Comparison in executive function in Chinese preterm and full-term infants at eight months

Yao Feng , Hong Zhou , Yan Zhang , Anthony Perkins , Yan Wang , Jing Sun

Front. Med. ›› 2018, Vol. 12 ›› Issue (2) : 164 -173.

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Front. Med. ›› 2018, Vol. 12 ›› Issue (2) : 164 -173. DOI: 10.1007/s11684-017-0540-9
RESEARCH ARTICLE
RESEARCH ARTICLE

Comparison in executive function in Chinese preterm and full-term infants at eight months

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Abstract

Executive function (EF) is increasingly recognized as being responsible for adverse developmental outcomes in preterm-born infants. Several perinatal factors may lead to poor EF development in infancy, and the deficits in EF can be identified in infants as young as eight months. A prospective cohort study was designed to study the EF in Chinese preterm infants and examine the relationship between EF in preterm infants and maternal factors during perinatal period. A total of 88 preterm infants and 88 full-term infants were followed from birth to eight months (corrected age). Cup Task and Planning Test was applied to assess the EF of infants, and the Bayley Scale of Infant Development (BSID-III) was used to evaluate cognitive (MDI) and motor abilities (PDI) of infants. In comparison with full-term infants, the preterm infants performed more poorly on all measures of EF including working memory, inhibition to prepotent responses, inhibition to distraction, and planning, and the differences remained after controlling the MDI and PDI. Anemia and selenium deficiency in mothers during pregnancy contributed to the differences in EF performance. However, maternal depression, hypertension, and diabetes during pregnancy were not related to the EF deficits in preterm infants. Future research should focus on the prevention of anemia and selenium deficiency during pregnancy and whether supplementing selenium in mothers during pregnancy can prevent further deterioration and the development of adverse outcomes of their offspring.

Keywords

executive function (EF) / preterm infant / working memory / inhibition to prepotent response / inhibition to distraction / planning

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Yao Feng, Hong Zhou, Yan Zhang, Anthony Perkins, Yan Wang, Jing Sun. Comparison in executive function in Chinese preterm and full-term infants at eight months. Front. Med., 2018, 12(2): 164-173 DOI:10.1007/s11684-017-0540-9

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References

[1]

Blencowe H, Cousens S, Oestergaard MZ, Chou D, Moller AB, Narwal R, Adler A, Vera Garcia C, Rohde S, Say L, Lawn JE. National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implications. Lancet 2012; 379(9832): 2162–2172

[2]

Saigal S, Doyle LW. An overview of mortality and sequelae of preterm birth from infancy to adulthood. Lancet 2008; 371(9608): 261–269

[3]

Doyle LW. Evaluation of neonatal intensive care for extremely-low-birth-weight infants. Semin Fetal Neonatal Med 2006; 11(2): 139–145

[4]

Bayless S, Stevenson J. Executive functions in school-age children born very prematurely. Early Hum Dev 2007; 83(4): 247–254

[5]

Sun J, Mohay H, O’Callaghan M. A comparison of executive function in very preterm and term infants at 8 months corrected age. Early Hum Dev 2009; 85(4): 225–230

[6]

Anderson SW, Damasio H, Tranel D, Damasio AR. Long-term sequelae of prefrontal cortex damage acquired in early childhood. Dev Neuropsychol 2000; 18(3): 281–296

[7]

Stuss DT. Biological and psychological development of executive functions. Brain Cogn 1992; 20(1): 8–23

[8]

Anderson V, Spencer-Smith M, Leventer R, Coleman L, Anderson P, Williams J, Greenham M, Jacobs R. Childhood brain insult: can age at insult help us predict outcome? Brain 2009; 132(1): 45–56

[9]

Diamond A, Churchland A, Cruess L, Kirkham NZ. Early developments in the ability to understand the relation between stimulus and reward. Dev Psychol 1999; 35(6): 1507–1517

[10]

Barkley RA. Behavioral inhibition, sustained attention, and executive functions: constructing a unifying theory of ADHD. Psychol Bull 1997; 121(1): 65–94

