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Nguyen, Nguyen, Kuo, and Chen: Impact of sarcopenia on outcomes following vertebral augmentation for osteoporotic vertebral compression fracture: a systematic review and meta-analysis

Abstract

Vertebral augmentation is a safe and effective treatment for osteoporotic vertebral compression fractures (OVCFs) in elderly patients. The impact of sarcopenia on post-procedure outcomes has been debated. This meta-analysis examined its effect on outcomes following vertebral augmentation in OVCF patients. Several electronic databases were searched until August 2024 for studies that compared patients with and without sarcopenia after kyphoplasty or vertebroplasty for OVCFs. The outcomes of interest were the rates of vertebral refracture and residual back pain (RBP), clinical outcomes, length of hospital stay, and mortality rate. The pooled results are presented as odds ratios (ORs) or mean differences with corresponding 95% confidence intervals (CIs). Fourteen studies involving 2197 patients with OVCF treated with vertebral augmentation were included. Of these patients, 813 had sarcopenia and 1384 did not, with a mean age of 73.06. Patients with sarcopenia exhibited a higher prevalence of refracture than those without sarcopenia (OR, 2.92; 95% CI, 1.34–6.34; p=0.007). Patients without sarcopenia had a 64% lower risk of RBP than those with sarcopenia (OR, 0.36; 95% CI, 0.23–0.56; p<0.001). Additionally, patients with sarcopenia demonstrated worse postoperative clinical outcomes, longer hospital stays, and a significantly higher risk of mortality. Sarcopenia adversely affects patients undergoing vertebral augmentation for OVCFs. Early diagnosis of sarcopenia in patients with OVCF and the adoption of comprehensive management strategies to improve and maintain muscle health are recommended (PROSPERO registry number: CRD42024578202).

Introduction

Osteoporotic vertebral compression fractures (OVCFs) are a common and serious consequence of osteoporosis and have become more prevalent as life expectancy increases. These fractures occur when weakened vertebrae collapse, frequently causing severe pain, restricted mobility, various morbidities, and even death [1,2].
Vertebral augmentation is a minimally invasive procedure to relieve pain and manage complications from OVCFs by injecting bone cement into the fractured vertebra to stabilize and restore height. There are two main types: vertebroplasty, in which bone cement is injected directly into the collapsed vertebra, and kyphoplasty, in which a balloon is first inserted into the fractured vertebra to create a cavity that is then filled with bone cement, which helps restore the original vertebral shape and reduce kyphosis [3]. Although these procedures offer benefits such as pain relief, vertebral height restoration, and boosted patient function, cement leakage, adjacent vertebral fracture, increased pain, and mortality are some complications that occur [4,5].
Sarcopenia is characterized by the progressive loss of skeletal muscle mass, quality, and strength associated with aging [6]. Recent studies indicate the negative impacts of sarcopenia on elderly patients undergoing orthopedic and trauma care, which contributes to increased risks of falls and fractures, resulting in decreased independence and decreased quality of life (QoL) [7,8]. Several studies have examined the effects of sarcopenia on patients undergoing vertebral augmentation for OVCFs, but their results are inconsistent. Some studies reported that sarcopenia did not affect outcomes after the procedures [912], while others showed significantly poorer results in patients with sarcopenia [1316]. Thus, we conducted this meta-analysis to thoroughly review all available publications on this topic and provide evidence on the impact of sarcopenia on these procedures. We hypothesized that the presence of sarcopenia negatively affects outcomes after kyphoplasty or vertebroplasty, specifically vertebral refracture, residual back pain (RBP), clinical performance, hospital stay, and mortality.

Materials and Methods

Registration and protocol

This study followed the Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) [17] and was registered with the International Prospective Register for Systematic Reviews (PROSPERO registry number: CRD42024578202).

