Daria Pašalić
Department of Medical Chemistry, Biochemistry and Clinical Chemistry
Zagreb University School of Medicine
Šalata ul 2.
10 000 Zagreb, Croatia
Phone +385 (1) 4590 205; +385 (1) 4566 940
E-mail: dariapasalic [at] gmail [dot] com

Useful links


Emina Colak1*, Nada Majkic-Singh1, Lepsa Zoric2, Aleksandra Radosavljevic2, Natalija Kosanovic-Jakovic2. The role of CRP and inflammation in the pathogenesis of age-related macular degeneration. Biochemia Medica 2012;22(1):39-48.
1Institute of Medical Biochemistry, Clinical Center of Serbia and Farmaceutical Faculty, University of Belgrade, Belgrade, Serbia
2Institute of Ophthalmology, Medical Retina Department, Clinical Center of Serbia and Medical Faculty, University of Belgrade, Belgrade, Serbia
*Corresponding author: eminacolak [at] sbb [dot] rs
Age-related macular degeneration (AMD) is a complex, degenerative and progressive disease involving the multiple genetic and environmental factors that can result in severe visual loss. The etiology of AMD is not well understood. Many theories exist and feature mechanisms of oxidative stress, atherosclerotic-like changes, genetic predisposition and inflammation. The most recent clinical studies appointed to a great role of inflammation and C-reactive protein (CRP) in the pathogenesis of AMD. There is a large body of evidence indicating the association of CRP with endothelial dysfunction, oxidative stress and production of reactive oxygen species (ROS), as well as with lipid status disorder in AMD patients. According to recent studies, CRP is definitely not only the inflammatory marker but also a mediator of development of the vascular disorders in the retinal circulation. The results obtained from the present studies may help our understanding the pathogenesis of the retinal vascular disease associated with high levels of CRP.
Key words:age-related macular degeneration; C-reactive protein; inflammation
Received: July 28, 2011                                                                                                                                          Accepted: November 30, 2011
Age-related macular degeneration (AMD) is the most common cause of visual impairment in the individuals over 50 years of age, with the prevalence of 0.05% before the age of 50 rising to 30% after 74 years of age. It is a complex, degenerative and progressive disease involving the multiple genetic and environmental factors that can result in severe visual loss. The molecular mechanisms causing the AMD remain unknown, although inflammatory processes have been implicated by identification of the AMD susceptibility genes encoding complement factors (1) and the presence of the complement proteins in drusen (2).
One of the pathological hallmarks of AMD is the focal deposition of the extracellular material between the retinal pigmented epithelium (RPE) and Bruch’s membrane called drusen. Drusen are visualised as yellow deposits under the retinal pigment epithelium and neurosensory retina and are associated with atrophy and depigmentation of the overlying retinal pigment epithelium. Although a few small (< 65 μm) hard drusen can be found in at least 96% of aged population, the presence of a numerous larger (> 125 μm) hard drusen, and especially large, soft drusen (125-250 μm) in the macula is considered particularly when accompanied by pigment irregularities or depigmentation a major risk factor for developing the advanced form of AMD (3). The material, referred to as drusen is composed of several cellular and humoural constituents of systemic inflammatory and immune mediated processes such as HLA-DR, immunoglobulin λ and κ light chains, complement components 5 and 9, amyloid A, amyloid P component, fibrinogen, vitronectin and C-reactive protein (4). Moreover, the accumulation of drusen can damage the surrounding structures, inculding Bruch’s membrane, and is associated with visual deficit that precede the loss of visual accuity in AMD (5).
The aetiology of AMD is not well understood. Many theories exist and feature mechanisms of oxidative stress, atherosclerotic-like changes, genetic predisposition and inflammation (6).
Risk factors for AMD
Several risk factors have been postulated to take an important role in development of AMD. Age is the strongest risk factor for AMD. The prevalence of AMD increases with age in white individuals (7). Female gender may be a risk factor in individuals aged over 75 years with the relative risk for neovascular form of AMD as much as twice that observed in age-matched men (8).
AMD is more common in white individuals than in people of other ethnic origin (9). It is postulated that increased levels of melanin could increase the free-radical scavenging potential of the RPE and Bruch’s membrane, thereby protecting against the risk of AMD (10). Several studies have found an association between advanced AMD and complement factor H, an integral component of the alternative pathway of complement activation (11). Other factors such as factor B and complement components C2 and C3 are also associated with AMD (12). A few clinical trials showed a relationship between the development of exudative lesions and a history of current cigarette smoking. Smoking increases the risk of the exudative type of AMD 2.8 times for females and 3.2 times for current smokers in men. Smoking cessation lowers the relative risk of AMD (13). Some studies have shown a direct association between age-related macular degeneration and raised concentration of cholesterol both in the serum (14) and in the diet (15). Increased concentration of HDL-cholesterol is considered to be cardioprotective have been shown to be associated with a reduced risk of AMD (16).
Several studies have described the beneficial effects of dietary carotenoids in slowing the course of the disease. A multicentre randomized trial has shown that oral supplementation with high levels of antioxidants and minerals are effective in slowing the progression of advanced stages of AMD (17). Some case-control studies have found evidence of decreasing risk of neovascular AMD among individuals reporting the highest intake of omega-3 fatty acids and fish (18). The use of exogenous supplements of oestrogen in post-menopausal women was associated with a lower risk of AMD in a study performed by the Eye Case Control Study Group (17).
