:: KoreaPediatrics.com - 부모도 반의사가 되어야 한다 ::
소아과학
새소식

C3 Glomerulopathy: Dense Deposit Disease and C3 Glomerulonephritis

C3 Glomerulopathy: Dense Deposit Disease and C3 Glomerulonephritis


NORD gratefully acknowledges Richard JH Smith, MD, Director of the Iowa Institute of Human Genetics and the Molecular Otolaryngology and Renal Research Laboratories at the University of Iowa, for assistance in the preparation of this report.


Synonyms of C3 Glomerulopathy: Dense Deposit Disease and C3 Glomerulonephritis
•C3G


Subdivisions of C3 Glomerulopathy: Dense Deposit Disease and C3 Glomerulonephritis
•dense deposit disease
•C3 glomerulonephritis


General Discussion

Over the past decade, important advances in our understanding of complement-mediated renal diseases have led to the adoption of new names or ‘disease categories’ to more precisely group diseases that appear to share a similar cause.  Consider, for example, dense deposit disease (DDD), a very rare kidney disease characterized on a renal biopsy test called ‘immunofluorescence’ by an abundance of a protein called C3 in the renal glomeruli, and named for the extremely dense ‘sausage-like’ deposits that are seen in the glomerular basement membrane (GBM) using electron microscopy.  In 2013, as a result of a consensus meeting, scientists recommended that DDD be sub-grouped under a new heading – C3 Glomerulopathy, abbreviated C3G.  The adoption of this new term was driven by the recognition that there is another group of patients with glomerular disease whose kidney biopsy is reminiscent of DDD.  On electron microscopy, the deposits in these patients are lighter in color and more widespread in location, but on immunofluorescence, as with DDD there is an abundance of C3 in the renal glomeruli. These patients are said to have C3 glomerulonephritis or C3GN.  In recognition of shared similarities, both DDD and C3GN are now classified as sub-types of C3G.

What happens in C3G?  Recall that the glomeruli are the filtering units of the kidney, where blood gets filtered under pressure through the GBM into another space, called Bowman's space, as urine.  About half a million glomeruli in each kidney do the filtering, creating a filtrate of water, sodium, potassium, chloride, glucose and small proteins.  In both DDD and C3GN, deposits of C3 and other proteins in the GBM disrupt kidney function.  Progressive damage to the glomeruli occurs and after about 10 years, enough damage has occurred so that about half of all persons with C3G have kidney failure.  When kidney failure occurs, dialysis must be started or transplantation must be performed.  The rate of progression to end-stage kidney failure and dialysis appears to be similar for both DDD and C3GN.

In addition to dense deposits in the kidney, persons with DDD can develop deposits in their eyes in an area called Bruch’s membrane.  This occurs because the ‘choriocapillaris-Bruch's membrane-retinal pigment epithelium’ interface in the eye is very similar to the capillary-GBM interface in the kidney.  The eye deposits are called drusen.  Whether they occur more or less frequently in patients with C3GN is not clear.


Signs & Symptoms



The signs and symptoms of DDD and C3GN are similar. They include: blood in the urine, which is called hematuria; dark foamy urine, which signifies the presence of protein or ‘proteinuria’; cloudiness of the urine, reflecting the presence of white blood cells; swelling or ‘edema’, initially of the legs although any part of the body can be affected; high blood pressure; decreased urine output; and decreased alertness.

As mentioned earlier, when a kidney biopsy is done in a person with the above signs and symptoms if C3G (either DDD or C3GN) is suspected, the immunofluorescence analysis should show abundant C3 in the glomerular capillaries. This finding is a requirement and in its absence, the diagnosis of C3G can be excluded. Sophisticated studies have been done to determine the precise composition of the electron-dense deposits in DDD and C3GN, and in addition to C3 the glomeruli contain many other proteins that belong to a system called the complement system. Proteins from both the alternative pathway of complement and the terminal pathway of the complement are found. This finding is in agreement with our understanding of the pathophysiology of DDD and C3GN.

As might be expected, since complement proteins are typically in the blood stream, if they become trapped in the kidneys, blood stream levels will often be correspondingly reduced; and in fact, in persons with both DDD and C3GN several complement proteins in the blood stream circulate at lower than expected levels. The most notable is the decrease in C3, which tends to be reduced to a greater extent in persons with DDD as compared to C3GN. Studies are currently being done to measure the levels of many different complement proteins in persons with DDD and C3GN and to compare these levels to persons without any kidney disease to determine whether the ‘profile’ for DDD and C3GN is unique. This technique is called ‘complement biomarker profiling’. Because the treatment of C3G is difficult, it is hoped that this type of information may provide clinicians with insight into what is happening at the level of the complement system in their patients with DDD and C3GN. One day, complement biomarker profiling may also help drive treatment decisions.


