American Journal of Respiratory and Critical Care Medicine

We examined whether the adverse effects of prenatal exposure to tobacco on lung development are limited to the last weeks of gestation by comparing respiratory function in preterm infants whose mothers had and had not smoked during pregnancy. Maximal forced expiratory flow (V˙max FRC) and time to peak tidal expiratory flow as a proportion of total expiratory time (Tptef:Te) were measured prior to discharge from hospital in 108 preterm infants (mean [SD] gestational age, 33.5 [1.8] wk), 40 of whose mothers had smoked during pregnancy. Infant urinary cotinine was less than 4 ng/ml in those born to nonsmokers, but it was as high as 458 ng/ml in exposed infants (p < 0.0001). Tptef:Te was significantly lower in infants exposed to tobacco in utero (mean [SD], 0.369 [0.109]) when compared with those who were not (0.426 [0.135]) (p ⩽ 0.02). V˙max FRC was also reduced in exposed infants (mean [SD], 85.2 [41.7] ml/s versus 103.8 [49.7] ml/s) (p = 0.07). After allowing for sex, ethnic group, body size, postnatal age, and socioeconomic status, Tptef:Te remained significantly diminished in infants exposed prenatally to tobacco (p < 0.05). Thus, impaired respiratory function is evident in infants born on average 7 wk prior to the expected delivery date, suggesting that the adverse effects of prenatal exposure to tobacco are not limited to the last weeks of pregnancy.

Maternal smoking during pregnancy is an avoidable risk factor for a number of adverse outcomes in infancy and later childhood, including low birthweight, preterm delivery, and sudden death in infancy (1, 2). The risk of lower respiratory illness, wheezing and asthma is increased among young children whose mothers smoke (3), and it has been suggested that these effects are mediated predominantly by prenatal effects on lung development (4, 5) and may operate by diminishing airway or alveolar growth, which is particularly rapid during fetal life.

Impaired airway function has been reported in infants of mothers who smoke (6-8), but most studies do not allow separation of the effects of prenatal and postnatal exposure. Although altered expiratory flow patterns during tidal breathing have been reported recently among term newborns (5, 9), the issue of how early in pregnancy these adverse effects may occur has not been addressed.

We now report a study examining the influence of maternal smoking during pregnancy on respiratory function during early life in preterm infants without known respiratory disease. The aim was to determine whether the adverse effects of maternal smoking on respiratory function are limited to the last weeks of pregnancy when placental function is likely to be most compromised.

Preterm infants (less than 36 completed weeks of gestation) without major congenital abnormalities or neonatal respiratory disease, whose parents were either both Northern European (white) or both Afro-Caribbean (black), were eligible for recruitment from the Special Care Baby Unit at the Homerton Hospital, London. Infants who, after delivery, required assisted ventilation for more than 6 h or supplemental oxygen for more than 24 h were ineligible, as were those whose parents did not speak English. The study was approved by the City and Hackney Local Research Ethics Committee. Written informed consent was obtained from the parents, who were usually present during respiratory measurements.

Information on maternal smoking during pregnancy was obtained retrospectively from maternal report at recruitment, as prospective documentation was not feasible in this study. Mothers were asked whether they had smoked at any time during pregnancy and, if so, the gestational age at stopping or starting smoking. Mothers were classified as smokers if they had smoked at any time after 4 wk of gestation, i.e., once they were aware that they might be pregnant. Indirect biochemical validation of maternal report of smoking was also performed by cotinine analysis (10) of urine obtained, whenever possible, from each infant within 24 h of delivery, and of maternal saliva, collected at infant respiratory function testing. Additional background information was obtained by the research midwife from mothers at recruitment, including paternal and maternal occupation, maternal age on leaving full-time education, and first degree family history of asthma.