It has been postulated that light plays a role in the development of AMD.It has been hypothesized that the photosensitization reactions may be involved in the development of AMD, via synthesis of the reactive oxygen species such as: superoxide, hydrogen peroxide, and singlet oxygen, which may damage the RPE and Bruch’s membrane (19). Blue iris color has been inconsistently implicated as a risk factor for AMD (20). Results from Beaver Dam Study suggest that people who spent leisure time outdoors were at increased risk of developing early AMD (21).
Chronic conditions and diseases such as atherosclerosis (22), diabetes (23) and cardiovascular diseases (24) as well are known as risk factors for AMD.
The pathological features of AMD
The pathology of age-related macular degeneration is characterized by degenerative changes involving the outer portion of the retina, retinal pigment epithelium, Bruch’s membrane, and less prominently the choriocapillaris. AMD may be classified into three forms: early, intermediate, and advanced. The early and intermediate forms account for 90% of all cases. In contrast, the advanced form accounts for 88% of all cases of blindness attributable to AMD. The earliest signs of AMD are discrete yellow deposits in the deep layers of the macula, known as drusen. Furthermore, areas of pigmentary disturbance may be observed in the underlying retinal pigment epithelium of the macula. Visual loss associated with these changes may be gradual, resulting from atrophy of the retinal pigment epithelium and the overlying photoreceptors. In addition, the early form of AMD may progress to the intermediate and advanced forms.
Although the advanced form of AMD is less common than the early and intermediate forms, the potential visual loss with advanced AMD is more significant. Advanced AMD has two clinical subtypes. Wet AMD (exudative or neovascular AMD) is the more common subtype and is characterized by proliferation of abnormal vessels in the choroid (a highly vascular area between the sclera and the retinal pigment epithelium). These choroidal neovascular membranes may proliferate into the subretinal space and retina and leak fluid and blood, causing damage and loss of vision. Other features of wet AMD are detachment of the retinal pigment epithelium and fibrosis, often termed a disciform scar, which forms in the late stages of the disease (25).
Pathologic states such as hypoxia, ischemia, or inflammation may tip the balance of proangiogenic and antiangiogenic factors in favor of the formation of new blood vessels. Vascular endothelial growth factor (VEGF) is pivotal in ocular angiogenesis because it is highly selective for endothelial cells, hypoxia drives its synthesis, it diffuses to its target, and it affects multiple components of angiogenesis such as endothelial cell proliferation, survival, and migration. Basic and clinical research implicates VEGF in the pathogenesis of choroidal neovascularization (CNV). Therefore, intravitreal drugs that block VEG have revolutionized the care of patients with neovascular AMD, decreasing growth and leakage from choroidal neovascular lesions and preventing moderate and severe vision loss associated with this process (26,27).
The second subtype of advanced AMD (the dry AMD form) involves atrophy, which progresses to visually significant structures of the retina, such as the fovea, which is responsible for the sharpest and central visual acuity. Progressive atrophy over a large area is termed geographic atrophy and may result in severe visual loss. Geographic atrophy is seen as normal RPE with hypotrophy, hypertrophy hypo- or hyperpigmentation, atrophy, migration, loss of outer retinal cells, attenuation of Bruch’s membrane and choriocapillaris degeneration (28).
The role of inflammation in the pathogenesis of AMD
There is mounting evidence from laboratory based studies that inflammation plays a key role in the pathogenesis of AMD (4,6,29). The inflammatory marker CRP has recently been shown to be an independent risk for cardiovascular and peripheral arterial disease (30-32) and a pathogenic factor leading to endothelial dysfunction in the cell culture model (33). Moreover, elevated concentration of CRP has been associated with an increased risk for hypertension (34), and for type 1 and type 2 diabetes mellitus (35). Because hypertension and diabetes are considered major risk factors for retinal vascular disorders, their association with inflammation and endothelial dysfunction has been suggested in humans with retinopathy (36).
Atherosclerosis is a known risk factor for AMD, most likely through decreased choroidal blood flow, directly or indirectly impairing the functioning of the RPE(37,38). Atherosclerosis is also associated with elevated hsCRP concentration, which may contribute to the higher risk of AMD (39).
Local inflammatory and immune-mediated events play a role in the development of drusen (40-42). Direct analysis by liquid chromatography and immunocytochemical analyses confirmed that drusen contain proteins associated with inflammation such as fibrinogen, vitronectin, complement components and C-reactive protein (CRP) (43). Some of these proteins seem to be locally produced by damaged retinal pigment epithelium cells (42). Drusen components have been found in atheroscerotic plaques and deposits in Alzheimer disease (44), and AMD, atherosclerosis and Alzheimer disease may partly share a similar inflammatory pathogenesis.
The AMD lesion formation has been conceptualized as sharing mechanisms with atheroscerotic plaque formation, where LDL retention within the arterial wall initiates a cascade of pathologic events called the “response to retention hypothesis” (45). In atheroscelrosis Apo B100 lipoproteins become oxidatively modified. This modification stimulates different biological processes including innate immune system-mediated inflammation which induce a cascade of pathological events than culminate in atherosclerotique plaques (46). In AMD, the following evidence supports the “response to retention” hypothesis:
·         Apo B100-containing lipoproteins accumulate in Bruch’s membrane in the same location as basal deposits in drusen;
·         oxidatively modified proteins and lipids are present in Bruch’s membrane and RPE inducing a pathologic phenotype to RPE cells (47); and
·         the accumulation of inflammatory mediators whitin drusen and basal deposites indicates a role for the innate immune response (48).
