Maternal Smoking During Pregnancy, Growth, and Bone Mass in Prepubertal Children

There have been no studies of smoking during pregnancy and bone mineralization in children. The objective of this population‐based longitudinal study was to determine whether maternal smoking during pregnancy is associated with bone mass and other growth variables in prepubertal children. We studied 330 8‐year‐old male and female children representing 47% of those who originally took part in a study of risk factors for Sudden Infant Death Syndrome in 1988. The main outcome measures were bone mineral density measured by a Hologic QDR2000 densitometer: birth weight, placental weight, height, and weight. Maternal smoking during pregnancy was associated with deficits in growth with these children having lower height (−1.53 cm, 95% confidence interval [CI] −3.03 to −0.03) and a trend to lower weight (−1.35 kg, 95% CI −2.75 to 0.11) at age 8. Furthermore, there was a disproportionate deficit in bone mass such that those children whose mothers smoked during pregnancy had lower size adjusted bone mass at the lumbar spine (−0.019 g/cm2, 95% CI −0.033 to −0.005) and femoral neck (−0.018 g/cm2, 95%CI −0.034 to −0.002) but not total body (−0.005 g/cm2, 95% CI −0.015 to 0.005). This association was only present for children born at term. Mothers who smoked during pregnancy also had lower placental weight (− 56 g, 95% CI −95 to −17), and further adjustment for placental weight led to nonsignificant results for smoking with both growth and bone parameters, suggesting that these associations may be mediated through placental size and function. Maternal smoking habit in 1996 was not significantly associated with bone mass at any site. In conclusion, this study has demonstrated a long‐term negative association between maternal smoking during pregnancy and both growth and bone mass in children born at term, and suggests that the timing of exposure rather than the dose or duration is critical. If these associations are present in other populations and they persist until the attainment of peak bone mass, then our findings suggest that osteoporosis prevention programs should start very early in the life cycle.

[1]  M. Law,et al.  A meta-analysis of cigarette smoking, bone mineral density and risk of hip fracture: recognition of a major effect , 1997, BMJ.

[2]  F. Speizer,et al.  Maternal smoking during pregnancy, urine cotinine concentrations, and birth outcomes. A prospective cohort study. , 1997, International journal of epidemiology.

[3]  J. Newnham,et al.  Prospective cohort study of factors influencing the relative weights of the placenta and the newborn infant , 1997, BMJ.

[4]  M. Griffiths,et al.  Correcting the Magnification Error of Fan Beam Densitometers , 1997, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[5]  R. Eastell,et al.  Growth in infancy and bone mass in later life , 1995, Annals of the rheumatic diseases.

[6]  O Johnell,et al.  Meta-analysis of how well measures of bone mineral density predict occurrence of osteoporotic fractures. , 1996, BMJ.

[7]  L. Vatten,et al.  Pre- and post-natal growth in children of women who smoked in pregnancy. , 1996, Early human development.

[8]  O. Johnell,et al.  Meta-analysis of how well measures of bone mineral density predict occurrence of osteoporotic fractures , 1996 .

[9]  C. Wild,et al.  Prevalence of smoking in early pregnancy by census area: measured by anonymous cotinine testing of residual antenatal blood samples. , 1996, The New Zealand medical journal.

[10]  S. Cnattingius,et al.  Effects on birthweights of maternal education, socio-economic status, and work-related characteristics , 1996, Scandinavian journal of social medicine.

[11]  B. Eskenazi,et al.  Passive and active maternal smoking during pregnancy, as measured by serum cotinine, and postnatal smoke exposure. I. Effects on physical growth at age 5 years. , 1995, American journal of epidemiology.

[12]  H. Hoffman,et al.  Do pregnant smokers eat differently from pregnant non-smokers? , 1995, Paediatric and perinatal epidemiology.

[13]  P. Egger,et al.  Childhood growth, physical activity, and peak bone mass in women , 1995, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[14]  S. Fisher,et al.  Maternal smoking inhibits early human cytotrophoblast differentiation. , 1995, Reproductive toxicology.

[15]  P. Steer,et al.  Placental nitric oxide metabolism. , 1995, Reproduction, fertility, and development.

[16]  J. Eisman,et al.  Lifestyle factors and bone density in the elderly: Implications for osteoporosis prevention , 1994, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[17]  R. Demir,et al.  Structural changes in placental barrier of smoking mother. A quantitative and ultrastructural study. , 1994, Pathology, research and practice.

[18]  J. Palmgren,et al.  Exercise, smoking, and calcium intake during adolescence and early adulthood as determinants of peak bone mass , 1994, BMJ.

[19]  E. Lieberman,et al.  Low birthweight at term and the timing of fetal exposure to maternal smoking. , 1994, American journal of public health.

[20]  H C Kemper,et al.  Weight‐bearing activity during youth is a more important factor for peak bone mass than calcium intake , 1994, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[21]  E. Seeman,et al.  The bone density of female twins discordant for tobacco use. , 1994, The New England journal of medicine.

[22]  D. Evain-Brion,et al.  Alteration of epidermal growth factor receptor in placental membranes of smokers: Relationship with intrauterine growth retardation , 1994 .

[23]  D. Evain-Brion,et al.  Alteration of epidermal growth factor receptor in placental membranes of smokers: relationship with intrauterine growth retardation. , 1994, American journal of obstetrics and gynecology.

[24]  J. Langhoff‐Roos,et al.  Effect of smoking on maternal glucose metabolism. , 1993, Gynecologic and obstetric investigation.

[25]  Role of peak bone mass and bone loss in postmenopausal osteoporosis: 12 year study. , 1992, BMJ.

[26]  F. Vio,et al.  Smoking during pregnancy and lactation and its effects on breast-milk volume. , 1991, The American journal of clinical nutrition.

[27]  T. Dwyer,et al.  Prospective cohort study of prone sleeping position and sudden infant death syndrome , 1991, The Lancet.

[28]  B. Dawson-Hughes,et al.  Smoking and bone loss among postmenopausal women , 1991, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[29]  R B Mazess,et al.  Bone density in premenopausal women: effects of age, dietary intake, physical activity, smoking, and birth-control pills. , 1991, The American journal of clinical nutrition.

[30]  J. Eisman,et al.  Effects of tobacco use on axial and appendicular bone mineral density. , 1989, Bone.

[31]  O. Miettinen,et al.  Theoretical Epidemiology: Principles of Occurrence Research in Medicine. , 1987 .

[32]  H. Meredith Relation between tobacco smoking of pregnant women and body size of their progeny: a compilation and synthesis of published studies. , 1975, Human biology.