- Top of page
- Supporting Information
Early epithelial injury after lung transplantation may contribute to development of bronchiolitis obliterans syndrome (BOS). We evaluated the relationship between early postoperative soluble receptor for advanced glycation end-product (sRAGE) levels, a marker of type I alveolar cell injury and BOS. We performed a cohort study of 106 lung transplant recipients between 2002 and 2006 at the University of Pennsylvania with follow-up through 2010. Plasma sRAGE was measured 6 and 24 h after transplantation. Cox proportional hazards models were used to evaluate the association between sRAGE and time to BOS, defined according to ISHLT guidelines. Sixty (57%) subjects developed BOS. The average time to BOS was 3.4 years. sRAGE levels measured at 6 h (HR per SD of sRAGE: 1.69, 95% CI: 1.11, 2.57, p = 0.02) and 24 h (HR per SD of sRAGE: 1.74, 95% CI: 1.14, 2.65, p = 0.01) were associated with an increased hazard of BOS. Multivariable Cox regression indicated this relationship was independent of potential confounders. Elevated plasma sRAGE levels measured in the immediate postoperative period are associated with the development of BOS. Early epithelial injury after transplantation may contribute to the development of fibrosis in BOS.
- Top of page
- Supporting Information
Bronchiolitis obliterans syndrome (BOS) following lung transplantation is a form of chronic lung allograft dysfunction characterized by progressive airflow obstruction . BOS is common, affecting almost 50% of recipients at 5 years . It is the leading cause of death after the first year of lung transplantation and it is a major contributor to the morbidity of lung transplant recipients . Several risk factors for BOS have been identified, including cytomegalovirus (CMV) infection , acute cellular rejection (ACR; Ref.  and primary graft dysfunction (PGD), a form of acute lung injury (ALI) occurring within 72 h of transplantation .
Although mechanisms underlying the development of BOS have not been completely elucidated, BOS may be related to either repeated episodes of epithelial injury or aberrant repair mechanisms . One hypothesis to explain the relationship between PGD and BOS is that the initial injury from PGD triggers an exuberant but dysregulated epithelial repair process. Persistence of the aberrant repair process in response to additional insults to the graft, such as viral infections and episodes of ACR, may eventually lead to BOS. This hypothesis is supported by recent work demonstrating aberrant epithelial cellular composition after an external injury in an animal model of BOS .
Prior studies of BOS have primarily focused on later risk factors, either months after transplantation or at the time of diagnosis of BOS . However, it is not clear when the epithelial injury leading to BOS begins, and the period immediately after transplantation may be important due to the inflammatory response related to ischemia reperfusion injury (IRI; Ref. . Although IRI is thought to be a major contributor to PGD , it may also be associated with sub-clinical epithelial injury independent of clinically significant PGD, triggering an abnormal epithelial repair process that leads to BOS.
The receptor for advanced glycation end products (RAGE) is a multi-ligand pattern recognition receptor implicated in acute and chronic inflammation . We have previously demonstrated an association with increased levels of soluble receptor for advanced glycation end products (sRAGE), the extracellular ligand-binding domain, with PGD after lung transplantation . sRAGE may have roles in endothelial injury and innate immune signaling. However, RAGE is highly expressed in epithelial cells in the lung  and is a recognized marker of type I alveolar epithelial injury in both animal models of ALI and human studies of ALI [14, 15]. In physiologic states, sRAGE is important in modulating adhesion of alveolar epithelial cells to the basement membrane . A role for sRAGE in fibrosis, during which this relationship is disrupted, has been postulated . Early changes in sRAGE may be a signal of early epithelial damage, as well as a marker of later lung injury, manifesting as BOS.
In this study, we aimed to evaluate the association between plasma sRAGE measured 6 and 24 h after transplantation with subsequent development of BOS. We hypothesized that plasma sRAGE levels would be associated with the development of BOS, independent of potentially confounding variables.
