key: cord-288931-d4fyitnk authors: Parisi, Valentina; Leosco, Dario title: Precision medicine in COVID-19: IL-1β a potential target date: 2020-04-18 journal: JACC Basic Transl Sci DOI: 10.1016/j.jacbts.2020.04.006 sha: doc_id: 288931 cord_uid: d4fyitnk nan On April 4, 2020, coronavirus disease 2019 (COVID-19) has been confirmed in 1.395 .136 people worldwide with a mortality of approximately 5.8 %. Since the COVID 19 dramatic outbreak, there is an urgent need for effective treatments. A wide spectrum of disease severity has been described, ranging from asymptomatic, mildly symptomatic, severe symptomatic requiring hospitalization, to respiratory failure from acute respiratory distress syndrome (ARDS). Furthermore, it has been widely reported that the prevalence of the disease is almost three times higher in males. Overall, these evidences suggest that the prognosis appears to be more conditioned by the host's response than by the infection itself, thus a precision medicine approach is highly desirable. In cardiovascular diseases, an important source of inflammatory mediators, including IL-1β, is the visceral adipose tissue (4) . Of note, activation of NLRP3 inflammasome in macrophages attenuates uncoupling protein 1 (UCP1) induction and mitochondrial respiration in cultures of primary adipocytes and the NLRP3 inflammasome activation appears to link obesity and dysfunctional thermogenesis (5). In conclusion, there are many open questions that merit to be explored: i) to verify the role of NLRP3 in the clinical variability of COVID-19; ii) to test the potential therapeutic effect in COVID-19 of IL-1β inhibition (canakinumab, anakinra); iii) to explore the role of visceral adipose tissue in the inflammatory response to SARS-CoV-2 infection. Bat coronaviruses and experimental infection of bats, the Philippines. Emerging infectious diseases Dampened NLRP3-mediated inflammation in bats and implications for a special viral reservoir host Mechanism of NLRP3 inflammasome activation Imbalance Between Interleukin-1β and Interleukin-1 Receptor Antagonist in Epicardial Adipose Tissue Is Associated With Non ST-Segment Elevation Acute Coronary Syndrome Inhibitory Effects of Toll-Like Receptor 4, NLRP3 Inflammasome, and Interleukin-1β on White Adipocyte Browning