This finding implies that the SI might be related to muscle function. However, we did not compare the SI with “gold” diagnostic criteria of sarcopenia such as the European Working Group on Sarcopenia in Older People (EWGSOP)8 or Asia Working Group for Sarcopenia (AWGS)9. Further studies were needed to determine the overall diagnostic accuracy of the SI for detecting sarcopenia, as well as the optimal cut-off points in hospitalized older adults.
Some limitations of our study need to be addressed. First, we did not adjust for some important confounders, such as frailty and activities of daily living. This may induce bias in our results. Second, the sample size of our study is relatively small, especially women. Third, it should be cautious to generalize our results into other ethnic populations or different clinical settings. Fourth, the readmission data were only based on self-reported information, which might be influenced by recall bias. Last, because an eGFR of 90 ml/min/1.73 m2 is the cut-off line of normal kidney function and mildly decreased33, we excluded patients with an eGFR < 90 ml/min/1.73 m2 (n = 40, 12.8%) from this study to minimize the impact of renal function on the results. Therefore, our results should not be used in older patients with an abnormal kidney function.
The SI based on serum cystatin C and creatinine is associated with long-term mortality but not readmission in a study population of hospitalized Chinese patients. However, whether the SI really reflects sarcopenia (or something else such as malnutrition) remains controversial. Further prospective studies are therefore needed to compare the SI to sarcopenia per se for predicting important clinical outcomes, such as quality of life and activities of daily living among older adults who living in different settings. Diagnostic accuracy studies of the SI against the classic diagnostic criteria of sarcopenia (or CT- or MRI-derived skeletal muscle mass) among older adults are also needed. There is still a long way to go before the SI can be applied in clinical practice to estimate either skeletal muscle mass or sarcopenia among older adults.
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
Cruz-Jentoft, A. J., Landi, F., Topinkova, E. & Michel, J. P. Understanding sarcopenia as a geriatric syndrome. Curr. Opin. Clin. Nutr. Metab. care 13, 1–7, https://doi.org/10.1097/MCO.0b013e328333c1c1 (2010).
Shafiee, G. et al. Prevalence of sarcopenia in the world: a systematic review and meta-analysis of general population studies. J. Diabetes Metab. Disord. 16, 21, https://doi.org/10.1186/s40200-017-0302-x (2017).
Landi, F. et al. Sarcopenia and mortality among older nursing home residents. J. Am. Med. Dir. Assoc. 13, 121–126, https://doi.org/10.1016/j.jamda.2011.07.004 (2012).
Landi, F. et al. Sarcopenia as a risk factor for falls in elderly individuals: results from the ilSIRENTE study. Clin. Nutr. 31, 652–658, https://doi.org/10.1016/j.clnu.2012.02.007 (2012).
Tsekoura, M., Kastrinis, A., Katsoulaki, M., Billis, E. & Gliatis, J. Sarcopenia and Its Impact on Quality of Life. Adv. Exp. Med. Biol. 987, 213–218, https://doi.org/10.1007/978-3-319-57379-3_19 (2017).
Cruz-Jentoft, A. J. et al. Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing 48, 16–31, https://doi.org/10.1093/ageing/afy169 (2019).
Vellas, B. et al. Implications of ICD-10 for Sarcopenia Clinical Practice and Clinical Trials: Report by the International Conference on Frailty and Sarcopenia Research Task Force. J. Frailty Aging 7, 2–9, https://doi.org/10.14283/jfa.2017.30 (2018).
Cruz-Jentoft, A. J. et al. Sarcopenia: European consensus on definition and diagnosis: Report of the European Working Group on Sarcopenia in Older People. Age Ageing 39, 412–423, https://doi.org/10.1093/ageing/afq034 (2010).
Chen, L. K. et al. Sarcopenia in Asia: consensus report of the Asian Working Group for Sarcopenia. J. Am. Med. Dir. Assoc. 15, 95–101, https://doi.org/10.1016/j.jamda.2013.11.025 (2014).
Studenski, S. A. et al. The FNIH sarcopenia project: rationale, study description, conference recommendations, and final estimates. J. Gerontol. A Biol. Sci. Med. Sci 69, 547–558, https://doi.org/10.1093/gerona/glu010 (2014).
Fielding, R. A. et al. Sarcopenia: an undiagnosed condition in older adults. Current consensus definition: prevalence, etiology, and consequences. International working group on sarcopenia. J. Am. Med. Dir. Assoc. 12, 249–256, https://doi.org/10.1016/j.jamda.2011.01.003 (2011).
Malmstrom, T. K. & Morley, J. E. SARC-F: a simple questionnaire to rapidly diagnose sarcopenia. J. Am. Med. Dir. Assoc. 14, 531–532, https://doi.org/10.1016/j.jamda.2013.05.018 (2013).
Ishii, S. et al. Development of a simple screening test for sarcopenia in older adults. Geriatr. Gerontol. Int. 14(Suppl 1), 93–101, https://doi.org/10.1111/ggi.12197 (2014).
Thongprayoon, C., Cheungpasitporn, W. & Kashani, K. Serum creatinine level, a surrogate of muscle mass, predicts mortality in critically ill patients. J. Thorac. Dis. 8, E305–311, https://doi.org/10.21037/jtd.2016.03.62 (2016).