- Top of page
- Supporting Information
There were 106 subjects in the cohort, 60 (57%, 95% CI: 47%, 66%) developed BOS. All subjects had a 24-h sRAGE measurement and 94 subjects had a 6-h sRAGE measurement. The average time to development of BOS was 3.4 ± 1.8 years. Subjects with BOS were older; more frequently had COPD as their pretransplant diagnosis, had a higher frequency of GERD and higher mean levels of sRAGE (Table 1).
Table 1. Demographic characteristics of the study population. The p values were calculated using t-test or chi-square test
| ||BOS||No BOS|| |
| ||(n = 60)||(n = 46)||p-Value|
|Time to BOS (yrs)||3.4 ± 1.8|| || |
|Age||57 ± 7||54 ± 11||0.06|
|Bilateral transplant||22 (51%)||21 (49%)||0.14|
|Race|| || || |
| Caucasian||53 (88%)||41 (89%)||0.63|
| African American||6 (10%)||3 (7%)|| |
| Hispanic||1 (2%)||1 (2%)|| |
| Other||0 (0%)||1 (2%)|| |
|Female gender||25 (42%)||13 (28%)||0.12|
|Native disease|| || ||0.19|
| COPD||42 (70%)||23 (50%)|| |
| CF||2 (3%)||4 (9%)|| |
| IPF||12 (20%)||16 (34%)|| |
| PPH||0 (0%)||1 (2%)|| |
| Sarcoid||2 (3%)||0 (0%)|| |
| CHD||1 (2%)||2 (4%)|| |
| Other||1 (1%)||0 (0%)|| |
|Grade 3 PGD at 72 h||4 (7%)||3 (6%)||0.98|
|AR grade 2 or higher (n = 104)||39 (65%)||23 (53%)||0.19|
|GERD||19 (32%)||4 (9%)||<0.01|
|sRAGE level at 6 h (pg/mL)||9112 ± 11405||6484 ± 6954||0.20|
|sRAGE level at 24 h (pg/mL)||5249 ± 7213||2897 ± 2576||0.04|
Plasma sRAGE levels at 6 h and 24 h were associated with an increased hazard of BOS (HR per SD of sRAGE at 6 h: 1.71, 95% CI: 1.12, 2.62, p = 0.02; HR per SD of sRAGE at 24 h: 1.75, 95% CI: 1.14, 2.68. p = 0.01). When analyzed by quartile, sRAGE at 6 h was not associated with time to BOS (log-rank p = 0.76), however, sRAGE at 24 h was (log-rank p = 0.01; Figure 1). Measured at 24 h, the highest quartile (quartile 4) of sRAGE had the greatest hazard of BOS (HR 3.09, 95% CI: 1.49, 6.43, p < 0.01) when compared to the lowest quartile (quartile 1). We were unable to detect a difference between quartile 2 (HR: 1.59, 95% CI: 0.75, 3.34, p = 0.23) or quartile 3 (HR: 1.27, 95% CI: 0.59, 2.76, p = 0.54) when compared to quartile 1.
Figure 1. Kaplan–Meier plot describing the association of quartiles of sRAGE with BOS. Quartile 1 is the lowest quartile of standardized sRAGE and quartile 4 is the highest. The p value was generated from log-rank test.
Download figure to PowerPoint
The association between sRAGE and time to BOS remained significant after bivariable adjustment for all evaluated potential confounders, including cardiopulmonary bypass use and volume of blood transfusion during the first 24 h (Table 2). Our multivariable model, after adjusting for hypothesized confounders, demonstrated a HR for time to BOS of 1.67 (95% CI: 1.51, 1.84, p < 0.01) for each SD of SRAGE measured at 6 h. Based on the results of our bivariable model, we added PASP and volume of blood transfusion to the 24-h analysis. The HR for time to BOS of 2.80 (95% CI: 2.39, 3.28, p < 0.01) for each SD of sRAGE measured at 24 h (Table 2). Exclusion of peak FEV1 from the model did not significantly change the analysis  hr HR: 1.73, 95% CI: 1.57, 1.91, p < 0.01), 24 hr HR: 2.70 (95% CI: 2.34, 3.12, p < 0.01).