Data sources and search strategies

Two independent reviewers comprehensively searched electronic databases (PubMed, Embase, Scopus, Cochrane Library, and Web of Science). The search utilized the keywords: “sarcopenia” and a combination of “vertebral augmentation,” “kyphoplasty,” or “vertebroplasty.” The search included all publications available until August 2024. Any discrepancies were resolved by a third author. The reviewers used EndNote version 20.5 (Clarivate, London, UK) to manage the retrieved studies, remove duplicates, and organize the references.

Inclusion and exclusion criteria

This meta-analysis reviewed original articles comparing the outcomes of kyphoplasty or vertebroplasty for OVCFs in patients with and without sarcopenia. Outcomes such as vertebral refracture, RBP rate, postoperative clinical outcomes, length of hospital stay, and mortality risk were compared between the two groups. Sarcopenia was diagnosed according to the specific criteria outlined in each study, as summarized in Table 1. Studies were excluded if they did not specify a diagnosis or definition of sarcopenia. Case reports, case series, expert opinions, reviews, letters, or systematic reviews were also excluded. Additionally, studies without the full text or necessary data were not included. No restrictions were placed on language or year of publication, and the third author resolved any disagreements.

Data extraction and methodological quality

Two reviewers independently reviewed potentially relevant studies and extracted data from the provided materials. The retrieved data included the year of publication, country, research design, number of patients with and without sarcopenia, mean age, sex distribution, follow-up time, sarcopenia diagnosis criteria, and outcome measurements. The Newcastle-Ottawa Scale was used to rate the quality of the included non-randomized studies [18]. Each study was assigned a rating between 0 and 9, with higher ratings indicating higher quality and a lower risk of bias. The reviewers evaluated the quality of each cohort or case-control study by examining three domains: the selection of study groups, comparability of the groups, and ascertainment of either the outcome of interest or exposure through a total of eight questions. In cases of disagreement, the reviewers consulted a third reviewer for the final decision.

Outcomes of interest

The primary outcome of this study was the vertebral refracture rate in the sarcopenia and non-sarcopenia groups after vertebral augmentation. The secondary outcomes were RBP (Visual Analog Scale [VAS] score of back pain >4 at follow-up), clinical performance 1 and 12 months after surgery, including pain measured by VAS, functional evaluation using the Oswestry Disability Index (ODI), length of hospital stay, and risk of all-cause mortality.

Statistical analysis, data synthesis, heterogeneity assessment, and publication bias evaluation

Our meta-analysis utilized Review Manager Software ver. 5.4 (Cochrane Collaboration, Oxford, UK). Continuous variables are represented as mean±standard deviation. The odds ratio (OR) and 95% confidence interval (CI) were estimated for dichotomous outcomes using the Mantel-Haenszel method. Continuous variables are presented as mean difference (MD) with 95% CI calculated using the inverse-variance method. The pooled odds ratio was also determined using the inverse-variance method for the given ORs. We assessed heterogeneity across the studies using the chi-square test, setting significance at a p-value under 0.1, and the Higgins I2 test, categorized as low (I2 under 25%), moderate (I2 between 25%–50%), or high (I2 above 50%) [19]. A random-effects model was applied when significant heterogeneity was observed (I2 >50% and p<0.05); in contrast, a fixed-effects model was used. Subgroup analysis was performed whenever possible. Sensitivity analysis was conducted by excluding one study at a time in cases of significant heterogeneity between studies. Statistical significance was set at p<0.05. Funnel plots and Egger’s regression tests were employed to evaluate publication bias using Comprehensive Meta-Analysis Software (BioStat, Englewood, NJ, USA).

