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. Author manuscript; available in PMC: 2011 Jan 1.
Published in final edited form as: Prev Med. 2009 Dec 21;50(1-2):13. doi: 10.1016/j.ypmed.2009.12.009

The Effects of Maternal Smoking During Pregnancy on Offspring Outcomes

Arpana Agrawal 1, Jeffrey Scherrer 1,2, Julia D Grant 1, Carolyn Sartor 1, Michele L Pergadia 1, Alexis E Duncan 1, Pamela AF Madden 1, Jon Randolph Haber 3, Theodore Jacob 3,4,*, Kathleen Bucholz 1,*, Hong Xian 1,2
PMCID: PMC2813884  NIHMSID: NIHMS166342  PMID: 20026103

Abstract

Objective:

To evaluate the possible association between maternal smoking during pregnancy (MSDP) and offspring outcomes of birth weight, pre-term birth, remediation, low scholastic achievement, regular smoking, attention deficit hyperactivity disorder (ADHD) and conduct problems (CD) while controlling for similar behaviors in parents.

Methods:

Using telephone interviews, data were collected, in 2001 and 2004, as a part of two U.S. offspring-of-twins projects. Fathers, who were twins participating in the Vietnam Era Twin Registry, their female spouse and their offspring were interviewed – information on 1342 unique pregnancies in mothers with a history of regular smoking was utilized for these analyses. The association between MSDP and birth weight, pre-term birth, remediation, low scholastic achievement, regular smoking, attention deficit hyperactivity disorder and conduct disorder while controlling for similar behaviors in parents, was examined using regression.

Results:

MSDP was associated with decreased birth weight, low scholastic achievement, regular smoking and ADHD. However, the association between MSDP and offspring ADHD was explained by maternal ADHD. MSDP was also associated with earlier age of offspring initiation of smoking and onset of regular smoking.

Conclusions:

MSDP may influence certain offspring outcomes via mechanisms that are independent from genetic risk attributable to comorbid conditions. Assisting expecting mothers with their smoking cessation efforts will likely provide widespread health benefits to both mother and offspring.

INTRODUCTION

In 2006, 17% of women giving birth reported cigarette smoking during pregnancy during their last trimester (Centers for Disease Control (CDC), 2004; PRAMS, 2007). While persistent cigarette smoking itself is one of the leading contributors to preventable death (Centers for Disease Control (CDC), 2002), maternal smoking during pregnancy (MSDP) has in and of itself been implicated as a potential risk factor associated with multiple offspring outcomes such as low birth weight, conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), offspring smoking and cognitive dysfunction (Knopik, 2009).

Low birth weight and other birth outcomes

There is considerable evidence supporting the hypothesis that offspring of mothers who smoke during their pregnancies have impaired fetal growth, pre-term birth and lower birth weight infants (Conter et al., 1995; D'Onofrio et al., 2003; Knopik et al., 2005; Bada et al., 2005; Salihu et al., 2005; Kyrklund-Blomberg et al., 2005; Stroud et al., 2009; McCowan et al., 2009; Thiriez et al., 2009), which, in turn, are correlated with a host of neuropsychological developmental delays. Of these, the association between MSDP and low birth weight appears to account for many of the associated outcomes, replicating consistently in prospective and retrospective studies.

Cognitive dysfunction and impaired learning

Some studies report impaired learning in those prenatally exposed to cigarette smoke, although results are equivocal (Bauman et al., 1991; Eskenazi and Trupin, 1995; Cornelius et al., 2001; Batstra et al., 2003; Mortensen et al., 2005; Lambe et al., 2006). Using an array of laboratory tasks, Cornelius et al., (Cornelius et al., 2001) found support for an association between MSDP and deficits in multiple aspects of learning and memory. In another study, MSDP was associated, via familial factors, with poor school performance (Lambe et al., 2006).

