Dynamic of Angiotensin type I receptor antibodies is associated with poor graft function following lung transplant

Lung transplantation (LTx) saves the lives of patients with end-stage lung disease, but the longevity of transplanted lungs is much lower than that of other transplanted organs. Antibodies to angiotensin type 1 receptor (AT1Rabs) have been linked to poorer graft outcome. This single-centre observational study assessed 49 patients that underwent LTx between July 2014 and October 2015 at The Alfred. AT1Rabs levels were measured pre-LTx and one-year post-LTx. AT1Rabs levels ≤10 U/ml were considered negative, >10 U/ml and ≤17U/ml intermediate, and >17 U/ml positive. The mean age at LTx was 59±9 and 53% were male. The mean follow up time was 7±3 years. There was a significant decrease in AT1Rabs levels after LTx and implementation of immunosuppressive therapy (12.3 U/l vs 9.8 U/l, p<0.001). The change in AT1Rabs levels between negative, intermediate and positive can be defined as increasing, stable or decreasing (Figure1):6% of patients had an increase in AT1Rabs levels, whereas 61% were stable and 33% had a decrease. A risk category increase was associated with a lower FEV1% predicted value at 12 months compared to patients with stable or decreasing risk category (60%vs92%vs82%, p=0.039). Additionally, a risk category increase was associated with baseline lung allograft dysfunction (p=0.025). An increase in risk according to AT1Rabs levels is associated with poor graft function following LTX. <fig><object-id>erj;64/suppl_68/PA578/F1</object-id><object-id>F1</object-id><object-id>F1</object-id><graphic></graphic></fig>

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Publication Details

Journal
Transplantation
Published
2024-09-14
DOI
https://doi.org/10.1183/13993003.congress-2024.pa578
Primary Topic
Transplantation: Methods and Outcomes
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article
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article

Dynamic of Angiotensin type I receptor antibodies is associated with poor graft function following lung transplant

Samantha Ennis, Helen Shingles, Andrei Darie, Glen Westall et al.
Transplantation
Transplantation: Methods and Outcomes
article

Dynamic of Angiotensin type I receptor antibodies is associated with poor graft function following lung transplant

Samantha Ennis, Helen Shingles, Andrei Darie, Glen Westall, Bronwyn Levvey, Kovi Levin, Lucy C. Sullivan, Steven Hiho, Miranda Paraskeva, Gregory Snell
article en

Abstract

Lung transplantation (LTx) saves the lives of patients with end-stage lung disease, but the longevity of transplanted lungs is much lower than that of other transplanted organs. Antibodies to angiotensin type 1 receptor (AT1Rabs) have been linked to poorer graft outcome. This single-centre observational study assessed 49 patients that underwent LTx between July 2014 and October 2015 at The Alfred. AT1Rabs levels were measured pre-LTx and one-year post-LTx. AT1Rabs levels ≤10 U/ml were considered negative, >10 U/ml and ≤17U/ml intermediate, and >17 U/ml positive. The mean age at LTx was 59±9 and 53% were male. The mean follow up time was 7±3 years. There was a significant decrease in AT1Rabs levels after LTx and implementation of immunosuppressive therapy (12.3 U/l vs 9.8 U/l, p<0.001). The change in AT1Rabs levels between negative, intermediate and positive can be defined as increasing, stable or decreasing (Figure1):6% of patients had an increase in AT1Rabs levels, whereas 61% were stable and 33% had a decrease. A risk category increase was associated with a lower FEV1% predicted value at 12 months compared to patients with stable or decreasing risk category (60%vs92%vs82%, p=0.039). Additionally, a risk category increase was associated with baseline lung allograft dysfunction (p=0.025). An increase in risk according to AT1Rabs levels is associated with poor graft function following LTX. <fig><object-id>erj;64/suppl_68/PA578/F1</object-id><object-id>F1</object-id><object-id>F1</object-id><graphic></graphic></fig>

Transplantation
Australian Red Cross Lifeblood (AU), The Alfred Hospital (AU), Alfred Health (AU)
No poverty
Openalex Percentile: Top 63%
Transplantation: Methods and Outcomes
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