Received 1 May 2010 | Accepted 28 October 2010 | Published 3 November 2010
Jiexi Zeng,1,3,4 Yuhong Chen,2,3,4 Zongzhong Tong,4 Xinrong Zhou,3 Chao Zhao,3,4 Kevin Wang,3 Guy Hughes,3 Daniel Kasuga,3 Matthew Bedell,3 Clara Lee,3 Henry Ferreyra,3 Igor Kozak,3 Weldon Haw,3 Jean Guan,3 Robert Shaw,3 William Stevenson,5 Paul D. Weishaar,5 Mark H. Nelson,6 Luosheng Tang,1 Kang Zhang3,4
1Department of Ophthalmology, Second Xiangya Hospital, Central South University, Changsha, China; 2Department of Ophthalmology & Vision Science, Eye and ENT hospital, Shanghai Medical School, Fudan University, Shanghai, China; 3Institute for Genomic Medicine and Shiley Eye Center, University of California San Diego, San Diego, CA; 4Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah School of Medicine, Salt Lake City, UT; 5Vitreo-Retinal Consultants & Surgeons, 530 North Lorraine, Wichita, KS; 6North Carolina Macular Consultants, Winston-Salem, NC
Correspondence to: Kang Zhang, Institute for Genomic Medicine (IGM), MC0838 Skaggs (SSPPS), room 4272,9500 Gilman Drive, La Jolla, CA, 92093-0838; Phone: (858)-2460823; FAX: (858)-2460873; email: firstname.lastname@example.org
Purpose: Age-related macular degeneration (AMD) is the most common cause of irreversible central vision loss worldwide. Research has linked AMD susceptibility with dysregulation of the complement cascade. Typically, complement factor H (CFH), complement factor B (CFB), complement component 2 (C2), and complement component 3 (C3) are associated with AMD. In this paper, we investigated the association between complement factor D (CFD), another factor of the complement system, and advanced AMD in a Caucasian population.
Methods: Six single nucleotide polymorphisms (SNPs), rs1683564, rs35186399, rs1683563, rs3826945, rs34337649, and rs1651896, across the region covering CFD, were chosen for this study. One hundred and seventy-eight patients with advanced AMD and 161 age-matched normal controls were genotyped. Potential positive signals were further tested in another independent 445 advanced AMD patients and 190 controls. χ2 tests were performed to compare the allele frequencies between case and control groups.
Results: None of the six SNPs of CFD was found to be significantly associated with advanced AMD in our study.
Conclusions: Our findings suggest that CFD may not play a major role in the genetic susceptibility to AMD because no association was found between the six SNPs analyzed in the CFD region and advanced AMD.
Age-related macular degeneration (AMD) is the most common cause of irreversible central vision loss worldwide . It can be divided into early and advanced (late) forms. Early AMD is characterized by the presence of drusen or pigmentary abnormalities in the retinal pigment epithelium (RPE), while advanced AMD includes two clinical types—geographic atrophy of the RPE (dry AMD) and choroidal neovascularization (wet AMD). Age-related macular degeneration is a complex disease caused by the combination of genetic predisposition and environmental factors [2-4]. The inheritance of AMD is polygenic and multifactorial: race, age, smoking, body mass, and body mass index have all been associated with AMD [2,5-9]. In the past five years, significant progress has been made in our understanding of AMD genetics through studies that identified specific single nucleotide polymorphisms (SNPs) significantly associated with AMD. The discovery of the strongest associations of AMD with the variants of complement factor H (CFH; OMIM 134370) [10-13] and ARMS2/HTRA1 (age-related maculopathy susceptibility 2, OMIM 611313; the high temperature requirement factor A1, OMIM: 602194) [14-17] has led to new hypotheses regarding the pathogenesis of this disease. CFH is primarily associated with the formation of drusen that often characterizes both types of advanced AMD in Caucasian populations, whereas ARMS2/HTRA1 is mainly associated with wet AMD . Other than these two major loci, three other members of the complement system, complement component 2 (C2; OMIM 217000), complement component 3 (C3; OMIM 120700), and complement factor B (CFB; OMIM 138470), were also found to be associated with AMD [10,19-21]. Most of these genes are complement pathway-associated genes, with the products participating in the alternative complement pathway and playing important roles in the complement system. Many studies have provided evidence that the complement system is involved in the pathogenesis of AMD and may have a pivotal effect on the formation and development of the disease [13,22-24]. However, the specific role of the complement system in the etiology of AMD is difficult to elucidate, and questions remain as to whether other components from this system are associated with AMD.
Complement factor D (CFD) is a protein of the trypsin family encoded by the CFDgene (OMIM 134350) and is involved in the alternative complement pathway of the complement system [25,26]. CFD is unique among serine proteases in that it requires neither enzymatic cleavage for expression of proteolytic activity nor inactivation by a serpin for its control . It is best known for its role in humoral suppression of infectious agents and has a high level of expression in fat, suggesting a role for adipose tissue in immune system biology (CFD). In this study, we investigated the association of CFD with advanced AMD in a Caucasian population.
