Effect of Supplementation of Preterm Formula With Long Chain Polyunsaturated Fatty Acids on Mineral Balance in Preterm Infants

BACKGROUNDIncorporation of long chain polyunsaturated fatty acids (LCP) into formulas may interfere with mineral metabolism. We investigate mineral balance in preterm infants who were fed a formula with LCP. METHODSInfants were randomized in a double-blind manner, 20 infants in each group, to receiv...

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Published in:Journal of pediatric gastroenterology and nutrition Vol. 35; no. 4; pp. 503 - 507
Main Authors: Martinez, Francisco Eulógio, Sieber, Vanessa Moura, Jorge, Salim Moysés, Ferlin, Maria Lúcia Silveira, Mussi-Pinhata, Marisa Márcia
Format: Journal Article
Language:English
Published: Hagerstown, MD Lippincott Williams & Wilkins, Inc 01-10-2002
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Abstract BACKGROUNDIncorporation of long chain polyunsaturated fatty acids (LCP) into formulas may interfere with mineral metabolism. We investigate mineral balance in preterm infants who were fed a formula with LCP. METHODSInfants were randomized in a double-blind manner, 20 infants in each group, to receive a formula with LCP (F+LCP) or without LCP (F) for 30 days. Plasma levels (at the beginning and after 30 days) and nutritional balance (after 1 week) for Ca, P, Mg, Zn, and Cu were obtained for all infants. RESULTSGroups were similar regarding birth weight, gestational age, weight, and corrected age at study start. During the 30-day study period, the groups had comparable milk intake and reached similar and satisfactory weight gains and longitudinal growth. Within each group, there was no change in plasma mineral concentrations over the course of the study, and there were no differences at each time point between groups. All values were within the normal range for age. No differences in mineral balance were detected between the F and F+LCP groups, with both groups demonstrating comparable intake, net retention, and fecal losses of each mineral. CONCLUSIONSAdding a content of LCP blend similar to that of human milk to a preterm formula caused no disturbance in Ca, P, Mg, Zn, or Cu nutritional balance.
AbstractList BACKGROUNDIncorporation of long chain polyunsaturated fatty acids (LCP) into formulas may interfere with mineral metabolism. We investigate mineral balance in preterm infants who were fed a formula with LCP. METHODSInfants were randomized in a double-blind manner, 20 infants in each group, to receive a formula with LCP (F+LCP) or without LCP (F) for 30 days. Plasma levels (at the beginning and after 30 days) and nutritional balance (after 1 week) for Ca, P, Mg, Zn, and Cu were obtained for all infants. RESULTSGroups were similar regarding birth weight, gestational age, weight, and corrected age at study start. During the 30-day study period, the groups had comparable milk intake and reached similar and satisfactory weight gains and longitudinal growth. Within each group, there was no change in plasma mineral concentrations over the course of the study, and there were no differences at each time point between groups. All values were within the normal range for age. No differences in mineral balance were detected between the F and F+LCP groups, with both groups demonstrating comparable intake, net retention, and fecal losses of each mineral. CONCLUSIONSAdding a content of LCP blend similar to that of human milk to a preterm formula caused no disturbance in Ca, P, Mg, Zn, or Cu nutritional balance.
Incorporation of long chain polyunsaturated fatty acids (LCP) into formulas may interfere with mineral metabolism. We investigate mineral balance in preterm infants who were fed a formula with LCP. Infants were randomized in a double-blind manner, 20 infants in each group, to receive a formula with LCP (F+LCP) or without LCP (F) for 30 days. Plasma levels (at the beginning and after 30 days) and nutritional balance (after 1 week) for Ca, P, Mg, Zn, and Cu were obtained for all infants. Groups were similar regarding birth weight, gestational age, weight, and corrected age at study start. During the 30-day study period, the groups had comparable milk intake and reached similar and satisfactory weight gains and longitudinal growth. Within each group, there was no change in plasma mineral concentrations over the course of the study, and there were no differences at each time point between groups. All values were within the normal range for age. No differences in mineral balance were detected between the F and F+LCP groups, with both groups demonstrating comparable intake, net retention, and fecal losses of each mineral. Adding a content of LCP blend similar to that of human milk to a preterm formula caused no disturbance in Ca, P, Mg, Zn, or Cu nutritional balance.
