Infant Wheeze, In-utero Nicotine, Pulmonary Function; Newborn, Abnormal, Second Hand Smoke
Conditions
Keywords
In-utero smoke;, Pulmonary function testing;, Wheeze;, Vitamin C;, Forced expiratory flows
Brief summary
Vitamin C supplementation (500 mg per day) given to pregnant women who can not quit smoking will improve the pulmonary function tests in their offspring measured at 3 months of age.
Detailed description
Smoking during pregnancy remains a major public health problem as at least 12% of pregnant women cannot quit smoking during pregnancy. This addiction is the largest preventable cause of childhood respiratory illness, including asthma, and children whose mothers smoked during pregnancy show lifetime decreases in pulmonary function. Smoking is a unique morbidity in that it is addictive, heavily advertised and recent genome studies show there are genotypes that significantly increase the likelihood of being unable to quit. Teen pregnancy, low income, low education, and living with another smoker are important factors increasing the odds of smoking during pregnancy. Pulmonary function tests done shortly after birth in babies born to mothers who smoked during pregnancy show decreased pulmonary function as measured by decreased respiratory flows and respiratory compliance and altered tidal breathing patterns. These changes can still be measured even after the infants have reached adulthood. Multiple epidemiologic studies show that these decreases in pulmonary function lead to increased respiratory disease and costs of hundreds of millions of dollars per year. The primary aim of this double-blind, placebo controlled, randomized, multi-site study is to demonstrate improved pulmonary function testing at 3 months of age, in infants delivered to smoking mothers who are randomized to 500 mg/day of supplemental vitamin C versus placebo at less than or equal to 22 weeks of pregnancy. We will recruit 278 smoking pregnant women into the study. Patients will meet with research personnel at each prenatal visit and smoking cessation will be actively encouraged. Patients will be monitored with a set of serial biomarkers to assess smoking and medication compliance, including urine cotinine levels, smoking questionnaires, pill counts and fasting plasma ascorbic acid levels. Pulmonary function tests will be done at 3 months of age and will measure forced expiratory flows. The infants will also be followed through one year of age with monthly validated respiratory questionnaires and a follow-up pulmonary function test at 12 months of age. Success of this study is supported by strong pilot data showing statistically significant improvements at about 48 hours of age in pulmonary function tests in infants born to smoking mothers who received vitamin C versus placebo, and preliminary data showing a lower incidence of wheezing at 12 months of age in these infants. Key genetic polymorphisms shown to increase sensitivity to in-utero smoke exposure will also be measured. The success of this study is also supported by animal models showing the effectiveness of vitamin C to preserve pulmonary function and genetic and epidemiologic studies linking the effects of smoking during pregnancy to oxidant mechanisms. The secondary aims of the study include: 1) to demonstrate a decreased incidence of wheezing through 12 months of age in infants delivered to smoking mothers who are randomized to 500mg/day of supplemental vitamin C versus placebo during pregnancy; 2) to demonstrate improved pulmonary function tests at 12 months of age in these infants.
Interventions
Pregnant smoking women will be randomized to daily vitamin C (500 mg) versus daily placebo
Sponsors
Study design
Eligibility
Inclusion criteria
At randomization: * Singleton gestation * ≥ 15 years old * Gestational age between 13 and 22 weeks * Receiving prenatal care * Current smoker * English speaking
Exclusion criteria
* Gestational age ≥ 23 and 0/7 weeks * Multiple gestation * Major fetal congenital anomalies * Current use of illicit drugs * Current alcohol abuse * Use of vitamin C (≥ 500 mg/day)\>3 days per week since last menstrual period * Refusal to abstain from vitamin or supplements containing significant vitamin C other than those provided through or approved by study staff * History of kidney stone in patient * Insulin dependent diabetes * Complex maternal medical conditions * Participation in other conflicting research projects * Unable to demonstrate stable method of communication * Pregnancy by in-vitro fertilization * Plan to terminate pregnancy * Failure of medication compliance trial * Failure to return in designated period during placebo run-in * Body mass index \> 50 at screening
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Forced Expiratory Flow at 75% of Expired Volume (FEF75) | 3 months of age | The primary outcome was the comparison of infant FEFs at 3 months of age obtained using the raised volume rapid thoracic compression (RVRTC) technique in offspring of pregnant smokers randomized to vitamin C versus placebo. The specific primary outcome parameter was the measurement of FEF at 75% of the expired volume (FEF75) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Forced Expiratory Flow at 75% of Expired Volume (FEF75) | 12 months of age | The measurement of forced expiratory flows and specifically FEF75 will be done at 12 months of age in infants born to pregnant smoking women randomized to vitamin C versus placebo during pregnancy. FEF75 will be measured with the raised volume rapid thoracic compression technique. |
| Incidence of Wheezing Through 12 Months of Age | 12 months of age | The incidence of wheezing through 12 months of age will be compared in the infants delivered to smoking pregnant women who were randomized to vitamin C (500 mg) versus placebo during pregnancy. |
Countries
United States
Participant flow
Recruitment details
Study staff screened women at prenatal clinics between December, 2012 and June, 2015 in the catchment area of the three clinical sites to identify eligible women who continued to smoke cigarettes.
