Skip to main content

Prevalence and associations of sarcopenia, obesity and sarcopenic obesity in end-stage knee osteoarthritis patients

Abstract

Objective

To identify the prevalence of obesity, sarcopenia, sarcopenic obesity in end-stage knee osteoarthritis (KOA) patients and analyze influences of obesity and sarcopenia in the progression of KOA.

Methods

A cross-sectional study was carried out among end-stage KOA patients who consecutively admitted to Orthopedic Department for TKA. We suppose that the level of decreased physical activities would be influenced by unilateral or bilateral KOA. Patient information, albumin, hemoglobin, pace, step frequency, number of comorbid conditions were collected. Bioelectrical impedance analyzer was used to analyze body composition. Obesity, sarcopenia, sarcopenic obesity rate were analyzed with accepted diagnosis criteria. Correlations between body mass index (BMI) or age and fat mass (FM), appendicular skeletal muscle mass (ASM) were analyzed.

Results

138 patients (male 30, female 108) in southwest of China including 67 patients with unilateral KOA and 71 patients with bilateral KOA were analyzed. No statistic difference was found in mean albumin, prealbumin and hematocrystallin, body composition values and number of comorbid conditions. We found that BMI was positively correlated with FM (Male: R2 = 0.7177, p < 0.0001, Female: R2 = 0.8898, p < 0.0001), ASM (Male: R2 = 0.2640, p = 0.0037, Female: R2 = 0.2102, p < 0.0001), FM index (FMI) (Male: R2 = 0.6778, p < 0.0001, Female: R2 = 0.8801, p < 0.0001), and ASM index (ASMI) (Male: R2 = 0.3600, p = 0.0005, Female: R2 = 0.4208, p < 0.0001) in end-stage KOA patients. However, age was not obviously correlated with FM or FMI (Male: FM, R2 = 0.006911, p = 0.3924; FMI, R2 = 0.7554, p = 0.0009196; Female: FM, R2 = 0.001548, p = 0.8412; FMI, R2 = 0.002776, p = 0.7822). And slightly negatively correlated with ASM (Male: R2 = 0.05613, p = 0.0136, Female: R2 = 0.01327, p = 0.5433) and ASMI (Male: R2 = 0.02982, p = 0.3615; Female: R2 = 0.03696, p = 0.0462). The prevalence of obesity, sarcopenia and obesity sarcopenia differs according to different diagnosis criteria. No difference in the occurrence rate of obesity was found between bilateral KOA and unilateral KOA patients, and occurrence rates of sarcopenia and sarcopenic obesity were statistically higher in bilateral KOA than that in unilateral KOA patients.

Conclusions

Obesity, sarcopenia and sarcopenic obesity are highly prevalent in end-stage KOA patients, sarcopenic obesity are more prevalent in bilateral KOA patients than that in unilateral KOA patients.

Introduction

Osteoarthritis (OA) is a degenerative joint disease, which is characterized by wear and tear and progressive loss of articular cartilage. Late-stage OA leads to disable condition that represents a substantial and increasing health burden with notable implications for individual affected, health-care systems, and wider socioeconomic costs [1, 2]. Worldwide, an estimated more than 240 million persons have symptomatic, activity-limiting OA, in which knee osteoarthritis (KOA) contribute the most of the overall burden [3, 4]. With the aging of population, increasing of obesity and joint injuries, symptomatic KOA increases gradually [1, 3, 4]. Current pharmacologic treatment such as non-steroidal anti-inflammatory drugs (NSIADs) mainly focus on pain relief, however, disease-modifying treatment is not yet available. As for late-stage KOA, total knee arthroplasty (TKA) is the main treatment method. It is known that the key treatments of KOA are education, exercise, and weight loss if needed [1, 4, 5].

As a degenerative disease of old age, many risk factors are associated with the prevalence of KOA, which including genetic factors, age, gender, immunometabolism, obesity, dyslipidaemia, hyperglycaemia and insulin resistance and dietary factors [6,7,8]. Obesity and sarcopenia are the two main syndromes caused by these risk factors, which are highly prevalent in the elderly population [9, 10]. Obesity is characterized by abnormal or excessive fat accumulation, and sarcopenia is characterized by loss of muscle mass and function, the relationship between these two syndromes is not clear. Recently, sarcopenic obesity, a phenotype of low muscle mass and high adiposity was identified as a bridge between obesity and sarcopenia, which may apply new guideline for the prevention of KOA [11,12,13].

