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Zinc, copper, selenium and manganese blood levels of preterm infants
  1. Lynne D Marriott (lynne.marriott1{at}ntlworld.com)
  1. MRC Epidemiology Resource Centre, United Kingdom
    1. Keith D Foote (footekd{at}doctors.org.uk)
    1. Royal Hampshire County Hospital, United Kingdom
      1. Alan C Kimber (a.c.kimber{at}soton.ac.uk)
      1. University of Southampton, United Kingdom
        1. Trevor H Delves (htdelves{at}netscape.net)
        1. Southampton General Hospital, United Kingdom
          1. Jane B Morgan (jane.b.morgan{at}btinternet.com)
          1. School of Biomedical and Molecular Sciences, United Kingdom

            Abstract

            Objective: To measure the zinc, copper, selenium and manganese blood levels in a cohort of 68 preterm infants; and to establish any associations with growth and/or dietary intakes.

            Design: Blood samples were collected at the infants’ expected dates of delivery (term) and 6 months later. Serum zinc, plasma copper and whole blood manganese were analysed by atomic absorption spectrometry, plasma and red cell selenium were determined by mass spectrometry. Growth and dietary intake determinations have been previously published.

            Setting: Hampshire, England.

            Results: The mean birth weight (SD) of the infants was 1.47 (0.434) kg, mean gestation (SD) 31.4 (2.9) weeks. Mean (SD) blood levels at the two ages were: serum zinc 12.0 (2.6) and 13.8 (2.5) µmol/l, plasma copper 10.1 (2.6) and 19.2 (3.6) µmol/l, plasma selenium 0.49 (0.15) and 0.72 (0.14) µmol/l, red cell selenium 1.68 (0.40) and 1.33 (0.19) µmol/l, blood manganese 320 (189) and 211 (68) nmol/l, respectively. There were no significant associations between levels of zinc and copper and dietary intakes of those nutrients at either age (dietary intakes of selenium and manganese were not determined). Only copper levels at term were significantly associated (r = 0.31, p = 0.05) with a growth parameter (head circumference).

            Conclusion: These results provide new information about trace element status in this vulnerable population.

            • copper
            • manganese
            • preterm
            • selenium
            • zinc

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