dc.contributor.author |
Schechter, Julia |
|
dc.contributor.author |
Do, Elizabeth K |
|
dc.contributor.author |
Zhang, Junfeng Jim |
|
dc.contributor.author |
Hoyo, Cathrine |
|
dc.contributor.author |
Murphy, Susan K |
|
dc.contributor.author |
Kollins, Scott H |
|
dc.contributor.author |
Fuemmeler, Bernard |
|
dc.date.accessioned |
2019-02-24T19:01:01Z |
|
dc.date.available |
2019-02-24T19:01:01Z |
|
dc.date.issued |
2018-12-24 |
|
dc.identifier |
5258109 |
|
dc.identifier.issn |
1462-2203 |
|
dc.identifier.issn |
1469-994X |
|
dc.identifier.uri |
https://hdl.handle.net/10161/18071 |
|
dc.description.abstract |
Introduction:Both prenatal smoke exposure and depression have been linked to lower
birth weight, a risk factor for morbidity and mortality. Few studies have looked at
the interaction between these risk factors and none have used a biomarker to objectively
measure prenatal smoke exposure. The current study sought to examine independent and
interactive effects of cotinine and depression on birth weight. The effect of race
was also explored. Method:Data were drawn from a prospective study of pregnant women
(N=568) in the southeastern U.S. Maternal demographic, health information, depressive
symptoms, and birth data were collected via self-report and medical record abstraction.
Prenatal blood samples were assayed for cotinine. Results:Controlling for covariates,
multiple regression analyses indicated that both cotinine and depressive symptoms
independently predicted lower birth weight and a significant interaction was also
observed. Upon probing the interaction, a negative association between cotinine levels
and birth weight was found in the context of higher depression but not lower depression
scores. Similarly, logistic regression analyses revealed a significant interaction
between cotinine and depression, such that cotinine predicted having a baby < 2500
g among women who fell above the indicated cut-off score. African American women had
the highest levels of cotinine and lowest weight babies; however, race was not a significant
moderator. Conclusions:Results suggest prenatal smoke exposure has a greater negative
effect on birth weight for women endorsing co-occurring depressive symptoms. Findings
can inform targeted interventions and assist medical providers with identifying women
at increased risk for poor perinatal outcomes. Implications:Despite the common occurrence
of smoking during pregnancy and prenatal depression, the interaction between these
risk factors on birth weight has rarely been examined. Further, the extant results
have been mixed, likely due in part to difficulties in measurement. The current study
was the first to use prenatal cotinine to assess bias-free, continuous levels of prenatal
smoke exposure. Results indicate that prenatal cotinine was a significant predictor
of birth weight only in the context of maternal depressive symptoms. These findings
have important implications for mitigating negative perinatal outcomes for pregnant
women and their children.
|
|
dc.language |
eng |
|
dc.publisher |
Oxford University Press (OUP) |
|
dc.relation.ispartof |
Nicotine & tobacco research : official journal of the Society for Research on Nicotine
and Tobacco
|
|
dc.relation.isversionof |
10.1093/ntr/nty267 |
|
dc.title |
Effect of Prenatal Smoke Exposure on Birth Weight: The Moderating Role of Maternal
Depressive Symptoms.
|
|
dc.type |
Journal article |
|
duke.contributor.id |
Schechter, Julia|0653050 |
|
duke.contributor.id |
Zhang, Junfeng Jim|0610071 |
|
duke.contributor.id |
Murphy, Susan K|0218826 |
|
duke.contributor.id |
Kollins, Scott H|0038487 |
|
dc.date.updated |
2019-02-24T19:00:59Z |
|
pubs.organisational-group |
School of Medicine |
|
pubs.organisational-group |
Duke |
|
pubs.organisational-group |
Psychology and Neuroscience |
|
pubs.organisational-group |
Trinity College of Arts & Sciences |
|
pubs.organisational-group |
Center for Child and Family Policy |
|
pubs.organisational-group |
Sanford School of Public Policy |
|
pubs.organisational-group |
Duke Cancer Institute |
|
pubs.organisational-group |
Institutes and Centers |
|
pubs.organisational-group |
Duke Clinical Research Institute |
|
pubs.organisational-group |
Duke Institute for Brain Sciences |
|
pubs.organisational-group |
University Institutes and Centers |
|
pubs.organisational-group |
Institutes and Provost's Academic Units |
|
pubs.organisational-group |
Psychiatry & Behavioral Sciences, Addictions |
|
pubs.organisational-group |
Psychiatry & Behavioral Sciences |
|
pubs.organisational-group |
Clinical Science Departments |
|
pubs.organisational-group |
Environmental Sciences and Policy |
|
pubs.organisational-group |
Nicholas School of the Environment |
|
pubs.organisational-group |
Pathology |
|
pubs.organisational-group |
Psychiatry, Child & Family Mental Health and Developmental Neuroscience |
|
pubs.publication-status |
Published |
|
duke.contributor.orcid |
Zhang, Junfeng Jim|0000-0003-3759-6672 |
|
duke.contributor.orcid |
Murphy, Susan K|0000-0001-8298-7272 |
|
duke.contributor.orcid |
Kollins, Scott H|0000-0001-6847-6935 |
|