BACKGROUNDIncorporation of long chain polyunsaturated fatty acids (LCP) into formulas may interfere with mineral metabolism. We investigate mineral balance in preterm infants who were fed a formula with LCP. METHODSInfants were randomized in a double-blind manner, 20 infants in each group, to receive a formula with LCP (F+LCP) or without LCP (F) for 30 days. Plasma levels (at the beginning and after 30 days) and nutritional balance (after 1 week) for Ca, P, Mg, Zn, and Cu were obtained for all infants. RESULTSGroups were similar regarding birth weight, gestational age, weight, and corrected age at study start. During the 30-day study period, the groups had comparable milk intake and reached similar and satisfactory weight gains and longitudinal growth. Within each group, there was no change in plasma mineral concentrations over the course of the study, and there were no differences at each time point between groups. All values were within the normal range for age. No differences in mineral balance were detected between the F and F+LCP groups, with both groups demonstrating comparable intake, net retention, and fecal losses of each mineral. CONCLUSIONSAdding a content of LCP blend similar to that of human milk to a preterm formula caused no disturbance in Ca, P, Mg, Zn, or Cu nutritional balance.
Author Ferlin, Maria Lúcia Silveira
Mussi-Pinhata, Marisa Márcia
Martinez, Francisco Eulógio
Jorge, Salim Moysés
Sieber, Vanessa Moura
AuthorAffiliation Department of Pediatrics, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Brazil; †Milupa GmbH & Co KG, Scientific Department, Friedrichsdorf, Germany
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10.1111/j.1365-2796.1989.tb01450.x
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10.1007/BF01651958
10.1093/ajcn/23.10.1322
10.1016/S0022-3476(35)80034-6
10.1016/0300-9629(82)90422-4
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10.1016/S0022-3476(05)81238-7
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Issue 4
Keywords Human
Pregnancy disorders
Nutrition
Calcium
Long chain
Polyunsaturated fatty acid
Phosphorus
Metabolism
Statistical study
Zinc
Humanized milk
Prematurity
Biological effect
Magnesium
Supplementation
Copper
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Snippet BACKGROUNDIncorporation of long chain polyunsaturated fatty acids (LCP) into formulas may interfere with mineral metabolism. We investigate mineral balance in...
Incorporation of long chain polyunsaturated fatty acids (LCP) into formulas may interfere with mineral metabolism. We investigate mineral balance in preterm...
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StartPage 503
SubjectTerms Alkaline Phosphatase - metabolism
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Calcium - blood
Copper - blood
Dietary Fats - administration & dosage
Dietary Fats - adverse effects
Dietary Fats - metabolism
Dietary Supplements
Double-Blind Method
Emergency and intensive care: metabolism and nutrition disorders. Enteral and parenteral nutrition
Fatty Acids, Unsaturated - administration & dosage
Fatty Acids, Unsaturated - adverse effects
Fatty Acids, Unsaturated - metabolism
Female
Humans
Infant Food
Infant Nutritional Physiological Phenomena
Infant, Newborn
Infant, Premature - metabolism
Intensive care medicine
Magnesium - blood
Male
Medical sciences
Minerals - blood
Minerals - metabolism
Phosphorus - blood
Prospective Studies
Zinc - blood
Title Effect of Supplementation of Preterm Formula With Long Chain Polyunsaturated Fatty Acids on Mineral Balance in Preterm Infants
URI http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00005176-200210000-00008
https://www.ncbi.nlm.nih.gov/pubmed/12394374
https://search.proquest.com/docview/72533610
Volume 35
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