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2017 ; 18
(1
): 199
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Screening for chronic kidney disease of uncertain aetiology in Sri Lanka:
usability of surrogate biomarkers over dipstick proteinuria
#MMPMID28629425
Ratnayake S
; Badurdeen Z
; Nanayakkara N
; Abeysekara T
; Ratnatunga N
; Kumarasiri R
BMC Nephrol
2017[Jun]; 18
(1
): 199
PMID28629425
show ga
BACKGROUND: The use of dipstick proteinuria to screen Chronic Kidney Disease of
uncertain aetiology (CKDu) in Sri Lanka is a recently debated matter of dispute.
The aim of this study was to assess the suitability of biomarkers: serum
creatinine, cystatin C and urine albumin to creatinine ratio (ACR) for screening
CKDu in Sri Lanka. METHODS: Forty-four male CKDu patients and 49 healthy males
from a CKDu-endemic region were selected. Meanwhile, 25 healthy males from a
non-endemic region were selected as an absolute control. The diagnostic accuracy
of each marker was compared using the above three study groups. RESULTS: In
receiver operating characteristics (ROC) plots for creatinine, cystatin C and
ACR, values of area under the curve (AUC) were 0.926, 0.920 and 0.737
respectively when CKDu was compared to non-endemic control. When CKDu was
compared to endemic control, AUCs of above three analytes were distinctly lower
as 0.718, 0.808 and 0.678 respectively. Cystatin C exhibited the highest
sensitivity for CKDu when analyzed against both control groups where respective
sensitivities were 0.75 against endemic control and 0.89 against non-endemic
control. ROC-optimal cutoff limits of creatinine, cystatin C and ACR in CKDu vs
non-endemic control were 89.0 ?mol/L, 1.01 mg/L and 6.06 mg/g-Cr respectively,
whereas in CKDu vs endemic control the respective values were 111.5 ?mol/L,
1.22 mg/L and 12.66 mg/g-Cr. CONCLUSIONS: Amongst the three biomarkers evaluated
in this study, our data suggest that Cystatin C is the most accurate functional
marker in detecting CKDu in endemic regions, yet the high cost hinders its
usability on general population. Creatinine is favorable over dipstick
proteinuria owing to its apparent accuracy and cost efficiency, while having the
ability to complement the kidney damage marker (ACR) in screening. ACR may not be
favorable as a standalone screening marker in place of dipstick proteinuria due
to its significant decline in sensitivity against the CKDu-endemic population.
However, creatinine and ACR in a complementary manner could overcome current
shortcomings of dipstick proteinuria and such a dual marker tool could be
commodious in screening CKDu-type tubulointerstital diseases. Furthermore, use of
ACR may also increase the ability to clinically discriminate CKDu from other
glomerular nephropathies.