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ORIGINAL RESEARCH article

Front. Med., 05 September 2025

Sec. Geriatric Medicine

Volume 12 - 2025 | https://doi.org/10.3389/fmed.2025.1644170

Correlation between metabolic syndrome indicators and locomotive syndrome in Chinese geriatric oncology inpatients

Ling Song&#x;Ling Song1Yu-Tong Jing&#x;Yu-Tong Jing2Ling LiLing Li1Yu-Ling YangYu-Ling Yang1Yun ChenYun Chen1Xiu-Feng WuXiu-Feng Wu3Ying ChenYing Chen1Hui YuHui Yu1Rui-Rong Wu
Rui-Rong Wu1*
  • 1Department of Oncology, Affiliated Hospital of Jiangnan University, Wuxi, Jiangsu Province, China
  • 2Wuxi Medical College of Jiangnan University, Lihu Avenue, Wuxi, Jiangsu Province, China
  • 3Department of Pharmacy, Affiliated Hospital of Jiangnan University, Wuxi, Jiangsu Province, China

Objective: To investigate the correlation between metabolic syndrome (MS) indicators and locomotive syndrome (LS) in geriatric oncology inpatients.

Methods: This study enrolled 430 geriatric oncology inpatients at risk of LS, admitted to the Department of Oncology at Affiliated Hospital of Jiangnan University from January 2024 and December 2024. Waist circumference, diastolic blood pressure, systolic blood pressure, total cholesterol (TC), triacylglycerols (TG), fasting glucose, high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C) were measured as MS indicators. The Geriatric Locomotive Function Scale (GLFS-25) was used to assess LS. Subjects were classified into two groups: those with LS (322 cases) and those without (87 cases), to analyze the correlation between MS indicators and LS.

Results: 409 geriatric oncology inpatients completed the study. One-way linear regression analysis revealed that waist circumference, systolic blood pressure, diastolic blood pressure, TG, and LDL-C were positively correlated with GLFS-25 (p < 0.05), while HDL-C was negatively correlated in geriatric oncology inpatients (p < 0.05). Logistic regression analysis identified waist, systolic blood pressure, TG, and LDL-C as risk factors for developing LS in geriatric oncology inpatients (p < 0.05).

Conclusion: Certain risk factors for MS are associated with increased GLFS-25 scores and the development of LS in geriatric oncology inpatients. Screening for LS is beneficial for the early diagnosis of MS and using LS as a focal point for intervention offers new insights into the comprehensive rehabilitation of geriatric oncology patients.

1 Background

Metabolic Syndrome (MS) is a complex clinical syndrome characterized by multiple concurrent pathologies, including abdominal obesity, elevated blood pressure, dyslipidemia, and hyperuricemia (1). These pathologic states constitute the core of MS, which stems from the pathophysiology of diverse metabolic disturbances. These disturbances are significant risk factors for promoting atherosclerosis, potentially leading to the progression of cardiovascular and cerebrovascular diseases, thus posing a serious threat to patients’ quality of life and life expectancy (2). Currently, MS represents a significant public health challenge in China, contributing to substantial medical and economic burdens and increasing socio-economic pressures by impacting workforce health and social productivity (3). Despite the lack of universally recognized treatment methods for MS, increasing research suggests that interventions aimed at improving musculoskeletal function (MF) in MS patients are both cost-effective and beneficial, and thus merit broader implementation (4).

In 2020, there were 19.29 million new cases of tumors globally and 4.57 million in China, predominantly among individuals aged 60–79 (5, 6). This demographic is expected to grow substantially in the coming decades due to changes in social life patterns and advances in medical technology (7, 8). Recent evidence indicates that hormonal changes associated with MS may increase cancer susceptibility through mechanisms, such as inflammatory responses, oxidative stress, growth hormone dysregulation, and vascular endothelial growth factor production (9, 10). Concurrently, as the survival of cancer patients increases, the prevalence of tumors coexisting with other chronic diseases is rising. MS significantly influences the relationship between cancer treatment and the morbidity and mortality associated with tumor-related chronic diseases, while also elevating the risk of other chronic conditions (11).

The current aim of geriatric oncology treatment is not only to improve prognosis but also to enhance the quality of life (QoL) (12). A crucial element in enhancing QoL involves maintaining and improving patients’ MF to support basic activities of daily living (ADL), thereby maximizing their ability to live independently and reducing the caregiving burden on family and society (13).

