Literature DB >> 10375364

Neonatal bilirubin production, reflected by carboxyhaemoglobin concentrations, in Down's syndrome.

M Kaplan1, H J Vreman, C Hammerman, D K Stevenson.   

Abstract

AIM: To determine whether increased bilirubin production, reflected by blood carboxyhaemoglobin (COHb) values, is responsible for hyperbilirubinaemia in cases of Down's syndrome with no obvious cause for excessive jaundice.
METHODS: Blood was sampled on the third day of life for COHb, total haemoglobin (tHb), and serum total bilirubin, from 19 consecutively born neonates with Down's syndrome (a subset of 34 term babies), who had developed hyperbilirubinaemia (serum bilirubin >/= 256 micromol), and from 32 term controls. COHb, measured by gas chromatography, was corrected for inspired CO (COHbc) and expressed as a percentage of tHb.
RESULTS: Significantly more of the Down's syndrome subset developed hyperbilirubinaemia than the controls (10/19 (52%) vs 7/32 (22%), relative risk 2.4, 95% confidence intervals (CI) 1.10 to 5.26). Third day serum bilirubin values (mean (SD)) were higher in the Down's syndrome neonates than in controls (214 +- 63 micromol/l vs 172 +- 54 micromol/l, respectively, p=0.015). Mean (SD) COHbc values were significantly higher in the Down's syndrome neonates than in controls (0.92 +- 0. 24% vs 0.63 +- 0.17%; p<0.0001). However, Down's syndrome neonates who became hyperbilirubinaemic had similar COHbc values to those who did not (0.87 +- 0.26% and 0.95 +- 0.23%, respectively). These values contrast with those of the controls, in whom a significant increase in COHbc was associated with hyperbilirubinaemia (0.74 +- 0. 15% vs 0.60 +- 0.16%, respectively; p<0.05). tHb values were similar in both groups.
CONCLUSIONS: Down's syndrome neonates had a greater risk of hyperbilirubinaemia, and higher COHbc values, than controls. However, excessive bilirubin production could not be exclusively responsible for the hyperbilirubinaemia. By inference, decreased bilirubin elimination probably plays a greater part in its pathogenesis than in controls. Down's syndrome neonates may have abnormal erythropoiesis, leading to increased haem turnover.

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Year:  1999        PMID: 10375364      PMCID: PMC1720958          DOI: 10.1136/fn.81.1.f56

Source DB:  PubMed          Journal:  Arch Dis Child Fetal Neonatal Ed        ISSN: 1359-2998            Impact factor:   5.747


  21 in total

1.  NEONATAL JAUNDICE IN DOWN'S SYNDROME.

Authors:  F PANIZON
Journal:  Lancet       Date:  1965-09-04       Impact factor: 79.321

2.  Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.

Authors:  M Kaplan; P Renbaum; E Levy-Lahad; C Hammerman; A Lahad; E Beutler
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

3.  Postnatal change of hemoglobins F and A2 in infants with Down's syndrome (G trisomy).

Authors:  M G Wilson; W A Schroeder; D A Graves
Journal:  Pediatrics       Date:  1968-08       Impact factor: 7.124

4.  Congenital marrow dysfunction in Down's syndrome.

Authors:  M M Weinberger; A Oleinick
Journal:  J Pediatr       Date:  1970-08       Impact factor: 4.406

Review 5.  Carbon monoxide and carboxyhemoglobin.

Authors:  H J Vreman; J J Mahoney; D K Stevenson
Journal:  Adv Pediatr       Date:  1995

6.  Intravenous immune globulin in neonatal ABO isoimmunization: factors associated with clinical efficacy.

Authors:  C Hammerman; M Kaplan; H J Vreman; D K Stevenson
Journal:  Biol Neonate       Date:  1996

7.  Contribution of haemolysis to jaundice in Sephardic Jewish glucose-6-phosphate dehydrogenase deficient neonates.

Authors:  M Kaplan; H J Vreman; C Hammerman; C Leiter; A Abramov; D K Stevenson
Journal:  Br J Haematol       Date:  1996-06       Impact factor: 6.998

Review 8.  Sources of carbon monoxide (CO) in biological systems and applications of CO detection technologies.

Authors:  P A Rodgers; H J Vreman; P A Dennery; D K Stevenson
Journal:  Semin Perinatol       Date:  1994-02       Impact factor: 3.300

9.  Carboxyhemoglobin determined in neonatal blood with a CO-oximeter unaffected by fetal oxyhemoglobin.

Authors:  H J Vreman; D K Stevenson
Journal:  Clin Chem       Date:  1994-08       Impact factor: 8.327

10.  Cu/Zn-superoxide dismutase and glutathione peroxidase during aging.

Authors:  J B de Haan; F Cristiano; R C Iannello; I Kola
Journal:  Biochem Mol Biol Int       Date:  1995-05
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