Chronic Kidney Disease
Also known as: CKD, kidney failure (stages 3–5), renal insufficiency
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Higher progression to end-stage renal disease in Black adults
Overview
Chronic kidney disease (CKD) is a progressive loss of kidney function, defined as eGFR below 60 mL/min/1.73 m² or evidence of kidney damage (such as urine albumin ≥30 mg/g) lasting more than three months. CKD is staged G1–G5 based on eGFR, with G5 representing kidney failure requiring dialysis or transplantation. Hypertension and diabetes are the two most common causes, accounting for roughly 70 percent of new kidney failure cases in the United States. Early CKD is usually silent; symptoms such as fatigue, edema, and decreased urine output emerge in later stages. Approximately 37 million Americans have CKD, and most are undiagnosed.
How Chronic Kidney Disease affects Black patients
Black adults are three times more likely than white adults to progress to end-stage renal disease (ESRD) requiring dialysis. A critical contributing factor is the APOL1 gene: variants G1 and G2, found predominantly in people with West African ancestry, dramatically increase the lifetime risk of kidney diseases including focal segmental glomerulosclerosis (FSGS), HIV-associated nephropathy, and lupus nephritis. Approximately 13 percent of Black Americans carry two high-risk APOL1 alleles. An equally important clinical issue resolved in 2021: the NKF-ASN Task Force recommended that the race coefficient be eliminated from the CKD-EPI eGFR equation, because the old formula systematically overestimated kidney function in Black patients, delaying nephrology referral, transplant waitlist placement, and drug dose adjustments by months to years. The race-free 2021 CKD-EPI equation is now the standard of care. Black patients also face documented disparities in transplant access — they wait longer for donor kidneys than white patients.
Symptoms
- Usually none until late stages (CKD is a 'silent' disease in stages G1–G3)
- Fatigue and decreased energy
- Swelling in ankles, feet, and legs (edema)
- Foamy or bubbly urine (proteinuria)
- Decreased urine output
- Shortness of breath (fluid accumulation)
- Nausea, loss of appetite, metallic taste (late-stage uremia)
- Persistent itching (uremic pruritus)
When to see a doctor
Annual eGFR and urine albumin-to-creatinine ratio (ACR) testing is recommended for anyone with diabetes, hypertension, a family history of kidney disease, or APOL1 high-risk variant status. Nephrology referral is recommended when eGFR drops below 30 mL/min/1.73 m² (CKD Stage G4), or earlier if eGFR is declining rapidly or there is heavy proteinuria.
Seek emergency evaluation for sudden severe decrease in urine output, extreme fatigue, confusion, or markedly elevated blood pressure, which may signal acute kidney injury.
Screening
KDIGO 2024 guidelines and the NKF recommend annual eGFR and urine ACR for all adults with diabetes or hypertension, plus for those with known CKD risk factors including obesity, APOL1 high-risk genotype, history of acute kidney injury, or a family member on dialysis. APOL1 genetic testing is clinically available and can identify Black patients at markedly elevated risk even before kidney disease is detectable — discuss with your nephrologist whether testing is appropriate for you.
Treatment overview
Slowing CKD progression centers on treating underlying causes and reducing intraglomerular pressure. ACE inhibitors or ARBs are essential for patients with proteinuric CKD and/or diabetes. SGLT2 inhibitors (empagliflozin, dapagliflozin, canagliflozin) reduce CKD progression and cardiovascular events independent of diabetes status — KDIGO 2024 designates them as first-line kidney-protective agents alongside ACE/ARB for appropriate patients. Finerenone, a non-steroidal mineralocorticoid antagonist, reduces CKD progression in diabetic kidney disease. Blood pressure target below 120/80 mmHg is recommended by SPRINT data. Avoidance of nephrotoxins (NSAIDs, IV contrast without precaution, certain antibiotics) is critical. When eGFR approaches 20, dialysis planning and transplant evaluation should begin promptly.
Questions to ask your doctor
Bring this list to your next appointment.
- What is my current eGFR and how has it trended over the past year?
- What is my urine albumin-to-creatinine ratio (ACR)?
- Is my eGFR being calculated with the race-free 2021 CKD-EPI equation?
- Should I be on an SGLT2 inhibitor for kidney protection?
- Which of my current medications could harm my kidneys?
- Should I be tested for APOL1 high-risk variants?
- At what eGFR should I be referred for transplant evaluation?
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This content is for informational and educational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider with questions about a medical condition. If you are experiencing a medical emergency, call 911 or your local emergency number immediately.