Infant respiratory function was measured prior to discharge from hospital, with the infant supine and naturally asleep, and with ambient temperature maintained at 23 to 25° C. Data were collected as described previously (11-13) during periods of behaviorally determined quiet sleep. The main outcome variables were maximal forced expiratory flow at functional residual capacity (V˙maxFRC) (13, 14), an index of peripheral airway function, and time to peak tidal expiratory flow as a proportion of total expiratory time (Tptef:Te) (12), an index of tidal expiratory flow patterns. The latter reflects the degree to which expiratory flow and timing are modulated in order to slow lung emptying during expiration. A reduction in Tptef:Te is associated with diminished airway function (15). V˙maxFRC was measured using the rapid thoraco-abdominal compression technique and reported as the mean of the three highest technically satisfactory measurements obtained (13, 14). Tptef:Te, together with respiratory rate and tidal volume, were measured via a face mask and flowmeter and reported as the mean of 60 consecutive regular breaths collected over two or three separate epochs (12). Passive respiratory compliance (Crs) was measured using the multiple occlusion test (11, 14), so that any observed differences in peripheral airway function might be interpreted with respect to the elastic recoil of the respiratory system.

Statistical Analysis

Background characteristics were examined in relation to maternal report of smoking during pregnancy (Minitab for Windows, Release 11), and the association between maternal smoking during pregnancy and V˙maxFRC or Tptef:Te examined using multiple regression analyses (SPSS for Windows, Release 7). The sample size was sufficient to detect a 1 standard deviation difference in V˙maxFRC or Tptef:Te between infants born to smoking or to nonsmoking mothers, with 90% power at the 5% level after adjustment for sex, ethnic group, body size, postnatal age, and socioeconomic status (16).

Tptef:Te was successfully measured in 108 infants, and V˙maxFRC and Crs in 89 and 101 infants, respectively. Failures were largely due to insufficient quiet sleep or technically unacceptable measurements (11). Of the entire group, 49 (45%) were male and 65 (60%) were white (Table 1). Nine infants had received low concentrations of oxygen for less than 24 h (inspired oxygen concentration < 0.30), five had been ventilated briefly, but none had been given surfactant. Forty (37%) infants were born to mothers who had smoked during pregnancy. The proportion of infants whose mothers smoked was similar in those with and without measurements of V˙maxFRC, as were all other background characteristics (data not shown). A similar proportion of mothers in the smoking and nonsmoking groups had received antenatal steroids just prior to delivery (18 and 19%, respectively).

Table 1. BACKGROUND CHARACTERISTICS ACCORDING TO MATERNAL SMOKING HABITS DURING PREGNANCY*

Maternal Smoking (n = 40)No Maternal Smoking (n = 68)
Smoking–Nonsmoking95% CI
Male, n (%)20 (50%)29 (43%)−16% – 23%
White, n (%)30 (75%)35 (51%)6% –  42%**
Paternal manual occupation, n (%) 23 (66%)27 (43%)2% –  44%**
Maternal education 16 (14–23)17 (15–31)   −2.3 – −0.3**
Maternal salivary cotinine, ng/ml§ 246.8 (0–673.3)0.2 (0–3.0)149 – 398,
Infant urinary cotinine, ng/ml 69.2 (1.5–458.0)0.4 (0–3.6) 62 – 125,

Definition of abbreviations: 95% CI = 95% confidence interval of the difference; maternal education = age in years on leaving full-time education.

*Values are shown as median with ranges shown in parentheses, unless otherwise stated.

n = 35, n = 63, respectively.

n = 38, n = 68, respectively.

§n = 28, n = 53, respectively.

n = 12, n = 38, respectively.

**p < 0.05.

F1-164p < 0.0001.

Of the 68 mothers who reported not smoking during pregnancy, one smoked up to but not after the third week of pregnancy. Two of 40 mothers classified as smokers had ceased smoking at 12 and 20 wk of gestation, respectively. Mothers reported smoking between 1 and 40 cigarettes a day (median, 10). Maternal salivary cotinine, available for 81 mothers, discriminated well between self-reported smokers and nonsmokers: median (range) in smokers being 246.8 ng/ml (0 to 673.3) compared with 0.2 ng/ml (0 to 3.0) in nonsmokers (p < 0.0001) (Table 1). Similarly, median (range) urinary cotinine within 48 h of birth was 69.2 ng/ml (1.5 to 458.0) in infants of smoking mothers and 0.4 ng/ml (0 to 3.6) in infants born to nonsmokers (p < 0.0001) (Table 1).