Locomotive Syndrome (LS), originally proposed by the Japanese Orthopaedic Association (JOA), is a high-risk condition characterized by difficulties in standing, walking, and other movements due to the weakening or impairment of the locomotor organs (bones, joints, muscles, and nerves, etc.). This condition leads to limited MF, increased care needs, and the potential for becoming bedridden (13, 14). Research indicates that LS is strongly associated with adverse outcomes such as decreased ADLs, fractures, and increased mortality (13, 15). Timely identification and intervention are crucial for successful rehabilitation (16, 17). LS focuses more on assessing an individual’s overall MF than on specific symptoms such as sarcopenia and debilitation (18, 19). The deterioration of muscles, bones, and other motor organs often progresses slowly and is difficult to detect (20). LS acts as a sensitive monitor of motor dysfunction and can provide early warnings of MF decline in patients who have not yet shown significant pathological changes (17). Studies have demonstrated that LS-1 and LS-2 states are reversible, and effective physical interventions at these stages can maintain or even improve an individual’s MF and ADL before irreversible physical impairment occurs (20).

LS and MS are both associated with aging (2, 14). Understanding the relationship between LS and MS in geriatric oncology patients facilitates the use of targeted interventions based on LS, leading to timely warnings and interventions that can prevent the regression of rehabilitation outcomes in these patients toward severity. Therefore, this study analyzed the occurrence of MS and LS in hospitalized elderly patients to provide new insights for the rehabilitation of elderly tumor patients.

2 Materials and methods

This investigation utilized a single-center, cross-sectional study design. Participants voluntarily joined the study and provided written informed consent. The Ethics Committee of the Affiliated Hospital of Jiangnan University approved the study (no. LS2023101), registered in the Chinese Clinical Trial Registry (no. ChiCTR2400079958) on 17/01/2024. The study adhered to the principles outlined in the Declaration of Helsinki.

2.1 Subjects

430 geriatric oncology inpatients at risk of LS were recruited from the Department of Oncology at the Affiliated Hospital of Jiangnan University between January 2024 and December 2024.

2.1.1 Inclusion criteria

① Patients must have had a definitive cancer diagnosis; ② Age > 60 years old; ③ Stable vital signs; ④ Cognitive clarity and coherent responsiveness; ⑤ Capability for autonomous self-care; ⑥ Absence of any MF disorder attributable to primary orthopedic diseases; ⑦ Provided informed consent and voluntarily participated in the study.

2.1.2 Exclusion criteria

① Patients with cognitive impairment or unconsciousness; ② Diagnosis of any incapacitating ailment contraindicating physical activity.

2.2 Measurements

A cross-sectional questionnaire, developed after a review of relevant literature on LS from databases such as Web of Science, Embase et al. and designed with input from clinical experts, was employed. This case report form included five parts:

2.2.1 General information

This section gathered data on the subjects’ gender, age, height, weight, self-care ability, marital status, initial tumor type, disease duration, metastatic recurrence, radiotherapy, and comorbidities (including hypertension, diabetes mellitus, dyslipidemia, stroke and chronic respiratory diseases).

2.2.2 LS

The presence of LS was assessed using the GLFS-25, a specialized screening scale recommended by the JOA (21). Validated by Chinese scholars, the GLFS-25 is deemed suitable for Chinese elderly tumor patients (22, 23). It consists of 25 items across four dimensions: physical pain, ADL, social activities, and mental health status. It employs a Likert 5-point scale, ranging from 0 (“no difficulty”) to 4 (“very difficult”), with a total score between 0 and 100. A score of ≥16 indicates LS; higher scores reflect worse MF and more severe LS. The GLFS-25 has demonstrated good reliability and validity: Cronbach’s α is 0.961, and retest correlation coefficients range from 0.712 to 0.924 (21). Subjects were categorized into an LS group (322 cases) and a non-LS group (87 cases) based on the presence of LS.

2.2.3 MS

Diagnosis of MS was based on the criteria set forth in the Chinese Guidelines for the Prevention and Control of Type 2 Diabetes Mellitus (2022 edition) (24): (1) Body mass index (BMI) ≥ 25 kg/m2; (2) Fasting plasma glucose (FPG) ≥ 6.1 mmol/L or diagnosed and treated diabetes; (3) Hypertension with systolic/diastolic blood pressure ≥140/90 mmHg or diagnosed and treated hypertension; (4) Dyslipidemia with fasting blood triglycerides ≥1.7 mmol/L and/or fasting blood HDL-C < 0.9 mmol/L for men and <1.0 mmol/L for women. MS is diagnosed when three or all four criteria are met. This study collected data on waist circumference, diastolic blood pressure, systolic blood pressure, total cholesterol (TC), triacylglycerols (TG), fasting glucose, high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C) from the study population.

