The estimation of glomerular filtration in acute and critical illness: Challenges and opportunities

Roy, Reuben; Macdonald, John S.; Dark, Paul; Kalra, Philip A.; Green, Darren

doi:10.1016/j.clinbiochem.2023.110608

Cited by 1 publication

(1 citation statement)

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“…An overestimation of mGFR could be demonstrated for creatinine‐based calculations in adolescent and adult MMA patients 9 . Serum CysC allows the calculation of estimated GFR (eGFR) and has been considered to be more accurate than serum creatinine determinations 26,31–34 …”

Section: Discussionmentioning

confidence: 99%

Kidney urinary biomarkers in patients with branched‐chain amino acid and cobalamin metabolism defects

Köpfer,

Garbade,

Klingbeil

et al. 2023

J of Inher Metab Disea

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There is a clinical need for early detection of chronic kidney disease (CKD) in patients with organic acidurias. We measured kidney markers in a longitudinal study over 5 years in 40 patients with methylmalonic aciduria (Mut0), propionic aciduria (PA), cobalamin A (CblA), and cobalamin C (CblC) deficiencies. Neutrophil gelatinase‐associated lipocalin (NGAL), calprotectin (CLP), kidney injury molecule‐1 (KIM‐1), dickkopf‐3 (DKK‐3), albumin and beta‐2‐microglobulin (B2MG) in urine, as well as cystatin C (CysC) in serum were quantified. In Mut0 patients, mean concentrations of B2MG, KIM‐1, and DKK‐3 were elevated compared with healthy controls, all markers indicative of proximal tubule damage. In PA patients, mean B2MG, albumin, and CLP were elevated, indicating signs of proximal tubule and glomerulus damage and inflammation. In CblC patients, mean B2MG, NGAL, and CLP were increased, and considered as markers for proximal and distal tubule damage and inflammation. B2MG, was elevated in all three diseases, and correlated with DKK‐3 in Mut0/CblA and with eGFR(CysC) and KIM‐1 in PA patients, respectively. None of the markers were elevated in CblA patients. Significant deterioration of kidney function, as determined by steady increase in CysC concentrations was noted in seven patients within the observation period. None of the investigated biomarker profiles showed a clear increase or added value for early detection. In conclusion, we identified disease‐specific biomarker profiles for inflammation, tubular, and proximal damage in the urine of Mut0, PA, and CblC patients. Whether these biomarkers can be used for early detection of CKD requires further investigation, as significant kidney function deterioration was observed in only a few patients.

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Section: Discussionmentioning

confidence: 99%