CgA100 - eGFR-adjusted serum chromogranin A

被引:0
|
作者
Asberg, Arne [1 ]
Mikkelsen, Gustav [1 ,2 ]
Lofblad, Lena [1 ,2 ]
机构
[1] Trondheim Reg & Univ Hosp, St Olav Hosp, Dept Clin Chem, Trondheim, Norway
[2] Norwegian Univ Sci & Technol, Fac Med & Hlth Sci, Dept Clin & Mol Med, Trondheim, Norway
关键词
Chromogranin A; estimated glomerular filtration rate; reference limits; indirect methods; finite mixture models; REFERENCE INTERVALS; EQUATION;
D O I
10.1080/00365513.2025.2466058
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The concentration of chromogranin A in serum (s-CgA) is a general marker of neuroendocrine neoplasms. Unfortunately, s-CgA is increased in several other clinical conditions, including renal failure. The physician who assesses s-CgA values must consider the patients' renal function. How this should be done is not clear. We developed an adjustment formula from the association between median s-CgA and the estimated glomerular filtration rate (eGFR) in 2708 patients where s-CgA was measured by the CgA II KRYPTOR method. We used multivariable fractional polynomial quantile regression with the model ln(s-CgA) = c(0) + c(1) x sex + c(2) x age + c(3) x eGFR, thus accounting for sex and age. The final adjustment formula could be simplified to s-CgA(100) = (eGFR / 100) x s-CgA, where s-CgA(100) is an indication of what s-CgA would be if eGFR in the same patient was 100 mL/minute/1.73 m(2). In patients with eGFR > 100 mL/minute/1.73 m(2) no adjustment was done. We tested the formula on another patient population (n = 1563), where s-CgA was measured by a RIA method. S-CgA(100) proved to be independent of eGFR in that population. The clinical validity of s-CgA(100) must await further investigations.
引用
收藏
页码:133 / 137
页数:5
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