Journal Article

Zinc Supplementation Inhibits Complement Activation in Age-Related Macular Degeneration

Daha, Mohamed R., van der Wilt, Gert Jan, van Huet, Ramon A. C., Berendschot, Tos T. J. M., van de Ven, Johannes P. H., Fauser, Sascha, de Bruijn, Chris, Blom, Anna M., Klevering, B. Jeroen, Groenewoud, Joannes M. M., Tian, Yuan, Mohlin, Frida C., van Asten, Freekje, Lechanteur, Yara T. E., Smailhodzic, Dzenita, den Hollander, Anneke I., Hoyng, Carel B.

2014

Overview

Age-related macular degeneration (AMD) is the leading cause of blindness in the Western world. AMD is a multifactorial disorder but complement-mediated inflammation at the level of the retina plays a pivotal role. Oral zinc supplementation can reduce the progression of AMD but the precise mechanism of this protective effect is as yet unclear. We investigated whether zinc supplementation directly affects the degree of complement activation in AMD and whether there is a relation between serum complement catabolism during zinc administration and the complement factor H (CFH) gene or the Age-Related Maculopathy susceptibility 2 (ARMS2) genotype. In this open-label clinical study, 72 randomly selected AMD patients in various stages of AMD received a daily supplement of 50 mg zinc sulphate and 1 mg cupric sulphate for three months. Serum complement catabolism-defined as the C3d/C3 ratio-was measured at baseline, throughout the three months of supplementation and after discontinuation of zinc administration. Additionally, downstream inhibition of complement catabolism was evaluated by measurement of anaphylatoxin C5a. Furthermore, we investigated the effect of zinc on complement activation in vitro. AMD patients with high levels of complement catabolism at baseline exhibited a steeper decline in serum complement activation (p<0.001) during the three month zinc supplementation period compared to patients with low complement levels. There was no significant association of change in complement catabolism and CFH and ARMS2 genotype. In vitro zinc sulphate directly inhibits complement catabolism in hemolytic assays and membrane attack complex (MAC) deposition on RPE cells. This study provides evidence that daily administration of 50 mg zinc sulphate can inhibit complement catabolism in AMD patients with increased complement activation. This could explain part of the mechanism by which zinc slows AMD progression. The Netherlands National Trial Register NTR2605.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: Age / Age related diseases / Aged / Aged, 80 and over / Andra medicinska och farmaceutiska grundvetenskaper / Basic Medicine / Biology and Life Sciences / Blindness / Catabolism / Cells, Cultured / Complement / Complement activation / Complement Activation - drug effects / Complement C3 - immunology / Complement C3 - metabolism / Complement C3d - immunology / Complement C3d - metabolism / Complement C5a - immunology / Complement C5a - metabolism / Complement component C3 / Complement component C5a / Complement Factor B - immunology / Complement Factor B - metabolism / Complement factor H / Complement Factor H - immunology / Complement Factor H - metabolism / Complement system / Copper Sulfate - administration & dosage / Dietary Supplements / Epithelial Cells - cytology / Epithelial Cells - drug effects / Epithelial Cells - immunology / Eye diseases / Fatty acids / Female / Gene Expression / Humans / Hypotheses / Inflammation / Laboratories / Macular degeneration / Macular Degeneration - blood / Macular Degeneration - diet therapy / Macular Degeneration - immunology / Macular Degeneration - pathology / Male / Medical and Health Sciences / Medicin och hälsovetenskap / Medicine and Health Sciences / Medicinska och farmaceutiska grundvetenskaper / Membrane attack complex / Mutation / Other Basic Medicine / Patients / Peritoneal dialysis / Proteins - genetics / Proteins - immunology / Retina / Retina - drug effects / Retina - immunology / Retina - pathology / Retinal Pigment Epithelium - cytology / Retinal Pigment Epithelium - drug effects / Retinal Pigment Epithelium - immunology / Sulfates / Systematic review / Zinc / Zinc Sulfate - administration & dosage