Skip to main content

Holiday schedule

Our Patient Service Centers will be closed on Wednesday, December 25, 2024 in observance of Christmas and Wednesday, January 1, 2025 in observance of New Year's Day. Have a healthy, happy holiday.

Hide

Test code(s) 39165

Components:
Creatinine, Serum (test code 375)
Albumin, Random Urine with Creatinine (test code 6517)

Chronic kidney disease (CKD) is defined as abnormalities of kidney structure or function, present for >3 months, withimplications for health.1 CKD can be diagnosed based on a glomerular filtration rate (GFR) <60 mL/min/1.73 m2 for >3 months, evidence of kidney damage for >3 months, or both.1

GFR is considered the best overall laboratory marker of kidney function.1 Because direct measurement of GFR can be problematic, an estimated GFR (eGFR) determined using creatinine- or cystatin C-based measurements is most commonly used to diagnose CKD in clinical practice. The Kidney Profile (test code 39165) incorporates creatinine-based eGFR.

Indications of kidney damage include a histologic abnormality, structural abnormality, history of kidney transplantation, abnormal urine sediment, tubular disorder-caused electrolyte abnormality, or an increased urinary albumin level (albuminuria). A urine albumin-creatinine ratio ≥30 mg/g (μg/mg) is considered evidence of albuminuria consistent with kidney damage.

Note that terminology has standardized to define a urine albumin-creatinine ratio result of ≥30 mg/g (albumin excretion rate ≥30 mg/24 h) as evidence of albuminuria; formerly, a ratio of 30-300 mg/g was referred to as “microalbuminuria,” and a ratio of >300 mg/g was defined as “macroalbuminuria.”1

KDIGO guidelines1 incorporate a risk map to

Stage CKD

Guide frequency of CKD monitoring

Identify conditions that would necessitate a cystatin C-based eGFR

Refer the patient to a nephrologist

Figure 1 provides an overview of recommended monitoring frequency for patients with CKD, based on risk of disease progression as assessed using eGFR and urine albumin-creatinine ratio. TestDirectory.QuestDiagnostics.com/HCP/IntGuide/DocLinks/TG_CKD_Fig1.pdf

The table below summarizes evidence-based suggestions for laboratory testing for complications and comorbidities in patients with CKD.


View Larger ▸

Being less influenced by diet and muscle mass, cystatin C-based eGFR testing is appropriate for patients in whom creatinine-based results may be misleading. These patients include pregnant people; persons with acute illness or suffering from malnutrition, serious comorbidities, or extremes of muscle mass (eg, bodybuilders, amputees, paraplegics, sufferers of a muscle-wasting disease or a neuromuscular disorder); or those taking creatine dietary supplements, or with a vegetarian or low-meat diet.1,5

However, cystatin C-based eGFR may be more affected by some non-GFR determinants, such as thyroid disorders, corticosteroid use, and smoking.3 In addition, small but significant associations of cystatin C levels with diabetes, obesity, and inflammation have been reported.6,7 For these reasons, creatinine-based eGFR is recommended for patients without contraindications.

Reference

  1. Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. KDIGO 2012 clinical practice guideline for the evaluation and management of chronic kidney disease. Kidney Int Suppl. 2013;3(1):1-150.
  2. Myers GL, Miller WG, Coresh J, et al. Recommendations for improving serum creatinine measurement: a report from the Laboratory Working Group of the National Kidney Disease Education Program. Clin Chem. 2006;52(1):5-18. doi:10.1373/clinchem.2005.0525144
  3. Vassalotti JA, Centor R, Turner BJ, et al. Practical approach to detection and management of chronic kidney disease for the primary care clinician. Am J Med. 2016;129(2):153-162.e7 doi:10.1016/j.amjmed.2015.08.025
  4. What is Hyperkalemia? National Kidney Foundation. Reviewed February 8, 2016. Accessed July 29, 2021. https://www.kidney.org/atoz/content/what-hyperkalemia
  5. Levey AS, Coresh J, Tighiouart H, et al. Measured and estimated glomerular filtration rate: current status and future directions. Nat Rev Nephrol. 2020;16(1):51-64. doi:10.1038/s41581-019-0191-y
  6. Shlipak MG, Matsushita K, Ärnlöv J, et al. Cystatin C versus creatinine in determining risk based on kidney function. N Engl J Med. 2013;369(10):932-943. doi:10.1056/NEJMoa1214234
  7. Stevens LA, Schmid CH, Greene T, et al. Factors other than glomerular filtration rate affect serum cystatin C levels. Kidney Int. 2009;75(6):652-660. doi:10.1038/ki.2008.638


This FAQ is provided for informational purposes only and is not intended as medical advice. A clinician’s test selection and interpretation, diagnosis, and patient management decisions should be based on his/her education, clinical expertise, and assessment of the patient.



Document FAQS.264 Version: 0
Version 0: effective 09/14/2021 to present