Results

A total of 103 records were identified. After removing duplicates, 43 records were screened for titles and abstracts. After excluding ineligible studies, we assessed the full texts of 23 records. Nine articles were excluded for several reasons. Finally, 14 studies were included in the meta-analysis. Fig. 1 summarizes the screening and selection processes for the study.
The characteristics of the included studies are presented in Table 1. The studies consisted of 2,197 patients with a pooled mean age of 73.06 years, and there were more females (n=1,600, 72.83%) than males (n=597, 27.17%). A total of 813 patients were diagnosed with sarcopenia and 1,384 without sarcopenia. The more common procedure was kyphoplasty, reported in 11 studies [9,1116,2023], followed by vertebroplasty, reported in five studies [10,20,21,24,25]. The follow-up time varied from 1 to 79 months.
Supplement 1 illustrates the methodological quality of all included studies. The Newcastle-Ottawa Scale was used to assess these studies because they were all observational in nature. Eight studies were rated as high-quality, with four scoring 7 points, four scoring 8 points, and three scoring 9 points. Three studies were deemed to have a high risk of bias, each scoring 6 points.
Table 2 shows the results of the meta-analysis of bone and muscle measurements in patients with OVCF. Patients with sarcopenia had significantly poorer bone and muscle health than those without sarcopenia, as demonstrated by a lower bone mineral density (MD, −0.42; 95% CI, −0.67 to −0.17; p<0.001), weaker handgrip strength (MD, −5.66; 95% CI, −9.42 to −1.89; p=0.003), and notably decreased in muscle mass.

Vertebral refracture

Fig. 2 shows the forest plot of vertebral refractures after vertebral augmentation in patients with and without sarcopenia. Eleven studies with 1,671 patients were included; 661 had sarcopenia and 1,010 did not [916,21,22,25]. The refracture rates were 29.35% for those with sarcopenia and 13.37% for those without sarcopenia. Patients with sarcopenia had a higher prevalence of refracture after the augmentation procedure than those without sarcopenia (OR, 2.92; 95% CI, 1.34–6.34; p=0.007). High heterogeneity was observed between the studies (I2=85%, p<0.001).
Subgroup analyses were performed. Among the Chinese population, patients with sarcopenia had more than four times the risk of refracture than patients without sarcopenia (OR, 4.33; 95% CI, 1.84–10.22; p<0.001). In contrast, studies conducted outside China showed no difference in refracture risk between the two groups (p=0.86). Patients under 70 years of age showed no difference in refracture risk between the two groups. However, patients over 70 years of age with sarcopenia had a higher risk than those without sarcopenia, with the risk increasing with age. Studies with less than 1-year follow-up found no significant refracture difference between the sarcopenic and non-sarcopenic groups (p=0.09). However, with follow-ups over 1 year, patients with sarcopenia showed a higher refracture risk (OR, 1.98; 95% CI, 1.22–3.21; p=0.006). Studies diagnosing sarcopenia with a single factor reported a lower refracture risk than those using multiple factors. Finally, patients with sarcopenia who underwent kyphoplasty had a higher refracture risk than those without sarcopenia (OR, 3.67; 95% CI, 1.46–9.22; p=0.006), while no difference was observed in vertebroplasty patients (p=0.88). The summary of the subgroup analysis is presented in Table 3.

Residual back pain

Five studies involving 836 patients (266 sarcopenic and 570 non-sarcopenic) examined RBP rates after vertebral augmentation [16,2225]. The forest plot in Fig. 3 shows that patients without sarcopenia had 64% lower odds of RBP than patients with sarcopenia (OR, 0.36; 95% CI, 0.23–0.56; p<0.001). No heterogeneity was observed between these studies (I2=0%, p=0.74).

Clinical outcomes

Five studies reported 1-month postoperative pain evaluation, revealing that patients with sarcopenia had significantly higher VAS scores than those without sarcopenia (MD, 1.06; 95% CI, 0.41–1.72; p<0.001) [11,12,16,22,25]. A high degree of heterogeneity was noted across the studies (I2=95%, p<0.001). Three studies assessed pain at 1-year postoperatively, and the pooled result suggested that patients with sarcopenia notably suffered more pain than those without sarcopenia (MD, 0.57; 95% CI, 0.49–0.66; p<0.001) [16,22,25]. No heterogeneity was detected between the studies (p=0.32). Forest plots illustrating the results are presented in Fig. 4.
Five studies investigated functional impairment due to low back pain 1 month after surgery [11,12,16,22,25]. Patients with sarcopenia demonstrated significantly higher ODI scores than those without sarcopenia, indicating worse outcomes (MD, 5.89; 95% CI, 4.11–7.67; p<0.001). These studies exhibited substantial heterogeneity (I2=85%, p<0.001). Three studies reported the ODI score 1-year postoperatively, and the result also showed a notably higher ODI score in patients with sarcopenia (MD, 5.49; 95% CI, 2.84–8.15; p<0.001) [16,22,25]. High heterogeneity was detected among the studies (I2=91%, p<0.001). Forest plots are shown in Fig. 5.

