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Cystatin C as a GFR Estimation Marker in Acute and Chronic Illness: A Systematic Review
Ogechi M Adingwupu1, Ernesto Rodolpho Barbosa2, Paul M Palevsky3
1Department of Medicine, Division of Nephrology, Tufts Medical Center, Boston, MA.
Insights
Creatinine-based GFR estimating equations are often inaccurate in ill patients. Combining creatinine and cystatin C (eGFRcr-cys) improves kidney function estimation in some conditions like cancer and HIV, indicating potential benefits of cystatin C testing.
Area of Science:
- Nephrology
- Clinical Chemistry
- Internal Medicine
Background:
- Creatinine-based estimated glomerular filtration rate (eGFRcr) equations exhibit inaccuracies in patients with acute or chronic illnesses.
- The performance of cystatin C-based (eGFRcys) and combined creatinine-cystatin C (eGFRcr-cys) equations in these populations remains understudied.
Purpose of the Study:
- To systematically review and evaluate the accuracy of eGFRcr, eGFRcys, and eGFRcr-cys equations compared to measured GFR (mGFR) in adult and pediatric populations with acute or chronic illnesses.
Main Methods:
- A systematic review of studies published since 2011, identified via PubMed and expert sources.
- Inclusion criteria focused on comparisons of eGFRcr, eGFRcys, and eGFRcr-cys against mGFR using standardized assays, excluding specific cohorts like CKD-only or diabetes-only populations.
Main Results:
- Twenty-six studies involving clinical populations (cancer, HIV, cirrhosis, liver transplant, heart failure, neuromuscular disease, critical illness, obesity) were included.
- eGFRcr-cys demonstrated greater accuracy than eGFRcr or eGFRcys in populations with cancer, HIV, and obesity.
- Performance was inconsistent in cirrhosis, liver transplant, heart failure, neuromuscular disease, and critical illness, with many studies showing poor performance and suggesting a need for more frequent mGFR.
Conclusions:
- The combined creatinine-cystatin C (eGFRcr-cys) equation enhances GFR estimation in various acute and chronic illnesses, supporting the utility of cystatin C measurements.
- The observed variability in performance highlights the need for careful consideration of GFR estimation methods and potentially more frequent measured GFR in certain clinical scenarios.
Rationale & Objective:
Creatinine-based GFR estimating (eGFRcr) equations may be inaccurate in populations with acute or chronic illness. The accuracy of GFR equations that use cystatin C (eGFRcys) or creatinine-cystatin C (eGFRcr-cys) is not well studied in these populations.
Study Design:
A systematic review of original articles identified from PubMed and expert sources. Two reviewers screened articles independently and identified those meeting inclusion criteria.
Setting & Study Populations:
Adults and children with acute or chronic illness.
Selection Criteria For Studies:
Studies published since 2011 that compared performance of eGFRcr, eGFRcys, and eGFRcr-cys relative to measured GFR (mGFR), used standardized assays for creatinine or cystatin C, and used eGFR equations developed using such assays. Studies of ambulatory clinical populations or research studies in populations with only CKD, kidney transplant recipients, only diabetes, kidney donor candidates, and community-based cohorts were excluded.
Data Extraction:
Data extracted from full text.
Analytical Approach:
Bias and percentages of estimates within 30% of mGFR (P30) of eGFR compared with mGFR were evaluated.
Results:
Of the 179 citations, 26 studies met the inclusion criteria: 24 in adults and 2 in children in clinical populations with cancer (n=5), HIV (n=5), cirrhosis (n=3), liver transplant (n=3), heart failure (n=2), neuromuscular diseases (n=1) critical illness (n=5), and obesity (n=2). In general, eGFRcr-cys had greater accuracy than eGFRcr or eGFRcys equations among study populations with cancer, HIV, and obesity, but did not perform consistently better in cirrhosis, liver transplant, heart failure, neuromuscular disease, and critical illness.
Limitations:
Participants were selected because of concern for inaccurate eGFRcr, which may bias results. Most studies had small sample sizes, limiting generalizability.
Conclusions:
eGFRcr-cys improves GFR estimation in populations with a variety of acute and chronic illnesses, providing indications for cystatin C measurement. Performance was poor in many studies, suggesting the need for more frequent mGFR.
Plain-Language Summary:
Kidney function, specifically glomerular filtration rate (GFR), estimated using creatinine (eGFRcr) is often inaccurate in people with acute and chronic illness. The accuracy of estimates using cystatin C alone (eGFRcys) or together with creatinine (eGFRcr-cys) is not well studied in these populations. We conducted a systematic review to address the knowledge gap. Of the 179 papers reviewed, we identified 26 studies in clinical populations with cancer (n=5); HIV (n=5); cirrhosis (n=3); liver transplant (n=3); heart failure (n=2); neuromuscular disease (n=1); critical illness (n=5); and obesity (n=2). In general, eGFRcr-cys improved the GFR estimation in HIV, cancer, and obesity, providing indications for cystatin C measurement. Performance was poor in many studies, suggesting the need for more frequent measured GFR.
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