Obesity is positively correlated with the development of KOA. Compared with normal weight individuals, obese individuals have 2.5–4.5 times increased risk for developing KOA. Meanwhile, overweight individuals are 1.5–2.5 times more likely to develop KOA than normal weight individuals [14,15,16]. On the other hand, most end-stage KOA patients are aged people with dramatically decreased physical activities, which resulted in the prevalence of sarcopenia in this population [3, 11, 13, 17,18,19]. We suppose that the level of decreased physical activities would be influenced by unilateral or bilateral KOA, which would result in different phenotypes among sarcopenia, obesity and sarcopenic obesity in KOA cohort. On the other hand, different diagnostic criterion may lead to different portion among these three types [9, 20]. The current study analyzed the prevalence of obesity, sarcopenia and sarcopenic obesity in end-stage KOA patients, and analyzed with different diagnostic criterion, through comparing nutrition associated indicators in unilateral and bilateral KOA patients, we found that sarcopenic obesity seems more prevalent in bilateral KOA patients.

Materials and methods

This is a cross-sectional study on end-stage KOA patients who consecutively admitted to Orthopedic Department of The First Affiliated Hospital of Chongqing Medical University for TKA. One hundred and forty-five (male 32, female 113) patients were participated this study. Patients diagnosed as rheumatoid arthritis (RA), traumatic arthritis, malignant tumor or other disease or condition which may affect the body fluid balance were excluded from the study. Finally, 138 patients (male 30, female 108) including 67 patients with unilateral KOA and 71 patients with bilateral KOA were analyzed. This study was approved by The Ethics Committee of The First Affiliated Hospital of Chongqing Medical University (NO. 2019-015) and informed consent was obtained from all the participants.

Patient information, including age, gender, weight, height and comorbid conditions were obtained from electronic medical record system. Prealbumin, albumin and hemoglobin were evaluated before surgery. Body composition was detected by Direct Segmental Multi-Frequency Bioelectrical Impedance Analyzer (DSM-BIA, Inbody 720, Korea) before surgery. Two hours before the determination, participants neither consume any liquids or solids nor do any intense activities. The same experienced technician performed the measurement for all participants as follows: supine position with bilateral ankle and wrist exposed, electrodes were placed on hairless sites of both left and right hands and feet. Phase angle, resistance, reactance, intracellular water (ICW), extracellular water (ECW), total body water (TBW), soft lean mass (SLM), fat free mass (FFM), skeletal muscle mass (SMM), body cell mass (BCM), Mineral, Bone Mineral Content, Waist Circle (Waist Cir.), basal metabolic rate (BMR), fat mass (FM), percent body fat (PBF) and visceral fat area (VFA), were measured in different frequency, as described previously [10, 21,22,23]. Step frequency and pace were calculated by recording time and frequency when patients walk 20 m.

Statistical analysis was performed with GraphPad Prism (GraphPad Software, La Jolla, CA) version 9.0. software. Quantitative data are shown as mean ± standard deviation (SD). There were no missing data on the patients included in the analyses. Normality of continuous variable was tested by Shapiroe-Wilk test. Between-group comparisons were conducted using Student's independent t-test, Chi-square, or Fisher's exact test, as appropriate, based on the distribution, variable type, and number in each group. Correlations were analyzed with simple linear regression. A two-tailed p value < 0.05 were considered statistically significant.

Results

 Flow chart of the current study was shown in Fig. 1, 138 patients diagnosed as end-stage KOA were included for the analysis, including 67 patients with unilateral KOA and 71 patients with bilateral KOA. Unilateral KOA group including 54 females and 13 males, and bilateral KOA group including 54 females and 17 males. Step frequency and pace in unilateral KOA were statistic higher than bilateral KOA patients (p < 0.0001). Patient characteristics were listed in Table 1, there were no statistic difference in mean age and BMI. No statistic difference was found in mean albumin, prealbumin and hematocrystallin values. Number of comorbid conditions and types of comorbid conditions were also listed in Table 1.

