Key result
Various biomarkers from radiology, tissue, bronchoalveolar lavage, and blood show promise for early detection and phenotyping of chronic lung allograft dysfunction, but require multicenter validation.
Why the study?
Chronic lung allograft dysfunction impairs lung transplant outcomes, driving an increasing need for biomarkers to assist in earlier detection, differential diagnosis of phenotypes, and prognostication.
Can biomarkers assist in the earlier detection, differential diagnosis, and prognostication of CLAD in lung transplant patients?
Can biomarkers assist in the earlier detection, differential diagnosis, and prognostication of CLAD in lung transplant patients?
A multimodal approach combining clinical data with various biomarkers is necessary for the early detection and prognostication of chronic lung allograft dysfunction.
CLAD biomarker research may aid phenotyping and prognostication; leaves open prospective validation before clinical use in lung transplant.
Chronic lung allograft dysfunction (CLAD) remains a major hurdle impairing lung transplant outcome. Parallel to the better clinical identification and characterization of CLAD and CLAD phenotypes, there is an increasing urge to find adequate biomarkers that could assist in the earlier detection and differential diagnosis of CLAD phenotypes, as well as disease prognostication. The current status and state-of-the-art of biomarker research in CLAD will be discussed with a particular focus on radiological biomarkers or biomarkers found in peripheral tissue, bronchoalveolar lavage' and circulating blood' in which significant progress has been made over the last years. Ultimately, although a growing number of biomarkers are currently being embedded in the follow-up of lung transplant patients, it is clear that one size does not fit all. The future of biomarker research probably lies in the rigorous combination of clinical information with findings in tissue, bronchoalveolar lavage' or blood. Only by doing so, the ultimate goal of biomarker research can be achieved, which is the earlier identification of CLAD before its clinical manifestation. This is desperately needed to improve the prognosis of patients with CLAD after lung transplantation.
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Verleden et al. (2022) conducted a review in Chronic lung allograft dysfunction (CLAD). Biomarkers was evaluated. Various biomarkers from radiology, tissue, bronchoalveolar lavage, and blood show promise for early detection and phenotyping of chronic lung allograft dysfunction, but require multicenter validation.
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