Key result
Novel circulating biomarkers show promise for guiding patient stratification and personalized therapy in circulatory shock.
Why the study?
High mortality in circulatory shock necessitates rapid identification of high-risk patients and early treatment monitoring, creating an unmet need for circulating biomarkers to improve stratification, predict responses, and guide personalized therapy.
Does assessment with circulating biomarkers improve patient stratification and predict treatment responses in critically ill patients with circulatory shock?
Does assessment with circulating biomarkers improve patient stratification and predict treatment responses in critically ill patients with circulatory shock?
Novel circulating biomarkers offer a promising approach to phenotype and personalize treatment for critically ill patients with circulatory shock.
Answers are grounded in this paper and cite their sources.
Biomarker assessment in circulatory shock remains investigational; leaves open prospective validation before guiding personalized therapy.
PURPOSE OF REVIEW: Circulatory shock is one of the most common reasons for ICU admission. Mortality rates in excess of 40% necessitate the rapid identification of high-risk patients, as well as the early assessment of effects of initiated treatments. There is an unmet medical need for circulating biomarkers that may improve patient stratification, predict responses to treatment interventions and may even be a target for novel therapies, enabling a better biological rationale to personalize therapy. RECENT FINDINGS: Apart from established biomarkers such as lactate, ScvO2 or NT-pro-BNP, novel biomarkers, including adrenomedullin, angiopoietins, angiotensin I/II ratios, renin and DPP3 show promise, as they are all associated with well defined, therapeutically addressable molecular pathways that are dysregulated during circulatory shock. Although some of the therapies related to these biomarkers are still in preclinical stages of development, they may represent personalized treatment opportunities for patients in circulatory shock. SUMMARY: From a molecular perspective, shock represents a highly heterologous syndrome, in which multiple unique pathways are dysregulated. Assessment of the status of these pathways with circulating biomarkers may provide a unique opportunity to detect specific phenotypes and implement personalized medicine in the treatment of circulatory shock.
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Lier et al. (2021) conducted a review in Circulatory shock. Circulating biomarkers (e.g., adrenomedullin, angiopoietins, renin, DPP3) was evaluated. Novel circulating biomarkers such as adrenomedullin, angiopoietins, renin, and DPP3 show promise for patient stratification and personalized therapy in circulatory shock.
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