Cystatin C proteoforms in chronic kidney disease

被引:5
作者
Dahl, Helene [1 ]
Meyer, Klaus [2 ]
Sandnes, Kristina [1 ]
Welland, Natasha Lervaag [1 ]
Arnesen, Iselin [1 ]
Marti, Hans-Peter [3 ,4 ]
Dierkes, Jutta [1 ,5 ,6 ]
Lysne, Vegard [6 ]
机构
[1] Univ Bergen, Ctr Nutr, Dept Clin Med, Bergen, Norway
[2] Bevital AS, Bergen, Norway
[3] Univ Bergen, Dept Clin Med, Bergen, Norway
[4] Haukeland Hosp, Dept Nephrol, Bergen, Norway
[5] Haukeland Hosp, Dept Med Biochem & Pharmacol, Bergen, Norway
[6] Univ Bergen, Mohn Nutr Res Lab, Bergen, Norway
关键词
GLOMERULAR-FILTRATION-RATE; TARGETED QUANTIFICATION; PROTEIN; ASSOCIATION; BIOMARKERS; CREATININE; PLASMA;
D O I
10.1371/journal.pone.0269436
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cystatin C, a cysteine protease inhibitor, is used as a biomarker of renal function. It offers several advantages compared to creatinine, and formulas for the estimation of the glomerular filtration rate based on cystatin C have been developed. Recently, several proteoforms of cystatin C have been discovered, including an intact protein with a hydroxylated proline at the N-terminus, and N-terminal truncated forms. There is little knowledge about the biological significance of these proteoforms. Methods: Cross-sectional study of patients with different stages of chronic renal disease (pre-dialysis n = 53; hemodialysis n = 51, renal transplant n = 53). Measurement of cystatin C proteoforms by MALDI-TOF MS, assessment of medicine prescription using the first two levels of the Anatomical Therapeutic chemical system from patients' records. Results: Patients receiving hemodialysis had the highest cystatin C concentrations, followed by pre-dialysis patients and patients with a renal transplant. In all groups, the most common proteoforms were native cystatin C and CysC 3Pro-OH while the truncated forms made up 28%. The distribution of the different proteoforms was largely independent of renal function and total cystatin C. However, the use of corticosteroids (ATC-L02) and immunosuppressants (ATC-H04) considerably impacted the distribution of proteoforms. Conclusion: The different proteoforms of cystatin C increased proportionally with total cystatin C in patients with chronic kidney disease. Prescription of corticosteroids and immunosuppressants had a significant effect on the distribution of proteoforms. The biological significance of these proteoforms remains to be determined.
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页数:13
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