Oxidized lipoproteins can trigger complement activation (46). CD36 is the major receptor implicated in uptaking the oxidized low density lipoproteins and is expressed also in RPE cells. It has been suggested that CD36 may have a role not only in the clearance of oxidized lipids from Bruch’s membrane (49) but also in the subsequently inducing an immune response (50).
In addition to aforementioned facts, the presence of matrix matalloproteinases (MMPs) in higher concentration in the Bruch’s membrane and RPE cells, especially MMP-2 and MMP-9 indicate to more similarity between atherosclerotic plaque and AMD lesion formation. It is known that MMP-2 and MMP-9 are implicated in the degradation of extracellular matrix components which can lead to plaque destabilization and rupture and subsequent future cardiovascular events, especially acute myocardial infarction (AMI) (51).
Chronic inflammation seems to be a causative factor for the development of AMD. Chronic inflammation results in endothelial dysfunction and facilitates the interactions between modified lipoproteins, monocyte-derived macrophages, T-cells and normal cellular elements of the retinal arterial wall (52). Macrophages are often seen in the area of geographic atrophy and are apparently phagocytosing pigment debris, as seen by electron microscopy or immunohistochemistry methods (44,53). Macrophages have been documented both morphologically and functionally in neovascular AMD (54). Activated macrophages and microglia may secrete chemokines and citokines, causing further cellular damage, Bruch’s membrane degradation and angiogenesis (55).
The human eye is known to produce significant quantities of 7-ketocholesterol and related substances as a direct result of photoreceptor function. In atherosclerosis oxysterols contribute to the conversion of macrophages into foam cells (56). 7-ketocholesterol has recently been found to be localized in deposits within the choriocapilaris and Bruch’s membrane of aging monkies (57). Oxysterols have cytotoxic and inflammatory properties on RPE cells inducing reactive oxygen species generation, glutathione depletion, and reduced mitochondrial membrane potential inflammation through activation of NFkB and eventually apoptotic-mediated cell death in cultured RPE cells (58).
Recently, a strong association between the Y402H single-nucleotide polymorphism in the complement factor H (CFH) gene and AMD was found in 3 clinic-based case control studies (59), and in a longitudinal population based study (60). Complement factor H is an essential regulator in the complement system. It activates C3b and functions as an activation inhibitor of the alternative complement pathway (61). This single-nucleotide polymorphism is located in a region that contains the binding sites for heparin and CRP. Complement factor H binds to CRP, which may help inhibit the CRP-dependent alternative pathway activation induced by damaged tissue (61). Complement factor H tends to prevent the assembly of complement complex in the arterial intima (62). It has been suggested that allele-specific changes in activities of the binding sites for heparin and CRP modify the protective action of complement factor H (63). Complement-related damage to choroidal vessels might lead to wet AMD (11). It is possible that reduction of CRP levels might lower the risk of AMD. Some recently published papers indicated that CFH binds to the denaturated rather than native CRP thus casting some doubt upon this link between CFH and CRP(64). It is also possible that persistent chronic inflammation that is a byproduct of attenuated complement-inhibitory activity may occur in those individuals with the risk-conferring CFH SNP Y402H and that this pro-inflammatory state, rather than impaired binding by CFH, leads to CRP accumulation in AMD retina. Alternatively, the role of CFH in AMD might be completely independent of CRP. Without a doubt, further studies are necessary to dissect the role, if any, of the CFH Y402H SNP in AMD pathogenesis. Deangelis and coworkers stated that there was a clear genetic influence on AMD, and the loci 1q33 (CFH) and 10q26 (PLEKHA1/ARMS2/HTRA1) were the most strongly associated with AMD, but the variation of these genomic regions alone were unable to predict disease development with high accuracy (65). Lederman et al. demonstrated that neovascular AMD was associated with altered gene expression in peripheral white blood cells that was not underlined by the major risk single nucleotide polymorphisms, and suggested that such altered expression may potentially serve as a biomarker for the disease (66). Increased levels of annexin A5 (ANXA5) mRNA transcripts were also found in the WBC of patients with AMD. ANXA5 which plays a role in the regulation of blood clot has been found in atherosclerotic plaques and is proposed to have and anti-inflammatory functions (67). Interestingly, other annexins were previously identified in drusen (68). Recent studies have revealed profound developmental consequences of mutations in genes encoding proteins of the lectin pathway of complement activation, a central component of the innate immune system. Apart from impairment of immunity against microorganisms, it is known that hereditary deficiencies of this system predispose one to autoimmune conditions. Polymorphisms in complement genes are linked to, for example, atypical hemolytic uremia and age-dependent macular degeneration. The recently discovered lectin pathway is less studied, but polymorphisms in the plasma pattern-recognition molecule mannan-binding lectin (MBL) are known to impact its level, and polymorphisms in the MBL-associated serine protease-2 (MASP-2) result in defects of complement activation (69).
