Minimal change disease overview
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Yazan Daaboul, Serge Korjian
Overview
Minimal change disease (MCD) is a podocytopathy that reveals foot process effacement on electron microscopy. It is the most common cause of nephrotic syndrome in children and less commonly in adults. Its name refers to the presence of nephrotic syndrome with the absence of any visible glomerular lesions on light microscopy and the absence of any staining on immunofluorescence, appearing similar to completely normal glomeruli on histopathology. Accordingly, it has also been called nil (nothing-in-light microscopy) disease. Other names, such as lipoid nephrosis (due to the presence of lipid-laden macrophages in the tubular epithelial cells and urine) and steroid-responsive/sensitive nephrotic syndrome (due to its generally excellent response to steroid therapy) may also refer to minimal change disease.
Historical Perspective
Minimal change disease was first described by F. Munk in 1913, when he coined the term “lipoid nephrosis” following the observation of lipid-laden macrophages in the proximal tubular epithelial cells and oval fat bodies in urine.[1] In 1925, Fahr and colleagues noted the resemblance of minimal change disease to focal segmental glomerulosclerosis (FSGS).[1] Ever since its early description, the term “lipoid nephrosis” has been criticized due to the clinical irrelevance of the lipid-laden cells seen on microscopy.
Classification
Minimal change disease can be classified based on the underlying clinical etiology of disease into primary and secondary. Minimal change disease currently has no pathological classification system. Based on the proposed Columbia classification, minimal change disease was considered an entity within the spectrum of focal segmental glomerulonephritis (FSGS).[2]
Pathophysiology
The exact pathogenesis of minimal change disease is not well-understood. T-cell dysfunction may mediate the pathogenesis of minimal change disease.[3] Due to the remarkable observation of disease recurrence after transplantation and the resolution of renal disease in recipients of kidneys from donors with MCD, it has been suggested that the presence of circulatory compounds may be attributable to the disease.[4][5][6] Factors associated with the pathophysiology of minimal change disease include glomerular permeability factor (GPF) from T cells,[7][8] hemopexin,[9][10] interleukin (IL)13,[11] cardiotrophin-like cytokine (CLC)-1,[12], and vascular endothelial growth factor (VEGF).[13]
Causes
Most cases of minimal change disease occur sporadically with no clear cause. Few cases occur due to genetic mutations.
Differential Diagnosis
The differential diagnosis of minimal change disease must always include other renal etiologies of nephrotic syndrome, such as focal segmental glomerulosclerosis (FSGS) and IgM nephropathy, and causes of peripheral edema and hypoalbuminemia, such as congestive heart failure, liver cirrhosis, and protein-losing enteropathy.
Epidemiology and Demographics
Minimal change disease (MCD) is considered a disease of childhood. It is responsible for up to 70-90% of nephrotic syndrome in patients less than 10 years of age, and up to 50% of older children.[14][15][16] Among children, several studies have shown a male predominance with approximately 2:1 male to female ratio.[17]
Natural History, Complications and Prognosis
Complications associated with the pathogenesis of the disease as a nephrotic syndrome include thromboembolic events and disorders of hemostasis, hyperlipidemia, vulnerability to infections, and hypertension.[17] Before the steroid era, patients died of renal failure and from infections.[18] Nowadays, patients have excellent renal outcomes when they are still steroid-responsive and virtually all patients survive with a normal creatinine clearance.[18][19] Although renal outcomes are considered excellent with appropriate therapy, the risk of chronic renal disease cannot be completely ruled out, especially among patients receiving nephrotoxic medications for prolonged periods of time.[19]
References
- ↑ 1.0 1.1 D'Agati V (2003). "Pathologic classification of focal segmental glomerulosclerosis". Semin Nephrol. 23 (2): 117–34. doi:10.1053/snep.2003.50012. PMID 12704572.
- ↑ D'Agati VD, Fogo AB, Bruijn JA, Jennette JC (2004). "Pathologic classification of focal segmental glomerulosclerosis: a working proposal". Am J Kidney Dis. 43 (2): 368–82. PMID 14750104.
- ↑ Shalhoub RJ (1974). "Pathogenesis of lipoid nephrosis: a disorder of T-cell function". Lancet. 2 (7880): 556–60. PMID 4140273.
- ↑ Hoyer JR, Vernier RL, Najarian JS, Raij L, Simmons RL, Michael AF (2001). "Recurrence of idiopathic nephrotic syndrome after renal transplantation. 1972". J Am Soc Nephrol. 12 (9): 1994–2002. PMID 11518795.
