N. Uzuner et al., URINARY NITRITE EXCRETION IN LOW-BIRTH-WEIGHT NEONATES WITH SYSTEMIC INFLAMMATORY RESPONSE SYNDROME, Biology of the neonate, 71(6), 1997, pp. 362-366
Increased nitric oxide (NO) levels are thought to play an important ro
le in the pathophysiology of the systemic inflammatory response syndro
me (SIRS) which is caused by disseminated vascular endothelial damage.
Clinical studies have shown that urinary nitrite (NO2-) and nitrate (
NO3-) excretions can be utilized as indexes of NO formation. The SIRS
and NO relationship was investigated in 15 neonates with SIRS, gestati
onal age 32.5 +/- 4.4 weeks and weight 1,737 +/- 753 g. The control gr
oup comprised 18 neonates with a gestational age of 32.8 +/- 3.5 weeks
and a weight of 1,778 +/- 538 g. There was no significant difference
in birth weights and gestational ages between the two groups (p > 0.05
and p > 0.05). The urinary nitrite levels obtained in the subjects we
re normalized for urinary creatinine concentrations. The mean urinary
nitrite levels in the control group neonates were found to be 4.22 +/-
1.8 mu mol/mmol creatinine on the Ist day, 4.09 +/- 2.28 on the 2nd,
3.62 +/- 1.6 on the 3rd, and 4.01 +/- 1.12 mu mol/mmol creatinine on t
he 7th day. There were no statistically significant differences betwee
n these levels (p > 0.05). We determined urinary levels of nitrite in
neonates in the study group within the first 24 h of SIRS symptoms and
found these levels (18.35 +/- 11.16 mu mol nitrite/mmol creatinine) t
o be elevated as compared with those of the control subjects on the 7t
h day of life (p < 0.0005). In conclusion, urinary nitrite excretion i
s significantly elevated in neonates with SIRS due to septic events, a
nd these results suggest that NO might play a part in SIRS.