Association of CRP with AMD
Several recent clinicalstudies suggest close association between serum CRP and ocular vascular disorders related to AMD.One recent study (70) demonstrated a close positive association between CRP and cholesterol levels (especially total cholesterol, LDL- and non-HDL cholesterol levels) in patients with AMD. AMD patients who had higher values of total-, LDL- and non-HDL-cholesterol values had also higher CRP values. This group of investigators succeeded to demonstrate a significant association between incidence of AMD and CRP levels, especially between occurrence of AMD and CRP levels higher than 3 mg/L. Several recent clinical studies reported that patients with the highest quartile of CRP (over 6.5 μg/mL) are at high risk of AMD (5,71). In addition, more than threefold higher incidence of AMD was found in women with serum CRP levels exceeding 5 μg/mL (5,71). The concentrations of CRP used in the study of Nagaoka (30) (0.7 and 7 μg/mL) covered the physiological and pathophysiological ranges, and only high level of CRP exhibited inhibitory action in endothelium-dependent vasomotor function. It appears that CRP levels known to predict cardiovascular events produce adverse effects on endothelial function in the retinal microvasculature. C-reactive protein (CRP) is an inflammatory marker known to be associated with cardiovascular disease, and a link between AMD and CRP has been suggested. Hong et al. (72) in his systematic review summarize the currently available evidence from clinic-based and population-based studies investigating this association. Their meta-analysis shows that high serum levels (> 3 mg/L) of CRP are associated with a two-fold likelihood of late onset AMD, compared to low levels (< 1 mg/L).
De Jong et al. (73) showed, in the Rotterdam study,the existence ofa small significantassociation between log CRP levels and AMD incident. Kikuchi et al. (74) demonstrated the trends of the increased risk of disease with the increase of CRP, which were statistically significant for both polypoidal choroidal vasculopathy (PCV) and neovascular AMD. The Rotterdam study (38) found that elevated baseline levels of high sensitive CRP (HsCRP) were associatedwith the development of early and late AMD in the large population-basedcohort. Boey et al. (75) demonstrated no associations betweenCRP and AMD or cataract in general population of the Asian people, while higherCRP was associated with AMD in individuals without diabetes.
Possible mechanism for CRP dependent-oxidative stress and lipid disorder
The inflammatory reaction is an important source of the oxygen-free radicals. Large amounts of superoxide radicals are secreted by activated phagocytic leukocytes, and also formed as by-product during biosynthesis of leukotrienes and prostaglandins and formation of lipid peroxides.
Proinflammatory cytokines play a central role in mediating the cellular and physiological responses. Non-enzymatic oxidative modification mediated by reactive oxygen speciestransforms low density lipoprotein (LDL) to an atherogenic molecule (E-LDL) that activates complement and macrophages and is present in the early atherosclerotic lesions and drusen. E-LDL accumulates in the human vascular smooth muscle cells (VSMC) where promotes angiotensin type 1 receptor (AT1-R) upregulation and stimulates VSMC migration proliferation and neointimal formation while concomitantly increasing reactive oxygen species (ROS) production. A growing body of evidence implicates CRP as a direct mediator of endothelial dysfunction. CRP directly upregulates endothelial cell adhesion molecules: ICAM-1, VCAM-1 and E-selectin, which play a key role in facilitating the leukocyte-endothelial interaction. CRP also promotes the release of MCP-1 a key chemoatractant chemokine which facilitates leukocyte transmigration through the endothelium (11,76). Recent studies suggest that CRP also promotes nuclear factor (NF)-κB upregulation in endothelial cells (77). In that way CRP functions as an active participant in lesion formation and hence is directlly linked to atherosclerosis.
CRP is capable of generating the TEMPOL-sensitive superoxide in the endothelial layer of the retinal arterioles. This finding is consistent with recent evidence showing that CRP can increase the production of superoxide in cultured human aortic endothelial cells and in porcine coronary arterioles (78). Clinical study of Fichtlscherer (79) reported that the increase of oxidative stress and the reduction of NO bioavailability were closely related to elevation of plasma CRP in patients with the coronary artery disease. The findings of Nagaoka (30) suggested that detrimental effects of CRP could also affect the ocular circulation and might partially contribute to development of the retinal vascular disease.
It has been demonstrated that CRP, in concentration known to predict vascular disease, directly inhibits the endothelium-dependent NO-mediated dilation of the isolated porcine retinal arterioles. The mechanism underlying the acute effect of CRP involves the activation of p38 kinase and the production of superoxide by vascular NAD(P)H oxidase. Recent clinical studies have demonstrated that statins are beneficial by preserving the endothelial function, possibly through the inactivation of the RhoA/Rho-kinase pathway and reduction of the oxidative stress. Since the impaired endothelium-dependent NO-mediated dilation is a key feature of the early vascular events, it is clear that CRP is not only an inflammatory marker but also a mediator of development of vascular disorders in the retinal circulation. Reductions in inflammation and oxidative stress or inhibition of RhoA/Rho-kinase activity (for example by statins) have been reported to improve endothelial function (80,81).
It has been demonstrated that human CRP could be bound with highest affinity to phosphocholine residues, but it also binds to a variety of other autologous and extrinsic ligands, and it aggregates or precipitates the cellular and molecular structures bearing these ligands. Autologous ligands include native and modified plasma lipoproteins, damaged cell membranes, a number of different phospholipids and related compounds, small nuclear ribonucleoprotein particles, and apoptotic cells. Binding of CRP to lipids, especially lecithin (phosphatidyl choline), and to plasma lipoproteins has been documented to be the first step in generation of foam cells and atherogenesis (82). It has been also demonstrated that aggregated, but not native, non-aggregated, CRP selectively binds only LDL and some VLDL particles from the whole serum. Native CRP does bind to oxidized LDL and to partly degraded LDL, as found in atheromatous plaques (83). When aggregated or bound to macromolecular ligands, human CRP is recognized by C1q and potently activates the classical complement pathway, engaging C3, the main adhesion molecule of the complement system, and the terminal membrane attack complex, C5–C9. Bound CRP may also provide secondary binding sites for factor H and thereby regulate alternative-pathway amplification and C5 convertases (84).