2.3 Statistical methods

SPSS 25.0 was applied for statistical analysis, the measurement data were expressed as mean ± standard deviation (Mean ± SD), the count data were expressed as frequency or frequency, t test was used to compare the means between the two groups, and χ2 test or consecutively corrected χ2 test was used to compare the rates. Linear regression analysis was conducted with GLFS-25 scores as the dependent variable and MS-related indices as independent variables. Logistic regression analysis was conducted with MS-related indices as independent variables, and LS as the dependent variable (Yes = 1, No = 0), using the backward method (Entry = 0.05, Removal = 0.10). The difference was considered statistically significant at p < 0.05.

3 Results

3.1 Prevalence of LS and MS

A total of 409 geriatric oncology inpatients completed the survey, achieving a questionnaire recovery rate of 95.1% (Figure 1). 13 participants withdrew due to privacy concerns, 6 failed to complete the GLFS-25 questionnaire, and 2 declined to disclose MS-related information. The diagnostic distribution was as follows: gastrointestinal neoplasm comprised 34.5% (141 cases); lung neoplasm 16.4% (67 cases); head and neck neoplasm 12.5% (51 cases); breast neoplasm 15.6% (64 cases); liver neoplasm 7.3% (30 cases); neoplasms of the reproductive system 7.6% (31 cases); and hematological malignancies 6.1% (25 cases) (Figure 2). 65.2% (267 cases) of the participants did not present any co-morbid chronic conditions, while 26.7% (109 cases) had one to two additional chronic conditions, and 8.1% (33 cases) reported three or more. The prevalence of LS was 78.7% (322/409), and the prevalence of MS was 42.8% (175/409). The prevalence of MS was higher in the LS group at 45.3% (146/322) compared to 33.3% (29/87) in the non-LS group, with this difference being statistically significant (p < 0.05).

Figure 1
Flowchart showing participant enrollment in a study on geriatric oncology inpatients. Initially, 430 were enrolled. Thirteen were excluded due to reluctance to complete the questionnaire, leaving 417. Six more were removed for lacking Geriatric Locomotive Function Scale data, leaving 411. Finally, two participants lacked Metabolic Syndrome data, resulting in 409 participants remaining.

Figure 1. Flow chart of study participants.

Figure 2
Bar chart showing the number of different neoplasms. Gastrointestinal neoplasms lead with 141, followed by lung (67), breast (64), head and neck (51), reproductive system (31), liver (30), and hematological malignancies (25).

Figure 2. The origin cancer of 409 geriatric cancer inpatients.

3.2 Clinical information

Patients in the LS group exhibited higher measures of gender, body mass, waist circumference, systolic and diastolic blood pressure, TG, and LDL-C compared to those in the non-LS group; these differences were statistically significant (p < 0.05). Differences in other clinical indicators were not statistically significant (p > 0.05). Details are provided in Table 1.

Table 1
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Table 1. Comparison of general information and metabolic syndrome indicators in patients with different locomotive syndrome statuses.

3.3 Linear regression analysis of MS indicators and GLFS-25 score

Linear regression analysis was conducted with GLFS-25 scores as the dependent variable and MS-related indices as independent variables. Results indicated that waist circumference, systolic and diastolic blood pressure, TG, and LDL-C were positively correlated with GLFS-25 scores (p < 0.05), while HDL-C was negatively correlated (p < 0.05). Details are provided in Table 2.

Table 2
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Table 2. Linear regression analysis of metabolic syndrome indicators and GLFS-25 scores.

3.4 Logistic regression analysis of MS indicators and LS

Logistic regression analysis was conducted with age, gender, waist circumference, systolic blood pressure, diastolic blood pressure, fasting blood glucose, TC, TG, HDL-C, and LDL-C as independent variables, and LS as the dependent variable (Yes = 1, No = 0), using the backward method (Entry = 0.05, Removal = 0.10). The assignment of values to the independent variables is detailed in Table 3. The multifactorial analysis identified waist circumference, systolic blood pressure, TG, and LDL-C as independent risk factors for the development of LS (p < 0.05). Further details are provided in Table 4.

