Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Published:

Pediatrics

Influence of aerobic exercise on maternal lipid levels and offspring morphometrics

Abstract

Background

Maternal BMI, lipid levels (cholesterol, triglyceride, LDL, HDL), and exercise amount are interrelated and each influence offspring body size. This study proposed to determine the influence of exercise on maternal lipid levels and infant body size.

Methods

We had 36 participants complete these measures. Participants in the aerobic exercise intervention (n = 14) completed three 50-min sessions weekly from 16 weeks gestation to delivery and were compared with a non-exercise control group (n = 22). Maternal lipid profiles were assessed at 16 and at 36 weeks gestation. Fetal body size was measured at 36 weeks gestational age using ultrasound assessment. Neonatal body size measures were acquired from birth records. Statistical analysis included two-sample t-tests, correlations, and regression models.

Results

Participants were similar in age, pre-pregnancy BMI, gravida, parity, education, and gestational weight gain (GWG). There were no differences in gestational age, Apgar scores at 1 and 5 min for infants of exercisers relative to controls. Exercisers had higher pre-training triglycerides (p = 0.004) and pregnancy change in triglycerides (p = 0.049) compared to controls. Head circumference was significantly larger in exercise exposed infants relative to infants of controls. Pregnancy METs had a positive relationship with birth length (r = .445, p = .006) and birth weight (r = .391, p = .02). GWG had a moderate, positive relationship with fetal abdominal circumference (r = .570, p = .004). Regression analysis indicated 5 predictors explained 61.7% of the variance in birth weight (Adj.R2 = 0.469, F(5,13) = 5,13, p = 0.02); it was found that pregnancy METs (β = .724, p = .007), 36 week cholesterol (β = 1.066, p = .02), and 36 week LDL (β = −1.267, p = .006) significantly predict birth weight. Regression analysis indicated 4 predictors explained 43.8% of the variance in birth length (Adj.R2 = 0.306, F(4,17) = 3.32, p = 0.04); it was found that pregnancy METs (β = .530, p = .03), and 36 week LDL (β = −.891, p = .049) significantly predict birth length.

Conclusion

The primary association and predictors of infant body size was related to pregnancy exercise and late pregnancy cholesterol and LDL levels. Considering these relationships, it is essential that women maintain aerobic exercise during pregnancy, but should also be cognizant of lipid levels during their pregnancy. Therefore intervention during pregnancy focused on infant body size should involve exercise and and quality nutritional intake foods during pregnancy.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1

Similar content being viewed by others

References

  1. Butler CL, Williams MA, Sorensen TK, Frederick IO, Leisenring. WM relation between maternal recreational physical activity and plasma lipids in early pregnancy. Am J Epidemiol. 2004;160:350–9.

    Article  Google Scholar 

  2. Mudd LM, Holzman CB, Catov JM, Senagore PK, Evans RW. Maternal lipids at mid-pregnancy and the risk of preterm delivery. Acta Obstet Gynecol Scand. 2012;91:726–35.

    Article  Google Scholar 

  3. Ryckman KK, Spracklen CN, Smith CJ, Robinson JG, Saftlas AF. Maternal lipid levels during pregnancy and gestational diabetes: a systematic review and meta-analysis. BJOG. 2015;122:643–51.

    Article  CAS  Google Scholar 

  4. Loprinzi PD, Fitzgerald EM, Woekel E, Cardinal BJ. Association of physical activity and sedentary behavior with biological markers among U.S. pregnant women. J Women’s Health. 2013;22:953–8.

    Article  Google Scholar 

  5. Nkwabong E. Maternal and neonatal complications of macrosomia. Trop Doct. 2014;44:201–4.

    Article  Google Scholar 

  6. Karakosta P, Chatzi L, Plana E, Margioris A, Castanas E, Kogevinas M. Leptin levels in cord blood and anthropometric measures at birth: a systematic review and meta-analysis. Paediatr Perinat Epidemiol. 2011;25:150–63.