Fig. 1
figure 1

Flow chart of subject selection. KOA: knee osteoarthritis

Table 1 Patients characteristics of unilateral and bilateral knee osteoarthritis (KOA)

BMI screens for weight categories that may lead to healthy problems. We firstly analyzed BMI distribution according to underweight (less than 18.0 kg/m2), normal weight (18–24.99 kg/m2), overweight (25.0–30.0 kg/m2) and obese (more than 30 kg/m2). As presented in Table 2, more than half (42 in 67 in unilateral and 39 in 71 in bilateral KOA) participates were classified to overweight or obesity, although no statistic difference was found when compare unilateral KOA group and bilateral KOA group according to BMI classification respectively. These results indicated the prevalence of obesity in KOA patients.

Table 2 BMI classification of unilateral and bilateral KOA patients

To further evaluate the nutritional condition of participates, body composition was detected by BIA. There was no significant statistic difference between unilateral KOA group and bilateral KOA group in BMR, ICW, ECW, TBW, SLM, FFM, SMM, ECW/TBW, BCM, protein, mineral, bone mineral content, Waist cir., Arm Cir., and Arm muscle Cir. (Table 3), which suggested no dramatic difference was exist for single nutritional marker.

Table 3 Basal Metabolic Rate (BMR) and body composition parameters in Unilateral and bilateral KOA patients

In different stage of KOA, body composition would change accordingly. Therefore, based on the cross-sectional data, we analyzed relationships between BMI and fat mass (FM), fat mass index (FMI), appendicular skeletal muscle mass (ASM) and appendicular skeletal muscle mass index (ASMI) respectively. As shown in Fig. 2, with the increasing of BMI, FM (Male: R2 = 0.7177, p < 0.0001, slope 95% CI 1.359–2.230, Female: R2 = 0.8898, p < 0.0001, slope 95% CI 1.676–1.933) and FMI (Male: R2 = 0.6778, p < 0.0001, slope 95% CI 0.4776–0.8255, Female: R2 = 0.8801, p < 0.0001, slope 95% CI 0.7105–0.8138) increased accordingly. Meanwhile, with the increasing of BMI, ASM (Male: R2 = 0.2640, p = 0.0037, slope 95% CI 0.2008–0.9349, Female: R2 = 0.2102, p < 0.0001, slope 95% CI 0.1828–0.4004) and ASMI (Male: R2 = 0.3600, p = 0.0005, slope 95% CI 0.08997–0.2819, Female: R2 = 0.4208, p < 0.0001, slope 95% CI 0.1017–0.1610) increased with lower correlation. These results indicated that with the increasing of BMI, fat mass, not appendicular skeletal muscle mass, was the main increasing in end-stage KOA patients, which imply the specific nutritional condition in end-stage KOA patients.

Fig. 2
figure 2

Correlation between FM, FMI, ASM, ASMI and BMI. FM: fat mass, FMI: fat mass index, ASM: appendicular skeletal muscle, ASMI: appendicular skeletal muscle mass index

Appendicular skeletal muscle mass and fat mass are the two main markers that stand for the balance between muscle and fat in aspect of body composition. We firstly analyzed muscle mass in KOA patients. With the using of appendicular skeletal muscle mass index by different diagnostic criteria (ASM by height2, weight, and BMI), we found that the diagnosis of reduced muscle mass (sarcopenia) differs from diagnostic criteria, however, the incidence rate of reduced muscle mass was higher in bilateral KOA than that in unilateral KOA patients (Table 4). As for the prevalence of obesity, we also use different diagnostic criteria (by BMI, Waist Cir, and PBF), the results showed that in incidence rate of obesity differs from different diagnostic criteria, with the lowest incidence rate by BMI (10.45% in Unilateral KOA and 7.04% in Bilateral KOA) and the highest incidence rate by Waist Cir. (74.63% in Unilateral KOA and 67.61% in Bilateral KOA). However, there was no statistic difference between unilateral KOA and bilateral KOA for the incidence rate of obesity with different diagnostic criteria (Table 5).

Table 4 Prevalence of reduced muscle mass by diagnostic criteria
Table 5 Prevalence of obesity by diagnostic criteria

To further analyze the incidence of sarcopenic obesity (SO) in KOA patients. We found that the prevalence of SO in the overall cohort varied according to diagnostic criteria. As shown in Table 6, a higher prevalence of SO was identified with ASM by BMI and PBF, and with the criteria of ASM by height2 and BMI no SO was identified. Alternatively, a higher prevalence of SO was found in bilateral male KOA patients with the criteria of ASM by height2 and Waist Cir., ASM by height2 and PBF, ASM by BMI and Waist Cir., and ASM by BMI and PBF.