Infants of smoking mothers were significantly more likely than those of nonsmoking mothers to be white (75% versus 51%), to have a father with a manual occupation (66% versus 43%), and to have a mother who left full-time education at a younger age (median [range], 16 yr (14 to 23) versus 17 yr [15 to 31]) (Table 1). They were equally likely to have a first degree relative with asthma (28% in each group). Infants of smoking mothers tended to be of lower birthweight (mean [SD]; 1,873 g [391] versus 1,959 g [457]) (p < 0.10), and at the time of respiratory function testing were significantly lighter (2,241 g [309] versus 2,363 g [356]) (p < 0.05) and shorter (44.9 cm [2.1] versus 45.9 cm [2.5]) (p < 0.05) compared with infants of non-smokers (Table 2).

Table 2. INFANT CHARACTERISTICS ACCORDING TO MATERNAL SMOKING HABITS DURING PREGNANCY*

Maternal Smoking(n = 40)
No Maternal Smoking(n = 68)
Nonsmoking 95% CI
Birth weight, g1,873 (391)1,959 (457)−255 –  83
Gestational age, wk33.4 (1.7)   33.6 (1.9)−0.9 – 0.5
Postnatal age, d     21 (11)   20 (9)−3 – 5
Postconceptional age, wk36.5 (1.5)   36.4 (1.3)−0.5 – 0.6
Test weight, g2,241 (309) 2,363 (356)−270 – −3
Test length, cm44.9 (2.1)   45.9 (2.5)−2.0 – −0.2

*Values are shown as mean with SD shown in parentheses, unless otherwise stated.

p < 0.05.

V˙maxFRC and Tptef:Te were diminished in infants exposed to tobacco in utero. Mean (SD) Tptef:Te was 0.369 (0.109) and 0.426 (0.135), respectively, in infants of mothers who did and did not smoke during pregnancy (p ⩽ 0.02), and mean (SD) V˙maxFRC was 85.2 (41.7) ml/s and 103.8 (49.7) ml/s (p = 0.07; Table 3). Compliance, tidal volume, respiratory rate, and total expiratory time did not differ according to maternal smoking in pregnancy when these variables were compared in absolute terms (Table 3). Similarly, when corrected for body weight, there was no significant difference between the groups for either Crs (11.5 versus 11.2 ml/kg/kPa for smoking versus nonsmoking) or tidal volume (7.2 versus 7.0 ml/kg, respectively).

Table 3. RESPIRATORY PARAMETERS ACCORDING TO MATERNAL SMOKING HABITS DURING PREGNANCY*

Maternal Smoking (n = 40)No Maternal Smoking (n = 68)Mean (95% CI) difference (smoking–nonsmoking)
V˙max FRC, ml/s85.2 (41.7)103.8 (49.7) 18.7 (−39.0 – 1.6)
Tptef:Te 0.369 (0.109)0.426 (0.135) 0.058 (−0.108 – −0.008)§
Respiratory compliance, ml/kPa 25.8 (5.2)26.7 (4.8)−0.9 (−2.9 – 1.2)
Tidal volume, ml16.1 (3.3)16.5 (3.3)−0.4 (−1.7 – 0.9)
Respiratory rate, breaths/min63 (13) 62 (14)   1 (−4 – 7)
Expiratory time, s0.571 (0.151)0.582 (0.166)−0.011 (−0.075 – 0.053)

Definition of abbreviations: V˙max FRC = maximal forced expiratory flow at functional residual capacity (n = 34, n = 55, respectively); Tptef:Te = the ratio of time to reach peak expiratory flow to total expiratory time.

*Values are shown as mean with SD shown in parentheses.

n = 37, n = 64, respectively.

p = 0.07.

§p < 0.02.

