Figures
Abstract
Background
We investigated the serological association of Chlamydia pneumoniae infection with age-related macular degeneration (AMD).
Methods
A systematic review and meta-analysis was performed. PubMed, Embase, Web of Science and the Association of Research in Vision and Ophthalmology abstracts were searched to identify studies investigating the serological association of Chlamydia pneumoniae infection with age-related macular degeneration. The quality of original studies was assessed using the Newcastle-Ottawa scale. Heterogeneity was explored with meta-regression. The odds ratios (ORs) and standardized mean differences (SMD) of Chlamydia pneumoniae infection between AMD patients and controls were pooled.
Results
In total, 9 studies met the inclusion criteria using the Newcastle-Ottawa scale scores ranging from 4 to 9. There was heterogeneity among studies due to a difference in the study designs and measurement of exposure to Chlamydia pneumoniae infection. The overall OR of Chlamydia pneumoniae infection with AMD was 1.11 (95% confidence interval: 0.78–1.57, P = 0.56). The overall SMD of antibody titer between AMD and control was 0.43 (95% confidence interval: −0.12 to 0.99, P = 0.13).
Citation: Chen X, Jhanji V, Chen C, Chen H (2014) Serological Association of Chlamydia pneumoniae Infection with Age-Related Macular Degeneration: A Systematic Review and Meta-Analysis. PLoS ONE 9(7): e103466. https://doi.org/10.1371/journal.pone.0103466
Editor: Paul Baird, Centre for Eye Research Australia, Australia
Received: August 16, 2012; Accepted: July 3, 2014; Published: July 25, 2014
Copyright: © 2014 Chen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was supported by the National Nature Science Foundation of China (30901646 and 81170853) and Guangdong Science and Technology Project (2011B031300013). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Age-related macular degeneration (AMD) is a leading cause of irreversible blindness worldwide. It is characterized by degeneration of photoreceptor/retinal pigment epithelium and, choroidal neovascularization. Several genetic and environmental factors have been found to be associated with the occurrence of AMD [1]. Age is by far the most important risk factor while smoking is another confirmed environmental factor associated with AMD [2]. In 2005, a genome-wide association study discovered that polymorphic variants in the complement factor H (CFH) [3] gene was associated with AMD. Later on, genetic polymorphisms in other factors in the complement pathway were also found to be associated with AMD, such as complement component 3 [4], complement factor B/complement component 2 [5]. Furthermore, serum level of C reactive protein was higher in AMD patients compared to the controls [6]. These results suggested that inflammation plays an important role in pathogenesis of AMD [7].
The hypothesis of association between Chlamydia pneumoniae and AMD originated from the role of Chlamydia pneumoniae infection in other inflammatory or autoimmune diseases such as arthritis [8] and atherosclerosis [9]. Chlamydia infection may trigger the activation of the alternate complement pathway, therefore potentially increasing an individual's risk of developing AMD. Two studies in 2003 found a serological association between AMD and anti-Chlamydia pneumoniae antibodies in American [10] and Japanese [11] populations respectively. However, the results reported from ensuing studies could not replicate these findings and consequently the role of Chlamydia in the causation of AMD remained controversial.
The purpose of this study was to systematically evaluate the association of Chlamydia pneumoniae infection with AMD through a meta-analysis of the published literature.
Methods
Inclusion criteria
We included studies that met the following criteria: 1) The study included subjects with early or advanced age-related macular degeneration and non-AMD controls; 2) The study investigated the association of Chlamydia pneumoniae infection with AMD; 3) Status of Chlamydia pneumoniae infection was determined by serology for measurement of IgG antibody or polymerase chain reaction (PCR) for detection of DNA in the serum. We excluded the following studies: 1) review articles or comments without original data; 2) animal studies or histological studies without data of serum infection; 3) studies investigating the association of Chlamydia pneumoniae infection and progression of AMD.