Externalizing behaviors

While the mechanism underlying their association is still under investigation, several studies report higher rates of externalizing behaviors, including attention deficit hyperactivity disorder (ADHD), conduct disorder (CD) as well as higher impulsivity and other problem behaviors in the offspring of mothers who smoked during their pregnancy (Milberger et al., 1996; Fergusson et al., 1998; Wakschlag et al., 2002; Batstra et al., 2003; Maughan et al., 2004; Knopik et al., 2005; Wakschlag et al., 2006; Cornelius et al., 2007; D'Onofrio et al., 2008; Knopik et al., 2009). Two recent studies have investigated the familial links between MSDP and externalizing disorders (Knopik et al., 2006; D'Onofrio et al., 2008) – broadly, these studies suggest that familial factors partially contribute to the association between MSDP and externalizing behavior, although the mechanisms are unclear. Multiple studies also report the association between MSDP and externalizing behaviors to be explained by maternal problem behaviors (Orlebeke et al., 1999; Silberg et al., 2003; Maughan et al., 2004).

Offspring smoking:

There is growing evidence that prenatal exposure to cigarette smoking increases the likelihood of cigarette smoking in the offspring (Cornelius et al., 2000; Cornelius et al., 2005). Given the high correlation between maternal nicotine dependence and MSDP (Agrawal et al., 2008; O'Callaghan et al., 2009), these youth represent a particularly vulnerable group of individuals with both increased genetic (inherited often from both parents who are smokers) and environmental risk (attributable to MSDP and potentially, via exposure to parents who smoke) risk.

In this study, using data on 1342 unique pregnancies, with offspring aged 12-32, their fathers and mothers, we investigate the association between MSDP and offspring outcomes of low birth-weight, pre-term birth, remediation, low scholastic achievement, ADHD, CD problems and regular smoking in the offspring. We highlight the importance of controlling for the influence of parental behaviors in studies of MSDP and offspring outcomes and, as a secondary analysis, also test for potential genetic and environmental links that may contribute to the relationship between MSDP and offspring outcomes.

METHODS AND MATERIALS

Sample

Offspring, with their biological mother and father, constituted the analytic sample. In 2001 and 2004 respectively, data collection was initiated from two offspring-of-twins (OOT) studies, which aimed to examine outcomes in the children of VETR twin fathers, who were members of the Vietnam Era Twin Registry (VETR) (Goldberg et al., 1987; Eisen et al., 1987; Henderson et al., 1990), which is a U.S. registry of male like-sex twin pairs in which both co-twins served in the military during the Vietnam Era (1965- 1975). Father twin pairs who (a) were concordant or discordant for alcohol dependence (AD, Project 1), or (b) were concordant or discordant for illicit drug dependence (DD, Project 2), along with (c) unaffected control twin pairs, were selected. Spouses and offspring of twin fathers were invited to participate. Fathers had already been interviewed by telephone, in 1992, with the Diagnostic Interview Schedule (DIS) (Robins et al., 1996). An adaptation of the Semi-Structured Assessment for the Genetics of Alcoholism (SSAGA)(Bucholz et al., 1994) was used to collect data from mothers and offspring. For both projects, biological mothers or custodial mothers (for e.g. step mothers) were eligible to participate if twins provided permission to contact them. Offspring were eligible to participate if the VETR twin father and biological and/or custodial mothers gave permission to contact them (In Project 2, permission was granted by either VETR twin father or mother). Parents provided written consent for their minor aged offspring to be interviewed. Due to the nature of data collection, there was some overlap of subjects (N=249) across the two studies – for these subjects, the more recently conducted Project 2 data were used. Descriptions of survey contents and response rates have been previously published (Jacob et al., 2003; Scherrer et al., 2004; Duncan et al., 2008).

Baseline data were used to create the database for the present study. Maternal data and offspring data were necessary to conduct these analyses and hence, any participants missing these components were excluded from the analyses. Additionally, to exclude spurious effects of a custodial mother reporting on MSDP or outcomes of her adoptive child, we excluded 9% of the mothers who were not the biological parent of the child. This yielded a sample size of 1741 offspring with maternal and paternal data – however, the key predictor, MSDP, was only assessed in the 1342 pregnancies (some offspring are related to each other, thus this total refers to 1342 unique pregnancies) in 1,122 mothers who previously reported smoking 100 or more cigarettes in a lifetime - this was our final sample.