There were no sex differences in ethnic group or paternal social class, however, significantly more girls than boys had a positive family history of asthma (32 and 14%, respectively; p ⩽ 0.05), and although of similar postnatal age, body weight, and length, the boys had lower V˙maxFRC, and Tptef:Te was significantly diminished. In boys and girls, respectively, mean (SD) V˙maxFRC was 87.0 (41.2) ml/s and 105.4 (51.4) ml/s (95% CI, boys-girls: −38.2 to 1.3 ml/s; p = 0.07) and Tptef:Te was 0.371 (0.125) and 0.433 (0.126) (95% CI, boys-girls: −0.110 to −0.013; p ⩽ 0.01). There were otherwise no significant sex differences in respiratory function.

More white than black mothers reported smoking during pregnancy (Table 1). V˙maxFRC and Tptef:Te were significantly lower in white infants. In white and black infants, respectively, mean (SD) V˙maxFRC was 87.3 (49.2) ml/s and 109.3 (42.3) ml/s (95% CI, white-black: −41.8 to −2.3 ml/s; p = 0.03), and mean (SD) Tptef:Te was 0.373 (0.108) and 0.452 (0.143) (95% CI, white-black: −0.127 to −0.031; p = 0.002). Weight-corrected compliance was higher (11.7 versus 10.7 ml/ kPa/kg; 95% CI, −0.02 to 2.00), respiratory rate lower (60 versus 66 breaths/min; 95% CI, −11.0, −0.4), and expiratory time was longer (0.596 versus 0.549 s; 95% CI, −0.015, 0.110) in white infants. Although maternal smoking during pregnancy was more prevalent in infants whose fathers were in manual occupations (Table 1), there were no social class differences in size at birth or at respiratory function testing, or in any of the respiratory function parameters measured except Tptef:Te.

Multiple regression analyses were undertaken before and after adjusting for those variables identified in univariate analyses as being significantly associated with maternal smoking and either V˙maxFRC or Tptef:Te. Within this population, postnatal age, body weight, and length at test were not significantly associated with Tptef:Te (p = 0.33, 0.93, and 0.76, respectively) and were therefore not included in the model, whereas ethnic group, sex and social class were. On univariate analysis, V˙maxFRC was not associated with weight at test (p = 0.21), or social class (p = 0.63), but there was a significant relationship with ethnic group, postnatal age, sex, and crown-heel length. After adjustment for these variables, there was no longer an association between maternal smoking and V˙maxFRC (Table 4). By contrast, after adjustment for all appropriate factors, Tptef:Te remained significantly diminished in infants whose mothers reported smoking during pregnancy, being a mean (95% CI) −0.046 (−0.092 to −0.001) lower than in those whose mothers did not smoke (p < 0.0) (Table 4).

Table 4. RESULTS OF REGRESSION ANALYSES

VariableEstimated Coefficient (95% CI)p Value
V˙max FRC
 Maternal smoking during pregnancy
  Unadjusted−18.7 (−39.0 – 1.6)0.071
  Adjusted* −6.5 (−24.3 – 11.2)0.467
 Ethnic group, white−23.5 (−41.3 – −5.6)0.011
 Postnatal age, per day−1.4 (−2.3 – −0.5)0.002
 Sex, male23.4 (−41.3 – −5.5)0.011
 Length, cm5.5 (1.7 – 9.3)0.005
Tptef:Te
 Maternal smoking during pregnancy
  Unadjusted−0.058 (−0.108 – −0.008)0.024
  Adjusted* −0.046 (−0.092 – −0.001)0.046
 Ethnic group, white−0.077 (−0.124 – −0.031)0.001
 Sex, male−0.064 (−0.109 – −0.018)0.007
 Paternal social class, manual0.043 (0.004 – 0.089)0.074

*Effect of maternal smoking during pregnancy after adjustment for variables identified in univariate analysis as being significantly associated with maternal smoking and either V˙max FRC or Tptef:Te.

In the United Kingdom, approximately one-third of mothers smoke during pregnancy, and this is more common among white women and those of lower socioeconomic status (3, 17). Although it is well recognized that mothers who smoke during pregnancy are at increased risk of low birthweight and preterm delivery, uncertainty remains regarding the contribution and timing of prenatal tobacco exposure to impaired respiratory function and respiratory morbidity in early childhood. By measuring respiratory function in preterm infants before hospital discharge, we were able to examine the effect of maternal smoking during pregnancy separately from that of postnatal exposure to environmental tobacco smoke. In addition, as infants in this study were born prematurely, we were able to examine whether adverse effects were limited to the last weeks of pregnancy.