Causes



The immediate cause of the symptoms of C3G is the change in the filtering mechanism of the kidney. The damaged glomeruli (the filters) permit protein and red and white blood cells to pass into the urine-containing space.

The most abundant protein in the blood stream is albumin. As albumin passes into the urine and is lost from the blood stream, hypoalbuminemia or ‘low albumin in the blood stream’ develops. One consequence of hypoalbuminemia is that water leaks out of the circulation and accumulates in the surrounding tissues. This process leads to edema. Because of gravity and hydrostatic pressure (water pressure), the effects of fluid leakage are most apparent in the feet and ankles, which become swollen. As kidney function further deteriorates and urine output decreases, sodium and water are retained and the swelling becomes magnified. High blood pressure also develops.

The specific cause of C3G is lack of regulation of the complement system. The causes of complement dysregulation can be divided into genetic and acquired factors. Amongst the former are changes in many of the complement genes, and amongst the latter are specific antibodies called C3 nephritic factors or C3Nefs that impair normal regulation of the complement system. It appears that patients with DDD are more likely to have C3Nefs, while patients with C3GN are more likely to have abnormalities in a group of proteins called the ‘Complement Factor H Related’ proteins, although more research needs to be done in this area.


Affected Populations



C3G affects persons of all ages, although the mean age appears to be lower in DDD patients as compared to C3GN patients. The prevalence of C3G is estimated at 2-3 per 1,000,000 people.


Related Disorders



Many types of glomerular injury mimic C3G and cause signs and symptoms of acute glomerulonephritis. For example, amongst children, acute glomerulonephritis may reflect underlying IgA nephropathy, Henoch-Schonlein purpura, hemolytic uremic syndrome or post-infectious glomerulonephritis. Amongst adults, the list of disorders that trigger acute glomerulonephritis is longer and more varied, and includes Goodpasture’s syndrome, viral diseases such as mononucleosis, measles, or mumps, infective endocarditis, and sexually transmitted diseases.

One disease process that warrants more detailed mention is post-infectious glomerulonephritis or PIGN. PIGN typically follows an infection at a site other than the kidneys, such as a skin or throat infection, usually with a specific type of bacterium known as ‘Group A hemolytic streptococcus bacterium’. As a consequence of the streptococcal infection, the glomeruli may become plugged and inflamed, leading to inefficient filtering by the kidneys. Protein and blood will be present in the urine, and edema may develop throughout the body. Hypertension will occur. Fortunately, PIGN is rare because of the common use of antibiotics for infections that trigger this disease. However it still occurs and affects people of any age, especially children 6-10 years old. The onset of renal problems is about 1-2 weeks after a throat infection and about 3-4 weeks after a skin infection. Most frequently, PIGN resolves without the need for renal biopsy. Occasional cases of PIGN never get better but instead ‘evolve’ into DDD or C3GN.


Diagnosis



C3G can ONLY be diagnosed by a kidney biopsy. The kidney deposits stain for the complement protein C3 and when examined under an electron microscope, dense deposits are present.


Standard Therapies



There is currently no specific therapy for C3G, however a number of non-specific treatments are appropriate. These treatments slow progression of chronic glomerular diseases through aggressive blood pressure control and reduction of proteinuria. Both angiotensin-converting enzyme (ACE) inhibitors and angiotensin II type-1 receptor blockers (ARBs) are first-line drugs to decrease spillage of protein into the urine and to improve kidney hemodynamics. These drugs may also limit the infiltration of white blood cells into the kidney. If hyperlipidemia (increased lipid in the blood stream) is present, lipid-lowering drugs can be used to reduce long-term atherosclerotic risks. These drugs may also delay progression of kidney disease.

Although widely used at one point, steroid therapy is not effective in C3G. However it is effective in a form of glomerulonephritis called juvenile acute non-proliferative glomerulonephritis (JANG), which can be confused with DDD. JANG can be distinguished from DDD because: 1) DDD is associated with low C3 levels; and, 2) persons with DDD often have nephrotic syndrome (greater than 3.5 gm of protein in the urine over 24 hours; hypoalbuminemia; edema). In JANG, C3 levels remain at the lower limit of normal.

