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Research Letter |

Subretinal Drusenoid Deposits Associated With Complement-Mediated IgA Nephropathy FREE

David R. Lally, MD1; Caroline Baumal, MD1
[+] Author Affiliations
1Department of Ophthalmology, New England Eye Center, Vitreoretinal Service, Tufts University School of Medicine, Boston, Massachusetts
JAMA Ophthalmol. 2014;132(6):775-777. doi:10.1001/jamaophthalmol.2014.387.
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Published online

Complement-mediated IgA nephropathy is the most common cause of chronic glomerulonephritis worldwide. The pathogenesis of renal damage is related to complement activation secondary to IgA immune complex deposition in the glomerulus. To our knowledge, this is the first report of IgA nephropathy associated with bilateral subretinal drusenoid deposits (SDDs). A hypothesis for the role of complement is proposed.

A 42-year-old asymptomatic Asian woman was referred for fundus abnormality noted on routine examination. Family history was noncontributory. Medical history was significant for proteinuria and stage III kidney disease secondary to IgA nephropathy diagnosed 2 years previously. Renal biopsy demonstrated mesangial IgA deposition, expansion of the mesangial matrix, and positive direct immunofluorescence for complement C3 and C1q. Oral prednisone therapy was unsuccessful, and long-term treatment with mycophenolate mofetil was initiated.

Visual acuity was 20/20 OU with mild myopic correction. There were well-defined clusters of small yellow deposits in the macula with relative sparing of the central fovea (Figure 1). Spectral-domain optical coherence tomography (Cirrus; Carl Zeiss Meditec) revealed perifoveal hyperreflective convex deposits internal to the retinal pigment epithelium (RPE)–Bruch membrane band corresponding to the yellow deposits (Figure 2) and secondary elevation of the ellipsoid band with reduced reflectivity. There was poorly delineated granular reflectivity between the ellipsoid and interdigitation bands adjacent to the deposit.

Place holder to copy figure label and caption
Figure 1.
Fundus Photographs

Color fundus photographs of the right (A) and left (B) eyes show small, clustered, well-defined macular deposits with relative sparing of the central fovea.

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Place holder to copy figure label and caption
Figure 2.
Spectral-Domain Optical Coherence Tomographic Images

Spectral-domain optical coherence tomographic images of the right (A) and left (B) eyes showing focal hyperreflectivity internal to the retinal pigment epithelium–Bruch membrane (white arrowheads). B, There is a small elevation of the ellipsoid band that has slightly reduced reflectivity (black arrowhead). There is poorly defined granular hyperreflectivity adjacent to the focal deposits and internal to the retinal pigment epithelium–Bruch membrane. Insets, Magnified views of the spectral-domain optical coherence tomographic images.

Graphic Jump Location

Complement-mediated IgA nephropathy presents in young adulthood with macroscopic hematuria, while older adults develop proteinuria, microscopic hematuria, and/or hypertension. Renal biopsy is diagnostic, demonstrating IgA deposits in the glomerular mesangium with complement C3 deposition. The pathogenesis of IgA nephropathy involves an error in IgA1 glycosylation resulting in IgA1 secretion into the systemic circulation. The IgA1 forms complex deposits attached to extracellular matrix and mesangial cells within the glomerulus. This induces mesangial cells to release proinflammatory mediators and activate the complement system via lectin and alternative pathways.1

The perifoveal deposits in our case are located above the RPE on spectral-domain optical coherence tomography and are consistent with SDDs. These differ from typical drusen in age-related maculopathy, which are focal elevations located between the basal lamina of the RPE and the inner collagenous layer of the Bruch membrane. The SDDs are the histopathologic correlate of reticular pseudodrusen.2 They are located perifoveally where rod density is highest and have been demonstrated in age-related macular degeneration, adult vitelliform macular degeneration, pseudoxanthoma elasticum, and fundus albipunctatus.3 Composition of the SDDs is similar to that of soft drusen containing unesterified cholesterol, apolipoprotein E, and complement factor H (CFH).

The renal glomerulus basement membrane and RPE–Bruch membrane complex are similar physiologically and exposed to immune complexes in the systemic circulation. The systemic circulation plays an important role in binding complement to drusen components. In cell culture, RPE cells have low complement immunoreactivity with drusen components. However, when RPE cells are exposed to human serum, a striking activation of terminal C5b-9 complex bound to drusen components is observed.4

Circulating serum IgA1 complexes should respect the blood-retinal barrier and would be unlikely to deposit in the subretinal space where SDDs are located. One hypothesis is that IgA1 complexes deposit on the basal surface of the RPE cell, causing activation similarly as in the renal mesangium. Activated RPE cells can bidirectionally secrete lipoproteins, and SDD formation may develop after apical secretion.2 This is supported by studies demonstrating that CFH plays a role in the subretinal space. The CFH regulates the alternative pathway by binding to C3b and acting as a cofactor for complement factor I. In cultured polarized RPE cells, CFH localizes to the cell’s apical surface, and in CFH knockout mice, photoreceptor damage is observed with minimal sub-RPE change.5,6 Complement cross-reactivity may provide a link between SDDs and IgA nephropathy.