In a group of otherwise healthy infants who were delivered on average 7 wk early, we found that respiratory function was impaired in those whose mothers had smoked during pregnancy. Both V˙maxFRC, a measure of peripheral airway function, and Tptef:Te, which reflects the degree to which expiratory flow and timing are modulated, were diminished. Maternal smoking habits were associated with paternal social class and ethnic origin of the parents, and V˙maxFRC and Tptef:Te with sex, ethnic origin, and, for V˙maxFRC alone, postnatal age and body length. After adjustment for these variables, Tptef:Te, but not V˙maxFRC, remained significantly reduced in infants whose mothers smoked.

A number of published studies have examined the association between maternal smoking and infant respiratory function (5-7, 18-20) but, with few exceptions (5, 9), have been unable to distinguish the effects of prenatal and postnatal exposure. Stick and colleagues (5) found a significant reduction in Tptef:Te at a postnatal age of 3 d among term infants exposed to maternal smoking in utero but not postnatally, with similar results being reported in awake full-term newborns by Lodrup and colleagues (9). Beyond the neonatal period, marked reductions in V˙maxFRC and/or increased bronchial responsiveness have been reported among infants whose mothers smoked in some (6, 7), but not all (18-20), studies. The current study is the first to have evaluated the impact of maternal smoking on respiratory function in preterm infants, and from our findings it would appear that there is a small but demonstrable effect on respiratory function by at least 33 wk of gestation.

Biochemical validation of maternally reported smoking habits (based on infants' urinary and maternal salivary cotinine) suggests that misclassification of smoking exposure is unlikely to account for the results of this study. Cotinine is a sensitive measure of recent smoke exposure and it discriminates well between active, passive, and nonsmokers (3, 10). As urine was collected any time up to 24 h postnatal age, and many mothers refrain from smoking during labour, infant urinary cotinine levels on the first day of life may underestimate in utero exposure. Despite this, values as great as 458 ng/ml were observed among some infants whose mothers reported smoking, similar to levels reported in actively smoking adults (10), suggesting marked in utero exposure. By contrast, among the non-smoking group, infant urinary and maternal salivary cotinine values were very low or undetectable, the former not exceeding 3 ng/ml, below the range of values reported in passive smokers (10). Because women who smoke during pregnancy usually continue to do so after the birth of their child, maternal salivary cotinine provided a proxy measure of smoking during pregnancy.

Because neonatal respiratory disease and its treatment may affect subsequent respiratory function (21), infants requiring such treatment were excluded from the study. This could potentially introduce bias because of a “healthy infant” effect if preterm infants with impaired respiratory function caused by maternal smoking were more likely to need ventilatory assistance at birth. Ideally, we would have compared the characteristics of infants recruited to the study with those of all age-eligible infants over the study period (with respect to sex, ethnic group, maternal smoking, size at birth, etc.). Regrettably, a systematic audit with reasons for exclusion was not maintained prospectively, and it was not feasible to collect such data reliably retrospectively. However, had any such bias occurred, it would have tended to strengthen rather than to diminish our findings. Although an association between maternal smoking and preterm delivery has been reported (3), an increased risk of neonatal ventilation has not. Indeed, maturation of lung surfactant may be enhanced in infants exposed to tobacco in utero, possibly through stress-related intrauterine steroid release (6, 22). In infants delivered prematurely, this may partially compensate for the adverse effects of in utero tobacco exposure on the lung, at least during the immediate neonatal period.

