Clinical Significance of Adropin and Afamin in Evaluating Renal Function and Cardiovascular Health in the Presence of CKD-MBD Biomarkers in Chronic Kidney Disease
Aim: The study aims to test the hypothesis that concentrations of adropin and afamin differ between patients in various stages of chronic kidney disease when compared with healthy controls. The study also investigates the association of the biomarkers (adropin and afamin) with CKD-MBD and traditiona...
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| Published in | Diagnostics (Basel) Vol. 13; no. 19; p. 3158 |
|---|---|
| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Basel
MDPI AG
09.10.2023
MDPI |
| Subjects | |
| Online Access | Get full text |
| ISSN | 2075-4418 2075-4418 |
| DOI | 10.3390/diagnostics13193158 |
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| Abstract | Aim: The study aims to test the hypothesis that concentrations of adropin and afamin differ between patients in various stages of chronic kidney disease when compared with healthy controls. The study also investigates the association of the biomarkers (adropin and afamin) with CKD-MBD and traditional cardiovascular risk parameters in CKD patients. Methodology: The cross-sectional study includes the subjects divided into four groups comprising the control group (healthy volunteers = 50), CKD stages 1–2 patients (n = 50), CKD stages 3–4 patients (n = 50), CKD stage 5 patients (n = 50). Serum concentrations of adropin and afamin were determined using ELISA. Clinical variables (renal, lipid, and CKD-MBD parameters) were correlated to adropin and afamin concentrations. Results: Afamin concentration was found to be higher in group IV, followed by groups III and II when compared to the control group, i.e., (83.243 ± 1.46, 64.233 ± 0.99, and 28.948 ± 0.72 vs. 14.476 ± 0.5) mg/L (p < 0.001), and adropin concentration was found to be lower in group IV as compared to groups III, II, and I (200.342 ± 8.37 vs. 284.682 ± 9.89 vs. 413.208 ± 12.32 vs. 706.542 ± 11.32) pg/mL (p < 0.001), respectively. Pearson correlation analysis showed that afamin was positively correlated with traditional cardiovascular risk biomarkers, while adropin showed a negative correlation. Conclusions: Adropin and afamin may potentially serve as futuristic predictors for the deterioration of renal function and may be involved in the pathological mechanisms of CKD and its associated complications such as CKD-MBD and high lipid levels. |
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| AbstractList | The study aims to test the hypothesis that concentrations of adropin and afamin differ between patients in various stages of chronic kidney disease when compared with healthy controls. The study also investigates the association of the biomarkers (adropin and afamin) with CKD-MBD and traditional cardiovascular risk parameters in CKD patients.AIMThe study aims to test the hypothesis that concentrations of adropin and afamin differ between patients in various stages of chronic kidney disease when compared with healthy controls. The study also investigates the association of the biomarkers (adropin and afamin) with CKD-MBD and traditional cardiovascular risk parameters in CKD patients.The cross-sectional study includes the subjects divided into four groups comprising the control group (healthy volunteers = 50), CKD stages 1-2 patients (n = 50), CKD stages 3-4 patients (n = 50), CKD stage 5 patients (n = 50). Serum concentrations of adropin and afamin were determined using ELISA. Clinical variables (renal, lipid, and CKD-MBD parameters) were correlated to adropin and afamin concentrations.METHODOLOGYThe cross-sectional study includes the subjects divided into four groups comprising the control group (healthy volunteers = 50), CKD stages 1-2 patients (n = 50), CKD stages 3-4 patients (n = 50), CKD stage 5 patients (n = 50). Serum concentrations of adropin and afamin were determined using ELISA. Clinical variables (renal, lipid, and CKD-MBD parameters) were correlated to adropin and afamin concentrations.Afamin concentration was found to be higher in group IV, followed by groups III and II when compared to the control group, i.e., (83.243 ± 1.46, 64.233 ± 0.99, and 28.948 ± 0.72 vs. 14.476 ± 0.5) mg/L (p < 0.001), and adropin concentration was found to be lower in group IV as compared to groups III, II, and I (200.342 ± 8.37 vs. 284.682 ± 9.89 vs. 413.208 ± 12.32 vs. 706.542 ± 11.32) pg/mL (p < 0.001), respectively. Pearson correlation analysis showed that afamin was positively correlated with traditional cardiovascular risk biomarkers, while adropin showed a negative correlation.RESULTSAfamin concentration was found to be higher in group IV, followed by groups III and II when compared to the control group, i.e., (83.243 ± 1.46, 64.233 ± 0.99, and 28.948 ± 0.72 vs. 14.476 ± 0.5) mg/L (p < 0.001), and adropin concentration was found to be lower in group IV as compared to groups III, II, and I (200.342 ± 8.37 vs. 284.682 ± 9.89 vs. 413.208 ± 12.32 vs. 706.542 ± 11.32) pg/mL (p < 0.001), respectively. Pearson correlation analysis showed that afamin was positively correlated with traditional cardiovascular risk biomarkers, while adropin showed a negative correlation.Adropin