Abstract:An objective assessment of exposure to tobacco smoke may be accomplished by means of examining particular biomarkers in body fluids. The most common biomarker of tobacco smoke exposure is urinary, or serum, cotinine. In order to distinguish non-smokers from passive smokers and passive smokers from active smokers, it is necessary to estimate cotinine cut-off points. The objective of this article was to apply statistical distribution of urinary cotinine concentration to estimate cut-off points distinguishing the… Show more
“…Other strengths include the relatively large sample size, which was also representative of the general population; the extended follow‐up enabling time‐to‐event analyses; exclusion of individuals with a baseline history of CVD; and measurements on a comprehensive panel of cardiovascular risk markers that enabled adequate adjustment for potential confounding. The cutoffs we employed to distinguish between no smoking and active smoking were appropriate (have high sensitivity and specificity values), conservative, and have been used in several previous studies 30, 31, 32, 33, 49. To enhance the validity of the findings, we restricted analyses to people with complete information on exposures, risk factors, and outcomes.…”
Section: Discussionmentioning
confidence: 99%
“…We categorized cotinine‐assessed smoking exposure as never smokers, former smokers, light current smokers, and heavy current smokers on the basis of cutoffs for urine cotinine reported in the literature. The cutoffs for urine cotinine were <100 ng/mL, 100 to 500 ng/mL, and >500 ng/mL for the categories of never smokers, former smokers, and current smokers, respectively, as employed in several previous reports 30, 31, 32, 33. Current smokers were then subdivided into light and heavy current smokers on the basis of the median cotinine level in current smokers, as reported in a previous study 31.…”
BackgroundWe aimed to compare the associations of smoking exposure as assessed by self‐reports and urine cotinine with cardiovascular disease (CVD) risk and determine the potential utility of cotinine for CVD risk prediction.Methods and ResultsSmoking status by self‐reports and urine cotinine were assessed at baseline in 4737 participants (mean age, 53 years) of the PREVEND (Prevention of Renal and Vascular End‐Stage Disease) prospective study. Participants were classified as never, former, light current (≤10 cigarettes/day), and heavy current smokers (>10 cigarettes/day) according to self‐reports and analogous cutoffs for urine cotinine. During a median follow‐up of 8.5 years, 296 first CVD events were recorded. Compared with self‐reported never smokers, the hazard ratios (95% confidence interval) of CVD for former, light current, and heavy current smokers were 0.86 (0.64–1.17), 1.28 (0.83–1.97), and 1.80 (1.27–2.57) in multivariate analysis. Compared with urine cotinine–assessed never smokers, the corresponding hazard ratios of CVD for urine cotinine–assessed former, light current, and heavy current smokers were 1.70 (1.03–2.81), 1.62 (1.15–2.28), and 1.95 (1.39–2.73) respectively. The C‐index change on adding urine cotinine–assessed smoking status to a standard CVD risk prediction model (without self‐reported smoking status) was 0.0098 (0.0031–0.0164; P=0.004). The corresponding C‐index change for self‐reported smoking status was 0.0111 (0.0042–0.0179; P=0.002).ConclusionsSmoking status as assessed by self‐reports and urine cotinine is associated with CVD risk; however, the nature of the association of urine cotinine with CVD is consistent with a dose‐response relationship. The ability of urine cotinine to improve CVD risk assessment is similar to that of self‐reported smoking status.