Length of hospital stay

Three studies compared the length of hospital stay between the groups [11,12,16], and the pooled result in Fig. 6 showed that patients with sarcopenia had longer hospital stays than patients without sarcopenia after the procedures (MD, 1.36; 95% CI, 1.05–1.67; p<0.001). No heterogeneity was observed in these studies (p=0.81).

Risk of mortality

Three studies reported mortality data [10,12,20]. We investigated the risk of mortality at 1-year and longer follow-up time points. At the 1-year follow-up, because the study by Yin et al. [12] showed no death between the two groups, only two studies were included in the meta-analysis. The results in Fig. 7A show that patients with sarcopenia had more than 30 times the odds of mortality 1 year after the procedure (OR, 30.72; 95% CI, 4.06–232.26; p<0.001). No heterogeneity was detected among the studies (I2=0%, p=0.94). For a more extended follow-up time point, we examined the mortality rate after 3 years, including the study by Bayram et al. [20] with a mean follow-up of 48 months, the study by Kara and Ozturk [10] with a timepoint of 40 months through the survival graph, and the study by Yin et al. [12] at their last follow-up of 3 years. The result in Fig. 7B shows that patients with sarcopenia had 14.4 times the odds of long-term mortality than patients without sarcopenia (OR, 14.4; 95% CI, 6.49–31.97; p<0.001). No heterogeneity was detected among the studies (I2=12%, p=0.32).

Sensitivity analysis and publication bias assessment

Supplements 2–5 presented the forest plots after sensitivity analysis of interest outcomes with high heterogeneity. No significant changes were observed in the pooled results. This consistency underscores the robustness of the finding. The funnel plot of the included studies (Supplement 6) and subsequent Egger’s regression test did not suggest evidence of publication bias (t=0.25, p=0.81).