Recent studies suggest that mycophenolate mofetil (MMF) is beneficial in patients with C3GN and can decrease the rate of progression to end-stage kidney failure. MMF inhibits inosine monophosphate dehydrogenase, the enzyme that controls the rate of synthesis of guanine monophosphate. Studies have not shown a similar effect for DDD.

One anti-complement drug is widely available. Called Eculizumab, it is a humanized monoclonal antibody against C5 that blocks activity of the terminal pathway of complement. In a small number of studies that have looked at the effect of Eculizumab in patients with C3G, it appears that Eculizumab is effective in decreasing proteinuria and the rate of progression of kidney disease in some but not all patients. Identifying those patients who are likely to respond to Eculizumab is difficult, but it appears that elevated levels of soluble C5b-9 may be indicative of a good response. Soluble C5b-9 is one of the biomarkers of complement activity that is regularly measured when complement biomarker profiling is done, as was mentioned earlier.

Persons with C3G who progress to end-stage kidney failure must receive dialysis – either peritoneal dialysis or hemodialysis – or a kidney transplantation. Transplantation is associated with a high rate of disease recurrence in the allograft and about half of transplants ultimately fail.


Investigational Therapies



To date, only one anti-complement drug is available for medical use (see above). One investigational therapy using a drug called CDX-1135 (also known as soluble CR1) is open to recruitment and another trial using a small molecule anti-C3 agent may soon start, however additional therapies for C3G are needed. All clinical trials receiving U.S. Government funding and some trials supported by private industry are posted on www.clinicaltrials.gov.

For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:

Tollfree: (800) 411-1222
TTY: (866) 411-1010
Email: prpl@cc.nih.gov

For information about clinical trials sponsored by private sources, contact:
www.centerwatch.com

For information about clinical trials conducted in Europe, contact:
https://www.clinicaltrialsregister.eu/

Contact for additional information about this condition:
Richard JH Smith, MD
Director of the Iowa Institute of Human Genetics and the Molecular Otolaryngology and Renal Research Laboratories
University of Iowa
richard-smith@uiowa.edu


Supporting Organizations
Genetic and Rare Diseases (GARD) Information CenterPO Box 8126
Gaithersburg, MD 20898-8126
Phone: (301) 251-4925
Toll-free: (888) 205-2311
Website: http://rarediseases.info.nih.gov/GARD/

KidneedsThe Greater Cedar Rapids Community Foundation
324 3rd St. SE
Cedar Rapids, IA 52401
Email: kidneedsMPGN@yahoo.com
Website: http://www.healthcare.uiowa.edu/kidneeds/index.htm

National Kidney Foundation30 East 33rd Street
New York, NY 10016
Phone: (212) 889-2210
Toll-free: (800) 622-9010
Email: info@kidney.org
Website: http://www.kidney.org



References



JOURNAL ARTICLES
Bomback AS, Smith RJH, Barile GR, Zhang Y, Heher EC, Herlitz L, Stokes MB, Markowitz GS, D’Agati VD, Canetta PA, Radhakrishnan J, Appel GB. Eculizumab for Dense Deposit Disease and C3 Glomerulonephritis. Clin J Am Soc Nephrol 2012 Mar 8 [Epub ahead of print]; 7(5):748-56, 2012.

Bu F, Borsa NG, Jones MB, Takanami E, Nishimura C, Hauer JJ, Azaiez H, Black-Ziegelbein EA, Meyer NC, Kolbe DL, Li Y, Frees K, Schnieders MJ, Thomas C, Nester CM, Smith RJ. High-throughput genetic testing for the thrombotic microangiopathies and C3 glomerulopathies. J Am Soc Nephrol 2015 Aug 17 [Epub ahead of print].

Gurkan S, Fyfe B, Weiss L, Xiao X, Zhang Y, Smith RJ. Eculizumab and recurrent C3 glomerulonephritis. Pediatr Nephrol 2013 May 22 [Epub ahead of print]; 28(10):1975-81, 2013.

Nester CM, Smith RJ. Diagnosis and treatment of C3 glomerulopathy. Clin Nephrol 2013 Sep 2 [Epub ahead of print]; 80:395-403, 2013.

Nester CM, Smith RJ. Treatment options for C3 glomerulopathy. Curr Opin Nephrol Hypertens 22(2): 231-7, 2013.

