Sarcopenia, characterized by an aging-related progressive decline of skeletal muscle mass, strength, and physical performance, is frequently encountered in patients undergoing peritoneal dialysis (PD) and is associated with adverse clinical outcomes. However, the best screening tools facilitating the rapid detection of sarcopenia among patients undergoing PD remain unknown.
Figure 1. The prevalence of low ASMI, low HGS, slow GS, and sarcopenia across four sarcopenia criteria among patients undergoing PD. ASMI, appendicular skeletal muscle index; HGS, handgrip strength; GS, gait speed; AWGS, Asian Working Group for Sarcopenia; EWGSOP, European Working Group on Sarcopenia in Older People; FNIH, Foundation for the National Institutes of Health; IWGS, International Working Group on Sarcopenia.
The prevalence of low ASMI, low HGS, slow GS, and sarcopenia across four sarcopenia criteria among patients undergoing PD. ASMI, appendicular skeletal muscle index; HGS, handgrip strength; GS, gait speed; AWGS, Asian Working Group for Sarcopenia; EWGSOP, European Working Group on Sarcopenia in Older People; FNIH, Foundation for the National Institutes of Health; IWGS, International Working Group on Sarcopenia. The correlations of SARC-F, SARC-CalF, and CC with anthropometric and skeletal muscle measurements are shown in Table 1. SARC-F correlated significantly with HGS (r = −0.363, p < 0.001) and GS (r = −0.452, p < 0.001) but not with ASMI (r = −0.125, p = 0.090) and anthropometric measurements. In contrast, SARC-CalF and CC correlated not only with HGS (r = −0.445, p < 0.001 for SARC-CalF; r = 0.522, p < 0.001 for CC) and GS (r = −0.293, p < 0.001 for SARC-CalF; r = 0.181, p = 0.019 for CC) but also with ASMI (r = −0.421, p < 0.001 for SARC-CalF; r = 0.683, p < 0.001 for CC).Table 1.
The correlations of SARC-F, SARC-CalF, and CC with anthropometric and skeletal muscle measurements.
Variables |
SARC-F |
|
SARC-CalF |
|
CC |
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r |
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p |
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r | p |
|
r |
p |
||||
Anthropometric measures |
|
|
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CC | ||||||||
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|
| |||||||
0.813 (0.749–0.866)a,b | ||||||||
|
|
| ||||||
<0.001* |
||||||||
Weight (kg) |
−0.029 |
0.692 |
|
−0.435 |
<0.001* |
|
0.721 |
<0.001* |
BMI (kg/m2) |
−0.009 |
0.900 |
|
−0.382 |
<0.001* |
|
0.625 |
<0.001* |
WC (cm) |
||||||||
SARC-CalF |
0.739 (0.670–0.801)a,c |
|||||||
0.120 |
0.104 |
|
−0.224 |
0.002* |
|
0.436 |
<0.001* |
|
MAMC (cm) |
−0.056 |
0.451 |
|
−0.395 |
<0.001* |
|
0.617 |
<0.001* |
FTI (kg/m2) |
0.136 |
0.067 |
|
−0.146 |
0.050* |
|
0.298 |
<0.001* |
<0.001* | ||||||||
SARC-F |
0.587 (0.513–0.659)b,c |
0.033* |
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EWGSOP2 |
|
|
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CC |
0.776 (0.709–0.834)b |
<0.001* |
||||||
SARC-CalF |
0.748 (0.679–0.809)c |
<0.001* |
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Skeletal muscle measures |
|
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SARC-F |
0.625 (0.551–0.695)b,c | |||||||
|
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0.003* | ||||||||
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|
|
|
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ASMI (kg/m2) |
−0.125 |
0.090 |
|
−0.421 |
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FNIH |
|
| ||||||
<0.001* |
| 0.683 |
<0.001* |
|||||
HGS (kg) |
−0.363 |
|||||||
CC | ||||||||
<0.001* | ||||||||
| ||||||||
0.652 (0.579–0.721) |
<0.001* | |||||||
−0.445 | <0.001* |
|
0.522 |
<0.001* |
||||
GS (m/s)a |
−0.452 |
|||||||
SARC-CalF | ||||||||
<0.001* | ||||||||
0.648 (0.575–0.717) | ||||||||
| −0.293 |
<0.001* |
|
0.181 |
0.019* |
Table 2. The diagnostic performance of SARC-F, SARC-CalF, and CC on sarcopenia based on four operational definitions in the overall study population.