Table 2. Association of plasma sRAGE levels at 6 and 24 h with time to BOS
| ||Hazard ratio (95% CI)|| ||Hazard ratio (95% CI)|| |
| ||sRAGE at 6 h|| ||sRAGE at 24 h|| |
|Variable||(n = 94)||p-Value||(n = 106)||p-Value|
|sRAGE per 1 SD||1.71 (1.12, 2.62)||0.02||1.75 (1.14, 2.68)||0.01|
|Adjusted for|| || || || |
| Grade 3 PGD at 72 h||1.69 (1.11, 2.57)||0.01||2.23 (1.24, 4.01)||0.01|
| ACR (per increase in grade by 1)|| || || || |
| or higher||1.76 (1.61, 1.93)||<0.01||1.68 (1.54, 1.84)||<0.01|
| Peak FEV1||1.57 (1.03, 2.38)||0.03||1.89 (1.24, 2.90)||<0.01|
| CBP||1.69 (1.11, 2.58)||0.02||2.08 (1.31, 3.32)||<0.01|
| Recipient race||1.70 (1.11, 2.60)||0.01||1.81 (1.14, 2.88)||0.01|
| Recipient diagnosis||1.65 (1.08, 2.53)||0.02||1.78 (1.16, 2.73)||0.01|
| Recipient sex||1.76 (1.15, 2.67)||0.01||1.88 (1.22, 2.92)||0.01|
| Recipient age||1.70 (1.11, 2.61)||0.01||1.73 (1.14, 2.63)||0.01|
| Donor sex||1.66 (1.09, 2.54)||0.02||1.71 (1.12, 2.61)||0.01|
| Donor age||1.72 (1.12, 2.64)||0.01||1.75 (1.14, 2.67)||0.01|
| Donor race||1.60 (0.98, 2.62)||0.06||1.78 (1.15, 2.75)||0.01|
| Blood (ml) during first 24 h||2.02 (1.23, 3.34)||0.01||2.35 (1.41, 3.90)||<0.01|
| Transplant type||1.66 (1.09, 2.54)||0.02||2.15 (1.36, 3.41)||<0.01|
| PASP at transplantation||1.73 (1.13, 2.64)||0.01||2.16 (1.29, 3.60)||<0.01|
| GERD||1.74 (1.13, 2.67)||0.01||1.61 (1.04. 2.49)||0.03|
|Multivariable model1||1.67 (1.51, 1.84)||<0.01||2.80 (2.39, 3.28)||<0.01|
Consistent with our previous findings, plasma sRAGE measured at 24 h was also associated with grade 3 PGD at 72 h (OR for each SD of sRAGE at 24hrs: 5.56, 95% CI: 1.82, 16.98 p < 0.01). Subjects in the highest quartile of sRAGE at 24 h had a greater frequency of grade 3 PGD at 72 h compared to subjects in all other quartiles (15% vs. 4%, p = 0.04). Higher sRAGE levels were associated with increasing grade of PGD (p for trend at 6 h = 0.01, p for trend at 24 h <0.01; Figure S1). We evaluated the relationship of sRAGE at 24 h and BOS while adjusting for grade 3 PGD at 72 h; and the association between sRAGE and BOS remained significant on adjustment (HR 2.23, 95% CI: 1.24, 4.01, p = 0.01; Table 2).
In analyses accounting for death as a competing risk, the association between sRAGE and BOS was unchanged at 24 h (HR: 1.82, 95% CI: 1.18, 2.79, p = 0.01), however, the association between sRAGE at 6 h and BOS was slightly attenuated (HR: 1.67, 95% CI: 0.95, 3.00, p = 0.08). In GEE analyses focusing on the relationship of sRAGE and changes in FEV1, the average FEV1 using all measurements after transplantation in quartile 4 of sRAGE measured at 6 h was 177cc smaller (p < 0.01) than quartile 1 and at 24 hours, the average FEV1 was 5-cc smaller in quartile 4 than quartile 1 (p = 0.90).