Table 6 Prevalence of sarcopenic obesity (SC) by diagnostic criteria

As we previously characterized that age is positively correlated with the prevalence of sarcopenia. Here, we also analyzed correlations between ages and FM, FMI, ASM and ASMI (Fig. 3). The results showed that age was not obviously correlated with FM or FMI in both female (FM, R2 = 0.006911, p = 0.3924, slope 95% CI − 0.2683 to 0.1061; FMI, R2 = 0.7554, p = 0.0009196, slope 95% CI − 0.09130 to 0.06645) and male patients (FM, R2 = 0.001548, p = 0.8412, slope 95% CI − 0.4021 to 0.3298; FMI, R2 = 0.002776, p = 0.7822, slope 95% CI − 0.1552 to 0.1180). As for ASM and ASMI, we found that age was slightly negatively correlated with ASM and ASMI in female patients (ASM, R2 = 0.05613, p = 0.0136, slope 95% CI − 0.1368 to − 0.01607; ASMI, R2 = 0.03696, p = 0.0462, slope 95% CI − 0.03915 to − 0.0003367, and not statistically correlation was found between age and ASM (R2 = 0.01327, p = 0.5433, slope 95% CI − 0.2467 to 0.1329) and ASMI (R2 = 0.02982, p = 0.3615, slope 95% CI − 0.07668 to 0.02887) in male patients. These results suggested that age should not be the main risk factor of sarcopenia or obesity in KOA cohort.

Fig. 3
figure 3

Correlation between FM, FMI, ASM, ASMI and age. FM: fat mass, FMI: fat mass index, ASM: appendicular skeletal muscle, ASMI: appendicular skeletal muscle mass index

Discussion

With the aging of population, morbidity of KOA increases gradually. Many factors, including age, genetic factors, gender, immunometabolism and obesity are correlated with the incidence of KOA. The relationship between obesity and KOA has been commonly studied, recently the relationship between sarcopenia and end-stage KOA has been noticed and reported, some of the studies explored one phenotype named sarcopenic obesity [13]. These studies indicated the complex relationships among sarcopenia, obesity and sarcopenic obesity [6, 13, 24]. We supposed that KOA induced decreased activities may accelerate the occurrence of sarcopenic obesity and compared sarcopenic obesity between unilateral and bilateral KOA patients. Our results found there is no difference in the occurrence rate of obesity between bilateral and unilateral end-stage KOA cohort, and occurrence rates of sarcopenia and sarcopenic obesity were statistically higher in bilateral KOA than that in unilateral KOA cohort. These results indicated that decreased activity is the risk factor for sarcopenic obesity in KOA cohort, in other words, bilateral KOA cohort with a higher risk of sarcopenia obesity.

KOA is one of the most prevalent forms of knee disease and a growing cause of disability worldwide. It is reported that nutritional condition is associated with the occurrence and progression of KOA on basis of that several nutrients participated cartilage metabolism [7]. On the other hand, obesity or overweight is another risk factor of KOA and sarcopenia is prevalent in older population [6, 12, 13]. Therefore, we analyzed the prevalence of obesity and sarcopenia in end-stage KOA cohort. We found that almost half end-stage KOA patients were diagnosed as obesity or overweight according to BMI criteria, and no obvious difference was found between unilateral and bilateral KOA cohort. As for the body composition analysis, there is no statistical difference between unilateral and bilateral KOA cohort. However, bilateral KOA patients with a higher incidence of sarcopenia compared with unilateral KOA patients. These results indicated that obesity is a risk factor of KOA, and sarcopenia may arise or aggravate with KOA progression. Decreased physical activity level is one of the key features of KOA cohort, which may cause or aggravate sarcopenia [13], through analyzing bilateral and unilateral KOA patients, we found obviously decreased pace and step frequency in bilateral KOA patients compared with unilateral KOA. However, we did not find statistic association between KOA side and decreased muscle mass side, this indicates sarcopenia in KOA patients is also characterized by systematic decreasing of muscle mass, rather than KOA affected limb muscle mass. On the other hand, sarcopenia is characterized as a geriatric syndrome and is a major challenge to healthy aging, which cause worse clinical outcomes and higher mortality than those without sarcopenia [9, 25]. The high incidence rate of sarcopenia in end stage KOA cohort needs to be pay attention to during perioperative recovery and functional training, prevention and treatment of sarcopenia and obesity may be beneficial for comprehensive treatment of KOA.