Literature search
A comprehensive literature search was performed in four databases, Medline in PubMed, Embase, Web of Science and abstracts of the Association of Research in Vision and Ophthalmology (ARVO) annual meetings. Search strategies used were, “Chlamydia pneumoniae” or “Chlamydophila pneumoniae” and, “macular degeneration”. The references of the included studies or reviews were reviewed as additional references. The literature search was performed for studies published until April 1, 2012 and was further updated up to April 21, 2014. No language limit was applied.
Screening of articles
All retrieved results were imported into the EndNote software (version X3, Philadelphia, PA). Two independent reviewers (HC and XC) assessed the titles and abstracts of all literature records retrieved from online search. Duplicate records and unrelated articles were excluded after the initial screening. Subsequently, full-texts of relevant records were obtained and a detailed review was performed. For multiple publications using all or part of the same study population, the most recent report was used. A third masked reviewer (VJ) was consulted when required in order to resolve any discrepancy.
Risk of bias assessment
The risk of bias was assessed by two independent reviewers (HC and XC) using a customized Newcastle-Ottawa scale [12]. The Newcastle-Ottawa scale has been identified [13] as one of the best tools for assessment of observational study designs. For our study, this scale included the following 9 items: 1) adequacy of case definition; 2) representativeness of cases; 3) community controls; 4) definition of controls; 5) comparability of age; 6) comparability of smoking; 7) ascertainment of measurement of Chlamydia pneumoniae infection; 8) same method employed for measurement for cases and controls; 9) non-response rate similar for cases and controls. One score was given to each item if the study met the criteria. If the study did not meet the criteria or did not provide clear information, zero score was given to this item. Any disagreement was resolved by discussion with a third reviewer (VJ).
Data extraction
The data from each included article was extracted by two reviewers independently, including characteristics of study population, diagnostic criteria and phenotype of cases and controls, sample size, and, measurement of Chlamydia pneumoniae infection in cases and controls. The measurement of Chlamydia pneumoniae infection was expressed as positive/negative, quintile [10] or trisection [14] or mean/standard deviation, in different studies. For quantitative data, we used the lowest quartile as negative. For continuous data, there were two different units used, titers [10], [15] and index [11]. We converted the index to titers by using the titer of 0.2 as a cut-off [16].
The primary outcome of interest in all the studies was association of Chlamydia with early or advanced AMD.
Data synthesis
Stata Software (version 12.0, StataCorp, College Station, TX) was used for the statistical analysis. The comparison of rate of positive Chlamydia pneumoniae infection was evaluated using odds ratio (OR) and 95% confidence interval (CI). Continuity correction was applied to the study with zero-cell counts by adding 0.5 to all cells of the study. The comparison of Chlamydia pneumoniae infection titers was evaluated using standardized mean difference (SMD) and 95% CI. Heterogeneity among the studies was assessed by the Chi-square test and I2 statistic. Meta-regression was used to explore the sources of heterogeneity if a statistically significant heterogeneity was observed (p<0.1 or I2>25%) [17], [18]. In meta-regression, the relationship between effect size and covariants including year, study design and method of detection of Chlamydia pneumoniae infection were explored. Random effect (DerSimonian and Laird) [19] models were used to pool the ORs or SMDs from individual studies if a statistically significant heterogeneity was found, otherwise, a fixed effect model was used. Funnel plots were used to assess the any publication bias. Egger's test [20] was used to quantify the possibility of publication bias.
Results
A total of 108 records were retrieved from online search, including 22 articles from PubMed, 49 from Web of Science, 25 from Embase and 12 from the ARVO annual meeting abstracts. During the initial screening, 41 records identified as ‘duplicate’, and 48 identified as ‘unrelated topic’, were excluded. Full texts of the remaining 19 records were retrieved and reviewed. Four records published as comments or review [21]–[24], 1 animal study [25], 3 histological studies [26]–[28], and 2 studies investigating the association of Chlamydia pneumoniae infection with AMD progression but not AMD prevalence [29], [30], were excluded (Figure 1).
