D plasma samples were compared using the Paired t test on log-transformed values. We evaluated the relationship between log10 UA levels, log10 parasite densities, log10 cytokine levels and log10 creatinine levels by Pearson’s correlation coefficient, and tested CI 1011 whether they were different from 0 using the t-distribution. To determine how parasite density and creatinine level predict UA level, we used a linear model with log 10 UA level as a response. Analyses were done in either GraphPad version 5.01 (GraphPad Software, La Jolla, CA) or R version 2.13.0 (R Core Development Team, http:/ www.r-project.org).ResultsParasite-derived UA stimulates the production of inflammatory cytokines from human PBMCs in vitro [11]. To explore whether this stimulation may occur in vivo, we measured plasma UA levels, parasite densities and plasma cytokine levels in a cohort of Malian children who developed P. falciparum malaria. Plasma samples were available for 90 (501/557) of children who developed a first episode of malaria in 2008. Of these samples, 473, 24 and 4 were from children with uncomplicated malaria (UM), non-cerebral severe malaria (NCSM) and cerebral malaria (CM), respectively. We included in this study an additional 5 plasma samples from children who developed CM in the 2009 malaria season, giving a total of 9 CM samples. Table 1 shows the characteristics of these children, stratified by clinical presentation. As expected, children with CM were younger (all were #3 years) than those with UM (p,0.0001). Compared tochildren with UM, median parasite densities were higher in children with NCSM (p = 0.0048) and CM (p = 0.0060). Median MedChemExpress SMER-28 hemoglobin levels at presentation did not differ between children with UM, NCSM and CM. The degree of anemia, however, worsened in all three groups of children after 72 hours of antimalarial therapy, and was significantly more severe in those children with CM (p = 0.0001) (Table 1). Compared to children with UM, those with NCSM and CM had higher and lower levels of plasma creatinine, respectively, but only the latter difference was statistically significant (Table 1). To determine whether plasma UA levels were associated with malaria severity, we compared them in groups of children that differed in clinical presentation. We found that UA levels were increased in children with NCSM (median 5.74 mg/dl, 1.21-fold increase, 95 CI 1.09?.35, p = 0.0007) and CM (median 5.69 mg/dl, 1.19-fold increase, 95 CI 0.97?.41, p = 0.0890) compared to those in children with UM (median 4.60 mg/dl) (Table 1 and Fig. 1a). Among these 501 children, we identified 39 children who provided a `baseline’ plasma sample in May 2008 when they were healthy and aparasitemic. In these paired plasma samples, we found that baseline UA levels increased 1.49-fold (95 CI 1.34, 1.65; p,0.0001) during a child’s malaria episode (GMT 3.14 mg/dl vs. 4.67 mg/dl) (Fig. 1b). To explore the cause of elevated UA levels during a malaria episode, we performed a series of univariate analyses on data obtained from children with UM. We found that log10 UA levels correlated significantly with log10 parasite densities (Pearson r = 0.1641, n = 438, p = 0.0006) but not age (r = 20.0144, n = 438, p = 0.7631). Since UA levels are known to be affected by renal function (which may be compromised during 
a malaria episode) [9,16,17], we also measured plasma creatinine levels. We found that log10 UA levels correlated significantly with log10 creatinine levels (r = 0.1634, n =.D plasma samples were compared using the Paired t test on log-transformed values. We evaluated the relationship between log10 UA levels, log10 parasite densities, log10 cytokine levels and log10 creatinine levels by Pearson’s correlation coefficient, and tested whether they were different from 0 using the t-distribution. To determine how parasite density and creatinine level predict UA level, we used a linear model with log 10 UA level as a response. Analyses were done in either GraphPad version 5.01 (GraphPad Software, La Jolla, CA) or R version 2.13.0 (R Core Development Team, http:/ www.r-project.org).ResultsParasite-derived UA stimulates the production of inflammatory cytokines from human PBMCs in vitro [11]. To explore whether this stimulation may occur in vivo, we measured plasma UA levels, parasite densities and plasma cytokine levels in a cohort of Malian children who developed P. falciparum malaria. Plasma samples were available for 90 (501/557) of children who developed a first episode of malaria in 2008. Of these samples, 473, 24 and 4 were from children with uncomplicated malaria (UM), non-cerebral severe malaria (NCSM) and cerebral malaria (CM), respectively. We included in this study an additional 5 plasma samples 
from children who developed CM in the 2009 malaria season, giving a total of 9 CM samples. Table 1 shows the characteristics of these children, stratified by clinical presentation. As expected, children with CM were younger (all were #3 years) than those with UM (p,0.0001). Compared tochildren with UM, median parasite densities were higher in children with NCSM (p = 0.0048) and CM (p = 0.0060). Median hemoglobin levels at presentation did not differ between children with UM, NCSM and CM. The degree of anemia, however, worsened in all three groups of children after 72 hours of antimalarial therapy, and was significantly more severe in those children with CM (p = 0.0001) (Table 1). Compared to children with UM, those with NCSM and CM had higher and lower levels of plasma creatinine, respectively, but only the latter difference was statistically significant (Table 1). To determine whether plasma UA levels were associated with malaria severity, we compared them in groups of children that differed in clinical presentation. We found that UA levels were increased in children with NCSM (median 5.74 mg/dl, 1.21-fold increase, 95 CI 1.09?.35, p = 0.0007) and CM (median 5.69 mg/dl, 1.19-fold increase, 95 CI 0.97?.41, p = 0.0890) compared to those in children with UM (median 4.60 mg/dl) (Table 1 and Fig. 1a). Among these 501 children, we identified 39 children who provided a `baseline’ plasma sample in May 2008 when they were healthy and aparasitemic. In these paired plasma samples, we found that baseline UA levels increased 1.49-fold (95 CI 1.34, 1.65; p,0.0001) during a child’s malaria episode (GMT 3.14 mg/dl vs. 4.67 mg/dl) (Fig. 1b). To explore the cause of elevated UA levels during a malaria episode, we performed a series of univariate analyses on data obtained from children with UM. We found that log10 UA levels correlated significantly with log10 parasite densities (Pearson r = 0.1641, n = 438, p = 0.0006) but not age (r = 20.0144, n = 438, p = 0.7631). Since UA levels are known to be affected by renal function (which may be compromised during a malaria episode) [9,16,17], we also measured plasma creatinine levels. We found that log10 UA levels correlated significantly with log10 creatinine levels (r = 0.1634, n =.