Table 3
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Table 3. Independent variable assignment.

Table 4
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Table 4. Logistic regression analysis of metabolic syndrome indicators and locomotive syndrome.

4 Discussion

In the current Chinese context, medical resources are primarily allocated to emergency oncology treatments, often at the expense of oncology rehabilitation, which remains underfunded. There is a pressing need for a highly sensitive, straightforward, and practical MF test indicator to quickly ascertain the health status of elderly tumor patients (25). Most existing MF assessment methods involve numerous specialized instruments and personnel, making the process complex and time-consuming. Many patients are hesitant to dedicate significant time and resources to MF testing, which may lead to unrecognized worsening of MF and missed opportunities for timely recovery, adversely affecting their prognosis (26). LS presents a viable solution by serving as an efficient and accessible indicator for detecting MF impairments. By providing early warnings of irreversible MF damage, LS can prevent severe MF injuries and their associated sequelae, thereby saving considerable time, money, and caregiving resources. Thus, LS was employed as a measure of MF in this study.

The results of the study indicated that the prevalence of MS among geriatric oncology inpatients was significantly higher in the LS group at 45.3% (146/322) compared to 33.3% (29/87) in the non-LS group. Furthermore, MS-related indicators (waist circumference, systolic blood pressure, diastolic blood pressure, TG, LDL-C, and HDL-C) were significantly correlated with GLFS-25 scores (p < 0.05). Waist circumference, systolic blood pressure, diastolic blood pressure, TG, and LDL-C were identified as risk factors for GLFS-25, while HDL-C acted as a protective factor. This suggests a positive association between MS and the occurrence of LS.

This may be attributed to the skeletal system and skeletal muscle, which constitute approximately 60% of body weight and are integral to adult musculoskeletal function (MF), influencing LS status (27). They also function as the body’s largest endocrine organ. Skeletal muscle synthesizes and secretes various cytokines, regulatory peptides, adipokines, growth factors, and proteins specific to bone and muscle regulation (28). These paracrine/autocrine factors are involved in the pathogenesis of central obesity, insulin resistance, dyslipidemia, hypertension, and microalbuminuria, forming a crucial pathophysiological foundation for MS (27).

Currently, public awareness and understanding of LS status in elderly tumor patients are inadequate, with limited knowledge on its scientific prevention and treatment. This study demonstrates a significant correlation between various MS indicators and LS, suggesting that addressing LS could illuminate new pathways for the rehabilitation of elderly tumor patients. Enhancing early screening and intervention for LS could also improve public knowledge and scientific understanding of LS.

JAMA suggests that physical activity serves as an effective non-pharmacological therapeutic approach, improving the overall physiological functions of patients with LS by regulating insulin resistance, adipocytokines, and lipid metabolism, thereby facilitating the prevention and treatment of MS. Developing tailored exercise prescriptions for LS also enhances the rehabilitation of geriatric oncology patients (17, 29). It is recommended that geriatric oncology patients select the appropriate type, intensity, and duration of exercise based on age, health status, and personal preference, utilizing heart rate monitoring as a guideline. Special attention should be given to their physical tolerance, adjusting exercise intensity to ensure safety and effectiveness, and to optimize metabolic indices and LS status continually. Exercise parameters such as intensity, duration, and frequency should adhere to the principles of individualization and gradual progression. If feasible, a professional cardiopulmonary exercise test may be performed prior to developing an exercise plan to scientifically tailor the exercise regimen.

5 Conclusion

In conclusion, our findings demonstrate an association between certain risk factors for MS and elevated GLFS-25 scores, suggesting a potential link with LS in geriatric oncology inpatients. While this cross-sectional study identifies these relationships, further longitudinal research is needed to determine whether LS screening could aid in early MS detection. Nevertheless, incorporating LS assessment into clinical evaluation may offer valuable insights for optimizing rehabilitation strategies in this vulnerable population.

6 Limitations

This study was limited to hospitalized elderly patients, representing a small sample size that does not reflect the broader population of geriatric oncology patients. Additionally, this study does not establish a causal relationship between abnormal metabolic indices and LS, necessitating further research with larger sample sizes and prospective designs.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving humans were approved by the Ethics Committee of the Affiliated Hospital of Jiangnan University approved the study (no. LS2023101). The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.