This study was approved by the Institutional Review Board of the University of California, San Diego. Informed consent was signed by all subjects before participation in the study. One hundred and seventy-eight nonfamilial advanced AMD patients and 161 age-matched normal controls (60 years or older with no drusen or RPE changes) as well as an independent replication cohort with 445 nonfamilial advanced AMD patients and 190 age-matched normal controls were recruited using the standard ophthalmic examination protocol. Grading was performed using a standard grid classification suggested by the International Age-related Maculopathy (ARM) Epidemiological Study Group for the age-related maculopathy and age-related macular degeneration group . All the participants were Caucasian.
Six SNPs, rs1683564, rs35186399, rs1683563, rs3826945, rs34337649, and rs1651896 at the CFD locus were chosen, which were either tag SNPs or those that might affect the function of CFD (Figure 1). A Caucasian cohort of 178 advanced AMD patients was genotyped and allele frequencies were compared with 161 age- and ethnicity-matched normal controls by laboratory personnel blinded to the case/control status. Potential positive findings were tested for replication in an independent cohort of 445 advanced AMD patients and 190 normal controls.
Genotypes of six SNPs were achieved by primer extension of multiplex PCR products followed with a SNaPshot using an ABI 3100 genetic analyzer (Applied Biosystems, Foster City, CA).
Deviation from Hardy–Weinberg equilibrium was assessed, with a statistical significance level of 0.01. A chi-square test was performed to assess evidence for association. The statistical significance level was adjusted by Bonferroni correction. Linkage disequilibrium (LD) patterns and haplotype blocks were defined using Haploview 4.1.
We genotyped six SNPs that tag the majority of CFD haplotypes and investigated allelic association with AMD. Four SNPs, rs1683564, rs35186399, rs1683563, and rs3826945, located either at the promoter region, exon, or intron of CFD, exhibited no association with advanced AMD in our study population. The SNP rs34337649, in exon 5 of CFD, showed no polymorphisms in our data (Table 1).
Of the six SNPs, rs1651896, which is located at the 3′ region of CFD, was found to be marginally associated with advanced AMD (P(allelic)=0.07, risk allele A: 37.4% in cases versus 30.7% in controls) in a Caucasian cohort of 178 advanced AMD cases and 161 normal controls. The result was further investigated in an independent replication cohort of 445 advanced AMD patients and 190 controls. No further significant association was observed for either the replication cohort (P(allelic)=0.882, risk allele A: 37.2% in cases versus 37.6% in controls) or the combined cohort (P(allelic)=0.223, risk allele A: 37.2% in cases versus 34.5% in controls, Table 2).
Linkage disequilibrium patterns and haplotype blocks were defined by combining the six SNPs (Figure 2). No significant association was found between the haplotypes and AMD phenotypes. The SNP rs34337649 was not shown in the plot because it was not a detected polymorphism in our data set.
The alternative complement pathway is one of three distinct complement pathways and is important in the clearance and recognition of pathogens in the absence of antibodies  (Figure 3). It is triggered by spontaneous C3 hydrolysis to form C3a and C3b, which makes C3b capable of binding to a pathogenic membrane surface. After binding with an activator membrane, C3b is bound by CFB to form C3bB. Complement factor H acts as one of the primary regulators by inhibiting the binding of CFB to C3b and also by degrading C3b. In the presence of CFD, C3bB is cleaved into C3bBa and C3bBb (C3 convertase). After hydrolysis of C3, C3 convertase and C3b become C3bBbC3b, which cleaves C5 into C5a and C5b. A membrane attack complex (MAC) is formed through subsequent reactions, which inserts into the cell membrane and initiates cell lysis [18,30,31]. In this pathway, CFB and CFD are involved in the activation and amplification loop, whereas CFH is a fluid phase inhibitor. To keep the complement activity under control, the competition between CFH and CFB binding to C3b on the host or pathogen cells needs to be tightly regulated. How this control is achieved is not completely clear .
Compared with other complement factors, CFH, C3, and CFB have been associated with AMD in many independent studies. However, the exact role they play in the pathogenesis of AMD and whether their effects are mediated through the complement system or through another pathway is poorly understood. Previously, CFD was studied using a CFD−/− mouse model, with the conclusion that eliminating the alternative pathway was neuroprotective and reduced photoreceptor susceptibility to light-induced damage . Contrary to this finding, no significant association between CFD SNPs and advanced AMD was found in this study. Due to the dearth of information about the relationship between CFD and AMD, further research in other populations may be warranted. Our results suggest it is unlikely that CFD is a major functional candidate gene conferring risk for AMD. However, due to the relatively small sample size, this study has limited power to detect minor effects. Extended cohorts will be needed to confirm the genetic role of CFD. Future research should also focus on a comprehensive understanding of genetic variants throughout all pathways of the complement system. By identifying high risk variants and improving our understanding of the complement system, early intervention for patients at risk of developing AMD and novel gene-based treatments may become a reality.
We thank all the participating AMD patients and their families. K.Z. is supported by grants from NIH, VA Merit Award, Foundation Fighting Blindness, the Macula Vision Research Foundation, Ruth and Milton Steinbach Fund, Research to Prevent Blindness, BWF Clinical Scientist Award in Translational Research. K.Z. has full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.