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Adrenomedullin, a 52 amino acid peptide, is a member of the calcitonin peptide family and is widely expressed in many tissues and organs.1 It can be upregulated by lipopolysaccharide (LPS) or pro-inflammatory cytokines during the course of bacterial, viral or fungal infections. Adrenomedullin has been shown to play a significant role in many physiological processes, including cellular growth, development, chemotaxis and migration.2-7 It also has potent anti-microbial activity, eliciting its response through membrane channel formation and lysis, as well as anti-apoptotic actions.8-11 However, two main actions are of significant interest in many disease conditions.
Growing evidence indicates that Adrenomedullin plays a key role in reducing vascular permeability and enhancing the stability of the endothelial system.
Adrenomedullin can reflect thepathophysiological changes occurring in the microcirculation duringdisease conditions, which may lead to organ dysfunction.Consequently, monitoring Adrenomedullin levels can be valuable inevaluating disease progression or assessing the efficacy oftherapeutic interventions on the host response.
Adrenomedullin is well-known for its vasodilatory properties. Increased circulating concentrations may result in potent and sustained hypotension, primarily due to the generation of nitric oxide in the vasculature. Transient concentration surges have been reported to contribute to the dramatic hypotension and vascular collapse observed in patients experiencing acute episodes of systemic capillary leak syndrome.20
Both acute and chronic increases in Adrenomedullin can lead to a significant decrease in total peripheral resistance, a drop in blood pressure, and an increase in heart rate, cardiac output, and stroke volume.
Therefore, fluctuations in Adrenomedullin levels can significantly impact blood supply to organs in certain disease settings.
Reliable and accurate measurement of Adrenomedullin is challenging/limited due to several factors, including its short half-life, fast metabolism, low concentrations, rapid degradation by proteases, and binding to compliment factor H. Consequently, Adrenomedullin levels are often underestimated.
The measurement of Mid-Regional proAdrenomedullin (MR-proADM) addresses some of these analytical issues.
MR-proADM is a fragment of 48 amino acids that splits from the proAdrenomedullin (proADM) molecule in a 1:1 ratio with Adrenomedullin, and therefore proportionally represents the levels and activity of Adrenomedullin. Its biological inactivity means that it does not bind to vessel walls and surfaces as found with Adrenomedullin. This biological inactivity, along with the longer half-life of MR-proADM results in a more stable estimation of plasma concentration levels compared to Adrenomedullin.2-3
This biological inactivity, along with the longer half-life of MR-proADM may provide a more stable estimation of plasma concentration levels compared to Adrenomedullin.2-3
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