[11]

van Wassenaer AG, Westera J, van Schie PEM, Houtzager BA, Cranendonk A, de Groot L, Ganzevoort W, Wolf H, de Vries JIP. Outcome at 4.5 years of children born after expectant management of early-onset hypertensive disorders of pregnancy. Am J Obstet Gynecol 2011;204(6):510.e1–.e9

[12]

Whitehouse AJO, Robinson M, Newnham JP, Pennell CE. Do hypertensive diseases of pregnancy disrupt neurocognitive development in offspring? Paediatr Perinat Epidemiol 2012; 26(2): 101–108

[13]

Robinson M, Mattes E, Oddy WH, de Klerk NH, Li J, McLean NJ, Silburn SR, Zubrick SR, Stanley FJ, Newnham JP. Hypertensive diseases of pregnancy and the development of behavioral problems in childhood and adolescence: the Western Australian Pregnancy Cohort Study. J Pediatr 2009; 154(2): 218–224.e2

[14]

Tuovinen S, Räikkönen K, Kajantie E, Henriksson M, Leskinen JT, Pesonen AK, Heinonen K, Lahti J, Pyhälä R, Alastalo H, Lahti M, Osmond C, Barker DJ, Eriksson JG. Hypertensive disorders in pregnancy and cognitive decline in the offspring up to old age. Neurology 2012; 79(15): 1578–1582

[15]

Gerner G, Baron IS. Pregnancy complications and neuropsychological outcomes: a review. Child Neuropsychol 2015; 21(3): 269–284

[16]

Polanska K, Krol A, Sobala W, Gromadzinska J, Brodzka R, Calamandrei G, Chiarotti F, Wasowicz W, Hanke W. Selenium status during pregnancy and child psychomotor development—Polish Mother and Child Cohort study. Pediatr Res 2016; 79(6): 863–869

[17]

Zhang Q, Ananth CV, Li Z, Smulian JC. Maternal anaemia and preterm birth: a prospective cohort study. Int J Epidemiol 2009; 38(5): 1380–1389

[18]

Freitas RG, Nogueira RJ, Antonio MA, Barros-Filho AA, Hessel G. Selenium deficiency and the effects of supplementation on preterm infants. Rev Paul Pediatr 2014; 32(1): 126–135

[19]

Schweizer U, Bräuer AU, Köhrle J, Nitsch R, Savaskan NE. Selenium and brain function: a poorly recognized liaison. Brain Res Brain Res Rev 2004; 45(3): 164–178

[20]

Watanabe C, Satoh H. Brain selenium status and behavioral development in selenium-deficient preweanling mice. Physiol Behav 1994; 56(5): 927–932

[21]

Willatts P. Effects of object novelty on the visual and manual exploration of infants. Infant Behav Dev 1983; 6(2-3): 145–149

[22]

Willatts P. The stage-IV infant’s solution of problems requiring the use of supports. Infant Behav Dev 1984; 7(2): 125–134

[23]

Willatts P. Stages in the development of intentional search by young infants. Dev Psychol 1984; 20(3): 389–396

[24]

Bayley N. Bayley Scale of Infant Development: Manual. 2nd ed. San Antonio, TX: The Psychological Corporation, 2006. 374

[25]

Cox JL, Holden JM, Sagovsky R. Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale. Br J Psychiatry 1987; 150(6): 782–786

[26]

Lee DT, Yip SK, Chiu HF, Leung TY, Chan KP, Chau IO, Leung HC, Chung TK. Detecting postnatal depression in Chinese women. Validation of the Chinese version of the Edinburgh Postnatal Depression Scale. Br J Psychiatry 1998; 172(5): 433–437

[27]

World Health Organization. Haemoglobin concentrations for the diagnosis of anaemia and assessment of severity. Vitamin and Mineral Nutrition Information System. Geneva: World Health Organization, 2011

[28]

Ge K. An Overview of Nutrition Sciences. Beijing: People’s Medical Publishing House, 2004

[29]