It is reported that men and women present different trajectories in the decline in skeletal muscle with aging. Women tend to have a sudden drop in muscle mass following menopause and men have a gradual decline especially in in sedentary individuals [26, 27]. In this study, we found that men presented a higher incidence of sarcopenia in bilateral KOA compared with unilateral KOA patients, and no obvious difference was found in women. This phenomenon may because sarcopenia in women was associated with estrogen level and activity level, in men was mainly associated with activity level.

Age is negatively corelated with the incidence of sarcopenia [28,29,30,31,32,33,34,35]. In end-stage KOA cohort, we found that age is negatively correlated with ASM and ASMI in female patients, however with a small correlation coefficient, and no statistic correlation was found in male patients. These results indicated that in end-stage KOA cohort, other risk factors, especially decreased activities and increased BMI were the main cause of sarcopenia. Meanwhile, we characterized that overweight or obesity is another feature of end-stage KOA cohort, and increased BMI is positively correlated with the increase of FM and FMI. Therefore, be similar with the previous studies [12, 13, 18], we also identified the prevalence of sarcopenia obesity in end-stage KOA cohort. As the diagnosis of SC differs from criteria, our data showed the high incidence of obesity by Waist Cir. or PBF, rather than by BMI, which indicates the high incidence of central obesity in end-stage KOA cohort. Be different with sarcopenia, obesity rates did not differ between unilateral and bilateral cohort, which indicates that obesity is one of the primary risk factors of KOA, and sarcopenia stand for relative severe activity limitation caused by KOA. In other words, obesity is a risk factor of KOA, and KOA, especially bilateral KOA is a risk factor of sarcopenia. Since sarcopenia is associated with fragility, fracture, osteoporosis, poor surgical outcomes etc. [32, 33, 35,36,37,38], the treatment or improve of SC in end-stage KOA patients is necessary for improving functional results perioperatively.

As one of the most important non-surgical treatment methods of KOA, therapeutic exercise is strongly recommended for the treatment or prevent of KOA [39]. The main advantages of exercise including enhance muscle strength, maintain joint stability etc. [39,40,41,42]. Meanwhile, physical exercise is essential for the prevention of sarcopenia [27]. In this study, the data also indicated the prevalence of sarcopenia in KOA patients, therefore, we deduce that lack of physical exercises not only induced the prevalence of sarcopenia, but also facilitated KOA progression. On the other hand, weight loss is strongly recommended for patients with KOA who are overweight or obese [39]. We found that obesity or overweight are highly prevalent in KOA cohort, which suggested that weight loss is a potential therapeutic target for KOA prevention and treatment. Taken together, rational physical exercise is beneficial for prevention of sarcopenia, obesity, sarcopenia obesity and knee osteoarthritis.

This study has some limitations. This is a cross sectional study, and we selected all the patient in the same hospital. Our study included Chinese people only, consequently, our data are not generalizable to the overall population who sustain hip fractures. We only analyzed end-stage OA patients and compared indicators between unilateral and bilateral KOA patients. Further studies focus on improving KOA progression through decreasing the occurrence of sarcopenia and/or obesity are needed.

In conclusion, this study showed that the prevalence of obesity, sarcopenia and sarcopenic obesity in end-stage KOA patients, although results do not conclusively establish weight loss and increased muscle mass as protective factors against osteoarthritis, procedures aimed to weight loss and increase muscle mass should be beneficial for KOA prevention and treatment.

Data availability

All data generated in this study are included in the article or supplementary materials.

References

  1. Hunter DJ, Bierma-Zeinstra S. Osteoarthritis. Lancet. 2019;393(10182):1745–59.

    Article  CAS  PubMed  Google Scholar 

  2. Martel-Pelletier J, Barr AJ, Cicuttini FM, Conaghan PG, Cooper C, Goldring MB, Goldring SR, Jones G, Teichtahl AJ, Pelletier JP. Osteoarthritis. Nat Rev Dis Prim. 2016;2:16072.

    Article  PubMed  Google Scholar 

  3. Long H, Liu Q, Yin H, Wang K, Diao N, Zhang Y, Lin J, Guo A. Prevalence trends of site-specific osteoarthritis from 1990 to 2019: findings from the Global Burden of Disease Study 2019. Arthrit Rheumatol. 2022;74:1172–83.

