Maternal and perinatal long-chain fatty acids: Possible roles in preterm birth - 10/09/11
Abstract |
OBJECTIVE: We conducted a case-control study to evaluate whether maternal and fetal ω-3 and ω-6 essential fatty acid status play possible roles in the pathogenesis of preterm birth.
STUDY DESIGN: Essential fatty acid status in blood and trophoblast tissues was measured in (1) women and their newborns with spontaneous preterm birth and (2) control women and newborns at 34 weeks' gestation (maternal blood) and at term delivery.
RESULTS: Thirty-seven preterm (mean gestational age 34 weeks) and 34 control mother-baby dyads (gestational age 40 weeks) were evaluated. The maternal percent of total arachidonic acid in red blood cells and plasma was increased in preterm cases versus controls at delivery (3.8- and 1.6-fold, respectively, p < 0.05). Maternal red blood cell eicosapentaenoic acid (1.98 ± 0.15, p < 0.0001) and ω-3/ω-6 ratios (0.58 ± 0.22, p < 0.009) were lower in preterm cases than in controls at delivery (4.64 ± 0.32 and 1.27 ± 0.12, respectively). Docosapentaenoic acid, a marker of ω-3 essential fatty acid deficiency, was higher in preterm maternal red blood cells (1.26 ± 0.18, p < 0.0001) and amnion (1.27 ± 0.19, p < 0.001) compared with term controls (0.12 ± 0.07 and 0.58 ± 0.13, respectively).
CONCLUSION: Women delivered preterm demonstrated higher arachidonic acid and docosapentaneoic acid levels in maternal blood and trophoblast tissue than did women delivered at term. This suggests (1) altered essential fatty acid intake or metabolism in a portion of women delivered preterm and (2) increased maternal red blood cell arachidonic acid is associated with an increased risk of preterm birth. (Am J Obstet Gynecol 1997;176:907-14.)
Le texte complet de cet article est disponible en PDF.Keywords : Prematurity, preterm birth, essential fatty acids, arachidonic acid, eicosanoids
Plan
From the Department of Food Science and Human Nutrition, Colorado State University,a and the Department of Obstetrics and Gynecology, University of Colorado Health Sciences Center.b |
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Supported by Colorado Agricultural Experiment Station, NC-167. |
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Reprint requests: M.A Harris, PhD, RD, Colorado State University, Department of Food Science and Human Nutrition, Fort Collins, CO 80523. |
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0002-9378/97 $5.00 + 0 6/1/79818 |
Vol 176 - N° 4
P. 907-914 - avril 1997 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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