- Top of page
- Supporting Information
In this study, we demonstrated an association between plasma sRAGE levels measured at both 6 and 24 h postoperatively with long-term risk for BOS. These findings suggest that early epithelial injury (within 24 h) after transplantation may be important in later development of BOS. The relationship between sRAGE and time to BOS remained significant despite adjustment for multiple potential confounders including ACR, cardiopulmonary bypass and blood transfusion.
RAGE is a pattern recognition receptor that is highly expressed in the lung during physiologic states . It is thought to be a biologic marker of type I alveolar cell injury, and is important in lung homeostasis through regulation of lung adhesion of alveolar epithelial cells to the basement membrane . Prior research has demonstrated a role for RAGE in chronic fibrotic lung diseases, such as IPF [22, 23]. Over-expression of RAGE has been demonstrated in lungs from subjects with IPF, particularly in the fibroblastic foci . Although there is also evidence indicating RAGE may have a protective effect against fibrosis , it may be that circulating plasma sRAGE is indicative of decreased RAGE in the epithelium in fibrotic disease. In this study, we found subjects with BOS had higher levels of sRAGE than those without, and higher levels than reported levels in healthy controls , adding to the literature supporting the role of sRAGE as a marker for the development of lung fibrosis and demonstrating the importance of early injury in long-term outcomes.
As we have previously published, sRAGE levels are associated with PGD , and others have demonstrated an association between RAGE in donor BAL fluid with PGD . In this study, we have demonstrated an association between sRAGE levels early after transplantation and BOS. Although the association between sRAGE and BOS was independent of grade 3 PGD, sRAGE may be a more sensitive marker of early epithelial injury than the clinical measures currently used to detect PGD. Therefore, the association between sRAGE and BOS may be useful in further clarifying the association between early sub-clinical epithelial injury and clinically apparent PGD with BOS.
If sRAGE is a mediator of the development of BOS, the mechanism may be via epigenetic changes occurring during ischemia reperfusion injury or clinically apparent PGD after lung transplantation leading to persistent changes in the RAGE pathway. Epigenetic changes have been demonstrated in a model of kidney transplant where DNA methylation after ischemia reperfusion injury persisted for up to 6 months . This type of change in regulation of RAGE isoforms may lead to up-regulation of the innate immune pathway leading to chronic inflammation and fibrosis . Further studies examining RAGE in bronchoalveolar lavage fluid at the time of transplant, genetic modifications of RAGE pre- and posttransplant and longitudinal measurements of sRAGE at later timepoints will be important in clarifying whether the association between sRAGE is a mediator of the development of BOS and important in the link between PGD and BOS, or a marker of another underlying process.
The association between sRAGE at 6 h and BOS was slightly attenuated when accounting for death as a competing risk. This may be because we excluded all early deaths, had limited power because we had fewer subjects at the 6-h timepoint, or that the relationship between sRAGE and BOS was truly confounded by death. Validation of this timepoint in a large sample size is necessary.
There are several limitations to this study. We did not measure sRAGE in plasma at later timepoints, therefore we cannot comment on changes in sRAGE levels over time. Not every subject in our cohort was uniformly screened for GERD, however, if they were not evaluated, it seems unlikely they had symptomatic GERD. This is a single-center study and may not be generalizable to other centers. As no one in this cohort had documented CMV pneumonitis; we were unable to evaluate the effect of CMV in mediating or confounding the relationship between sRAGE and BOS. This study focused only on the BOS phenotype and did not account for other types of chronic allograft dysfunction, such as restrictive allograft syndrome (RAS; Ref. . Finally, though we did not have a committee to adjudicate BOS, we took into account factors, including ACR and GERD that may have contributed to the development of BOS.
In conclusion, early plasma sRAGE levels are associated with increased hazard of BOS. Early epithelial injury, either sub-clinical or manifesting as concurrent PGD, may be a risk factor for later BOS. Our study prioritizes a focus on epithelial injury and RAGE for longitudinal studies aimed at understanding the link between early lung injury and BOS.