According to recent studies, CRP is definitely not only the inflammatory marker but also a mediator for development of the vascular disorders in the retinal circulation. The results obtained from the present studies may help our understanding the pathogenesis of the retinal vascular disease associated with high levels of CRP. Since there is no cure for AMD, prevention is the first approach to reduce vision loss. Control of modifiable risk factors such as smoking, hypertension, hyperlipoproteinemia, oxidative stress and chronic inflammation could reduce the risk of developing AMD.
·         The choroid, also known as the choroidea or choroid coat, is the vascular layer of the eye, containing connective tissue, and lying between the retina and the sclera (85).
·         Retina is a light-sensitive tissue lining the inner surface of the eye. The optics of the eye create an image of the visual world on the retina, which serves much the same function as the film in a camera (86).
·         The pigmented layer of retina or retinal pigment epithelium (RPE) is the pigmented cell layer just outside the neurosensory retina that nourishes retinal visual cells, and is firmly attached to the underlying choroid and overlying retinal visual cells (87).
·         The fovea centralis, also generally known as the fovea, is a part of the eye, located in the center of the macula region of the retina. The fovea is responsible for sharp central vision (also called foveal vision), which is necessary in humans for reading, watching television or movies, driving, and any activity where visual detail is of primary importance (88).
·         The macula or macula lutea (from Latin macula, “spot” + lutea, “yellow”) is an oval-shaped highly pigmented yellow spot near the center of the retina of the human eye, and acts as a natural sunblock (analogous to sunglasses) for this area of the retina. The yellow colour comes from its content of lutein and zeaxanthin (89).
·         The sclera (from the Greek skleros, meaning hard, also known as the white or white of the eye, is the opaque (usually white, though certain animals, such as horses and lizards, can have black sclera), fibrous, protective, outer layer of the eye containing collagen and elastic fiber (90).
·         Bruch’s membrane is located between RPE and choroid and it represents a semipermeable filtration barrier through which major metabolic exchange take place (91).
This work was supported by the Ministry of Science of Serbia through contract No175036.
Potential conflict of interest
None declared.
 1. Gu J, Pauer GJT, Yue X, Narendra U, Sturgill GM, Bena J, et al. Proteomic and Genomic Biomarkers for Age-Related Macular Degeneration. Adv Exp Med Biol 2010;664:411–7.
 2. Edwards AO, Ritter R III, Abel KJ, Manning A, Panhuysen C, Farrer LA. Complement factor H polymorphism and age-related macular degeneration. Science 2005;308:421–4.
 3. Nowak J. Age-related macular degeneration (AMD): pathogenesis and therapy. Pharmacol Rep 2006;58:353-63.
 4. McGwin G, Hall TA, Xie A, Owsley C. The regulation between C reactive protein and age related macular degeneration in the Cardiovascular Health Study. Br J Ophthalmol 2005;89:1166–70.
 5. Seddon J, Gensler G, Milton R, Klein ML, Rifai N. Association between C-reactive protein and age-related macular degeneration. JAMA 2004;291:704–10.
 6. Zarbin MA. Current concepts in the pathogenesis of age-related macular degeneration. Arch Ophthalmol 2004;122:598–614.
 7. Coleman HR, Chan CC, Ferris FL, Chew EY. Age-related macular degeneration. Lancet 2008;372:1835–45.
 8. Smith W, Assink J, Klein R, Mitchell P, Klaver CC, Klein BE, et al. Risk factors for age-related macular degeneration: pooled findings from three continents. Ophthalmology 2001;108:697–704.
 9. Klein R, Klein BE, Jenson SC, Mares-Perlman JA, Cruickshanks KJ, Palta M, et al. Age-related maculopathy in a multiracial United States population: the National Health and Nutrition Examination Survey III. Ophthalmology 1999;106:1056–65.
10. Hu DN, Simon JD, Sarna T. Role of ocular melanin in ophthalmic physiology and pathology. Photochem & Photobiol 2008;84:639–44.
11. Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, et al. Complement factor H polymorphism in age-related macular degeneration. Science 2005;308:385–9.
12. Yates YR, Sepp T, Matharu BK. Complement C3 variant and the risk of age-related macular degeneration. N Engl J Med 2007;357:19–27.
13. O’Shea JG. Age-related macular degeneration. Postgrad Med J 1998;74:203-7.
14. Tomany SC, Wang JJ, van Leeuwen R, Klein R, Mitchell P, Vingerling JR, et al. Risk factors for incident age-related macular degeneration. Pooled findings from 3 continents. Ophthalmology 2004;111:1280–7.
15. Mares-Perlman JA, Brady WE, Klein R, VandenLangenberg GM, Klein BE, Palta M. Dietary fat and age-related maculopathy. Arch Ophthalmol 1995;113:743–8.
16. Hyman L, Schachat AP, He Q, Leske MC. Hypertension, cardiovascular disease, and age-related macular degeneration. Arch Ophthalmol 2000;118:351–8.
17. Age-Related Eye Disease Study Research Group. The Age-Related Eye Disease Study Research Group. A randomized, placebo-controlled, clinical trial of high-dose supplementation with vitamins C and E, beta carotene, and zinc for age-related macular degeneration and vision loss. Arch Ophthalmol 2001;119:1417–36.
18. SanGiovanni JP, Chew EY, Clemons TE, Davis MD, Ferris FL 3rd, Gensler GR, et al. The relationship of dietary lipid intake and age-related macular degeneration in a case-control study. Arch Ophthalmol 2007;125:671–9.
