» Articles » PMID: 35297568

Serum Creatinine and Cystatin C-based Diagnostic Indices for Sarcopenia in Advanced Non-small Cell Lung Cancer

Overview
Date 2022 Mar 17
PMID 35297568
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Sarcopenia is an important prognostic factor of lung cancer. The serum creatinine/cystatin C ratio (CCR) and the sarcopenia index (SI, serum creatinine × cystatin C-based glomerular filtration rate) are novel screening tools for sarcopenia; however, the diagnostic accuracy of the CCR and SI for detecting sarcopenia remains unknown. We aimed to explore and validate the diagnostic values of the CCR and SI for determining sarcopenia in non-small cell lung cancer (NSCLC) and to explore their prognostic values for overall survival.

Methods: We conducted a prospective cohort study of adult patients with stage IIIB or IV NSCLC. Levels of serum creatinine and cystatin C were measured to calculate the CCR and SI. Sarcopenia was defined separately using CCR, SI, and the Asian Working Group for Sarcopenia (AWGS) 2019 criteria. Participants were randomly sampled into derivation and validation sets (6:4 ratio). The cutoff values for diagnosing sarcopenia were determined based on the derivation set. Diagnostic accuracy was analysed in the validation set through receiver operating characteristic (ROC) curves. Cox regression models and survival curves were applied to evaluate the impact of different sarcopenia definitions on survival.

Results: We included 579 participants (women, 35.4%; mean age, 58.4 ± 8.9 years); AWGS-defined sarcopenia was found in 19.5% of men and 10.7% of women. Both CCR and SI positively correlated with computed tomography-derived and bioimpedance-derived muscle mass and handgrip strength. The optimal cutoff values for CCR and SI were 0.623 and 54.335 in men and 0.600 and 51.742 in women, with areas under the ROC curves of 0.837 [95% confidence interval (CI): 0.770-0.904] and 0.833 (95% CI: 0.765-0.901) in men (P = 0.25), and 0.808 (95% CI: 0.682-0.935) and 0.796 (95% CI: 0.668-0.924) in women (P = 0.11), respectively. The CCR achieved sensitivities and specificities of 73.0% and 93.7% in men and 85.7% and 65.7% in women, respectively; the SI achieved sensitivities and specificities of 75.7% and 86.5% in men and 92.9% and 62.9% in women, respectively. CCR-defined, SI-defined, and AWGS-defined sarcopenia were independently associated with a high mortality risk [hazard ratio (HR) = 1.75, 95% CI: 1.25-2.44; HR = 1.55, 95% CI: 1.11-2.17; and HR = 1.76, 95% CI: 1.22-2.53, respectively].

Conclusions: CCR and SI have satisfactory and comparable diagnostic accuracy and prognostic values for sarcopenia in patients with advanced NSCLC. Both may serve as surrogate biomarkers for evaluating sarcopenia in these patients. However, further external validations are required.

Citing Articles

Lower creatinine levels are associated with an increased risk of depression: evidence from the China Health and Retirement Longitudinal Study.

Liu F, Zhong X, Wang C Front Psychiatry. 2025; 16:1446897.

PMID: 40071279 PMC: 11894454. DOI: 10.3389/fpsyt.2025.1446897.


The systemic oxidative stress index predicts clinical outcomes of esophageal squamous cell carcinoma receiving neoadjuvant immunochemotherapy.

Feng J, Wang L, Yang X, Chen Q Front Immunol. 2025; 16:1535507.

PMID: 39958338 PMC: 11825508. DOI: 10.3389/fimmu.2025.1535507.


Identification of risk factors and development of a predictive nomogram for sarcopenia in Alzheimer's disease.

Chen S, Ou R, Wei Q, Fu J, Zhao B, Chen X Alzheimers Dement. 2025; 21(2):e14503.

PMID: 39778036 PMC: 11848345. DOI: 10.1002/alz.14503.


Serum creatinine- and cystatin C-based indices are associated with the risk of subsequent sarcopenia: evidence from the China Health and Retirement Longitudinal Study.

Ning X, Xie C, Kong Y Front Nutr. 2024; 11:1471068.

PMID: 39634549 PMC: 11614666. DOI: 10.3389/fnut.2024.1471068.


Lower creatinine-to-cystatin c ratio associated with increased risk of incident amyotrophic lateral sclerosis in the prospective UK biobank cohort.

Wang Z, Cao W, Deng B, Fan D Sci Rep. 2024; 14(1):28289.

PMID: 39550435 PMC: 11569255. DOI: 10.1038/s41598-024-79910-1.


References
1.
Chen L, Woo J, Assantachai P, Auyeung T, Chou M, Iijima K . Asian Working Group for Sarcopenia: 2019 Consensus Update on Sarcopenia Diagnosis and Treatment. J Am Med Dir Assoc. 2020; 21(3):300-307.e2. DOI: 10.1016/j.jamda.2019.12.012. View

2.
Udy A, Scheinkestel C, Pilcher D, Bailey M . The Association Between Low Admission Peak Plasma Creatinine Concentration and In-Hospital Mortality in Patients Admitted to Intensive Care in Australia and New Zealand. Crit Care Med. 2015; 44(1):73-82. DOI: 10.1097/CCM.0000000000001348. View

3.
Fielding R, Vellas B, Evans W, Bhasin S, Morley J, Newman A . Sarcopenia: an undiagnosed condition in older adults. Current consensus definition: prevalence, etiology, and consequences. International working group on sarcopenia. J Am Med Dir Assoc. 2011; 12(4):249-56. PMC: 3377163. DOI: 10.1016/j.jamda.2011.01.003. View

4.
Studenski S, Peters K, Alley D, Cawthon P, McLean R, Harris T . The FNIH sarcopenia project: rationale, study description, conference recommendations, and final estimates. J Gerontol A Biol Sci Med Sci. 2014; 69(5):547-58. PMC: 3991146. DOI: 10.1093/gerona/glu010. View

5.
Tang T, Zhuo Y, Xie L, Wang H, Yang M . Sarcopenia index based on serum creatinine and cystatin C is associated with 3-year mortality in hospitalized older patients. Sci Rep. 2020; 10(1):1260. PMC: 6985114. DOI: 10.1038/s41598-020-58304-z. View