    Article  Google Scholar 

  7. Renault KM, Norgaard K, Nilas L, Carlsen EM, Cortes D, Pryds O, et al. The treatment of obese pregnant women (TOP) study: a randomized controlled trial of the effect of physical activity intervention assessed by pedometer with or without dietary intervention in obese pregnant women. Am J Obstet Gynecol. 2014;210:134 e1–9.

    Article  Google Scholar 

  8. Fay RA, Dey PL, Saadie CM, Buhl JA, Gebski VJ. Ponderal index: a better definition of the ‘at risk’ group with intrauterine growth problems than birth-weight for gestational age in term infants. Aust N Z J Obstet Gynaecol. 1991;31:17–9.

    Article  CAS  Google Scholar 

  9. Muktabhant B, Lawrie TA, Lumbiganon P, Laopaiboon M. Diet or exercise, or both, for preventing excessive weight gain in pregnancy. Cochrane Database Syst Rev. 2015;6:CD007145.

  10. de Oliveria Melo AS, Silva JL, Tavares JS, Barros VO, Leite DF, Amorim MM. Effect of a physical exercise program during pregnancy on uteroplacental and fetal blood flow and fetal growth: a randomized controlled trial. Obstet Gynecol. 2012;120(2 Pt 1):302–10.

    Article  Google Scholar 

  11. Ruiz JR, Perales M, Pelaez M, Lopez C, Lucia A, Barakat R. Supervised exercise-based intervention to prevent excessive gestational weight gain: a randomized controlled trial. Mayo Clin Proc. 2013;88:1388–97.

    Article  Google Scholar 

  12. Barakat R, Pelaez M, Montejo R, Luaces M, Zakynthinaki M. Exercise during pregnancy improves maternal health perception: a randomized controlled trial. Am J Obstet Gynecol. 2011;204:402 e1–7.

    Article  Google Scholar 

  13. Pinzon DC, Zamora K, Martinez JH, Florez-Lopez ME, de Plata AC, Mosquera M, et al. Type of delivery and gestational age is not affected by pregnant Latin-American women engaging in vigorous exercise: a secondary analysis of data from a controlled randomized trial. Rev Salud Publica. 2012;14:731–43.

    Google Scholar 

  14. Stafne SN, Salvesen KA, Romundstad PR, Eggebo TM, Carlsen SM, Morkved S. Regular exercise during pregnancy to prevent gestational diabetes: a randomized controlled trial. Obstet Gynecol. 2012;119:29–36.

    Article  Google Scholar 

  15. Practice ACoO. Physical Activity and exercise during pregnancy and the postpartum period. Obstet Gynecol. 2015;650:8.

    Google Scholar 

  16. Moyer C, Livingston J, Fang X, May LE. Influence of exercise mode on pregnancy outcomes: ENHANCED by Mom project. BMC Pregnancy Childbirth. 2015;15:133.

    Article  Google Scholar 

  17. Pescatello LS, American College of Sports Medicine. ACSM’s guidelines for exercise testing and prescription. 9th ed. Philadelphia: Wolters Kluwer/Lippincott Williams & Wilkins Health; 2014. pp. xxiv, 456.

  18. Mottola MF, Davenport MH, Brun CR, Inglis SD, Charlesworth S, Sopper MM. VO2peak prediction and exercise prescription for pregnant women. Med Sci Sports Exerc. 2006;38:1389–95.

    Article  Google Scholar 

  19. Cramp AG, Bray SR. A prospective examination of exercise and barrier self-efficacy to engage in leisure-time physical activity during pregnancy. Ann Behav Med. 2009;37:325–34.

    Article  Google Scholar 

  20. Kriska AM, Knowler WC, LaPorte RE, Drash AL, Wing RR, Blair SN, et al. Development of questionnaire to examine relationship of physical activity and diabetes in Pima Indians. Diabetes Care. 1990;13:401–11.

