eMedicine Specialties > Nephrology > Glomerular Diseases

Glomerulonephritis, Chronic: Differential Diagnoses & Workup

Author: Moro O Salifu, MD, MPH, FACP, Associate Professor, Department of Internal Medicine, Chief, Division of Nephrology, Director of Nephrology Fellowship Program and Transplant Nephrology, State University of New York Downstate Medical Center
Coauthor(s): Barbara G Delano, MD, MPH, Director of Home Hemodialysis and Peritoneal Dialysis, Professor, Department of Internal Medicine, Division of Nephrology, State University of New York at Brooklyn
Contributor Information and Disclosures

Updated: Oct 23, 2009

Differential Diagnoses

Azotemia
Glomerulonephritis, Nonstreptococcal Associated With Infection
Chronic Renal Failure
Glomerulonephritis, Poststreptococcal
Glomerulonephritis, Acute
Glomerulonephritis, Rapidly Progressive
Glomerulonephritis, Crescentic
Uremia
Glomerulonephritis, Diffuse Proliferative
Glomerulonephritis, Membranoproliferative
Glomerulonephritis, Membranous

Other Problems to Be Considered

Mesangial glomerulonephritis

Workup

Laboratory Studies

  • Urinalysis
    • The presence of dysmorphic RBCs, albumin, or RBC casts suggests glomerulonephritis as the cause of renal failure.
    • Waxy or broad casts are observed in all forms of CKD, including chronic glomerulonephritis.
    • Low urine-specific gravity indicates loss of tubular concentrating ability, an early finding in persons with CDK.
  • Urinary protein excretion
    • This can be estimated by calculating the protein-to-creatinine ratio on a spot morning urine sample. The ratio of urinary protein concentration (in mg/dL) to urinary creatinine (in mg/dL) reflects 24-hour protein excretion in grams. For instance, if the spot urine protein value is 300 mg/dL and the creatinine value is 150 mg/dL, then the ratio is 300 divided by 150, which equals 2. Thus, in this example, the 24-hour urine protein excretion is 2 g.
    • The estimated creatinine clearance rate is used to assess and monitor the GFR. The 2 formulas available to calculate the value are the Cockroft-Gault formula, which estimates creatinine clearance, and the Modification of Diet in Renal Disease Study (MDRD) formula, which is used to calculate the GFR. The Cockroft-Gault formula is simple to use but overestimates the GFR by 10-15% because creatinine is both filtered and secreted. The MDRD formula is much more complex but is available as a PDA through the National Kidney Foundation or can be calculated online through the Hypertension, Dialysis, and Clinical Nephrology Web site.
    • The estimated creatinine clearance rate is also used to monitor response to therapy and to initiate an early transition to renal replacement therapy (eg, dialysis access placement, transplantation evaluation). The degree of proteinuria, especially albuminuria, helps predict renal prognosis in patients with chronic glomerulonephritis. Patients with greater than 1 g/d have an increased risk of progression to ESRD.

      In a study of 38 patients with chronic glomerulonephritis, Hayakawa et al examined the relationship between plasma adiponectin, leptin, and proteinuria levels; glomerular filtration rate; and metabolic risk factors.2 They found that plasma adiponectin levels were much higher in patients with heavy proteinuria (38.8 +/- 27.8 μ g/mL) than they were in patients who had mild (13.3 +/- 5.1 μ g/mL, P <0.001) or moderate proteinuria (18.1 +/- 8.0 μ g/mL, P <0.01). Serum leptin levels, however, did not differ according to the degree of proteinuria.
  • CBC count
    • Anemia is a significant finding in patients with some decline in the GFR.
    • Physicians must be aware that anemia can occur even in patients with serum creatinine levels of less than 2 mg/dL. Even severe anemia can occur at low serum creatinine levels. Anemia is the result of marked impairment of erythropoietin production.
  • Serum chemistry
    • Serum creatinine and urea nitrogen levels are elevated.
    • Impaired excretion of potassium, free water, and acid results in hyperkalemia, hyponatremia, and low serum bicarbonate levels, respectively.
    • Impaired vitamin D-3 production results in hypocalcemia, hyperphosphatemia, and high levels of parathyroid hormone.
    • Low serum albumin levels may be present if uremia interferes with nutrition or if the patient is nephrotic.

Imaging Studies

  • Renal ultrasonogram

    • Obtain a renal ultrasonogram to determine renal size, to assess for the presence of both kidneys, and to exclude structural lesions that may be responsible for azotemia.
    • Small kidneys often indicate an irreversible process.

Procedures

  • Kidney biopsy
    • If the kidney is small, kidney biopsy is usually unnecessary; no specific pattern of disease can be discerned at this point.
    • A kidney biopsy may be considered in the minority of patients who exhibit an acute exacerbation of their chronic disease. This may be particularly pertinent to patients with preserved kidney size and in those with lupus nephritis.