The characteristics of the remaining 9 articles [10], [11], [14], [15], [31]–[35] that were included for meta-analysis are shown in table 1. Overall, the study population was from United States of America (n = 4), United Kingdom (n = 1), Austria (n = 1), Australia (n = 1), Japan (n = 1) and Turkey (n = 1). Seven studies [10], [11], [14], [32]–[35] were case control studies and the other 2 were nested case-control studies [15], [31]. The methodology quality scores of the included studies ranged from 4 to 9 (Table 2).
The inclusion criteria of AMD were clearly defined in all studies except 1 study [11]. However, the criteria were not consistent. Six out of 9 studies [10], [15], [31]–[34] included both early and advanced AMD, 2 studies [14], [35] included only advanced AMD but both geographic atrophy and choroidal neovascularization were included, and 1 study [11] included only choroidal neovascularization. There were 2 population based nested case-control studies [15], [31] and their cases represented the population well. One study selected cases according the genotypes and was therefore likely to have selection bias [34]. The controls were community controls in the two population-based studies [15], [31] but hospital controls in other studies. Definition of controls was clear in all studies except one [34]. The cases and controls were comparable for age in all except three studies [10], [34], [35]. Matching for smoking was reported in two studies [15], [31].
Serology testing was used to measure Chlamydia pneumoniae infection exposure in 8 studies, including ELISA in 7 studies [10], [11], [14], [15], [31]–[33], and micro-immunofluorescent assay in one study [34], whereas PCR was used in 1 study [35]. The methodology was same in cases and controls in all studies. The non-response rate was reported in all studies.
Seven out of 9 studies [10], [14], [31]–[35] reported the categorical data (Figure 2A), with a total 758 cases and 637 controls. The individual ORs of having AMD with Chlamydia pneumoniae ranged from 0.61 to 2.66. Of these, only one study reported a statistically significant association of Chlamydia pneumoniae infection with AMD [35]. The heterogeneity test showed a p value of 0.13, I2 = 40%. It was found by meta-regression that the method of measurement might be the source of heterogeneity (I2 = 0, p = 0.065), but not the year of study (I2 = 48.7%, p = 0.796) or the study design (I2 = 41.5%, p = 0.565).
A: Forest plot comparing the positive rate of Chlamydia pneumoniae infection between AMD cases and controls; squares indicate study-specific odds ratio (OR). B: Funnel plots for positive rate of Chlamydia pneumoniae infection between AMD cases and controls; C: Forest plot comparing the IgG antibody titers of Chlamydia pneumoniae infection between AMD cases and controls; squares indicate study-specific standardized mean difference (SMD). The size of the box is proportional to the weight of the study; horizontal lines indicate 95% confidence interval (CI); diamond indicates summary OR or SMD with its corresponding 95% CI.
We used a random effect model to pool the individual results. The overall OR was 1.11 (95% CI: 0.78–1.57, P = 0.56), suggesting no significant association between Chlamydia pneumoniae and AMD. We further performed a sensitivity analysis to exclude the only study using PCR [35]. The results showed I2 = 0% and the OR = 0.94 (95% CI: 0.728–1.23, P = 0.65). Funnel plot did not suggest any asymmetry (Figure 2B). No significant publication bias was found in Egger's test (p = 0.538).
Three studies [10], [11], [15] reported continuous data (Figure 2C) with a total of 249 cases and 473 controls. Significant SMD of Chlamydia pneumoniae antibody titer between AMD cases and controls were reported in two [10], [11] out of these three studies. The heterogeneity test showed P = 0.01, I2 = 80%. We used a random effect model to pool the individual results. The overall SMD was 0.43 (95% CI: −0.12 to 0.99, P = 0.13), suggesting no significant difference of Chlamydia pneumoniae antibody titer in serum of AMD cases and controls. It was found by meta-regression that the study design (I2 = 0, p = 0.447) was the source of heterogeneity. The two studies reporting a significant difference were case-control studies and the third study with a negative result was a nested case-control study. No significant publication bias was found in Egger's test (p = 0.181).