“…Other strengths include the relatively large sample size, which was also representative of the general population; the extended follow‐up enabling time‐to‐event analyses; exclusion of individuals with a baseline history of CVD; and measurements on a comprehensive panel of cardiovascular risk markers that enabled adequate adjustment for potential confounding. The cutoffs we employed to distinguish between no smoking and active smoking were appropriate (have high sensitivity and specificity values), conservative, and have been used in several previous studies 30, 31, 32, 33, 49. To enhance the validity of the findings, we restricted analyses to people with complete information on exposures, risk factors, and outcomes.…”
Section: Discussionmentioning
confidence: 99%
“…We categorized cotinine‐assessed smoking exposure as never smokers, former smokers, light current smokers, and heavy current smokers on the basis of cutoffs for urine cotinine reported in the literature. The cutoffs for urine cotinine were <100 ng/mL, 100 to 500 ng/mL, and >500 ng/mL for the categories of never smokers, former smokers, and current smokers, respectively, as employed in several previous reports 30, 31, 32, 33. Current smokers were then subdivided into light and heavy current smokers on the basis of the median cotinine level in current smokers, as reported in a previous study 31.…”
BackgroundWe aimed to compare the associations of smoking exposure as assessed by self‐reports and urine cotinine with cardiovascular disease (CVD) risk and determine the potential utility of cotinine for CVD risk prediction.Methods and ResultsSmoking status by self‐reports and urine cotinine were assessed at baseline in 4737 participants (mean age, 53 years) of the PREVEND (Prevention of Renal and Vascular End‐Stage Disease) prospective study. Participants were classified as never, former, light current (≤10 cigarettes/day), and heavy current smokers (>10 cigarettes/day) according to self‐reports and analogous cutoffs for urine cotinine. During a median follow‐up of 8.5 years, 296 first CVD events were recorded. Compared with self‐reported never smokers, the hazard ratios (95% confidence interval) of CVD for former, light current, and heavy current smokers were 0.86 (0.64–1.17), 1.28 (0.83–1.97), and 1.80 (1.27–2.57) in multivariate analysis. Compared with urine cotinine–assessed never smokers, the corresponding hazard ratios of CVD for urine cotinine–assessed former, light current, and heavy current smokers were 1.70 (1.03–2.81), 1.62 (1.15–2.28), and 1.95 (1.39–2.73) respectively. The C‐index change on adding urine cotinine–assessed smoking status to a standard CVD risk prediction model (without self‐reported smoking status) was 0.0098 (0.0031–0.0164; P=0.004). The corresponding C‐index change for self‐reported smoking status was 0.0111 (0.0042–0.0179; P=0.002).ConclusionsSmoking status as assessed by self‐reports and urine cotinine is associated with CVD risk; however, the nature of the association of urine cotinine with CVD is consistent with a dose‐response relationship. The ability of urine cotinine to improve CVD risk assessment is similar to that of self‐reported smoking status.
“…A major metabolite of nicotine that is present in tobacco smoke, cotinine has a half-life of 16 to 20 hours in the body but can remain in the system for up to 2 weeks (Zielinska-Danch et al, 2007). The concentration of cotinine found in the serum, urine, or even saliva is directly related to the extent of an individual's smoking.…”
Background: Lung cancer is a major cause of Korean female mortality and is clearly associated with smoking. The Korean National Health and Nutrition Examination Survey (KNHANES IV-2,3), which included both self-reports of smoking and urinary cotinine data, revealed a significant discrepancy between the prevalence of self-reported and biochemically-verified female smokers. The factors associated with accurate self-reporting of current smoking status remain poorly understood, however. Materials and Methods: We assessed the prevalence of smoking in KNHANES using both self-report and urinary cotinine data. Subsequently, using univariate and multivariate tests, we assessed whether age, intensity of smoking, marital status, relationship with cohabitants, education, occupation, residential area, or annual household income were associated with inaccurate selfreporting in Korean females. We also investigated whether the prevalence of inaccurate self-reports changed over the survey period
“…However, as those studies primarily focused on a simple linear correlation, there is a lack of data showing how cotinine levels independently predict severity of nicotine dependence after adjustment of potential confounding factors. Furthermore, the standard cut-off values for cotinine levels as an indicator of high nicotine dependence have not been set yet, whereas there have been mainly several reports on urinary cotinine cut-off points discriminating non-smokers/smokers or passive/ active smokers (Zielinska-Danch et al, 2007).…”
Background: Although nicotine dependence plays a role as a main barrier for smoking cessation, there is still a lack of solid evidence on the validity of biomarkers to determine nicotine dependence in clinical settings. This study aimed to investigate whether urinary cotinine levels could reflect the severity of nicotine dependence in active smokers. Materials and Methods: Data regarding general characteristics and smoking status was collected using a self-administered smoking questionnaire. The Fagerström test for nicotine dependence (FTND) was used to determine nicotine dependence of the participants, and a total of 381 participants were classified into 3 groups of nicotine dependence: low (n=205, 53.8%), moderate (n=127, 33.3%), and high dependence groups (n=49, 12.9%). Stepwise multiple linear regression model and receiver operating characteristic (ROC) curves analyses were used to determine the validity of urinary cotinine for high nicotine dependence. Results: In correlation analysis, urinary cotinine levels increased with FTND score (r=0.567, P<0.001). ROC curves analysis showed that urinary cotinine levels predicted the high-dependence group with reasonable accuracy (optimal cut-off value=1,000 ng/mL; AUC=0.82; P<0.001; sensitivity=71.4%; specificity=74.4%). In stepwise multiple regression analysis, the total smoking period (β=0.042, P=0.001) and urinary cotinine levels (β=0.234, P<0.001) were positively associated with nicotine dependence, whereas an inverse association was observed between highest education levels (>16 years) and nicotine dependence (β=-0.573, P=0.034). Conclusions: The results of this study support the validity of using urinary cotinine levels for assessment of nicotine dependence in active smokers.
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