Clinical Trial Details
— Status: Recruiting
Administrative data
| NCT number |
NCT00563966 |
| Other study ID # |
smokingmothers-HMO-CTIL |
| Secondary ID |
|
| Status |
Recruiting |
| Phase |
N/A
|
| First received |
November 25, 2007 |
| Last updated |
May 9, 2008 |
| Start date |
April 2008 |
| Est. completion date |
December 2008 |
Study information
| Verified date |
November 2007 |
| Source |
Hadassah Medical Organization |
| Contact |
David Mankuta, MD |
| Phone |
97226776484 |
| Email |
mankutad[@]gmail.com |
| Is FDA regulated |
No |
| Health authority |
Israel: Ministry of Health |
| Study type |
Observational
|
Clinical Trial Summary
It is generally understood that smoking during pregnancy has deleterious effects on the
developing fetus, although research on smoking during pregnancy has been limited in focus,
with most studies focused on birth weight of newborns and children's behavioral
disturbances. However, little is known about the neurobiological underpinnings of
nicotine-related developmental deficits and even less is known about genetic and
environmental factors that may exacerbate the risk for such deficits in some children. In
this study, we propose to examine the relation between antenatal exposure to nicotine and
infants' stress-responses before and after birth (2-days, 6-months) and its moderation of by
family-based stressors and genes related to nicotine metabolism and stress responsivity.
We hypothesize that the risk imposed on infants by antenatal exposure to nicotine is
moderated by genotype that influences functioning of the HPA axis, metabolism of nicotine,
and stress-levels and parenting that influence the development of neural substrates (HPA
axis) and infants' capacity to cope with stress. There is a growing consensus that Gene x
Environmental (G x E) interplay likely mediated by epigenetic effects constitute one of the
central mechanism by which complex disorders develop. Our proposal offers an exceptional
paradigm to explore the association between genes, environment, and G x E interactions on
the neural and behavior response of children to stressful challenges.
Description:
Detailed Description of the Proposed Research
Design overview. A large cohort of pregnant women will be recruited, and those who meet
criteria will be divided into two groups according to their testimony regarding their
smoking behavior and saliva cotinine screening, as in our previous studies. At 3-time
points, the antenatal period, 2-days and 6-months of age; we will assess infants' responses
to challenges using biochemical, behavioral, and subjective measures. The challenges
selected are "proven" stressors and previous research has demonstrated their effectiveness
in eliciting stress-reactions (e.g., increased cortisol). In parallel, we will obtain an
obstetric history (from medical records), demographics, measure of symptomology, information
on smoking and drinking habits, life stresses, and family cohesion at each time point, plus
information about mothers' feelings/behavior and mothers' ratings of infants "regulatory"
behavior after birth. The antenatal and neonatal sessions will be carried out in Hadassah
Hospital and the 6-month session in the developmental laboratory at Hebrew University.
Genetic material will be collected from parents and their infant at childbirth.
Recruitment Women smokers will be recruited will be recruited by nurses in well-baby clinics
(where physicians do routine prenatal check-ups), gynecologists, midwives, and by
advertisement. In addition, we will recruit women at the time of routine checks in Hadassah
hospital (Nuchal translucency test) at 12 weeks, triple/quadra test blood testing at 16
weeks, early (14-16 weeks) and advanced (20-22 week) fetal anatomy scan, and glucose test at
24-28 weeks) (supervised by Dr. Mankuta). In all, we will recruit 150 women for the
"smoking" group, using the following inclusion criteria: smokes at least 10 cigarettes a day
(i.e., habitual smokers) no abuse of alcohol or drugs, no chronic physical disability, 22-35
years of age, living with partner, speaks English, Hebrew, or Russian, natural conception).
A (second) group of 150 women who meet inclusion criteria (except smoking) and matched in
age, education, gender of infant, and parity to the "smokers" will serve as controls. At
recruitment and each time-point, mothers (and their spouses) who agree to participate in the
research protocol will be interviewed for smoking habits (Fagerstrom Tolerance
Questionnaire, FTQ) as detailed in our previous studies on smoking. At recruitment, women
will be explicitly told that we are not encouraging smoking and will provide resources if,
at any time, during the study, they want to stop smoking.
Antenatal period (Dr. David Mankuta)
The prenatal session will be carried out at 34-36 weeks of gestation (by last menstrual
period and confirmed by early ultrasound) and will consist of 3 phases: (1) waiting room- in
which mothers receive instructions, (2) ultrasound- to evaluate limb movement before and
after vibroacoustic stimulation (VAS), as well as measures of fetuses' well-being
(cardiotocograph test, biophysical profile), and (3) post exam- administration of
questionnaires.
Limb movement. Measures of fetal limb movement are good reflections of infant state, are
stable from late gestation out to 4-weeks postnatal age 80 , are affected by antenatal
stress 81, and forecast infants' state regulation 2 weeks after birth. Ultrasound (ATL 3500
and 5000) will be used to visualize and film the fetus for offline coding of limb movements.
To begin testing, infant must be in state 1F, characterized by minimal fetal movement for 2
minutes. When this criterion is met, baseline the VAS (Fetal Acoustic Corometrics Stimulator
Model 146; ≈75 HZ, ≈82 db) will be presented for 5 s. Fetal movements will be videotaped
with the recorder built into the scanner. During off-line time-event coding, each limb
movement will be counted. From these raw counts, we will average the number of movements
observed in 10 s intervals during the 1 min prior to (baseline) and during the 5 min after
stimulation. Reactivity will be derived by calculating the difference between the mean
baseline count and the mean count recorded during the 5 s of stimulation. Regulation will be
calculated as (1) the slope of the counts across the post stimulation period (5 minutes),
and (2) the difference between the mean baseline count and the mean count of last three 10
second epochs. for first time point. Previous studies have shown limb-counts to be stable
(24-36 weeks), reliable, and sensitive to maternal stress.
Questionnaires