Pre-assignment details
To exclude highly non-compliant subjects, consented patients entered a medication compliance trial of 14 ± 7 days. Placebo tablets were given to participants and they were excluded if they failed to return for a post compliance visit within 14 ± 7 days of the screening visit or if they took \< 75% of the required tablets.
Participants by arm
| Arm | Count |
|---|---|
| Placebo Tablet+Prenatal Vitamin A daily placebo tablet
Placebo tablet+prenatal vitamin | 126 |
| Vitamin C +Prenatal Vitamin Vitamin C +prenatal vitamin: Pregnant smoking women will be randomized to daily vitamin C (500 mg) versus daily placebo | 125 |
| Total | 251 |
Baseline characteristics
| Characteristic | Placebo Tablet+Prenatal Vitamin | Total | Vitamin C +Prenatal Vitamin |
|---|---|---|---|
| Age, Categorical <=18 years | 10 Participants | 16 Participants | 6 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 116 Participants | 235 Participants | 119 Participants |
| Age, Continuous | 26.4 years STANDARD_DEVIATION 5.9 | 26.5 years STANDARD_DEVIATION 5.6 | 26.6 years STANDARD_DEVIATION 5.2 |
| BMI at Enrollment | 30.0 kg/m^2 STANDARD_DEVIATION 7.3 | 29.3 kg/m^2 STANDARD_DEVIATION 6.9 | 28.6 kg/m^2 STANDARD_DEVIATION 6.5 |
| Cigarette Smoking 3 months prior to Pregnancy | 17.7 cigarettes per day STANDARD_DEVIATION 10.8 | 16.8 cigarettes per day STANDARD_DEVIATION 9.4 | 15.9 cigarettes per day STANDARD_DEVIATION 7.7 |
| Cigarette Smoking at Enrollment | 7.8 cigarettes per day STANDARD_DEVIATION 4.9 | 7.9 cigarettes per day STANDARD_DEVIATION 4.9 | 8.0 cigarettes per day STANDARD_DEVIATION 5 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 7 Participants | 9 Participants | 2 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 119 Participants | 241 Participants | 122 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 1 Participants | 1 Participants |
| Gestational Age at Enrollment | 16.4 weeks STANDARD_DEVIATION 2.9 | 16.5 weeks STANDARD_DEVIATION 3 | 16.7 weeks STANDARD_DEVIATION 3.1 |
| Gestational Age at Randomization | 18.2 weeks STANDARD_DEVIATION 2.8 | 18.3 weeks STANDARD_DEVIATION 2.9 | 18.4 weeks STANDARD_DEVIATION 3 |
| Gravida | 3.5 pregnancies STANDARD_DEVIATION 2.4 | 3.4 pregnancies STANDARD_DEVIATION 2.2 | 3.3 pregnancies STANDARD_DEVIATION 2 |
| Health Insurance Type Government Assistance | 106 Participants | 218 Participants | 112 Participants |
| Health Insurance Type None or Self Pay | 2 Participants | 2 Participants | 0 Participants |
| Health Insurance Type Private Insurance | 18 Participants | 31 Participants | 13 Participants |
| Highest Education Level Attained Bachelor's Degree | 6 Participants | 9 Participants | 3 Participants |
| Highest Education Level Attained Graduate School | 0 Participants | 0 Participants | 0 Participants |
| Highest Education Level Attained High School or GED | 40 Participants | 99 Participants | 59 Participants |
| Highest Education Level Attained Less than High School | 31 Participants | 51 Participants | 20 Participants |
| Highest Education Level Attained Some College | 49 Participants | 92 Participants | 43 Participants |
| Marital Status Divorced | 7 Participants | 15 Participants | 8 Participants |
| Marital Status Married | 31 Participants | 53 Participants | 22 Participants |
| Marital Status Significant Other | 39 Participants | 95 Participants | 56 Participants |
| Marital Status Single | 49 Participants | 88 Participants | 39 Participants |
| Maternal History of Alcohol Abuse No | 126 Participants | 247 Participants | 121 Participants |
| Maternal History of Alcohol Abuse Yes | 0 Participants | 4 Participants | 4 Participants |