Corresponding Author: David R. Lally, MD, New England Eye Center, 260 Tremont St, Boston, MA 02116 (david.lally@gmail.com).

Author Contributions: Dr Lally had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Study concept and design: Lally, Baumal.

Acquisition, analysis, or interpretation of data: Lally, Baumal.

Drafting of the manuscript: Lally, Baumal.

Critical revision of the manuscript for important intellectual content: Lally, Baumal.

Statistical analysis: Lally, Baumal.

Administrative, technical, or material support: Lally.

Study supervision: Baumal.

Conflict of Interest Disclosures: None reported.

Funding/Support: This work was supported in part by an unrestricted award to the New England Eye Center, Tufts University School of Medicine from Research to Prevent Blindness.

Role of the Sponsor: Research to Prevent Blindness was involved in the design and conduct of the study but had no role in collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

Wyatt  RJ, Julian  BA.  IgA nephropathy. N Engl J Med. 2013;368(25):2402-2414.
PubMed   |  Link to Article
Curcio  CA, Messinger  JD, Sloan  KR, McGwin  G, Medeiros  NE, Spaide  RF.  Subretinal drusenoid deposits in non-neovascular age-related macular degeneration: morphology, prevalence, topography, and biogenesis model. Retina. 2013;33(2):265-276.
PubMed   |  Link to Article
Zweifel  SA, Spaide  RF, Yannuzzi  LA.  Acquired vitelliform detachment in patients with subretinal drusenoid deposits (reticular pseudodrusen). Retina. 2011;31(2):229-234.
PubMed   |  Link to Article
Johnson  LV, Forest  DL, Banna  CD,  et al.  Cell culture model that mimics drusen formation and triggers complement activation associated with age-related macular degeneration. Proc Natl Acad Sci U S A. 2011;108(45):18277-18282.
PubMed   |  Link to Article
Coffey  PJ, Gias  C, McDermott  CJ,  et al.  Complement factor H deficiency in aged mice causes retinal abnormalities and visual dysfunction. Proc Natl Acad Sci U S A. 2007;104(42):16651-16656.
PubMed   |  Link to Article
Kim  YH, He  S, Kase  S, Kitamura  M, Ryan  SJ, Hinton  DR.  Regulated secretion of complement factor H by RPE and its role in RPE migration. Graefes Arch Clin Exp Ophthalmol. 2009;247(5):651-659.
PubMed   |  Link to Article

Figures

Place holder to copy figure label and caption
Figure 1.
Fundus Photographs

Color fundus photographs of the right (A) and left (B) eyes show small, clustered, well-defined macular deposits with relative sparing of the central fovea.

Graphic Jump Location
Place holder to copy figure label and caption
Figure 2.
Spectral-Domain Optical Coherence Tomographic Images

Spectral-domain optical coherence tomographic images of the right (A) and left (B) eyes showing focal hyperreflectivity internal to the retinal pigment epithelium–Bruch membrane (white arrowheads). B, There is a small elevation of the ellipsoid band that has slightly reduced reflectivity (black arrowhead). There is poorly defined granular hyperreflectivity adjacent to the focal deposits and internal to the retinal pigment epithelium–Bruch membrane. Insets, Magnified views of the spectral-domain optical coherence tomographic images.

Graphic Jump Location

Tables

References

Wyatt  RJ, Julian  BA.  IgA nephropathy. N Engl J Med. 2013;368(25):2402-2414.
PubMed   |  Link to Article
Curcio  CA, Messinger  JD, Sloan  KR, McGwin  G, Medeiros  NE, Spaide  RF.  Subretinal drusenoid deposits in non-neovascular age-related macular degeneration: morphology, prevalence, topography, and biogenesis model. Retina. 2013;33(2):265-276.
PubMed   |  Link to Article
Zweifel  SA, Spaide  RF, Yannuzzi  LA.  Acquired vitelliform detachment in patients with subretinal drusenoid deposits (reticular pseudodrusen). Retina. 2011;31(2):229-234.
PubMed   |  Link to Article
Johnson  LV, Forest  DL, Banna  CD,  et al.  Cell culture model that mimics drusen formation and triggers complement activation associated with age-related macular degeneration. Proc Natl Acad Sci U S A. 2011;108(45):18277-18282.
PubMed   |  Link to Article
Coffey  PJ, Gias  C, McDermott  CJ,  et al.  Complement factor H deficiency in aged mice causes retinal abnormalities and visual dysfunction. Proc Natl Acad Sci U S A. 2007;104(42):16651-16656.
PubMed   |  Link to Article
Kim  YH, He  S, Kase  S, Kitamura  M, Ryan  SJ, Hinton  DR.  Regulated secretion of complement factor H by RPE and its role in RPE migration. Graefes Arch Clin Exp Ophthalmol. 2009;247(5):651-659.
PubMed   |  Link to Article

Correspondence

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