Udy, A. A. et al. The Association Between Low Admission Peak Plasma Creatinine Concentration and In-Hospital Mortality in Patients Admitted to Intensive Care in Australia and New Zealand. Crit. Care Med. 44, 73–82, https://doi.org/10.1097/CCM.0000000000001348 (2016).
Kashani, K. B. et al. Evaluating Muscle Mass by Using Markers of Kidney Function: Development of the Sarcopenia Index. Crit. Care Med. 45, e23–e29, https://doi.org/10.1097/CCM.0000000000002013 (2017).
Kashani, K., Sarvottam, K., Pereira, N. L., Barreto, E. F. & Kennedy, C. C. The sarcopenia index: A novel measure of muscle mass in lung transplant candidates. Clin. Transplant. 32, e13182, https://doi.org/10.1111/ctr.13182 (2018).
He, Q., Jiang, J., Xie, L., Zhang, L. & Yang, M. A sarcopenia index based on serum creatinine and cystatin C cannot accurately detect either low muscle mass or sarcopenia in urban community-dwelling older people. Sci. Rep. 8, 11534, https://doi.org/10.1038/s41598-018-29808-6 (2018).
Barreto, E. F. et al. Validation of the sarcopenia index to assess muscle mass in the critically ill: A novel application of kidney function markers. Clin. Nutr. 38, 1362–1367, https://doi.org/10.1016/j.clnu.2018.05.031 (2018).
Yang, M. et al. Sarcopenia predicts readmission and mortality in elderly patients in acute care wards: a prospective study. J. Cachexia Sarcopenia Muscle 8, 251–258, https://doi.org/10.1002/jcsm.12163 (2017).
Atkinson, H. H. et al. Cognitive function, gait speed decline, and comorbidities: the health, aging and body composition study. J. Gerontol. A Biol. Sci. Med. Sci 62, 844–850 (2007).
Kaiser, M. J. et al. Validation of the Mini Nutritional Assessment short-form (MNA-SF): a practical tool for identification of nutritional status. J. Nutr. Health Aging 13, 782–788 (2009).
Liu, H. C. et al. Prevalence and subtypes of dementia in Taiwan: a community survey of 5297 individuals. J. Am. Geriatr. Soc. 43, 144–149 (1995).
Chan, A. C. Clinical validation of the Geriatric Depression Scale (GDS): Chinese version. J. Aging Health 8, 238–253, https://doi.org/10.1177/089826439600800205 (1996).
Curcio, F. et al. Biomarkers in sarcopenia: A multifactorial approach. Exp. Gerontol. 85, 1–8, https://doi.org/10.1016/j.exger.2016.09.007 (2016).
Patel, S. S. et al. Serum creatinine as a marker of muscle mass in chronic kidney disease: results of a cross-sectional study and review of literature. J. Cachexia Sarcopenia Muscle 4, 19–29, https://doi.org/10.1007/s13539-012-0079-1 (2013).
Barreto, E. F. et al. Sarcopenia Index Is a Simple Objective Screening Tool for Malnutrition in the Critically Ill. J. Parenter. Enter. Nutr. 43, 780–788, https://doi.org/10.1002/jpen.1492 (2018).
Amado, C. A. et al. The Ratio Serum Creatinine/Serum Cystatin C (a Surrogate Marker of Muscle Mass) as a Predictor of Hospitalization in Chronic Obstructive Pulmonary Disease Outpatients. Respiration 97, 1–8, https://doi.org/10.1159/000494296 (2018).
Suzuki, K. et al. Utility of creatinine/cystatin C ratio as a predictive marker for adverse effects of chemotherapy in lung cancer: A retrospective study. J. Int. Med. Res. 43, 573–582, https://doi.org/10.1177/0300060515579116 (2015).
Komorita, Y. et al. The serum creatinine to cystatin C ratio predicts bone fracture in patients with type 2 diabetes: The Fukuoka Diabetes Registry. Diabetes Res. Clin. Pract. 146, 202–210, https://doi.org/10.1016/j.diabres.2018.10.021 (2018).
Yanishi, M. et al. The creatinine/cystatin C ratio provides effective evaluation of muscle mass in kidney transplant recipients. Int. Urol. Nephrol. 51, 79–83, https://doi.org/10.1007/s11255-018-2015-6 (2019).
Osaka, T. et al. Decreased the creatinine to cystatin C ratio is a surrogate marker of sarcopenia in patients with type 2 diabetes. Diabetes Res. Clin. Pract. 139, 52–58, https://doi.org/10.1016/j.diabres.2018.02.025 (2018).
KDIGO Group. Chapter 2: Definition, identification, and prediction of CKD progression. Kidney Int. Suppl. 3, 63–72, https://doi.org/10.1038/kisup.2012.65 (2013).
This work is supported by the National Key R&D Program of China (No.2018YFC2002104) and the Health Commission of Sichuan Province (No. ZH2018-102). The sponsors had no role in the design, methods, data collection, analysis, and preparation of this work.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Tang, T., Zhuo, Y., Xie, L. et al. Sarcopenia index based on serum creatinine and cystatin C is associated with 3-year mortality in hospitalized older patients. Sci Rep 10, 1260 (2020). https://doi.org/10.1038/s41598-020-58304-z