Author contributions

LS: Data curation, Formal analysis, Investigation, Methodology, Writing – original draft, Writing – review & editing. Y-TJ: Data curation, Investigation, Writing – original draft, Writing – review & editing. LL: Data curation, Formal analysis, Investigation, Writing – original draft. Y-LY: Formal analysis, Funding acquisition, Methodology, Resources, Writing – original draft. YuC: Data curation, Formal analysis, Investigation, Methodology, Writing – original draft. X-FW: Data curation, Funding acquisition, Investigation, Methodology, Writing – original draft. YiC: Funding acquisition, Investigation, Methodology, Writing – review & editing. HY: Formal analysis, Investigation, Methodology, Writing – review & editing. R-RW: Funding acquisition, Methodology, Writing – original draft, Writing – review & editing.

Funding

The author(s) declare that financial support was received for the research and/or publication of this article. This research project was funded by the Regional Medical Center Development Program under the partnership between Jiangnan University Affiliated Hospital and Donghai County People’s Hospital (No. DHBFH202501, No. DHBFH202503, No. DHBFG202504 and No. DHBFM202504), Research Project on Hospital Management Innovation in Jiangsu Province (No. JSYGY-3-2024-601), Scientific and Technological Achievements Promotion Project of Wuxi Municipal Health Commission Project Program (No. T202336), Jiangsu Provincial Traditional Chinese Medicine Science and Technology Development Plan Project (No. MS2024063), Wuxi Municipal Health Commission Youth Research Project (Q202201) and Jiangsu Pharmaceutial Association- Aosaikang Hospital Pharmaceutical Fund (No. A202134). The funders had no role in considering the study design or in the collection,analysis, interpretation of data, writing of the report, or decision to submit the article for publication. We also appreciate all participants for their time and efforts.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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References

1. Seravalle, G, and Grassi, G. Sympathetic nervous system, hypertension, obesity and metabolic syndrome. High Blood Press Cardiovasc Prev. (2016) 23:175–9. doi: 10.1007/s40292-016-0137-4

PubMed Abstract | Crossref Full Text | Google Scholar

2. Saklayen, MG. The global epidemic of the metabolic syndrome. Curr Hypertens Rep. (2018) 20:12. doi: 10.1007/s11906-018-0812-z

PubMed Abstract | Crossref Full Text | Google Scholar

3. Lu, J, Wang, L, Li, M, Xu, Y, Jiang, Y, Wang, W, et al. China Noncommunicable Disease Surveillance Group. Metabolic syndrome among adults in China: the 2010 China noncommunicable disease surveillance. J Clin Endocrinol Metab. (2017) 102:507–515. doi: 10.1210/jc.2016-2477

Crossref Full Text | Google Scholar

4. Roberts, CK, Hevener, AL, and Barnard, RJ. Metabolic syndrome and insulin resistance: underlying causes and modification by exercise training. Compr Physiol. (2013) 3:1–58. doi: 10.1002/j.2040-4603.2013.tb00484.x

PubMed Abstract | Crossref Full Text | Google Scholar

5. Taber, JM, Klein, WMP, Suls, JM, and Ferrer, RA. Lay awareness of the relationship between age and cancer risk. Ann Behav Med. (2017) 51:214–25. doi: 10.1007/s12160-016-9845-1

PubMed Abstract | Crossref Full Text | Google Scholar

6. Qiu, H, Cao, S, and Xu, R. Cancer incidence, mortality, and burden in China: a time-trend analysis and comparison with the United States and United Kingdom based on the global epidemiological data released in 2020. Cancer Commun (Lond). (2021) 41:1037–48. doi: 10.1002/cac2.12197

PubMed Abstract | Crossref Full Text | Google Scholar

7. Wildiers, H, Heeren, P, Puts, M, Topinkova, E, Janssen-Heijnen, MLG, Extermann, M, et al. International Society of Geriatric Oncology consensus on geriatric assessment in older patients with cancer. J Clin Oncol. (2014) 32:2595–603. doi: 10.1200/JCO.2013.54.8347

PubMed Abstract | Crossref Full Text | Google Scholar

8. Diaz, FC, Hamparsumian, A, Loh, KP, Verduzco-Aguirre, H, Abdallah, M, Williams, GR, et al. Geriatric oncology: a 5-year strategic plan. Am Soc Clin Oncol Educ Book. (2024) 44:e100044. doi: 10.1200/EDBK_100044