Discussion

Our meta-analysis reviewed 14 studies that included 2,197 patients who underwent vertebral augmentation for OVCFs. The findings revealed that patients with sarcopenia had elevated risks of vertebral refracture, RBP, poorer postoperative clinical performance, longer hospital stays, and mortality following the procedures compared to those without sarcopenia. The refracture risk increased with age in patients with sarcopenia undergoing vertebral augmentation. Additionally, the impact of sarcopenia on vertebral refracture was more pronounced following kyphoplasty than following vertebroplasty.
Sarcopenia is a progressive age-related condition characterized by decreased skeletal muscle mass, strength, and function [6]. After the age of 65 years, individuals typically lose 1.4% of muscle mass and 1.4%–2.5% of muscle strength annually [26]. Therefore, the prevalence of sarcopenia rises with age, impacting a significant portion of the elderly population. This, combined with increasing life expectancy, has made sarcopenia a significant public health concern. The consequences of sarcopenia extend beyond physical frailty, as affected individuals face higher risks of falls, fractures, chronic diseases, and disability, leading to a diminished QoL and greater dependence on others [27]. The economic burden associated with caring for sarcopenic individuals is also considerable [28].
Vertebral refracture is one of the most common complications after vertebral augmentation, with incidence rates reported as high as 52%. It is associated with various factors, including advanced age, low body mass index, bone loss, fracture in the thoracolumbar junction, and so forth [2933]. Many studies have highlighted the critical role of bone health in preventing refracture. Previous studies have reported a significant connection between bone and muscle health, showing considerable bone loss following muscle deterioration [3436]. These findings support our observations in this meta-analysis among patients with OVCF, where those with sarcopenia exhibited significantly worse bone and muscle conditions than those without sarcopenia. Additionally, losing muscle mass and strength increases fall risk and weakens the paraspinal and core muscles, reducing spinal stability and adding stress to the vertebrae, possibly leading to fractures [21,27,37,38]. Our study has confirmed that patients with sarcopenia have a substantially higher risk of postoperative refracture than those without sarcopenia, with increasing risk with age, which is also consistent with previous research linking these factors to an elevated risk of spine fractures [3941]. A key finding in our meta-analysis was that poor muscle health was more strongly linked to increased refracture risk in patients who undergo kyphoplasty than in those who undergo vertebroplasty, indicating that it may be a risk factor for poorer outcomes after kyphoplasty. Restoring vertebral height in the context of poor muscle quality, combined with changes in vertebral stiffness caused by cement augmentation, can compromise spinal stability and increase stress on adjacent vertebrae, ultimately leading to a significantly higher risk of refracture [4244]. However, this result should be interpreted cautiously, as fewer studies and participants were involved in vertebroplasty than in kyphoplasty (two studies with 248 participants versus eight studies with 1,334 participants). This underscores the need for additional research to explore the impact of sarcopenia on outcomes after vertebroplasty.
RBP is recognized as a significant global issue, severely impacting QoL, leading to disability, and reducing physical performance [45]. Previous studies have identified factors contributing to RBP after kyphoplasty or vertebroplasty, such as low bone density, bone cement volume, or dorsal fascia injury [4648]. Recently, attention has turned to the role of sarcopenia in RBP following spine surgery. Our study found that patients with sarcopenia experienced RBP after vertebral augmentation compared to those without sarcopenia. Muscles are crucial for stabilizing the spine and facilitating its functional movement. When these muscles weaken, the spine loses essential support, leading to misalignment and increased stress on the vertebral disks and joints, exacerbating pain. This can create a vicious cycle where pain reduces physical activity, further contributing to muscle atrophy and increased pain sensitivity [37,48]. Moreover, muscle loss worsens bone quality, which was associated with RBP because of the changes in alignment and stability of the spine [46,49,50].
In this study, patients with sarcopenia experienced longer hospital stays than those without sarcopenia. They also exhibited significantly poorer clinical outcomes at 1 month and 1 year after surgery, reporting higher pain levels and more severe functional impairments following vertebral augmentation. Increased pain and reduced functional recovery indicate that sarcopenia may intensify the physical strain and healing difficulties associated with spinal procedures and postoperative rehabilitation, resulting in prolonged recovery times. These findings are consistent with previous studies, which have repeatedly highlighted the adverse impact of sarcopenia on lumbar spinal diseases and surgical outcomes [12,5154].
Patients with sarcopenia were shown to have a higher risk of mortality at 1-year and longer-term follow-up after vertebral augmentation. The presence of sarcopenia was also reported to increase the risk of mortality after spinal surgery [5557]. Sarcopenia adversely affects patients due to associated morbidities, frailty, chronic systemic inflammation, and hormonal changes, leading to hospital readmissions, poorer health conditions, and mortality [5860]. Moreover, sarcopenia, which causes gait and balance impairments, significantly increases the risks of falls and severe injuries [61].
This study has several limitations. First, most studies were retrospective, which may have introduced bias. Second, all the included studies were observational, making them susceptible to various biases that could affect the reliability of the findings. Third, there was significant heterogeneity among the studies included in our analysis. For instance, most of the studies that investigated the influence of sarcopenia on refracture were from China, showing a higher refracture risk in patients with sarcopenia, while studies outside China found no difference. The overrepresentation of the Chinese population highlights the need for further research on other populations to help generalize these findings. Additionally, studies with a longer mean follow-up (over 1 year) showed a more significant impact of sarcopenia on vertebral refracture, unlike those with shorter follow-ups. Finally, the use of various tools for muscle assessment created diagnostic inconsistencies [7,62,63]. Among the studies reviewed, six combined two or three factors-muscle mass measurement and muscle strength or physical performance [9,1115] while the rest relied solely on muscle mass measurement to diagnose sarcopenia [10,16,2025]. These differing methodologies contributed to the considerable heterogeneity in the meta-analysis, underscoring the necessity for a standardized and effective tool for detecting sarcopenia across the general population.
It is crucial to recognize that sarcopenia significantly affects outcomes after vertebral augmentation. Early diagnosis and timely intervention are essential to improve muscle mass and quality, thereby minimizing adverse outcomes, preventing patient dependency, and enhancing QoL. Regular physical activity, particularly resistance training, and a protein-rich diet are vital for building and maintaining muscle mass after the procedure [6466].