Measures

Offspring Outcomes

Several outcomes were examined in the offspring: Birth weight (BW); Preterm birth (PREM); Remediation (i.e. taking remedial classes/a speech/language therapist, REM); Conduct problems (CD); ADHD (ADHD); Low scholastic achievement (EDU) and Regular smoking (REGSMK).

Definitions for each measure are listed in Table 1.

TABLE 1.

Prevalence of offspring outcomes, paternal and maternal measures in 1,342 offspring of 1,122 mothers from two U.S. offspring of twins studies conducted in 2001 and 2004.

Measure Abbreviation %
Maternal smoking during pregnancy MSDP 14.2
Self-reported whether they had smoked during the 1st, 2nd and the 3rd trimester of pregnancy.
Maternal drinking during pregnancy MDDP 12.3
Self-reported whether they had consumed alcoholic beverages even on one day after knowing they were
pregnant (during any pregnancy).
Maternal heavy smoking MHSI 16.7
A score of 4 or more on the Heaviness of Smoking Inventory (H.S.I.) (Heatherton et al., 1989) indicating
risk for nicotine dependence (Chabrol et al., 2005).
Maternal current smoking MCUR 15.5
Self-reported smoking at time of interview.
Maternal lifetime drug use MDRG 43.3
Self-reported use of cannabis, cocaine, stimulants, sedatives, opiates, heroin, psychedelics, inhalants or
hallucinogens.
Maternal alcohol dependence MAD 8.6
Meeting criteria for lifetime DSM-IV alcohol dependence based on self-reported symptoms
Maternal attention deficit hyperactivity disorder MADHD 7.8
Self-reported meeting criteria for ADHD prior to age 7 years.
Maternal conduct problems MCDP 22.8
Self-reported, endorsing one or more items from a conduct problems behavior checklist.
Paternal DSM-IIIR nicotine dependence PND 47.4
Meeting criteria for nicotine dependence from self-reported symptoms.
Paternal alcohol dependence PAD Grp 1: 31.7, Grp 2: 11.6,
Grp 3: 13.2
High-risk sampling.
Paternal drug dependence PDD Grp 1: 69.1, Grp 2: 5.4,
Grp 3: 6.8
High-risk sampling.
Paternal current smoking PCUR 24.6
Self-reported smoking at time of interview.
Paternal conduct disorder PCD 9.4
Meeting criteria for DSM-IIIR conduct disorder based on self-reported symptoms.
Offspring birth weight BW* Mean: 121.9 ounces (SE
0.6) **
Maternal report of birth weight (in ounces).
Offspring premature birth PREM 7.9
Maternal report that the offspring was born 3 or more weeks prior to their due date.
Offspring attention deficit hyperactivity disorder problem ADHD 10.5
Maternal endorsement of 6 or more DSM-IV inattention or hyperactivity/impulsivity symptoms (with or
without impairment).
Offspring conduct disorder (3+ symptoms) CD 13.5
Self-report of 3 or more DSM-IV symptoms of conduct disorder.
Offspring regular smoking REGSMK 18.5
Self-report of having smoked 21 or more cigarettes over the lifetime and smoking three or more times per week
for a minimum of three weeks.
Offspring remediation/remedial classes REM 20.3
Maternal report of offspring using a speech/language therapist or using remedial/special education.
Offspring low scholastic achievement EDU 16.4
Self-report of consistently receiving C's or lower grades in school.
*

4.5% of the offspring had a birthweight that was less than 88 ounces (approximately 2496 grams).

**

121.9 ounces ≈ 3, 456 grams

Maternal Covariates

The primary maternal predictor was maternal smoking during pregnancy (MSDP). Mothers self-reported whether they had smoked during the 1st, 2nd and the 3rd trimester of pregnancy, only if they had previously reported smoking a 100 or more cigarettes in their lifetime (N=1,342 pregnancies in 1,122 biological mothers). Due to the distribution of the data (85.8% didn't report MSDP, 2.4% reporting 1st trimester only, 2% reporting 1st or 2nd trimester but not 3rd and 10.3% reporting MSDP into the 3rd trimester) a dichotomous measure reflecting any MSDP was coded. The prevalence of MSDP (14.2%) is comparable to U.S. population estimates (Centers for Disease Control (CDC), 2004). Secondary analyses used multi-level variables that excluded any smoking in the 1st trimester that may have occurred prior to knowledge of pregnancy.

