Predictive value of circulating fibroblast growth factor-23 and Klotho on protein-energy wasting in patients undergoing hemodialysis

被引:0
|
作者
Zhou, Xiaoling [1 ]
Luo, Yang [1 ]
Guo, Yidan [1 ]
Jia, Meng [1 ]
Zhang, Chunxia [1 ]
Shi, Zhihua [1 ]
Du, Ye [2 ,3 ]
机构
[1] Capital Med Univ, Beijing Shijitan Hosp, Dept Nephrol, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Chest Hosp, Dept Med Oncol, Beijing, Peoples R China
[3] Beijing TB & Tumor Res Inst, Beijing, Peoples R China
来源
FRONTIERS IN NUTRITION | 2025年 / 11卷
关键词
hemodialysis; protein-energy wasting; fibroblast growth factor-23; Klotho; malnutrition; CHRONIC KIDNEY-DISEASE; INTERNATIONAL SOCIETY; RENAL NUTRITION; BONE; INFLAMMATION; MASS;
D O I
10.3389/fnut.2024.1497869
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: As a state of metabolic and nutritional derangements, protein-energy wasting (PEW) is highly prevalent and associated with increased morbidity and mortality in hemodialysis patients. Fibroblast growth factor-23 (FGF-23) and Klotho have been proven to contribute to chronic kidney disease-mineral and bone disorder (CKD-MBD) in patients undergoing hemodialysis. Previous evidence suggested that FGF-23 and Klotho may also contribute to the malnutritional status among these patients; however, the inter-relationship between the FGF-23-Klotho axis and PEW remains unclear. Therefore, we conducted this cross-sectional study to evaluate the association between plasma FGF-23 and Klotho levels and PEW in hemodialysis patients and to explore whether these markers could predict the presence of PEW. Methods: Plasma concentrations of FGF-23 and Klotho were measured, and their associations with PEW were assessed. PEW was evaluated based on body weight, muscle mass, biochemical data, and protein and energy intake, according to the 2008 criteria from the International Society of Renal Nutrition and Metabolism (ISRNM). Results: In this study, 147 hemodialysis patients (mean age 61.05 +/- 13.32 years) were enrolled, of whom 66 (44.90%) had PEW. PEW was significant positively correlated with FGF-23 (r = 0.403, p < 0.001), age (r = 0.225, p = 0.006), C-reactive protein (r = 0.236, p = 0.004), intact parathyroid hormone (r = 0.237, p = 0.004), and single-pool Kt/V (r = 0.170, p = 0.040), while it was negatively correlated with Klotho (r = -0.361, p < 0.001), hemoglobin (r = -0.215, p = 0.009), and serum creatinine (r = -0.278, p = 0.001). Logistic regression analyses showed that plasma FGF-23 and Klotho were independently associated with PEW, even after adjusting for covariables. The area under the ROC curve (AUC) of FGF-23 and Klotho in predicting PEW was 0.734 and 0.710 (p < 0.001), respectively. When the combination of FGF-23 and Klotho was used to predict PEW, its sensitivity was 81.8%, specificity was 60.5%, and the AUC was 0.746. Conclusion: Plasma levels of FGF-23 and Klotho are associated with PEW in hemodialysis patients. Higher plasma FGF-23 levels and lower Klotho levels may serve as valuable predictors of PEW in these patients.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] Protein-energy wasting in maintenance hemodialysis patients - etiology and diagnosis
    Radjen, Slavica
    Ristic-Medic, Danijela
    Terzic, Brankica
    Djurovic, Branka
    Mijuskovic, Mirjana
    VOJNOSANITETSKI PREGLED, 2018, 75 (04) : 404 - 409
  • [32] Gelsolin and Adipokines Are Associated With Protein-Energy Wasting in Hemodialysis Patients
    Chiu, Terry Ting-Yu
    Liao, Shang-Chih
    Lee, Wen-Chin
    Lee, Po-Shun
    Ng, Hwee-Yeong
    Chien, Yu-Su
    Lee, Chien-Te
    ARTIFICIAL ORGANS, 2015, 39 (02) : 150 - 155
  • [33] High circulating level of fibroblast growth factor-23 promotes renal excretion of phosphate in hemodialysis patients with residual renal function
    Wang Mengjing
    You Li
    Li Haiming
    Lin Yong
    Zhang Zhijie
    Hao Chuanming
    Chen Jing
    XVI INTERNATIONAL CONGRESS ON NUTRITION AND METABOLISM IN RENAL DISEASE (ICRNM), 2012, : 67 - 70
  • [34] Fibroblast growth factor-23 and Alpha-Klotho concentrations in dogs with canine Leishmaniasis
    Gultekin, Gamze
    Ulutas, Pinar Alkim
    RESEARCH IN VETERINARY SCIENCE, 2024, 171
  • [35] Clinical Potential of Targeting Fibroblast Growth Factor-23 and αKlotho in the Treatment of Uremic Cardiomyopathy
    Law, Jonathan P.
    Price, Anna M.
    Pickup, Luke
    Radhakrishnan, Ashwin
    Weston, Chris
    Jones, Alan M.
    McGettrick, Helen M.
    Chua, Winnie
    Steeds, Richard P.
    Fabritz, Larissa
    Kirchhof, Paulus
    Pavlovic, Davor
    Townend, Jonathan N.
    Ferro, Charles J.
    JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2020, 9 (07):
  • [36] Prevalence of Protein-Energy Wasting in Patients with CKD on Hemodialysis in Mexico
    Luna, Gabriela
    Solis, Edgar
    Martin-Alemany, Geovana
    Davalos, Karla
    Munoz, Alondra
    Escobar, Maria
    Lagunes, Laura
    Sepulveda, Tania
    Flores, Diana
    Pina, Luz
    Diez, Ingrid
    Romero, Ludwig
    Navarro, Jorge
    Ardavin Ituarte, Juan M.
    Hernandez-Estrada, Sergio
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2024, 35 (10):
  • [37] PROTEIN-ENERGY WASTING AND SURVIVAL IN DIABETES MELLITUS HEMODIALYSIS PATIENTS
    Elian, Viviana
    Ditu, Georgiana
    Bodnarescu, Mihaela
    Calin, Adina
    Serafinceanu, Cristian
    Cioca, Gabriela
    Pantea-Stoian, Anca
    INTERDIAB 2016: DIABETES MELLITUS AS CARDIOVASCULAR DISEASE, 2016, : 521 - 535
  • [38] ROLE OF FIBROBLAST GROWTH FACTOR-23 AND SOLUBLE ALPHA KLOTHO IN CHRONIC KIDNEY DISEASE
    Scholze, Alexandra
    Petersen, Lise
    Hocher, Berthold
    Rasmussen, Lars M.
    Tepel, Martin
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2014, 29 : 120 - 121
  • [39] Pathophysiological Implications of Fibroblast Growth Factor-23 and Klotho and Their Potential Role as Clinical Biomarkers
    Donate-Correa, Javier
    Muros de Fuentes, Mercedes
    Mora-Fernandez, Carmen
    Navarro-Gonzalez, Juan F.
    CLINICAL CHEMISTRY, 2014, 60 (07) : 933 - 940
  • [40] FIBROBLAST GROWTH FACTOR-23 AND KLOTHO LEVELS IN CHILDREN BEFORE AND AFTER RENAL TRANSPLANTATION
    Sawires, H.
    Essam, R.
    Ishak, M.
    PEDIATRIC TRANSPLANTATION, 2015, 19 : 105 - 106