Conclusions

Sarcopenia adversely affects patients undergoing vertebral augmentation for OVCFs, increasing the likelihood of vertebral refracture, particularly with advancing age. These patients are also more prone to RBP, poor clinical outcomes, prolonged hospital stay, and higher mortality risk. Early diagnosis of sarcopenia in high-risk patients and the implementation of comprehensive management strategies to enhance and sustain muscle health are advised to prevent adverse outcomes.

Key Points

  • This meta-analysis compared outcomes of vertebral augmentation for osteoporotic vertebral compression fractures in sarcopenic versus non-sarcopenic patients.

  • Sarcopenia was associated with significantly worse outcomes after the procedures.

  • Early detection and comprehensive management strategies are recommended to preserve muscle health and improve patient outcomes.

Notes

Conflict of Interest

No potential conflict of interest relevant to this article was reported.

Acknowledgments

The authors express their gratitude to the Wan Fang Hospital for providing financial support for this research.

Funding

This study was financially supported by the Wan Fang Hospital (Grant number: 114-wf-eva-09).

Author Contributions

Conceptualization: YJK, YPC. Methodology: BTTN, TTN. Formal analysis and investigation: BTTN. Resources: BTTN. Visualization: BTTN, YPC. Writing–original draft preparation: BTTNg. Writing–review and editing: TTN, YJK, YPC. Supervision: YJK, YPC. Funding acquisition: YPC. All authors reviewed the manuscript.

Supplementary Materials

Supplementary materials can be available from https://doi.org/10.31616/asj.2024.0467.
Supplement 1. Methodological quality assessment of included studies using the Newcastle-Ottawa Scale for Non-Randomized Controlled Trials.
Supplement 2. Forest plot of vertebral refracture prevalences after sensitivity analysis.
Supplement 3. Forest plot of Visual Analog Scale score 1 month after vertebral augmentation between the two groups after sensitivity analysis.
Supplement 4. Forest plot of Oswestry Disability Index 1 month after surgery between the two groups after sensitivity analysis.
Supplement 5. Forest plot of Oswestry Disability Index 1 month after surgery between the two groups after sensitivity analysis.
Supplement 6. Funnel plot of included studies.
asj-2024-0467-Supplement.pdf