    Article  CAS  Google Scholar 

  21. Bauer PW, Broman CL, Pivarnik JM. Exercise and pregnancy knowledge among healthcare providers. J Women’s Health. 2010;19:335–41.

    Article  Google Scholar 

  22. Davies GA, Wolfe LA, Mottola MF, MacKinnon C. Society of O, gynecologists of Canada SCPOC. Joint SOGC/CSEP clinical practice guideline: exercise in pregnancy and the postpartum period. Can J Appl Physiol. 2003;28:330–41.

    Article  Google Scholar 

  23. Amiel-Tison C, Gosselin J, Infante-Rivard C. Head growth and cranial assessment at neurological examination in infancy. Dev Med Child Neurol. 2002;44:643–8.

    Article  Google Scholar 

  24. Bartholomeusz HH, Courchesne E, Karns CM. Relationship between head circumference and brain volume in healthy normal toddlers, children, and adults. Neuropediatrics. 2002;33:239–41.

    Article  CAS  Google Scholar 

  25. May LE, Suminski RR, Langaker MD, Yeh HW, Gustafson KM. Regular maternal exercise dose and fetal heart outcome. Med Sci Sports Exerc. 2012;44:1252–8.

    Article  Google Scholar 

  26. Labonte-Lemoyne E, Curnier D, Ellemberg D. Exercise during pregnancy enhances cerebral maturation in the newborn: a randomized controlled trial. J Clin Exp Neuropsychol. 2017;39:347–54.

    Article  Google Scholar 

  27. Kunugi H, Takei N, Murray RM, Saito K, Nanko S. Small head circumference at birth in schizophrenia. Schizophr Res. 1996;20:165–70.

    Article  CAS  Google Scholar 

  28. Martyn CN, Gale CR, Sayer AA, Fall C. Growth in utero and cognitive function in adult life: follow up study of people born between 1920 and 1943. BMJ. 1996;312:1393–6.

    Article  CAS  Google Scholar 

  29. Raikkonen K, Kajantie E, Pesonen AK, Heinonen K, Alastalo H, Leskinen JT, et al. Early life origins cognitive decline: findings in elderly men in the Helsinki Birth Cohort Study. PLoS One. 2013;8:e54707.

    Article  CAS  Google Scholar 

  30. Broekman BF, Chan YH, Chong YS, Quek SC, Fung D, Low YL, et al. The influence of birth size on intelligence in healthy children. Pediatrics. 2009;123:e1011–6.

    Article  Google Scholar 

  31. Gale CR, O’Callaghan FJ, Bredow M, Martyn CN. Avon Longitudinal Study of P, Children Study T. The influence of head growth in fetal life, infancy, and childhood on intelligence at the ages of 4 and 8 years. Pediatrics. 2006;118:1486–92.

    Article  Google Scholar 

  32. Heinonen K, Raikkonen K, Pesonen AK, Kajantie E, Andersson S, Eriksson JG, et al. Prenatal and postnatal growth and cognitive abilities at 56 months of age: a longitudinal study of infants born at term. Pediatrics. 2008;121:e1325–33.

    Article  Google Scholar 

  33. Clapp JF 3rd. Morphometric and neurodevelopmental outcome at age 5 years of the offspring of women who continued to exercise regularly throughout pregnancy. J Pediatr. 1996;129:856–63.

    Article  Google Scholar 

  34. Barakat R, Pelaez M, Lopez C, Lucia A, Ruiz JR. Exercise during pregnancy and gestational diabetes-related adverse effects: a randomised controlled trial. Br J Sports Med. 2013;47:630–6.

    Article  Google Scholar 

  35. Barakat R, Pelaez M, Cordero Y, Perales M, Lopez C, Coteron J, et al. Exercise during pregnancy protects against hypertension and macrosomia: randomized clinical trial. Am J Obstet Gynecol. 2016;214:649 e1–8.