| Maternal History of Asthma No | 88 Participants | 169 Participants | 81 Participants |
| Maternal History of Asthma Yes | 38 Participants | 82 Participants | 44 Participants |
| Maternal History of Substance Abuse No | 110 Participants | 215 Participants | 105 Participants |
| Maternal History of Substance Abuse Yes | 16 Participants | 36 Participants | 20 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 2 Participants | 3 Participants | 1 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 15 Participants | 35 Participants | 20 Participants |
| Race (NIH/OMB) More than one race | 8 Participants | 15 Participants | 7 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 1 Participants | 1 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 100 Participants | 197 Participants | 97 Participants |
| Region of Enrollment United States | 126 participants | 251 participants | 125 participants |
| Sex: Female, Male Female | 126 Participants | 251 Participants | 125 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk |
|---|---|---|---|---|
| deaths Total, all-cause mortality | 1 / 126 | 1 / 125 | 1 / 123 | 1 / 120 |
| other Total, other adverse events | 54 / 126 | 59 / 125 | 0 / 123 | 0 / 120 |
| serious Total, serious adverse events | 30 / 126 | 20 / 125 | 31 / 123 | 33 / 120 |
Outcome results
Forced Expiratory Flow at 75% of Expired Volume (FEF75)
The primary outcome was the comparison of infant FEFs at 3 months of age obtained using the raised volume rapid thoracic compression (RVRTC) technique in offspring of pregnant smokers randomized to vitamin C versus placebo. The specific primary outcome parameter was the measurement of FEF at 75% of the expired volume (FEF75)
Time frame: 3 months of age
Population: Population included in analysis were infants who were able to complete technically acceptable PFT/FEF measurements at 3 months of age.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Placebo Tablet+Prenatal Vitamin | Forced Expiratory Flow at 75% of Expired Volume (FEF75) | 188.7 ml/s | Standard Deviation 66.4 |
| Vitamin C +Prenatal Vitamin | Forced Expiratory Flow at 75% of Expired Volume (FEF75) | 200.7 ml/s | Standard Deviation 71.1 |
Forced Expiratory Flow at 75% of Expired Volume (FEF75)
The measurement of forced expiratory flows and specifically FEF75 will be done at 12 months of age in infants born to pregnant smoking women randomized to vitamin C versus placebo during pregnancy. FEF75 will be measured with the raised volume rapid thoracic compression technique.
Time frame: 12 months of age
Population: These measurements were performed at the 12 month visit.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Placebo Tablet+Prenatal Vitamin | Forced Expiratory Flow at 75% of Expired Volume (FEF75) | 324 mL/s | Standard Deviation 84.1 |
| Vitamin C +Prenatal Vitamin | Forced Expiratory Flow at 75% of Expired Volume (FEF75) | 351.6 mL/s | Standard Deviation 71.1 |
Incidence of Wheezing Through 12 Months of Age
The incidence of wheezing through 12 months of age will be compared in the infants delivered to smoking pregnant women who were randomized to vitamin C (500 mg) versus placebo during pregnancy.
Time frame: 12 months of age
Population: Population is infants who have reached 12 months of age, and whose parent/caregiver has completed at least 1 respiratory questionnaire past 122 days after birth.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Placebo Tablet+Prenatal Vitamin | Incidence of Wheezing Through 12 Months of Age | 63 Participants |
| Vitamin C +Prenatal Vitamin | Incidence of Wheezing Through 12 Months of Age | 51 Participants |