19. Winkler BS, Boulton ME, Gottsch JD, Sternberg P. Oxidative damage and age-related macular degeneration. Molecular Vision 1999;5:32–45.
20. Klein R, Klein BE, Jensen SC, Cruickshanks KJ. The relationship of ocular factors to the incidence and progression of age-related maculopathy. Arch Ophthalmol 1998;116:506–13.
21. Klein R, Klein BE, Jensen SC, Cruickshanks KJ. Sunlight and the 5-year incidence of early age-related maculopathy: the Beaver Dam Eye Study. Arch Ophthalmol 2001;119:246–50.
22. Chakravarthy U, Wong TY, Fletcher A, Piault E, Evans C, Zlateva G, et al. Clinical risk factors for age-related macular degeneration: A systemic review and meta-analysis. BMC Ophthalmol 2010;10:31.
23. Choi JK, Lym YL, Moon JW, Shin HJ, Cho B. Diabetes mellitus and early age-related macular degeneration. Arch Ophthalmol 2011; 129:196-9.
24. Tan JS, Mitchell P, Smith W, Wang JJ. Cardiovascular risk factors and long-term incidence of age.related macular degeneration: the Blur Mountains Eye Study. Ophthalmology 2007;114:1143-50.
25. Bourla DH, Young TA. Age-Related Macular Degeneration:a practical approuch to a challenging disease. J Am Geriatr Soc 2006;54:1130–5.
26. Bressler SB. Introduction: Understanding the Role of Angiogenesis and Antiangiogenic Agents in Age-Related Macular Degeneration. Ophthalmology 2009;116:S1-7.
27. Yuan A, Kaiser PK. Emerging therapies for the treatment of neovascular age related macular degeneration. Semin Ophthalmol 2011;26:149-55.
28. McLeod DS, Taomoto M, Otsuji T, Green WR, Sunness JS, Lutty GA. Quantifying changes in RPE and choroidal vasculature in eyes with age-related macular degeneration. Invest Ophthalmol Vis Sci 2002;43:1986–93.
29. Johnson LV, Ozaki S, Staples MK, Erickson PA, Anderson DH. A potential role for immune complex pathogenesis in drusen formation. Exp Eye Res 2000;70:441–9.
30. Nagaoka T, Kuo L, Ren Y, Yoshida A, Hein TW. C-reactive protein inhibits endothelium-dependent nitric oxide-mediated dilatation of retinal arterioles via enhanced superoxide production. Invest Ophthalmol Vis Sci 2008;49:2053–60.
31. Simundic AM. New insights in the pathophysiology of inflammation. Biochem Med 2011;21:243-4.
32. Thiruvagounder M, Khan S, Sheriff DS. The prevalence of metabolic syndrome in a local population in India. Biochem Med 2010;20:249-52.
33. Mueck AO, Seeger H, Wallwiener D. Further evidence for direct vascular actions of statins: effect on endothelial nitric oxide synthase and adhesion molecules. Exp Clin Endocrinol Diabetes 2001;109:181–3.
34. Sesso HD, Buring JE, Rifai N, Blake GJ, Gaziano JM, Ridker PM. C-reactive protein and the risk of developing hypertension. JAMA 2003;290:2945–51.
35. Chase HP, Cooper S, Osberg I, Stene LC, Barriga K, Norris J, et al. Elevated C-reactive protein levels in the development of type 1 diabetes. Diabetes 2004;53:2569–73.
36. Yasukawa T. Inflammation in age-related macular degeneration: pathological or physiological? Expert Rev Ophthalmol 2009;4:107-12.
37. van Leeuwen R, Ikram MK, Vingerling JR, Witteman JC, Hofman A, de Jong PT. Blood pressure, atherosclerosis, and the incidence of age-related maculopathy: The Rotterdam Study. Invest Ophthalmol Vis Sci 2003;44:3771–7.
38. Boekhoom SS, Vingerling JR, Witteman JC, Hofman A, de Jong P. C-reactive protein level and risk of aging macula disorder: The Rotterdam Study. Arch Ophthalmol 2007;125:1396–401.
39. Van der Meer IM, de Maat MP, Bots ML, Breteler MM, Meijer J, Kiliaan AJ, et al. Inflammatory mediators and cell adhesion molecules as indicators of severity of atherosclerosis: The Rotterdam Study. Arterioscler Thromb Vasc Biol 2002;22:838–42.
40. Jovicic S, Ignjatovic S, Dajak M, Kangrga R, Majkic-Singh N. Factor analysis of cardiovascular risk determinants associated with elevated C-Reactive protein concentraction. J Med Biochem 2010;29:447-8.
41. Ali A, Sultan P, El-Napoli M, Fahmy MA. Lipoprotein metabolism abnormalities in patients with chronic renal insufficiency. J Med Biochem 2011;30:38-44.
42. Penfold PL, Madigan MC, Gillies MC, Provis JM. Immunological and aetiological aspects of macular degeneration. Prog Retin Eye Res 2001;20:385–414.
43. Anderson DH, Mullins RF, Hageman GS, Johnson LV. A role for local inflammation in the formation of drusen in the aging eye. Am J Ophthalmol 2002;134:411–31.
44. Roth F, Bindewald A, Holz FG. Key pathophysiologic pathways in age-related macular disease Graefes Arch Clin Exp Ophthalmol 2004;242:710–6.
45. Curcio CA, Johnson M, Huang JD, Rudolf M. Aging, age-related macular degeneration, and the response-to-retention of apolipoptotein B-containing lipoproteins. Prog Ret Eye Res 2009;28:393-422.