Discussion
In this systematic review and meta-analysis, we summarized the current literature on the association of Chlamydia pneumoniae infection with AMD. Nine studies with a total of 785 cases and 659 controls were identified. Neither the pooled results of OR of infection positivity rate nor the MD of titers were statistically significant. Therefore, the current literature does not support the association of AMD with Chlamydia pneumoniae infection.
Of the nine studies that investigated the association of Chlamydia pneumoniae and AMD, statistically significant association was reported in 3 studies [10], [11], [35] whereas the remaining 6 studies did not find a significant association [14], [15], [31]–[34]. The discrepancy in the results reported in different studies may be attributed to a small sample size and/or heterogeneity across the studies. Meta-regression suggested that study design as well as methodology for detection of Chlamydia pneumoniae infection were the major causes of heterogeneity. There were 7 case-control studies and the two nested case-control studies. Eight studies measured the IgG antibody [10], [11], [14], [15], [31]–[34] and only one study used the PCR for DNA [35]. The category of AMD was also inconsistent among studies. Some studies included cases with choroidal neovascularization [10], while others included subjects with advanced AMD [35] or both early and advanced AMD [15], [34].
Although our study found no association of Chlamydia pneumoniae infection and prevalence of AMD, we believe that it cannot completely exclude the role of Chlamydia pneumoniae infection in the pathogenesis of AMD. In a previously reported prospective study in an Australian cohort, the subjects in the upper tertiles of Chlamydia pneumoniae antibody titers had two to three times higher risk of AMD progression than those in the lowest tertile. [30] Furthermore, this risk might interact with the genotypes of Complement factor H, which is a major associated gene for AMD [29]. The pathological studies of Chlamydia pneumoniae detection in human eyes add further controversy. In a previous study on identification of Chlamydia pneumoniae within human choroidal neovascularization tissues, Chlamydia pneumoniae was detected in four out of nine AMD choroidal neovascularization tissues by immunohistochemistry and, two out of nine tissues by PCR. Chlamydia was not detected in any of the 22 non-AMD specimens [26]. However, in another study, Chlamydia pneumoniae DNA was detected in 2/59 (3.3%) AMD samples and in 1/16 (6.2%) control samples. [35] A later PCR report in 13 choroidal neovascularization cases did not detect Chlamydia pneumoniae in any of the samples [27]. The relationship between Chlamydia pneumoniae and AMD was also investigated in cellular and animal studies. It was reported that Chlamydia pneumoniae infection induced production of vascular endothelial growth factor (VEGF) by human macrophages, and, IL-8 and MCP-1 by the retinal pigment epithelium (RPE) cells [26]. In another study, treatment of mouse RPE cells with Chlamydia pneumoniae antigen induced expression of IL-6 and VEGF. Vitreous injection of Chlamydia pneumoniae antigen increased the size of laser-induced CNV in mice via Toll like receptor-2. [25]
There are some limitations of our study. Firstly, the quality of original research was moderate in some studies. Secondly, pooling results were based on high heterogeneity, with a small number of included studies thereby limiting the exploration of sources of heterogeneity. The characteristics of study subjects were also variable in different studies and the original studies did not report the result of association in each AMD categories. Furthermore, the prevalence of Chlamydia pneumoniae may vary according to the geographical location [36]. Although we found that there was no statistically significant association between Chlamydia pneumoniae and AMD, this conclusion was based on data from cross-sectional studies. Further prospective or functional studies may be required to further investigate the role of Chlamydia pneumoniae in the pathogenesis of AMD.
Author Contributions
Conceived and designed the experiments: CC HC. Performed the experiments: XC VJ. Analyzed the data: XC VJ CC. Contributed reagents/materials/analysis tools: XC VJ CC HC. Wrote the paper: VJ HC. Final approval of the manuscript: XC VJ CC HC.
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