Cotinine versus questionnaire: early-life environmental tobacco smoke exposure and incident asthma
© Carlsten et al.; licensee BioMed Central Ltd. 2012
Received: 1 June 2012
Accepted: 28 November 2012
Published: 5 December 2012
The use of biomarkers has expanded considerably, as an alternative to questionnaire-based metrics of environmental tobacco smoke (ETS); few studies have assessed the affect of such alternative metrics on diverse respiratory outcomes in children, and we aimed to do so.
We evaluated various measures of birth-year ETS, in association with multiple respiratory endpoints early years of life, in the novel context of a birth cohort at high risk for asthma. We administered questionnaires to parents, both at the end of pregnancy and at one year of life, and measured cotinine in cord blood (CCot; in 275 children) and in urine (UCot; obtained at 12 months in 365 children), each by radioimmunoassay. Multiple logistic regression was used to assess the association of the various metrics with recurrent wheeze at age 2 and with bronchial hyperresponsiveness (BHR) and asthma at age 7.
Self-reported 3rd trimester maternal smoking was associated with significantly increased risk for recurrent wheeze at age 2 (odds ratio 3.5 [95% confidence interval = 1.2,10.7]); the risks associated with CCot and 3rd trimester smoking in any family member were similar (OR 2.9 [1.2,7.0] and 2.6 [1.0,6.5], respectively). No metric of maternal smoking at 12 months appeared to significantly influence the risk of recurrent wheeze at age 2, and no metric of ETS at any time appeared to significantly influence risk of asthma or BHR at age 7.
Biomarker- and questionnaire-based assessment of ETS in early life lead to similar estimates of ETS-associated risk of recurrent wheeze and asthma.
KeywordsChildren Exposure to environmental tobacco smoke Bronchial hyperresponsiveness Wheeze Asthma
Exposures that confer risk for incident childhood asthma include early-life stressors and infections, allergens, outdoor pollutants, and tobacco smoke . In our previous work , we focused on the lattermost and demonstrated that questionnaire-based exposure to environmental tobacco smoke (ETS) at year 7, administered to parents within a birth cohort of high-risk children, was not a risk factor for asthma at year 7. An alternative to questionnaire-based data is to examine cotinine as a direct metric of exposure. A recent comprehensive meta-analysis , which included studies of older children, converted cotinine measures to approximate cigarette dose as an alternative to comparing the effect of the various metrics on risk estimates directly. However, few studies have assessed the effect of multiple ETS exposure metrics on diverse respiratory outcomes over a number of years. We hypothesized that biomarker-based assessment of ETS and questionnaire-based assessment of ETS would lead to different estimates of ETS-associated asthma risk. The purpose of the paper is to compare questionnaire-based ETS estimates with biomarkers of ETS, in terms of associated risk for recurrent wheeze, physician-diagnosed asthma, and measures of bronchial hyperresponsiveness (BHR), using a unique birth cohort.
Risk of asthma, recurrent wheeze and bronchial hyperreactivity with various metrics of environmental tobacco smoke
Measures at 3rd trimester/birth
Maternal smoking (self-reported) during 3rd trimester
3.5 (1.2,10.7) p=0.025
Any family member smoking (self-reported) during 3rd trimester
2.9 (1.2,7.0) p=0.015
Cord blood cotinine above 50th percentile
2.6 (1.0,6.5) p=0.045
Measures at 12 months
Maternal smoking (self-reported) at 12 months
Any family member smoking (self-reported) at 12 months
Urinary cotinine:Cr above 50th percentile at 12 months
Reported maternal smoking at any timepoint assessed was infrequent (8% during the 3rd trimester and 9% at one year of age). Amongst those mothers who smoked during the 3rd trimester, the mean (± SD) number of cigarettes per day was 10 (± 7). 69% of those reduced smoking during pregnancy. The Pearson correlation (r) between a positive self-report of maternal smoking during the third trimester of pregnancy and CCot was 0.89 (p < 0.0001). CCot ranged from 0 (below the detection limit) to 330 ng/ml; UCot ranged from 0 (below the detection limit) to 2821 ng/mg. The r between a positive self-report of maternal smoking at 12 months and urinary cotinine was 0.48 (p < 0.0001). The correlations between any family member reporting smoking during 3rd trimester or at 12 months, and CCot or UCot (respectively), were 0.52 (p < 0.0001) and 0.47 (p < 0.0001). The r between UCot and CCot was 0.54 (p < 0.0001).