PubMed Abstract | Crossref Full Text | Google Scholar

9. Hirode, G, and Wong, RJ. Trends in the prevalence of metabolic syndrome in the United States, 2011-2016. JAMA. (2020) 323:2526–8. doi: 10.1001/jama.2020.4501

PubMed Abstract | Crossref Full Text | Google Scholar

10. Reddy, P, Lent-Schochet, D, Ramakrishnan, N, McLaughlin, M, and Jialal, I. Metabolic syndrome is an inflammatory disorder: a conspiracy between adipose tissue and phagocytes. Clin Chim Acta. (2019) 496:35–44. doi: 10.1016/j.cca.2019.06.019

PubMed Abstract | Crossref Full Text | Google Scholar

11. Esposito, K, Chiodini, P, Colao, A, Lenzi, A, and Giugliano, D. Metabolic syndrome and risk of cancer: a systematic review and meta-analysis. Diabetes Care. (2012) 35:2402–11. doi: 10.2337/dc12-0336

PubMed Abstract | Crossref Full Text | Google Scholar

12. Firkins, J, Hansen, L, Driessnack, M, and Dieckmann, N. Quality of life in "chronic" cancer survivors: a meta-analysis. J Cancer Surviv. (2020) 14:504–17. doi: 10.1007/s11764-020-00869-9

PubMed Abstract | Crossref Full Text | Google Scholar

13. Hirano, K, Imagama, S, Hasegawa, Y, Ito, Z, Muramoto, A, and Ishiguro, N. The influence of locomotive syndrome on health-related quality of life in a community-living population. Mod Rheumatol. (2013) 23:939–44. doi: 10.1007/s10165-012-0770-2

PubMed Abstract | Crossref Full Text | Google Scholar

14. Akahane, M, Maeyashiki, A, Tanaka, Y, and Imamura, T. The impact of musculoskeletal diseases on the presence of locomotive syndrome. Mod Rheumatol. (2019) 29:151–6. doi: 10.1080/14397595.2018.1452173

PubMed Abstract | Crossref Full Text | Google Scholar

15. Ono, R, Murata, S, Uchida, K, Endo, T, and Otani, K. Reciprocal relationship between locomotive syndrome and social frailty in older adults. Geriatr Gerontol Int. (2021) 21:981–4. doi: 10.1111/ggi.14273

PubMed Abstract | Crossref Full Text | Google Scholar

16. Morita, Y, Ito, H, Kawaguchi, S, Nishitani, K, Nakamura, S, Kuriyama, S, et al. Systemic chronic diseases coexist with and affect locomotive syndrome: the Nagahama study. Mod Rheumatol. (2023) 33:608–16. doi: 10.1093/mr/roac039

PubMed Abstract | Crossref Full Text | Google Scholar

17. Hirahata, M, Imanishi, J, Fujinuma, W, Abe, S, Inui, T, Ogata, N, et al. Cancer may accelerate locomotive syndrome and deteriorate quality of life: a single-Centre cross-sectional study of locomotive syndrome in cancer patients. Int J Clin Oncol. (2023) 28:603–9. doi: 10.1007/s10147-023-02312-2

PubMed Abstract | Crossref Full Text | Google Scholar

18. Tokida, R, Ikegami, S, Takahashi, J, Ido, Y, Sato, A, Sakai, N, et al. Association between musculoskeletal function deterioration and locomotive syndrome in the general elderly population: a Japanese cohort survey randomly sampled from a basic resident registry. BMC Musculoskelet Disord. (2020) 21:431. doi: 10.1186/s12891-020-03469-x

PubMed Abstract | Crossref Full Text | Google Scholar

19. Cruz-Jentoft, AJ, Bahat, G, Bauer, J, Boirie, Y, Bruyère, O, Cederholm, T, et al. Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing. (2019) 48:16–31. doi: 10.1093/ageing/afy169

PubMed Abstract | Crossref Full Text | Google Scholar

20. Yurube, T, Ito, M, Takeoka, T, Watanabe, N, Inaoka, H, Kakutani, K, et al. Possible improvement of the sagittal spinopelvic alignment and balance through "locomotion training" exercises in patients with "locomotive syndrome": a literature review. Adv Orthop. (2019) 2019:1–7. doi: 10.1155/2019/6496901

PubMed Abstract | Crossref Full Text | Google Scholar

21. Seichi, A, Hoshino, Y, Doi, T, Akai, M, Tobimatsu, Y, and Iwaya, T. Development of a screening tool for risk of locomotive syndrome in the elderly: the 25-question geriatric locomotive function scale. J Orthop Sci. (2012) 17:163–72. doi: 10.1007/s00776-011-0193-5