and afamin may potentially serve as futuristic predictors for the deterioration of renal function and may be involved in the pathological mechanisms of CKD and its associated complications such as CKD-MBD and high lipid levels.CONCLUSIONSAdropin and afamin may potentially serve as futuristic predictors for the deterioration of renal function and may be involved in the pathological mechanisms of CKD and its associated complications such as CKD-MBD and high lipid levels. Aim: The study aims to test the hypothesis that concentrations of adropin and afamin differ between patients in various stages of chronic kidney disease when compared with healthy controls. The study also investigates the association of the biomarkers (adropin and afamin) with CKD-MBD and traditional cardiovascular risk parameters in CKD patients. Methodology: The cross-sectional study includes the subjects divided into four groups comprising the control group (healthy volunteers = 50), CKD stages 1–2 patients (n = 50), CKD stages 3–4 patients (n = 50), CKD stage 5 patients (n = 50). Serum concentrations of adropin and afamin were determined using ELISA. Clinical variables (renal, lipid, and CKD-MBD parameters) were correlated to adropin and afamin concentrations. Results: Afamin concentration was found to be higher in group IV, followed by groups III and II when compared to the control group, i.e., (83.243 ± 1.46, 64.233 ± 0.99, and 28.948 ± 0.72 vs. 14.476 ± 0.5) mg/L (p < 0.001), and adropin concentration was found to be lower in group IV as compared to groups III, II, and I (200.342 ± 8.37 vs. 284.682 ± 9.89 vs. 413.208 ± 12.32 vs. 706.542 ± 11.32) pg/mL (p < 0.001), respectively. Pearson correlation analysis showed that afamin was positively correlated with traditional cardiovascular risk biomarkers, while adropin showed a negative correlation. Conclusions: Adropin and afamin may potentially serve as futuristic predictors for the deterioration of renal function and may be involved in the pathological mechanisms of CKD and its associated complications such as CKD-MBD and high lipid levels. |
| Author | Singh, Tanveer Ahmad, Sheikh F. Krishan, Pawan Kumari, Pratima Singh, Ravinder Kaur, Rupinder Singh, Varinder |
| AuthorAffiliation | 2 Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala 147002, Punjab, India; pawankrishan@rediffmail.com 5 Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia; fashaikh@ksu.edu.sa 3 Department of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M Health Science Center, Bryan, TX 77807, USA; tanveersingh1988@gmail.com 4 Department of Pharmaceutical Sciences and Technology, Maharaja Ranjit Singh Punjab Technical University, Bathinda 151001, Punjab, India; varinderjassal17@gmail.com 1 Chitkara College of Pharmacy, Chitkara University, Rajpura 140401, Punjab, India; rupinder@chitkara.edu.in (R.K.); pratima.kumari@chitkara.edu.in (P.K.) |
| AuthorAffiliation_xml | – name: 2 Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala 147002, Punjab, India; pawankrishan@rediffmail.com – name: 4 Department of Pharmaceutical Sciences and Technology, Maharaja Ranjit Singh Punjab Technical University, Bathinda 151001, Punjab, India; varinderjassal17@gmail.com – name: 1 Chitkara College of Pharmacy, Chitkara University, Rajpura 140401, Punjab, India; rupinder@chitkara.edu.in (R.K.); pratima.kumari@chitkara.edu.in (P.K.) – name: 3 Department of Neuroscience and Experimental Therapeutics, College of Medicine, Texas A&M Health Science Center, Bryan, TX 77807, USA; tanveersingh1988@gmail.com – name: 5 Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia; fashaikh@ksu.edu.sa |
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| Cites_doi | 10.1038/s41598-020-66254-9 10.2147/IJNRD.S101808 10.1002/jcla.22672 10.3390/nu11010152 10.1177/15593258221127568 10.14336/AD.2017.0523 10.3390/molecules25030549 10.1016/j.mce.2019.110532 10.2217/bmm-2018-0126 10.1038/oby.2012.31 10.2147/IJNRD.S191156 10.3390/ijms23158318 10.22452/mjcs.sp2022no1.10 10.1016/j.ekir.2021.05.012 10.1016/j.diabres.2018.02.034 10.1155/2021/6644631 10.1152/ajpheart.00449.2020 10.1186/s12958-018-0338-x 10.3390/biom12010116 10.17219/acem/104551 10.1016/j.molmet.2017.12.002 10.1093/ndt/gfac212 10.3389/fendo.2021.670425 10.3389/fcell.2021.644363 10.1177/1557988316664074 10.3390/diagnostics10070483 10.3390/biomedicines10092094 10.1016/j.mvr.2020.104105 10.1186/s12882-022-02948-8 10.3390/jcm12062231 10.3390/biomedicines9040404 10.1507/endocrj.EJ18-0060 10.3389/fphys.2021.696163 |
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| SubjectTerms | adropin afamin biomarker Biomarkers Blood pressure Blood vessels Calcification cardiovascular Cardiovascular disease Cholesterol CKD CKD-MBD Clinical significance Diabetes Heart High density lipoprotein Homeostasis Hyperlipidemia Hypertension Inflammation Kidney diseases Kinases Lipids Metabolic disorders Metabolic syndrome Mortality Proteins Smooth muscle Variance analysis Vitamin D Vitamin E |
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| Title | Clinical Significance of Adropin and Afamin in Evaluating Renal Function and Cardiovascular Health in the Presence of CKD-MBD Biomarkers in Chronic Kidney Disease |
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