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Original Article

Serum concentration of chromogranin A at admission: An early biomarker of severity in critically ill patients

, , , , , , & show all
Pages 38-44 | Received 19 Dec 2007, Published online: 08 Jul 2009

Figures & data

Figure 1.  Flow chart of the study. A total of 100 consecutive intensive care unit (ICU) admissions over a 2-month period were screened and 14 healthy controls from our medical staff were also analyzed. Patients were excluded who had former chronic renal, hepatic, or cardiac failures, if they were undergoing treatment with steroids or proton pump inhibitors and if they had a medical history with neuroendocrine tumors. Finally, patients with recent multiple stress or a surgical intervention were also excluded.

Figure 1.  Flow chart of the study. A total of 100 consecutive intensive care unit (ICU) admissions over a 2-month period were screened and 14 healthy controls from our medical staff were also analyzed. Patients were excluded who had former chronic renal, hepatic, or cardiac failures, if they were undergoing treatment with steroids or proton pump inhibitors and if they had a medical history with neuroendocrine tumors. Finally, patients with recent multiple stress or a surgical intervention were also excluded.

Table I.  Characteristics of participants. Data are mean values±SEM. Pairwise comparisons are shown.

Table II.  Biological values in the study population. Data are median (interquartile range). The comparisons are versus the healthy control group (HC).

Figure 2.  Serum concentrations of chromogranin A (CGA) on admission in critically ill patients. Controls (SIRS-, Infection -; n=23) included healthy controls (n = 14) and patients with self-poisoning (n=9) without SIRS; SIRS patients (SIRS+, Infection-; n=13) were those with systemic inflammatory response syndrome from non-septic origin; septic patients (n=31) are in gray. The medians (interquartile ranges) for the three groups were 40.0 µg/L (35.0–52.5) for controls, 110.0 µg/L (81.0–143.0) for SIRS patients, and 138.5 µg/L (65–222.3) for septic patients respectively. * P < 0.01; # P < 0.001.

Figure 2.  Serum concentrations of chromogranin A (CGA) on admission in critically ill patients. Controls (SIRS-, Infection -; n=23) included healthy controls (n = 14) and patients with self-poisoning (n=9) without SIRS; SIRS patients (SIRS+, Infection-; n=13) were those with systemic inflammatory response syndrome from non-septic origin; septic patients (n=31) are in gray. The medians (interquartile ranges) for the three groups were 40.0 µg/L (35.0–52.5) for controls, 110.0 µg/L (81.0–143.0) for SIRS patients, and 138.5 µg/L (65–222.3) for septic patients respectively. * P < 0.01; # P < 0.001.

Figure 3.  Influence of serum chromogranin A (CGA) concentration at admission on survival time. Kaplan-Meier analysis in the ICU patients (n=53) with inframedian (dashed line) or supramedian (solid line) values (71 µg/L). These data confirmed that the lower the serum concentration on admission, the longer the survival time (log rank test, P=0.0013). Survival time is plotted against survival rate.

Figure 3.  Influence of serum chromogranin A (CGA) concentration at admission on survival time. Kaplan-Meier analysis in the ICU patients (n=53) with inframedian (dashed line) or supramedian (solid line) values (71 µg/L). These data confirmed that the lower the serum concentration on admission, the longer the survival time (log rank test, P=0.0013). Survival time is plotted against survival rate.

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