46. Ebrahimi KB, Handa JT. Lipids, lipoproteins and age-related macular degeneration. J Lipids 2011;2011:802059.
47. Olofsson SO, Boren J. Apolipoprotein B: a clinically important apolipoprotein which assembles atherogenic lipoproteins and promotes the development of atherosclerosis. J Int Med 2005;258:395-410.
48. Lommatzsch A, Hermans P, Muller KD, Bornfeld N, Bird AC, Pauleikhoff D. Are low inflammatory reactions involved in exudative age-related macular degeneration? Morphological and immunohistochemical analysis of AMD associated with basal deposits. Gre Arch Clin Exp Ophthalmol 2008;246:803-10.
49. Picard E, Houssier M, Bujold K, Sapieha P, Lubell W, Dorfman A, et al. CD36 plays an important role in the clearance of oxLDL and associated age-dependent sub-retinal deposits. Aging 2010;2:981-9.
50. Srewart CR, Stuart LM, Wilkinson K, van Gils JM, Deng J, Halle A, et al. CD36 ligands promote sterile inflammation through assembly of a tool-like receptor 4 and 6 heterodimer. Nat Immunol 2010;11:155-61.
51. Chau KY, Sivaprasad S, Patel N, Donaldson TA, Luthert PJ, Chong NV. Plasma levels of matrix metalloproteinase-2 and –9 (MMP-2 and MMP-9) in age-related macular degeneration. Eye 2007;21:1511-5.
52. Verna S, Yeh ETH. C-reactive protein and atherotrombosis–Beyond a biomarker: an actual partaker of lesion formation. Am J Physiol Regul Integr Comp Physiol 2003;285:R1253-6.
53. Kim SY, Sadda S, Pearlman J, Humayun MS, de Juan E Jr, Melia BM, Green WR. Morphometric analysis of the macula in eyes with disciform age-related macular degeneration. Retina 2002;22:471–7.
54. Allikmets R, Dean D. Bringing age-related macular degeneration into focus. Nat Genet 2008;40:820–1.
55. Chen J, Connor KM, Smith LE. Overstaying their welcome: defective CX3CR1 microglia eyed in macular degeneration. J Clin Invest 2007;117:2758–62.
56. Larrayouz IM, Huang JD, Lee JW, Pascual I, Rodriguez IR. 7-ketocholesterol-induced inslammation: involvement of multiple kinase signaling pathways via NFkB but independetly of reactive oxygen species formation. Invest Ophthalmol Vis Sci 2010;51:4942-55.
57. Moreira EF, Larrayoz IM, Lee JW, Rodriguez IR. 7-ketocholesterol is present in lipid deposits in the primate retina: potential implication in the induction of VEGF and CNV formation. Invest Ophthalmol Vis Sci 2009;50:523-32.
58. Dasari B, Prasanthi JR, Marwarha G, Singh BB, Ghribi O. The oxysterol 27-hydroxycholesterol increase β-amyloid and oxidative stress in retinal pigment epithelial cells. BMC Ophthalmol 2010;10:22.
59. Edwards AO, Ritter R III, Abel KJ, Manning A, Panhuysen C, Farrer LA. Complement factor H polymorphism and age-related macular degeneration. Science 2005;308:421–4.
60. Despriet DD, Klaver CC, Witteman JC, Bergen AA, Kardys I, de Maat MP, et al. Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration. JAMA 2006;296:301–9.
61. Rodrıguez de Cordoba S, Esparza-Gordillo J, Goicoechea de Jorge E, Lopez-Trascasa M, Sanchez-Corral P. The human complement factor H: functional roles, genetic variations and disease associations. Mol Immunol 2004;41:355–67.
62. Oksjoki R, Jarva H, Kovanen PT, Laine P, Meri S, Pentikainen MO. Association between complement factor H and proteoglycans in early human coronary atherosclerotic lesions: implications for local regulation of complement activation Arterioscler Thromb Vasc Biol 2003;23:630–6.
63. Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, et al. Complement factor H variant increases the risk of age-related macular degeneration. Science 2005;308:419–21.
64. Hakobyan S, Harris CL, van der Berg CW, Fernandez-Alonso MC, de Jorge EG, de Cordoba SR, et al. Complement factor H binds to denaturated rather than to native pentametric C-reactive protein. J Biol Chem 2008; 283:30451-60.
65. Deangelis MM, Silveira AC, Carr EA, Kim IK. Genetics of age-related macular degeneration: current concepts, future directions. Semin Ophthalmol 2011;26:77-93.
66. Lederman M, Weiss A, Chowers I. Association of neovascular age-related macular degeneration with specific gene expression patterns in peripheral white blood cells.Invest Ophthal Vis Sci 2010;51:53-8.
67. Cederholm A, Frostegard J. Annexin A5 in cardiovascular disease and systemic lupus erythematosus. Immunology 2005;210:761-8.
68. Rayborn Me, Sakaguchi H, Shadrach KG, Crabb JW, Hollyfield JG. Annexins in Bruch’s membrane and drusen. Adv Exp Med Biol 2006;572:75-8.
69. Degn SE, Jensenius JC, Thiel S. Disease-causing mutations in genes of the complement system. Am J Hum Genet 2011;68:689-705.
70. Colak E, Kosanovic-Jakovic N, Zoric L, Radosavljevic A, Stankovic S, Majkic-Singh N. The association of lipoprotein parameters and C-reactive protein in patients with age-related macular degeneration. Ophthalmic Res 2011;46:125–32.