Other covariates were Maternal drinking during pregnancy (MDDP); Maternal Heavy Smoking (MHSI); Maternal Current smoking (MCUR); Maternal Drug Use (MDRG); Maternal Alcohol Dependence (MAD); Maternal ADHD (MADHD) and Maternal CD problems (MCDP). These are defined in Table 1. Data on maternal drug use during (any) pregnancy were available but rates were very low (1.9%) and hence, we did not include this measure in the current study.

Paternal Covariates

Covariates from the father included Paternal Lifetime Nicotine Dependence (PND); Paternal Current Smoking (PCUR) and Paternal conduct disorder (PCD), each defined in Table 1. As the original studies selected father twins on the basis of their alcohol or drug dependence status, sample selection bias was controlled by adjusting for the ascertainment strategy, using the 4-group design(Jacob et al., 2003). According to this design, fathers, who were the VETR twin pairs, were designated as:

  • Group 1 if the father of the offspring had alcohol dependence (AD) or drug dependence (DD) – the offspring in this instance is at high genetic and environmental risk.

  • Group 2 if the father of the offspring was unaffected but his identical co-twin (who shares 100% of his genes identical-by-descent) had a diagnosis of AD or DD – the offspring here is at high genetic risk but low environmental risk.

  • Group 3 if the father of the offspring was unaffected but his fraternal co-twin (who shares 50% of his genes identical-by-descent) had a diagnosis of AD or DD – the offspring is at moderate genetic but low environmental risk.

  • Group 4, where irrespective of zygosity, both the father and his cotwin are unaffected – the offspring is at low genetic and environmental risk.

Two 4-group design variable sets, one each for AD (PAD) and for DD (PDD), were included as covariates representing paternal alcohol and drug dependence and to control for sampling design. Ethnicity (Caucasian – 94.4%), paternal (63.8%) and maternal (70.5%) education representing 13 or more years of educational attainment were used as covariates.

Statistical analyses

A series of logistic regression models were fitted to the data. The offspring outcome was predicted by MSDP as well as the remaining maternal and paternal covariates – all analyses controlled for PAD, PDD as well as ethnicity and parental education. In instances where an offspring outcome was highly correlated with another outcome measure (for e.g. offspring smoking correlated with offspring ADHD), the mediating influence of the correlated measure was tested in a subsequent model.

For any offspring outcome (except birth weight and pre-term birth) that was significantly associated with MSDP in the multivariate models, we also fit Kaplan-Meier survival curves to examine whether MSDP also influenced age at onset of the outcome (for e.g. if MSDP associated with regular smoking in the offspring, is it also associated with earlier onset of regular smoking). All analyses were done in STATA with a robust variance estimator that allowed for clustered observations (i.e. adjusting standard errors when related offspring/siblings are treated as independent observations).

RESULTS

Correlation between measures

MSDP was negatively correlated with birth weight and positively with regular smoking in the offspring (Table S1-S3). Correlations between MSDP and ADHD or CDP were modest, however correlations between offspring ADHD and maternal ADHD (MADHD) and maternal CD (MCDP) were higher. MSDP as well as mother's H.S.I. (MHSI) and current smoking (MCUR) was also correlated with nicotine dependence and current smoking in the father, suggesting positive assortative mating (i.e. tendency for smokers to marry smokers). Finally, CD, ADHD, regular smoking (REGSMK) and low scholastic achievement (EDU) were correlated with each other in the offspring, likely representing a general predisposition to externalizing behaviors. EDU was also correlated parental education.