Fig. 1
Preferred Reporting Items for Systematic Reviews and Meta-analysis flowchart. WOS, Web of Science.
asj-2024-0467f1.jpg
Fig. 2
Forest plot of vertebral refracture after augmentation procedures comparing patients with and without sarcopenia. M-H, Mantel-Haenszel; CI, confidence interval; df, degree of freedom.
asj-2024-0467f2.jpg
Fig. 3
Forest plot of the association between the presence of sarcopenia and residual back pain after vertebral augmentation. SE, standard error; IV, inverse variance; CI, confidence interval; df, degree of freedom.
asj-2024-0467f3.jpg
Fig. 4
Forest plots of Visual Analog Scale (VAS) scores 1 month (A) and 1 year (B) postoperatively between sarcopenic and non-sarcopenic patients. SD, standard deviation; IV, inverse variance; CI, confidence interval; df, degree of freedom.
asj-2024-0467f4.jpg
Fig. 5
Forest plots of ODI scores 1 month (A) and 1 year (B) postoperatively between sarcopenic and non-sarcopenic patients. ODI, Oswestry Disability Index; SD, standard deviation; IV, inverse variance; CI, confidence interval; df, degree of freedom.
asj-2024-0467f5.jpg
Fig. 6
Forest plot comparing the length of hospital stay after vertebral augmentation between sarcopenic and non-sarcopenic patients. SD, standard deviation; IV, inverse variance; CI, confidence interval; df, degree of freedom.
asj-2024-0467f6.jpg
Fig. 7
Forest plots of 1-year (A) and long-term (B) mortality rates following vertebral augmentation between sarcopenic and non-sarcopenic patients. M-H, Mantel-Haenszel; CI, confidence interval; df, degree of freedom.
asj-2024-0467f7.jpg
Table 1
Included study characteristics
Study (year) Country Study design Vertebral augmentation No. of participants (n=2,197) Mean age (yr) (73.06±6.25) Gender Follow-up time Sarcopenia diagnosis criteria
S (n=813) Non-S (n=1,384) Male (n=597) Female (n=1,600)
Bayram et al. [20] (2020) Turkiye R cohort Vertebroplasty, kyphoplasty 51 52 72.13±8.82 39 64 48.28±38.67 PLVI at the lumbar 4 level: (1) high (≥0.603); (2) low (<0.603)
Bo et al. [24] (2022) China R cohort Vertebroplasty 40 116 69.73±6.03 54 102 1 yr SMI at the thoracic 12 level: <42.6 cm2/m2 (male) or <30.6 cm2/m2 (female)
Chen et al. [13] (2022) China R cohort Kyphoplasty 69 145 77.98±3.92 60 154 ≥3 mo AWGS: (1) handgrip strength: <26 kg (male) or <18 kg (female); (2) 6-m gait speed: <0.8 m/sec; (3) AMI: <7.0 kg/m2 (male) or <5.4 kg/m2 (female)
Wang et al. [11] (2021) China R cohort Kyphoplasty 34 43 76.97±6.45 36 41 1 yr (1) Handgrip strength: <27 kg (male) or <16 kg (female); (2) SMI: <42.6 cm2/m2 (male) or <30.6 cm2/m2 (female)
Jing et al. [14] (2024) China R cohort Kyphoplasty 177 199 70.30±8.33 71 305 1 mo EWGSOP: (1) handgrip strength: <27 kg (male) or <16 kg (female); (2) SMI at the thoracic 12 level: <42.6 cm2/m2 (male) or <30.6 cm2/m2 (female)
Kara et al. [10] (2023) Turkiye R cohort Vertebroplasty 50 54 76.64±7.70 30 74 30.57±19.84 PMI at the lumbar 3 level: <540 mm2/mm2 (male) or <360 mm2/mm2
Lidar et al. [21] (2022) Israel R case-control Vertebroplasty, kyphoplasty 41 48 80.20±7.10 31 58 1–79 mo Psoas nCSA <quartile 2
Ohyama et al. [9] (2021) Japan P cohort Kyphoplasty 39 21 77.80±5.80 13 47 6 mo AWGS: (1) SMI: <7.0 kg/m2 (male) or 5.7 kg/m2 (female); (2) handgrip strength: <26 kg (male) or <18 kg (female); (3) 6-m gait speed: <0.8 m/sec
Peng et al. [22] (2023) China R cohort Kyphoplasty 45 56 69.05±6.66 46 55 ≥1 yr SMI: <36 cm2/m2 (male) or <29 cm2/m2 (female)
Sun et al. [25] (2024) China R cohort Vertebroplasty 72 72 73.48±9.24 42 102 1 yr PLVI: (1) high: >0.79; (2) low: ≤0.79
Tu et al. [23] (2024) China R cohort Kyphoplasty 61 206 71.27±3.75 46 221 3 mo TPA: <385 mm2/m2 (female) or <545 mm2/m2 (male)
Wang et al. [15] (2019) China R cohort Kyphoplasty 48 189 70.61±8.87 36 201 1 yr (1) SMI at the lumbar 3 level: ≤36.0 cm2/m2 (male) or ≤29.0 cm2/m2 (female); (2) handgrip strength: <26 kg (male) or <18 kg (female); (3) 6-m gait speed: <0.8 m/sec
Wu et al. [16] (2024) China R cohort Kyphoplasty 43 125 74.33±8.25 43 125 15.82±3.19 AMI: <7.0 kg/m2 (male) or <5.4 kg/m2 (female)
Yin et al. [12] (2024) China R cohort Kyphoplasty 43 58 75.64±6.65 50 51 3 yr (1) Handgrip strength: <27 kg (male) or <16 kg (female); (2) SMI: <42.6 cm2/m2 (male) or <30.6 cm2/m2 (female)

