Details

Autor(en) / Beteiligte

• García-García, P.M
• Martín-Izquierdo, E
• de Basoa, C.M.-F
• Jarque-López, A
• Pérez-Suárez, G
• Rivero-González, A
• González-Posadas, J.M
• Macía-Heras, M
• García-Nieto, V.M
• Navarro-Gónzález, J.F

Titel

Urinary Clara Cell Protein in Kidney Transplant Patients: A Preliminary Study

Ist Teil von

• Transplantation proceedings, 2016-11, Vol.48 (9), p.2884-2887

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2016

Quelle

MEDLINE

Beschreibungen/Notizen

• Abstract Objective The aim of this exploratory study was to analyze the urinary excretion of Clara cell protein (CC16), a new marker of proximal tubular dysfunction (PTD), in kidney transplantation (KT). Materials and Methods Urinary concentrations of CC16, β2-microglobulin (β2m), and N-acetyl-glucosaminidase (NAG) were measured in 50 KT patients (72% men; mean age 50.4 ± 12.4 years; diabetes in 24%; duration of KT 4.3 ± 3.1 years) and 10 healthy controls (6 men; mean age 33.6 ± 13.4 years). Results Urinary levels of β2m, NAG, and CC16 were significantly higher in KT patients than in controls: β2m: 0.77 (interquartile range [IQ] 0.22 to 4.62) g/g vs 0.069 (IQ 0.05 to 0.10) g/g; NAG: 3.16 (IQ 2.09 to 5.33) U/g vs 1.73 (IQ 1.25 to 2.07) U/g; CC16: 26.01 (IQ 8.62 to 123.3) g/g vs 2.51 (IQ 0.83 to 7.18) g/g ( P  < .001). Elevated levels of β2m, NAG, and CC16 were found in 81%, 28%, and 71% of KT patients, respectively. Urinary levels of β2m, NAG, and CC16 significantly increase as glomerular filtration rate (GFR) decreases. Interestingly, in patients with GFR >60 mL/min, we still found high levels of β2m, NAG, and CC16 in 77%, 13%, and 52%, respectively. Diabetic subjects had significant higher levels of the 3 markers compared with nondiabetic subjects, without differences in albumin excretion or GFR. CC16 showed a positive correlation with urinary albumin ( r  = 0.42, P  < .001), NAG ( r  = 0.352, P  < .05), and β2m ( r  = 0.75, P  < .001). Conclusion PTD is highly prevalent in KT patients. This is the first study that analyzes CC16 in KT patients, showing that the urinary excretion of this protein is significantly increased in this population. Further studies are needed to examine the clinical value of CC16 in KT patients.