Two measures of outcome were selected for this study. V˙maxFRC, which provides a measure of peripheral airway function that is relatively independent of upper airway and nasal resistance (11, 14), is determined largely by the geometry and resistive pressure losses along the small airways under conditions of dynamic compression. This measure has been widely used to characterise the normal growth and development of the airway during infancy, and the pulmonary abnormalities associated with acute and chronic lung disorders during early childhood (14). However, the caliber of the small intrathoracic airways is determined not only by their anatomic dimensions but by the structure and compliance of the airway wall and the distending pressures surrounding them, with the latter being influenced by the lung volume at which measurements are made. We did not consider lung volume measurements to be feasible in this study of small unsedated preterm infants, but we conclude that a significant reduction in lung volume is unlikely since respiratory rate, tidal volume, and respiratory compliance did not vary according to maternal smoking habits. Despite the narrow age range studied, there was a positive correlation between V˙maxFRC and length (but not weight). Once corrected for length, the association between V˙maxFRC and maternal smoking disappeared (Table 4). However, it is debatable whether it is appropriate to adjust for body size since in both the current and previous (6) studies, infants of smoking mothers have been shown to be significantly shorter at birth and at testing.

V˙maxFRC was diminished in boys and white infants, and was inversely related to postnatal age at testing. The observed sex differences are consistent with previously published reports of diminished airway function in boys during infancy and childhood (8, 13, 18, 20, 23) and may contribute to the higher prevalence of wheezing and asthma reported in boys at all ages to puberty (23, 24). We have previously reported that V˙maxFRC tends to be higher in black than in white preterm infants (13). This may be a transient difference reflecting the measurement of flows at a slightly higher end-expiratory lung volume among the black babies because of their different pattern of breathing, with more marked expiratory braking (longer Tptef:Te) during the neonatal period. A similar mechanism may explain the relatively high flows previously reported in newborns (19) and the negative correlation of V˙maxFRC with postnatal age noted in this study (Table 4).

In the East Boston cohort study (6, 8, 25), V˙maxFRC was reduced in infants of mothers who smoked during pregnancy to a much greater extent than in this study. This may reflect the fact that infants in the current study were delivered before the full impact of prenatal exposure to maternal smoking on somatic and airway growth had occurred, and they had not been exposed to any tobacco smoke postnatally. Furthermore, in the current study, but not in the East Boston study, the adjusted model included body length.

We found that Tptef:Te was significantly lower in preterm infants whose mothers had smoked, a reduction of similar magnitude to that reported in full-term newborns (5, 9). The ratio was also reduced in boys, as has been previously reported (20), in white infants (13), and in those whose fathers had a manual occupation. After allowing for these variables, Tptef:Te remained significantly diminished in infants of mothers who smoked, suggesting an underlying alteration in respiratory mechanics or control of breathing that had occurred several weeks before the infants were due to be delivered.

Tptef:Te reflects the degree to which expiration is actively modulated by the upper airways and diaphragm, and it was first noted to be diminished in adults with chronic obstructive airways disease (15). Martinez and colleagues (20, 26) reported that a reduced ratio among infant boys preceded and predicted an increased risk of wheezing during the first 3 yr of life. In the presence of severe airflow limitation, the tidal breathing curve is defined by intrathoracic airway mechanics. However in healthy subjects, it represents an integrated response of the entire respiratory system, includes neural, laryngeal, and intrathoracic components, and is strongly influenced by respiratory rate and postnatal age (12, 27).

The potential effects of smoking during pregnancy on lung and airway development may include structural alterations (28) as well as interference with the control of respiration (29, 30) and the developing immune system (4). A marked reduction in fetal movements, indicative of exposure to hypoxia, has been reported for at least an hour after the mother has smoked (31). Prenatal or postnatal exposure to nicotine can induce changes in central nervous system sensitivity to blood gases, resulting in impaired control of breathing (29, 30). In addition, nicotine may act as a vasoconstrictor, resulting in reduced placental blood flow, reduced supply of nutrients and oxygen to the fetus, and growth retardation. In the rat model, maternal smoking during pregnancy causes not only fetal growth retardation but marked structural changes to the developing lung, even when identical calorific intake is taken by control and experimental animals (28). Thus, the observed reduction in Tptef:Te among infants exposed prenatally to tobacco may reflect altered maturation of the lung and control of breathing as much as structural changes in airway development (27, 32).