Kiselev SY, L'Vova O A, Gliga T, Bakushkina NI, Suleimanova EV, Grishina KI, Baranov DA, Ksenofontova OL, Martirosyan SV. The assessment of neurocognitive functions in premature infants in the first year of life using Bayley Scales. Zh Nevrol Psikhiatr Im S S Korsakova 2016;116(4 Pt 2):62–67 (in Russian)

[30]

Heikura U, Hartikainen AL, Nordström T, Pouta A, Taanila A, Järvelin MR. Maternal hypertensive disorders during pregnancy and mild cognitive limitations in the offspring. Paediatr Perinat Epidemiol 2013; 27(2): 188–198

[31]

Koren G. Systematic review of the effects of maternal hypertension in pregnancy and antihypertensive therapies on child neurocognitive development. Reprod Toxicol 2013; 39: 1–5

[32]

Tuovinen S, Eriksson JG, Kajantie E, Räikkönen K. Maternal hypertensive pregnancy disorders and cognitive functioning of the offspring: a systematic review. J Am Soc Hypertens 2014; 8(11): 832–847.e1

[33]

Petrides M. Frontal lobe and working memory: evidence from investigations of the effects of cortical excisions in nonhuman primates. In: Boller F, Spinnler H, Hendler JA. Handbook of Neuropsychology. Vol. 9. Amsterdam: Elsevier Science, 1994. 59–82

[34]

Milner B. Effects of different brain lesions on card sorting. Arch Neurol 1963; 9(1): 90–100

[35]

Shallice T, Burgess PW. Deficits in strategy application following frontal lobe damage in man. Brain 1991; 114(Pt 2): 727–741

[36]

Bastian TW, Santarriaga S, Nguyen TA, Prohaska JR, Georgieff MK, Anderson GW. Fetal and neonatal iron deficiency but not copper deficiency increases vascular complexity in the developing rat brain. Nutr Neurosci 2015;18(8): 365–375

[37]

Mensink GBM, Fletcher R, Gurinovic M, Huybrechts I, Lafay L, Serra-Majem L, Szponar L, Tetens I, Verkaik-Kloosterman J, Baka A, Stephen AM. Mapping low intake of micronutrients across Europe. Br J Nutr 2013; 110(4): 755–773

[38]

Gu J, Royland JE, Wiggins RC, Konat GW. Selenium is required for normal upregulation of myelin genes in differentiating oligodendrocytes. J Neurosci Res 1997; 47(6): 626–635

[39]

Watanabe C, Satoh H. Brain selenium status and behavioral development in selenium-deficient preweanling mice. Physiol Behav 1994; 56(5): 927–932

[40]

Yang X, Yu X, Fu H, Li L, Ren T. Different levels of prenatal zinc and selenium had different effects on neonatal neurobehavioral development. Neurotoxicology 2013; 37: 35–39

[41]

Skröder HM, Hamadani JD, Tofail F, Persson, Vahter ME, Kippler MJ. Selenium status in pregnancy influences children’s cognitive function at 1.5 years of age. Clin Nutr 2015; 34(5): 923–930

[42]

Rao R, de Ungria M, Sullivan D, Wu P, Wobken JD, Nelson CA, Georgieff MK. Perinatal brain iron deficiency increases the vulnerability of rat hippocampus to hypoxic ischemic insult. J Nutr 1999; 129(1): 199–206

[43]

Collette F, Van der Linden M. Brain imaging of the central executive component of working memory. Neurosci Biobehav Rev 2002; 26(2): 105–125

[44]

Lie CH, Specht K, Marshall JC, Fink GR. Using fMRI to decompose the neural processes underlying the Wisconsin Card Sorting Test. Neuroimage 2006; 30(3): 1038–1049

[45]

Rothmayr C, Sodian B, Hajak G, Döhnel K, Meinhardt J, Sommer M. Common and distinct neural networks for false-belief reasoning and inhibitory control. Neuroimage 2011; 56(3): 1705–1713

[46]

Spreng RN, Mar RA, Kim AS. The common neural basis of autobiographical memory, prospection, navigation, theory of mind, and the default mode: a quantitative meta-analysis. J Cogn Neurosci 2009; 21(3): 489–510

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