    Article  Google Scholar 

  36. Cavalcante SR, Cecatti JG, Pereira RI, Baciuk EP, Bernardo AL, Silveira C. Water aerobics II: maternal body composition and perinatal outcomes after a program for low risk pregnant women. Reprod Health. 2009;6:1.

    Article  Google Scholar 

  37. Cordero Y, Mottola MF, Vargas J, Blanco M, Barakat R. Exercise is associated with a reduction in gestational diabetes mellitus. Med Sci Sports Exerc. 2015;47:1328–33.

    Article  Google Scholar 

  38. Clapp JF 3rd, Kim H, Burciu B, Lopez B. Beginning regular exercise in early pregnancy: effect on fetoplacental growth. Am J Obstet Gynecol. 2000;183:1484–8.

    Article  Google Scholar 

  39. Price BB, Amini SB, Kappeler K. Exercise in pregnancy: effect on fitness and obstetric outcomes—a randomized trial. Med Sci Sports Exerc. 2012;44:2263–9.

    Article  Google Scholar 

  40. Murtezani A, Pacarada M, Ibraimi Z, Nevzati A, Abazi N. The impact of exercise during pregnancy on neonatal outcomes: a randomized controlled trial. J Sports Med Phys Fit. 2014;54:802–8.

    CAS  Google Scholar 

  41. Nascimento SL, Surita FG, Parpinelli MA, Siani S, Pinto e Silva JL. The effect of an antenatal physical exercise programme on maternal/perinatal outcomes and quality of life in overweight and obese pregnant women: a randomised clinical trial. BJOG. 2011;118:1455–63.

    Article  CAS  Google Scholar 

  42. Oostdam N, van Poppel MN, Wouters MG, Eekhoff EM, Bekedam DJ, Kuchenbecker WK, et al. No effect of the FitFor2 exercise programme on blood glucose, insulin sensitivity, and birthweight in pregnant women who were overweight and at risk for gestational diabetes: results of a randomised controlled trial. BJOG. 2012;119:1098–107.

    Article  CAS  Google Scholar 

  43. Petrella E, Malavolti M, Bertarini V, Pignatti L, Neri I, Battistini NC, et al. Gestational weight gain in overweight and obese women enrolled in a healthy lifestyle and eating habits program. J Matern Fetal Neonatal Med. 2014;27:1348–52.

    Article  CAS  Google Scholar 

  44. Vinter CA, Jensen DM, Ovesen P, Beck-Nielsen H, Jorgensen JS. The LiP (Lifestyle in Pregnancy) study: a randomized controlled trial of lifestyle intervention in 360 obese pregnant women. Diabetes Care. 2011;34:2502–7.

    Article  Google Scholar 

  45. Clapp JF 3rd, Schmidt S, Paranjape A, Lopez B. Maternal insulin-like growth factor-I levels (IGF-I) reflect placental mass and neonatal fat mass. Am J Obstet Gynecol. 2004;190:730–6.

    Article  CAS  Google Scholar 

  46. Perichart-Perera O, Munoz-Manrique C, Reyes-Lopez A, Tolentino-Dolores M, Espino YSS, Ramirez-Gonzalez MC. Metabolic markers during pregnancy and their association with maternal and newborn weight status. PLoS One. 2017;12:e0180874.

    Article  Google Scholar 

  47. Catov JM, Bodnar LM, Kip KE, Hubel C, Ness RB, Harger G, et al. Early pregnancy lipid concentrations and spontaneous preterm birth. Am J Obstet Gynecol. 2007;197:610 e1–7.

    Article  Google Scholar 

  48. Zeljkovic A, Vekic J, Spasic S, Jelic-Ivanovic Z, Spasojevic-Kalimanovska V, Gojkovic T, et al. Changes in LDL and HDL subclasses in normal pregnancy and associations with birth weight, birth length and head circumference. Matern Child Health J. 2013;17:556–65.

