Cytokine Profiles as Potential Prognostic and Therapeutic Markers in SARS-CoV-2-Induced ARDS

被引:59
作者
Salton, Francesco [1 ,2 ]
Confalonieri, Paola [1 ,2 ]
Campisciano, Giuseppina [3 ]
Cifaldi, Rossella [1 ]
Rizzardi, Clara [2 ,4 ]
Generali, Daniele [2 ,4 ]
Pozzan, Riccardo [1 ,2 ]
Tavano, Stefano [1 ,2 ]
Bozzi, Chiara [1 ,2 ]
Lapadula, Giulia [1 ,2 ]
Meduri, Gianfranco Umberto [5 ]
Confalonieri, Marco [1 ,2 ]
Comar, Manola [2 ,3 ]
Lerda, Selene [6 ]
Ruaro, Barbara [1 ,2 ]
机构
[1] Univ Trieste, Univ Hosp Trieste, Pulmonol Unit, I-34149 Trieste, Italy
[2] Univ Trieste, Dept Med Surg & Hlth Sci, I-34149 Trieste, Italy
[3] Inst Maternal & Child Hlth IRCCS Burlo Garofolo, Dept Adv Translat Microbiol, I-34137 Trieste, Italy
[4] Univ Hosp Trieste, Dept Pathol, I-34149 Trieste, Italy
[5] Univ Tennessee, Dept Med, Pulm Crit Care & Sleep Med Div, Hlth Sci Ctr, Memphis, TN 38163 USA
[6] 24Ore Business Sch, Via Monte Rosa 91, I-20149 Milan, Italy
关键词
acute respiratory distress syndrome (ARDS); cytokines; glucocorticoids; COVID-19; non-invasive ventilation (NIV); RESPIRATORY-DISTRESS-SYNDROME; RESISTANCE;
D O I
10.3390/jcm11112951
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Glucocorticoids (GCs) have been shown to reduce mortality and the need for invasive mechanical ventilation (IMV) in SARS-CoV-2-induced acute respiratory distress syndrome (ARDS). It has been suggested that serum cytokines levels are markers of disease severity in ARDS, although there is only limited evidence of a relationship between the longitudinal cytokine profile and clinical outcomes in patients with SARS-CoV-2-induced ARDS treated with GC. Methods. We conducted a single-center observational study to investigate serial plasma cytokine levels in 17 patients supported with non-invasive ventilation (NIV) in order to compare the response in five patients who progressed to IMV versus 12 patients who continued with NIV alone. All patients received methylprednisolone 80 mg/day continuous infusion until clinical improvement. Results. The study groups were comparable at baseline. All patients survived. Although IL-6 was higher in the NIV group at baseline, several cytokines were significantly higher in the IMV group on day 7 (IL-6, IL-8, IL-9, G-CSF, IP-10, MCP-1, MIP-1 alpha) and 14 (IL-6, IL-8, IL-17, G-CSF, MIP-1 alpha, RANTES). No significant differences were observed between groups on day 28. Conclusions. Patients in the IMV group had higher inflammation levels at intubation than the NIV group, which may indicate a higher resistance to glucocorticoids. Higher GC doses or a longer treatment duration in these patients might have allowed for a better control of inflammation and a better outcome. Further studies are required to define the prognostic value of cytokine patterns, in terms of both GC treatment tailoring and timely initiation of IMV.
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