As noted in Table 1, the choice of ETS metric during a given exposure time-frame influences the estimate of asthma risk only modestly; within a given exposure time-frame the various measures generally confer similar risk for a given respiratory outcome. For exposures near the time of birth, all 3 metrics were associated with significantly increased risk for recurrent wheeze at year 2, but none was associated with significant risk of wheeze or asthma of the year 7 outcomes. Regarding the measures determined at 12 months, there is a trend towards increased risk for recurrent wheeze at 2 years, with the objective measure of UCot being associated with a borderline significant risk for recurrent wheeze (OR 2.2, [0.99, 4.7], p = 0.051). Regarding asthma and BHR at 7 years, no metric was significantly associated with risk. There was a suggestion that self-reported metrics conferred relative “protection” for asthma at 7 years (borderline statistical significance) while the opposite trend was apparent based on the biomarkers. We did sensitivity analyses using alternate cutoffs for elevated CCOt and UCot, based on prior literature [6, 7], but this did not appreciably change the results.
In the 1980’s large cohort studies showed that ETS exposure, assessed by parental questionnaire, was associated with increased risk for BHR in children . Subsequently, investigators moved to gathering biomarkers of exposure from the children themselves. Children’s urinary cotinine was demonstrated as a biomarker of risk for asthma and wheeze . Subsequently, the use of biomarkers for ETS has expanded considerably and several reports have directly compared the various measures as exposure metrics [6, 7, 10], revealing complex dynamics dependent on several variables. In our initial analysis of risk factors for asthma at age seven , we were surprised to find that questionnaire data suggested that maternal smoking was not a significant risk factor and could be a significant “protective” factor. The questionnaire-based data in the current study again suggests “protection” from maternal smoking, though with a less focused confidence interval due to a smaller sample size (in our previous paper  biomarkers were not required for inclusion in analysis). As we speculate that maternal smoking is unlikely to be truly protective, these findings motivated our exploration of more objective measurement of exposure, and our findings reinforce that motivation.
Limitations to our data include lack of questionnaire data regarding maternal smoking from the period prior to the 3rd trimester and sample size affecting the confidence limits for the effect of various metrics. This is important because Neuman and colleagues  have documented a time-dependency to ETS exposures during early life, though their analysis focused on pregnancy versus post-pregnancy ETS rather than on trimester-specific ETS. Duijts and colleagues  did look at trimester-specific effects but for wheeze only (not asthma). Note however that given our specific motivation to compare questionnaire-based data versus that biological sampling, the 3rd trimester would correspond most closely with cord-blood at birth. Another potential limitation is that concern for familial asthma risk led to behavioral changes (decreased smoking) of some family members to reduce the risk of asthma in their children, thus limiting generalizability of our findings in this cohort of children at high risk for asthma, relative to other cohorts with average asthma risk and more typical smoking prevalence. Finally, we did note that amongst those 31 children in the cohort that had both frequent “colds”, defined as at least 3 per year, the risk for wheeze at 2 years (45%) was higher than in those with fewer colds (6% of these children had wheeze at 2 years). Though we were underpowered for a specific analysis of interactions between ETS and upper respiratory tract infections, potential such interactions remain an important concern, as highlighted by Ciprandi and others .
In spite of these limitations, our study is unique in evaluating various measures of ETS, in association with multiple respiratory endpoints; we believe that this is further unique in the context of a birth cohort at high risk for asthma but with modest maternal smoking rates. In spite of self-reported maternal smoking occurring in reportedly less than 10% of the families, this metric appears to be the robust for predicting early life recurrent wheeze, and similar risk estimates for this endpoint were noted when ETS was represented by either a broader sampling of family members or by cord blood cotinine. This latter similarity in risk is remarkable since cotinine, while more comprehensively measuring inhaled ETS (including that due to paternal and incidental exposures), has a relatively short half-life of approximately 20 hours  and thus may not represent averaged exposure over the specific time period.
In conclusion, various metrics of ETS exposure focused on the time of birth, but not those focused at 1 year of age, seem to confer increased risk for recurrent wheeze at 2 years, but none of these ETS metrics appear to confer risk for later respiratory outcomes. As recent work by others suggest , this pattern may be explained by ETS exposure leading to transient inflammation in the context of underdeveloped 2-year-old airways (precipitating wheezing at age 2), rather than to changes resulting in persistently hyperreactive airways at age 7; ETS exposure may be particularly influential in early-life wheeze, but such influence may be less strong (relative to other exposures that influence respiratory outcomes) by 7 years of life in high risk children. Biomarker- and questionnaire-based assessment of ETS in early life lead to similar estimates of ETS-associated risk of recurrent wheeze and asthma in this high-risk cohort.
Environmental tobacco smoke
Cotinine in cord blood
Cotinine in urine
Pearson correlation coefficient.
The study was supported by the Canadian Institutes of Health Research, the BC Lung Association and the Manitoba Medical Service Foundation.
The study was funded by the Canadian Institutes of Health Research, the BC Lung Association and the Manitoba Medical Service Foundation.
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