In conclusion, the findings of this study suggest that, in infants of mothers who smoke during pregnancy, changes in respiratory function are evident by at least 7 wk prior to the expected date of delivery. At the time of testing, none of these infants had been exposed to tobacco smoke postnatally. However, many had been heavily exposed in utero as reflected by infant urinary cotinine levels at birth of a magnitude comparable to that reported in active smokers. Thus, prenatal exposure to tobacco has adverse effects that are evident some 2 mo before most babies are born. Because diminished respiratory function in very early life has been shown to precede and predict wheezing lower respiratory illnesses in early childhood (20), it is likely that these infants are also at increased risk of such illnesses. This would suggest that the incidence and severity of respiratory illnesses in preterm infants might be diminished by programs to reduce the prevalence of maternal smoking in pregnancy. These findings highlight the need to identify effective strategies to help women stop smoking.

The writers would like to thank Angie Wade for statistical advice and assistance, Liane Pilgrim for help in data collection and analysis, the staff on the Special Care Baby Unit at Homerton Hospital who collected the urine specimens, Colin Feyerabend at the Poison's Unit, New Cross Hospital, who performed the cotinine analyses, and all the parents who allowed their babies to participate in this study.

Supported by the Foundation for the Study of Infant Death, the Dunhill Medical Trust, the Muirhead Trust, and the Deutsche Forschungsgemeinschaft.