    Article  Google Scholar 

  49. Ortega RM, Gaspar MJ, Cantero M. Influence of maternal serum lipids and maternal diet during the third trimester of pregnancy on umbilical cord blood lipids in two populations of Spanish newborns. Int J Vitam Nutr Res. 1996;66:250–7.

    CAS  Google Scholar 

  50. Ye K, Bo QL, Du QJ, Zhang D, Shen Y, Han YP, et al. Maternal serum lipid levels during late pregnancy and neonatal body size. Asia Pac J Clin Nutr. 2015;24:138–43.

    CAS  Google Scholar 

  51. Ophir E, Dourleshter G, Hirsh Y, Fait V, German L, Bornstein J. Newborns of pre-eclamptic women: a biochemical difference present in utero. Acta Obstet Gynecol Scand. 2006;85:1172–8.

    Article  Google Scholar 

  52. Bansal N, Charlton-Menys V, Pemberton P, McElduff P, Oldroyd J, Vyas A, et al. Adiponectin in umbilical cord blood is inversely related to low-density lipoprotein cholesterol but not ethnicity. J Clin Endocrinol Metab. 2006;91:2244–9.

    Article  CAS  Google Scholar 

  53. Balsan GA, Vieira JL, Oliveira AM, Portal VL. Relationship between adiponectin, obesity and insulin resistance. Rev Assoc Med Bras. 2015;61:72–80.

    Article  Google Scholar 

  54. Kriketos AD, Gan SK, Poynten AM, Furler SM, Chisholm DJ, Campbell LV. Exercise increases adiponectin levels and insulin sensitivity in humans. Diabetes Care. 2004;27:629–30.

    Article  Google Scholar 

  55. Zhang S, Rattanatray L, McMillen IC, Suter CM, Morrison JL. Periconceptional nutrition and the early programming of a life of obesity or adversity. Prog Biophys Mol Biol. 2011;106:307–14.

    Article  CAS  Google Scholar 

  56. Mehta SH. Nutrition and pregnancy. Clin Obstet Gynecol. 2008;51:409–18.

    Article  Google Scholar 

  57. Fazzi C, Saunders DH, Linton K, Norman JE, Reynolds RM. Sedentary behaviours during pregnancy: a systematic review. Int J Behav Nutr Phys Act. 2017;14:32.

    Article  Google Scholar 

  58. Knopp RH, Warth MR, Charles D, Childs M, Li JR, Mabuchi H, et al. Lipoprotein metabolism in pregnancy, fat transport to the fetus, and the effects of diabetes. Biol Neonate. 1986;50:297–317.

    Article  CAS  Google Scholar 

  59. McConville P, Walker NP. The reliability of case register diagnoses: a birth cohort analysis. Soc Psychiatry Psychiatr Epidemiol. 2000;35:121–7.

    Article  CAS  Google Scholar 

  60. Starling AP, Engel SM, Whitworth KW, Richardson DB, Stuebe AM, Daniels JL, et al. Perfluoroalkyl substances and lipid concentrations in plasma during pregnancy among women in the Norwegian Mother and Child Cohort Study. Environ Int. 2014;62:104–12.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

Supported by grants from American Heart Association (15GRNT24470029) and KCUMB and internal funds from East Carolina Univeristy. We would like to thank the pregnant women for their participation.

Funding

This study was funded, in part, by the American Heart Association (AHA grant #15GRNT24470029) and by East Carolina University (ECU) internal funds. This study was not supported by NIH, Wellcome Trust, Howard Hughes Medical Institute, or other external funds.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Linda E May.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Clark, E., Isler, C., Strickland, D. et al. Influence of aerobic exercise on maternal lipid levels and offspring morphometrics. Int J Obes 43, 594–602 (2019). https://doi.org/10.1038/s41366-018-0258-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41366-018-0258-z

This article is cited by

Search

Quick links