Pickering MC, D’Agati VD, Nester CM, Smith RJ, Haas M, Appel GB, Alpers CE, Bajema IM, Bedrosian C, Braun M, Doyle M, Fakhouri F, Fervenza FC, Fogo AB, Frémeaux-Bacchi V, Gale DP, Goicoechea de Jorge E, Griffin G, Harris CL, Holers VM, Johnson S,Lavin PJ, Medjeral-Thomas N, Morgan BP, Nast CC, Noel L-H, Peters DK, Rodríguez de Córdoba S, Servais A, Sethi S, Song W-C, Tamburini P, Thurman JM, Zavros M, Cook TH. C3 glomerulopathy: consensus report. Kidney Inter 2013 Oct 30 [Epub ahead of print]; 84:1079-89, 2013.

Prasto J, Kaplan BS, Russo P, Chan E, Smith RJH, Meyers KEC. Streptococcal infection as possible trigger for Dense Deposit Disease (C3 glomerulopathy). Eur J Pediatr 2014 Jan 3 [Epub ahead of print]; 173(6):767-72, 2014.

Rabasco C, Cavero T, Román E, Rojas-Rivera J, Olea T, Espinosa M, Cabello V, Fernández-Juarez G, González F, Ávila A, Baltar JM, Díaz M, Alegre R, Elías S, Antón M, Frutos MA, Pobes A, Blasco M, Martín F, Bernis C, Macías M, Barroso S, de Lorenzo A, Ariceta G, López-Mendoza M, Rivas B, López-Revuelta K, Campistol JM, Mendizábal S, de Córdoba SR, Praga M. Effectiveness of mycophenolate mofetil in C3 glomerulonephritis. Kidney Int. 2015 Jul 29. doi: 10.1038/ki.2015.227.[Epub ahead of print].

Ruseva MM, Peng T, Lasaro MA, Bouchard K, Liu-Chen S, Sun F, Yu ZX, Marozsan A, Wang Y, Pickering MC. Efficacy of Targeted Complement Inhibition in Experimental C3 Glomerulopathy. J Am Soc Nephrol. 2015 Jun 5. pii: ASN.2014121195. [Epub ahead of print].

Sethi S, Fervenza FC, Zhang Y, Zand L, Meyer NC, Borsa N, Nasr SH, Smith RJH. Atypical post-infectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement. Kidney Inter 2012 Dec 12 [Epub ahead of print].

Sethi S, Fervenza FC, Zhang Y, Zand L, Vrana JA, Nasr SH, Theis JD, Dogan A, Smith RJH. C3 Glomerulonephritis: clinicopathologic findings, complement abnormalities, glomerular proteomic profile, treatment and follow-up. Kidney Inter 2012 Jun 6 [Epub ahead of print]; 82:465-73, 2012.

Xiao X, Pickering MC, Smith RJH. C3 Glomerulopathy: The genetic and clinical findings in Dense Deposit Disease and C3 Glomerulonephritis. Semin Thromb Hemost 2014 May 5 [Epub ahead of print]; 40(4):465-71, 2014.

Zand L, Lorenz EC, Cosio FG, Fervenza FC, Nasr SH, Gandhi MJ, Smith RJH, Sethi S. Clinical findings, pathology and outcomes of C3 glomerulonephritis following kidney transplantation. J Am Soc Nephrol 2013 Dec 19 [Epub ahead of print]; 25(5): 1110-7, 2014.

Zand L, Kettah A, Fervenza FC, Smith RJH, Nasr S, Zhang Y, Vrana JA, Leung N, Cornell LD, Sethi S. C3 glomerulonephritis associated with monoclonal gammopathy. Am J Kid Dis 2013 Apr 25 [Epub ahead of print]; 62(3):506-14, 2013.

Zhang Y, Meyer NC, Wang K, Nishimura C, Frees K, Jones M, Katz LM, Sethi S, Smith RJH. Causes of alternative pathway dysregulation in Dense Deposit Disease. Clin J Am Soc Nephrol 2012 Jan 5 [Epub ahead of print]; 7:265-74, 2012.

Zhang Y, Nester CM, Holanda DG, Marsh HC, Hammond RA, Thomas LJ, Meyer NC, Hunsicker LG, Sethi S, Smith RJH. Soluble CR1 therapy improves complement regulation in C3 glomerulopathy. J Am Soc Nephrol 2013 Aug 1 [Epub ahead of print]; 24:1820-1829, 2013.