- ↑ Mauer SM, Hellerstein S, Cohn RA, Sibley RK, Vernier RL (1979). "Recurrence of steroid-responsive nephrotic syndrome after renal transplantation". J Pediatr. 95 (2): 261–4. PMID 376811.
- ↑ Ali AA, Wilson E, Moorhead JF, Amlot P, Abdulla A, Fernando ON; et al. (1994). "Minimal-change glomerular nephritis. Normal kidneys in an abnormal environment?". Transplantation. 58 (7): 849–52. PMID 7940721.
- ↑ Koyama A, Fujisaki M, Kobayashi M, Igarashi M, Narita M (1991). "A glomerular permeability factor produced by human T cell hybridomas". Kidney Int. 40 (3): 453–60. PMID 1787645.
- ↑ Lagrue G, Xheneumont S, Branellec A, Hirbec G, Weil B (1975). "A vascular permeability factor elaborated from lymphocytes. I. Demonstration in patients with nephrotic syndrome". Biomedicine. 23 (1): 37–40. PMID 1174637.
- ↑ Cheung PK, Stulp B, Immenschuh S, Borghuis T, Baller JF, Bakker WW (1999). "Is 100KF an isoform of hemopexin? Immunochemical characterization of the vasoactive plasma factor 100KF". J Am Soc Nephrol. 10 (8): 1700–8. PMID 10446937.
- ↑ Lennon R, Singh A, Welsh GI, Coward RJ, Satchell S, Ni L; et al. (2008). "Hemopexin induces nephrin-dependent reorganization of the actin cytoskeleton in podocytes". J Am Soc Nephrol. 19 (11): 2140–9. doi:10.1681/ASN.2007080940. PMC 2573012. PMID 18753258.
- ↑ Lai KW, Wei CL, Tan LK, Tan PH, Chiang GS, Lee CG; et al. (2007). "Overexpression of interleukin-13 induces minimal-change-like nephropathy in rats". J Am Soc Nephrol. 18 (5): 1476–85. doi:10.1681/ASN.2006070710. PMID 17429054.
- ↑ McCarthy ET, Sharma M, Savin VJ (2010). "Circulating permeability factors in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis". Clin J Am Soc Nephrol. 5 (11): 2115–21. doi:10.2215/CJN.03800609. PMID 20966123.
- ↑ Parikh SM (2012). "Circulating mediators of focal segmental glomerulosclerosis: soluble urokinase plasminogen activator receptor in context". Am J Kidney Dis. 59 (3): 336–9. doi:10.1053/j.ajkd.2011.09.011. PMID 22033283.
- ↑ Cho MH, Hong EH, Lee TH, Ko CW (2007). "Pathophysiology of minimal change nephrotic syndrome and focal segmental glomerulosclerosis". Nephrology (Carlton). 12 Suppl 3: S11–4. doi:10.1111/j.1440-1797.2007.00875.x. PMID 17995521.
- ↑ Cameron JS (1996). "Nephrotic syndrome in the elderly". Semin Nephrol. 16 (4): 319–29. PMID 8829270.
- ↑ Cameron JS, Turner DR, Ogg CS, Sharpstone P, Brown CB (1974). "The nephrotic syndrome in adults with 'minimal change' glomerular lesions". Q J Med. 43 (171): 461–88. PMID 4422336.
- ↑ 17.0 17.1 Waldman M, Crew RJ, Valeri A, Busch J, Stokes B, Markowitz G; et al. (2007). "Adult minimal-change disease: clinical characteristics, treatment, and outcomes". Clin J Am Soc Nephrol. 2 (3): 445–53. doi:10.2215/CJN.03531006. PMID 17699450.
- ↑ 18.0 18.1 Kyrieleis HA, Löwik MM, Pronk I, Cruysberg HR, Kremer JA, Oyen WJ; et al. (2009). "Long-term outcome of biopsy-proven, frequently relapsing minimal-change nephrotic syndrome in children". Clin J Am Soc Nephrol. 4 (10): 1593–600. doi:10.2215/CJN.05691108. PMC 2758253. PMID 19808243.
- ↑ 19.0 19.1 Niaudet P (2009). "Long-term outcome of children with steroid-sensitive idiopathic nephrotic syndrome". Clin J Am Soc Nephrol. 4 (10): 1547–8. doi:10.2215/CJN.05950809. PMID 19808239.