Key result
A novel allysine-binding gadolinium chelate (GdOA) MRI probe can non-invasively detect and quantify lung fibrogenesis, with signal enhancement correlating with disease extent and therapeutic response.
Why the study?
Can a novel allysine-binding gadolinium chelate (GdOA) non-invasively detect and quantify lung fibrogenesis using MRI?
Can a novel allysine-binding gadolinium chelate (GdOA) non-invasively detect and quantify lung fibrogenesis using MRI?
A novel allysine-binding gadolinium chelate (GdOA) enables non-invasive detection and quantification of lung fibrogenesis via MRI, correlating with disease extent and therapeutic response.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for molecular MRI in fibrosis; leaves open human translation and validation.
Fibrogenesis is the active production of extracellular matrix in response to tissue injury. In many chronic diseases persistent fibrogenesis results in the accumulation of scar tissue, which can lead to organ failure and death. However, no non-invasive technique exists to assess this key biological process. All tissue fibrogenesis results in the formation of allysine, which enables collagen cross-linking and leads to tissue stiffening and scar formation. We report herein a novel allysine-binding gadolinium chelate (GdOA), that can non-invasively detect and quantify the extent of fibrogenesis using magnetic resonance imaging (MRI). We demonstrate that GdOA signal enhancement correlates with the extent of the disease and is sensitive to a therapeutic response.
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Waghorn et al. (2017) studied Lung Fibrogenesis. Allysine-binding gadolinium chelate (GdOA) MRI probe was evaluated on Detection and quantification of fibrogenesis via GdOA signal enhancement. A novel allysine-binding gadolinium chelate (GdOA) MRI probe can non-invasively detect and quantify lung fibrogenesis, with signal enhancement correlating with disease extent and therapeutic response.
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