71. Schaumberg DA, Christen WG, Buring JE, Glynn RJ, Rifai N, Ridker PM. High-sensitivity C-reactive protein, other markers of inflammation, and the incidence of macular degeneration in women. Arch Ophthalmol 2007;125:300–5.
72. Hong T, Tan AG, Mithchell P, Wang JJ. A review and meta-analysis of the association between C-reactive protein and age-related macular degeneration. Surv Ophthalmol 2011;56:184-94.
73. De Jong PT, Boekhoorn SS, Vingerling JR, Witteman JCM, Hofman A. C-reactive protein and incident aging macular disease (AMD): The Rotterdam Study. Invest Ophthalmol Vis Sci 2005;46:E-Abstract 2379.
74. Kikuchi M, Nakamura M, Ishikawa K, Suzuki T, Nishihara H, Yamakoshi T, et al. Elevated C-reactive protein levels in patients with polypoidal choroidal vasculopathy and patients with neovascular age-related macular degeneration. Ophthalmol 2007;114:1722–7.
75. Boey PY, Tay WTT, Lamoureux E, Tai S, Mitchell P, Wang JJ, et al. C-Reactive protein and age-related macular degeneration and cataract: The Singapore Malay eye study. Invest Ophthalmol Vis Sci 2010;51:1880–5.
76. Pasceri V, Chang J, Willerson JT, Yeh ET. Modulation of C-reactive protein-mediated monocyte chemoattractant protein-1 induction in human endothelial cells by anti-atherosclerosis drugs. Circulation 2001;103:2531–4.
77. Verma S, Badiwala MV, Weisel RD, Li SH, Fedak PWM, Li RK, Mickle DAG. C-reactive protein upregulates the NF-κB signaling pathwayin saphenous vein endothelial cells: implications for atherosclerosis and restenosis. J Thorac Cardiovasc Surg 2003;126:1886–91.
78. Qamirani E, Ren Y, Kuo L, Hein TW. C-reactive protein inhibits endothelium-dependent NO-mediated dilation in coronary arterioles by activating p38 kinase and NAD(P)H oxidase. Arterioscler Thromb Vasc Biol 2005;25:995–1001.
79. Fichtlscherer S, Breuer S, Schachinger V, Dimmeler S, Zeiher AM. C-reactive protein levels determine systemic nitric oxide bioavailability in patients with coronary artery disease. Eur Heart J 2004;25:1412–8.
80. Wassmann S, Ribaudo N, Faul A, Laufs U, Bohm M, Nickenig G. Effect of atorvastatin 80 mg on endothelial cell function (forearm blood flow) in patients with pretreatment serum low-density lipoprotein cholesterol levels < 130 mg/dL. Am J Cardiol 2004;93:84–8.
81. Zoric L, Kosanovic-Jakovic N, Colak E, Radosavljevic A, Jaksic V, Stevic S. Oksidativni stres u sklopu faktora rizika od nastanka i razvoja senilne degeneracije makule. Vojnosanit pregl 2008;65:313-8
82. Pepys MB, Hirschfield GM. C-reactive protein: a critical update. J Clin Invest 2003;111:1805–12.
83. Chang MK, Binder CJ, Torzewski M, Witzum JL. C-reactive protein binds to both oxidized LDL and apoptotic cells through recognition of a commom ligand:phosphorylcholine of oxidized phospholipids. Proc Natl Acad Sci U.S.A. 2002;99:13043–8.
84. Scholl HPN, Charbel Issa P, Walier M, Janzer S, Polloh-Kopp B, Börncke F et al. Systemic complement activation in age-related macular degeneration. PloS ONE 2008;3:e2593.
85. Choroid. Available at: Accessed: November 25, 2011.
86. Retina. Available at: Accessed: November 25, 2011.
87. Retinal_pigmented_epithelium. Available at: Accessed: November 25, 2011.
88. Fovea_centralis. Available at: Accessed: November 25, 2011.
89. Macula_of_retina. Available at: Accessed: November 25, 2011.
90. Sclera. Available at: Accessed: November 25, 2011.
91. Eye. Available at: Accessed: November 25, 2011.
Uloga CRP i upale u patogenezi makularne degeneracije povezane sa starošću
Makularna degeneracija povezana sa starošću (engl. age-related macular degeneration, AMD) kompleksna je, degenerativna i progresivna bolest koja uključuje višestruke genetske i okolišne čimbenike te može rezultirati ozbiljnim gubitkom vida. Etiologila AMD još se ne razumije u potpunosti. Postoje mnoge teorije koje ističu mehanizme oksidativnog stresa, promjene nalik na aterosklerotske promjene, genetske predispozicije i upalu. Najnovija klinička istraživanja proučavaju važnu ulogu upale i C-reaktivnog proteina (CRP) u patogenezi AMD. Postoji veliki broj dokaza koji ukazuju na povezanost CRP-a s endotelnom disfunkcijom, oksidativnim stresom i stvaranjem reaktivnih kisikovih spojeva kao i s poremećajem lipidnog statusa kod bolesnika oboljelih od AMD. Prema navodima novijih istraživanja CRP definitivno nije samo upalni biljeg, već i posrednik u razvoju vaskularnih poremećaja u retinalnoj cirkulaciji. Rezultati dobiveni nedavno provedenim istraživanjima mogu pomoći pri razumijevanju patogeneze retinalne vaskularne bolesti povezane s visokom koncentracijom CRP-a.
Ključne riječi: makularna degeneracija povezane sa starošću; C-reaktivni protein; upala