PubMed Abstract | Crossref Full Text | Google Scholar

22. Yang, Y-L, Su, H, Lu, H, Yu, H, Wang, J, Zhou, YQ, et al. Current status and risk determinants of locomotive syndrome in geriatric cancer survivors in China-a single-center cross-sectional survey. Front Public Health. (2024) 12:1421280. doi: 10.3389/fpubh.2024.1421280

PubMed Abstract | Crossref Full Text | Google Scholar

23. Yang, Y-L, Wang, H-H, Su, H, Lu, H, Yu, H, Wang, J, et al. Reliability and validity tests of the Chinese version of the geriatric locomotive function scale (GLFS-25) in tumor survivors. Heliyon. (2014) 10:e29604. doi: 10.1016/j.heliyon.2024.e29604

Crossref Full Text | Google Scholar

24. Chinese Elderly Type 2 Diabetes Prevention and Treatment of Clinical Guidelines Writing Group, Geriatric Endocrinology and Metabolism Branch of Chinese Geriatric Society, Geriatric Endocrinology and Metabolism Branch of Chinese Geriatric Health Care Society, Geriatric Professional Committee of Beijing Medical Award Foundation, National Clinical Medical Research Center for Geriatric Diseases (PLA General Hospital). Clinical guidelines for prevention and treatment of type 2 diabetes mellitus in the elderly in China (2022 edition). Zhonghua Nei Ke Za Zhi. (2022) 61:12–50. doi: 10.3760/cma.j.cn112138-20211027-00751

PubMed Abstract | Crossref Full Text | Google Scholar

25. Fusco, D, Ferrini, A, Pasqualetti, G, Giannotti, C, Cesari, M, Laudisio, A, et al. Comprehensive geriatric assessment in older adults with cancer: recommendations by the Italian Society of Geriatrics and Gerontology (SIGG). Eur J Clin Investig. (2021) 51:e13347. doi: 10.1111/eci.13347

PubMed Abstract | Crossref Full Text | Google Scholar

26. Outlaw, D, Abdallah, M, Gil-Jr, LA, Giri, S, Hsu, T, Krok-Schoen, JL, et al. The evolution of geriatric oncology and geriatric assessment over the past decade. Semin Radiat Oncol. (2022) 32:98–108. doi: 10.1016/j.semradonc.2021.11.002

PubMed Abstract | Crossref Full Text | Google Scholar

27. Frontera, WR, and Ochala, J. Skeletal muscle: a brief review of structure and function. Calcif Tissue Int. (2015) 96:183–95. doi: 10.1007/s00223-014-9915-y

PubMed Abstract | Crossref Full Text | Google Scholar

28. Nishikawa, H, Asai, A, Fukunishi, S, Nishiguchi, S, and Higuchi, K. Metabolic syndrome and sarcopenia. Nutrients. (2021) 13:3519. doi: 10.3390/nu13103519

PubMed Abstract | Crossref Full Text | Google Scholar

29. Expert Panel on Detection E, and Treatment of High Blood Cholesterol in Adults. Executive summary of the third report of the national cholesterol education program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (adult treatment panel III). JAMA. (2001) 285:2486–97. doi: 10.1001/jama.285.19.2486

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: locomotive syndrome, metabolic syndrome, aging, geriatric oncology inpatients, correlation

Citation: Song L, Jing Y-T, Li L, Yang Y-L, Chen Y, Wu X-F, Chen Y, Yu H and Wu R-R (2025) Correlation between metabolic syndrome indicators and locomotive syndrome in Chinese geriatric oncology inpatients. Front. Med. 12:1644170. doi: 10.3389/fmed.2025.1644170

Received: 10 June 2025; Accepted: 25 August 2025;
Published: 05 September 2025.

Edited by:

Sachchida Nand Rai, Banaras Hindu University (BHU), India

Reviewed by:

Vivek K. Chaturvedi, Banaras Hindu University, India
Reda Elbadawy, Benha University, Egypt
Payal Singh, Banaras Hindu University, India

Copyright © 2025 Song, Jing, Li, Yang, Chen, Wu, Chen, Yu and Wu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Rui-Rong Wu, MTgyMDUwMzkyMzFAMTYzLmNvbQ==

These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.