Association between MSDP and offspring outcomes

In univariate models (Table 2) and after adjusting for PAD, PDD, ethnicity and parental education, MSDP was associated with decreasing birth weight, ADHD, low scholastic achievement and with regular smoking in the offspring. In multivariate models, controlling for all maternal and paternal covariates, MSDP had a sustained influence on decreasing birth weight and offspring's regular smoking. The effects of MSDP on offspring ADHD was attributable to mother's self-reported ADHD, maternal CDP and with low paternal education. Maternal ADHD, maternal low education and paternal current smoking were associated with low scholastic achievement. MDDP was not associated with these offspring outcomes.

TABLE 2.

Univariate and multivariate association between MSDP and offspring outcomes in 1,342 offspring from two U.S. offspring of twins studies conducted in 2001 and 2004.

Birth weight*


(BW)
Preterm birth


(PREM)
Attention Deficit
Hyperactivity
Disorder
(ADHD)
Conduct
problems

(CD)
Regular smoking


(REGSMK)
Remediation


(REM)
Low Scholastic
Achievement

(EDU)
Univariate

MSDP −7.72
[−11.13, −4.31]
1.38
[0.76, 2.49]
1.74
[1.10, 2.75]
1.27
[0.82, 1.96]
2.25
[1.54, 3.27]
1.16
[0.79, 1.72]
1.51
[1.01-2.25]

Adjusting for ethnicity, parental education and study design

MSDP −8.00
[−11.46,−4.55]
1.14
[0.79, 1.65]
1.53
[1.00,2.35]
1.18
[0.76, 1.18]
2.09
[1.43, 3.07]
1.20
[0.81, 1.77]
1.53
[1.02, 2.30]

Adjusting for all maternal and paternal covariates

MSDP −7.63
[−11.12,−4.14]
- 1.74
[1.18, 2.58]
-
MDDP - - - -
HSI - - - -
MCUR - - - -
MDRG - - 1.74
[1.26, 2.39]
-
MAD - - - -
MADHD - 4.10
[2.50, 6.72]
- 2.03
[1.31, 3.16]
MCD - 1.29
[1.10, 1.52]
- -
PND - - 1.76
[1.28, 2.42]
1.41
[1.01, 1.97]
PAD - - - -
PDD - - - -
PCUR - - - -
PASPD - - - -
*

Continuous measure – coefficient shown.

Kaplan-Meier curves for survivor function were tested for initiation of cigarette smoking and regular smoking (Figure 1). MSDP was also associated with earlier onset of regular smoking (hazard ratio of 1.48, 95% C.I. [1.13-1.94]) in the offspring.

FIGURE 1.

FIGURE 1

Nelson-Aelan curves representing hazards of regular smoking at various ages of onset in 1342 offspring of mothers reporting maternal smoking during pregnancy (MSDP) and those without MSDP from two U.S. offspring of twins studies conducted in 2001 & 2004.

DISCUSSION

Previous studies have attempted to disentangle the etiology of the relationship between MSDP and smoking as well as externalizing behaviors in the offspring (see Knopik, 2009 for a review). While, using a subset of these data, Knopik et al (2009) recently showed univariate associations between ADHD problems and MSDP, a preponderance of studies, including ours, support the hypothesis that for externalizing behaviors, such as ADHD and CD, transmission of risk may be attributable to a latent predisposition to non-normative behaviors (Silberg et al., 2003; Maughan et al., 2004; Knopik et al., 2005; Knopik et al., 2006; D'Onofrio et al., 2008) – in other words, women with a predisposition to non-normative/problem behaviors tend to also smoke during their pregnancy and their offspring are at increased risk for externalizing psychopathology via a direct transmission of genetic risk from mother (and father) to offspring. A recent study found no differences in rates of externalizing behaviors between siblings discordant for MSDP also alluding to the possible role of family environment that may jointly increase likelihood of MSDP as well as later externalizing behaviors in the offspring (D'Onofrio et al., 2008) – the potential role of parental behaviors or general permissive parenting may be explored in this context.

