Folic Acid Intake, Fetal Brain Growth, and Maternal Smoking in Pregnancy: A Randomized Controlled Trial

Korede K Yusuf, Hamisu M Salihu, Roneé Wilson, Alfred Mbah, William Sappenfield, Karen Bruder, Usman J Wudil, Muktar H Aliyu, Korede K Yusuf, Hamisu M Salihu, Roneé Wilson, Alfred Mbah, William Sappenfield, Karen Bruder, Usman J Wudil, Muktar H Aliyu

Abstract

Background: Folic acid supplementation during pregnancy plays an important role in fetal growth and development. To our knowledge, no experimental study has examined the effect of folic acid on fetal brain growth in women who smoke cigarettes during pregnancy.

Objectives: The aim of this study was to investigate the efficacy of higher-dose compared with standard-dose folic acid supplementation on prenatal fetal brain growth, measured by head circumference, brain weight, and brain-body weight ratio (BBR).

Design: In this randomly assigned, double-blind, controlled clinical trial, we recruited 345 smoking pregnant women attending a community health center in Tampa, FL between 2010 and 2014. Participants were randomly assigned in a 1:1 ratio to receive either 0.8 mg folic acid/d (standard of care at the study center) or 4 mg folic acid/d (higher strength). Participants were also enrolled in a smoking cessation program. A 2-level linear growth model was used to assess treatment effect and factors that predict intrauterine growth in head circumference over time. Multiple linear regression analyses were conducted to estimate the effect of higher-strength folic acid on head circumference at birth, fetal brain weight, and fetal BBRs.

Results: Mothers who received the higher dose of folic acid had infants with a 1.18 mm larger mean head circumference compared with infants born to mothers who received the standard dose, but this difference was not statistically significant (P = 0.2762). Higher-dose folic acid also had no significant effect on brain weight. The BBR of infants of mothers who received higher-dose folic acid was, however, 0.33 percentage points lower than that for infants of mothers who received the standard dose of folic acid (P = 0.044).

Conclusions: Infants of smokers in pregnancy may benefit from higher-strength maternal folic acid supplementation. We noted a decrease in the proportion of infants with impaired BBR among those on higher-dose folic acid. This trial was registered at clinicaltrials.gov as NCT01248260.

Keywords: brain growth; brain-to-body weight ratio; fetal brain weight; folic acid; head circumference; smokers.

Figures

FIGURE 1
FIGURE 1
Enrollment, randomization, and follow-up of participants.
FIGURE 2
FIGURE 2
Longitudinally derived cotinine trajectories in the modified intention-to-treat population (n = 319). Each straight line reflects an individual cotinine trajectory: 1, low level; 2, moderate level; and 3, high level.