    Article  Google Scholar 

  4. Katz JN, Arant KR, Loeser RF. Diagnosis and treatment of hip and knee osteoarthritis: a review. JAMA. 2021;325(6):568–78.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Hawker GA. Osteoarthritis is a serious disease. Clin Exp Rheumatol. 2019;37 Suppl 120(5):3–6.

    PubMed  Google Scholar 

  6. Bortoluzzi A, Furini F, Scire CA. Osteoarthritis and its management—epidemiology, nutritional aspects and environmental factors. Autoimmun Rev. 2018;17(11):1097–104.

    Article  CAS  PubMed  Google Scholar 

  7. Messina OD, Vidal Wilman M, Vidal Neira LF. Nutrition, osteoarthritis and cartilage metabolism. Aging Clin Exp Res. 2019;31(6):807–13.

    Article  PubMed  Google Scholar 

  8. Matsunaga M, Lim E, Davis J, Chen JJ. Dietary quality associated with self-reported diabetes, osteoarthritis, and rheumatoid arthritis among younger and older US adults: a cross-sectional study using NHANES 2011–2016. Nutrients. 2021;13(2):545.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Chen LK, Woo J, Assantachai P, Auyeung TW, Chou MY, Iijima K, Jang HC, Kang L, Kim M, Kim S, et al. Asian Working Group for Sarcopenia: 2019 consensus update on sarcopenia diagnosis and treatment. J Am Med Dir Assoc. 2020;21(3):300–7.

    Article  PubMed  Google Scholar 

  10. Chen Y, Wu X, Chen J, Xu W, Liang X, Huang W, Liao J. Nutritional condition analysis of the older adult patients with femoral neck fracture. Clin Nutr. 2020;39(4):1174–8.

    Article  PubMed  Google Scholar 

  11. Roubenoff R. Sarcopenic obesity: the confluence of two epidemics. Obes Res. 2004;12(6):887–8.

    Article  PubMed  Google Scholar 

  12. Batsis JA, Mackenzie TA, Lopez-Jimenez F, Bartels SJ. Sarcopenia, sarcopenic obesity, and functional impairments in older adults: National Health and Nutrition Examination Surveys 1999–2004. Nutr Res. 2015;35(12):1031–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Godziuk K, Prado CM, Woodhouse LJ, Forhan M. Prevalence of sarcopenic obesity in adults with end-stage knee osteoarthritis. Osteoarthr Cartil. 2019;27(12):1735–45.

    Article  CAS  Google Scholar 

  14. Oliveira MC, Vullings J, van de Loo FAJ. Osteoporosis and osteoarthritis are two sides of the same coin paid for obesity. Nutrition. 2020;70:110486.

    Article  CAS  PubMed  Google Scholar 

  15. Zheng H, Chen C. Body mass index and risk of knee osteoarthritis: systematic review and meta-analysis of prospective studies. BMJ Open. 2015;5(12):e007568.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Cawsey S, Padwal R, Sharma AM, Wang X, Li S, Siminoski K. Women with severe obesity and relatively low bone mineral density have increased fracture risk. Osteoporos Int J Establ Result Cooper Eur Found Osteoporos Natl Osteoporos Found USA. 2015;26(1):103–11.

    Article  CAS  Google Scholar 

  17. Williams V, Ying S, Stahlman S. Update: osteoarthritis and spondylosis, active component, U.S. Armed Forces, 2016–2020. MSMR. 2021;28(12):2–13.

    PubMed  Google Scholar 

  18. Godziuk K, Prado CM, Woodhouse LJ, Forhan M. The impact of sarcopenic obesity on knee and hip osteoarthritis: a scoping review. BMC Musculoskelet Disord. 2018;19(1):271.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Ryu M, Jo J, Lee Y, Chung YS, Kim KM, Baek WC. Association of physical activity with sarcopenia and sarcopenic obesity in community-dwelling older adults: the Fourth Korea National Health and Nutrition Examination Survey. Age Ageing. 2013;42(6):734–40.

    Article  PubMed  Google Scholar 

  20. Cho BW, Kim DS, Kwon HM, Yang IH, Lee WS, Park KK. Cross-sectional association between hypercholesterolemia and knee pain in the elderly with radiographic knee osteoarthritis: data from the Korean National Health and Nutritional Examination Survey. J Clin Med. 2021;10(5):933.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Altay MA, Erturk C, Sert C, Oncel F, Isikan UE. Bioelectrical impedance analysis of basal metabolic rate and body composition of patients with femoral neck fractures versus controls. Eklem hastaliklari ve cerrahisi = Jt Dis Relat Surg. 2012;23(2):77–81.