1. Haglund B., Cnattingius S.Cigarette smoking as a risk factor for sudden infant death syndrome: a population based study. Am. J. Public Health8019902932
2. Blair P. S., Fleming P. J., Bensley D., Smith I., Bacon C., Taylor E., Berry J., Golding J., Tripp J.Smoking and the sudden infant death syndrome: results from 1993–5 case-control study for confidential inquiry into stillbirths and deaths in infancy. B.M.J.3131996195198
3. Royal College of Physicians. 1992. Smoking and the Young: A Report of a Working Party of the Royal College of Physicians. Royal College of Physicians, London.
4. Taylor B., Wadsworth J.Maternal smoking during pregnancy and lower respiratory tract illness in early life. Arch. Dis. Child.621987786791
5. Stick S. M., Burton P. R., Gurrin L., Sly P. D., LeSouëf P. N.Effects of maternal smoking during pregnancy and a family history of asthma on respiratory function in newborn infants. Lancet348199610601064
6. Hanrahan J. P., Tager I. B., Segal M. R., Tosteson T. D., Castile R. G., Van V. H., Weiss S. T., Speizer F. E.The effect of maternal smoking during pregnancy on early infant lung function. Am. Rev. Respir. Dis.145199211291135
7. Young S., LeSouëf P. N., Geelhoed G. C., Stick S. M., Turner K. J., Landau L. I.The influence of a family history of asthma and parental smoking on airway responsiveness in early infancy. N. Engl. J. Med.324199111681173
8. Tager I. B., Hanrahan J. P., Tosteson T. D., Castile R. G., Brown R. W., Weiss S. T., Speizer F. E.Lung function, pre- and post-natal smoke exposure, and wheezing in the first year of life. Am. Rev. Respir. Dis.1471993811817
9. Lodrup Carlsen, K. C., J. J. K. Jaakkola, P. Nafstad, and K.-H. CarlsenIn utero exposure to cigarette smoking influences lung function at birth. Eur. Respir. J.10199717741779
10. Jarvis M. J., Tunstall-Pedoe H., Feyerabend C., Vesey C., Saloojee Y.Comparison of tests used to distinguish smokers from nonsmokers. Am. J. Public Health77198714351438
11. Stocks, J., P. D. Sly, R. S. Tepper, and W. J. Morgan. 1996. Infant Respiratory Function Testing. John Wiley & Sons, New York.
12. Stocks J., Dezateux C. A., Jackson E. A., Hoo A., Costeloe K. L., Wade A. M.Analysis of tidal breathing parameters in infancy: how variable is Tptef:Te? Am. J. Respir. Crit. Care Med.150199413471354
13. Stocks J., Henschen M., Hoo A. F., Costeloe K., Dezateux C.The influence of ethnicity and gender on airway function in preterm infants. Am. J. Respir. Crit. Care Med.156199718551862
14. American Thoracic Society/European Respiratory SocietyRespiratory mechanics in infants: physiologic evaluation in health and disease. Am. Rev. Respir. Dis.1471993474496
15. Morris M. J., Lane D. J.Tidal expiratory flow patterns in airflow obstruction. Thorax361981135142
16. Cohen, J. 1988. Statistical Power Analysis for the Behavioural Sciences. Erlbaum Associates, Hillsdale, NJ.
17. Balarajan R., Yuen P.British smoking and drinking habits: variations by country of birth. Comm. Med.81986237239
18. Clarke J. R., Salmon B., Silverman M.Bronchial responsiveness in the neonatal period as a risk factor for wheezing in infancy. Am. J. Respir. Crit. Care Med.151199514341440
19. Tepper R. S., Reister T.Forced expiratory flows and lung volumes in normal infants. Pediatr. Pulmonol.151993357361
20. Martinez F. D., Morgan W. J., Wright A. L., Holberg C. J., Taussig L. M.The Group Health Medical Associates' PersonnelDiminished lung function as a predisposing factor for wheezing respiratory illness in infants. N. Engl. J. Med.319198811121117
21. Parat S., Moriette G., Delaperche M. F., Escourrou P., Denjean A., Gaultier C.Long-term pulmonary functional outcome of bronchopulmonary dysplasia and premature birth. Pediatr. Pulmonol.201995289296
22. Lieberman E., Torday J., Barbieri R., Cohen A., Van Vunakis H., Weiss S. T.Association of intrauterine cigarette smoke exposure with indices of fetal lung maturation. Obstet. Gynecol.791992564570
23. Hibbert M., Lannigan A., Raven J., Landau L., Phelan P.Gender differences in lung growth. Pediatr. Pulmonol.191995129134
24. Gold D. R., Rotnitzky A., Damokosh A. I., Ware J. H., Speizer F. E., Ferris J. B. G., Dockery D. W.Race and gender differences in respiratory illness prevalence and their relationship to environmental exposures in children 7 to 14 years of age. Am. Rev. Respir. Dis.14819931018
25. Brown R. W., Hanrahan J. P., Castile R., Tager I. B.Effect of maternal smoking during pregnancy on passive respiratory mechanics in early infancy. Pediatr. Pulmonol.1919952328
26. Martinez F. D., Wright A. L., Taussig L. M., Holberg C. J., Halonen M., Morgan W. J.The Group Health Medical AssociatesAsthma and wheezing in the first six years of life. N. Engl. J. Med.3321995133138
27. Clarke J., Silverman M.Infant lung function and tidal breathing patterns. Pediatr. Pulmonol.201995135136
28. Collins M. H., Moessinger A. C., Kleinerman J.Fetal lung hypoplasia associated with maternal smoking: a morphometric analysis. Pediatr. Res.191985408412
29. Milerad J., Larsson H., Lin J., Sundel H. W.Nicotine attenuates the ventilatory response to hypoxia in the developing lamb. Pediatr. Res.371995652660
30. Lewis K. W., Bosque E. M.Deficient hypoxia awakening response in infants of smoking mothers: possible relationship to sudden infant death syndrome. J. Pediatr.1271995691699
31. Thaler I., Goodman J. D. S., Dawes G. S.Effects of maternal cigarette smoking on fetal breathing and fetal movements. Am. J. Obstet. Gynecol.1381980282287
32. Mikkilineni S., England S.On tidal expiratory flow measurements in infants. Pediatr. Pulmonol.1819947172
Correspondence and requests for reprints should be addressed to Ah-Fong Hoo, Portex Anaesthesia, Intensive Therapy and Respiratory Medicine Unit, Institute of Child Health and Great Ormond Street Hospital, NHS Trust, 30 Guilford Street, London WC1N 1EH, UK.

Dr. Stocks is supported by SIMS Portex Plc.

Dr. Dezateux is supported by the Wellcome Trust.

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American Journal of Respiratory and Critical Care Medicine
158
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