References

    1. Ekblad M, Korkeila J, Parkkola R, Lapinleimu H, Haataja L, Lehtonen L; PIPARI Study Group. Maternal smoking during pregnancy and regional brain volumes in preterm infants. J Pediatr 2010;156:185–90.e1.
    1. Ekblad M, Korkeila J, Lehtonen L. Smoking during pregnancy affects foetal brain development. Acta Paediatr 2015;104(1):12–18.
    1. Lindley AA, Becker S, Gray RH, Herman AA. Effect of continuing or stopping smoking during pregnancy on infant birth weight, crown-heel length, head circumference, ponderal index, and brain:body weight ratio. Am J Epidemiol 2000;152(3):219–25.
    1. Luck W, Nau H, Hansen R, Steldinger R. Extent of nicotine and cotinine transfer to the human fetus, placenta and amniotic fluid of smoking mothers. Dev Pharmacol Ther 1985;8(6):384–95.
    1. England LJ, Aagaard K, Bloch M, Conway K, Cosgrove K, Grana R, Gould TJ, Hatsukami D, Jensen F, Kandel D, Lanphear B et al. .. Developmental toxicity of nicotine: A transdisciplinary synthesis and implications for emerging tobacco products. Neurosci Biobehav Rev 2017;72:176–89.
    1. Banderali G, Martelli A, Landi M, Moretti F, Betti F, Radaelli G, Lassandro C, Verduci E. Short and long term health effects of parental tobacco smoking during pregnancy and lactation: a descriptive review. J Transl Med 2015;13:327.
    1. Liu J, Leung PW, McCauley L, Ai Y, Pinto-Martin J. Mother's environmental tobacco smoke exposure during pregnancy and externalizing behavior problems in children. Neurotoxicology 2013;34:167–74.
    1. McDonald SD, Perkins SL, Jodouin CA, Walker MC. Folate levels in pregnant women who smoke: an important gene/environment interaction. Am J Obstet Gynecol 2002;187(3):620–5.
    1. Jauniaux E, Johns J, Gulbis B, Spasic-Boskovic O, Burton GJ. Transfer of folic acid inside the first-trimester gestational sac and the effect of maternal smoking. Am J Obstet Gynecol 2007;197(1):58.e1–6.
    1. Ozerol E, Ozerol I, Gokdeniz R, Temel I, Akyol O. Effect of smoking on serum concentrations of total homocysteine, folate, vitamin B12, and nitric oxide in pregnancy: a preliminary study. Fetal Diagn Ther 2004;19(2):145–8.
    1. Stark KD, Pawlosky RJ, Beblo S, Murthy M, Flanagan VP, Janisse J, Buda-Abela M, Rockett H, Whitty JE, Sokol RJ et al. .. Status of plasma folate after folic acid fortification of the food supply in pregnant African American women and the influences of diet, smoking, and alcohol consumption. Am J Clin Nutr 2005;81(3):669–77.
    1. Bailey LB, Gregory JF 3rd.. Folate metabolism and requirements. J Nutr 1999;129(4):779–82.
    1. Schlotz W, Jones A, Phillips DI, Gale CR, Robinson SM, Godfrey KM. Lower maternal folate status in early pregnancy is associated with childhood hyperactivity and peer problems in offspring. J Child Psychol Psychiatry 2010;51(5):594–602.
    1. Roza SJ, van Batenburg-Eddes T, Steegers EA, Jaddoe VW, Mackenbach JP, Hofman A, Verhulst FC, Tiemeier H. Maternal folic acid supplement use in early pregnancy and child behavioral problems: the generation R study. Br J Nutr 2010;103(3):445–52.
    1. Suren P, Roth C, Bresnahan M, Haugen M, Hornig M, Hirtz D, Lie KK, Lipkin WI, Magnus P, Reichborn-Kjennerud T et al. .. Association between maternal use of folic acid supplements and risk of autism spectrum disorders in children. JAMA 2013;309(6):570–7.
    1. Steenweg-de Graaff J, Roza SJ, Walstra AN, El Marroun H, Steegers EA, Jaddoe VW, Hofman A, Verhust FC, Tiemeier H, White T. Associations of maternal folic acid supplementation and folate concentrations during pregnancy with foetal and child head growth: the generation R study. Eur J Nutr 2017;56(1):65–75.
    1. Bartholomeusz HH, Courchesne E, Karns CM. Relationship between head circumference and brain volume in healthy normal toddlers, children, and adults. Neuropediatrics 2002;33:23, 9–41.
    1. Cooke RW, Lucas A, Yudkin PL, Pryse-Davies J. Head circumference as an index of brain weight in the fetus and newborn. Early Hum Dev 1977;1(2):145–149.
    1. Dinc D, Schulte PFJ.. The use of anticonvulsants and the levels of folate, vitamin B12 and homocysteine. Tijdschr Psychiatr 2018;60:20–28.
    1. Gilles FH, Leviton A, Dooling EC. The developing human brain: growth and epidemiologic neuropathology. Boston (MA): J Wright-PSG; 1983
    1. Elliott JA, Vink R, Jensen L, Byard RW. Brain weight-body weight ratio in sudden infant death syndrome revisited. Med Sci Law 2012;52(4):207–9.
    1. Studer J, Bartsch C, Haas C. Aquaporin-4 polymorphisms and brain/body weight ratio in sudden infant death syndrome (SIDS). Pediatr Res 2014;76(1):41–45.
    1. WHO. Serum and red blood cell folate concentrations for assessing folate status in populations. WHO/NMH/NHD/EPG/15.01. Geneva: WHO; 2015.
    1. Kozinszky Z, Dudas RB.. Validation studies of the Edinburgh Postnatal Depression Scale for the antenatal period. J Affect Disord 2015;176:95–105.
    1. Cohen S, Kamarck T, Mermelstein R. A global measure of perceived stress. J Health Soc Behav 1983;24(4):385–96.
    1. Russell T, Crawford M, Woodby L. Measurements for active cigarette smoke exposure in prevalence and cessation studies: why simply asking pregnant women isn't enough. Nicotine Tob Res 2004;6 Suppl 2:S1, 41–51.
    1. Harel S, Tomer A, Barak Y, Binderman I, Yavin E. The cephalization index: a screening device for brain maturity and vulnerability in normal and intrauterine growth retarded newborns. Brain Dev 1985;7(6):580–4.
    1. Castanys-Munoz E, Kennedy K, Castaneda-Gutierrez E, Forsyth S, Godfrey KM, Koletzko B, Ozanne SE, Ruedda R, Schoemaker M, van der Beek EM et al. .. Systematic review indicates postnatal growth in term infants born small-for-gestational-age being associated with later neurocognitive and metabolic outcomes. Acta Paediatr 2017;106(8):1230–8.
    1. Rice D, Barone S Jr.. Critical periods of vulnerability for the developing nervous system: Evidence from humans and animal models. Environ Health Perspect 2000;108 Suppl 3:511–33.
    1. Zhang J, Bowes WA Jr.. Birth-weight-for-gestational-age patterns by race, sex, and parity in the united states population. Obstet Gynecol 1995;86(2):200–8.
    1. van Uitert EM, Steegers-Theunissen RP. Influence of maternal folate status on human fetal growth parameters. Mol Nutr Food Res 2013;57(4):582–95.

Source: PubMed

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