    Google Scholar 

  22. Tasar PT, Sahin S, Karaman E, Ulusoy MG, Duman S, Berdeli A, Akcicek F. Prevalence and risk factors of sarcopenia in elderly nursing home residents. Eur Geriatr Med. 2015;6(3):214–9.

    Article  Google Scholar 

  23. Shi K, Liu L, He Y-J, Li D, Yuan L-X, Lash GE, Li L. Body composition and bone mineral status in patients with Turner syndrome. Sci Rep. 2016;6(1):38026.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Thomas S, Browne H, Mobasheri A, Rayman MP. What is the evidence for a role for diet and nutrition in osteoarthritis? Rheumatology. 2018;57(suppl_4):iv61–74.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Chen LK, Lee WJ, Peng LN, Liu LK, Arai H, Akishita M, Asian Working Group for S. Recent advances in sarcopenia research in Asia: 2016 update from the Asian Working Group for Sarcopenia. J Am Med Direct Assoc. 2016;17(8):e761-767.

    Article  Google Scholar 

  26. Laviano A, Gori C, Rianda S. Sarcopenia and nutrition. Adv Food Nutr Res. 2014;71:101–36.

    Article  CAS  PubMed  Google Scholar 

  27. Rolland Y, Czerwinski S, Abellan Van Kan G, Morley JE, Cesari M, Onder G, Woo J, Baumgartner R, Pillard F, Boirie Y, et al. Sarcopenia: its assessment, etiology, pathogenesis, consequences and future perspectives. J Nutr Health Aging. 2008;12(7):433–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Sawaya Y, Ishizaka M, Kubo A, Shiba T, Hirose T, Onoda K, Maruyama H, Urano T. The Asian working group for sarcopenia’s new criteria updated in 2019 causing a change in sarcopenia prevalence in Japanese older adults requiring long-term care/support. J Phys Ther Sci. 2020;32(11):742–7.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Chang HK, Lee JY, Gil CR, Kim MK. Prevalence of sarcopenia in community-dwelling older adults according to simplified algorithms for sarcopenia consensus based on Asian Working Group for Sarcopenia. Clin Interv Aging. 2020;15:2291–9.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Shiota A, Nakayama N, Saito Y, Maeda T, Maeda Y, Nakayama K. Prevalence and associated factors of malnutrition and sarcopenia in a daycare facility: a cross-sectional study. Healthcare. 2020;8(4):576.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Ontan MS, Dokuzlar O, Ates Bulut E, Soysal P, Isik AT. The relationship between osteoporosis and sarcopenia, according to EWGSOP-2 criteria, in outpatient elderly. J Bone Miner Metab. 2021;39:684–92.

    Article  CAS  PubMed  Google Scholar 

  32. Harvey NC, Orwoll E, Kwok T, Karlsson MK, Rosengren BE, Ribom E, Cauley JA, Cawthon PM, Ensrud K, Liu E, et al. Sarcopenia definitions as predictors of fracture risk independent of FRAX((R)), falls, and BMD in the osteoporotic fractures in men (MrOS) study: a meta-analysis. J Bone Miner Res Off J Am Soc Bone Miner Res. 2021;36:1235–44.

    Article  Google Scholar 

  33. Zhang S, Tan S, Jiang Y, Xi Q, Meng Q, Zhuang Q, Han Y, Sui X, Wu G. Sarcopenia as a predictor of poor surgical and oncologic outcomes after abdominal surgery for digestive tract cancer: a prospective cohort study. Clin Nutr. 2019;38(6):2881–8.

    Article  PubMed  Google Scholar 

  34. Kuwada K, Kuroda S, Kikuchi S, Yoshida R, Nishizaki M, Kagawa S, Fujiwara T. Sarcopenia and comorbidity in gastric cancer surgery as a useful combined factor to predict eventual death from other causes. Ann Surg Oncol. 2018;25(5):1160–6.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Nakashima Y, Saeki H, Nakanishi R, Sugiyama M, Kurashige J, Oki E, Maehara Y. Assessment of sarcopenia as a predictor of poor outcomes after esophagectomy in elderly patients with esophageal cancer. Ann Surg. 2018;267(6):1100–4.