Definitions |
AUC (95% CI) |
p |
AWGS 2019 | ||
0.002* | ||
SARC-F | ||
0.587 (0.513–0.659) |
0.063 |
|
IWGS |
|
|
CC |
0.750 (0.682–0.811)b |
<0.001* |
SARC-CalF |
0.710 (0.639–0.774)c |
<0.001* |
SARC-F |
0.621 (0.547–0.691)b,c |
0.004* |
AUC, area under curve; CI, confidence interval; AWGS, Asian Working Group for Sarcopenia; CC, calf circumference; EWGSOP, European Working Group on Sarcopenia in Older People; FNIH, Foundation for the National Institutes of Health; IWGS, International Working Group on Sarcopenia. a p < 0.05 indicates significant difference of AUCs between CC and SARC-CalF. b p < 0.05 indicates significant difference of AUCs between CC and SARC-F. c p < 0.05 indicates significant difference of AUCs between SARC-CalF and SARC-F. *The AUC was significantly different from 0.5.
In patients undergoing HD, Yamamoto et al. have reported that the AUCs of the SARC-F questionnaire for muscle weakness and poor physical performance range from 0.76 to 0.87, indicating its good diagnostic performance for identifying patients undergoing HD with physical disability [19]. Furthermore, a close relationship between SARC-F scores and overall mortality in patients undergoing HD has been demonstrated in our previous study [20]. Unfortunately, the AUCs of SARC-F for sarcopenia, defined as both low muscle mass and strength, were less satisfactory in geriatric and dialysis populations [20][21]. Similarly, in our PD cohort, the diagnostic performance of SARC-F on sarcopenia was generally poor across the four different criteria. In patients undergoing HD, Marini et al. have reported that SARC-F is more closely associated with muscle functionality than muscle mass [22]; similarly, we disclosed a poor correlation of SARC-F with skeletal muscle mass, including MAMC and ASMI, in patients undergoing PD. These findings suggest that the score of SARC-F primarily reflected the status of skeletal muscle strength and physical performance rather than muscle mass, the latter of which is considered as an essential criterion for sarcopenia diagnosis. In contrast, CC yielded the highest correlation with ASMI in our analysis. In this regard, SARC-CalF, which adds the CC item into SARC-F, could improve the weakness of SARC-F in the aspect of skeletal muscle mass assessment. Not surprisingly, the improved performance of SARC-CalF over SARC-F exhibited in our PD cohort had been consistently reported in the geriatric and cancer population [12][13][14][15]. In particular, CC is considered a strong and reliable marker for skeletal muscle mass in the general population, which exhibited a high correlation with appendicular lean mass in a large-scale NHANES 1999–2006 cohort [23]. The good diagnostic performance of CC for detecting sarcopenia was affirmed in middle-aged and older adults [9][10][11][24] and in patients with chronic liver disease [25] and stroke [26]. In our patients undergoing PD, CC yielded the best correlation not only with ASMI but also with HGS among the three screening tools. The discriminative power of CC was even significantly better than that of SARC-CalF when we adopted the AWGS 2019—the criteria that may be most suitable for our Taiwanese population over the other three definitions. These findings emphasize that CC could be a simple-to-measure and valuable tool for the initial screening of sarcopenia among patients undergoing PD.Among the widely used screening tools for sarcopenia, CC and SARC-CalF outperformed SARC-F in the diagnostic accuracy of sarcopenia among patients undergoing PD, and both could serve as optimal screening tools for sarcopenia in clinical settings.