The literature surrounding the impact of MSDP on birth weight and other birth complications is quite robust. We validate those findings here - offspring whose mothers reported MSDP, on average, weighed 215.5 grams (7.6 ounces) less at birth when compared to offspring whose mothers may have been regular smokers but did not report MSDP. Animal studies demonstrate the effects of nicotine on fetal and placental development – a common hypothesis here posits that nicotine exerts anorexigenic effects on both mother and fetus (Perkins et al., 1994; Ernst et al., 2001) exacerbated by hypoxia related to respiratory difficulties in the fetus (Abel, 1980; Byrd and Howard, 1995; Cnattingius, 2004). Some studies have also considered the possible mediating role of lower maternal weight gain, lower maternal BMI and premature birth – however, the effect of MSDP on low birth weight appears to be independent and direct.

After adjusting for maternal and paternal covariates, low scholastic achievement, via self-reported school grade was not associated with MSDP, suggesting that other familial factors that correlate with both MSDP and offspring scholastic achievement may be at play. While early studies (Butler and Goldstein, 1973; Fogelman, 1980; Fogelman and Manor, 1988)demonstrated strong associations between MSDP and scholastic achievement, recently, Lambe et al., (2006) have reported that MSDP during the first but not the second pregnancy is associated with low scholastic achievement in the second offspring. Additionally, consistent with our finding, another study (Braun et al., 2009) reported that maternal education attenuated the relationship between MSDP and intellectual abilities, further reinforcing the role of correlated familial factors.

The findings of the present study should be viewed with some limitations in mind. First, the parent studies were designed to study outcomes in the offspring of twin pairs - while this can be particularly useful in disentangling the role of genetic factors from environmental influences, we were limited in our ability to do this due to (a) reduced power and (b) because the fathers, but not the mothers, were twins. Thus, a formal test of genetic influences of MSDP on offspring outcome is not possible (Eaves et al., 2005). Additionally, the fathers were members of the VETS – this, as well as strategies for contacting mothers and offspring, may influence the generalizability of our findings. Second, reports of MSDP were retrospective and cross-sectional and may have been influenced by recall bias or other personal factors. While studies show high reliability in self-reported smoking during pregnancy (Heath et al., 2003; Reich et al., 2003; Pickett et al., 2009), recent increases in dissemination of information on adverse consequences of MSDP on offspring may have discouraged some mothers from disclosing it. Third, maternal gestational weight was not available on all participants and hence could not be used as a control. Fourth, maternal nicotine dependence was assessed using the H.S.I and DSM-based nicotine dependence measures were not available. Finally, as the mother often reported on the offspring and herself (e.g. ADHD), rater bias may have influenced our findings to some extent.

MSDP increases neonatal intensive care unit admissions by 20%(Adams et al., 2002). There continues to be a clear need for health care professionals to counsel expectant mothers (and where possible, fathers/spouses/partners of expectant mothers) regarding the adverse consequences of smoking during their pregnancy and offer behavioral counseling or safe pharmacological aids. Not only does MSDP, directly and indirectly, influence the well-being of the offspring (from fetal stages through young adulthood) but also has key health consequences for the expecting mother. As articulated in the core objectives of Healthy People 2010 (Healthy People 2010, 2000), reducing risk behaviors and increasing education surrounding prenatal health, will be vital in attaining better quality of life for mothers, their offspring and consequently, families in general.

Supplementary Material

01

ACKNOWLEDGEMENTS

This study was funded by grants DA020810, DA18660, DA14363, DA18267 and DA019951, DA23668 & DA19951 from the National Institute on Drug Abuse (NIDA), grants AA11667, AA11822, AA007580, and AA11998 from the National Institute on Alcohol Abuse and Alcoholism (NIAAA), and from a Merit Review Grant (Jacob) from the Department of Veterans Affairs Medical Research Service. The United States Department of Veterans Affairs has provided financial support for the development and maintenance of the VET Registry. Numerous organizations have provided invaluable assistance in the conduct of this study, including: Department of Defense, National Personnel Records Center, National Archives and Records Administration, the Internal Revenue Service, National Opinion Research Center, National Research Council, National Academy of Sciences, and the Institute for Survey Research at Temple University. Most importantly, the authors gratefully acknowledge the continued cooperation and participation of the members of the VET Registry and their families.

Footnotes

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