Histologic Findings

In early stages, the glomeruli may still show some evidence of the primary disease.

In advanced stages, the glomeruli are hyalinized and obsolescent. The tubules are disrupted and atrophic, and marked interstitial fibrosis and arterial and arteriolar sclerosis occur.

More on Glomerulonephritis, Chronic

Overview: Glomerulonephritis, Chronic
Differential Diagnoses & Workup: Glomerulonephritis, Chronic
Treatment & Medication: Glomerulonephritis, Chronic
Follow-up: Glomerulonephritis, Chronic
References
Further Reading

References

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  2. Hayakawa K, Ohashi H, Yokoyama H, et al. Adiponectin is increased and correlated with the degree of proteinuria, but plasma leptin is not changed in patients with chronic glomerulonephritis. Nephrology (Carlton). Apr 2009;14(3):327-31. [Medline].

  3. Wolf G. Antiproteinuric response to dual blockade of the renin-angiotensin system in primary glomerulonephritis. Nat Clin Pract Nephrol. Sep 2008;4(9):474-5. [Medline].

  4. Cho ME, Smith DC, Branton MH, et al. Pirfenidone slows renal function decline in patients with focal segmental glomerulosclerosis. Clin J Am Soc Nephrol. Sep 2007;2(5):906-13. [Medline].

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  7. Boulware LE, Troll MU, Jaar BG, Myers DI, Powe NR. Identification and referral of patients with progressive CKD: a national study. Am J Kidney Dis. 2006;48:192. [Medline].

  8. Cameron JS. The Long-Term Outcome of Glomerular Diseases. In: Schrier RW, Gottschalk CW, ed. Diseases of the Kidney. 6th ed. Little, Brown & Company: Boston, Mass; 1997:1919.

  9. Campbell NR, Burgess E, Choi BC, Taylor G, Wilson E, Cléroux J, et al. Lifestyle modifications to prevent and control hypertension. 1. Methods and an overview of the Canadian recommendations. Canadian Hypertension Society, Canadian Coalition for High Blood Pressure Prevention and Control, Lab Centre for Disease Control. CMAJ. May 4 1999;160(9 Suppl):S1-6. [Medline].

  10. Contreras G, Pardo V, Leclercq B, Lenz O, Tozman E, O'Nan P, et al. Sequential therapies for proliferative lupus nephritis. N Engl J Med. Mar 4 2004;350(10):971-80. [Medline].

  11. Coppo R, Gianoglio B, Porcellini MG, Maringhini S. Frequency of renal diseases and clinical indications for renal biopsy in children (report of the Italian National Registry of Renal Biopsies in Children). Nephrol Dial Transplant. Feb 1998;13(2):293-7. [Medline].

  12. Coresh J, Walser M, Hill S. Survival on dialysis among chronic renal failure patients treated with a supplemented low-protein diet before dialysis. J Am Soc Nephrol. Nov 1995;6(5):1379-85. [Medline].

  13. Gharavi AG, Yan Y, Scolari F, Schena FP, Frasca GM, Ghiggeri GM, et al. IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23. Nat Genet. Nov 2000;26(3):354-7. [Medline].

  14. Imbasciati E, Gregorini G, Cabiddu G, Gammaro L, Ambroso G, Del Giudice A, et al. Pregnancy in CKD stages 3 to 5: fetal and maternal outcomes. Am J Kidney Dis. 2007;49:753-62. [Medline].

  15. Jafar TH, Stark PC, Schmid CH, Landa M, Maschio G, Marcantoni C, et al. Proteinuria as a modifiable risk factor for the progression of non-diabetic renal disease. Kidney Int. 2001;60:1131-40. [Medline].

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  20. Nakao N, Yoshimura A, Morita H, Takada M, Kayano T, Ideura T. Combination treatment of angiotensin-II receptor blocker and angiotensin-converting-enzyme inhibitor in non-diabetic renal disease (COOPERATE): a randomised controlled trial. Lancet. 2003;361(9352):117-24. [Medline].

  21. Obrador GT, Pereira BJ. Early referral to the nephrologist and timely initiation of renal replacement therapy: a paradigm shift in the management of patients with chronic renal failure. Am J Kidney Dis. Mar 1998;31(3):398-417. [Medline].

  22. Peterson JC, Adler S, Burkart JM, Greene T, Hebert LA, Hunsicker LG, et al. Blood pressure control, proteinuria, and the progression of renal disease. The Modification of Diet in Renal Disease Study. Ann Intern Med. Nov 15 1995;123(10):754-62. [Medline].

  23. Polenakovic M, Grcevska L. Survival rate of patients with glomerulonephritis. Acta Med Croatica. 1992;46(1):15-20. [Medline].

  24. Remuzzi G, Bertani T. Pathophysiology of progressive nephropathies. N Engl J Med. Nov 12 1998;339(20):1448-56. [Medline].