S, sarcopenia; R cohort, retrospective cohort; PLVI, psoas-lumbar vertebral index; SMI, skeletal muscle mass index; AWGS, Asian Working Group for Sarcopenia; AMI, appendicular muscle mass index; EWGSOP, the European Sarcopenia Working Group in Older People; PMI, psoas muscle index; nCSA, normalized cross-sectional area; P cohort, prospective cohort; TPA, total psoas area.

Table 2
Bone and muscle measurement meta-analyses comparing sarcopenic and non-sarcopenic patients undergoing vertebral augmentation
Variable No. of studies No. of participants Model Combined effect (mean difference) 95% confidence interval p-value Heterogeneity I2 (%) p-value
Bone mineral density 6 [9,13,15,16,22,25] 924 Random −0.42 −0.67 to −0.17 <0.001 91 <0.001
Handgrip strength 5 [9,1113,15] 689 Random −5.66 −9.42 to −1.89 0.003 95 <0.001
Gait speed 1 [9] 60 Fixed −0.1 −0.24 to 0.04 0.17 NA NA
Muscle mass measurements 1,062
 SMI (cm2/m2) 4 [11,12,15,22] 516 Random −12.86 −15.49 to −10.23 <0.001 90 <0.001
 AMI (kg/m2) 3 [9,13,16] 442 Random −1.70 −1.97 to −1.44 <0.001 70 0.04
 PMI (mm2/m2) 1 [10] 104 Fixed −211.99 −247.19 to −176.79 <0.001 NA NA

NA, not applicable; SMI, skeletal muscle index; AMI, appendicular muscle index; PMI, psoas muscle index.

Table 3
Summary of the subgroup analysis for vertebral refracture (primary outcome)
Subgroup No. of studies No. of participants Model Pooled odds ratio (95% CI) p-value Heterogeneity I2 (%) p-value
Country Random
 China 8 [1116,22,25] 1,418 4.33 (1.84–10.22) <0.001 82 <0.001
 Out of China 3 [9,10,21] 253 1.10 (0.38–3.20) 0.86 73 0.02
Mean age (yr) Random
 <70 1 [22] 101 6.49 (0.30–138.78) 0.23 NA NA
 70–80 9 [916,25] 1,481 2.79 (1.14–6.81) 0.02 88 <0.001
 >80 1 [21] 89 3.07 (1.18–7.97) 0.02 NA NA
Mean follow-up time Random
 Under 1 year 3 [9,13,14] 650 6.46 (0.74–56.24) 0.09 94 <0.001
 1 year and above 8 [1012,15,16,21,22,25] 1,021 1.98 (1.22–3.21) 0.006 43 0.09
Sarcopenia definition Random
 1 factor 5 [10,16,21,22,25] 606 1.74 (1.10–2.74) 0.02 64 0.02
 More than 1 factor 6 [9,1115] 1,065 4.63 (3.31–6.46) <0.001 89 <0.001
Vertebral augmentation procedures Random
 Kyphoplasty 8 [9,1116,22] 1,334 3.67 (1.46–9.22) 0.006 85 <0.001
 Vertebroplasty 2 [10,25] 248 1.14 (0.22–5.85) 0.88 76 0.04

CI, confidence interval; NA, not available.

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