Zhang Y, Nester CM, Martin B, Skjoedt MO, Meyer NC, Shao D, Borsa N, Palarasah Y, Smith RJ. Defining the complement biomarker profile of C3 glomerulopathy. Clin J Am Soc Nephrol 2014 Oct 23 [Epub ahead of print]; 9 (11):1876-82, 2014.

Zhang Y, Shao D, Ricklin D, Hilkin BM, Nester CM, Lambris JD, Smith RJH. Compstatin analog Cp40 inhibits complement dysregulation in vitro in C3 glomerulopathy. Immunobiol 2015 May 5 [Epub ahead of print]; 220(8):993-8, 2015.

Years Published
2005, 2010, 2013, 2015


The information in NORD’s Rare Disease Database is for educational purposes only and is not intended to replace the advice of a physician or other qualified medical professional.

The content of the website and databases of the National Organization for Rare Disorders (NORD) is copyrighted and may not be reproduced, copied, downloaded or disseminated, in any way, for any commercial or public purpose, without prior written authorization and approval from NORD. Individuals may print one hard copy of an individual disease for personal use, provided that content is unmodified and includes NORD’s copyright.

National Organization for Rare Disorders (NORD)
55 Kenosia Ave., Danbury CT 06810 • (203)744-0100

번호 제목 날짜
2659 어린이들이 잘 자라고 행복해야 그 나라가 좋은 나라가 될수 있습니다. 2017.05.24
2658 부부 관계를 원만하고 행복하는 데 필요한 중요한 12가지 조건을 나열하면 2017.05.11
2657 “3~5세 소아 성교육, 이럴 땐 어떻게 해야”에 관한 인터넷 소아청소년 건강상담 질의응답의 예 입니다. 2017.05.11
2656 제 19대 대한민국 대통령 문 재인 취임 말씀에서 2017.05.10
2655 ' 아들 딸 조건 없는 진정한 사랑라으로 키우세요 그리고 인성교육은 이렇게' 양서각 출간 2017.05.09
2654 다음은 “칭찬과 질투 우리아이 어떡하면”에 관한 인터넷 소아청소년 건강상담 질의응답의 예 입니다. 2017.05.08
2653 13장 가정과 학교 훈련을 위한 벌과 체벌 Punishment, Corporal punishment for training in Home and School 2017.05.07
2652 아기가 태어 날 때 모든 아빠는 분만하는 부인의 곁에서 기다리고 있다가 갓 태어난 아기와 부모-자녀 사랑 반딩을 형성하는 분만방법을 국가적인 차원에서 법으로 정하면 어떨까. 2017.05.07
2651 제12장 부모와 자녀의 대화 (부모-자녀 간 대화) 2017.05.07
2650 자녀 훈련을 시키는 부모의 자세와 방법 2017.05.07
2649 ▣ 아이들은 보는 대로 듣는 대로 배우고 자란다.Children are growing and learning what they see and what they hear 2017.05.06
2648 제10장 폴 통가스 미 상원의원의 자녀 사랑 Honorable Senator Paul Tsongus's love for his children 2017.05.06
2647 그릇 된 자녀 사랑 - 소유적 사랑, 유혹적 사랑, 대리적 사랑, 역할 전도적 사랑 Wrong love- Possessive love, Vicarious love, Seductive love, Role reversal love 2017.05.06
2646 제5장 타고난 9가지 기질, 25 퍼센타일 개성과 75 퍼센타일 개성 9 Inherent Different Temperaments, 25 Percentile Personality and 75 Percentile Personality 2017.05.05
2645 부부간에 조건 없는 진정한 사랑을 하는 법 2017.05.05
2644 다음은 “분노발작”에 관한 인터넷 소아청소년 건강상담 질의응답의 예 입니다. 2017.05.05
2643 ‘아들 딸 조건 없는 진정한 사랑으로 키우세요 그리고 인성교육은 이렇게’ 2017.05.05
2642 소아 학대와 소아 무관심(아동 학대와 아동 무관심/어린이 학대 와 어린이 무시 방치/아동 학대와 아동 무시) 2017.05.03
» C3 Glomerulopathy: Dense Deposit Disease and C3 Glomerulonephritis 2017.05.03
2640 안면도 출생 이상원 TOP 미국 소아청소년과 전문의가 되기까지 2017.05.03