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  26. Research Group on Progressive Chronic Renal Disease. Nationwide and long-term survey of primary glomerulonephritis in Japan as observed in 1,850 biopsied cases. Nephron. 1999;82(3):205-13. [Medline].

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  28. Schöll U, Wastl U, Risler T, Braun N, Grabensee B, Heering P, et al. The "point of no return" and the rate of progression in the natural history of IgA nephritis. Clin Nephrol. Nov 1999;52(5):285-92. [Medline].

  29. Troyanov S, Wall CA, Miller JA, Scholey JW, Cattran DC. Idiopathic membranous nephropathy: definition and relevance of a partial remission. Kidney Int. Sep 2004;66(3):1199-205. [Medline].

  30. Wolf G, Ritz E. Combination therapy with ACE inhibitors and angiotensin II receptor blockers to halt progression of chronic renal disease: pathophysiology and indications. Kidney Int. 2005;67:799-812. [Medline].

Further Reading

Clinical guidelines:
ACR Appropriateness Criteria® renal failure. American College of Radiology - Medical Specialty Society. 1995 (revised 2008). 10 pages. NGC:007019

Clinical trials:
Efficacy and Safety Study of Abatacept to Treat Lupus Nephritis

Etanercept for the Treatment of Lupus Nephritis

Retinoids for Minimal Change Disease and Focal Segmental Glomerulosclerosis

Keywords

glomerulonephritis, chronic glomerulonephritis, IgA nephropathy, membranous nephropathy, membranoproliferative glomerulonephritis, poststreptococcal glomerulonephritis, glomerulonephritis treatment, crescentic glomerulonephritis, glomerulosclerosis, rapidly progressive glomerulonephritis, RPGN, focal segmental glomerulosclerosis, FSGS, glomerular fibrosis, tubulointerstitial fibrosis, lupus nephritis, azotemia, uremia

Contributor Information and Disclosures

Author

Moro O Salifu, MD, MPH, FACP, Associate Professor, Department of Internal Medicine, Chief, Division of Nephrology, Director of Nephrology Fellowship Program and Transplant Nephrology, State University of New York Downstate Medical Center
Moro O Salifu, MD, MPH, FACP is a member of the following medical societies: American College of Physicians-American Society of Internal Medicine, American Medical Association, American Society for Artificial Internal Organs, American Society of Diagnostic and Interventional Nephrology, American Society of Nephrology, American Society of Transplantation, and National Kidney Foundation
Disclosure: Nothing to disclose.

Coauthor(s)

Barbara G Delano, MD, MPH, Director of Home Hemodialysis and Peritoneal Dialysis, Professor, Department of Internal Medicine, Division of Nephrology, State University of New York at Brooklyn
Barbara G Delano, MD, MPH is a member of the following medical societies: American Society of Nephrology, International Society of Nephrology, National Kidney Foundation, and Sigma Xi
Disclosure: Nothing to disclose.

Medical Editor

Frank C Brosius III, MD, Nephrology Program Director, Professor of Internal Medicine and Physiology, Department of Internal Medicine, Division of Nephrology, University of Michigan School of Medicine
Frank C Brosius III, MD is a member of the following medical societies: Alpha Omega Alpha, American Diabetes Association, American Society of Nephrology, and Phi Beta Kappa
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

George R Aronoff, MD, Director, Professor, Departments of Internal Medicine and Pharmacology, Section of Nephrology, Kidney Disease Program, University of Louisville School of Medicine
George R Aronoff, MD is a member of the following medical societies: American Federation for Medical Research, American Society of Nephrology, Kentucky Medical Association, and National Kidney Foundation
Disclosure: Nothing to disclose.

CME Editor

Rebecca J Schmidt, DO, FACP, FASN, Professor of Medicine, Section Chief, Department of Medicine, Section of Nephrology, West Virginia University School of Medicine
Rebecca J Schmidt, DO, FACP, FASN is a member of the following medical societies: American College of Osteopathic Internists, American College of Physicians, American Medical Association, American Society of Nephrology, International Society of Nephrology, National Kidney Foundation, Renal Physicians Association, and West Virginia State Medical Association
Disclosure: Abbott Grant/research funds Speaking and teaching; Genzyme Honoraria Consulting; Amgen Honoraria Speaking and teaching; Ortho Biotech Honoraria Speaking and teaching

Chief Editor

Vecihi Batuman, MD, FACP, FASN, Professor of Medicine, Section of Nephrology-Hypertension, Tulane University School of Medicine; Chief, Medicine Service, Southeast Louisiana Veterans Health Care System
Vecihi Batuman, MD, FACP, FASN is a member of the following medical societies: American College of Physicians, American Society of Hypertension, American Society of Nephrology, and International Society of Nephrology
Disclosure: Nothing to disclose.

 
 
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