    Article  PubMed  Google Scholar 

  36. Chou SE, Rau CS, Tsai YC, Hsu SY, Hsieh HY, Hsieh CH. Risk factors and complications contributing to mortality in elderly patients with fall-induced femoral fracture: a cross-sectional analysis based on trauma registry data of 2,407 patients. Int J Surg. 2019;66:48–52.

    Article  PubMed  Google Scholar 

  37. Kanis JA, Borgstrom F, De Laet C, Johansson H, Johnell O, Jonsson B, Oden A, Zethraeus N, Pfleger B, Khaltaev N. Assessment of fracture risk. Osteoporos Int J Estab Result Coop Eur Found Osteoporos Natl Osteoporos Found USA. 2005;16(6):581–9.

    Article  Google Scholar 

  38. Sakurai K, Kubo N, Tamura T, Toyokawa T, Amano R, Tanaka H, Muguruma K, Yashiro M, Maeda K, Hirakawa K, et al. Adverse Effects of low preoperative skeletal muscle mass in patients undergoing gastrectomy for gastric cancer. Ann Surg Oncol. 2017;24(9):2712–9.

    Article  PubMed  Google Scholar 

  39. Kolasinski SL, Neogi T, Hochberg MC, Oatis C, Guyatt G, Block J, Callahan L, Copenhaver C, Dodge C, Felson D, et al. 2019 American College of Rheumatology/Arthritis Foundation guideline for the management of osteoarthritis of the hand, hip, and knee. Arthritis Care Res. 2020;72(2):149–62.

    Article  Google Scholar 

  40. Vincent KR, Vasilopoulos T, Montero C, Vincent HK. Eccentric and concentric resistance exercise comparison for knee osteoarthritis. Med Sci Sports Exerc. 2019;51(10):1977–86.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Kan HS, Chan PK, Chiu KY, Yan CH, Yeung SS, Ng YL, Shiu KW, Ho T. Non-surgical treatment of knee osteoarthritis. Hong Kong Med J = Xianggang yi xue za zhi. 2019;25(2):127–33.

    CAS  PubMed  Google Scholar 

  42. Alcalde GE, Fonseca AC, Boscoa TF, Goncalves MR, Bernardo GC, Pianna B, Carnavale BF, Gimenes C, Barrile SR, Arca EA. Effect of aquatic physical therapy on pain perception, functional capacity and quality of life in older people with knee osteoarthritis: study protocol for a randomized controlled trial. Trials. 2017;18(1):317.

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

The authors express their sincere gratitude to medical and nursing stuff of Orthopaedic surgery of The First Affiliated Hospital of Chongqing Medical University and all patients who participated in the study.

Funding

The reported work was supported by the Medicine Program of Chongqing Municipal Health Commission (#2022wsjk010), Joint Foundation of Chongqing Science and Technology Commission and Municipal Health Commission (#2022DBXM002), and Appropriate Technology Promotion Program of Chongqing Municipal Health Commission (#2019jstg017). This project was also supported by the Top Talent Award from The First Affiliated Hospital of Chongqing Medical University (BJRC2021-04) and Cultivating Program of Postdoctoral Research of The First Affiliated Hospital of Chongqing Medical University (CYYY-BSHPYXM-202202). JY was supported by a Postdoctoral Fellowship from Chongqing Medical University and rewarded by China Postdoctoral Science Foundation (No. 2022M720605).

Author information

Authors and Affiliations

Authors

Contributions

JYL was responsible for conceiving and designing the experiments, performing the experiments, collecting data, analyzing data, and writing the manuscript. JC was responsible for collecting data, analyzing data, and writing the manuscript. WX was responsible for analyzing. JC was responsible for performing the experiments. QC was responsible for analyzing and reviewing the manuscript. YLT was responsible for analyzing and contributing reagents/materials/analysis tools. WH was responsible for designing the experiments, analyzing the data, contributing reagents/materials/analysis tools, and reviewing the manuscript.

Corresponding authors

Correspondence to Qiang Cheng, Yongli Tang or Wei Huang.

Ethics declarations

Ethics approval and consent to participate

The ethics committee of The First Affiliated Hospital of Chongqing Medical University approved the study (NO. 2019-015).

Competing interests

The authors declare no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Liao, J., Chen, J., Xu, W. et al. Prevalence and associations of sarcopenia, obesity and sarcopenic obesity in end-stage knee osteoarthritis patients. J Health Popul Nutr 42, 108 (2023). https://doi.org/10.1186/s41043-023-00438-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s41043-023-00438-7

Keywords